Marie Charlotte Bonnevie (c1703-after 1742): One Fourth Native & Not Her Sister Marie – 52 Ancestors #421

Marie Charlotte Bonnevie was born about 1703 to Jacques Bonnevie and Françoise dit d’Azy Mius, probably in Port Royal, Acadia. However, the Port Royal parish records begin in 1702 and she’s not there, so it’s possible that Marie Charlotte was born elsewhere, probably Pobomcoup, an outpost, where her mother’s parents lived.

Marie Charlotte Bonnevie should not be confused with her slightly younger sister, Marie Bonnevie, who was born on May 12, 1706, in Port Royal, Acadia, to the same parents.

Yes, I know, it’s quite confusing. In this article, I’ll either call Marie Charlotte by that name or Charlotte, and her sister will always be Marie.

Given that these two females both survived, we can rest assured that Marie Charlotte was called Charlotte. In fact, in most records, including her marriage, she’s listed by the name of Charlotte Bonnevie.

Her sister, Marie, born in 1706, didn’t have a middle name, at least not that we know of. Marie married François Duguay around 1737, probably in Beaubassin, and was having children there by 1740.

In the 1703 Port Royal census, Marie Charlotte’s father, Jacques Bonnevie is listed with a wife, 2 daughters, and one arms bearer, which would be him.

One daughter would be Marie Charlotte’s older sister, Françoise, and the younger of the two daughters would be Marie Charlotte.

On May 31, 1704, Marie Charlotte’s younger brother, Jacques Bonnevie, was born. As an adult, he was a blacksmith and married the niece of Marie Charlotte’s husband.

In 1707, the Port Royal census showed Jacques Bonneur, his wife, 1 boy less than 14, 3 girls less than 12, 1 arpent of land, 2 cattle, and 6 hogs. This is probably the same family and the known children fit.

This man is very clearly not a farmer because you can’t support a family on 1 arpent of land, which is similar to an acre.

In the 1714 census, we find “Beaumont,” which is probably his dit name, with no first name, a wife, 1 son, and 3 daughters. Based on the location and number of children, this is probably him.

Now we have three “surnames,” Bonnevie, Bonneur, and Beaumont.

Marie Charlotte’s brother, Charles, was born and baptized on October 13, 1715, but we never find a record of him again, so he apparently died, and his death was not recorded.

Marie Charlotte’s oldest sibling, Françoise, married Pierre Olivier in Port Royal in 1718, so we know the family was still there at that time. By at least 1741, Françoise was in Beaubassin, where she remarried Jean Pierre Helie.

On August 25, 1719, Charlotte stood as godmother for her sister’s firstborn child, Marie Joseph Olivier, who had been born the day before. I can see the two sisters hugging joyfully after that solemn moment, promising to watch over each other’s children forever. Either her father, Jacques, or her brother, Jacques, stood with her. Her brother Jacques would only have been 15 at that time, so I suspect this was her father.

Where was Charlotte’s mother?

The church, which was located on a hill at far right, overlooked the bay and the fort. The cemetery was adjacent to the church, in the small rolling hills behind those trees. Perhaps Charlotte’s brother, Charles, and her mother were already there, although there is no death or burial record for either of them. Maybe after the baptism, Charlotte, Françoise, and Jacques took a walk in the cemetery and introduced the baby to family members who had already passed over. After all, this would have been Françoise Mius’s first grandchild.

There are only two baptisms for Charlotte’s sister Françoise’s children, in 1719 and 1722. We really don’t know where she and her husband, Pierre Olivier, a tailor, were through 1732 when their last child was born. We do know that by 1741, Françoise was in Beaubassin, where she married Jean Pierre Helie.

Marie Charlotte married on August 18, 1721 in that same church in Port Royal to Jacques Lord, and her brother, Jacques Bonnevie married Jacques Lord’s niece, Marguerite Lord about 1729. These families probably lived near one another.

Marie Charlotte’s Parents

There’s something of a mystery surrounding Marie Charlotte’s parents.

According to Stephen White, we know that in 1732, Charlotte’s father, Jacques Bonnevie, was living on Île Royale and was listed as a retired disabled veteran of the French army, having served 17 years. He suffered a wound to his thigh, which caused his disability. Île Royale is now Cape Breton Island.

Cape Breton Island is located at the furthest eastern point of Nova Scotia, then Acadia.

Based on that same record, Jacques’s birth year is estimated to be 1660. We know he is not found in records prior to his presumed marriage to Françoise Mius, whose father, Philippe, lived in Pobomcoup, now Pubnico, on the opposite end of Nova Scotia, some 450 miles distant.

Somehow, Jacques had to have met Françoise.

Was he somehow connected to Philippe Mius? Perhaps through his profession as a soldier? He would have been about 40 when he married.

Why did Jacques Bonnevie and his bride, whose family lived in Pobomcoup, settle in Port Royal, which was no place close to her parents? Was Jacques Bonnevie serving at or stationed at the fort there?

On the 1758 map above, the fort is shown along with the approximate location of Julien Lord/Lore’s home with the red star, just slightly upriver, 3 or 4 miles away.

If Jacques Bonnevie served 17 years, does that mean he was disabled sometime around, say, 1716 or 1717, which would be about the time no more children were baptized?

Based on Marie Charlotte’s mother’s estimated birth year between 1684 and 1687, this probably means that her mother died between 1715 and 1717 when she would have been expected to have born the next child.

Was Jacques Bonnevie’s wound somehow related to his wife’s death?

We have so many unanswered questions.

One thing we can say, fairly confidently, is that the Bonnevie family must have lived in relatively close proximity to the Lord/Lore family on what is now the Annapolis River for two of Jacque Bonnevie’s children to have married Julien Lord’s son and granddaughter.

Of course, they would all have attended the Catholic Church together.

Marie’s Maternal Grandmother

One thing we know for sure is that Marie Charlotte’s mother was half-Native, making Charlotte and her siblings one-fourth, and Charlotte’s maternal grandmother was Mi’kmaq.

Acadian history relates this story, but the mitochondrial DNA of Marie Charlotte’s descendants through all females confirms it.

Mitochondrial haplogroup X2a2 is unquestionably Native American, found primarily in Atlantic Maritime Canada, but with one sample found in New Mexico, based on my analysis in the book, DNA for Native American Genealogy.

Warfare

Marie Charlotte’s first memories may have been of warfare. After all, her father was a soldier, and conflict ebbed and flowed in Acadia, sometimes erupting in full-throated battle, but never ending.

The English attacked Acadia in 1704, and raids continued intermittently until 1707, when an attack by soldiers from New England failed.

The Acadians began beefing up the fort and built a store within the fort in 1708, expecting more of the same. Charlotte’s father was assuredly one of those soldiers.

Prisoners taken from English corsairs reported that the English were planning attacks in either 1708 or 1709.

In 1710, when Marie Charlotte would have been about 7 or 8 years old, the English routed the Acadians with 3400 English soldiers pitted against the 300 Acadian soldiers.

Marie Charlotte’s father was among those brave soldiers who managed to hold the fort for 19 days in spite of being outnumbered more than 100-fold. Surely they, and their families, expected them to die, but miraculously, they didn’t. Charlotte must have been terrified.

Beginning in 1710, the English ruled the land and initially “encouraged” the Acadians to leave. Then, the English changed their mind and didn’t want the Acadians to leave because they realized they needed the Acadians to feed them.

About the same time, the Acadians changed their minds too, and decided they WANTED to leave. They tried various methods of moving themselves and their households to Les Mines and Beaubassin, none of which succeeded.

In 1711, the local priest was kidnapped during a skirmish and taken to Boston, along with some other Acadian captives, where they were held for two years.

This means that anyone who was born during this time would have to be baptized later and burials would certainly have occurred, but not recorded in the parish register. Acadia had no priest during this time, so the records are incomplete.

In 1713, Acadia was officially passed to the English, along with her people.

In 1715, the Fort gates were shut, and no trade was allowed with anyone, including Native people.

By 1720, Port Royal had been renamed Annapolis Royal and the Acadians were again being pressured to take a loyalty oath to the British crown. Refusal meant they had to leave within 3 months and take nothing with them.

They still refused, and they also refused to leave.

Acadians were nothing if not stubborn, a trait that is clearly heritable!

Marriage and Children

The Bonnevie family lived near the Lord family. Marie Charlotte was godmother to Pierre Laure’s baby born in February 1720 when she was about 17 or 18.

By this time, Marie Charlotte’s mother had probably died, her father was disabled, and she married Jacques Lord/Lore/Lor/L’Or, Laur or Laure the following year on August 18, 1721.

Register – RG 1 volume 26 page 327
Priest – Charlemagne Cuvier
Registration Date – 18 August 1721
Event – Marriage
Groom – Jacques L’Or, widower of Angelique Comeau
Bride – Charlotte Bonnevie
Father – Jacques de Bonnevie
Mother – Françoise Mius

Marie Charlotte is referred to as Charlotte in her marriage record.

Jacques was a widower, and Marie inherited two stepchildren: Jacques Lore, born in 1709, and Angelique, born in 1711. They were just a few years younger than Charlotte.

Marie Charlotte’s children began arriving 15 months later and were all born and baptized in the Catholic church in Annapolis Royal:

  • Charles Lord/Lore, born November 23, 1722, married Marguerite Garceau on January 20, 1755, in Port Royal, and died on November 9, 1797, in Three Rivers, Quebec.
  • Joseph Lord/Lore, born February 19, 1725, married Marie-Josephe Garceaux on February 3, 1750, in Port Royal, and died sometime after 1752. His last known child was born in January 1753, but additional children could have been born during or after the Acadian Removal in 1755.
  • Pierre Benjamin Lord/Lore was born on January 25, 1728, married Marie-Josephe Blanchard on May 31, 1763, in L’Acadie, Quebec, and died on July 20, 1813, in St.-Gregoire-de-Nicolet, Canada.
  • Jean or Jean-Baptiste Lord/Lore was born August 9, 1730, married Marie-Josephe Garceau in 1765 in New York, and died on May 12, 1809, in St-Ours, Quebec, Canada.
  • Paul Lord/Lore was born on December 21, 1733. Marie Charlotte’s brother, Jacques Bonnevie, stood up as the Godfather. Nothing more is known of this child.
  • Claude-Poncy Lord/Lore was born on September 21, 1736, but nothing more is known of this child.
  • François Lord/Lore was born on August 10, 1739. Nothing more is known.
  • Honoré Lord/Lore, the youngest child, was born June 17, 1742, married Appoline dit Hippolite Garceau in 1765 in New York, and died on May 20, 1818, in Saint-Jean-sur-Richelieu, Quebec, Canada.

We do have parish records for Annapolis Royal fairly reliably up until the Expulsion, so it’s likely that we don’t know anything about Marie Charlotte’s children born in 1733, 1736, and 1739 because they had not yet married in 1755 when the expulsion occurred.

They could have died either during that horrific event or afterward in New England, assuming they were in exile with their siblings.

However, if they got separated, it’s hard to tell where they might have wound up or if they even survived.

They could also have survived, married in the colonies, and not followed their siblings to Quebec, meaning we have no record of them. Perhaps one day DNA testing of their descendants will reveal that someone survived.

1731, 1732 and 1733

Marie Charlotte’s siblings, who lived to adulthood, eventually wound up in the Northern Acadian settlements, specifically Beaubassin and Île Saint-Jean.

Charlotte’s brother, Jacques Bonnevie, stayed in Port Royal, where his children were baptized from 1730-1741. On September 21, 1731, Marie Charlotte, called Charlotte, was the Godmother for Jacques’ daughter, Marguerite Bonnevie who had been born on September 18th and was named after her mother, Marguerite Laure.

Marie Charlotte’s father, Jacques Bonnevie, is shown on Île Royal in 1732, aged 72, listed as a retired and disabled veteran of the French Army. He reportedly died there at Louisbourg on April 23, 1733.

Jacques’s adult children had not made their way to Île Royal, so why did he? Who would have been there to help him?

Or had they?

We know that Marie Bonnevie was born in 1706, and the first sighting of her after this was her marriage to François Duguay who was from Île Saint-Jean. They settled in Saint-Pierre-du-Nord and are listed in 1752 in Riviere du Nord-Est.

Still, Île Saint-Jean, Prince Edward Island today, isn’t Île Royal, today’s Cape Breton Island.

This map shows Acadia just before the expulsion and the locations where Acadians were deported to and from, beginning in 1755.

Life Deteriorates at Port Royal, ummm, I mean Annapolis Royal

By 1745, life in Acadia had deteriorated significantly and was getting worse. It’s no wonder so many had left for points North and East.

A 1745 report from Port Royal said the Acadian homes were “wretched wooden boxes, without conveniences, and without ornaments, and scarcely containing the most necessary furniture …” A visitor in the 1750s stated that “the houses of the village (Annapolis Royal) … are mean, and in general built of wood.”

The situation deteriorated significantly under Governor Charles Lawrence, who wanted to get rid of the Acadians. He used acts of individuals to make charges against the whole population. He revoked the former governor’s orders not to use military force if the Acadians refused to comply. One example was that if an Acadian was ordered to get firewood, and he didn’t do it promptly … his house would be used for fuel.

That’s horrifically brutal.

This explains why most of Marie Charlotte’s siblings had left before 1750.

The Last Record of Marie Charlotte Bonnevie

The last actual record we have for Marie Charlotte is the birth of her last child in 1742.

We have absolutely nothing for either her or her husband, Jacques Lord/Lore, from that time forward other than this oral history for Jacques:

“He suffered the great disturbance that occurred in Acadia in 1755, when the oppressor forced the family to go into exile in New York, United States. He returned to Canada with his son Pierre-Benjamin and they settled in Kamouraska The three children of Angelique Comeau (Corriveau) did not have an heir.”

Note that we only know of two children from Jacques’ first marriage, but it’s certainly possible that there were three.

If this is accurate, and if this is the same Jacques Lord/Lore who was married to Marie Charlotte Bonnevie, then he would have been 108 in 1786.

The problem is that the burial record shows this man’s age to be 79, not 108. This would be Jacques son, Jacques, but that doesn’t mean that Jacques Sr. didn’t also die there, perhaps somewhat earlier. There is a record with both Jacques and Pierre Lore witnessing a marriage in L’Ile-Dupas in 1764.

If indeed this is the same man, he would have been deported from the Port Royal region along with the other Lore males, including son Honoré.

If Jacques and his youngest son, Honoré, were deported from Port Royal, there’s no reason to think that Marie Charlotte Bonnevie, Honoré’s mother, was living far away from her children on Île Royal during or after the deportation. In fact, that’s contra-indicated.

If this Jacques is Charlotte’s step-son, born in 1709, not her husband, which is the most likely scenario, this group of people together actually provides evidence that Charlotte was NOT on Île Royal and that she and her family were all deported from Port Royal.

There is absolutely no evidence that any of her children or step-children left the Port Royal area before the expulsion began.

The Deportation

Charlotte’s brother Jacques Bonnevie, who was found near Beaubassin but did not move to Île Royal, was deported to South Carolina in 1755. He was one of only five or six families who returned to Canada in 1756. That trickle was immediately stopped before it turned into a river. Jacques was at Ristigouche in 1760 and reportedly a prisoner at Fort Edward (Pisiguit) with his wife and five children in 1761, although I have been unable to verify that.

The deportation meant death for Charlotte’s sisters and their families.

Marie Charlotte’s Death

Everywhere I look, Marie Charlotte is reported to have died at sea on or about December 13, 1758. I know where this comes from, but I think it’s inaccurate.

There are two issues.

First, I think most people have conflated the two Maries, literally combining or at least confusing them. Our Marie Charlotte born about 1703, and her younger sister, Marie, born in 1706.

Let’s summarize what we know about where the children of Jacques Bonnevie and Françoise Mius were in the 1755 deportation era.

  • Françoise Bonnevie, born about 1701, lived in Beaubassin in 1741, where she remarried Jean Pierre Hélie dit Nouvelle. Her last child was born in Beaubassin in 1742. In 1752, she and her husband were in the La Roque census, age 50, in Rivière-du-Nord-Est, Île Saint-Jean, Prince Edward Island.
  • Marie Charlotte Bonnevie and her husband Jacques Lord/Lore have no records found after 1742. We do know that four of their children married Garceau children, one in Acadia and three in exile. I believe these families were on the Brigge Experiment together, which departed from Annapolis Royal and sailed for New York. We know positively that Honoré, born in 1742, fought at Albany, New York, in the Revolutionary War.
  • Jacques Bonnevie, born in 1704, was in Beaubassin by 1746 and at Petitcodiah in 1752. He married Anne Melanson about 1755 and was subsequently deported to South Carolina. Ships with Acadians that arrived in South Carolina departed from either Chignecto, which is near Beaubassin, or Annapolis Royal. The surname Bonnevie does appear on the roster of the ship Cornwallis, which left Chignecto on October 13, 1755.
  • Marie Bonnevie, born in 1706 and married François Duguay, was living in Riviere du Nord-Est, Isle Saint-Jean, in 1748 and 1752, probably near her sister. Today, that’s Hillsborough River or North East River, near Charlottetown, Prince Edward Island.

So, given this information, where did this 1758 death date originate?

The information came from Stephen A. White, Dictionnaire généalogique des familles acadiennes (Moncton, N.-B.: Centre d’études acadiennes, Université de Moncton, 1999) p. 178-179.

Françoise Bonnevie (Jacques Bonnevie dit Beaumont and Françoise Mius) born around 1702, (On 1752 La Roque census age 50). Married (1) Pierre Olivier (Pierre & Geneviève Roussel) on 18 Oct 1718 in Port-Royal. Married (2) at 39 years of age, Jean Hélie dit Nouvelle (Étienne & Marguerite Laporte), widower of Anne-Marie Lalande, on 16 Jan 1741 in Beaubassin. She died (according to S.A. White), around 13 Dec 1758 when the ship Violet sank during the crossing to France.

Note from S.A. White: Françoise Bonnevie and Marie Bonnevie, their husbands and many of their children are among the Acadian families from Île Saint-Jean [Prince Edward Island] who disappeared without a trace after 1758. We believe that they were among the unfortunate passengers aboard one of the two British ships that sank. (see SHA vol II, p. 286-299) Jan, Feb, Mar 1968

Click to access 18cahier_total.pdf

AHA!

Well, that explains that, but no place is Marie Charlotte Bonnevie, her husband, or her children mentioned.

Marie Charlotte Bonnevie is NOT Marie Bonnevie.

What About Marie Charlotte?

I do not believe that Marie Charlotte drowned when those two ships went down.

Why?

I don’t believe she was a passenger on those ships or ever on Île Saint-Jean (Prince Edward Island) or Île Royal (Cape Breton Island).

We have no evidence whatsoever that Marie Charlotte, her husband, nor any of her children were ever lived on Île Royal or in Louisbourg, where both the ship Violet, with 280-400 people, and Duke William, with more than 360 people, sailed from en route to France.

Her father was in Louisbourg in 1732 before his death, but that does not equate to any of his children being there then or two decades later.

By 1758, three years into the deportations, the English no longer deported Acadians to the colonies but shipped them directly back to France. The Île Saint-Jean Acadians may have thought they had escaped deportation.

Given that Marie Charlotte’s sisters were indeed on Île Saint-Jean just before the expulsion began, unless they died before those ships sailed following the Siege of Louisbourg, it stands to reason that they were on those ships. There’s no record that they ever made it to France, and we know the ships sank with hundreds of Acadians on board.

Louisbourg fell on July 26th, and over the next few weeks and months, the residents were rounded up and loaded onto overcrowded, poorly maintained transport ships. Floating death traps.

Families on Prince Edward Island were rounded up and deported as well. Only 30 families managed to remain hidden. The rest sank aboard those two cursed death ships.

Marie Charlotte’s sisters, husbands, children, and grandchildren were almost certainly among them, wiping entire families off the face of the earth.

Thankfully, Marie Charlotte was probably spared that horrific fate and may have been waiting to greet them on the other side. Perhaps this time, an early death was a blessing.

It’s also possible that Marie Charlotte had already been deported with her children back in 1755 and was living somewhere in New England. At least, I hope if she got deported, she was loaded onto a ship with her children, not separated.

Her six youngest children were unmarried, the 4 youngest were minors, and all but one of those is lost to us. Honoré, her youngest, was only 13. He would have been terrified regardless, but even more so if both of his parents were already deceased and he faced that alone.

If Charlotte was deported with them, she probably died sometime between 1755 and 1764, when her children began making their way north into Quebec, settling near Montreal.

Of course, Honoré married about that time in New York and had children baptized in 1768 in Yamachiche, Quebec, but there was no sign of Marie Charlotte.

One way or another, the record and circumstances of her death are lost to us. It seems she either died in the 13 years between Honoré’s birth and the 1755 deportation or was lost during the resulting exile.

Either way, she didn’t enjoy a long life and died someplace between the age of 40 and about 63. I hope her family was at least able to provide her with the Catholic sacraments, even if they couldn’t bury her in consecrated ground and erect a stone or wooden cross in her memory.

Maybe the “Indian quilt” found in her son Honoré’s 1818 estate was a tiny piece of her mother’s family line that she was able to salvage and pass down to her son. Perhaps it warmed and comforted them on that horrific voyage into the unknown and warmed their hearts as they remembered long-lost but much-loved family members.

RIP Marie Charlotte, wherever you lay.

_____________________________________________________________

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RootsTech 2024 – Celebrating 25 Years of Genetic Genealogy

On the first day of RootsTech, we celebrated the milestone anniversary of 25 years of genetic genealogy. Right now, we are at the intersection of two incredibly powerful tools: genetics and AI. Both technologies are revolutionary and have changed and are changing the genealogical world overnight. What an amazing time to be alive!

Day 1 is Just Beginning

Day 1 is just the beginning, although pre-show activities have been occurring for a day or two. Everyone is excited. The energy on the show floor and as attendees talk is palpable – a form of human electricity.

I’m going to share some of RootsTech’s flavor with you, so come along with me as I attend a few sessions, give my dozen sessions, and meet people.

First, I need to provide some caveats.

  • I wasn’t able to attend very many sessions
  • I didn’t get to half the expo floor booths
  • I was only at one keynote, but fortunately, most were recorded

I managed to overcommit myself “just a bit,” and I just couldn’t be in two places at once. Thankfully, recorded sessions are available here.

One of the reasons that I didn’t get as much done as I had hoped is because I kept running into people. There was more hugging at RootsTech than at a bear-hug festival. The fun of taking selfies is a thing – a modern-day bonding experience and lots of group selfies are floating around on social media.

I truly love my fellow genealogists, many of whom I’ve discovered are cousins, and some of whom have become lifelong friends. They are brothers and sisters of heart -people who I can’t imagine NOT having in my family. This group of troublemakers is the perfect example of that, with Lianne Krüger, Mags Gaulden, and me in the back and Janine Cloud in front. I think we look like a girl band. Perhaps we’ll call ourselves The Chromosomes. 😊

The first thing on my agenda for Thursday was a book signing for my book, DNA for Native American Genealogy.

Penny Walters wandered by while I was signing and said hello.

Penny, the queen of selfies, constantly has to instruct me on how to do this successfully. It seems I either shut my eyes or I’m smiling so hard I’m laughing. One day, Penny, one day!

Thanks, Penny, for taking this picture of me with my book.

Following the book signing, Janine Could, Groups and Events Manager at FamilyTreeDNA, and I had an AMA, Ask Me Anything session in the FamilyTreeDNA booth about determining if you have Native American ancestors. Our stories are so complementary.

I was raised with and participated in Native cultural traditions. Janine wasn’t, but she is an enrolled Cherokee tribal member. After we had known each other for several years, we discovered that we’re related, but not through that line – at least not that we know of.

The great thing about AMA sessions is that the speakers are literally there to answer your questions. During the conference, lots of people took advantage of the expertise of speakers and their fellow attendees.

Remember

Last year, I met Charis, in the middle between me and Janine. Charis made my day when she told me that she was driving by the Salt Palace a week or so before RootsTech, saw that I was giving a Native American session, and knew she had to attend.

We talked for a long time, and I wondered if I would see her again this year.

Sure enough!

I saw her walking down an aisle, so I knew she was attending. I wanted to give her a hug but I couldn’t at that moment.

She stopped by the FamilyTreeDNA booth and asked Janine if she thought I’d remember her.

You remember people that make you feel good, and she really did.

Someone once told me that people often remember you for how you make them feel.

This year, Charis attended my sessions, and it felt good to see a friendly, smiling face in the audience.

After one class, she waited for me until everyone’s questions were answered. I asked if we could sit down in the quiet at a vacant table in the back of that hall for a few minutes to visit.

Charis pulled out a bag with a card and gave it to me, saying she hoped I didn’t think it was weird or anything. I was stunned and quite moved.

Her name is Remember, the theme of Rootstech this year.

I cried. Charis’s gift was so thoughtful in so many ways, as was the card – and she had no idea how personally this touched me.

We talked for a long time, and while I’m not going to share details, I remembered how it felt to be young and have your life’s trajectory shifted in ways you can’t control.

I remembered what it was like to have hopes dashed.

I remembered when I was “just doing what I was doing” every day, not realizing that I was making memories – not just for me but for others as well.

I remember when Douglas explained the concept of GodMothers to me – and I wasn’t young.

Douglas told me that I had GodMothered people through our combined educational ministry (and I’m not talking about church here) and through my own individual work. Of course, the first thing I thought when Douglas said that was, “No, no, not me,” but then I remembered my mother’s “simple” ministry to others. I remembered how my step-father changed my life both with his actions and a few simple, well-placed words. I remembered the kindness of others when I desperately needed it – and still do.

I remembered.

I remembered that we all have a mission, a ministry, even if we don’t realize it. Even if we don’t understand it. Even if “all we do” is a simple kindness every day.

I remembered that some people’s lives are meant to intersect.

Charis is doing GodMother work, or maybe God’s Mother’s work, every day of her life.

Charis gives me hope for the future.

Thank you Charis, for Remember, and for helping me remember. And for being the next generation of GodMothers and shining your light for others to follow in generations of GodMother footsteps.

Remember.

Genetic Genealogy Turns 25

A few weeks before RootsTech, Diahan Southard emailed and asked me if I’d be interested in and willing to write a short, roughly 3-page “chapter” for a book she was preparing for RootsTech, celebrating the 25th anniversary of genetic genealogy.

Additionally, Diahan would be hosting a panel where some of the contributors would share our remembrances, beginning with the earliest days and ending with more recent innovations.

You can watch the session here.

It’s not hyperbole to say that genetic genealogy changed my life. It also changed the trajectory of my career.

I was very proud to be included on this panel with Diahan and Bennett Greenspan, both of whom I have known since the beginning. Never in my wildest dreams could I have imagined an event like this – let alone being on this stage on this incredibly memorable day.

Diahan shared her story about beginning her career at Sorenson Molecular Institute with Scott Woodward, who joined us and told his story via video.

Bennett Greenspan spoke about his inspiration as a genealogist, and how and why he founded FamilyTreeDNA in 1999.

Bennett introduced Y-DNA and mitochondrial DNA to the consuming public, planting the seeds of an industry that would flourish and ultimately become a household word in the genealogy community.

Tim Janzen spoke about the role of Y-DNA from the first 12-marker panels to the Big Y-700 today. The landmark discovery that Thomas Jefferson had fathered children with Sally Hemmings occurred as a result of Y-DNA testing and drew attention to the possibilities for solving long-standing mysteries – known or unknown.

Leah Larkin discussed the tipping point of autosomal DNA in the genetic genealogy industry.

Aimee Haynes with DNA Angels, an adoption search organization, explained how autosomal DNA, in particular, answers questions for adoptees, giving identities and histories to millions of people who “don’t know who they are.”

Diahan asked me to speak about ethnicity and genetic genealogy, and I actually managed to find my original ethnicity test from 2003. That image in the middle with the red dot and “parenthesis” bands was the extent of the information returned, in addition to the percentages. By the way, those percentages weren’t accurate either, but it was a beginning.

However, ethnicity, with associated segment information at FamilyTreeDNA and 23andMe, has paved the way for painting both ethnicity and match segments with Jonny Perl’s DNAPainter.

Jonny spoke about his inspiration for DNAPainter and how he initially developed it for his own use. Now, just a few years later, everyone loves it!

Lori Napolitano spoke about the evolution of Forensic Investigative Genetic Genealogy (FIGG), also known as IGG, including a collage of people whose remains have been identified and a separate collage of perpetrators of violent crime who are now off the streets. She addressed the successes along with the challenges.

Lori’s 3 or 4 minutes were extremely balanced, presenting both sides of the coin, and I strongly encourage you to listen beginning at about minute 36.

Diahan has compiled these people’s contributions along others for a total of 34 vignettes in the book So Far: Genetic Genealogy – The First 25 Years 1999-2024.

  • Megan Smolenyak-Smolenyak
  • Scott Woodward
  • Bennett Greenspan
  • Ann Turner
  • Ugo Perego
  • Diahan Southard
  • Scott Fisher
  • Roberta Estes
  • Tim Janzen
  • Jim Bartlett
  • Blaine Bettinger
  • Daniel Horowitz
  • Debbie Kennett
  • Kitty Cooper
  • Angie Bush
  • Michelle Leonard
  • Paul Woodbury
  • Kelli Bergheimer
  • Judy Russell
  • Dana Leeds
  • Drew Smith
  • Diana Elder
  • Nicole Dyer
  • Leah Larkin
  • Nathan Dylan Goodwin
  • Mary Eberle
  • Mags Gaulden
  • Aimee-Rose-Haynes
  • Jonny Perl
  • Brianne Kirkpatrick
  • Laura Olmsted
  • Cheryi Hudson-Passey
  • Margaret Press
  • Penny Walters

The stories and visions of these pioneers and industry influencers are fascinating.

The eBook is free by scanning the QR code below or click here.

The following day, I found Diahan’s booth and was able to thank her for this labor of love.

Printed copies of Diahan’s book were available for sale in her booth, Your DNA Guide, and I was surprised how many people sought out attendees who wrote mini-chapters and asked us to sign our pages. What fun!

Diahan and I go back a long way. In the greatest of ironies, in the very early days, the Skidmore Family Association retained Diahan to “tell them what she could” about early Y-DNA tests of 51 Skidmore men. Initially, I was very concerned that the family association might have gotten themselves aligned with someone who was less than competent – but then thrilled when I discovered that consultant was Diahan. Better yet, my own line was one of 8 individual Skidmore lines that Diahan identified and was represented by several testers. Back then, Diahan was working with only a few STR markers and of course, today, we have Big Y-700 tests.

Sunny Morton, another author, joined us for a lovely photo in Diahan’s booth.

I’ve always been incredibly grateful to Sunny for taking me under her wing during my first year speaking at RootsTech, where I had 4 or 5 days to prepare a presentation to cover for another speaker who was unexpectedly unable to attend. Baptism by fire, for sure.

Another reminder that people remember you for how you make them feel.

Expo Hall Show Floor

In between sessions and events, I wandered around the show floor to see the booths, their offerings, and my friends. Many of these people are probably your friends, too, or you have seen their names in the community.

Near Diahan’s booth, I found Diana Elder and Nicole Dyer, pictured above, a lovely mother-daughter professional genealogist pair who founded Family Locket. Should I say this? I especially love the baby genealogist peeking at us from behind. I’m thinking in another year or so, it will be a three-generation endeavor.😊

I was excited to run into Marian Pierre-Louis, who facilitates the smooth running of Legacy Family Tree Webinars and slays technology gremlins left and right! Another person I’m grateful to!

Geoff Rasmussen, founder of Legacy Family Tree, both the Legacy Family Tree Software and the webinars, was staffing the booth. If you haven’t tried these amazing genealogy webinars, all webinars are free initially and for 7 days and are then available by subscription in the webinar library.

Here, Geoff and Marian appear together. What a wonderful team. I’ll have a new webinar in the library before year-end.

Further down the row, I found Geneanet. If you’re not familiar with Geneanet, they are the last totally free resource that I’m aware of that allows the free uploading of your tree, regardless of size.

I use Geneanet often, especially when searching for Europeans. One of my favorite trees at Geneanet belongs to professional genealogist Karen Theriot Reader, and it documents more than 166,000 Acadians and their descendants—along with sources.

Yes, there was food, although not as much as in earlier years. However, these lovely mini-bundt cakes were TO DIE FOR. Unfortunately, I never did manage to purchase a chocolate one.

Maybe I’ll just have to cross my fingers for next year.

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FamilyTreeDNA 2023 Update – Past, Present and Future

At the FamilyTreeDNA International Conference on Genetic Genealogy, held November 3-5 in Houston for group project administrators, product and feature updates were scattered across both days in various presentations.

I’ve combined the updates from FamilyTreeDNA into one article.

I’ve already written two articles that pertain to the conference.

FamilyTreeDNA has already begun rolling the new Y DNA haplogroups from Family Finder autosomal tests, which I wrote about here:

I still have at least two more articles to publish from this conference that was chocked full of wonderful information from a wide range of talented speakers.

Past, Present, and Future with Katy Rowe-Schurwanz

Katy Rowe-Schurwanz, FamilyTreeDNA’s Product Manager, provided an update on what has been accomplished in the four and a half years since the last conference, what’s underway now, and her wish list for 2024.

Please note the word “wish list.” Wish list items are NOT commitments.

Recent Milestones

A lot has been happening at FamilyTreeDNA since the last conference.

Acquisition and Wellness Bundles

As everyone is aware, at the end of 2020, myDNA acquired Gene by Gene, the parent company of FamilyTreeDNA, which included the lab. As a result, the FamilyTreeDNA product menu has expanded, and wellness bundles are now available for FamilyTreeDNA customers.

If you’re interested, you can order the Wellness product in a bundle with a Family Finder test, here.

You can add the Wellness product for $39 if you’ve already tested.

New TIP (Time Prediction) STR Report

Did you notice that the old TIP report for Y DNA STR markers was replaced with an updated version several months ago?

To view the new report, sign on and select your Y DNA matches. At the far right of each match you’ll see these three icons representing a pedigree chart, notes, and the TIP (Time Predictor) report.

The updated TIP report includes wonderful new graphs and age estimates for each match category, which you can read about, here. Each category, such as 67-marker matches, has time estimates in which a common ancestor might have lived at each possible genetic distance.

Math is our friend, and thankfully, someone else has done it for us!

Please note that the Big Y SNP dates are MUCH more accurate for a variety of reasons, not limited to the instability and rapid mutation rate of STR mutations.

MyOrigins3

MyOrigins3, FamilyTreeDNA’s ethnicity offering, added over 60 new reference populations for a total of 90, plus chromosome painting. You can read about MyOrigins features here, and the white paper, here.

This is one of my favorite improvements because it allows me to identify the segment location of my population ancestries, which in turn allows me to identify people who share my minority segments such as Native American and African.

Due to a lack of records, these relationships are often exceedingly difficult to identify, and MyOrigins3 helps immensely.

Additional Releases

Additional products and features released since the last conference include:

Discover

Released in July 2022, Discover is the amazing new free product that details your ancestor’s Y DNA “story” and his walk through time and across the globe.

In the past 18 months, all of the Discover features are new, so I’m only making a brief list here. The great thing is that everyone can use Discover if you know or can discover (pardon the pun) the haplogroup of your ancestral lines. Surname projects are often beneficial for finding your lineages.

  • Haplogroup Story includes haplogroup location, ages derived from the earliest known ancestor (EKA) of your matches, and ancient DNA samples. Please be sure you’ve entered or updated your EKA, and that the information is current. You can find instructions for how to update or add your EKA here.
  • A recent addition to the haplogroup story includes Haplogroup Badges.
  • Country Frequency showing where this haplogroup is found with either a table view or an interactive map
  • Famous and infamous Notable Connections, including Mayflower passengers, Patriots from the American Revolution, US presidents, royal houses, artists, musicians, authors, pirates, sports figures, scientists, and more.

If you know of a proven connection to a notable figure, contact customer support and let them know! Notable connections are added every week.

One famous Discover connection is Ludwig von Beethoven which resulted from a joint academic study between FamilyTreeDNA and academic researchers. It’s quite a story and includes both a mystery and misattributed parentage. You can see if you match on Discover and read about the study, here.

  • Updated Migration Map, including locations of select ancient DNA sites
  • The Time Tree, probably the most popular Discover report, shows the most current version of the Y DNA phylotree, updated weekly, plus scientifically calculated ages for each branch. Tree node locations are determined by your matches and their EKA countries of origin. I wrote about the Time Tree, here.
  • Anticipated in early 2024, the EKA and block tree matches will also be shown on the Time Tree in Discover for individual Big Y testers, meaning they will need to sign in through their kits.
  • The Group Time Tree, visible through group projects, takes the Time Tree a step further by including the names of the EKA of each person on the Time Tree within a specific project. Information is only displayed for project members who have given permission to include their data. You can select specific project groupings to view, or the entire project. I wrote about the Group Time Tree here and here.
  • Globetrekker is an exclusive Big Y mapping feature discussed here, here, here, and here.
  • Ancient Connections includes more than 6,100 ancient Y DNA results from across the globe, which have been individually analyzed and added for matching in Discover. Ancient Connections serve to anchor haplogroups and provide important clues about matches, migration paths and culture. New connections are added weekly or as academic papers with adequate Y DNA coverage are released.
  • Your Ancestral Path, which lists the haplogroups through every step from the tester back to Y Adam and beyond. Additional information for each haplogroup in your path includes “Time Passed” between haplogroups, and “Immediate Descendants,” meaning haplogroups that descend from each subclade. New columns recently added include “Tested Modern Descendants” and “Ancient Connections.”
  • Suggested Projects include surname, haplogroup, and geographic projects. Katy said that people joining projects are more likely to collaborate and upgrade their tests. You can also see which projects other men with this haplogroup have joined, which may well be projects you want to join too.
  • Scientific Details provides additional information, such as each branch’s confidence intervals and equivalent variables (SNPs). You can read more here.
  • Compare Haplogroups is the most recent new feature, added just last month, which allows you to enter any two haplogroups and compare them to determine their most recent common ancestral haplogroup. You can read about Compare Haplogroups, here.

Please note that the Studies feature is coming soon, providing information about studies whose data has been included in Discover.

You can read about Discover here, here, here, and here.

If you’re interested, FamilyTreeDNA has released a one-minute introduction to Y DNA and Discover that would interest new testers, here.

Earliest Known Ancestor (EKA) Improvement

Another improvement is that the earliest known ancestor is MUCH easier to enter now, and the process has been simplified. The EKAs are critical for Discover, so PLEASE be sure you’ve entered and updated your EKA.

Under the dropdown beside your name in the upper right-hand corner of your personal page, select Account Settings, then Genealogy and Earliest Known Ancestors. Complete the information, then click on “Update Location” to find or enter the location on a map to record the coordinates.

It’s easy. Just type or drop a pin and “Save.”

Saving will take you back to the original EKA page. Save that page, too.

Recommended Projects on Haplogroups & SNPs Page

You’re probably aware that Discover suggests projects for Y DNA testers to join, but recommended haplogroup projects are available on each tester’s pages, under the Y DNA Haplotree & SNPs page, in the Y DNA STR results section.

If there isn’t a project for your immediate haplogroup, just scroll up to find the closest upstream project. You can also view this page by Variants, Surnames and Countries.

This is a super easy tool to use to view which surnames are clustered with and upstream of your haplogroup. With Family Finder haplogroups being assigned now, I check my upstream haplogroups almost daily to see what has been added.

For example, my Big Y Estes results are ten branches below R-DF49, but several men, including Estes testers, have been assigned at this level, thanks to Y DNA haplogroups from Family Finder testing. I can now look for these haplogroups in the STR and Family Finder matches lists and see if those men are receptive to Big Y testing.

Abandoned Projects

Sometimes group project administrators can no longer function in that capacity, resulting in the project becoming abandoned. FamilyTreeDNA has implemented a feature to help remedy that situation.

If you discover an abandoned project, you can adopt the project, spruce things up, and select the new project settings. Furthermore, administrators can choose to display this message to recruit co-administrators. I need to do this for several projects where I have no co-admin.

If you are looking for help with your project, you can choose to display the button
through the Project Profile page in GAP. For non-project administrators, if you’d like to help, please email the current project administrators.

New Kit Manager Feature

FamilyTreeDNA has added a “Kit Manager” feature so that an individual can designate another person as the manager of their kit.

This new setting provides an avenue for you to designate someone else as the manager of your DNA test. This alerts FamilyTreeDNA that they can share information with both of you – essentially treating your designated kit manager the same as you.

If you’re the kit manager for someone else, you NEED to be sure this is completed. If that person is unavailable for some reason, and support needs to verify that you have legitimate access to this kit, this form and the Beneficiary form are the ONLY ways they can do that.

If your family member has simply given you their kit number and password, and for some reason, a password reset is required, and their email address is the primary contact – you may be shut out of this kit if you don’t complete this form.

Beneficiary Page

Additionally, everyone needs to be sure to complete the Beneficiary page so that in the event of your demise, FamilyTreeDNA knows who you’ve designated to access and manage your DNA account in perpetuity. If you’ve inherited a kit, you need to add a beneficiary to take over in the event of your death as well.

What is FamilyTreeDNA working on now?

Currently in the Works

Katy moved on to what’s currently underway.

Privacy and Security

Clearly, the unauthorized customer data exposure breach at 23andMe has reverberated through the entire online community, not just genetic genealogy. You can read about the incident here, here, here, and here.

FamilyTreeDNA has already taken several steps, and others are in development and will be released shortly.

Clearly, in this fast-moving situation, everything is subject to change.

Here’s what has happened and is currently planned as of today:

  • Group Project Administrators will be required to reset their password soon.

Why is this necessary?

Unauthorized access was gained to 23andMe accounts by people using the same password for multiple accounts, combined with their email as their user ID. Many people use the same password for every account so that they can remember it. That means that all a hacker needs to do is breach one account, and they can use that same information to “legitimately” sign in to other accounts. There is no way for the vendor to recognize this as unauthorized since they have both your user ID and password.

That’s exactly what happened at 23andMe. In other breaches, this information was exposed, and hackers simply tried the same username and password combination at 23andMe, exposing the entire account of the person whose account they signed in “as.” This includes all of their matches, genetic tree, shared matches, matches of matches, ethnicity, and segments. They could also have downloaded both the match list and the raw DNA file of the compromised account.

At FamilyTreeDNA, project administrators can select their own username, which could be their email, so they will be required to reset their password.

Additional precautions have been put in place on an interim basis:

  • A pause in the ability to download match and segment information.
  • A pause in accepting 23andMe uploads.

Administrators will also be required to use two-factor authentication (2FA.) To date, two of the four major vendors are requiring 2FA. I would not be surprised to see it more broadly. Facebook recently required me to implement 2FA there, too, due to the “reach” of my postings, but 2FA is not required of everyone on Facebook.

Please note that if you received an email or message that is supposedly from any vendor requiring 2FA, GO DIRECTLY TO THAT VENDOR SITE AND SIGN IN.  Never click on a link in an email you weren’t expecting. Bad actors exploit everything.

Customers who are not signing in as administrators are not required to implement 2FA, nor will they be required to reset their password.

Personally, I will implement 2FA as soon as it’s available.

While 2FA is an extra step, it’s easy to get used to, and it has already literally saved one of my friends from an authorized hack on their primary and backup email accounts this week. Another friend just lost their entire account on Facebook because someone signed in as them. Their account was gone within 15 minutes.

2FA is one of those things you don’t appreciate (at all) until it saves you, and then, suddenly, you’re incredibly grateful.

At this point in time, FamilyTreeDNA users will NOT be required to do a password reset or implement 2FA. This is because customers use a kit number for sign-in and not a username or email address. I would strongly recommend changing your password to something “not easy.” Never reuse passwords between accounts.

I really, really want you to visit this link at TechRepublic and scroll down to Figure A, which shows how long it takes a hacker to crack your password. I guarantee you, it’s MUCH quicker than you’d ever expect.

Kim Komando wrote about this topic two years ago, so compare the two charts to see how much easier this has become in just two years.

Again, if you receive an email about resetting your password, don’t click on a link. Sign in independently to the vendor’s system, but DO reset your password.

FamilyTreeDNA also engages in additional security efforts, such as ongoing penetration testing.

New Permissions

Additionally, at FamilyTreeDNA, changes were already in the works to separate out at least two permissions that testers can opt-in to without granting project administrators Advanced rights.

  • Download data
  • Purchase tests

The ability to purchase tests can be very important because it allows administrators to order and pay for tests or upgrades on behalf of this tester anytime in the future.

Family Finder Haplogroups

FamilyTreeDNA has already begun releasing mid-level Y DNA haplogroups for autosomal testers in a staggered rollout of several thousand a day.

I wrote about this in the article, FamilyTreeDNA Provides Y DNA Haplogroups from Family Finder Autosomal Tests, so I’m not repeating all of that information here – just highlights.

  • The Family Finder haplogroup rollout is being staggered and began with customers on the most recent version of the testing chip, which was implemented in March of 2019.
  • Last will be transfers/uploads from third parties.
  • Haplogroups resulting from tests performed in the FTDNA labs will be visible to matches and within projects. They will also be used in both Discover and the haplotree statistics. This includes Family Finder plus MyHeritage and Vitagene uploads.
  • Both MyHeritage and Vitagene are uploaded or “transferred” via an intracompany secure link, meaning FamilyTreeDNA knows that their information is credible and has not been manipulated.
  • Haplogroups derived from tests performed elsewhere will only be visible to the user or a group administrator viewing a kit within a project. They will not be visible to matches or used in trees or for statistics.
  • Any man who has taken a Y DNA STR test will receive a SNP-confirmed, updated haplogroup from their Family Finder test that replaces their predicted haplogroup from the STR test.

Please read this article for more information.

New Discover Tools and Updates

Discover content continues to be updated, and new features are added regularly, creating an increasingly robust user experience.

Soon, group administrators will be able to view all Discover features (like Globetrekker) when viewing kits of project members who have granted an appropriate level of access.

Ancient and Notable connects are added weekly, and a new feature, Study Connections, will be added shortly.

Study Connections is a feature requested by customers that will show you which study your academic matches came from. Today, those results are used in the Y DNA tree, but the source is not detailed.

Anticipated in early 2024, the EKA and block tree matches will also be shown on the Time Tree in Discover for individual Big Y testers (not publicly).

Big Y FaceBook Group

FamilyTreeDNA has ramped up its social media presence. They launched the Big Y Facebook group in July 2023, here, which currently has just under 9000 members. Several project administrators have volunteered their time to help manage the group.

FamilyTreeDNA Blog

In addition, FamilyTreeDNA is publishing at least one blog article each week, and sometimes more. You can view or subscribe here. Some articles are written by FamilyTreeDNA staff, but project administrators and customers author other content.

Multi-Language Support

Translation of the main FamilyTreeDNA website and results pages to Spanish has begun, with more languages planned soon.

Paypal, Payments, and Gift Cards

Paypal has been added as a payment selection, along with a PayPal option that provides the ability to make payments.

Additionally, a gift card can be purchased from the main page.

Million Mito Project & Mitotree

Work on the Million Mito Project is ongoing.

The Million Mito Project was launched in 2020 as a collaborative effort between FamilyTreeDNA’s Research & Development Team and the scientific portion of the Genographic Project. I’m a team member and wrote about the Million Mito Project, here.

We’re picking up from where the Phylotree left off in 2016, analyzing 20 times more mtDNA full sequences and reimagining the mtDNA Haplotree. By examining more mtDNA data and applying the processes that allowed FamilyTreeDNA to build the world’s largest Y DNA Haplotree, we can also create the world’s largest Mitotree.

In 2022, the first update was released, authored by the Million Mito team, with the discovery of haplogroup L7. You can read about this amazing discovery rooted deep in the tree here, here, and here. (Full disclosure: I’m a co-author.)

Not only that, but “Nature Scientific Reports” selected this article as one of five named Editor’s Choice in the Mitogenomics category, here. In the science world, that’s a HUGE deal – like the genetic Emmy.

Here’s one example of the type of improvements that can be expected. Currently, the formation of haplogroup U5a2b2a reaches back to about 5000 years ago, but after reanalysis, current branches originated between 500 and 2,500 years ago, and testers are clustered more closely together.

This is SOOO exciting!!!

Just as Discover for Y DNA results was built one feature at a time, the same will be true for MitoDiscover. That’s my name, not theirs.

As the new Mitotree is rolled out, the user interface will also be updated, and matching will function somewhat differently. Specifically, it’s expected that many more haplogroups will be named, so today’s matching that requires an exact haplogroup match to be a full sequence match will no longer work. That and other matching adjustments will need to be made.

I can hardly wait. I have so many results I need to be able to view in a tree format and to place in a timeframe.

You can be included in this exciting project, learn more about your matrilineal (mother’s) line, and hopefully break down some of those brick walls by taking the full sequence mitochondrial DNA test, here.

After the new Mitotree is rolled out and the Y DNA Family Finder haplogroups are completed, Family Finder customers, where possible, will also receive at least a basic-level mitochondrial haplogroup. Not all upload files from other vendors include mtDNA SNPs in their autosomal files. The mitochondrial Family Finder haplogroup feature isn’t expected until sometime in 2025, after the new tree and MitoDiscover are complete.

The Future

What’s coming later in 2024, or is ongoing?

Privacy Laws

Most people aren’t aware of the new privacy laws in various states, each of which has to be evaluated and complied with.

The effects of these changes will be felt in various areas as they are implemented.

New Kits Opted Out of IGG

Since late August, all new FTDNA kits are automatically opted OUT of Investigative Genetic Genealogy (IGG) by default.

Regular matching consent and IGG matching consent have been separated during onboarding.

Biobanking Separate Consent

Another consent change is to have your sample biobanked. FamilyTreeDNA has always maintained your sample for “roughly 25 years.” You could always ask to have your sample destroyed, but going forward, you will be asked initially if you want your sample to be retained (biobanked.) It’s still free.

Remember, if someone declines the biobanking option, their DNA will be disposed of after testing. They can’t order upgrades without submitting a new sample. Neither can their family after they’re gone. I ordered my mother’s Family Finder test many years after she had gone on to meet our ancestors – and I’m incredibly grateful every single day.

MyHeritage Tree Integration

An exciting change coming next year is tree integration with MyHeritage.

And no, before any rumors get started, FAMILYTREEDNA IS NOT MERGING WITH MYHERITAGE. It’s a beneficial marriage of convenience for both parties.

In essence, one of the primary focuses of MyHeritage is trees, and they do that very well. FamilyTreeDNA is focused on DNA testing and their existing trees have had issues for years. MyHeritage trees are excellent, support pedigree collapse, provide search capabilities that are NOT case sensitive, SmartMatching, and much more.

If you don’t have a MyHeritage account, creating one is free, and you will be able to either port your existing FamilyTreeDNA tree, or begin one there. If you’re already a MyHeritage member, FamilyTreeDNA and MyHeritage are planning together for a smooth integration for you. More detailed information will be forthcoming as the integration progressed and is released to customers.

You’ll be able to connect multiple kits to your tree at MyHeritage, just like you can at FamilyTreeDNA today, which enables family matching, aka bucketing.

You can also have an unlimited number of different trees at MyHeritage on the same account. You’re not limited to one.

After you link your initial FamilyTreeDNA kit to the proper person in your MyHeritage tree, you’ll be able to relink any currently linked kits.

MyHeritage will NOT receive any DNA information or match information from FamilyTreeDNA, and yes, you’ll be able to use the same tree independently at MyHeritage for their DNA matching.

You’ll still be able to view your matches’ trees, except it will actually be the MyHeritage tree that will be opened at FamilyTreeDNA in a new tab.

To the best of my knowledge, this is a win-win-win, and customers of both companies aren’t losing anything.

One concern is that some FamilyTreeDNA testers have passed away and cannot transition their tree, so a view-only copy of their tree will remain at FamilyTreeDNA so that their matches can still see their tree.

Big Y Infrastructure

Katy mentioned that internal discussions are taking place to see what changes could be made to improve things like matching and test processing times.

No changes are planned for SNP or STR coverage, but discussions are taking place about a potential update to the Telomere to Telomere (T2T) reference. No promises about if or when this might occur. The last part of the human genome to be fully sequenced, the T2T reference model includes the notoriously messy and unreliable region of the Y chromosome with many repeats, duplications, gaps, and deletions. Some data from this region is probably salvageable but has previously been omitted due to the inherent problems.

I’m not sure this shouldn’t be in the next section, the Wishlist.

Wishlist

There are lots of good things on the Wishlist – all of which I’d love.

I’d have difficulty prioritizing, but I’d really appreciate some Family Finder features in addition to the items already discussed. I’d also like to see some GAP (administrator) tool updates.

Which items do you want to see most?

Katy said that FamilyTreeDNA is NOT planning to offer a Whole Genome Sequencing (WGS) test anytime soon. So, if you’re holding your breath, please don’t. Based on what Katy did say, WGS is very clearly not a consideration in 2024 and I don’t expect to see it in 2025 either unless something changes drastically in terms of technology AND pricing.

While WGS prices have come down, those consumer tests are NOT scanned at the depth and quality required for advanced tests like the Big Y or even Family Finder. Normally consumer-grade WGS tests are scanned between 2 and 10 times, where the FamilyTreeDNA lab scans up to 30 times in order to obtain a quality read. 30X scans are in the same category as medical or clinical grade whole genome scans. Significantly higher quality scans mean significantly higher prices, too, so WGS isn’t ready for genealogy prime time yet.

Additionally, commercially available WGS tests are returned to the customer “as is,” and you’re left to extract the relevant SNPs and arrange them into files, or find someone else to do that. Not to mention, in order to preserve the integrity of their database, FamilyTreeDNA does not accept Y or mitochondrial DNA uploads.

Recently, I saw two WGS files with a 20-25% no-call rate for the autosomal SNPs required for the Family Finder test. Needless to say, that’s completely unacceptable. Some tools attempt to “fix” that mess by filling in the blanks in the format of either a 23andMe or Ancestry file so you can upload to vendors, but that means you’re receiving VERY unreliable matches.

The reason none of the major four vendors offer WGS testing for genealogists is because it’s not financially feasible nor technologically beneficial. The raw data file alone won’t fit on most home computers. WGS is just not soup yet, and it won’t be for the general consuming public, including relevant tools, for at least a few years.

I’ve had my whole genome sequenced, and trust me, I wish it were feasible now, but it just isn’t.

Suggestions Welcomed

Katy said that if you have suggestions for items NOT on the wishlist today to contact her through support.

I would add that if you wish to emphasize any specific feature or need above others, please send that feedback, politely, to support as well.

Katy ended by thanking the various teams and individuals whose joint efforts together produce the products we use and enjoy today.

Lab Update

Normally, DNA testing companies don’t provide lab updates, but this conference is focused on group project administrators, who are often the most dedicated to DNA testing.

A lab update has become a tradition over the years.

Linda Jones, Lab Manager, provided a lab update.

You may or may not know that the FamilyTreeDNA lab shifted gears and stepped up to handle Covid testing.

Supply-chain shortages interfered, but the lab ran 24×7 between 2020 and 2022.

Today, the lab continues to make improvements to processes with the goal of delivering the highest quality results in a timely manner.

On Monday, after the conference, attendees could sign up for a lab tour. You might say we are a rather geeky bunch and really enjoy the science behind the scenes.

Q&A and Thank You

At the end of the conference, the FamilyTreeDNA management team answered questions from attendees.

Left to right, Daniel Au, CTO; Linda Jones, Lab Manager; Katy Rowe-Schurwanz, Product Manager; Clayton Conder, VP Marketing; Goran Runfeldt, Head of R&D; and Andrew Gefre, Development Manager. Not pictured, Jeremy Balkin, Support Manager; Kelly Jenkins, VP of Operations; and Janine Cloud, Group Projects Manager. Janine is also responsible for conferences and events, without whom there would have been no 2023 FamilyTreeDNA conference. Janine, I can’t thank you enough!

A huge thanks to all of these people and many others, including the presenters, CSRs,  IT, and other FamilyTreeDNA team members for their support during the conference, enabling us to enjoy the conference and replenish the well of knowledge.

_____________________________________________________________

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FamilyTreeDNA Provides Y DNA Haplogroups from Family Finder Autosomal Tests

Big News! FamilyTreeDNA is delivering holiday gifts early!

Y DNA haplogroups are beginning to be delivered as a free benefit to men who took the Family Finder test at FamilyTreeDNA. This is the first wave of a staggered rollout. Haplogroup results will be delivered to several thousand people at a time, in batches, beginning today.

This is no trivial gift and includes LOTS of information that can be used in various ways for your genealogy. Please feel free to share this article. The new Family Finder haplogroups are another reason to take a Family Finder test and to encourage other family members to do so as well.

How is this Even Possible?

Clearly, Y DNA is not autosomal DNA, so how is it possible to obtain a Y DNA or mitochondrial DNA haplogroup from an autosomal test? Great question!

Many autosomal DNA processing chips include a limited number of targeted Y and mitochondrial DNA SNP locations. Generally, those locations are haplogroup predictive, which is how haplogroup information can be obtained from an autosomal DNA test.

Compared to the actual Y DNA and mitochondrial DNA tests, only a small fraction of the information is available through autosomal tests. Only the full sequence mitochondrial DNA test or the Big Y-700 test will provide you with the full story, including your most refined haplogroup, additional information, and matching with other customers.

Having said that, haplogroups obtained from Family Finder provide important clues and genealogical information that will hopefully whet recipients’ appetites for learning even more.

Delivery Schedule

This first group of men to receive haplogroup results consists of testers who have purchased the Family Finder test since March 2019 when the most recent chip was put into production.

FamilyTreeDNA will be rolling haplogroups out in batches of a few thousand each day until everyone’s is complete, in the following order:

  • Family Finder tests purchased since March 2019 (their V3 chip)
  • Family Finder tests purchased between the fall of 2015 to March 2019 (their V2 chip)
  • Family Finder tests purchased from 2010 to the fall of 2015 (their V1 chip)
  • Autosomal uploads from other vendors for customers who have unlocked the advanced Family Finder features for $19

Uploaded DNA Files from Other Vendors

After the results are available for all males who have tested at FamilyTreeDNA, haplogroups will begin to be rolled out to customers who uploaded autosomal DNA files from other companies, meaning MyHeritage, Vitagene, 23andMe, and Ancestry.

To receive haplogroups for files uploaded from other vendors, the Family Finder advanced tool unlock must have been (or can be) purchased for $19. In addition to haplogroups, the unlock also provides access to the chromosome browser, myOrigins (ethnicity), Chromosome painting for myOrigins ethnicity, and ancient Origins.

Both MyHeritage and Vitagene tests are performed in the Gene by Gene lab. Those “uploads” are actually a secure business-to-business transaction, so the file integrity is assured.

Ancestry and 23andMe DNA files are downloaded from those companies, then uploaded to FamilyTreeDNA. Some people build “composite” files in the format of these companies, so FamilyTreeDNA has no way to assure that the original DNA upload file hasn’t been modified and it is a legitimate, unmodified, file from either 23andMe or Ancestry. Hence, in some situations, they are treated differently.

Both Ancestry and 23andMe utilize different chips than FamilyTreeDNA, covering different SNPs. Those results may vary slightly from results available from native FamilyTreeDNA tests, and will also vary from each other. In other words, there’s no consistency, and therefore haplogroup accuracy cannot be confirmed.

Haplogroups resulting from tests performed in the FamilyTreeDNA lab will be visible to matches and on the SNP pages within projects. They will also be used in both Discover and the haplotree statistics. This includes Family Finder plus MyHeritage and Vitagene DNA file uploads.

Tests performed elsewhere will receive haplogroups that will only be visible to the user, or a group administrator viewing a kit within a project. They will not be visible to matches, used in trees or for statistics.

At their recent conference, FamilyTreeDNA provided this slide during an update about what to expect from Family Finder haplogroups.

Today, only Y DNA haplogroups are being provided, but after the new mitochondrial tree is available, customer haplogroups are updated, and MitoDiscover (my name, not theirs) is released, FamilyTreeDNA is planning to provide mitochondrial DNA haplogroups for Family Finder customers as well. The current haplogroup estimate is late 2024 or even into 2025.

Unfortunately, some of Ancestry’s DNA files don’t include mitochondrial DNA SNPs, so some customers who’ve uploaded Ancestry files won’t receive mitochondrial haplogroups.

STR Haplogroups to be Updated

All FamilyTreeDNA customers who have taken Y DNA STR tests, meaning 12, 25, 37, 67, or 111 markers, receive predicted haplogroups. Often, the Family Finder extracted results can provide a more refined haplogroup.

When that is possible, STR test predicted haplogroup results will be updated to the more refined Family Finder haplogroup.

Furthermore, while STR results are quite reliably predicted, Family Finder results are SNP-confirmed.

Notification

When your Family Finder test has received a haplogroup or your STR-derived haplogroup has been updated, you’ll receive an email notification with a link to a short, less than 2-minute video explaining what you’re receiving.

You can also expect emails in the following days with links to additional short videos. If you’d like to watch the videos now, click here.

You can also check your results, of course. If you should have received an email and didn’t, check your spam folder, and if it’s not there, notify FamilyTreeDNA in case your email has managed to get on the bounce list.

Group project administrators will receive notifications when a haplogroup is updated for a member in a project that they manage. This doesn’t just apply to Family Finder haplogroup updates for STR results – notifications will arrive when Big Y haplogroups are updated, too.

Emails about haplogroup updates will include both the old and the updated haplogroup.

Haplogroups may change as other testers receive results, forming a new haplogroup. The Big Y-700 test is evergreen, meaning as the Y tree grows, testers’ results are updated on an ongoing basis.

New View

Let’s take a look at what customers will receive.

In one of my surname projects, one male has taken a Family Finder test, but not the Y DNA test.

Several other men in that same paternal line, who are clearly related (including his brother), have taken Y DNA tests – both STR and the Big Y-700.

We have men who have taken the Big Y-700 test, STR tests only (no Big Y), and one with only a Family Finder test, so let’s compare all three, beginning with the man who has taken a Family Finder test but no Y DNA tests.

He has now been assigned to haplogroup I-BY1031, thanks to his Family Finder test.

Before today, because he has not taken a Y DNA test, he had no haplogroup or Y DNA Results section on his personal page.

Today, he does. Of course, he doesn’t have STR results or matches, but he DOES have confirmed SNP results, at least part way down the tree.

He can view these results on the Haplotree & SNPs tab or in Discover. Let’s look at both.

Haplotree & SNPs

By clicking on the Haplotree & SNPs link, you can view the results by variants (mutations,) as shown below, or by countries, surnames, or recommended projects for each haplogroup.

Of course, as more Family Finder results are rolled out, the more names and countries will appear on the Haplotree.

Recommended Projects

It’s easy to determine which haplogroup projects would be a good fit for people with these new haplogroups to join.

Just view by Recommended Projects, then scan up that column above the selected haplogroup. You can even just click right there to join. It’s that easy!

Results still won’t show on the public project page, because these testers don’t have STR results to display. Perhaps this will encourage additional testing in order to match with other men.

Download SNP Results

If you’re interested, you can download your SNP results in spreadsheet format.

I’m only showing four of my cousin’s positive SNPs, but FamilyTreeDNA was able to extract 358 positive SNPs to assign him to haplogroup I-BY1031.

Are Family Finder Haplogroups Better Than STR Test Predicted Haplogroups?

How do Family Finder haplogroups stack up against STR-predicted haplogroups?

Viewing the Y DNA results of related cousins who have taken STR tests, but not the Big Y-700, we see that their Y DNA haplogroup was predicted as I-M253.

We also know that the haplogroup determined by the Big Y-700 for this line is I-BY73911.

How can we use this information beneficially, and what does it mean?

Discover

Family Finder haplogroups can access Discover, which I wrote about, here.

Clicking on the Discover link takes you to your haplogroup story.

Let’s look at the new Family Finder Haplogroup Story for this tester.

Haplogroup I-BY1031 is about 3100 years old and is found in England, Sweden, the US, and 14 other countries. Of course, as more Family Finder haplogroups are provided to customers, this information will change for many haplogroups, so check back often.

Of course, you’ll want to review every single tab, which are chapters in your ancestral story! The Time Tree shows your haplogroup age in perspective to other haplogroups and their formation, and Ancient Connections anchors haplogroups through archaeology.

You can share any Discover page in several ways. This is a good opportunity to excite other family members about the discoveries revealed through DNA testing and genealogy. Prices are reduced right now with the Holiday Sale, too, so it’s a great time to gift someone else or yourself.

Compare – How Good is Good?

Ok, so how much better is the Family Finder haplogroup than the STR-predicted haplogroup, and how much better is the Big Y-700 haplogroup than the other two?

I’ll use the Discover “Compare” feature to answer these questions.

First, let’s compare the STR-predicted haplogroup of I-M253 to the Family Finder haplogroup of I-BY1031.

I clicked on Compare and entered the haplogroup I wish to compare to I-BY1031.

I-M253 I-BY1031 I-BY73199
Haplogroup Source STR Predicted Family Finder Big Y-700
Formation Year 2600 BCE 1100 BCE 1750 CE
Age – Years ago 4600 3100 270
Era Stone Age, Metal Age Metal Age Modern
Ancestral Locations England, Sweden, Germany, UK, +100 Sweden, England, US, +14 Netherlands
Tested Descendants 26,572 121 2
Branches 6779 69 0 – this is the pot-of-gold end leaf on the branch today

I created this chart to compare the major features of all three haplogroups.

The STR-predicted haplogroup, I-M253, takes you to about 2,600 BCE, or about 4,600 years ago. The Family Finder haplogroup shifts that significantly to about 1100 BCE, or 3100 years ago, so it’s about 1500 years more recent. However, the Big Y haplogroup takes you home – from 3100 years ago to about 270 years ago.

Notice that there’s a LOT of room for refinement under haplogroup I-M253. A Big Y tester might wind up on any of those 6779 branches, and might well be assigned to a newly formed branch with his test. The Family Finder haplogroup, I-BY1031, which was, by the way, discovered through Big Y testing, moved the autosomal test taker forward 1500 years where there are 121 descendants in 69 branches. The Big Y-700 test is the most refined possible, moving you directly into a genealogically relevant timeframe with a very specific location.

I-M253 is found in over 100 countries, I-BY1031 in 17 and I-BY73199 is found only in one – the Netherlands.

Based on confirmed genealogy, the common ancestor of the two men who have Big Y-700 haplogroup I-BY73199 was a man named Hendrik Jans Ferwerda, born in 1806 in the Netherlands, so 217 years ago. Of course, that haplogroup itself could have been born a generation or two before Hendrik. We simply won’t know for sure until more men test. More testers refine the haplotree, haplogroup ages, and refine our genealogy as well.

Haplogroup Comparison and Analysis

Let’s look at the Discover “Compare” feature of the three haplogroups from my family line from the Netherlands. Please note that your results will differ because every haplogroup is different, but this is a good way to compare the three types of haplogroup results and an excellent avenue to illustrate why testing and upgrades are so important.

The haplogroup ages are according to the Discover Time Tree.

Y-Adam to Haplogroup I1 I-M253 STR Haplogroup  to I-BY1031 Family Finder Haplogroup I-BY1031 Family Finder Haplogroup to BY73199 Big Y Haplogroup
Y-Adam (haplogroup A-PR2921) lived about 234,000 years ago
A0-T
A1
A1b
CT
CF
F
GHIJK
HIJK
IJK
IJ
I
M170
Z2699
L840
I1 I1
I-M253 lived about 4600 years ago
DF29
Z58
Z2041
Z2040
Z382
Y3643
Y2170
FT92441
FT45372
PH1178
BY1031 I-BY1031 lived about 3100 years ago
FT230048
BY65928
BY61100
I-BY73199 lived about 270 years ago

 All of the base haplogroups in the first column leading to Haplogroup I span the longest elapsed time, about 230,000 years, from Y-Adam to I-M253, the STR-predicted haplogroup, but are the least relevant to contemporary genealogy. They do tell us where we came from more distantly.

The second column moves you about 1500 years forward in time to the Family Finder confirmed haplogroup, reducing the location from pretty much everyplace in Europe (plus a few more locations) with more than 6700 branches, to 69 branches in only 17 countries.

With the fewest haplogroups, the third column spans the most recent 2800 years, bringing you unquestionably into the genealogically relevant timeframe, 270 years ago, in only one country where surnames apply.

If we had more testers from the Netherlands or nearby regions, there would probably be more branches on the tree between BY1031 and BY73199, the Big Y-700 haplogroup.

The second column is clearly an improvement over the first column which gets us to I-M253. The Family Finder upgrade from I-M253 to BY1031 provides information about our ancestors 3000-4500 years ago, where they lived and culturally, what they were doing. Ancient Connections enhance that understanding.

But the third column moves into the modern area where surnames are relevant and is the holy grail of genealogy. It’s a journey to get from Adam to the Netherlands in one family 270 years ago, but we can do it successfully between Family Finder and the Big Y-700.

Family Finder Matching

Given that these new haplogroups result from Family Finder, how do these results show in Family Finder matching? How do we know if someone with a haplogroup has taken a Y DNA test or if their haplogroup is from their Family Finder test?

  • All Family Finder haplogroups will show in the results for people who tested at FamilyTreeDNA as soon as they are all rolled out
  • All MyHeritage and Vitagene uploads, because they are processed by the Gene by Gene lab, will be shown IF they have purchased the unlock.
  • No Ancestry or 23andMe haplogroups will be shown to Family Finder matches

To determine whether or not your matches’ haplogroups result from a Y DNA test or a Family Finder haplogroup, on your Family Finder match page, look just beneath the name of your matches.

The first man above received the Family Finder haplogroup. You can see he has no other tests listed. The second man has taken the Big Y-700 test. You can see that he has a different haplogroup, and if you look beneath his name, you’ll see that he took the Big Y-700 test.

For other men, you may see the 67 or 111 marker tests, for example, so you’ll know that they are available for Y-DNA matching. That may be important information because you can then visit the appropriate surname project to see if they happen to be listed with an earliest known ancestor.

After the rollout is complete, If you have a male Family Finder match with no haplogroup shown, you know that:

  • They did not test at FamilyTree DNA
  • If they uploaded from MyHeritage or Vitagene, they did not unlock the advanced Family Finder features
  • Or, they tested at either 23andMe or Ancestry, and uploaded their results

You can always reach out to your match and ask.

How to Use This Information

There are several great ways to utilize this new information.

I have a roadblock with my Moore line. Moore is a common surname with many, many origins, so I have autosomal matches to several Moore individuals who may or may not be from my Moore line.

I do know the base haplogroup of my Moore men, but I do not have a Big Y, unfortunately, and can’t upgrade because the tester is deceased. (I wish I had ordered the Big Y out the gate, but too late now.)

As soon as the results are complete for all of the testers, I’ll be able, by process of elimination to some extent, focus ONLY on the testers who fall into Family Finder haplogroup of my Moore cousins, or at least haplogroup close for Ancestry or 23andMe upload customers. In other words, I can eliminate the rest.

I can then ask the men with a similar haplogroup to my proven Moore cousins for more information, including whether they would be willing to take a Y DNA test.

  • Second, as soon as the Family Finder processing is complete, I will know that all male Family Finder matches and uploads from MyHeritage and Vitagene that have paid for the unlock will have haplogroups displayed on the Family Finder Match page. Therefore, if there’s a male Moore with no haplogroup, I can reach out to see where they tested and if a haplogroup has been assigned, even if it’s from Ancestry or 23andMe and isn’t displayed in Family Finder.

If so, and they share the haplogroup with me, I’ll be able to include or exclude them. If included, I can then ask if they would consider taking a Y DNA test.

  • Third, for lines I don’t yet have Y DNA testers for, I can now peruse my matches, and my cousins’ matches for that line. See items one and two, above. Even if they don’t reply or agree to Y DNA testing, at least now I have SOME haplogroup for that missing line.

Discover will help me flesh out the information I have, narrow regions, find projects, look at ancient DNA for hints, and more.

  • Fourth, the haplogroups themselves. I don’t know how many million tests FamilyTreeDNA has in their database, but if we assume that half of those are male, some percentage won’t have taken a Y DNA test at all. We’ll be able to obtain Y-DNA information for lines where there may be no other living descendant. I have at least one like that. He was the end of the surname line and is deceased, with no sons.

I’m literally ecstatic that I’ll be able to obtain at least something for that line. If it’s anything like my example Netherlands lineage, the Family Finder haplogroup may be able to point me to an important region of Europe – or maybe someplace else very unexpected.

The Bottom Line

Here’s the bottom line. You don’t know what you don’t know – and our ancestors are FULL of surprises.

I can’t even begin to tell you how MUCH I’m looking forward to this haplogroup rollout.

To prepare, I’m making a list of my genealogical lines:

  • If the paternal line, meaning surname line, is represented by any match in any database
  • If that line is represented by a known person in the FamilyTreeDNA database and by whom
  • If they or someone from that line has joined a surname or other FamilyTreeDNA project, and if so, which one
  • If they’ve taken a Y DNA test, and what kind – watch STR results for an updated haplogroup
  • If they’ve taken a Family Finder test – my cousin is a good example of a known individual whose kit I can watch for a new haplogroup
  • Old and new haplogroup, if applicable

If my only relative from that line is in another vendor’s database, I’ll ask if they will upload their file to FamilyTreeDNA – and explain why by sharing this article. (Feel free to do the same.) A Y DNA haplogroup is a good incentive, and I would be glad to pay for the unlock at FamilyTreeDNA for cousins who represent Y and mitochondrial DNA lines I don’t already have.

One way I sweeten the pie is to offer testing scholarships to select lines where I need either the Y DNA or mitochondrial DNA of relevant ancestors. It’s a good thing these haplogroups are being rolled out a few thousand at a time! I need to budget for all the scholarships I’ll want to offer.

I feel like I won the lottery, and FamilyTreeDNA is giving me a free haplogroup encyclopedia of information about my ancestors through my cousins – even those who haven’t taken Y DNA tests. I can’t even express how happy this makes me.

What lines do you want to discover more about, and what is your plan? Tests are on sale now if you need them!

_____________________________________________________________

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I receive a small contribution when you click on some of the links to vendors in my articles. This does NOT increase the price you pay but helps me to keep the lights on and this informational blog free for everyone. Please click on the links in the articles or to the vendors below if you are purchasing products or DNA testing.

Thank you so much.

DNA Purchases and Free Uploads

Genealogy Products and Services

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Holiday DNA Sales Are Here!!!

I apologize for the brevity of this posting, but I came home from the FamilyTreeDNA Conference this past weekend with “conference crud.”

I’ll catch you up on that great conference later, but sales won’t wait, and the holiday sales have already begun. This is a great time to order. These prices are the lowest ever.

MyHeritage

The MyHeritage autosomal test is only $36, and shipping is free if you order two or more DNA tests. That’s a GREAT deal. Click here to order.

If you’ve already tested elsewhere, you can upload your raw DNA file from that vendor to MyHeritage, here. I’ve provided step-by-step instructions, here. After you’ve uploaded, be sure to purchase the $29 unlock for advanced autosomal features, including the MyHeritage chromosome browser and Theories of Family Relativity, which shows you how you connect with DNA matches who share the same ancestor in MyHeritage’s collection of 52 million trees.

If you’re new to MyHeritage, you can also purchase a data or records subscription here, including a free trial.

I use this combination of DNA, trees, and tools almost daily and love that MyHeritage sends me regular record matches from their billions of genealogy records.

FamilyTreeDNA

Every test is on sale at FamilyTreeDNA.

As you know, FamilyTreeDNA provides Y-DNA, mitochondrial, and autosomal testing through their Family Finder test. They also accept autosomal DNA file uploads from Ancestry and MyHeritage. You’ll find easy download and upload instructions for each vendor, here. The advanced feature unlock is on sale now for just $9!

You can order each test individually or bundle tests for a better price.

Note that the introductory Y-DNA 37-marker test is available for $99, and can later be upgraded to the Big-Y test. However, the Big Y-700 is on sale for $399 which is a great price. Y-DNA testing unlocks your paternal ancestor’s history revealed in FamilyTreeDNA‘s world-class Discover tools.

If you’ve already tested at FamilyTreeDNA and would like to add another test for yourself or upgrade, say to the Big-Y test, just click here, sign on, and click on the Add Ons and Upgrade button in the upper right-hand corner.

I hope I’m not spilling the beans, but all sale prices, including upgrades and autosomal transfer unlocks, are shown below:

Genealogy Goals

The holidays are coming! Take a look at what you need for your genealogy.

I decided a long time ago it’s absolutely fine to “gift myself” with purchases and upgrades for my cousins. Especially the Big Y-700 at FamilyTreeDNA and the mitochondrial DNA test, which is vastly underutilized. This helps my genealogy immensely, as well as theirs. Most people are happy to swab, especially if you’re doing the genealogy work.

My goal is to:

  • Have the autosomal DNA of each of my family members and cousins in both databases that provide chromosome browsers so that I can confirm ancestors at FamilyTreeDNA and MyHeritage.
  • Find male cousins to test for the Y-DNA, the surname lineage of each of my ancestral lines. Males who descend paternally from each male ancestor can usually be tracked by their surname.
  • Mitochondrial DNA for each of my ancestors. For mitochondrial DNA testing, we need testers descended through all females from each female ancestor, although males in the current generation can test. Everyone has their mother’s direct matrilineal line mitochondrial DNA.

To find testing candidates for your lineages, check projects at FamilyTreeDNA, autosomal matches at all vendors, your ancestors at WikiTree, ThruLines at Ancestry, even though ThruLines is still having issues, and Theories of Family Relativity at MyHeritage.

With DNAtests on sale right now, this is a great time to purchase tests at MyHeritage and FamilyTreeDNA.

_____________________________________________________________

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Share the Love!

You’re always welcome to forward articles or links to friends and share on social media.

If you haven’t already subscribed (it’s free,) you can receive an email whenever I publish by clicking the “follow” button on the main blog page, here.

You Can Help Keep This Blog Free

I receive a small contribution when you click on some of the links to vendors in my articles. This does NOT increase your price but helps me keep the lights on, and this informational blog free for everyone. Please click on the links in the articles or to the vendors below if you are purchasing products or DNA testing.

Thank you so much.

DNA Purchases and Free Uploads

Genealogy Products and Services

My Book

Genealogy Books

Genealogy Research

Ancestry’s ThruLines Are a Hot Mess Right Now – But Here Are Some Great Alternatives

Right now, ThruLines at Ancestry is one hot mess.

Aside from the inherent frustration, especially over a holiday weekend when many people had planned to work on their genealogy, I’d like to say, “don’t panic.”

I don’t have any inside information about what’s going on at Ancestry, and I’ve attempted to make contact through their support page with no luck. They make talking to a person exceedingly difficult; plus, it’s a holiday weekend, and they are probably inundated.

Regardless, I have an idea of what is happening. Ancestry has been in the midst of recalculating “things,” perhaps in relation to their other changes, which I’ll write about separately in a few days.

In any event, Ancestry SURELY MUST KNOW there’s a significant problem because I imagine thousands of their customers are screaming right about now. Adding another voice won’t be helpful.

Symptoms

  • You may not have ThruLines at all.
  • If you do have ThruLines, don’t trust the information, or more to the point, don’t trust that it’s in any way complete.

I have two tests at Ancestry, both connected to different trees so that my matches and Thrulines are calculated separately for each test.

Test One

My first Ancestry test is connected to my primary tree. I’ve been amassing Thrulines cousins ever since the feature was released. I have hundreds of cousin matches descended from some of my more prolific ancestors.

Additionally, my sister’s grandchildren have tested, as have other close relatives who have connected their tests to their trees.

Today, those people are still showing on my match list, but are NOT showing as matches in ThruLines. None of them. Most of my ThruLines ancestors are showing zero matches, and the rest are only showing very few. Ancestors who had hundreds before now have 2, for example.

Here’s an example with my cousin, Erik.

My grandfather, William George Estes, shown in Erik’s tree, above, is his great-grandfather. Erik is my half first cousin, once removed, and we share 417 cM over 16 segments.

Yet, looking at my ThruLine for William George Estes, neither he nor my other cousins are shown as matches. Same for William George’s parents, and so forth.

ThruLines is VERY ill right now.

Test Two

My second DNA test at Ancestry is even worse. There are no ThruLines calculated, even though my DNA is tree-attached, and I had ThruLines previously.

I see this message now, and I can’t even begin to tell you how irritating this is – in part because it suggests the problem is my fault. It’s clearly not. My tree hasn’t changed one bit. I’m not alone, either. I’ve seen other people posting this same message.

And yes, if you’re thinking that there is absolutely no excuse for this – you’re right.

However, outrage isn’t good for us and won’t help – so let’s all do something else fun and productive instead.

Productive Genealogy Plans

Here are some productive suggestions.

At MyHeritage:

At FamilyTreeDNA:

  • Build your haplogroup pedigree chart by locating people through different companies descended from each ancestor in your tree through the appropriate line of descent, and see if they have or will take a Y-DNA or mtDNA test.
  • Tests are on sale right now, and there’s no subscription required at FamilyTreeDNA for anything.
  • Check Y-DNA and mtDNA tests to see if there are new matches and if you share a common ancestor.

At 23andMe:

  • Check for new matches and triangulation.
  • Check to see if 23andMe has added any of your new matches to your genetic tree.

Remember, the parental sides are typically accurate, but the exact placement may not be, and 23andMe deals poorly with half-relationships. It’s certainly still worth checking though, because 23andMe does a lot of heavy lifting for you.

DNAPainter

For me, the most productive thing to do this weekend would be to copy the segment information from new matches with whom I can identify common ancestors at FamilyTreeDNA, MyHeritage and 23andMe – the vendors who provide segment data – and paint those segments to DNAPainter.

Not only does DNAPainter allow me to consolidate my match data in one place, DNAPainter provides the ability for me to confirm ancestors through triangulation, and to assign unknown matches to ancestors as well.

As you can see, I’ve successfully assigned about 90% of my segments to an ancestor, meaning I’ve confirmed descent from that ancestor based on my autosomal matches’ descent from that same ancestor – preferably through another child. Will new matches propel me to 91%? I hope so.

What percentage can you or have you been able to assign?

If you need help getting started, or ideas, I’ve written about DNAPainter several times and provided a compiled resource library of those articles, here.

Have fun!!!

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Haplogroups: DNA SNPs Are Breadcrumbs – Follow Their Path

Recently a reader asked some great questions.

If Y-DNA is unchanged, then why isn’t the Y-DNA of every man the same today? And if it’s not the same, then how do we know that all men descend from Y-Adam? Are the scientists just guessing?

The scientists aren’t guessing, and the recent scientific innovations behind how this works is pretty amazing, so let’s unravel these questions one at a time.

The first thing we need to understand is how Y-DNA is inherited differently from autosomal DNA, and how it mutates.

First, a reminder that:

  • Y-DNA tests the Y chromosome passed from father to son in every generation, unmixed with any DNA of the mother. This article focuses on Y-DNA.
  • Mitochondrial DNA tests the mitochondria passed from mothers to all of their children, but is only passed on by the females, unmixed with the DNA of the father. This article also pertains to mitochondrial SNPS, but we will cover that more specifically later in another article.
  • Autosomal DNA is passed from both parents to their children. Each child inherits half of each parent’s autosomal DNA.

Let’s look at how this works.

Autosomal vs Y-DNA Inheritance

Click on image to enlarge

Autosomal DNA, shown here with the green (male) and pink (female) images, divides in each generation as it’s passed from the parent to their child. Each child inherits half of each parent’s autosomal DNA, meaning chromosomes 1-22. For this discussion, each descendant shown above is a male and has a Y chromosome.

This means that in the first generation, which would be the great-grandfather, about 700,000 locations of his green autosomal DNA are tested for genealogy purposes.

His female partner (pink) also has about 700,000 locations. During recombination, they each contribute about 350,000 SNPs (Single Nucleotide Polymorphisms) of autosomal DNA to their child. Their offspring then has a total of 700,000 SNPs, 350,000 green and 350,000 pink contributed by each parent.

This process is repeated for each child, whether male or female (with the exception of the X chromosome, which is beyond the scope of this article), but each child does not receive exactly the same half of their parents’ autosomal DNA. Recombination is random.

In the four generations shown above, the green autosomal DNA of generation one, the great-grandfather, has been divided and recombined three times. The original 700,000 locations of great-grandfather’s green DNA has now been whittled down to about 87,500 locations of his green DNA.

Y-DNA in the Same Generation

Looking now at the blue Y-DNA at left, the Y-DNA remains the same in each generation with the exception of one mutation approximately every two or three generations.

As you can see in the chart, in the exact same number of generations, the Y-DNA of each male, which he inherited from his father:

  • Never recombines with any DNA from the mother
  • Never divides and gets smaller in subsequent generations
  • Remains essentially unchanged in each generation

The key word here is “essentially.”

Y-DNA

The Y chromosome consists of about 59 million locations or SNPs of DNA. STR tests, Short Tandem Repeats, which are essentially insertions and deletions, test limited numbers of carefully curated markers selected for the fact that they mutate in a genealogically relevant timeframe. These markers are combined in panels of either 67 or 111 marker tests available for purchase at FamilyTreeDNA today, or historically 12, 25, 37, 67, and 111 marker panels. The STR test was the original Y-DNA test for genealogy and is still used as an introductory test or to see if a male matches a specific line, or not.

From the STR tests, in addition to matching, FamilyTreeDNA can reliably predict a relatively high-level haplogroup, or genetic clan, based on the frequency of the combinations of those marker values in specific STR locations.

SNPs are much more reliable than STRs, which tend to be comparatively unstable, mutating at an unreliable rate, and back mutating, which can be very disconcerting for genealogy. We need reliable consistency to be able to assign a male tester to a specific lineage with confidence. We can, however, find genealogically relevant matches that may be quite important, so I never disregard STR tests or testers. STR tests aren’t relevant for deeper history, nor can they reliably discern a specific lineage within a surname. SNP tests can and do.

The Big Y-700 SNP test gives us that and more, along with the earlier Big Y-500 test which scanned about 30 million locations. The Big Y-700 is a significant improvement; men can upgrade from the Big Y-500 or STR tests.

The Big Y-700 test scans about 50 million Y-DNA locations, known as the gold standard region, for all mutations. It reports 700 or more STR markers for matching, but more importantly, it scans for all SNP mutations in those 50 million locations.

All mutations are confirmed by at least five positive repeat scans and are then assigned a haplogroup name if found in two or more men.

Y-DNA Testing

If Y-DNA remained exactly the same, then the Y-DNA of men today would be entirely indistinguishable from each other – essentially all matching humankind’s first common ancestor. With no changes, Y-DNA would not be useful for genealogy. We need inherited mutations to be able to compare men and determine their level of relatedness to each other.

Fortunately, Y-DNA SNPs do mutate. Y-DNA is never divided or combined, so it stays essentially the same except for occasional mutations which are inherited by the following generations.

Using SNP markers scanned in the Big Y test, one new mutation happens on the average of every two or three generations. Of course, that means that sometimes there are no mutations for a few generations, and sometimes there are two mutations between father and son.

What this does, though, very effectively, is provide a trail of SNP mutations – breadcrumbs essentially – that we can use for matching, AND for tracking our mutations, which equate to ancestors, back in time.

Estes Male Breadcrumb Trail

I’ve tested several Estes men of known lineage, so I’m going to use this line as an example of how mutations act as breadcrumbs, allowing us to track our ancestors back in time and across the globe.

Multiple cousins in my Estes line have taken the Big Y-700 test.

My closest male cousin matches two other men on a unique mutation. That SNP has been named haplogroup R-ZS3700.

We know, based on our genealogy, that this mutation occurred in Virginia and is found in the sons of Moses Estes born in 1711.

How do we know that?

We know that because three of Moses’s descendants have tested and all three of those men have the same mutation, R-ZS3700, and none of the sons of Moses’s brothers have that mutation.

I’ve created a chart to illustrate the Estes pedigree chart, and the haplogroups assigned to those men. So, it’s a DNA pedigree chart too. This is exactly what the Big-Y DNA test does for us.

In the red-bordered block of testers, you can see the three men that all have R-ZS3700 (in red), and all are sons of Moses born in 1711. I have not typed the names of all the men in each generation because, for purposes of this illustration, names aren’t important. However, the concept and the fact that we have been able to connect them genealogically, either before or because of Y-DNA testing, is crucial.

Directly above Moses born in 1711, you can see his father Abraham born in 1647, along with Moses’ brothers at right and left; John, Richard, Sylvester, and Elisha whose descendants have taken the Big Y-700 test. Moses’s brothers’ descendants all have haplogroup R-BY490 (in blue), but NOT R-ZS3700. That tells us that the mutation responsible for R-ZS3700 happened between Abraham born in 1647, and Moses born in 1711. Otherwise, Moses’s brothers would have the mutation if his father had the mutation.

Moses’s descendants also have R-BY490, but it’s NOT the last SNP or haplogroup in their lineage. For Moses’s descendants, R-ZS3700 occurred after R-BY490.

You can see haplogroup R-BY490 boxed in blue.

We know that Moses and his father, Abraham, both have haplogroup R-BY490 because all of Abraham’s sons have this haplogroup. Additionally, we know that Abraham’s father, Silvester also had haplogroup R-BY490.

How do we know that?

Abraham’s brother, Richard’s descendant, tested and he has haplogroup R-BY490.

However, Silvester’s father, Robert born in 1555 did NOT have R-BY490, so it formed between him and his son, Silvester.

How do we know that?

Robert’s other son, Robert born in 1603 has a descendant who tested and has haplogroup R-BY482, but does NOT have R-BY490 or R-ZS3700.

All of the other Eates testers also have R-BY482, blocked in green, in addition to R-BY490, so we know that the mutation of R-BY490 developed between Robert born in 1555 and his son, Silvester born in 1600, because his other son’s descendant does not have it.

Looking at only the descent of the haplogroups, in order, we have

  • R-BY482 (green) found in Robert born in 1555 and all of his descendants.
  • R-BY490 (blue) found in Silvester born in 1600 and all of his descendants, but not his brother
  • R-ZS3700 (red) found in Moses born in 1711 and all of his descendants, but not his brothers

If we had Estes men who descend from the two additional documented generations upstream of Robert born in 1555, we might discover when R-BY482 occurred, but to date, we don’t have any additional testers from those lines.

Now that we understand the genesis of these three haplogroups in the Estes lineage, what else can we discover through our haplogroup breadcrumbs?

The Discover Reports

By entering the haplogroup in the Discover tool, either on the public page, here, or clicking on Discover on your personal page at FamilyTreeDNA if you’ve taken the Big-Y test, you will see several reports for your haplogroup.

I strongly suggest reviewing each category, because they cumulatively act as chapters to the book of your haplogroup story, but we’re going to skip directly to the breadcrumbs, which is called the Ancestral Path.

The Ancestral Path begins with your haplogroup in Line 1 then lists the first upstream or parent haplogroup in Line 2. In this case, the haplogroup I entered is R-ZS3700.

You can see the estimated age of the haplogroup, meaning when it formed, at about 1700 CE. Moses Estes who was born in 1711 is the first Estes man to carry haplogroup R-ZS3700, so that’s extremely close.

Line 2, R-BY490 occurred or was born about 1650, and we know that it actually occurred between Robert and Silvester born in 1600, so that’s close too.

Scanning down to Line 3, R-BY482 is estimated to have occurred about 1500 CE, and we know for sure it had occurred by 1555 when Robert was born.

We see the parent haplogroup of R-BY487 on Line 4, dating from about 750 CE. Of course, if more men test, it’s possible that more haplogroups will emerge between BY482 and BY487, forming a new branch. Given the time involved, those men wouldn’t be expected to carry the Estes surname, as surnames hadn’t yet been adopted in that timeframe.

Moving down to Line 9, we see R-ZP18 from 2250 BCE, or about 4250 years ago. Looking at the right column, there’s one ancient sample with that haplogroup. The location of ancient samples anchors haplogroups definitively in a particular location at a specific time.

Haplogroup by haplogroup, step by step, we can follow the breadcrumbs back in time to Y-Adam, the first homo sapiens male known to have descendants today, meaning he’s the MRCA, or most recent common ancestor for all men.

Neanderthals and Denisovans follow, but their Y-DNA is only available through ancient samples. They have no known direct male survivors, but someday, maybe someone will test and their Y-DNA will be found to descend from Neanderthals or Denisovans.

Now that we know when those haplogroups occurred, how did our ancestors get from Africa 232,000 years ago to Kent, England, in the 1400s? What path did they take?

The new Globetrekker tool answers that question.

The Breadcrumb Trail

In Globetrekker, each haplogroup’s location is placed by a combination of testers’ results, their identified earliest known ancestor (EKA) country and location, combined with ancient samples, climatic factors like glaciers and sea levels, and geographic features. You can read about Globetrekker here and here.

To view the Globetrekker tool, you must sign it to an account that has taken the Big Y test. It’s a tool exclusively provided for Big-Y testers.

You can click at the bottom of your Globetrekker map to play the animated video.

Beginning in Africa, our ancestors began their journey with Y-Adam, then migrated through the Near East, South Asia, East Asia, then west through central Asia into Europe. The Estes ancestors crossed the English Channel and migrated around what is now England before settling in Deal, on the east coast.

Clicking on any haplogroup provides a description of that haplogroup and how it was placed in that location.

Enabling the option for ancient DNA shows those locations as well, near the haplogroups they represent when the animation is playing.

Clicking on the shovel icon explains about that particular ancient DNA sample, what is known, and how it relates to the haplogroup it’s connected to by a dotted line on the map.

Pretty cool, huh!!

End to End

As you can see from this example, Big Y results are an end-to-end tool.

We can use the Big Y-700 haplogroups very successfully for recent genealogy – assigning testers to specific lines in a genealogy timeframe. Some haplogroups are so specific that, without additional information, we can place a man in his exact generation, or within a generation or two.

Not shown in my Estes pedigree chart is an adoptee with a different surname, of course. We know that he descends from Moses’s line because he carries haplogroup R-ZS3700, but we are still working on the more recent generations using autosomal DNA to connect him accurately.  If more of Moses’s descendants tested, we could probably place him very specifically. Without the Big Y-700 test, he wouldn’t know his biological surname or that he descends from Moses. That’s a HUGE breakthrough for him.

There’s more about the Estes line to learn, however.

If our Estes cousins tested their brothers, uncles or other Estes males in their line, they would likely receive a more refined haplogroup that’s relevant only to that line.

Using Big-Y test results, we can place men within a couple of generations and identify a common ancestor, even when all men within a haplogroup don’t know their genealogical lineage. Using those same test results, we can follow the breadcrumbs all 50 steps back in time more than 230,000 years to Y-Adam.

End to end, the Big-Y test coupled with breadcrumbs in Discover, Globetrekker, and other amazing tools is absolutely the most informative and powerful test available to male testers for their paternal line genealogy.

These amazing innovations tracking more than 50,000 haplogroups across the globe answer the original questions about how we know.

The more people who take or upgrade to the Big Y-700 test, the more haplogroup branches will be added, and the more refined the breadcrumbs, ages, and maps will become. In other words, there’s still more to learn.

Test if you haven’t, and check back often for new matches and breadcrumbs, aka updates.

_____________________________________________________________

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New Information About Philip Jacob Miller (c1726-1799) and Magdalena Possibly Rochette (c1730-1800/1808) – 52 Ancestors #404

I’ve written about Philip Jacob Miller and his wife, Magdalena, whose birth surname has been reported forever as Rochette.

One of the reasons I publish such extensive articles, including literally everything I know or can find about each ancestor, is to cast a trail of breadcrumbs. There’s always a chance that a future researcher will come across something new. I may or may not be here, but I really do want accurate information to outlive me.

Recently, that’s exactly what happened. Christine Berwanger, Ph. D., a descendant of Philip Jacob Miller and Magdalena through daughters Christena who married Henry Snell, and Hannah who married Arnold Snider, contacted me with information I did not previously have. I’m very grateful to both Christine and Doris Sullivan Bache, who Christine credits with doing a great deal of the original research back in the 1980s.

Doris, an avid researcher and descendant of Philip Jacob Miller and Magdalena through the Snider line passed away in 2009 and is memorialized here.

Thankfully, Doris shared with Christine, who shared with me and has graciously granted me permission to share with you.

Let’s start with Philip Jacob Miller’s estate packet.

Philip Jacob Miller’s Estate Packet

Christine said that Doris ordered Philip Jacob’s entire estate packet and sent her copies of receipts along with a letter in 1989.

From Christine’s May 2023 email to me:

An ancestor’s estate file provides perhaps the most complete picture we will have of his life. Hence, I include the transcribed inventory and settlement of Philip Jacob Miller’s worldly possessions, in addition to his generous bequeaths of land to his children and their families. Note the Bible. Also of interest, the descriptions of the animals, the smoothbore gun, and the coffee mill.

Note the large sum due from Col. Thomas Hart to the estate. Thomas Hart was a prominent merchant in Hagerstown, Maryland, and an associate of Daniel Boone, who removed to Lexington, Kentucky in 1794. He was the father-in-law of Henry Clay. Henry Snell purchased his Fleming County land from Hart[i] There was clearly a relationship with this prominent person and the Miller/Snell family.

Receipt No. 54, 22 Nov 1795[ii], includes payment for a trip to Annapolis, and a payment of 9.15.1 to Nathaniel Rochester – who was a close associate and partner of Col. Hart, Hagerstown Postmaster 1793-1803, Washington County Maryland Sheriff 1804-1806, the first president of the Hagerstown Bank founded in 1807, and founder of Rochester, New York.[iii]

Other prominent persons are named in the estate. Martin Baum, born in Hagerstown in 1765 and later mayor of Cincinnati, was a witness to:

Receipt No. 33, 20 Sep 1808[iv]

Received at Cincinnati Septr 20th 1808 of Abraham Miller one of the Administrators of Philip Jacob Millers Estate Twenty Dollars being part of my legacy of the said Estate In witness whereof I hereunto set my hand

                                               his

Martin Baum            Arnold      x    Snider

                                             Mark

The estate was a complex one: the inventory was conducted in Sep 1799, but the settlement was not completed until Sep 1808. Abraham, as Administrator, documented thirty-nine days travel back to Hagerstown, Maryland, three trips to Lexington, Kentucky, four days travel to Chillicothe, Ohio (state Capitol and location of a land office), four days to the Court in Newport, Kentucky, and four days showing the land to appraisers. He charged the estate $88.50 for travel and expenses. David Miller, as Administrator, spent eighteen days travelling to Lexington, eight days to Fleming County, fifteen days going to Court, two days to the Sheriff of Campbell County, recording a deed in Williamsburg, four days to Chillicothe, for expenses of $58.18 ¾. He also credited himself with $8 paid to his mother.[v] Abraham and David had families and farms and were active in their Brethren Church. These duties must have been onerous, yet they persisted.

Collecting debts owed to the estate involved several transactions. The estate paid Nicholas Rochester 5.7.6 for collecting $699 2/100. (The image clearly reads Nicholas; I have been unable to match a Nicholas Rochester. Nathaniel did not have a son or a brother by that name. If Nathaniel was meant, this is a different transaction than the one in 1795.) Surveyor General of the Virginia Military District and prominent landowner William Lytle signed a receipt pertaining to the debt owed the estate by Col Thomas Hart. Witness James Taylor was a prominent resident of Newport, Kentucky.

Receipt No. 55, 14 Apr 1800[vi]

Received of Daniel Miller by the hands of David Miller an order for Two hundred dollars on Colo Thomas Hart of Lexington Kentucky, which if accepted, is to be in full for the one hundred acres of land on which the said Daniel now lives as witness my hand this 14th of April 1800

Teste James Taylor                   Wm. Lytle

Summary, Life and Estate of Philip Jacob Miller:

Philip Jacob Miller was devoted to his family, his religion, his land, his community, and his country. He, in accordance with the principles of the German Baptist Brethren and other sects such as the Amish and Mennonites, chose to live a simple life. His estate inventory attests to that. Yet, he accrued wealth. He loaned money rather than spent it. He accrued enough to bequest each of his ten children 200 acres and further distributions from his estate.

He moved in the circles of the merchants and landowners of his time as well as the circles of his neighbors and co-religionists. His simple lifestyle did not mean he did not participate in the life of the broader community. Records attest that he did. We use our understanding of history to understand the context of the lives our ancestors lived; yet our ancestor’s lives influenced that history.

Mary Christine Berwanger

[1] Editor James F. Hopkins and Associate Editor Mary W. M. Hargreaves, editor, The Papers of Henry Clay. 2, The Rising statesman, 1815-1820 (Lexington, Kentucky: University Press of Kentucky, 1961).

2 Receipts, Estate of Philip Jacob Miller, Campbell County KY Estate Administration, Settlement Drawer 1817-1836, envelope 1828 (should be 1808), Alexandria, Kentucky. 22 Feb 1989, Doris S. Bache mailed to me a transcript of receipts No. 27 through No. 66, typed pages 7 through 13, mostly distributions from the estate to family beneficiaries. Pages 1 through 6 were not included, presumably because they did not pertain to family members. This was in the day of taking handwritten notes, typing them up, and going to the library to make copies to mail to other researchers.

3 Biography at Sheriff Nathaniel Rochester’s Records, Washington County, 1804-1806

http://www.whilbr.org/rochester/index.aspx

4 Receipt No. 33, Receipts, Estate of Philip Jacob Miller.

5 Receipt No. 66, Receipts, Estate of Philip Jacob Miller.

6 Receipt No. 55, Receipts, Estate of Philip Jacob Miller.

[i] Editor James F. Hopkins and Associate Editor Mary W. M. Hargreaves, editor, The Papers of Henry Clay. 2, The Rising statesman, 1815-1820 (Lexington, Kentucky: University Press of Kentucky, 1961).

[ii] Receipts, Estate of Philip Jacob Miller, Campbell County KY Estate Administration, Settlement Drawer 1817-1836, envelope 1828 (should be 1808), Alexandria, Kentucky. 22 Feb 1989, Doris S. Bache mailed to me a transcript of receipts No. 27 through No. 66, typed pages 7 through 13, mostly distributions from the estate to family beneficiaries. Pages 1 through 6 were not included, presumably because they did not pertain to family members. This was in the day of taking handwritten notes, typing them up, and going to the library to make copies to mail to other researchers.

[iii] Biography at Sheriff Nathaniel Rochester’s Records, Washington County, 1804-1806

http://www.whilbr.org/rochester/index.aspx

[iv] Receipt No. 33, Receipts, Estate of Philip Jacob Miller.

[v] Receipt No. 66, Receipts, Estate of Philip Jacob Miller.

[vi] Receipt No. 55, Receipts, Estate of Philip Jacob Miller.

Rochette

The source of Magdalena’s oft-reported surname as Rochette has baffled me and many other researchers for decades.

Christine, thanks to Doris, has been able to provide what is probably the original source for that surname. I’m saying it now, and I’ll say it again – this by no means proves that Magdalena’s surname was Rochette. It does, however, provide one more piece of evidence and an answer to the question of where that name came from.

From Christine:

Rochette – from a “loose paper in a family bible”

Click on the image to enlarge

This may be a copy of the “loose paper in a family bible.”

Doris S. Bache mentioned in her letter of 22 Feb 1989: “When I heard from Sharon Biggs in reference to the maiden name of Magdalena Miller, the name “Rochette” had come from a loose paper in a family bible. Author unknown, also. I am accepting the maiden name, but as you will note, most of the earlier information is incorrect, with the alternating of Phillip and Jacob in the generations before 1729. Of course, the name Morgan has been proven to be Maugens.” Doris is referring to the two pages above, taped together, which was included with her letter. She received this from Sharon Biggs.

Philip Jacob Miller married Magdalena Rochette, born in Sedan, France. Their children are listed (pencil checkmarks) with Abraham underlined. Both the name Rochette and the place Sedan, France are specific. If this is a copy of the loose paper from the bible, the (presumably) descendent who wrote it, knew the names of Philip and Magdalen’s children, so might indeed have known Magdalena’s surname and place of birth.

Sedan, France was a source of Huguenot refugees following the revocation of the Edict of Nantes in 1685.

French Huguenots relocated throughout Europe and to the Americas. It is possible that Magdalen’s family fled to Germany or America.

Philip Jacob Miller and Magdalena Rochette are apparently the Miller ancestors of the author. Listed below their names are the Maugans / Morgan ancestors: Conrad Morgan, said to be born in Virginia, and wife. Listed are some of their known children, with Katherine underlined. The wife named, “Margaret Mynne or Marie” does not match other sources, who give his wife as Anna Rebecca Hoffman (1739–1810).

Next, Abraham Miller, son of Philip Jacob and Magdalena, married Katherine Morgan, daughter of Conrad and wife. Their son Matthias Miller is underlined. He married Elizabeth Gorman. Their daughter Emma Miller (1849-1925) is underlined. She married Elihu T. Hedrick.

The paper comprises a direct line Ahnentafel from Emma Miller to her great-grandparents. The author of the paper is likely Emma herself or one of her children. It is certainly possible for a person to know from family history the names and origins of his or her great-grandparents. It is also possible for confusion on the part of the person writing down notes from memory.

Abraham Miller’s entry gives his birthdate and place as 28 Apr 1764 in Frederick County, Maryland, which agrees with the entry in Philip Jacob Miller’s Bible: “My son Abraham was born April 28, 1764.” Katherine Morgan his wife, was born 16 Jul 1767 in Frederick County. The note further states, “Their children were born in Clermont Co. Ohio, on bounty land given to Abraham Miller’s father by King George 2.” This statement is a confusion of time and place, but as with most oral history, there is some truth in it.

Abraham’s father, Philip Jacob Miller, intended each of his children to have a 200-acre parcel. Sons Abraham and David, as administrators of his estate, purchased 2000 acres, most in Virginia Military Survey 3790. The Virginia Military District was established as bounty land for Virginia Revolutionary soldiers. Often, they did not occupy the land but sold it to someone else. “Survey 3790, for Taylor, James et. al for Jacob Miller, C. C. [chain carrier], Jacob Snyder, C. C. [chain carrier], and Abraham Miller, M [marker]. With William Lytle, D. S. [Deputy Surveyor], and dates February 20, 1880 and June 9, 1802. These survey crews were comprised of: The D. S. Deputy Surveyor, C. C. chain carriers, and M. marker. The crews were often early settlers in the area.”  Hence Survey of 3790, from which Philip Jacob’s estate subsequently purchased 2000 acres of William Lytle, was in the Virginia Military District, hence bounty land. Abraham sold his 200-acre lot from his father’s estate to William Spence for $400, 22 Apr 1805. He instead resided in Clermont County, but I have not tracked his deeds.

In 1808, Abraham and David surveyed part of the Virginia Military District in Goshen Township, Clermont County, Survey 5959. “Abraham Miller was marker, David Miller was Chain Carrier.”

Perhaps land that Philip Jacob Miller’s father Michael Miller bought in Pennsylvania was originally granted by George the Second. I have not seen his Chester County deeds. Stinchcomb’s deed was in 1725, sold to Michael Miller et al in 1744. George II reigned from 1727-1760.

Summary, Questions, and Coincidences: This document records family history, and most of the information is verified by other sources.

The name Rochette and origin in Sedan, France is too specific to disregard out of hand, especially since this document existed prior to the Internet, when one could search a name and connect it to a person with no other evidence than the surname.

Coincidence?

There was a French Huguenot Rochet family from Sedan, France, and daughter Suzanne was smuggled out, married, and settled in Virginia.

“The most interesting story relating to the Huguenots of Manakin Town [Virginia] is that of Suzanne Rochet. After Revocation of Edict of Nantes in 1658, the refugee daughters of Moses Rochet wrote from Amsterdam to their father in France to send them their youngest sister, Suzanne. Since the French government was keeping strict watch to prevent the escape of Huguenots from the country, the Rochets always referred to Suzanne as “the Little Nightcap.” After several unsuccessful attempts to send his daughter past the Guards, Rochet finally smuggled her out of the country to Holland with the aid of a friendly ship-captain. In the French Church Amsterdam, Suzanne married July 1692 Abraham Michaux, a Huguenot refugee from Sedan. By 1705 they and their children had joined the colony at Manakin Town” [Virginia].

Source: “The Little Nightcap” by the Rev. W. Twyman Williams recorded here.

“At the same time, her sisters in Holland became very much concerned about her. They had found refuge in Amsterdam and wished to have her in safety there with them. So they wrote to their father, but for fear that the letter might be read by spies and informers, they did not refer to Suzanne. Instead, they asked their father to make every effort to send them “the little nightcap” they had left behind when they made their escape. But how? At last, Jean Rochet hit upon a plan. He found a ship’s captain.” “This man, though not a Huguenot, was kindly enough disposed to help. So Jean Rochet had his daughter set into a hogshead marked “merchandise,” fastened down the head of the large barrel, and hauled it to the ship. The captain had it taken aboard and stowed away. The ship was searched, but the hidden girl was not discovered. As soon as the danger of further search was over, the captain let her out of her uncomfortable hiding place and got her safely to Holland.”

This paper says Conrad Maugans / Morgan was born in Virginia. Some ancestry trees claim Magdalena Rochette was his sister. Is there any evidence that the Maugans were Huguenot? Or that they were in Virginia?

The name Rochette is sometimes given as LaRoche, which broadens the search possibilities.

French Huguenots went to Germany, and went to Pennsylvania, where they married into German families. It is possible that Philip Jacob Miller married a French woman, known to the family in Germany or met in Pennsylvania. “The French Element among the Pennsylvania Germans” should be understood before concluding that Philip Jacob Miller did not marry a French woman.

There is a German site dedicated to Huguenot genealogy, which contains the name Rochette.

Sources:

Alma A. Smith, The Virginia Military Surveys of Clermont and Hamilton Counties, Ohio 1787-1849 (Cincinnati, Ohio: A.A. Smith, 1985), p. 141, 20 Feb 1800.

 Alma A. Smith, The Virginia Military Surveys of Clermont and Hamilton Counties, Ohio 1787-1849, p. 174, 19 May 1808.

Excellent description of the connections and intermarriages of the French and Germans. George G. Struble, “The French Element among the Pennsylvania Germans” Pennsylvania History: A Journal of Mid-Atlantic Studies, Vol 22 (July 1955)pp, 267–76,  https://journals.psu.edu/phj/article/view/22432/22201.

Deutsche Hugenotten-Gesellschaft e.V., https://www.hugenotten.de/genealogie/arbeitsgemeinschaft-datenbank.php

Click to access 2018-08-namensliste-pro-gen.pdf

My Analysis

I’m incredibly grateful to Christine, Doris, and Sharon Biggs. I’m especially impressed that Christine can actually find a letter from 1989!

Let’s take a look at this information.

The analysis of Philip Jacob Miller’s estate packet brings his life into perspective in a new and different light. The information I had previously was a list of inventory items and a list of bills. Doris clearly possessed the entire packet that included receipts with additional information, not to mention the additional research into the identities of the various people mentioned in the estate settlement.

It appears that Philip Jacob was quite well-off later in his life. I can’t help but wonder if the fact that he reluctantly served in the Revolutionary War may have opened doors that allowed him to purchase the 2000 acres, providing a 200-acre farm to each of his children.

Let’s look at the information in that unsourced but clearly authentic Bible record.

Philip Jacob’s birth location is likely incorrect. Philip Jacob Miller’s parents were living in Krotelbach, Germany, when they were married in 1714, with their first child baptized the following year. In April of 1719, another son was baptized in Kallstadt. A third son was born on the farm by the name of Weilach near Bad Durkheim in April of 1721. There is absolutely nothing to indicate that the family settled in the Netherlands before immigrating to the US. Therefore, it’s highly unlikely that Philip Jacob was born in the Netherlands between 1723 and 1727.

The second questionable item from that Bible record involves Conrad Maugans, sometimes referred to as Morgan. This man was born around 1735 and was clearly German. It’s unlikely, but not impossible, that he was born in Virginia. It’s also very unlikely that Magdalena was his sister. Three of her children married Conrad’s children. David Miller married Conrad’s daughter Magdalene Maugans.  Additionally, her son Abraham Miller married Catherine Maugans. A third child, Esther Miller, married Gabriel Maugans. First-cousin marriages did occur in Brethren families so that alone does not rule out Magdalena and Conrad being siblings. However, it is interesting that she has no child named Conrad, nor do her children who did not marry his children.

I have found no evidence whatsoever to indicate that Philip Jacob’s wife, Magdalena, was a Maugans. I’ve seen that rumor for years as well.

I strongly suspect the confusion arose because Conrad’s daughter, Magdalene married a Miller and was therefore Magdalene Miller. Conrad’s will was written in German, but has been translated by an anonymous researcher.

Next, let’s do some math. We know that Magdalena Miller was born sometime around 1730, and that she and Philip Jacob Miller likely married in York County, PA, around 1750 but no later than July of 1751 based on the birth date of their first child. It’s also possible that they married in Lancaster Co., PA or Frederick Co., MD. Unfortunately, Brethren did not register their marriages.

Philip Jacob was Brethren, so she would have to have been Brethren too, or converted, in order for them to be married and remain within the church. What I do know, absolutely, positively, is that there is no Rochette surname of any family in any of these three counties in a relevant timeframe. Women in that time and place did NOT travel around without their family. If Magdalena was a Rochette, then where was her father or other family members?

Furthermore, if Magdalena was indeed the Suzanne Rochet, Huguenot from Sedan, she was born sometime around 1658 and married Abraham Michaux in 1692, so she clearly is not the Magdalena born around 1730. The “little nightcap” story, however, is lovely and excellent history all by itself.

There is some discussion that the Magdalena in question is Suzanne’s daughter, but then her surname would be Michaux, not Rochette.

I’m highly skeptical based on that, in addition to the fact that the Magdalena who married Philip Jacob had to have been Brethren, either before or certainly at the time of their marriage.

I’d feel a lot better about the Rochette surname and the Sedan location if the rest of that Bible information was accurate. Doris mentioned that she had found additional discrepancies.

Having said that, the information is very specific, including the Sedan location. Perhaps this information is not entirely wrong, just a generation or two offset?

If Magdalena’s surname was Rochette or something similar, I would expect to have at least a few DNA matches. I have MANY Miller matches from Philip Jacob’s father, Michael Miller, through is other children.

However, I don’t have matches to someone with the surname of Rochette, or similar, with two exceptions.

Unfortunately, at Ancestry, I can’t search by ancestor, so while I do have matches to people with Rochette in their trees, the ones I reviewed are Magdalena listed as Rochette. What I really need to do is be able to filter by Rochette matches not=Magdalena Rochette who is married to Philip Jacob Miller.

I did find a Rochette match at MyHeritage, but the match to this person could be through a different line. Another French match that could be helpful has a private tree, so no cigar there, either.

At FamilyTreeDNA, my mother’s matches to Rochette are only trees reflecting Magdalena as a Rochette.

I checked Filae and found nothing for a Magdalena Rochette of the right age, but Christine jumped right into serious research.

Christine’s French Huguenot Research

From Christine:

Note: Madeleine or Magdeleine are French versions of Magdalena.

The Huguenots were Calvinist Protestants, and their Reformed Churches recorded sacramental records.

“On October 18, 1685, the Edict of Nantes was revoked and French Huguenots could either convert to Catholicism, face life in a prison or convent, or flee the country. At this time, there were about 800,000 Huguenots in France, and nearly one-fourth of them left the country.”

French Reformed sacramental records are available from Sedan, Ardennes, France, from the 1500s and 1600s, indexed on FamilySearch (link here) but not (on FamilySearch) after the Edict of Nantes when the French Reformed Churches were suppressed. The baptism records which documented “the Little Nightcap” family are amazingly easy to read.

From these records and online ancestry or FamilySearch trees, this Sedan Rochette family included men who did not marry or die in Sedan (from these records) who might have moved elsewhere to become the grand-father, father, uncle of Magdalena / Madeleine. [Chart below is incomplete, not verified with original sources.]

Little Night Cap had a daughter Anne Madeleine. [I did not record all her children. Daughter Olive Judith married an Anthony Morgan, who does not seem to be related to the Maugans/ Morgans of the Miller lines.]

Little Night Cap is not the only Rochette woman to come to the New World [see Susanna daughter of Isaac] and it is likely some of the Rochette men came also. Having their baptismal dates and relationships from the Sedan records makes it more likely to match them to other men of the same name and age.

Did Magdalena/Madeleine’s family also leave before 1685? Did the Huguenots who remained in France continue to record their sacramental records? If so, where might those be?

They migrated to Protestant Countries, so in those places their later sacraments would have been recorded, such as in the Netherlands (cited in Little Night Cap’s family), parts of Germany, etc., and their churches in the New World. They did end up assimilating.

Descendancy Narrative of Moses Thiery Rochet

From Christine:

Moses Thiery1 ROCHET was born in 1615. He married Suzanne RONDEAU on 7 Feb 1638 at Sedan, Ardennes, France.1 He died on 31 Dec 1649.

Jean2 ROCHET was born in 1641 at Sedan, Ardennes, France. He married Marie TRUFET on 21 Dec 1664 at Sedan, Ardennes, France.2

Susan3 “Little Night Cap” ROCHET. Her married name was MICHAUX. She was baptized on 13 Apr 1667 at Sedan, Ardennes, France.3 She married Abraham MICHAUX on 13 Jul 1692 at Amsterdam, Netherlands. She immigrated on 8 May 1701 to London, England. She died on 18 Dec 1744 at Virginia at age 77.4

      1. Olive Judi4 MICHAUX married Anthony MORGAN. Her married name was MORGAN. She was born in 1706 at Virginia.5 She died on 27 Oct 1760 at Virginiia.6
      2. Anne Madeline4 MICHAUX was born in 1706 at Virginia. She died in 1796 at Virginia.

Isaac3 ROCHET died in 1672. He was baptized on 30 Aug 1672 at Sedan, Ardennes, France.7

Louis3 ROCHET was baptized on 5 May 1676 at Sedan, Ardennes, France.8 He died on 1 Oct 1726 at age 50.9

Daniel3 ROCHET was baptized on 5 Jan 1679 at Sedan, Ardennes, France.10

Jacques2 ROCHET was born in 1642. He died in 1647.

Isaac2 ROCHET was also known as Isaac DE LA ROQUET. He was born in 1641 at Sedan, Ardennes, France.11 He was baptized on 10 Jan 1644 at Sedan, Ardennes, France.12 He married Jeanne DUFRAY on 16 May 1666 at Reformed Protestant Church, Sedan, Ardennes, France. He married Jeanne DUFRAY on 16 May 1666 at Sedan, Ardennes, France.2 He died in Nov 1695 at age 51.

    1. Susanna3 ROCHET. Her married name was GARRIGUES. She was born in 1686 at Sedan, Ardennes, France.13 She married Matthieu GARRIGUES on 28 May 1702 at Netherlands. She died on 30 Sep 1746 at Philadelphia, Pennsylvania.14

Marie2 ROCHET was born on 22 Aug 1645.15 She died in 1763 at Sedan, Ardennes, France.

Vincent2 ROCHET was born on 18 Sep 1646.

Charles2 ROCHET was born on 29 Dec 1647.16 He died on 12 Jul 1670 at Sedan, Ardennes, France, at age 22.17

Printed on: 13 May 2023

Prepared by: Mary Christine Berwanger, Ph.D.

Endnotes:

  1. Ardennes: Sedan – Tables alphabétique des mariages, Ms 664/index, 1573-1682 family search.
  2. Ardennes: Sedan – Tables alphabétique des mariages, Ms 664/index, 1573-1682 familysearch.
  3. Name Susane Rochet
    Sex     Female
    Father’s Name     Jean Rochet
    Mother’s Name     Marie Trufet
    Event Baptism, 13 Apr 1667, Sedan, Ardennes, France
    “France, registres protestants, 1536-1897,” database with images, FamilySearch (https://familysearch.org/ark:/61903/1:1:QVN3-4BVH : 19 February 2021), Susane Rochet, 13 Apr 1667; citing Baptism, Societe de L’histoire du Protestantisme Francais (Society of the History of French Protestantism), Paris.
  4. Suzanne Laroche ROCHETTE (1667–1744)
    Birth 13 APR 1667 • Sedan, Ardennes, Champagne-Ardenne, France
    Death 18 DEC 1744 • Manakin Sabot, Goochland, Virginia, USA.
  5. Olive Judi Morgan (1706–1760) Birth 1706 • Manakin, Goochland County, Virginia, USA.
  6. Death 27 OCTOBER 1760 • Cumberland County, Virginia, USA.
  7. Name Isaac Rochet
    Sex     Male
    Father’s Name     Jean Rochet
    Mother’s Name     Marie Trufet
    Event    Baptism, 30 Aug 1672, Sedan, Ardennes, France.
  8. Name Louis Rochet
    Sex     Male
    Father’s Name     Jean Rochet
    Mother’s Name     Marie Truffet
    Event  Baptism 05 May 1676, Sedan, Ardennes, France.
  9. 1 October 1726.
  10. Christening • 1 Source 5 January 1679Sedan, Ardennes, Champagne-Ardenne, France.
  11. Isaac De La Roquet (Rochet) (1641–1695)
    Birth 1641 • Sedan, Ardennes, Champagne-Ardenne, France
    Death NOV 1695.
  12. 10 January 1644, familysearch.
  13. Birth 1686 • Sedan, Ardennes, Champagne-Ardenne, France.
  14. Death 30 SEP 1746 • Christ Church, Philadelphia, Pennsylvania, Colonial America.
  15. Birth 22 August 1645 Sedan, Ardennes, Champagne-Ardenne, France
    Death 1763 Sedan, France.
  16. 29 December 1647.
  17. 12 July 1670 Sedan, Ardennes, Champagne-Ardenne, France.

Rochette, or Not?

Combining the information provided by Christine and Doris along with additional research provides additional information but no smoking gun. The jury is still out. However, we now have additional information, including the probable source of the surname, Rochette.

At this point, I’m no more convinced that her surname was Rochette than I was before. I am, however, very grateful to have solved the mystery of where the Rochette rumor originated.

I’m hoping that some of the Miller researchers will be able to provide additional information about the source of the Bible or maybe even more about the source of Rochette.

I’m also VERY hopeful that someone will discover information about Magdalena’s origins. Or, perhaps someone has additional Rochette information that might be helpful. I was unable to find Rochette information in the relevant counties, but maybe other researchers have or can.

Just putting this out there and hoping that this update finds its way to the right researcher and that one day, we can actually solve the mystery of Magdalena’s parents.

However, we do have another clue…

Can DNA Help?

We have the mitochondrial DNA of Magdalena. Mitochondrial DNA is inherited from your mother through a direct line of females – so her mother, and her mother, on up the tree.

We know that Magdalena’s mitochondrial DNA is an exact match with a descendant of Mary Myers born February 8, 1775, in Pennsylvania and who died on September 28, 1849, in Montgomery County, Ohio. Unfortunately, we don’t know who Mary Myer’s parents were. Maybe one of you descends from this line or has information about the Myers family. Also spelled Meyers, Moyers.

Of course, mitochondrial DNA can reach far back in time, but the migration path from Pennsylvania to Montgomery County, Ohio, is the path the Brethren took to settle that region, and is where Magdalena’s descendant lives who tested. Montgomery County was the dispersion point for the Brethren North into Indiana and westward as well.

Another mitochondrial match also connects to the Zircle/Meyer family in Rockingham/Augusta County, VA where several Brethren families settled about the time of the Revolutionary War. These families originated in the Lancaster/York County, PA region or the Frederick County, MD region.

Tracking a match back to the earliest ancestor, I found that Peter Zirkle (c1745-c1818)’s wife’s name was “Fanny” and she is reported to be Frene “Fannie” Meyer. I have found several attributions, but no place can I find how the Meyer surname was attributed to her, or who here parents were. Assuming Fanny was born about 1745 as well, Magdalena born about 1730 could have been her sister or maybe a cousin.

Meyer/Moyer is noted as one of the founding Brethren families in York County, PA where Philip Jacob Miller was living when he married. It’s VERY likely that he married within the Brethren families.

The History of York Co, PA, written in 1907 tells us that the first Brethren congregation in York (now Adams) County was the Conewago Church which was established in 1738, “20 miles west from the town of York, on the Little Conewago,” which was in the vicinity of Hanover.

Surnames of the families who were among the early church members were Eldrick, Dierdorff, Bigler, Gripe (Cripe), Studsman (Stutzman) and others.

Prominent members include Jacob Moyer, James Henrick, preachers; Hans Adam Snyder, George Wine, Daniel Woods, Henry Geing, Joseph Moyer, Nicholas Hostetter, Christian Hostetter, Rudy Brown, Dobis Brother, Jacob Miller, Michael Koutz, Stephen Peter, Henry Tanner, Michael Tanner, John Moyer, Jacob Souder, Henry Hoff, John Swartz.  The wives of these persons named were also members of the church.

Unmarried members were Barbara Snyder John Geing, Maud Bowser, George Peter, Hester Wise, Christian Etter, John Peter Weaver, Barbara Bear, Elizabeth Boering, Grace Hymen. Their first preacher was Daniel Leatherman, Sr, followed by Nicholas Martin, Jacob Moyer (Meyers) and James Hendrich (Henry.)

In 1741, a new church was founded “on the Great Conewago, about 14 miles west from the new town of York.”  Founding members there include John Neagley, Adam Sower, Jacob Sweigard, Peter Neiper and Joseph Latshaw. The first elder was George Adam Martin followed by Daniel Leatherman Jr. and Nicholas Martin. In 1770 members included George Brown, John Heiner, Peter Fox, Anthony Dierdorff, Nicholas Moyer, Manasseh Brough, Michael Bosserman, David Ehrhard, Daniel Baker, Abraham Stauffer, Henry Dierdorff, John Burkholder, Andrew Trimmer, Eastace Rensel, Peter Dierdorff, Barnett Augenbaugh, John Neagley, Michael Brissel, Welty Brissel, Matthias Bouser, Laurence Baker, Philip Snell, Nicholas Baker Jr., Adam Sower, Adam Dick, Henry Brissel, David Brissel, Henry Radibush, George Wagner and George Reeson.  Unmarried members were Peter Wertz, Ann Mummert, Christian Fray, Samuel Arnold, Mary Latshaw, Catharine Studabaker, Nicholas Baker, Marillas Baker, Sarah Brissel, Jacob Miller, Rudolph Brown.

Can anyone tell me what happened to the Moyer men listed above?

  • Jacob Moyer
  • Joseph Moyer
  • John Moyer
  • Nicholas Moyer

Are they related? Who is their father? Who were their wives?  And perhaps more importantly, did they have a sibling or child, Magdalena, born about 1730?

Does anyone know if any of these men wound up in Rockingham County, VA by 1773 or so?

Please reach out if you descend from these families, and especially if you descend from these families through all females to the current generation, which can be male or female. If you do, you carry the mitochondrial DNA of their wife and daughters. Please reach out to me.

Do You Descend from a Brethren Female Line?

Do you descend matrilineally from a Brethren female line, meaning through all females beginning with your mother? If so, your mitochondrial DNA descends from a Brethren family.

If you have already taken the mitochondrial DNA test at FamilyTreeDNA, please join the Miller-Brethren DNA project. If you have not tested, please order a mitochondrial DNA test, here, and join the Miller Brethren DNA Project.

Based on the Brethren cultural handicap of not registering marriages, mitochondrial DNA testing is critically important. It provides the tools to identify and place Brethren females with their families. DNA, in this case, promises to do what traditional genealogy cannot.

_____________________________________________________________

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Which DNA Test Should I Buy? And Why?

Which DNA test should I buy, and why?

I receive questions like this often. As a reminder, I don’t take private clients anymore, which means I don’t provide this type of individual consulting or advice. However, I’m doing the next best thing! In this article, I’m sharing the step-by-step process that I utilize to evaluate these questions so you can use the process too.

It’s important to know what questions to ask and how to evaluate each situation to arrive at the best answer for each person.

Here’s the question I received from someone I’ll call John. I’ve modified the wording slightly and changed the names for privacy.

I’m a male, and my mother was born in Charleston, SC. My maternal grandmother’s maiden name was Jones and a paternal surname was Davis. The family was supposed to have been Black, Dutch, Pennsylvania Dutch, and Scots-Irish…only once was I told I was 3/16 Indian, with Davis being 3/4 and Jones being full Indian.

Do I have enough reasonable information to buy a test, and which one?

Please note that it’s common for questions to arrive without all the information you need to provide a sound answer – so it’s up to you to ask those questions and obtain clarification.

Multiple Questions

There are actually multiple questions here, so let me parse this a bit.

  1. John never mentioned what his testing goal was.
  2. He also never exactly said how the paternal line of Davis was connected, so I’ve made an assumption. For educational purposes, it doesn’t matter because we’re going to walk through the evaluation process, which is the same regardless.
  3. John did not include a tree or a link to a tree, so I created a rudimentary tree to sort through this. I need the visuals and normally just sketch it out on paper quickly.
  4. Does John have enough information to purchase a test?
  5. If so, which test?

There is no “one size fits all” answer, so let’s discuss these one by one.

Easy Answers First

The answer to #4 is easy.

Anyone with any amount of information can purchase a DNA test. Adoptees do it all the time, and they have no prior information.

So, yes, John can purchase a test.

The more difficult question is which test, because that answer depends on John’s goals and whether he’s just looking for some quick information or really wants to delve into genealogy and learn. Neither approach is wrong.

Many people think they want a quick answer –  and then quickly figure out that they really want to know much more about their ancestors.

I wrote an article titled DNA Results – First Glances at Ethnicity and Matching for new testers, here.

Goals

Based on what John said, I’m going to presume his goals are probably:

  • To prove or disprove the family oral history of Black, Dutch, Pennsylvania Dutch (which is actually German,) Scots-Irish, and potentially Native American.
  • John didn’t mention actual genealogy, which would include DNA matches and trees, so we will count that as something John is interested in secondarily. However, he may need genealogy records to reach his primary goal.

If you’re thinking, “The process of answering this seemingly easy question is more complex than I thought,” you’d be right.

Ethnicity in General

It sounds like John is interested in ethnicity testing. Lots of people think that “the answer” will be found there – and sometimes they are right. Often not so much. It depends.

The great news is that John really doesn’t need any information at all to take an autosomal DNA test, and it doesn’t matter if the test-taker is male or female.

To calculate each tester’s ethnicity, every testing company compiles their own reference populations, and John will receive different results at each of the major companies. Each company updates their ethnicity results from time to time as well, and they will change.

Additionally, each company provides different tools for their customers.

The ethnicity results at different companies generally won’t match each other exactly, and sometimes the populations look quite different.

Normally, DNA from a specific ancestor can be found for at least 5 or 6 generations. Of course, that means their DNA, along with the DNA from all of your other ancestors is essentially combined in a communal genetic “pot” of your chromosomes, and the DNA testing company needs to sort it out and analyze your DNA for ethnicity.

DNA descended from ancestors, and their populations, further back in people’s trees may not be discerned at all using autosomal DNA tests.

A much more specific “ethnicity” can be obtained for both the Y-DNA line, which is a direct patrilineal line for men (blue arrow,) and the mitochondrial DNA line (pink arrows,) which is a direct matrilineal line for everyone, using those specific tests.

We will discuss both of those tests after we talk about the autosomal tests available from the four major genealogy DNA testing companies. All of these tools can and should be used together.

Let’s Start with Native American

Let’s evaluate the information that John provided.

John was told that he “was 3/16 Indian, with Davis being 3/4 and Jones being full Indian.”

We need to evaluate this part of his question slightly differently.

I discussed this in the article, Ancestral DNA Percentages – How Much of Them is in You?

First, we need to convert generations to 16ths.

You have two ancestors in your parent’s generation, four in your grandparents, and so forth. You have 16 great-great-grandparents. So, if John was 3/16th Native, then three of his great-great-grandparents would have been fully Native, or an equivalent percentage. In other words, six ancestors in that generation could have been half-Native. Based on what John said, they would have come from his mother’s side of the tree. John is fortunate to have that much information to work with.

He told us enough about his tree that we can evaluate the statement that he might be 3/16ths Native.

Here’s the tree I quickly assembled in a spreadsheet based on John’s information.

His father, at left, is not part of the equation based on the information John provided.

On his mother’s side, John said that Grandfather Davis is supposed to be three-quarters Native, which translates to 12/16ths. Please note that it would be extremely beneficial to find a Y-DNA tester from his Davis line, like one of his mother’s brothers, for example.

John said that his Grandmother Jones is supposed to be 100% Native, so 16/16ths.

Added together, those sum to 28/32, which reduces down to 14/16th or 7/8th for John’s mother.

John would have received half of his autosomal DNA from his mother and half from his non-Native father. That means that if John’s father is 100% non-Native, John would be half of 14/16ths or 7/16ths, so just shy of half Native.

Of course, we know that we don’t always receive exactly 50% of each of our ancestors’ DNA (except for our parents,) but we would expect to see something in the ballpark of 40-45% Native for John if his grandmother was 100% Native and his grandfather was 75%.

Using simple logic here, for John’s grandmother to be 100% Native, she would almost assuredly have been a registered tribal member, and the same if his grandfather was 75% Native. I would think that information would be readily available and well-known to the family – so I doubt that this percentage is accurate. It would be easy to check, though, on various census records during their lifetimes where they would likely have been recorded as “Indian.” They might have been in the special “Indian Census” taken and might be living on a reservation.

It should also be relatively easy to find their parents since all family members were listed every ten years in the US beginning with the 1850 census.

The simple answer is that if John’s grandparents had as much Native as reported, he would be more than 3/16th – so both of these factoids cannot simultaneously be accurate. But that does NOT mean neither is accurate.

John could be 7/8th or 40ish%, 3/16th or 18ish%, or some other percentage. Sometimes, where there is smoke, there is fire. And that seems to be the quandary John is seeking to resolve.

Would  Ethnicity/Population Tests Show This Much Native?

Any of the four major testing companies would show Native for someone whose percentage would be in the 40% or 18% ballpark.

The easiest ethnicities to tell apart from one another are continental-level populations. John also stated that he thinks he may also have Black ancestry, plus Dutch, Pennsylvania Dutch (German), and Scots-Irish. It’s certainly possible to verify that using genealogy, but what can DNA testing alone tell us?

How far back can we expect to find ethnicities descending from particular ancestors?

In this table, you can see at each generation how many ancestors you have in that generation, plus the percentage of DNA, on average, you would inherit from each ancestor.

All of the major DNA testing companies can potentially pick up small trace percentages, but they don’t always. Sometimes one company does, and another doesn’t. So, if John has one sixth-generation Native American ancestor, he would carry about 1.56% Native DNA, if any.

  • Sometimes a specific ethnicity is not found because, thanks to random recombination, you didn’t inherit any of that DNA from those ancestors. This is why testing your parents, grandparents, aunts, uncles, and siblings can be very important. They share your same ancestors and may have inherited DNA that you didn’t that’s very relevant to your search.
  • Sometimes it’s not found because the reference populations and algorithms at that testing company aren’t able to detect that population or identify it accurately, especially at trace levels. Every DNA testing company establishes their own reference populations and writes internal, proprietary ethnicity analysis algorithms.
  • Sometimes it’s not found because your ancestor wasn’t Native or from that specific population.
  • Sometimes it’s there, but your population is called something you don’t expect.

For example, you may find Scandinavian when your ancestor was from England or Ireland. The Vikings raided the British Isles, so while some small amount of Scandinavian is not what you expect, that doesn’t mean it‘s wrong. However, if all of your family is from England, it’s not reasonable to have entirely Scandinavian ethnicity results.

It’s also less likely as each generation passes by that the information about their origins gets handed down accurately to following generations. Most non-genealogists don’t know the names of their great-grandparents, let alone where their ancestors were from.

Using a 25-year average generation length, by the 4th generation, shown in the chart above, you have 16 ancestors who lived approximately 100 years before your parents were born, so someplace in the mid-1800s. It’s unlikely for oral history from that time to survive intact. It’s even less likely from a century years earlier, where in the 7th generation, you have 128 total ancestors.

The best way to validate the accuracy of your ethnicity estimates is by researching your genealogy. Of course, you need to take an ethnicity test, or two, in order to have results to validate.

Ethnicity has a lot more to offer than just percentages.

Best Autosomal Tests for Native Ethnicity

Based on my experience with people who have confirmed Native ancestry, the two best tests to detect Native American ethnicity, especially in smaller percentages, are both FamilyTreeDNA and 23andMe.

Click images to enlarge

In addition to percentages, both 23andMe and FamilyTreeDNA provide chromosome painting for ethnicity, along with segment information in download files. In other words, they literally paint your ethnicity results on your chromosomes.

They then provide you with a file with the “addresses” of those ethnicities on your chromosomes, which means you can figure out which ancestors contributed those ethnicity segments.

The person in the example above, a tester at FamilyTreeDNA, is highly admixed with ancestors from European regions, African regions and Native people from South America.

Trace amounts of Native American with a majority of European heritage would appear more like this.

You can use this information to paint your chromosome segments at DNAPainter, along with your matching segments to other testers where you can identify your common ancestors. This is why providing trees is critically important – DNA plus ancestor identification with our matches is how we confirm our ancestry.

This combination allows you to identify which Native (or another ethnicity) segments descended from which ancestors. I was able to determine which ancestor provided that pink Native American segment on chromosome 1 on my mother’s side.

I’ve provided instructions for painting ethnicity segments to identify their origins in specific ancestors, here.

Autosomal and Genealogy

You may have noticed that we’ve now drifted into the genealogy realm of autosomal DNA testing. Ethnicity is nice, but if you want to know who those segments came from, you’ll need:

  • Autosomal test matching to other people
  • To identify your common ancestor with as many matches as you can
  • To match at a company who provides you with segment information for each match
  • To work with DNAPainter, which is very easy

The great news is that you can do all of that using the autosomal tests you took for ethnicity, except at Ancestry who does not provide segment information.

Best Autosomal Test for Matching Other Testers

The best autosomal test for matching may be different for everyone. Let’s look at some of the differentiators and considerations.

If you’re basing a testing recommendation solely on database size, which will probably correlate to more matches, then the DNA testing vendors fall into this order:

If you’re basing that recommendation on the BEST, generally meaning the closest matches for you, there’s no way of knowing ahead of time. At each of the four DNA testing companies, I have very good matches who have not tested elsewhere. If I weren’t in all four databases, I would have missed many valuable matches.

If you’re basing that recommendation on which vendor began testing earliest, meaning they have many tests from people who are now deceased, so you won’t find their autosomal tests in other databases that don’t accept uploads, the recommended testing company order would be:

If you’re basing that recommendation on matches to people who live in other countries, the order would be:

Ancestry and 23andMe are very distant third/fourth because they did not sell widely outside the US initially and still don’t sell in as many countries as the others, meaning their testers’ geography is more limited. However, Ancestry is also prevalent in the UK.

If you’re basing that recommendation on segment information and advanced tools that allow you to triangulate and confirm your genetic link to specific ancestors, the order would be:

Ancestry does NOT provide any segment information.

If you’re basing that recommendation on unique tools provided by each vendor, every vendor has something very beneficial that the others don’t.

In other words, there’s really no clear-cut answer for which single autosomal DNA test to order. The real answer is to be sure you’re fishing in all the ponds. The fish are not the same. Unique people test at each of those companies daily who will never be found in the other databases.

Test at or upload your DNA to all four DNA testing companies, plus GEDmatch. Step-by-step instructions for downloading your raw data file and uploading it to the DNA testing companies who accept uploads can be found, here.

Test or Upload

Not all testing companies accept uploads of raw autosomal DNA data files from other companies. The good news is that some do, and it’s free to upload and receive matches.

Two major DNA testing companies DO NOT accept uploads from other companies. In other words, you have to test at that company:

Two testing companies DO accept uploads from the other three companies. Uploads and matching are free, and advanced features can be unlocked very cost effectively.

  • FamilyTreeDNA – free matching and $19 unlock for advanced features
  • MyHeritage – free matching and $29 unlock.for advanced features

I recommend testing at both 23andMe and Ancestry and uploading one of those files to both FamilyTreeDNA and MyHeritage, then purchasing the respective unlocks.

GEDmatch

GEDmatch is a third-party matching site, not a DNA testing company. Consider uploading to GEDmatch because you may find matches from Ancestry who have uploaded to GEDmatch, giving you access to matching segment information.

Other Types of DNA

John provided additional information that may prove to be VERY useful. Both Y-DNA and mitochondrial DNA can be tested as well and may prove to be more useful than autosomal to positively identify the origins of those two specific lines.

Let’s assume that John takes an autosomal test and discovers that indeed, the 3/16th Native estimate was close. 3/16th equates to about 18% Native which would mean that three of his 16 great-great-grandparents were Native.

John told us that his Grandmother Jones was supposed to be 100% Native.

At the great-great-grandparent level, John has 16 ancestors, so eight on his mother’s side, four from maternal grandmother Jones and four from his maternal grandfather Davis.

John carries the mitochondrial DNA of his mother (red boxes and arrows,) and her mother, through a direct line of females back in time. John also carries the Y-DNA of his father (dark blue box, at left above, and blue arrows below.)

Unlike autosomal DNA which is admixed in every generation, mitochondrial DNA (red arrows) is inherited from that direct matrilineal line ONLY and never combines with the DNA of the father. Mothers give their mitochondrial DNA to both sexes of their children, but men never contribute their mitochondrial DNA to offspring. Everyone has their mother’s mitochondrial DNA.

Because it never recombines with DNA from the father, so is never “watered down,” we can “see” much further back in time, even though we can’t yet identify those ancestors.

However, more importantly, in this situation, John can test his own mitochondrial DNA that he inherited from his mother, who inherited it from her mother, to view her direct matrilineal line.

John’s mitochondrial DNA haplogroup that will be assigned during testing tells us unquestionably whether or not his direct matrilineal ancestor was Native on her mother’s line, or not. If not, it may well tell us where that specific line originated.

You can view the countries around the world where Y-DNA haplogroups are found, here, and mitochondrial haplogroups, here.

If John’s mitochondrial DNA haplogroup is Native, that confirms that one specific line is Native. If he can find other testers in his various lines to test either their Y-DNA or mitochondrial DNA, John can determine if other ancestors were Native too. If not, those tests will reveal the origins of that line, separate from the rest of his genealogical lines.

Although John didn’t mention his father’s line, if he takes a Y-DNA test, especially at the Big Y-700 level, that will also reveal the origins of his direct paternal line. Y-DNA doesn’t combine with the other parent’s DNA either, so it reaches far back in time too.

Y-DNA and mitochondrial DNA tests are laser-focused on one line each, and only one line. You don’t have to try to sort it out of the ethnicity “pot,” wondering which ancestor was or was not Native.

My Recommendation

When putting together a testing strategy, I recommend taking advantage of free uploads and inexpensive unlocks when possible.

  • To confirm Native American ancestry via ethnicity testing, I recommend testing at 23andMe and uploading to FamilyTreeDNA, then purchasing the $19 unlock. The free upload and $19 unlock are less expensive than testing there directly.
  • For matching, I recommend testing at Ancestry and uploading to MyHeritage, then unlocking the MyHeritage advanced features for $29, which is less expensive than retesting. Ancestry does not provide segment information, but MyHeritage (and the others) do.

At this point, John will have taken two DNA tests, but is now in all four databases, plus GEDmatch if he uploads there.

  • For genealogy research on John’s lines to determine whether or not his mother’s lines were Native, I recommend an Ancestry and a MyHeritage records subscription, plus using WikiTree, which is free.
  • To determine if John’s mother’s direct matrilineal female line was Native, I recommend that John order the mitochondrial DNA test at FamilyTreeDNA.
  • When ordering multiple tests, or uploading at FamilyTreeDNA, be sure to upload/order all of one person’s tests on the same DNA kit so that those results can be used in combination with each other.

Both males and females can take autosomal and mitochondrial DNA tests.

  • To discover what he doesn’t know about his direct paternal, meaning John’s surname line – I recommend the Big Y-700 test at FamilyTreeDNA.

Only males can take a Y-DNA test, so women would need to ask their father, brother, or paternal uncle, for example, to test their direct paternal line.

  • If John can find a male Davis from his mother’s line, I recommend that he purchase the Big Y-700 test at FamilyTreeDNA for that person, or check to see if someone from his Davis line may have already tested by viewing the Davis DNA Project. Like with mitochondrial DNA, the Y-DNA haplogroup will tell John the origins of his direct Davis male ancestor – plus matching of course. He will be able to determine if they were Native, and if not, discover the origins of the Davis line.
  • For assigning segments to ancestors and triangulating to confirm descent from a common ancestor, I recommend 23andMe, MyHeritage, FamilyTreeDNA and GEDmatch, paired with DNAPainter as a tool.

Shopping and Research List

Here are the tests and links recommended above:

More Than He Asked

I realize this answer is way more than John expected or even knew to ask. That’s because there is often no “one” or “one best” answer. There are many ways to approach the question after the goal is defined, and the first “answer” received may be a bit out of context.

For example, let’s say John has 2% Native ancestry and took a test at a vendor who didn’t detect it. John would believe he had none. But a different vendor might find that 2%. If it’s on his mother’s direct matrilineal line, mitochondrial DNA testing will confirm, or refute Native, beyond any doubt, regardless of autosomal ethnicity results – but only for that specific ancestral line.

Autosomal DNA can suggest Native across all your DNA, but Y-DNA and mitochondrial DNA confirm it for each individual ancestor.

Even when autosomal testing does NOT show Native American, or African, for example, it’s certainly possible that it’s just too far back in time or has not been passed down during random recombination, but either Y-DNA or mitochondrial DNA will unquestionably confirm (or refute) the ancestry in question if the right person is tested.

This is exactly why I attempt to find a cousin who descends appropriately from every ancestor and provide testing scholarships. It’s important to obtain Y-DNA and mitochondrial DNA information for each ancestor.

Which Test Should I Order?

What steps will help you decide which test or tests to take?

  1. Define your testing goal.
  2. Determine if your Y-DNA or mitochondrial DNA will help answer the question.
  3. Determine if you need to find ancestors another generation or two back in time to get the most benefit from DNA testing. In our example, if John discovered that both of his grandparents were enrolled tribal members, that’s huge, and the tribe might have additional information about his family.
  4. Subscribe to Ancestry and MyHeritage records collections as appropriate to perform genealogical research. Additional information not only provides context for your family, it also provides you with the ability to confirm or better understand your ethnicity results.
  5. Extend your tree so that you can obtain the best results from the three vendors who support trees; Ancestry, FamilyTreeDNA, and MyHeritage. All three use trees combined with DNA tests to provide you with additional information.
  6. Order 23andMe and Ancestry autosomal DNA tests.
  7. Either test at or upload one of those tests to MyHeritage, FamilyTreeDNA, and GEDmatch.
  8. If a male, order the Big Y-700 DNA test. Or, find a male from your ancestral line who has taken or will take that test. I always offer a testing scholarship and, of course, share the exciting results!
  9. Order a mitochondrial DNA test for yourself and for appropriately descended family members to represent other ancestors. Remember that your father (and his siblings) all carry your paternal grandmother’s mitochondrial DNA. That’s often a good place to start after testing your own DNA.
  10. If your parents or grandparents are alive, or aunts and uncles, test their autosomal DNA too. They are (at least) one generation closer to your ancestors than you are and will carry more of your ancestors’ DNA.
  11. Your siblings will carry some of your ancestors’ DNA that you do not, so test them too if both of your parents aren’t available for testing.

Enjoy!!!

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Comparing DNA Results – Different Tests at the Same Testing Company

Several people have asked about different tests at the same DNA testing company. They wondered if matching is affected, meaning whether your matches are different if you have two different tests at the same company. Specifically, they asked if you are better off purchasing a test AT a DNA testing vendor that allows uploads, rather than uploading a test from a different vendor. Does it make a difference to the tester or their matches? Do they have the same matches?

These are great questions, and the answer isn’t conclusive. It varies based on several factors.

Having multiple tests at the same DNA testing company can occur in three ways:

  • The same person tests twice at the same DNA testing company.
  • The same person tests once at the DNA testing company and uploads a test from a different testing company. Only two of the primary four DNA testing companies accept uploads from other vendors – FamilyTreeDNA and MyHeritage.
  • The same person uploads two different files from other DNA testing companies to the DNA testing company in question. For example, the DNA company could be FamilyTreeDNA and the two uploaded DNA files could be from either MyHeritage, 23andMe or Ancestry.

All DNA testing companies allow users to download their raw DNA data files. This enables the tester to upload their DNA file to the vendors who accept uploaded files. Both FamilyTreeDNA and MyHeritage provide matching for free, but advanced tools require a small unlock fee of $19 and $29, respectively.

Testing Company Accepts Uploads from Other Companies Download Upload Instructions
23andMe No Instructions here
Ancestry No Instructions here
FamilyTreeDNA Yes, some Instructions here
MyHeritage Yes, some Instructions here

I wrote about developing a DNA testing and transfer/upload strategy, here, and about which companies accept which tests, here.

Not all DNA files are created equal. Therefore, not all files from vendors are compatible with other vendors for various reasons.

Multiple Tests at the Same DNA Testing Company

I have at least two tests at each of the four major vendors. I did this for research purposes, meaning to write articles to share with you.

If you actually test twice at a vendor, meaning purchase two separate tests and take them yourself, you will have two test results at that testing company. At some companies, specifically 23andMe, if you purchase a new test through their “upgrade” procedure, you won’t have two tests, just the newer one.

However, if you’re testing at the DNA testing company, and also uploading, I generally don’t recommend more than one test at each vendor. All it really does is clog up people’s match lists with no or little additional benefit. At 23andMe, with their restrictions on the size of your match list, if everyone had two tests, the effective match limit would be half of their stated limit of about 1500 matches for earlier testers and about 5000 for current testers with subscriptions.

So, in essence, I’m telling you to “do as I say, not as I do.” We all have better things to do with our money rather pay for the same test twice. If you haven’t tested your Y-DNA or mitochondrial DNA, that’s much more beneficial than two autosomal tests at one vendor.

Chips and Chip Evolution

Before we begin the side-by-side comparison, let’s briefly discuss DNA testing chips and how they work.

Each DNA testing company purchases DNA processing equipment. Illumina is the big dog in this arena. Illumina defines the capacity and structure of each chip. In part, how the testing companies use that capacity, or space on each chip, is up to each company. This means that the different testing companies test many of the same autosomal DNA SNP locations, but not all of the same locations.

Furthermore, the individual testing companies can specify a number of “other” locations to be included on their chip, up to the chip maximum size limit. The testing companies who offer Y-DNA or mitochondrial DNA haplogroups from autosomal tests use part of their chip array space for selected known haplogroup-defining SNP locations. This does NOT mean that Y-DNA or mitochondrial DNA is autosomal, just that the testing company used part of their chip array space to target these SNPs in your genome. Of course, for your most refined haplogroup and Y-DNA or mitochondrial DNA matching, you have to take those specific tests at FamilyTreeDNA .

This means that each testing company includes and reports many of the same, but also some different SNP locations when they scan your DNA.

In the lab, after your DNA is extracted from either your saliva or the cheek swab, it’s placed on this array chip which is then placed in the processing equipment.

There are several steps in processing your DNA. Each DNA location specified on the chip is scanned and read multiple times, and the results are recorded. The final output is the raw DNA results file that you see if/when you download your raw DNA file.

Here’s an example from my file. The RSID is the reference SNP cluster ID which is the naming convention used for specific SNPs. It’s not relevant to you, but it is to the lab, along with the chromosome number and position, which is in essence the address on the chromosome.

In the Result column, your file reports one nucleotide (T, A, C or G) that you inherited from each parent at each tested position. They are not listed in “parent order” because your DNA is not organized in that fashion. There’s no way for the lab to know which nucleotide came from which parent, unless they are the same, of course. You can read about nucleotides, here.

When you upload your raw DNA file to a different DNA testing company (vendor), they have to work with a file that isn’t entirely compatible with the files they generate, or the other files uploaded from other DNA testing companies.

In addition to dealing with different file formats and contents from multiple DNA vendors, companies change their own chips and file structure from time to time. In some cases, it’s a forced change by the chip manufacturer. Other times, the vendors want to include different locations or make improvements. For example, with 23andMe’s focus on health, they probably add new medically related SNP locations regularly. Regardless of why, some DNA files include locations not included in other files and are not 100% compatible.

Looking at the first few entries in my example file above, let’s say that the testing vendor included the first ten positions, but an uploaded file from another company did not. Or perhaps the chip changed, and a different version of the company’s own file contains different positions.

DNA testing companies have to “fill in the blanks” for compatibility, and they do this using a technique called imputation. Illumina forced their customers to adopt imputation in 2017 when they dropped the capacity of their chip. I was initially quite skeptical, but imputation has worked surprisingly well. Some of the matching differences you will see when comparing the results of two different DNA files is a result of imputation.

I wrote about imputation in an early article here. Please note the companies have fixed many issues with imputation and improved matching greatly, but the concepts and imputation processes still apply. The downloaded raw data files are your results BEFORE imputation, meaning that it’s up to any company where you upload to process your raw file in the same way they would process a file that they generated. A lot goes on behind the scenes when you upload a file to a DNA testing company.

At both 23andMe and Ancestry, you know that all of your matches tested there, meaning they did not upload a file from another testing company. You don’t know and can’t tell what chip was utilized when your matches tested. The only way to determine a chip testing version, aside from knowing the date or remembering the chip version from when you tested, is to look at the beginning of the raw data download file, although not all files contain that information.

Ok, now that you understand the landscape, let’s look at my results at each company.

23andMe

I tested twice at 23andMe on two different chip versions, V3 and V4, which tested some different locations of my DNA. Neither of these chips is the current version. I originally tested twice to evaluate the differences between the two test versions which you can read about, here.

23andMe named their ethnicity results Ancestry Composition.

They last updated my V3 test’s Ancestry Composition results on July 28, 2021.

The percentages are shown at left, and the country locations are highlighted at right for my 23andMe V3 test.

Click to enlarge any graphic

The 23andMe V4 test was also updated for the last time on July 28, 2021.

The ethnicity results differ substantially between the two chip versions, even though they were both updated on the same date.

In October of 2020, in an effort to “encourage” their customers to pay for a new test on their V5 chip, 23andMe announced that there would be no ethnicity updates on older tests. So, I really don’t know for sure when my tests were actually updated. Just note how different the results are. It’s also worth mentioning that 23andMe does not show trace amounts on their map, so even though my Indigenous American results were found, they aren’t displayed on the map.

Indigenous is, however, shown in yellow on their DNA Chromosome Painting.

No other testing company restricts updates, penalizing their customers who purchased earlier versions of tests.

Matches at 23andMe

23andMe limits your matches to about 1500 unless you have purchased the current test, including health AND pay for an annual $69 subscription which buys you about 5000 matches. I have not purchased this test.

Your number of actual matches displayed/retained is also affected by how many people you have communicated with, or at least initiated communications with. 23andMe does not roll those people off of your match list.

I have 1803 matches on both of my tests, meaning I’ve reached out to about 300 people who would have otherwise been removed from my match list. 23andMe retains your highest matches, deleting lower matches after you reach the maximum match threshold.

I’ve randomly evaluated several of the same matches at each vendor, at least five maternal and five paternal, separated by a blank row. I wanted to determine whether they match me on the same number of centimorgans, meaning the same amount of DNA, on both tests, and the same number of segments.

Match 23and Me V3 23and Me V4
Patricia 292 cM – 12 segments Same as V3
Joe 148 cM, 8 segments Same
Emily 73 cM, 4 segs 72 cM, 4 seg
Roland 27 cM, 1 seg Same
Ian 62 cM, 4 seg Same
Stacy 469 cM, 16 segments 482 cM, 16 segments
Harold 134 cM, 6 segments Same
Dean 69 cM, 3 seg Same
Carl 95 cM, 4 seg Same
Debbie 83 cM, 4 seg 84 cM, 4 seg

As you can see, the matches are either exact or xclose.

Please note that bolded matches are also found at another company. I will include a summary table at the end comparing the same match across multiple vendors.

23and Me Summary

The 23andMe V3 and V4 match results are very close. Since the match limit is the same, and the results are so close between tests, they are essentially identical in terms of matching.

The ethnicity results are similar, but the V4 test reflects a broader region. Italian baffles me in both versions.

Ethnicity should never be taken at face value at any DNA testing company, especially with smaller percentages which could be noise or a combination of other regions which just happens to resemble Italy, in my case.

I don’t know what type of comparison the current chip would yield since I suspect it has more medical and less genealogical SNPs on board.

Reprocessing Tests

This is probably a good place to note that it’s very expensive for any company to update their customer’s ethnicity results because every single customer’s DNA results file must be completely rerun. Note that this does not mean their DNA itself is retested. The output raw data file is reprocessed using a new algorithm.

Rerunning means reprocessing that specific portion of every test, meaning the vendors must rent “time in the cloud.” We are talking millions of dollars for each run. I don’t know how much it costs per test, but think about the expense if it takes $1 to rerun each test in the vendor’s database. Ancestry has more than 20 million tests.

While we, as consumers, are always chomping at the bit for new and better ethnicity results – the testing companies need to be sure it really is “better,” not just different before they invest the money to reprocess and update results.

This is probably why 23andMe decided to cease updating older kits. The newer tests require a subscription which is recurring revenue.

The same is true when DNA testing companies need to rematch their entire user base. This happens when the criteria for matching changes. For example, Ancestry purged a large number of matches for all of their customers back in 2020. While match algorithm changes necessitate rematching, with associated costs, this change also provided Ancestry with the huge benefit of eliminating approximately half of their customer’s matches. This freed up storage space, either physically in their data center or space rented in the cloud, representing substantial cost-savings.

How long can a DNA testing company reasonably be expected to continue investing in a product which never generates additional revenue but for which the maintenance and reinvestment costs never end?

Ancestry and MyHeritage both hope to offset the expenses of maintaining their customer’s DNA tests and providing free updates by selling subscriptions to their record services. 23andMe wants you to purchase a new test and a yearly subscription. FamilyTreeDNA wants you to purchase a Big Y-DNA and mitochondrial DNA test.

OK, now let’s look at my matches at Ancestry.

Ancestry

I’ve taken two Ancestry tests, V1 and V2. There were some differences, which I wrote about here and here. V2 is no longer the current chip.

Except for 23andMe who wants their customers to purchase their most current test, the other companies no longer routinely announce new chip versions. They just go about their business. The only way you know that a vendor actually changed something is when the other companies who accept uploads suddenly encounter an issue with file formats. It always takes a few weeks to sort that out.

My Ancestry V1 test’s ethnicity results don’t show my Native American ethnicity.

Ancestry results were updated in June 2022

However, my V2 results do include Native American ethnicity.

Matches at Ancestry

I have many more matches on my V1 test at Ancestry because I took steps to preserve my smaller matches when Ancestry initiated its massive purge in 2020. I wrote about that here and here.

Ancestry’s SideView breaks matches down into maternal, paternal, and unassigned based on your side selection. You tell Ancestry which side is which. You may be able to determine which “side” is maternal or paternal either by your ethnicity or shared matches. While SideView is not always accurate, it’s a good place to begin.

Match Category Ancestry V1 Test Ancestry V2 Test
Maternal 15,587 15,116
Paternal 42,247 41,870
Both 2 2
Unassigned 48,999 4,127
Total 106,835 61,115

Ancestry either displays all your matches or your matches by side, which I used to compile the table above. I suspect that Ancestry is not assigning any of the smaller preserved matches to “sides” based on the numbers above.

Ancestry implemented a process called Timber that removes DNA that they feel is “too matchy,” meaning you match enough people in this region that they think it’s a pileup region for you personally, and therefore not useful. In some cases, enough DNA is removed causing that person to no longer be considered a match because they fall beneath the match threshold. I am not a fan of Timber.

Your match amount shown is AFTER Timber has removed those segments. Unweighted shared DNA is your pre-Timber match amount.

You can view the Unweighted shared DNA by clicking on the amount of shared DNA on your match list.

You can read Ancestry’s Matching White Paper, here.

Let’s take a look at my matches. I’ve listed both weighted and unweighted where they are different.

Match Ancestry V1 Ancestry V2
Michael 755 cM, 35 seg 737 cM, 33 seg
Edward 66 cM, 4 seg (unweighted 86 cM) 65 cM, 4 seg (unweighted 86 cM)
Tom 59 cM, 3 seg (unweighted 63) Same
Jonathon 43 cM, 4 seg, (unweighted 52 cM) Same
Matthew 20 cM, 2 seg (unweighted 35 cM) Same
Harold 132 cM, 7 seg 135 cM, 6 seg
Dean 67 cM, 4 seg (unweighted 78 cM) 66 cM, 4 seg (unweighted 78 cM)
Debbie 93 cM, 5 seg Same
Valli 142 cM, 3 seg Same
Jared 20 cM, 1 seg (unweighted 22 cM) Same

Timber only removes DNA when the match is under 90 cM. Almost every match under 90 cM has some DNA removed.

Ancestry Summary

The results of the two Ancestry tests are very close.

In some circumstances, no DNA is removed by Timber, so the unweighted is the same as the weighted. However, in other cases, a significant amount is removed. 15 cM of Matthew’s 35 cM was removed by Timber, reducing his total to 20 cM.

Remember that Ancestry does not show shared matches unless they are greater than 20 cM, which is different than any other DNA testing company.

At one point, Ancestry was selling a health test that was also a genealogy test. That test utilized a different chip that is not accepted for uploads by other vendors. The results of that test might well be different that the “normal” Ancestry tests focused on genealogy. The Ancestry health test is no longer offered.

Companies that Accept Uploads

DNA testing companies that accept uploaded DNA files from other DNA testing companies need to process the uploaded file, just like a file that is generated in their own lab. Of course, they must deal with the differences between uploaded files and their own file format. The processing includes imputation and formulates the uploaded file so that it works with the tools that they provide for their customers, including ethnicity (by whatever name they use) matching, family matching (bucketing), advanced matching, the match matrix, triangulation, AutoClusters, Theories of Family Relativity, and other advanced tools.

Of course, the testing company accepting uploads can only work with the DNA locations provided by the original DNA testing company in the uploaded file.

Matching and some additional tools are free to uploaders, but advanced tools require an inexpensive unlock.

FamilyTreeDNA

I took a test at FamilyTreeDNA, plus uploaded a copy of both of my Ancestry DNA files.

FamilyTreeDNA named their population (ethnicity) test myOrigins and the current version is V3. I wrote about the rollout and comparison in September of 2020, here.

My DNA test taken at FamilyTreeDNA, above, reveals Native American segments that match reference populations found both in North and South America and the Caribbean Islands.

At FamilyTreeDNA, my Ancestry V1 uploaded file results show Native American population matches only in North America.

Interestingly, my Ancestry V1 file processed AT Ancestry did not reveal Native American ancestry, but the same file uploaded to and processed at FamilyTreeDNA did show Native American results, reflecting the difference between the vendors’ internal algorithms and reference populations utilized.

My myOrigins results from my Ancestry V2 uploaded file at FamilyTreeDNA also include my North American Native American segments. The V2 test also showed Native American ethnicity at Ancestry, so clearly something changed in Ancestry’s algorithm, locations tested, and/or reference populations between V1 and V2.

Fortunately, FamilyTreeDNA provides both chromosome painting and a population download file so I can match those Native segments with my autosomal matches to identify which of my ancestors contributed those specific segments.

One of my Native segments is shown in pink on Chromosome1. My mother has a Native segment in exactly the same location, so I know that this segment originated with my mother’s ancestors.

I downloaded the myOrigins population segment file and painted my results at DNAPainter, along with the matches where I can identify our common ancestor. This allowed me to pinpoint the ancestral line that contributed this Native segment in my maternal line. You can read about using DNAPainter, here.

FamilyTreeDNA Matches

I have significantly more matches at FamilyTreeDNA on their test than on either of my Ancestry tests that I uploaded. However, nearly the same number are maternally or paternally assigned through Family Matching, with the remainder unassigned. You can read about Family Matching here.

Match Category FamilyTreeDNA Test Ancestry V1 at FamilyTreeDNA Ancestry V2 at FamilyTreeDNA
Paternal 3,479 3,572 3,422
Maternal 1,549 1,536 1,477
Both 3 3 3
All 8,154 6,397 6,579

Family matching, aka bucketing, automatically assigns my matches as maternal and paternal by linking known relatives to their place in my tree.

I completed the following match chart using my original test taken at FamilyTreeDNA, plus the same match at FamilyTreeDNA for both of my Ancestry tests.

In other words, Cheryl matched me at 467 cM on 21 segments on the original test taken at FamilyTreeDNA. She matched me on 473 cM and 21 segments on my Ancestry V1 test uploaded to FamilyTreeDNA and on 483 cM and 22 segments on the Ancestry V2 test uploaded to FamilyTreeDNA.

Match FamilyTreeDNA Ancestry V1 at FTDNA Ancestry V2 at FTDNA
Cheryl 467 cM, 21 seg 473 cM, 21 seg 483 cM, 22 seg
Patricia 195 cM, 11 seg 189 cM, 11 seg 188 cM, 11 seg
Tom 77 cM, 4 seg 71 cM, 4 seg 76 cM, 4 seg
Thomas 72 cM, 3 seg 71 cM, 3 seg 74 cM, 3 seg
Roland 29 cM, 1 seg 35 cM, 2 seg 35 cM, 2 seg
Rex 62 cM, 4 seg 55 cM, 3 seg 57 cM, 3 seg
Don 395 cM, 18 seg 362 cM, 15 seg 398 cM, 18 seg
Ian 64 cM, 4 seg 56 cM, 4 seg 64 cM, 4 seg
Stacy 490 cM, 18 seg 494 cM, 15 seg 489 cM, 14 seg
Harold 127 cM, 5 cM 133 cM, 6 seg 143 cM, 6 seg
Dean 81 cM, 4 seg 75 cM, 3 seg 83 cM, 4 seg
Carl 103 cM, 4 seg 101 cM, 4 seg 102 cM, 4 seg
Debbie 99 cM, 5 seg 97 cM, 5 seg 99 cM, 5 seg
David 373 cM, 16 seg 435 cM, 19 seg 417 cM, 18 seg
Amos 176 cM, 7 seg 177 cM. 8 seg 177 cM, 7 seg
Buster 387 cM, 15 seg 396 cM, 16 seg 402 cM, 17 seg
Charlene 461 cM, 21 seg 450 cM, 21 seg 448 cM, 20 seg
Carol 65 cM, 6 seg 64 cM, 6 seg 65 cM, 6 seg

I have tested many of my cousins at FamilyTreeDNA and encouraged others to test or upload. I’ve attempted to include enough people so that I can have common matches at least at one other DNA testing company for comparison.

FamilyTreeDNA Summary

The matches are relatively close, with a few being exact.

Interestingly, some of the segment counts are different. In most cases, this results from one segment being broken into multiple segments by one or more of the tests, but not always. In the couple that I checked, the entire segment seems to descend from the same ancestral couple, so the break is likely a result of not all of the same DNA locations being tested, plus the limits of imputation.

MyHeritage

I have two tests at MyHeritage. One taken at MyHeritage, and an uploaded file from FamilyTreeDNA.

MyHeritage displays both ethnicity results and Genetic Groups which maps groups of people that you match. I left the Genetic Groups setting at the highest confidence level. Shifting it to lower displays additional Genetic Groups, some of which overlap with or are within ethnicity regions.

My test taken at MyHeritage, above, shows several ethnicities and Genetic Groups, but no Native American.

My FamilyTreeDNA kit processed at MyHeritage shows the same ethnicity regions, one additional Genetic Group, plus Native American heritage in the Amazon which is rather surprising given that I don’t show Native in North American regions where I’m positive my Native ancestors lived.

MyHeritage Matching

At MyHeritage, I compared the results of the test I took with MyHeritage, and a test I uploaded from FamilyTreeDNA. Fewer than half of my matches can be assigned to a parent via shared matching.

Matches MyHeritage Test FamilyTreeDNA at MyHeritage
Paternal 4,422 6,501
Maternal 2,660 3,655
Total 13,233 16,147

I have rounded my matches at MyHeritage to the closest cM.

Match MyHeritage Test FamilyTreeDNA at MyHeritage
Michael 801 cM, 32 seg 823 cM, 31 segments
Cheryl 467 cM, 23 seg 477 cM, 23 seg
Roland No match 28 cM, 1 seg
Patty 156 cM, 9 seg 151 cM, 9 seg
Rex 43 cM, 4 seg 53 cM, 3 seg
Don 369 cM, 16 seg 382 cM, 17 seg
 
David 449 cM, 17 seg 460 cM, 17 seg
Charlene 454 cM, 23 seg 477 cM, 24 seg
Buster 408 cM, 15 seg 410 cM, 16 seg
Amos 183 cM, 8 seg Same
Carol 78 cM, 6 seg 87 cM, 7 seg

MyHeritage Summary

I was surprised to discover that Roland had no match with the MyHeritage test, but did with the FamilyTreeDNA test. I wonder if this is a searching or matching glitch, especially since both companies use the same chip. 28 cM in one segment is a reasonably large match, and even if it was divided in two, it would still be over the matching threshold. I know this is a valid match because Roland triangulates with me and several cousins, I’m positive of our common ancestor, and he also matches me at both FamilyTreeDNA and 23andMe.

Other than that, the matches are reasonably close, with one being exact.

Your Matches Aren’t Everyplace

I unsuccessfully searched for someone who was a match to me in all four databases. Ancestry does not permit match downloads, so I had to search manually. People don’t always use the same names in different databases.

Surprisingly, I was unable to find one match who is in all of the databases. Many people only suggest testing at Ancestry because they have the largest database, but if you look at the following comparison chart that I’ve created, you’ll see that 16 of 26 people, or 62% were not at Ancestry. Conversely, many people were at Ancestry and not elsewhere. I could not find five maternal and five paternal matches at Ancestry that I could identify as matches in another database. 40% were not elsewhere.

If you think for one minute that it doesn’t matter for genealogy if you’re in all four major databases, please reconsider. It surely does matter.

Every single vendor has matches that the others don’t. Substantial, important matches. I have found first and second-cousin matches in every database that weren’t elsewhere.

Many of the original testers have passed away and can’t test again. My mother can never test at either 23andMe or Ancestry, but she is at both FamilyTreeDNA and MyHeritage because I could upgrade her kit at FamilyTreeDNA after she died. I uploaded her to MyHeritage. Of course, because she is a generation closer to our ancestors, she has many valuable matches that I don’t.

Each vendor provides either an email address or a messaging platform for you to contact your matches. Don’t be discouraged if they don’t answer. Just today, I received a reply that was years in the making.

Genealogists hope for immediate gratification, but we are actually in this for the long game. Play it with every tool at your disposal.

The Answer

Does it matter if you test at a DNA testing company, or upload a file?

I know this was a very long answer to what my readers hoped was a simple yes or no question.

There is no consistent answer at either FamilyTreeDNA or MyHeritage, the two DNA testing companies that accept uploads. Be sure you’re in both databases. My closest two matches that I did not test were found at MyHeritage. Here’s a direct link to upload at MyHeritage.

Of the vendors, those two should be the closest to each other because they are both processed in the GenebyGene lab, but again, the actual chip version, when the test was originally taken, and each vendor’s internal processing will result in differences. Neither the original test at the DNA testing company nor the uploaded files have consistently higher or lower matches. Neither type of test or upload appears to be universally more or less accurate. Differences in either direction seem to occur on a match-by-match basis. Many are so close as to be virtually equivalent, with a few seemingly random exceptions. Of course, we always have to consider Timber.

If you upload, unlock the advanced features at both FamilyTreeDNA and MyHeritage.

If you upload to a DNA testing company, you may discover in the future that some features and functions will only be available to original testers.

Personally, if I had the option, I would test at the company directly simply because it eliminates or at least reduces the possibility of future incompatibilities – with the exception of 23andMe which has chosen to not provide consistent updates to older tests. I’m incredibly grateful I didn’t test my mother or now deceased family members at 23andMe, and only there. I would be heartsick, heartbroken, and furious.

Our DNA is an extremely valuable resource for our genealogy. It’s the gift that truly keeps on giving, day after day, even when other records don’t exist. Be sure you and your family members are in each database one way or another, and test your Y-DNA (for males) and mitochondrial DNA (for everyone) to have a complete arsenal at your disposal.

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