Category Archives: Y DNA

Ancient Connections: Where Archaeology Meets Your Ancestors

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Ancient Connections, a report found on FamilyTreeDNA’s Discover platform for both Y-DNA and mitochondrial DNA (mtDNA), can be used in multiple ways to enhance your genealogy and unlock secrets.

It’s exciting to examine ancient burials linked to our ancestors and understand how we connect to them. Ancient Connections offer a wealth of information, providing clues that can help unravel long-standing mysteries.

Today, there are more than 12,960 Y-DNA Ancient Connections in Discover, along with more than 25,310 mitochondrial Ancient Connections, and that number increases weekly.

Why the disparity, you ask? Remember, everyone has mitochondrial DNA, but only males have Y-DNA.

In addition to matches, your DNA results hold something even more powerful – evidence of where your ancestors and their cousins lived in the distant past, when they lived, and the cultural context surrounding them. These essential insights are unavailable through any other means. Ancient Connections help us answer the age-old question, “Where did I come from?”

Could These People Be My Ancestors?

I’ll show you how to answer another question, too. Which of these Ancient Connections could potentially be your ancestors, and which ones are your “haplo-cousins”?

Regardless, they all help us understand our ancestors’ past, and that of their descendants.

Discover is for Everyone

FamilyTreeDNA provides a free version of Discover that everyone can use. There’s also an enriched version with additional information for their customers who have purchased Y-DNA and mitochondrial DNA tests.

Discover has something to offer for everyone.

Mitochondrial DNA is passed from mothers to all of their children of both sexes – unmixed with the DNA of the father.

Everyone has their mother’s mitochondrial DNA, which is passed intact, except for an occasional mutation, directly down through generations of mothers. It’s not admixed like autosomal DNA, so we don’t lose some portion in each generation. This is exactly why we can track mitochondrial DNA infinitely far back in time and why it’s so crucial for understanding the origins of your mother’s specific line.

Y-DNA is passed from fathers only to their sons, which is what makes males male. Like mitochondrial DNA, Y-DNA is not admixed with any DNA from the mother, so we get a laser line-of-sight view of the direct patrilineal line back in time. The Y-DNA direct paternal line is the male’s surname line in cultures where males carry their father’s surname.

If you’ve tested at or upgraded to either the Big Y-700 level or the mtFull, full mitochondrial sequence test, you will receive the most granular haplogroup possible, meaning the closest in time and most informative. You’ll also match with other testers who have taken the less-refined lower-level tests.

The most informative and precise results occur when both people have taken the premium tests. As more people test and science advances, you may receive a new haplogroup from time to time when you and another tester share a rare mutation – so these tests are evergreen.

Both Y-DNA and mitochondrial DNA testers at any level have access to Discover on their dashboard for those products, although the results of lower-level tests provide less information.

The Free Version of Discover Compared to the Premium Version for Testers

Here’s a comparison of lower-level Y-DNA tests and the Big Y-700.

Click any image to enlarge

Y-DNA testers who have only taken the 12-111 STR panel tests receive a predicted haplogroup, and when clicking through to Discover, receive up to 10 Ancient Connections.

For example, If your Y-DNA haplogroup is predicted as R-M269, the most common male lineage in Europe that arose some 6450 years ago, your Ancient Connections begin with the closest genetic match to R-M269. Viewing Ancient Connections that are 6500 years ago will certainly be interesting, so please do look, but probably not terribly useful for genealogy.

However, if that same person were to upgrade to the Big Y-700, they would receive a much more recent haplogroup, and along with it, up to 30 Ancient Connections within their major haplogroup lineage, R in this case, plus the oldest sample in the database. For some haplogroups, there may not yet be 30 Ancient Connections, although new ancient samples are added weekly for both Y-DNA and mitochondrial DNA.

All Ancient Connections begin with the matches who are genetically closest to the haplogroup requested.

The same scenario holds true for mitochondrial DNA testers who previously tested at the HVR1/HVR2 level, but not at the full sequence level, which is the only test available today.

This article focuses on testers at the higher levels, meaning the Big Y-700 and the mtFull tests, and how to utilize their 30 closest Ancient Connections. We’ll walk through step-by-step examples using both.

However, before we begin evaluating our Ancient Connections, we need to cover two fundamental concepts.

BCE, CE and Converting to “Years Ago”

It’s helpful to understand date structures and how they are used.

It’s easy to get confused when seeing the dates of CE, current era, and BCE, before current era, which means we misinterpret the information.

For example, the year 100 CE is the year 100 that occurred roughly 1900 years ago. We round 2026 to 2000 for these types of calculations. The year 100 BCE, before current era, occurred approximately 2100 years ago. I often prefer to work in “years ago”, because it equalizes the numbers, meaning you’re less likely to get confused about how long ago someone lived or something happened.

To do the calculations from BCE dates to “years ago,” add 2000, so 2250 BCE equals 4250 years ago.

For CE dates, subtract from 2000. The date 500 CE occurred 1500 years ago.

This can be especially confusing when you’re dealing with the same number on either side of the current era, which began in the year 1. There is no year zero. For example, we need to be vigilant not to confuse 500 BCE, which was 2500 years ago, and 500 CE, which was 1500 years ago.

Now, on to our second concept.

Haplogroup Age and Burial Age Are Not the Same

When viewing Ancient Connections, the genetic age of the haplogroup, meaning when it was formed, and age of the burial are two different things.

Haplogroup R-ZP18 is about 4250 years old, and this Late Iron Age, pre-Roman burial which is also R-ZP18, occurred about between 2337 and 2043 years ago.

Haplogroup ages and the date they emerged, which show on the Timeline, sometimes mature and are refined with additional testers and branching.

Burials are dated using various techniques, and sometimes the ages provided in the academic papers are earlier than the genetic age of the haplogroup, shown on the Timeline at the bottom of the Connections page.

Discover makes no attempt to “fix” this situation, because it’s unclear which age should be changed. It’s not unusual to be unable to fully analyze ancient remains. For example, let’s say a sample is determined to have the SNP for R-ZP18, but simultaneously lacks downstream SNPs and some upstream SNPs, and the burial was dated from surrounding soil or artifacts. In that case, it would be impossible to know what is precisely “accurate”, but the sample is accurate enough to be included in Ancient Connections. This is also why some samples aren’t included in Globetrekker calculations. Some low-quality samples are excluded entirely.

Every ancient sample is individually analyzed by R&D team members before being included in the phylogenetic tree and Ancient Connections. Sometimes, the scientists at FamilyTreeDNA can assign a more specific haplogroup than was available to the paper authors at the time of publication because the tree has since branched.

As you receive new Ancient Connections, your older ones, except your final or oldest connection, will roll off of your list.

That’s one reason I devised a process for analyzing and recording my Ancient Connections, and for determining which ones might be actual ancestors – or at least aren’t precluded from it.

First Peek at Ancient Connections

Sign in to your FamilyTreeDNA account and click on the Discover link on the dashboard for the type of test you wish to view.

In the Y-DNA example, I’m using my male Estes cousins. As a female, I can’t test for the Estes Y chromosome, so I recruited others to represent my line. You can see the results in the Estes DNA project.

After signing in, click on Discover, then on Ancient Connections.

Y-DNA Ancient Connections 

It’s a bonanza!

Your Ancient Connections are displayed at the top of the page, ordered from genetically closest to most distant. These are archaeological samples whose data has been extracted from academic papers and analyzed before being include in Discover.

You’ll see a description of the first sample, or any sample you click on. The Timeline for that sample, along with your haplogroup and your common ancestor’s haplogroup, is displayed at the bottom of the page.

The first, meaning closest, Ancient Connection is highlighted, so let’s take a look.

  • “You” are shown in the dark purple frame (with purple arrows) at right, with your haplogroup, in this case R-ZS3700, which is placed on the Timeline at the bottom of the page in the appropriate location.
  • The Ancient Connection named “North Berwick 16499”, whose name was taken from the academic paper in which it was found, is shown in a red frame and placed on the timeline based on information provided in the paper.

“North Berwick” has been assigned to haplogroup R-ZP18, either in the paper, or by the FamilyTreeDNA R&D team if a more refined haplogroup can be determined, and is this tester’s closest Ancient Connection based on its position on the list.

Note that you may have other Ancient Connections who are genetically equivalent in age, meaning they too would be R-ZP18. In our case, only one sample is assigned to that haplogroup.

  • Your Shared Ancestor, in the green frame, is the first man who carried R-ZP18, which emerged about 2250 BCE, or 4250 years ago.

Notice that I said, “the first man.” That man’s sons, grandsons and so forth were also haplogroup R-ZP18. Some went on to develop new downstream haplogroups, but apparently, North Berwick, by the time he lived, had not. Either that, or a downstream haplogroup cannot yet be determined due to a lack of other testers in that lineage.

Men with downstream SNPs (mutations), meaning downstream haplogroups, also descended from R-ZP18. Those SNP mutations become downstream haplogroups when two or more men who carry the same SNP mutation match each other. For example, our Estes ancestor who carries haplogroup R-ZS3700 descends from R-ZP18 through a distinct series of downstream SNPs (mutations). While we carry R-ZP18 in our lineage, it’s not our most refined haplogroup.

However, for North Berwick, haplogroup R-ZP18 is his most refined haplogroup.

Because of this, we know for sure that North Berwick and the Estes men both descend from the original R-ZP18 man who lived about 4250 years ago, but we can’t tell when they shared a common ancestor between 4250 years ago and 3750 years ago when the next downstream haplogroup R-BY342, was formed in the Estes lineage.

Because North Berwick does not belong to a different downstream haplogroup, it’s genetically possible that the Estes men could descend from him during that 500-year timeframe. There’s nothing to exclude that possibility based on his haplogroup alone, but looking at when North Berwick lived is another matter.

North Berwrock lived between 2337 and 2043 years ago, which is 1400 years LATER than when the first downstream haplogroup, R-BY342 was formed, about 3750 year ago, in the Estes lineage. This precludes North Berwick from being our direct ancestor. Instead, he’s our “haplocousin.” We share a common upstream ancestor.

What we we absolutely CAN confirm, though, is that between 500 and 1300 years earlier than North Berwick lived, between when haplogroups R-BY342 and R-ZP18 were formed, both North Berwick and our Estes ancestor descended from the same man.

This kind of information is like waving a red flag in a genealogist’s face. We immediately need to know more.

This is just the beginning, and we have so many questions!

Revealing More Information

Did our common ancestor live in or near North Berwick, or someplace else? What do we know about the history of North Berwick?

What can we discern about North Berwick?

  • When did this man live, and where?
  • What do we know about him?
  • Who was he?
  • Did he live close to where my earliest known ancestor in this line is found?
  • What can I tell about his culture?
  • Were there grave goods that provide at least a peek into his life?

So many questions!

Discover tells us that he lived between 337 and 43 BCE, so between 2337 and 2043 years ago, during the Late Iron Age, and is associated with the Iron Age Britain cultural group.

The Ancient Connections “Reference” provides information about the paper where the North Berwick sample was found. No links are provided because sometimes the paper is behind a paywall, and you can’t access it without paying, and sometimes it’s a preprint and will appear later elsewhere. Sometimes one paper actually uses data from an earlier paper, and it gets complicated.

The first thing I do is Google the paper – Patterson et al. 2022. Google provides two links – one that’s free, and one that isn’t. Many times, the sample data is found in the supplementary material, which may also be behind a paywall, even if the paper isn’t.

I know you’re going to think it’s a pain, but I strongly encourage you to read every paper, though sometimes they can be challenging to understand, so read them when you’re fresh, not tired, and can concentrate. If nothing else, at least read the abstract. There’s so much great information buried in academic papers, including nice maps and discussions of the burial site. You can also learn more sometimes by Googling the burial site itself.

Let me give you an example from this paper’s abstract. I’ve added the brackets [ ] for clarity, from the body of the paper:

Between 1000 and 875 BC[E], EEF [Early European Farmer] ancestry increased in southern Britain [England and Wales] but not northern Britain [Scotland] due to incorporation of migrants who arrived at this time and over previous centuries, and who were genetically most similar to ancient individuals from France. These migrants contributed about half the ancestry of people of England and Wales from the Iron Age, thereby creating a plausible vector for the spread of early Celtic languages into Britain.

How does this information align with our North Berwick man? He lived between 2337 and 2043 years ago, and the EEF ancestry increased in southern Britain between 3000 and 2875 years ago. The authors do add “over previous centuries” which probably accounts for the 500-year gap and gets closer to when R-ZP18 lived. North Berwick is found in Scotland, not England or Wales, so not part of the group of people most closely aligned with the ancient French migrants from this timeframe. Maps in the paper confirm this as well.

Googling the paper and sample name provided additional sourced information. This paper incorporates samples from earlier papers and performed a different type of analysis.

Ironically, I wrote about this in detail in 2022, here, before Discover was introduced, so I had absolutely no idea that North Berwick 16499, discovered on Law Road in North Berwick, was related to my ancestors, and therefore, to me.

In that article, I researched and mapped the samples. North Berwick 16499 is located on the coast, along the harbour, not far from Edinburgh.

The burial was excavated in the cemetery of the original St. Andrew’s Church in North Berwick, originally built in the 1100s, but now in ruins.

This paper’s supplementary material explains that:

Excavation of a substantial square cist at Law Road, North Berwick, uncovered the remains of four inhumations of Late Iron Age date (Richardson et al. 2005). Two adult males 3603 (Skeletons C46 and C51) and a female around 16–18 years of age at death (Skeleton C50) appeared to have been displaced for the burial of an adult female (Skeleton C47), wearing an iron brooch. One of the males (C46) had been buried with a bone-handled iron knife.

What I wouldn’t give to see that iron brooch and bone-handled knife.

C51 is North Berwick 16499, “our” skeleton. A cist grave is a small, stone-lined burial box, and this one was preserved beneath medieval deposits.

That reference gave the even more precise location of Law Road and St. Andrews Street and informs us that the remains are held by National Museums Scotland. Checking their collections confirms that they hold these items, plus the bones. However, there are no photos shown. Contacting them for images might yield results.

What the paper did not say is that little was known prior to these excavations about early North Berwick.

By Stefan Schäfer, Lich – Own work, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=19450589

North Berwick was known to exist as a ferry landing from the 7th century, but an archaeological survey of Berwick Law, a hill that overlooks the town, revealed much earlier information:

The earliest features on North Berwick Law comprise a pair of newly discovered cup-marked rocks and the scanty remains of a prehistoric hilltop fort discovered by RCAHMS (1957, xv), whose outworks appear to be more limited than suggested by previous authorities (Feachem 1963, 119; OS 1975). The lower SW flank of the Law is dotted with the remains of a prehistoric settlement comprising at least 12 hut circles or house platforms and fragments of an associated field system of small cairns and banks.

Unfortunately, the perimeters of Berwick Law have been settled and farmed since, and the hilltop has served recently in the same capacity as it probably served initially – as a lookout across the firth. The residents would have been watching from this highest point for invaders arriving by sea.

It’s about half a mile from the foot of the hill to the burial cist.

The survey also mentioned that they found “stray bronze age finds” that had likely been disrupted by subsequent settlement. The bronze age in Northern Scotland began about 4200 years ago, about the time that R-ZP18 lived, until about 2800 years ago. Whoever North Berwick 16499 was, the man who was buried here some 2400 years ago, he was probably associated with this hilltop fort, perhaps farming at the base, probably living in one of those huts or nearby. His body wouldn’t have been taken far for burial.

We are left to wonder how long his family had lived here, and how they had arrived. Was his cist burial a sign of status? Was he sent to commend the fort, or had his family settled here centuries earlier? Did our ancestor descend from this location, too?

After our analysis, we know that our ancestor did not descend from North Berwick 16499 himself, but North Berwick definitely descended from our ancestor.

If you’re thinking this is a rabbit hole, it definitely is – but what a rabbit hole! There is so much to be gleaned from these Connections.

The Evaluation Process

I needed a process to keep track of these Ancient Connections, my findings, and how they relate to my Estes ancestors. Who begat, or might have begat whom, and where?

I created a spreadsheet as I read and analyzed each Ancient Connection relative to my ancestral line. I include what I know about it, and what I THINK I know about it. Those can be two vastly different things. I follow this same process for every ancestral line where I can find a representative Y-DNA or mitochondrial DNA tester.

For example, there’s a persistent rumor that the Estes family line descends from the d’Este family of Italy. That rumor was spun up long before we had genetic proof that our line was found in Kent, England, in records dating back to about 1495. Fortunately, church records, for the most part, and some civil records still exist.

The first known record is the will of our Nycholas Ewstas written on January 1, 1533/1534 in Deal, Kent, England. We confirmed that this is our Estes line by testing the Y-DNA of his descendant who still lives a few miles up the road, compared with the descendants of Abraham Estes (1647-1720), the man who immigrated to Virginia in 1673. We believed that Abraham Estes, who married in 1672, then immigrated 14 months later, was one and the same person.

Based on the details of the d’Este rumor, the Estes line was supposed to descend from one Francesco d’Este (Esteuse), an illegitimate royal son, exiled to France about 1471 after the death of his father, Azzo VI of Este, by a jealous half-brother, complete with a royal allowance. There are mentions of him in the Dutch and French courts, then nothing. Silence.

Apparently, various Estes lines in England liked the idea that he crossed the English Channel and settled in the fishing village of Deal, with his descendants carrying the surname Estes, a derivative of d’Este. King James apparently believed there was a connection and made that suggestion himself in one instance, although it’s unclear if that Estes man was from our Estes line.

It’s difficult to prove a negative, so we need to rely on the evidence we do have, much of which has been discovered and accumulated in more recent years, since the genesis of that rumor which was widely believed.

To begin with, it makes no sense that between 1471 and 1495, the family suddenly went from being a wealthy exiled royal circulating at court in France and the Netherlands, to peasant fishermen on the coast across the channel.

There is a legitimate royal lineage that does descend from the d’Este family in Italy, but until and unless someone who is a descendant of the direct male line of the House of Hanover, which reaches back to the Azzo line of Ferrara, takes the Y-DNA test, there’s no proof positive. Either their Y-DNA would match the Estes line, or not. I’d wager that it does not, but I’d love to find out for sure.

I’m hopeful that some nugget in Ancient Connections might add weight to either side of the argument.

Creating a Spreadsheet

First, I’ll show you the Ancient Connections spreadsheet built for the Estes line, then I’ll demonstrate how to build it.

Here’s the finished spreadsheet. Every haplogroup’s spreadsheet will be different.

I placed the four confirmed Estes haplogroups at the bottom because that’s the base from which the Ancient Connections are built, beginning with the closest Connection first.

“My” haplogroup, meaning for my ancestor’s Estes male line, is R-ZS3700, but there’s one additional downstream haplogroup, which I’ve included for completeness.

Let me alert you now that you WILL receive new Ancient Connections, which means that for every new Connection you receive, one more distant Connection rolls off the end because it’s outside of your 30 genetically closest Connections threshold. I’ve received new Ancient Connections in the past three months, between the time I originally began gathering this information and when I published this article.

The underlying message, in addition to maintaining your spreadsheet, is to set a calendar alert to check your Ancient Connections regularly. One rolled off that was more distant genetically, but was located only 10 miles away from where my Estes ancestors originated in Deal, England.

We’ll build the spreadsheet so you can easily expand it as new Connections are added.

Also, note that you may receive multiple matches from the same archaeological excavation site, which, of course, is highly suggestive of a family. If the multiple burials are in the same exact location and from roughly the same timeframe, I only record them on the spreadsheet once to reduce clutter, but I add a note that there are multiples.

The Build Process

Referencing the image above, haplogroups in the column directly above the originating haplogroup, R-BY154784, then R-ZS3700, colored apricot, are parent haplogroups – meaning that these haplogroups descend from the haplogroups above them. Look at R-ZP18, North Berwick, above R-BY482 as an example. This means two things.

  1. It’s possible that my ancestors could descend from these individuals in this column. However, all things considered, it’s more likely that they are a “cousin” of my ancestor who lived at that time and carried that haplogroup before a new mutation happened and branched into a new downstream haplogroup. That’s exactly what we proved about North Berwick based on when he lived and our downstream haplogroup formation date.
  2. Every man who shares that haplogroup, R-ZP18, absolutely DOES descend from the original man who carried that haplogroup-defining mutation that arose about 2250 BCE or about 4250 years ago. That one man in whom R-ZP18 occurred is noted above North Berwick, in red, indicating that both North Berwick and the Estes men descend from the man whose name is now R-ZP18.

On my spreadsheet, I’ve colored the cells of the haplogroups that I do descend from, and the burials I might descend from, apricot. The common haplogroups that burials and contemporary testers downstream descend from are in bold red text (R-ZP18 and R-DF49).

Burials who carry a different branching haplogroup, meaning they aren’t R-ZP18, but branch FROM from R-ZP18, are shown with their branches in blue. My ancestors cannot descend from blue haplogroups because we are on different branches of R-ZP18. Our branch is apricot.

Let’s add the next Ancient Connection.

Here’s the Time Tree Timeline of the second Ancient Connection, named Mount Pleasant 746, found at All Saints, Cambridgeshire, England, who lived between 940 and 1365 CE.

This shows two things.

  • My R-ZS3700 ancestor cannot descend from the Mount Pleasant burial, since R-ZS3700 doesn’t carry the mutation for R-BY173525, found in the Mount Pleasant burial.
  • However, since R-BY173525 branched from R-ZP18, we DO SHARE a common ancestor who lived about 4250 years ago. This means that between 4250 years ago and 940-1385 CE, the man found in Cambridgeshire, and my ancestor found in Kent around 1495 CE, both migrated in different directions from where their common ancestor, R-ZP18, lived, wherever that was.

The next closest Ancient Connection is Vor Frue Kirkegård 336, buried in the yard of a former monastic church in Vor Frue Kirkegård, Aalborg, Denmark, which dates from the 12th century. This man lived between 1536 and 1806 CE.

Again, my Estes ancestor who carries R-ZS3700 can’t descend directly from this man. Three things preclude Vor Frue Kirkegård 336 from being our ancestor:

  • The fact that Vor Frue Kirkegard 336 carries R-BY203953, but the Estes line does not.
  • Vor Frue Kirkegard 336 does not carry, R-BY342, the next downstream SNP for the Estes line.
  • Vor Frue Kirkegard 336 lived between 1536 and 1806 CE, which is contemporary with or after the earliest documented Estes ancestor was living in Kent, England circa 1495.

In this case, the locations are not in close proximity, over 500 miles apart by a combination of land and water. This distance would be less compelling as an elimination factor if the men were further separated by time.

In this case, any one of the first three pieces of evidence, alone, would preclude Vor Frue Kirkegard from being our ancestor.

Once again, R-ZS3700 shares the common ancestor of R-ZP18 with Vor Frue Kirkegård 336, along with Mount Pleasant 746 and North Berwick 16499. All of those men shared one common ancestor 4250 years ago.

Now, we have the bottom portion of our tree built out – meaning everyone who either carries haplogroup R-ZP18 as their primary haplogroup, or descends from that man.

Moving up the tree in the apricot column, you’ll notice that I’ve left spaces that leave room for the branching haplogroups in blue on the right. You won’t know how many spaces you need or the configuration until you start building the tree in your spreadsheet.

I listed both “5 haplogroups” and “3 haplogroups,” in the apricot column. You can spell those haplogroups out if you wish, but for my Ancient Connections, they didn’t matter. They may matter in the future, though, if you have an Ancient Connection who descends from or branches from one of them.

If you need an easy way to determine your ancestral lineage, the Ancestral Path is just the thing for you adn will help build your spreadsheet.

Your Ancestral Path

It’s easy to view which haplogroups are in your direct ancestral line. Just click on the “Ancestral Path” link in Discover’s sidebar.

Your haplogroup is shown at the top, with the parent haplogroups in order beneath. I’ve boxed the “5 haplogroups” between R-BY482 and R-ZP18 here, and then the “3 haplogroups” between R-ZP18 and R-DF49, which is where we find the next closest Ancient Connections.

One bonus of the Ancestral Path display is that you can see how many Ancient Connections are in the database for each haplogroup, at far right.

As I continue to build out my spreadsheet, the next four burials are all R-DF49, a haplogroup that was formed about 4400 years ago. Three of those burials are in England, and the fourth is in the Orkney Islands. They are all apricot, meaning:

  • They don’t carry any downstream haplogroups
  • They all descend from R-DF49
  • Based on haplogroups alone, nothing precludes the Estes line from descending from any of those men

Evaluating each Ancient Connection in the same way we did for North Berwick, when they lived, as compared to our Estes men, and where, may eliminate some of these burials as possible direct ancestors.

The balance of the Ancient Connections descend from R-DF49 through different branches and are colored blue, removing them as possible ancestors of R-ZS3700.

Regardless, we all share an ancestor, R-DF49, about 4400 years ago, just shortly before R-ZP18 lived some 4250 years ago. It would make sense that R-DF49 and R-ZP18 lived in relatively close proximity, given that they only lived about 200 years apart.

What else can we learn about these Ancient Connections?

Migration Map

To view all of your Ancient Connections on a map, just click on “Migration Map” in Discover’s sidebar.

The haplogroup whose path you are viewing, in this case, R-DF13, is the red dot on the bar at the top and is shown on the map with a red circle, but is mostly obscured here by the blue and red circles with numbers in the British Isles.

That haplogroup’s migration map, and your Ancient Connections, are displayed together. Individual burials not in close proximity to others are shown with individual trowels, and multiple burials are shown with blue and red circles, with the number indicating how many burials are found at that location.

Expanding the map shows more detail. I placed a red star to indicate the Estes lineage in Deal, at the bottom right.

Many of the blue and red circles have expanded, too.

By clicking on the blue circle, you can see which samples are found there. In this case, these 7 matching samples were all found in the same archaeological dig.

By clicking on any sample, you’ll see additional information.

One of my original questions was whether or not there was any indication whatsoever, even a smidgen of possibility that the d’Este rumor might be true. Some Estes researchers are not convinced by other arguments.

Given that our closest Ancient Connection lived about 2000 years ago in the British Isles, as do most, but not all, of the other Ancient Connections, it’s exceptionally unlikely that the progenitor of the Estes lineage was living in Italy in the 1400s, just a generation before our Estes ancestors are found in the records in Deal, and some 2000 years after the parent haplogroups of R-ZS3700 were already well-established in the British Isles.

There’s another place to check for additional information.

Notable Connections

Sometimes Notable Connections includes people who are either “ancient” themselves, and whose haplogroups have been identified through their descendants, or are from burials, or a combination of both. The difference is that their identity is not entirely a mystery.

When evaluating Notable Connections for genealogy, focus on:

  • Their haplogroup
  • Your shared haplogroup
  • When and where they lived
  • Any precluding factors like we found when analyzing North Berwick

Notable Connections are all interesting, but only a few may be relevant to your genealogy or your ancestors’ journey to where you first found them.

Speaking of their journey, Globetrekker shows you the most likely path of your ancestor’s haplogroup over time.

Globetrekker

Globetrekker is currently only available for Y-DNA, and only for those who have taken the Big Y test.

Clicking on Globetrekker through my cousin’s account shows the path of his haplogroup, through Europe, in this case, into England and, if I enable them, includes relevant Ancient Connections. One Ancient Connection, Mount Pleasant 746, at Cambridgeshire, is found on the estimated genetic haplogroup path.

We’ve already determined that the Estes line cannot descend from Mount Pleasant 746, but the locations of the descendants of our common ancestor, R-ZP18 can still provide substantial clues about where our common ancestor might have lived, and his culture.

I’ve also enabled Globetrekker’s “Sibling Lines” which indicate haplogroup siblings with the thinner lines. These display options are easy to toggle on and off.

Note that this is an estimated genetic path. In other words, it’s not exact. Especially, paths of the newer haplogroups can and will change over time as more testers test, and earliest known ancestors (EKAs) are added. I wrote about how to add EKAs in the article, “Earliest Known Ancestors” at FamilyTreeDNA in 3 Easy Steps. Please add yours, along with their location.

Sometimes the most refined haplogroup did not emerge in England, R-ZS3700 in this case, but in America. However, since the descendants have noted their EKA correctly as originating in England, that’s where the most refined haplogroup is also shown.

Furthermore, other than for Native Americans who are indigenous to the Americas, Globetrekker and the Migration Map both stop at the originating land mass for both Y-DNA and mitochondrial DNA.

You can read more about Globetrekker, here.

What About the d’Este Family Story?

Now, about that d’Este family story.

Globetrekker utilizes the “least cost” migration methodology, which means the easiest, least risky, route of passage from place to place for our ancestors. The Strait of Dover is the closest link to the European mainland, and was shallower at that time as well.

There’s absolutely no genetic evidence that points to Italy or anyplace south for the Estes ancestral line. In fact, haplogroup R-S552 emerged about 4650 years ago, and appeared about the time that this lineage crossed from continental Europe into what is today England. There’s no evidence that this line back-migrated to the continent, to then remigrate back to the British Isles after 1471.

Ancient Connections show us that there’s evidence of the Estes ancestral haplogroups in many locations across the British Isles, long before Frencesco d’Este was being exiled from Italy. Multiple Estes family members appear in the earliest records in the Deal area, so it’s certain that they were well established and probably fishing on those same shores hundreds, if not thousands, of years earlier, based on Ancient Connections these various migration maps.

These provide one more very large nail in the coffin of that much-loved but extremely unlikely family story.

The final piece of evidence would be if a proven male descendant of the d’Este line tested and did or didn’t match. I’m not holding my breath.

Mitochondrial DNA

The methodology for building your Ancient Connections spreadsheet is exactly the same for mitochondrial DNA, with one exception.

You immediately know that you cannot descend from any male burial, because men don’t pass their mitochondrial DNA on to their children of either sex. You could, however, potentially be descended from his mother, or sister, or cousin, etc. Otherwise, the guidelines are the same.

Sometimes, Ancient Connections can resolve long-standing conflicts.

The Conflict Surrounding Radegonde Lambert

For a very long time, it was believed that Radegonde Lambert, an early Acadian woman born around 1621, was Native American because there were no known people, other than her, with that surname in Acadia. Based on the birth years of her children, she married Jean Blanchard, a French man, around 1642.

It doesn’t help any that French soldiers arrived in 1632, family settlement began about 1636, but there are virtually no records until the 1671 census, nearly 40 years later. Lots of people perished during that 40 year window.

Radegonde could have married before her arrival in Acadia, and Lambert may not be spelled accurately. We are fortunate that French women are referenced by their birth surnames, not their married surnames, so she is listed as Radegonde Lambert, the wife of Jean Blanchard on the 1671, 1678 and 1686 censuses.

Based on the conflict swirling around her presumed Native American ancestry, plus early mitochondrial DNA HVR1/HVR2 results that pointed to haplogroup “X”, which has both Native American and European branches, Radegonde began to be reported as “DNA confirmed Native”. However, that was incorrect, and she was NOT DNA confirmed as Native. Haplogroup X2a and subclades are Native American, while other haplogroup X AND X2 subclades are European, as can be viewed in the Acadian AmerIndian DNA Project.

By the time full mitochondrial sequence testing became available, that incorrect “confirmation” was firmly entrenched in family trees and among researchers, leading me to pen the article, Haplogroup X2b4 is European, Not Native American.

While ho-hum with a yawn today, it was radical at the time and greeted with quite the kerfluffle. After all, Radegonde was proven Native and HOW DARE ME! 😊

Prior to Mitotree, Radegonde’s haplogroup was X2b4, but now it’s been extended to X2b4t2, which arose about the year 500, or around 1500 years ago.

X2b4 and subclades are quite rare, with only 353 descendants today, including subclades.

X2b4t2 only has 65 members.

Clicking on the “Other Countries” link takes you to the Country Frequency report.

Click on “Table View.”

Note that the 36 “Other Countries” includes people who have listed “Unknown Origin,” who are counted individually. People listing United States often mean they are brick walled here. Some people interpret this as Native American, but there is a separate United States Native American category. Not everyone selects the correct category.

These locations are user-reported in the Earliest Known Ancestor (EKA) information, which is critical for Discover reports. I wrote about how to complete that information in 3 easy steps, here. Please add yours, including location!

One person has reported that Radegonde Lambert is “United States Native American.” She’s not Native, and she never lived in the United States either. During her lifetime, Acadians lived in Nova Scotia, where three censuses accurately reflect her residence.  Perhaps that incorrect information was entered by someone years ago, and never changed. Most people don’t think to update their EKA information.

Unfortunately, when misinformation is provided, or not corrected after we learn more, new testers view that as nuggets of evidence, and the misinformation cycle continues.

One of the benefits of Ancient Connections is that they are NOT based on trees, historical records, or genealogy of any sort. Ancient Connections are based on archaeological digs, and the location of the excavation is not subject to question.

So, let’s take a quick look at Radegonde Lambert’s Ancient Connections and see what we find.

A Quick Sneak Preview

Because I’m interested primarily in a quick view of locations, I’m skipping right to the Migration Map where all of the Ancient Connections are shown.

Radegonde’s Ancient Connections are scattered all over Europe, but there’s absolutely nothing in the Americas.

Given that Native burial excavations are culturally frowned upon in many locations, we might not see any in the US, but we also wouldn’t see any recent burials in Europe, given that the Native people have been in the Americas for well over 10,000 years.

Generally, even when Ancient Connections are missing in the US, we still find some contemporary testers with proven genealogy who carry that haplogroup, and at least a few ancient burials in Canada, Mexico, Central and South America.

The first seven Ancient Connection matches carry haplogroup X2b4, and the rest are European subgroups of X2b4. There are no closer matches as of today, but that doesn’t mean there won’t be eventually.

X2b4 emerged sometime before 5200 years ago, clearly someplace in Europe, possibly central Europe.

Radegonde’s X2b4 match locations are:

  • Malá Ohrada site in Prague – the individual lived 5800-5400 years ago
  • Hetty Peglers Tump, Gloucestershire, England – lived 5639-5383 years ago
  • Sorsum, Hildesheim, Lower Saxony, Germany – lived 5350-5100 years ago
  • Passage Tomb, Carrowkeel, Cairn K, Sligo, Ireland – lived 5100-4600 years ago
  • Kolín I-7b, Bohemia, Czech Republic – lived 4835-4485 years ago
  • De Tuithoorn, Oostwoud, Netherlands – lived 4579-4421 years ago

It’s unquestionable that X2b4 was found across Europe, not in the Americas, 5000 years ago.

This image is NOT from Radegonde Lambert’s Ancient Connections. I’ve included it to illustrate a Native American branch of haplogroup X2.

The descendants of Native American haplogroup X2a, shown above, match Kennewick Man, who is also X2a, as their closest Ancient Connection. He lived between 9250 and 8390 years ago along the river in present-day Kennewick, Washington. Their second-closest Ancient Connection is with an X2a1 burial found in Windsor, Ontario, who lived between 1223 and 1384 CE.

Neither of these unquestionably Native burials are found in the Ancient Connections of Radegonde Lambert’s descendants.

It’s worth noting here that when evaluating rare haplogroups, their Ancient Connections may reach far back in time. For example, if a Native American haplogroup only has a few Ancient Connections within the Americas, the rest of their Ancient Connections, if any, will be found on another continent. Failing to read the results thoroughly and thoughtfully could lead to an inappropriate and incorrect conclusion.

For example, haplogroup X is found in Eurasia prior to the migrated of people across Beringia, the now-submerged landmass connecting Asia with Alaska, to become the indigenous people of the Americas. Therefore, if there are less than 30 closer X2a Ancient Connections, one would expect to find Ancient Connections reflecting that continental Asian, or even Eurasian, heritage far back in time.

Notable Connections

One final tip for both Y-DNA and mitochondrial DNA is to check Notable Connections and selectively add them to your spreadsheet, if appropriate. Sometimes you’ll find people there that are both Notable and Ancient.

Not that we need more evidence about whether Radegonde Lambert’s matrilineal ancestors were Native or European, but Notable Connections provides us with one more corroborating piece of evidence.

Cangrande della Scala was an Italian nobleman who lived around 1300. He and Radegonde share a haplogroup X2b1″79 ancestor in Europe around 9000 years ago, which was after the Native people had crossed Siberia and Beringia to begin settling Canada and the Americas.

If there was any question left about Radegonde Lambert’s origins, Ancient Connections resolved it, with a backup volley from Notable Connections.

Radegonde Lambert was my ancestor, so I’m going to build her Ancient Connections spreadsheet and savor every discovery, but if I were simply seeking confirmation of or the answer to the question of whether Radegonde Lambert was Native American or European, I need look no further.

Mitochondrial DNA Case Study

In the article, Mitochondrial DNA A-Z: A Step-by-Step Guide to Matches, Mitotree and mtDNA Discover, I wrote in detail about utilizing mitochondrial DNA to break through genealogy brick walls.

My goal was to detremine if Catherine LeJeune, Edmee LeJeune and Jeanne LeJeune dit Briard were sisters or at least matrilineal relatives. Fortunately, we had several testers.

As it turned out, Catherine and Edmee were European sisters, but Jeanne did not share a matrilineal ancestor with Catherine and Edmee. Jeanne was Native American.

Next, we wanted to discover as much information about the LeJeune sisters as possible.

I created an Ancient Connections spreadsheet for the LeJeune sisters and included those results in my analysis, so please take a look. Their Ancient Connections were unexpected and simply astounding.

You literally never know who is waiting for you, nor the message they hold, just waiting to be delivered.

Ancient Connections are clues from your ancestors.

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Sixteen Unique Trees at FamilyTreeDNA: How and When to Use Each

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I love all the various trees at FamilyTreeDNA – and I’m not referring just to traditional genealogy trees with people, names, and dates. I’m talking about phylogenetic or haplogroup trees – the ones you use to understand your Y-DNA and mitochondrial DNA haplogroups, origins – and more. These trees tell you ABOUT your ancestors, those people in the more traditional genealogy tree, and the combination of both is powerful.

This article introduces the various trees available at FamilyTreeDNA, when and where you’ll find them, and what they can do for you.

Haplogroup Trees

Phylogenetic, or haplogroup trees, provide a genetic path from you, or the tester, today, back in time to Y-Line Adam, or Mitochondrial Eve – the first two humans who lived AND have descendants today.

Let’s start by explaining about Y-DNA and mitochondrial DNA (mtDNA), their inheritance path, and what they mean to you.

Y-DNA

Only men have a Y-chromosome, so only biological males can test their Y-DNA.

Y-Line Adam, Y-DNA haplogroup A-PR2921, lived about 232,000 BCE, or 234,000 years ago.

Is it possible that one day someone will test whose results push that date back somewhat? Yes, of course, as we are always learning, and many testers split branches.

Today, all 711,000+ modern descendants who have tested carry the mutation named A-PR2921 as their oldest SNP (single nucleotide polymorphism), or haplogroup-defining mutation in their Y-DNA. That’s because we all descend from that one man.

If you’re a male, Y-DNA testing tells you about your direct paternal line by matching with other men who have also taken a Y-DNA test, and by revealing valuable information from before the adoption of surnames. There’s no other way to reach that far back in time.

If you’re a female, you can recruit males in your family to test.

The Big Y-700 test provides the deepest-reaching and most refined Y-DNA test available, which is essential for both genealogy and tree-building.

Mitochondrial DNA

All people have mitochondrial DNA, inherited from their mother directly through her matrilineal line – meaning her mother, her mother, her mother, and so forth – directly up your tree through all mothers.

Everyone inherits their mitochondrial DNA (mtDNA) from their mother, but only females pass it on. Both males and females in the current generation, meaning you, can (and should) test their mitochondrial DNA.

Mitochondrial Eve, mitochondrial DNA haplogroup L, lived about 141,000 BCE, or about 143,000 years ago. All 315,000 testers descend from this one woman.

Like with Y-Line Adam, one day the results of future testers may push this date further back in time. A full sequence mitochondrial DNA test, mtFull, is necessary to test all 16,569 mitochondrial locations.

Test Types

FamilyTreeDNA has been in business for more than 25 years. Technology has advanced dramatically during that time. While they continue to offer new tests and products, they strive to maintain value for their original testers.

Even though some early testers may have joined their ancestors, matching with their test results is still beneficial to us.

Present-day DNA testers can still derive value by matching the earlier, lower-level, lower-resolution tests. Not as much value as if the original tester had taken a higher-level test, but those tests may not have been available at that time.

Matches, surnames, genealogy, locations, and haplogroups provide us with valuable information. The more people who test, the larger the pool becomes, and the better our chances of discovering something that refines our understanding of our ancestors – and identifies who they are.

Before we look at the trees available, let’s take a look at where haplogroups come from. Different level tests assign different levels of haplogroups, based on how much is tested.

Let’s answer two common questions:

  1. Where can you find your haplogroup, and what does it mean?
  2. How can haplogroups be different for people who descend from the same ancestor?

Where Do Haplogroups Come From?

Since the beginning, FamilyTreeDNA has always provided their customers with haplogroup information. Haplogroups are very genealogically useful today, but initially, 25 years ago, they were only able to provide essentially continental-level origin information for your particular line. That too was useful, and helped to identify and eliminate common lineages – just not as useful as today.

Science and testing have both come a long way. Present-day testers still match with people who only tested at a lower level. You never know what you might find at that level – a match to someone who has not taken the current tests, but is still very relevant because they share your ancestor. In fact, they may be the only tester who does.

For Y-DNA testers, you’ll notice several match categories that reflect different testing levels – along with the number of matches at each level. At one time, you could purchase each one of these tests individually, then later upgrade to higher-level tests. Today, only the 37 and 111 marker tests, and the Big Y-700, which scans the entire gold-standard region of the Y chromosome, are available. Higher level tests include the lower-level tests.

Click any image to enlarge

Different types of tests provide either a predicted or a confirmed haplogroup which shows on your match list.

Without getting all sciency on you – the 12-111 marker tests test targeted STRs, or short tandem repeats, which can’t be used for haplogroup assignment and confirmation. They can and are used to compare to other testers for matching because the number of repeats, or stutters, are inherited on the Y chromosome. The Big Y test scans the Y chromosome for SNPs, single nucleotide polymorphisms, which are stable mutations that define haplogroups. I wrote about this in the article, STRs vs SNPs, Multiple DNA Personalities.

Some haplogroups are much further down the tree, or more current, than others. Your most current haplogroup, only available with the Big Y-700 test, is the best because it brings you the closest to current in time, often placing you within family branches. The Big Y-700 scans about 23 million locations on the Y chromosome, revealing both known and unknown mutations, not just a few markers, making it the most refined and relevant test genealogically.

Each higher-level test includes the lower-level tests. You can see what tests your matches have taken by looking beneath their names on your match list. In this case, these Estes men who match my cousin have taken the Family Finder (or uploaded an autosomal transfer), and taken the mtFull test. One match initially took the Big Y-500 but has since upgraded to the Big Y-700, and the other originally tested at the 111 marker level, and has since upgraded as well.

The Big Y-700 includes all lower-level tests, such as the Big Y-500 (now obsolete), the 111, 67, 37, 25, and 12 marker STR tests. You still match with people who only tested at those levels, plus everyone else who ordered a more refined test.

The haplogroup you receive is more or less refined, based on the test level you take.

Y-DNA Test Type Haplogroup Provided Relevance Upgradable
Y-DNA STR 12-111 marker tests (only 37 and 111 are available today – the rest are obsolete) Predicted based on STRs – very reliable at the level predicted Predicted (not confirmed) haplogroup that was generally formed a couple thousand years ago, or earlier Yes, if enough quality DNA remains. Only 37, 111, and the Big Y-700 tests are available today. Recommend the upgrade to Big Y-700.
Individual SNP test (now obsolete) Confirms a predicted haplogroup or tests a single SNP to confirm a closer haplogroup Relevant at the level tested – either positive or negative result was reported Individual SNP tests have now been replaced by Big Y-700, which covers all individual SNPs that were available to test, plus much more.
Big Y-500 test (now obsolete) Confirmed haplogroup within range of that test’s ability, replaced by much more granular Big Y-700 Big Y-700 is more refined and moves the tester towards more current haplogroups, so more genealogically significant Yes, upgrade to Big Y-700 if enough DNA remains, or tester can re-swab
Big Y-700 – scans the entire gold-standard region of the Y chromosome – approximately 23 million base pairs Top-of-the-line SNP-confirmed test, most granular and refined. Scans for known and previously unknown mutations. Extremely accurate. Generally advances the tester into a genealogical timeframe, and often divides testers into multiple lineages descended from a known common ancestor No more advanced test is available.
Family Finder autosomal test or transfer Confirmed to mid-range level if possible. Not all transfer files have Y-DNA or mtDNA SNPs so you get what you get. Useful in autosomal matching for locating people you may be related to you with that surname. Ask the match if they are willing to take a Y-DNA test, if relevant, or sponsor a testing scholarship for them.

Family Finder haplogroups are relatively new at FamilyTreeDNA. Each chip level that FamilyTreeDNA has used for testing over the years, and the chips that other vendors have used, contain different SNPs (or none at all on the Ancestry test) that can be measured for some level of haplogroup. Other vendors generally don’t quality-control for either Y-DNA or mtDNA SNPs because they don’t use them. This is a “you get what you get” freebie.

That said, most Family Finder haplogroups are closer in time, or “better” than the predicted R-M269, the most common haplogroup in Europe, often reported with STR testing.

Not everyone with a transfer kit receives a haplogroup. Due to quality and reliability issues, you cannot see haplogroups on your autosomal match list for those who only have a haplogroup through an autosomal transfer.

Using our male Estes testers as an example, we find the following haplogroup results at the various testing levels:

Haplogroup Haplogroup Formation Date Ancestor or Haplogroup Formation Location Haplogroup Source
R-M269 4450 BCE (6450 years ago) Between Ukraine and Kazakhstan, north of the Black and Caspian Seas Predicted from 12-111 STR marker tests
R-BY487 700 CE (1300 years ago) UK, Scotland/England Family Finder DNA SNP Confirmed
R-BY482 1550 CE Robert Eastye b 1555 Ringwould, Kent, England Big Y-700
R-BY490 1700 CE Silvester Eastye b 1596 Kent, England Big Y-700
R-ZS3700 1750 CE Moses Estes 1711 VA Big Y-700
R-BY154784 1850 CE Joseph Estes b c 1790 VA or TN Big Y-700

All of these are valid and accurate haplogroups – some are just closer in time and much more useful than others. All of these men have R-M269, because it is a parent haplogroup of all of those downstream haplogroups. The Big-Y tested men beginning with R-BY482 don’t share the haplogroups below them, because they don’t have those mutations that are downstream on the tree. However, the men at the bottom with R-BY154784 have all of the SNPs above them.

Note that all haplogroup formation dates are ranges. I’m showing the midpoint here.

When upgrading, if the original tester is deceased, select the highest-level test available, as there may not be enough DNA to run more than one test. When I offer scholarships now, I always just offer the Big Y-700 test to avoid future issues.

If the tester you need is no longer available, consider the possibility that other people, family members perhaps, might be available to test to represent this same line.

Next, let’s look at mitochondrial test levels and haplogroups.

Mitochondrial DNA Test Type Haplogroup Provided Relevance Upgradable
HVR1 & HVR2 tests (no longer available) Predicted based on around 1000 markers – very reliable at the level predicted Predicted haplogroup, not confirmed, generally formed a couple thousand years ago or earlier Yes, if enough quality DNA remains. Only the mtFull test is available today.
mtFull, full sequence test Tests all 16,569 SNP locations in the entire mitochondria. Most granular and refined. Extremely accurate. Often brings tester into genealogical timeframe, especially with the new Mitotree. Divides testers into multiple haplotype lineages, sometimes descended from known common ancestor. No upgrade needed to receive new Mitotree and mtDNA Discover benefits.
Family Finder autosomal test or transfer Coming soon. Will be the same criteria and caveats as Y-DNA SNPs. May be able to find a similar or upstream haplogroup that might point to a common ancestor. Ask autosomal match if they are willing to take a mtFull test, if relevant, or sponsor a scholarship for them.

Ok, now that we understand more about haplogroups, how they are determined, and where yours came from, let’s look at all of the trees at FamilyTreeDNA.

Trees Within Your Y-DNA and Mitochondrial DNA Account

Let’s start with trees found within your personal account, so sign in.

Each tree has a different purpose and unique benefits.

Tree #1 – Your Matches Genealogy Trees

Each of your matches may have provided links to genealogical trees. They may show trees in multiple places too; at MyHeritage, an archived tree at FamilyTreeDNA, and a WikiTree link. I makes notes about their trees in the comments field, and I also keep a spreadsheet to look for commonalities.

Tree #2 – Haplogroups and SNPs for Y-DNA Testers

Next, for Y-DNA testers, click on the Y-DNA Results and Tools.

You’ll see the Haplotree & SNPs tile on the dashboard.

The Haplotree and SNPs link takes you to a phylogenetic tree that defaults to your haplogroup, where you can view:

  • Variants – SNP mutations that define your haplogroup
  • Surnames with this haplogroup – so long as there are multiple public testers
  • Countries – self-reported for earliest known ancestors (EKA)
  • Recommended Projects – haplogroup projects only – others such as surname projects are found in Discover under Suggested Projects

Tree #3 – The Block Tree for Big Y Testers

People who have taken the Big Y-700 test have a separate section that includes tools for the Big-Y test that aren’t relevant for the 12-111 STR marker tests.

Big Y testers will see the Block Tree tile on their dashboard.

The block tree is an alternative way of displaying matches on a phylogenetic tree. While the Discover Time Tree is viewed left to right, this tree is displayed top to bottom, with each mutation being represented by one grey bar on the scale at left. Each mutation corresponds to approximately 100 years, which is a rough average for the frequency of Y-chromosomal mutations.

People with 30 mutations or fewer are shown as matches, with the goal of reaching back about 1500 years.

Each large block shows the mutation for which the haplogroup is named, such as R-BY482, at the top. The mutations, known as variants, shown below that haplogroup name, are found in the results of each person in that haplogroup, but in the future, people without those mutations, or with additional mutations, will form a new branching haplogroup.

The green “Private Variants” at the bottom of the branches display the average number of mutations of people within that group awaiting another tester to have the same mutations, so a new branch can be formed. I view Private Mutations as “haplogroups in waiting.”

Discover

In addition to the haplogroup trees shown in your account at FamilyTreeDNA, there are several additional trees in Discover for both Y-DNA and mitochondrial DNA. Discover, updated weekly, is a suite of tools for both Y-DNA and mitochondrial DNA that, cumulatively, provides a book about your haplogroup results.

Discover comes in two flavors:

  • The publicly available free version with limited functionality
  • Your private version with expanded functionality available from within your account

You can access Discover, here if you’d like to follow along.

Discover is a publicly available free tool introduced in the fall of 2023 that provides more than a dozen reports, enabling a deeper understanding of all haplogroups.

Just select Y-DNA or mtDNA and enter your haplogroup of choice.

Think of these menu choices, in the sidebar, as chapters in your personal book. Every chapter has something interesting to tell you. Please read them – don’t just scan.

In addition to the free version, if you have taken a Big-Y or mitochondrial DNA full sequence test at FamilyTreeDNA, you’ll have additional information available.

For mitochondrial DNA results, just click on the pink Discover tile.

For Y-DNA results, click on the blue Discover tile.

Within Discover, you’ll find three distinct trees.

Trees #4 and #5 – Y-DNA and Mitochondrial DNA Time Trees

The Time Tree shows your Y-DNA or mitochondrial DNA haplogroup displayed on a timeline, along with:

  • A self-reported ancestral country indicator for every person’s DNA in that haplogroup
  • Haplotype groupings indicating exact matches between everyone in that haplotype.

A haplotype is a grouping of people whose DNA matches exactly, including unstable or hypervariable locations too unreliable to use for haplogroup formation. However, those mutations may be relevant for genealogical matching.

I wrote about haplogroups and haplotypes here and here.

Tree #6 and #7 – Y-DNA and Mitochondrial DNA Class Tree View

The Classic Tree is available for both Y-DNA and mitochondrial DNA.

On the Classic Mitotree View, you can display and filter the tree, including haplotypes, in seven ways, as shown in the dropdown “Display Options.”

Tree #8 and #9 – Y-DNA and Mitochondrial DNA Tree Branch Comparison

Have you ever seen two haplogroups and wondered how closely they are related? Compare provides that answer.

Here, I’m comparing my haplogroup to that of a family member. Everyone is related, but how long ago are we related on our matrilineal lines?

Haplogroup J1c2f compared with haplogroup V216a shows that our common ancestor lived a VERY long time ago – about 55,000 years in the past, someplace in the fertile crescent.

For either Y-DNA or mitochondrial DNA, you can compare two haplogroups. This provides specific information about those two branches of the tree, and where they intersect. To view more about the common ancestor, just pop R+10398 into Discover and learn more about when and where that ancestor lived.

Trees #10 and #11 – Match Time Trees

Match Time Trees are one of the most useful Discover features.

In addition to the Time Trees and Classic Trees provided for everyone in Discover, test takers will also have a Match Time Tree that shows all of your matches, organized genetically.

For mtFull testers, your matches are organized by haplotype cluster. People in your haplotype cluster are your exact matches.

I have over 100 full sequence matches, so I’m only showing the first few in this screenshot. In addition to the match’s name, their EKA (earliest known ancestor) is shown, if provided.

On the Y-DNA Match Time Tree, links are provided to genealogical trees of the tester, which could be an archived FamilyTreeDNA tree, a MyHeritage tree, WikiTree, or some combination.

You can actually see your matches’ WikiTree tree on your Match Time Tree by enabling another feature.

Trees #12 and #13 – WikiTree Tree Integration

While you’re still on the Match Time Tree page for either Y-DNA or mitochondrial DNA, click on Display Options, above the Time Tree, and enable WikiTree Connections. Unfortunately, the default for this great feature is “off.”

I’ve enabled “Share Mode” at the top to obfuscate the names of the testers, and I’ve adjusted the vertical spacing so you can see more in my examples. You’ll notice the grey lines with dots inside circles. I think of these as beads or maybe knots on a rope, but they actually represent a line of ancestors.

Each tester with one of those grey dot bars has connected themselves to their ancestors at WikiTree, a public one-world tree. Living people are not shown, hence the dash marks to the immediate left of the tester’s name.

By mousing over any of the dots, aka ancestors, you can view information about this ancestor of this Estes tester at WikiTree. Ancestors appear in genealogical order in their relevant place on the Time Tree. How cool is that!!!

WikiTree, like any tree, public or private, can have errors. Always verify any tree using original source documents.

As far as I’m concerned, the Match Time Tree is one of the very best features of both Y-DNA and mitochondrial DNA testing and matching. There are so many options to select from, so take some time to look around.

Your Personal Version of Discover is Best

Y-DNA Discover and mtDNA Discover can both be useful for any level of haplogroup, but the best results are obtained when clicking through from the tester’s FamilyTreeDNA account. Big Y and full sequence mitochondrial DNA customers receive additional information, not available in the free, public version of Discover, including

  • The Match Time Tree
    • Including WikiTree integration
  • Globetrekker (Y-DNA, mtDNA coming eventually)
  • Up to 30 Ancient Connections, as compared to 3 in the free version
  • Up to 30 Notable Connections, as compared to 3 in the free version

Tree #14 – Group Time Trees

I absolutely love Group Time Trees. They are similar to Match Time Trees, but unlike Match Time Trees, are publicly viewable for Group Projects if the volunteer project administrators have enabled this feature for the project.

There are two ways to access Group Time Trees – through publicly accessible Discover or directly through any project.

In Discover, select Group Project in the dropdown.

Then type the name of the surname project you’re seeking. You’ll be presented with a menu if the surname you’ve entered is found in multiple projects, or administrators have listed it as “of interest” in their project.

I clicked on the Estes project.

Viewing the Estes DNA Project, under DNA Results, you can see the various options.

Selecting Y-DNA Results Overview displays the project results by administrator-defined group. The teal groups all descend through Abraham Estes through various sons.

However, by clicking the Group Time Tree instead, you can view all these testers and their results in a Match Time Tree format, arranged genetically.

Clicking on the Group Time Tree link takes you to the Group Time Tree for this project. A menu is displayed at left, based on how the administrator has grouped the project.

I’ve selected several groups that I know descend from the original Estes ancestor from Kent, England. Testers who have joined the Estes project and granted permission for their results to be displayed publicly are automatically grouped genetically, at right, with their surname and EKA (earliest known ancestor), assuming they have entered that information.

Earliest Known Ancestors (EKA)

You’ve probably noticed that earliest known ancestors, along with their locations, are used in many places.

Please enter both your direct paternal (father, father, to father’s line) and direct matrilineal (mother, mother, to mother’s line) earliest known ancestors, along with their locations. I wrote about how to do that in “Earliest Known Ancestors” at FamilyTreeDNA in 3 Easy Steps, here.

Trees #15 and #16 – Public Trees

In addition to trees within testers’ accounts, Discover trees, Group Time Trees, and WikiTree tree integration, FamilyTreeDNA provides two additional public trees.

FamilyTreeDNA made the Y-DNA and mitochondrial DNA haplogroup trees freely available years ago, at the bottom of their main company public page – without signing in.

These trees are still actively maintained today and are free for everyone to use.

To find these trees, scroll all the way to the very bottom of the page, in the footer, to the Community section. Yes, I know, it’s a bit like a scavenger hunt!

You can select to view either the Y-DNA or mtDNA tree. I love this tree, because it shows how many SNP-confirmed people have been tested. That number does not include the thousands of academic and public samples that may be utilized to help define haplogroups, and that you’ll sometimes see in your Ancient and Notable Connections.

So, if you receive a new haplogroup, but you don’t see a new match on your list or on the Block Tree, it’s probably because you match a high-quality academic sample.

The trees display from the root, meaning the oldest haplogroup is shown at the top. In the Y-DNA tree, above, haplogroup A-PR2921 is “Y-Adam”.

You can select any haplogroup on the bar across the top, search by country, or select a specific branch name to view.

The tree itself is viewable by country, as shown above, or by variant, meaning the haplogroup-defining mutations, shown below.

Additionally, for the Y-DNA tree, you can choose to display by surname, so long as there are two or more testers with that identically spelled surname who share this haplogroup and who have given permission for public display.

Please note that these people are all SNP-tested and confirmed at the level reported, but they are NOT all Big-Y testers.

This feature alone can be genealogy-changing because they may be surnames associated with your ancestors in records, or they may just be neighbors. Or maybe you thought they were “just neighbors,” but they are actually related.

At one time, customers could order an individual SNP test for R-M269 to confirm their predicted haplogroup. That test is no longer available, but anyone who took that test to confirm R-M269 and never tested or received results (like Family Finder) at a more granular level will be reported at R-M269. Note that 687 is the number of distinct surnames shown, not the total number of testers.

The three “hamburger dots” on the right side provide options for a user-reported Country Report based on the location of their earliest known ancestor, and a Surname Report. The surname report for R-M269 shows a total of 2448 testers who share those 687 surnames.

It’s a Whole Forest

Who knew there were 16 unique trees available at FamilyTreeDNA!

Each tree has a unique purpose and provides information not available elsewhere.

Take a look and see what kind of information is waiting for you – and don’t forget to check back often.

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The New FamilyTreeDNA NGS Family Finder Test

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Click on any image to enlarge

Recently, in a press release, FamilyTreeDNA announced a new version of their Family Finder autosomal test that increases coverage from about .02% to about 9% of the human genome. Increasing coverage to this level using precision genomics holds great promise for the future.

Everyone who has purchased a Family Finder test since the beginning of March is automatically tested using the new technology – and it doesn’t cost any more than the earlier test.

As shown in this slide presented by Dave Vance, Senior VP and General Manager at FamilyTreeDNA, the new test covers 400 times more DNA locations than the industry-standard microarray chip-based test.

The typical vendor microarray autosomal DNA test covers somewhere between 400,000 and 750,000 locations.

Utilizing this new technology is an investment in the future.

You Don’t Know What You Don’t Know

To quote Dave:

Two numbers I want you to remember.

0.02 is the percent of your whole genome reported by standard autosomal tests today. All of your ancestry estimates, shared segments, and autosomal matches come from that small fraction.

9 is the percent of your genome that our new Family Finder test reports at high quality coverage. Starting right now — that’s over 400 times more data, from the very same test.

And the real point isn’t the number. It’s what that data makes possible. This gives us the foundation to unlock deeper, more meaningful insights — not just today, but for years to come. And when it becomes possible to go even further, I want FamilyTreeDNA to lead the way.

But what does that 9% mean for your genealogy research?

It means fewer unexplained matches, a clearer understanding of how people are related, and more confidence in the conclusions you draw from your autosomal DNA. Moving from connections to explanations, and from data to answers.

And until we can start rolling out those deeper insights, for now you’ll still get the same trusted Family Finder experience you’re used to — but you’ll also have the benefit of data that’s ready to unlock even more as new insights become possible.

In fact, you can watch Dave for yourself, at RootsTech, on the mainstage, here, having the unenviable position of following the Irish-step-dancing Gardiner Brothers. Yea, Dave, I didn’t get that gene either!

What makes NGS sequencing so special?

Sequencing Types

NGS is the abbreviation for Next Generation Sequencing, also called massive parallel sequencing. Rather than using individual probes, NGS is a high-throughput technology that simultaneously sequences millions of DNA fragments while still allowing targeting of specific regions.

Dave wrote about the differences between different types of sequencing, here.

All vendors select or target locations in the human genome that are most relevant for their product set, purpose or goals.

The older microarray sequencing machines have been in use for many years. They use probes to read specific targeted addresses, one by one, identifying which of four nucleotides is present at each location on your two copies of each chromosome.

The four nucleotides, adenine (A), thymine (T), cytosine (C), and guanine (G) are the building blocks of DNA, and you receive one from each parent at every location on chromosomes 1-22. Chromosome 23, the sex selection chromosome is a little bit different due to X-DNA and Y-DNA, but the locations are still read the same way using NGS technology.

The results of DNA testing are essentially a downloadable output file with the following information for each read:

  • The RSID SNP cluster ID chromosome
  • The chromosome number
  • The position (think street address) on the chromosome
  • The results, which are the abbreviations for the nucleotide found on the first and second strands of your DNA at that location

In autosomal DNA testing, positions on strands cannot inherently be identified as maternal or paternal without additional techniques such as parental comparison or phasing.

This data file is not meant for you to analyze, but for computers to compare to other DNA testers. Needless to say, the power of the data lies in the information it holds, such as ethnicity, haplogroup-identifying mutations, and matching with other testers.

The output files must be compatible with each other, or the vendors must make accommodations for any incompatibility.

Regardless of the sequencing type, currently, all genetic genealogy vendors’ download files use this same pattern.

The difference between the files and file types from each vendor is:

  • The technology used for the test
  • How much DNA is tested
  • How many rows of data are provided in the download file
  • The quality of the results

Sequencing Type Differences

Let’s put this in terms that we all understand.

With microarray sequencing, a utility worker is sent to each address to read the two nucleotides.

With both NGS and whole-genome sequencing, many addresses are read at the same time. Think of a fleet of drones flying over a neighborhood and reading what is written on the rooftops of each house address.

The difference between the type of NGS sequencing utilized by FamilyTreeDNA, and whole-genome sequencing is threefold:

  1. NGS targets specific addresses and neighborhoods in a controlled manner, because we know they are useful and are specifically interested in the data at those locations. In other words, it omits oceans, deserts, and other places that we know aren’t useful for genealogy.
  2. Whole-genome sequencing covers the majority of the genome, even though more than 90% of the genome is identical in all humans. In other words, the fleet of whole-genome sequencing drones flies over everything, including oceans and deserts, reading and storing everything.
  3. The number of times the drones fly over each address.

For example, a low-pass whole-genome test would fly over the entire world (your genome), scanning it once or twice, but there will be cloud cover and weather in some locations. Typically, you want at least two complete reads from each address to compare to ensure a minimum level of quality. The missed areas need to be estimated with tools like imputation to fill in the blanks.

The breadth of DNA covered is known as “coverage”, or “pass coverage”. So, whole-genome testing covers all or most of the genome, including more than 90% that is not genealogically relevant because it’s identical in all humans.

With NGS sequencing, you specify which locations or neighborhoods you want the drones to read, and you instruct them to fly over just those regions, say, 5 or 10 times. Even if there’s weather or another issue, chances are that at least some of those passes will be able to read both nucleotides.

How many times a particular location, or base, is read is known as “read depth” or “sequencing depth”. The greater the depth, the higher the quality and accuracy of the targeted locations, which means less imputation or “fixing” is needed.

Within the industry, confidence to coverage correlation is about 93% confidence of accuracy for both alleles at a given location at a depth of 5X, which rises to about 99% accuracy at a depth of 10X.

Using our examples, whole-genome sequencing covers about 98% of the genome, at a depth specified by the vendor. Low-pass whole-genome testing is typically performed at a depth of 2X, meaning each location is scanned twice.

NGS combines the best aspects of both “drone style” and “targeted” reads, providing the highest accuracy for the areas that are most important for genetic genealogy at an affordable price, while also targeting enough of the human genome to allow for new discoveries that may be important to either population genetics for ethnicity identification, or to identify your own family lineage mutations.

Yes, you can get both high coverage and very deep reads. That’s called medical-grade whole-genome sequencing, where your entire genome is sequenced to a depth of at least 30X, but it’s both expensive and not useful for genealogy. None of the genealogy vendors are prepared to, or need to, process the massive amount of data generated by a medical-grade whole-genome test, so there is no benefit to taking that type of test for genealogical purposes.

Why is NGS Sequencing Important?

FamilyTreeDNA has moved from the 700,000+ SNPs previously read on their microarray chip, to more than 280 million base pairs. So, from about .02% to about 9% of the 3.1 billion base pairs of the human genome.

Technology has improved to the point where NGS sequencing is no more expensive than microarray sequencing and provides substantially more results.

In other words, there’s no reason NOT to implement this technology now. The new Family Finder test is fully compatible with their earlier Family Finder tests, so everything is painless.

Plus, NGS allows FamilyTreeDNA to target specific locations that benefit their customers, such as both Y-DNA and mitochondrial DNA SNPs. Of course, you’ll still need to take the Big Y-700 or the full sequence mitochondrial DNA (mtDNA) test for full results and matching – but males will receive a confirmed Y-DNA mid-level haplogroup now, with midrange mtDNA haplogroups coming in the future for Family Finder testers. This is a feature that other vendors don’t target or provide at the same level.

I’m very hopeful that these foundation haplogroups will serve as an “appetizer” and will encourage more people to take both the Big Y-700 (males only) and the mtFull test (for everyone), as applicable, to receive those types of specific matches and learn more about their ancestors.

Speaking of the future, how do you future-proof your DNA?

Future-Proofing Your DNA

If you’ve already tested, should you purchase a new Family Finder test for yourself now?

No.

I know you didn’t expect that answer, but here’s why.

Everyone who purchases a Family Finder test, which uses NGS technology, receives the same matching and features as the legacy test.

FamilyTreeDNA doesn’t yet know the benefits and discoveries that will eventually be available, and they won’t know until after they have results of customers to work with.

Having said that, you will definitely want to future-proof your DNA and the results of anyone whose results you count on to help sort through your own.

So, let’s make a plan!

Assuring Future Compatibility

Plan 1 – Test Your Relatives:

Your closest relatives are your best assets. They help you determine how you match others, who you share ancestors with, and the identities of those ancestors. You absolutely need to test the following relatives if they are available:

  • Parents
  • Grandparents
  • Siblings, both full and half – test all of them if both parents aren’t available for testing.
  • If your sibling(s) are deceased or not available, their children carry half of their DNA, but not the same half, so test everyone available. You don’t need to test your siblings’ children if that sibling is available to test.
  • Aunts and uncles, or their descendants if they are not available
  • Great-aunts and uncles, or their descendants if they are not available
  • First and second cousins

Plan 2 – Person Has Never Tested:

Plan 3 – Already Tested at FamilyTreeDNA:

  • If they or you have already taken a Family Finder test at FamilyTreeDNA, an upgrade offer will be forthcoming soon. You don’t need to do anything now.
  • If the person is critical for your research, elderly, or there is some other reason for concern, the tester or kit manager can contact FamilyTreeDNA customer support now and inquire whether or not there is an unopened vial of DNA.
  • To assure that there is enough DNA left for the future, or that the DNA sample is not too old, you can request that a “C/D vial” set be sent to you/them just in case. Be sure the current address is valid.
  • This is also a good time to be sure that your/their Beneficiary Information and/or Kit Manager information is current as well. You’ll find both under Account Settings beside the name in the upper right corner of the page.

Plan 4 – Uploaded From Another Vendor:

  • If you uploaded your DNA file to FamilyTreeDNA from another vendor instead of testing there, hold your horses for now. You’ll clearly have to swab, because when you do an upload, only the data file is uploaded. No DNA is actually transferred or uploaded. I’m not sure what process will be put in place for transfer/uploaded testers, but FamilyTreeDNA will let you know when something is available.

What NOT to Do

I contacted FamilyTreeDNA and this is what they ask customers NOT to do:

  1. Don’t request that your current test be deleted so you can order a new one. This removes everything – linkages, trees, family matching, permissions, project membership, other tests, and notes. Not just for you, but for your matches who have done work on their match with you as well.
  2. Don’t order a second kit, which causes “twins” in the system. I don’t have inside knowledge, but I’ll bet there will be special upgrade pricing if you just wait a bit!

I’m Excited

I don’t know what the future holds, but I’m hoping for:

  • More granular ethnicity (we always want that, right?)
  • More confident matching
  • Improved relationship identification
  • Additional tools to identify descendants of specific ancestors
  • Tools to identify missing ancestors

As a contract member of the R&D team, I’ll let you know when my NGS results are back and how they compare to my matches on the current chip. You know I’m building that spreadsheet already!!

_____________________________________________________________

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I receive a small commission when you click a vendor link in my articles and purchase that item. This does NOT increase your price but helps me keep the lights on and this informational blog free for everyone. Please click on the affiliate links in the articles or to the vendors below if you are purchasing products or DNA testing.

Thank you so much.

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RootsTech 2026 – The Wind Beneath Our Wings

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I started writing this article on Sunday evening, the day after RootsTech ended, and I’m basking in the afterglow. Also, my back and feet may never forgive me.

As a tongue-in-cheek comment, I think someone coined the word “exhausterwhelmulated” and defined it as being exhausted, overwhelmed, and overstimulated all at once. Yep, that’s me.

However, I need to add another couple of words to this – gratitude and joy.

Gratitude and Joy

I’m going to try to express this without sounding too sappy.

Do you recall the joy you used to feel when you spotted a relative you loved dearly but didn’t get to see often? Think of the unbridled joy as you piled out of your parents’ car and spotted your grandmother coming out of the door because she saw the car pull up. You ran as fast as your little legs could carry you directly into her arms, and got hugged so tightly it nearly squeezed the breath out of you.

I don’t know what the word for that would be, but it’s similar to how RootsTech feels.

Let me explain. Continue reading →

RootsTech 2026 Schedule: Online and In-Person Sessions Plus Book Signing – You’re Invited!

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RootsTech is right around the corner.

Like always, there’s so much energy swirling around RootsTech, whether you’re attending in person or virtually. I can hardly wait!

If you’re attending RootsTech in Salt Lake City, I hope we have the opportunity to connect. Please be sure to say hello.

I have a few DNAeXplain badge ribbons left, so be sure to ask me for one. When they are gone, they’re gone and will soon become a RootsTech collector’s item!.

Register

Be sure to register for the free online conference, here, if you aren’t attending in Salt Lake City. All of the in-person only sessions have a syllabus available, and many speakers include their slides. So be sure to check everything out, even sessions that are in-person only.

Join Relatives at RootsTech

Oh, and while you’re at it, sign up for Relatives at RootsTech, here, and see which of your cousins are attending either virtually or in-person. I’ve written several articles about how I utilize Relatives at RootsTech, here.

Roberta’s Schedule

Here’s my presentation, appearance and book-signing schedule.

“Monday’s with Myrt”, hosted by Pat Richley-Erickson (Myrt), a RootsTech tradition, is always broadcast from the FamilySearch Library in SLC on the Monday before RootsTech. Myrt live-streams interviews and discussions with lots of people you know. 

I’ll be discussing something completely out of the ordinary for me – with surprise visuals! Here’s the link. Come join us for the fun!

Thursday is a VERY Busy Day With Four Sessions

This recorded session is available for everyone at this link, beginning when RootsTech opens and throughout the conference. This session is sponsored by FamilyTreeDNA, which makes sense because they are the only vendor that offers X-DNA matching.

Show Floor

Two of my events will take place in booths on the show floor. The book-signing in in the GenealogyBank booth, at far right, and the MyHeritage session is right inside the main entrance where you can’t miss it!

You can purchase my books during the signing while supplies last. If you’ve previously purchased a book and would like it signed, you can bring the book, of course, or I will have some bookplates with me that I will gladly sign for you.

  • Thursday, March 5 – 2 PM Mountain Time (SLC), MyHeritage booth #900, Everything I Love About MyHeritage

Ok, so this session might not include quite EVERYTHING I love about MyHeritage. I’m going to begin in an unexpected place with an underutilized tool, Cousin Finder, and work my way through using the rest of the MyHeritage DNA (and supporting) tools successfully. Two fun case studies in my own family with an unexpected twist that every genealogist dreams about. MyHeritage makes it easy to jump the pond!

Mitochondrial DNA to Z is in-person only, so not recorded or livestreamed. Here’s the link which includes my slides. (You’re welcome!).

Friday Holds Two Great Sessions – Including One That’s Livestreamed

Y-DNA to Z is in-person only, so not recorded or livestreamed. Here’s the link which includes my slides. (You’re welcome!).

Mapping Maternal Connections, sponsored by FamilyTreeDNA, is available both in person and online. As a contract member of the R&D team, and as a genetic genealogist, I’m really excited to share the latest updates with you, as well as how I’m using the new MitoTree, matching and Discover to solve long-standing mysteries. Here’s the link, which includes a syllabus.

Just so you know, recordings of online sessions will be available after the event, so if you miss it, come back to view later.

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Thank you so much.

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A Forest of Fathers: FamilyTreeDNA’s Y-DNA Tree Tops 100,000 Branches

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Congratulations to FamilyTreeDNA and all of their customers who contributed to this absolutely monumental milestone. The Y-DNA tree has now reached 100,000 branches.

Chart courtest of FamilyTreeDNA

I knew they were getting close because the official January numbers were 99,777.

Congratulations to the entire team, but especially to Michael Sager, Senior Phylogeneticist, who has been the chief architect of the tree “forever.” This is definitely his baby.

Here’s Michael in 2020 at RootsTech discussing the Y-DNA tree construction methodology.

The Y-DNA tree is built using the results of 698,000 individual Y-DNA testers, plus thousands of both academic and ancient results.

These 100,000 tree branches are built from 857,000 variants, known as SNP mutations. Think of those as a huge 857,000-piece puzzle that Michael Sager has spent the past decade assembling into the Y-DNA tree of mankind, reaching all the way back to Y-DNA Adam.

In the tree today, haplogroup A-PR2021, named for variant or SNP (single nucleotide polymorphism) PR2921, is Y-DNA Adam, who lived in Africa about 234,000 years ago.

Click on any image to enlarge

FamilyTreeDNA has made their entire Y-DNA tree public and free, and that’s in addition to the baker’s dozen reports available through Discover for each haplogroup.

Let’s take a look!

The Public Y-DNA Tree by Country

You can view the public Y-DNA tree, here, and can select to view the tree by:

  • Variants (mutations) that define each haplogroup
  • Country
  • Surname

For example, here is the oldest, or top portion of the tree, using “by Country,” the first of three options.

Notice two things at far right:

  • There may be a “+” when there are too many countries to display
  • The 3 dots

Clicking on the three dots provides you with the option for a “Country Report” or “Surname Report” for that specific haplogroup.

The Country Report shows the number of haplogroup members from each country. Remember that countries are self-reported by the testers. The country should be the location where the tester’s earliest known paternal ancestor (EKA) was living or from.

You can see how many people are members of this specific branch, and in the next column, how many people are members of this branch plus all “son” or downstream branches. One column excludes new haplogroup letters (when a different base haplogroup is formed), and the other includes all downstream haplogroups, even if the beginning branch letter changes. The final “Distribution” column shows the percentage of people in that haplogroup who originated from each country.

In this case, 43% are from the US, which probably means that they are brick-walled here, given that the only people originally “from” the United States were Native Americans who fall into specific subclades of haplogroups C and Q.

If you’d like more information about A-V148, or any other haplogroup, you can go to Discover and enter a haplogroup name. I always check the Ancient Connections because archaeological remains anchor haplogroups in a particular place at a particular time. We’ll cover more about Discover in a minute.

The Public Y-DNA Tree by Variant

This haplotree view “by Variant” shows the variants, or SNP mutations, that identify each haplogroup.

You can see that Haplogroup A-PR2921, the granddaddy of the tree, is based on only one mutation, PR2921, which is also the haplogroup name. This means two things:

  • Every haplogroup beneath this branch on the tree also has the mutation, PR2921, which is how we know it’s the “original” founding mutation
  • This haplogroup cannot be split further, because there are no additional variants

For example, look at the branch, A-L1090, the first “child haplogroup” of A-PR2921. A-L1090 has the 26 mutations displayed, plus more, for a total of 695.

This means that as more men test, there are literally more than 695 opportunities for various men to match on a unique subset of those mutations, plus new mutations never discovered before, forming new haplogroups.

Some lines have died out over time, and others may be quite rare. This is the perfect example of why it’s important for every male to take the Big Y test, aside from genealogy.

Looking on down the tree to the next haplogroup “generation,” we can see that haplogroup A-V148 has 21 descendant haplogroups, but its sibling subclade, A-V168 has 99,967 – essentially the rest of the tree.

The Public Y-DNA Tree by Surname

Viewing the tree “by Surname” can be very useful. Surnames are shown beside their haplogroup if there are two or more individuals:

  • With the same spelling of the surname who are assigned to this haplogroup
  • Who are members of a public DNA Group Project
  • Who have given permission for their information to be displayed publicly within the project

You can see that haplogroup A-V148 has one surname showing – Goddard.

Haplogroup A-M31 shows four: Bass, Johnson, Evans and Cruise.

Clicking on the three dots shows the Surname Report.

This report reveals that there are seven men with the Goddard surname and no other surnames are currently lissted for this haplogroup.

You might be a member of this haplogroup even if your surname isn’t Goddard. Surnames were only adopted in the past few hundred years, and many have changed during that time for a wide variety of reasons, including spelling variations. Not everyone who is in the matching database has joined a project, so they may show up on your match list, but not be visible here.

Since we know that several Goddard men are in some project, how do we figure out which project or projects they have joined?

Discover’s Suggested Projects

Go to Discover and enter the haplogroup. Click the big orange “Search” button, which will display the Haplogroup Story page for that haplogroup.  .

From the Discover menu at left, select “Suggested Projects”.

For haplogroup A-V148, 10 projects are listed based on which projects members of this haplogroup have joined or on project administrator settings. Those projects alone may provide ancestral hints. Many people, if not most, join multiple projects, such as haplogroup projects, surname projects, and geographic or ethnic projects.

You can click through to any of the projects listed for any haplogroup to take a look. I use my browser search function to search for specific surnames on project pages.

You may find that someone who descends from your ancestor has tested and is waiting for you to match them – plus other genealogical hints as well.

Is Your Surname in the Database?

How can you tell whether your surname is in the database? That’s a great question!

In the public tree, there’s a “Search by Surname” feature. I searched for Estes, and discovered that Estes appears on 8 different branches of haplogroup R. Next, I need to click on haplogroup R, which is directly beneath the search box.

This doesn’t mean there are only 8 men who have tested, but that they are found on 8 different tree branches.

Remember that men who obtain a Family Finder haplogroup are also included on the free Public Tree, so I’ll probably find some Estes men on higher branches of the tree than they would appear if they had taken a Big Y-700 DNA test. Hopefully, they will upgrade, which will help them and all Estes descendants by piecing together our Estes lineages.

Sure enough, using my browser search to search for “Estes”, I discovered the name included with 500 other surnames in haplogroup R-L21, in R-DF49, in R-1690, and then the goldmine – four haplogroups that have ONLY the surname Estes listed.

These are our Estes twigs on the haplotree’s branches, and define four lines that begin with Silvester Estes born in 1522 in Kent, England. These haplogroups are how we proved where our line originated, and how we place testers who are uncertain about their genealogy on their correct tree branches today.

Don’t forget about both the surname and country reports available to the right when searching by surname in the Public Tree. You can also navigate to Discover to learn more about any of these haplogroups in which your surname appears.

Iff you’re an Estes male, you may or may not land in one of these haplogroups. You might even be a member of a different lineage altogether. The only way you’ll know is to take the Big Y-700 test, or minimally, the introductory 37 and 111 marker tests to view your matches. These entry-level tests provide a predicted haplogroup based on STR markers, but you’ll only be placed in your proper place in the tree with the definitive Big Y-700 test. I wrote about the difference between STRs and SNPs here.

Obviously, Y-DNA is only applicable to biologically male testers who have a Y chromosome, and you’ll only see surnames on the tree if multiple people with that exact surname have tested and joined projects, but there’s one more place to look if you want to see how many people with your surname have tested at FamilyTreeDNA.

Group Projects Search

In the footer of every FamilyTreeDNA page, under Community, you’ll find “Group Projects.” No, I don’t know why they buried this tool here, because I find it very useful, and you’ll never find it if you don’t know where to look. But now you do!

Enter the surname you are seeking and click “Search.”

You’ll see at the bottom of the search results page that 391 people whose surname is spelled exactly “Estes” have taken a DNA test at FamilyTreeDNA.

Clearly, some will be males, and others female, and they may have:

  • Taken the autosomal Family Finder test
  • Uploaded an autosomal test from another vendor
  • Taken the mitochondrial DNA direct matrilineal test (your mother’s mother’s mother’s direct line through all females)
  • Taken a Y-DNA test (males only) for the direct patrilineal (surname) line

Lots of people in the database will be descended from Estes ancestors, but won’t carry the surname. This search is an invaluable resource for genealogists seeking their ancestors’ surnames and lineages. Check it out by entering the surnames of your four grandparents and see what’s there!

I use this search tool, combined with projects to find actual testers who represent my ancestral lines and their haplogroups. Then I search the public tree and use Discover to learn about my ancestors. Which brings me back to why this milestone is so important.

Congratulations on a HUGE Milestone for Mankind

The trip to 100,000 haplotree branches was a long and sometimes challenging road. What an amazing accomplishment! Today, the tree is growing at warp speed, but it began with “horses and buggies” in 2003.

  • In 2003, the YCC Consortium published a paper defining the structure of the Y-DNA tree which, then, consisted of 153 branches based only on 243 SNPs. That’s all that had been discovered in academia at the time. But citizen science was coming into its own and many more haplogroup discoveries would soon follow, thanks to our testing pioneers.
  • In 2006, ISOGG committed to developing and maintaining a public, manually curated haplotree based on SNPs discovered at different labs. The ISOGG tree was published annually, with the final version released in July 2020.
  • In 2006, there were about 250 branches on the Y-DNA tree and SNP discoveries were rare events. Today, with the Big Y-700, new SNP discoveries occur at the rate of several hundred per week, thanks to the testing public.
  • In 2010, the YCC consortium released its final tree that included only 440 branches.
  • In 2013, FamilyTreeDNA introduced the Big Y test, which used the newer NGS (next generation sequencing) scanning technique instead of targeting specific locations on the Y-chromosome. The Big Y-700 test scans millions of locations in the gold standard region of the Y chromosome. It reads known Y-DNA SNP locations for haplogroup placement, but also identifies mutations not previously discovered that are often lineage-specific. That’s the key to identifying new haplogroups. Haplogroups are literally named after their SNP.
  • 2018 was a banner year. There were 17,966 branches on the tree.
  • By 2018, the haplotree was benefiting from what was termed a “SNP tsunami,” which rapidly expanded the tree. In June, 2018, FamilyTreeDNA named their 100,000th SNP. That too was a huge milestone, which I wrote about, here. Not every SNP discovered becomes its own haplogroup, of course, but they all must be placed appropriately on the tree.
  • In September of 2018, FamilyTreeDNA introduced their Public Tree.
  • That avalanche of SNP discovery meant that the volunteer-maintained ISOGG tree was struggling mightily to keep up with the onslaught, publishing one final tree in 2020. The landscape had changed. A yearly, independent tree that compiled information from multiple sources was no longer necessary. Haplogroup and SNP discoveries were being made almost exclusively at FamilyTreeDNA, who publishes and maintains their Y-DNA tree organically as SNPs are discovered and added to the tree.
  • In December 2021, the FamilyTreeDNA Y-DNA haplotree reached 50,000 branches. I wrote about that milestone, here.
  • In just over four years, that has doubled at a rate of about about 1000 new branches per month. That’s mind-boggling!
  • On February 5, 2026, the haplotree reached 100,000 branches! I checked earlier today (Feb. 6th) and there are already 39 more haplogroups. No moss growing under their feet. They’ve reached for the treetops and gone beyond!

Reaching 100,000 branches on the Y-DNA tree is an absolutely amazing achievement, both scientifically and genealogically. Perhaps best of all, reconstructing the lineage and paths of our ancestors is the only way we can reach indefinitely back in time. Beyond surnames and far beyond what autosomal DNA can touch.

Based on that, we can add genetic anthropology to the fields that have benefited immensely from the achievements of the tree. Conversely, genetic anthropology has contributed to the construction of the tree with the sequencing of ancient DNA results, allowing thousands of ancient samples to be incorporated.

Every contemporary haplogroup descends from Y-DNA Adam. Given that Adam lived at least 234,000 years ago, that represents about 9,360 direct-line ancestors (at 25 years per generation) for each one of us. At 20 years per generation, we have 11,700. Wouldn’t Y-line Adam be utterly dumbstruck to learn that he has 8 billion descendants, of which slightly more than half are males who still carry his defining haplogroup mutation, A-PR2021!

Thanks to the FamilyTreeDNA public Y-DNA tree and searches, plus the amazing Discover tools, we can now peel back the curtain of time on both recent and distant ancestors by walking our haplogroups back one at a time until we meet our earliest ancestor of all – Adam

Want to Meet Adam? Here’s How You Can Participate

You can participate in building the Y-DNA tree of humankind and meet Adam by taking a Big Y-700 DNA test, which you can order here. If you’re a female, you can sponsor a Y-DNA test for a male relative, such as a father, uncle, or brother who represents one of your surname lines. But don’t stop with your own paternal line – reach out and make those same discoveries for all of your ancestral lines! Your ancestors are waiting to meet you!!

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Getting Ready for RootsTech 2026

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RootsTech, March 5-7, 2026, will be here before you know it. Behind the scenes, people are scurrying around like crazy!

Let’s take a peek!

You’d Think January Would Be Quiet…

January seems like it would be a quiet, “down” time, after the holidays, but for many of us, it’s not. It would seem like the holidays would be a time to relax and catch up, but I always get further behind and face a ton of emails in January. (I’m still very behind with those.)

No small part of my January issue is self-imposed, though not all of it.

Let me explain.

  • I’ve always strived for one industry or technical blog article each week. Something about a tool, a product, a how-to article, industry news, something useful and educational. I can’t write an article without using and understanding the tools, so these articles take a substantial amount of time to prepare.
  • I also strive for one “52 Ancestors” article each week, typically published on the weekend. While these articles reconstruct the lives of my ancestors, they include a great deal of genealogy research, instructional content, and a substantial amount of history that affected the lives of anyone who lived in that location or during that time. While the topic is my ancestor, these articles are useful far beyond my own genealogy.

As an aside, many people read these articles as a short-story series. Working on each article draws me close to each ancestor individually. I literally walk through their life beside them – joys, sorrows, deaths, where they lived, what was happening around them – birth to burial.

  • Of course, then there’s “everything else.” Other articles, interviews, my contractual work, collaborating with others, and of course, some smidgen of personal time.

January is Different

But the reason January is different, on steroids, is threefold:

  • It’s the month that speakers begin planning and preparing for sessions they will be giving during the rest of the year.
  • For US business owners, it’s when we begin gathering the information for business taxes, which are due March 15th, a week after RootsTech, which means that we have to get the information to our preparer long before RootsTech. I’m not exaggerating to say this is one of my LEAST favorite activities ever.
  • However, the third challenge is RootsTech itself.

RootsTech 2026

RootsTech, held March 5-7 this year in Salt Lake City, is the granddaddy of all genealogy conferences. I’m fortunate to be able to attend and present – and I’m grateful for that opportunity. But there’s a huge amount of prep, and while some of it happens in December, most of it falls in January.

I’m often asked about what it takes to create a presentation, or put more bluntly, “Why does it take so long? All you have to do is throw together a few Powerpoints.” So, here’s the backstory.

I can’t speak for other presenters, but every 45-minute presentation that I create takes about a week.

If you’re stunned, every one of my slides includes images and often graphics that I create. The slide content needs to be balanced, readable, and not distracting form the point I’m trying to make. It needs to flow smoothly from the prior slide, and to the next one.

It goes without saying that I have to verify everything, sometimes with a vendor, sometimes making sure features still work the way I think they do, or did, the logic is accurate, and that any math maths.

Many screenshots used for articles and presentations need to be blurred, and I need to be sure I don’t accidentally compromise someone’s privacy.

It seems there are 1000 little things. Ok, so maybe only 100!

Syllabus: Oh, you want a syllabus too? Well, that’s another document which often has to be formatted in a specific way, and must be between x and y pages long. Some requirements for different conferences are very specific, down to the font.

The presentation must “fit” into its allocated time, say, generally 45 or 50 minutes, without me talking at 150 MPH with the audience feeling rushed, and provide enough information to be both useful and entertaining. This means that presenters must practice, refine, practice. You get the drift.

Additionally, when working in a tech field, like DNA, vendors change things, often, and you need to review your presentation just before the conference to be sure the screenshots and information are still current. Speakers watch every announcement between presentation creation and the conference with an eye to changes. I swear, it never fails that the night before, I’m always trying to update my presentation because a vendor updated their website. One time it was literally at the podium. That was way too close for comfort.

RootsTech must manage and coordinate hundreds of presenters, their presentations and syllabi, lots of technology, and massive logistics. In order to do so:

  • Pre-recorded sessions are due to RootsTech at the end of December.
  • For other speakers, copies of their PowerPoint presentations and syllabi are due by January 25th so RootsTech can review, check for any issues, and make any last-minute changes. (Hint – you may not see another blog article for the next 10 days.)

All things considered, RootsTech does a great job, but last-minute schedule changes do occur, so be sure to check your planned schedule closer to and daily during RootsTech.

My 2026 RootsTech Sessions

Pre-Recorded Session:

  • X-DNA Basics for Genealogists, a recorded session that will be available in the FamilyTreeDNA virtual booth, which means that everyone will be able to watch. The great news is that the vendor booths and their contents will be visible in the Expo Hall, both in person and virtually, entirely free. You don’t need to register to attend RootsTech to view the vendor booths, but there’s no reason not to, because online registration is free.

Live-Streamed Session:

  • I’ll be presenting Mapping Maternal Connections: Where Science Meets Genealogy on the Updated mtDNA Tree of Humankind for FamilyTreeDNA as a member of the R&D team that developed the new Mitotree. This will be a fun session that explains why mitochondrial DNA matters, covers the latest update, and how the new Mitotree, along with Discover, provides genealogists with new tools to break through brick walls.

The date and time for this session have not yet been confirmed, so check the schedule moving forward.

You must register for RootsTech Online to access live-streamed sessions remotely. They are added to the RootsTech on-demand library for later viewing.

In-Person Sessions

I’m fortunate to have two in-person sessions this year. Neither are being live-streamed or recorded, so I hope to see you in person.

  • Mitochondrial DNA to Z: My Results Are Back, Now What? Everyone is excited when their DNA test results are back, but what do you do next? How do you use them most effectively? What do those numbers means and why are they important? If these questions sound familiar, this is just the class for you. We will take results, step-by-step through all of the reports and tools and help you interpret what they mean and how to use them for genealogy using a case study.

This session is currently scheduled on March 5th, at 4:30 PM, Mountain Time. Please see the Schedule Warning section below.

  • Y-DNA to Z: My Results Are Back, Now What? Would you like to understand how to use your Y-DNA results for genealogy? What do those numbers mean and why are they important? This is just the class for you. We will take Y-DNA results, including the Big Y-700, step-by-step through all of the reports and tools and help you interpret what they mean and how to use them for genealogy. We’ll close with “next steps”, so you have a plan to understand your own Y-DNA message, PLUS how to create a genetic tree to reveal the messages from your other ancestors too. Females don’t have a Y chromosome, but we have fathers, brothers and male family members to test.

This session is currently scheduled on March 6th, at 3 PM, Mountain Time. Please see the Schedule Warning below.

Schedule Warning!!

When viewing sessions on the RootsTech website, the date and time displayed on your computer is the date and time that the event occurs USING YOUR LOCAL TIME!! The RootsTech website uses the time on your computer and adjusts the RootsTech session time displayed to your local time.

That’s fine if you’re attending online, but it’s NOT fine if you’re trying to plan an in-person schedule around travel time and other commitments.

For example, here’s the time displayed for my Y-DNA session. You can see that it says 5 PM, which is GMT-5, and that’s the time where I live, not in Salt Lake City which, during RootsTech, is GMT-7.

This session is NOT available virtually, so anyone who wants to attend will need to do so in person in Salt Lake City. However, the local time, in Salt Lake City, that this session will be taking place is 3 PM, not 5 PM.

In prior years, when I’ve scheduled these sessions in my phone, I wound up having to go back and change the time of every session after arriving in SLC – so that just adds to the confusion. Check your phone after arriving to be sure your sessions are shown in their correct time slot.

One more possible glitch this year is that Salt Lake City time changes at 2 AM on the day following RootsTech. Be sure to factor this time difference into your schedule if you’re planning to fly on Sunday, March 8, the day after RootsTech.

Bottom line – when planning your RootsTech events, be sure to calculate the local time and not your system time, unless you’ll be attending virtually. Also, be sure to check your schedule often in case either schedule or room changes have been made.

Register

Be sure to register for RootsTech. Online is free, and in-person only costs $129 for a 3-day pass, which is a great value for everything that’s offered.

When you register for RootsTech, you’ll be able to use their complimentary conference schedule planning feature which is infinitely helpful. If you’re planning to attend any session, adding it to your RootsTech calendar helps RootsTech with room size planning – getting the right speakers in the right rooms to properly accommodate the audience size.

If you have more questions, here’s the RootsTech FAQ.

Personal Note

On a personal note, RootsTech isn’t just a conference, it’s a clan gathering, a homecoming for genealogists where we meet and mingle with other genealogists. Where we find cousins, both new and old. It’s a place to bask in the genealogy glow with our peeps and discuss historical events, new technology, old maps and common ancestors. It’s a reunion, a place of excited greetings and infinite hugs.

Me with Mags Gaulden in 2018

I know this sounds sappy, but it’s absolutely true. It’s the only place many of us see each other. We have a great deal of fun and cherish every minute!

Come make some priceless memories.

I hope to see you there!

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2025 Genetic Genealogy Retrospective: Wow – What a Year!

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2025 has been quite a year in genetic genealogy. Genetic genealogy, per se, really isn’t a separate “thing” anymore. DNA testing is now an integral part of genealogy, with the potential to answer questions that nothing else can!

The 76 articles I wrote in 2025 fall into multiple categories and focus on different topics based on what was happening in the industry.

From my perspective, here are the most notable announcements and trends in genetic genealogy, and genealogy more broadly.

#1 for 2025 – Mitochondrial DNA: The Million Mito Project Released the New Mitotree, Updates, and mtDNA Discover

The biggest genealogy news items this year, both industry-wide and genealogy-changing are definitely the release of the new Mitotree, plus two tree updates. But that’s not all.

In addition, full sequence mitochondrial DNA testers received new Mitotree haplogroups, if appropriate, and everyone received a haplotype – a new feature. Along with Mitotree, FamilyTreeDNA introduced mtDNA Discover which provides 13 individual reports based on your haplogroup and matches.

It’s no wonder that mitochondrial DNA articles led the pack with the most views based on the eleven articles about that topic. If you haven’t yet tested your mitochondrial DNA at FamilyTreeDNA, there’s no better time! You never know what you’re going to discover and the more testers, the more matches for everyone.

You don’t know what you don’t know, and you’ll never know if you don’t test. Remember, mitochondrial DNA is for both males and females and tests your mother’s direct matrilineal line (mother to mother to mother, etc.) – reaching beyond known surnames.  Click here to order or upgrade.

#2 – MyHeritage Low Pass Whole Genome Sequence Test Charges into the Future

Another big hitter is the new MyHeritage low-pass whole genome test (WGS) test. It’s new and innovative, but we haven’t seen comparative results yet.

My results from the new low-pass whole genome test just came back, and I haven’t had the opportunity to review them yet, as compared to the earlier tests. That said, I do have roughly the same number of matches, but I need to determine if they are the same matches, and how well they track. I’ll be working on that review soon.

The new whole genome test may be more about future proofing and preparedness than additional current benefit – but we will see. I definately wanted to take the whole genome test so I can receive and benefit from whatever new is coming down the pike.

MyHeritage allows you to maintain multiple DNA tests on your account, so the new whole genome won’t “replace” your older or uploaded test. That way, you can easily compare the results of the whole genome against any DNA test that you curently have at MyHeritage.

Click here to order the new test.

#3 – 23andMe Experiences Problems

On a less positive note, but still quite newsworthy is the bankruptcy of 23andMe and subsequent repurchase of 23andMe by the original founder after setting up a new nonprofit. I have real mixed feelings about this topic. However, 23andMe was really never about genealogy, and now, matching segment information is no longer available. Those searching for unknown parents or family may want to test there if they are unsuccessful elsewhere.

Best Genealogy Tool

The FamilySearch full text search continues to have a HUGE impact for genealogists. This tool is not one-and-done, but provides increasing amounts of rich information as more records are added to the “fully scanned” collection. If you haven’t tried it, please do. It’s a game-changer and continues to improve.

A Cautionary Word About AI – Artificial Intelligence

AI is such a hot topic right now that I feel it needs to be included.

The FamilySearch full text search uses a form of AI. However, you’ll quickly notice that it can’t read everything, gets words and names wrong, and if you actually need to fully depend on it for accuracy, you cannot. (That said, it’s still an amazing tool, and I’m not picking on FamilySearch.)

Aside from FamilySearch, AI in its current form is both wonderful and terrible. I’ll be writing about AI in the new year, but for now, don’t ever rely on AI for anything that you can’t verity. It’s your assistant, not an expert, no matter how insistent it is. Never trust and always verify.

This is ESPECIALLY TRUE WHEN RELATED TO GENETICS and genetic related topics. I can’t even begin to tell you how very wrong it has been, and how much people fall in love with inaccurate results. No, just no – at least for now.

You need to know your AI tool, your skill set, your understanding of AI broadly, the tool’s limitations, and yours, and that’s all before verifying the actual AI results. If you want to educate yourself, and everyone should, treat yourself to anything, anyplace by either Mark Thompson or Steve Little, the dynamic AI duo. They offer YouTube videos and classes in a wide variety of places – but keep in mind that AI tools and technology literally change every few weeks.

AI is, indeed, a specialty all unto itself, much like genetic genealogy. And right now, it’s not soup yet, but it is cooking.

Tried and True Genetic Genealogy Staples – DNAPrint and Genetic Affairs

I haven’t written about either one this year, but I use both DNAPainter and Genetic Affairs regularly.

I consistently paint segments from matches at both MyHeritage, FamilyTreeDNA, and GEDmatch that are newly identified to an ancestor or ancestral couple at DNAPainter.

Unfortunately, neither Ancestry nor 23andMe provide matching cM location information for your matches (chromosome browser), but you may find some people who have tested at those companies at both FamilyTreeDNA and GEDmatch if they have uploaded to either of those vendors. Both vendors provide segment information and a Chromosome Browser, enabling you to paint that information to DNAPainter when you can identify your common ancestor.

MyHeritage also provides a Chromosome Browser, but unfortunately, no longer accepts uploads from any other vendor. You can paint segments from MyHeritage, but no longer upload DNA files to MyHeritage.

Thanks to DNAPainter, I have 90% of my segments identified to specific ancestors – which is actually rather remarkable given that my mother’s grandfather was a Dutch immigrant, and her great-grandparents on her other side were German immigrants, meaning we don’t have many matches on either of those lines.

Genetic Affairs continues to develop new, advanced clustering tools, one of which I’ll be reviewing soon.

Major Vendor Releases

Aside from what’s listed above, most of the major vendors released new features.

MyHeritage released a VERY COOL new tool called Cousin Finder that finds your relatives in the MyHeritage database, whether they match you on a DNA test, or not. They may not have even taken a DNA test. Cousin Finder identifies your common ancestor and shows your relationships. It’s a wonderful way to initiate communications, discuss your common ancestors, and ask about DNA testing.

Of my 378 Cousin Finder matches, only 23 (about 6%) are on my DNA match list, so that leaves 355 people to message, several of whom represent Y-DNA and mtDNA lines I don’t have. You can bet I’ll be offering testing scholarships.

Additionally, MyHeritage released a new ethnicity version.

FamilyTreeDNA, in addition to the new Mitotree, Discover, and associated features, released a new match matrix so you can see if and how selected matches are related to each other in a grid format. In other words, you can create your own cluster.

A new built-in “Share” feature blurs private information to make sharing easier both on the website and in Discover.

Discover improvements include thousands of new Y-DNA and mtDNA tree branches, plus thousands of new Ancient DNA samples. Discover is evergreen, so once you’ve taken that Big Y-700 test or the mitochondrial DNA test, your learning never stops as more content is added.

Tree integration with WikiTree is super-easy and means you don’t have to choose between trees. You can choose to retain your archived tree at FamilyTreeDNA, or move your tree to MyHeritage, PLUS link yourself to your family at WikiTree.

Ancestry released match clustering and a new beta pedigree view of ThruLines, but that’s back in the shop for more work. I’d expect to see it rereleased in 2026.

Conferences

RootsTech is the granddaddy of genealogy conferences, and it’s always fun to attend and write about the experience. Many vendors release new tools or products during the conference.

The ECGGC (East Coast Genetic Genealogy Conference), held in the fall, is the only conference that focuses entirely on genetic genealogy, new tools, how to use existing tools, and more. The 2025 conference was virtual and provided a great deal of focused content. Attendees particularly appreciate the deep dive in a particular topic presented in DNA Academy.

I’ll be at RootsTech in 2026, will write about that soon, and hope to see you there.

Concepts, Techniques and Plain Old Genealogy

In the past, my Concepts series and genealogy “how to” articles have been very popular, so, in 2025, I penned a half-dozen articles focusing on frequently asked questions about relationships and DNA.

For example, how does one go about finding DNA testing candidates? The number of options may surprise you and includes both Cousin Finder and Relatives at RootsTech.

By testing ONE PERSON for either Y-DNA or mitochondrial DNA that represents an ancestor, you actually receive information about that entire lineage of ancestors. So, on my Estes line, by locating an Estes male from my line to test, I received relevant information for every Estes male in my line, back to and beyond the progenitor.

Eventually, we hit a brick wall in every line, and those tools are the perfect way to break through those brick walls.

Other articles discuss things like how to use Discover’s Ancient Connections, and the difference between half and full relationships, both in your tree and genetically. Plus, what does a cousin “once removed” mean anyway? And why do I care?

Another question I receive is how far back, based on the shared amount of DNA, should I look in my matches’ trees for our common ancestor? In other words, how many generations back should I click? That article was fun and produced some unexpected results.

Memorial Articles

Because we are part of a community, I write memorial articles when one of our friends passes on. This year, sadly, Schelly Talalay Dardashti, well-known Jewish genealogist, and another very close friend joined the ancestors, so I’ve recognized the best in both of their lives which constitutes their legacy.

Be the Storyteller

Last, but not least, I wrote about my ancestors in the “52 Ancestors” series, which launched several years ago with Amy Johnson Crow’s challenge to write about one ancestor per week. She hosts this every year, and you can join (free) now.

I’m now on ancestor #467, so yes, it’s addictive, but it’s also AMAZING how many wonderful cousins I’ve met who have information that I did not. Not only that, but after publishing about an ancestor, I’ve discovered that I’m related to people I’ve known for years. We were SOOOooo excited!

I’ve been writing about the lives of my ancestors for several years now, and the articles include attempts to identify Y-DNA and mtDNA testers for each ancestor, where appropriate. There’s so much to learn that can’t be revealed any other way.

Plus, people seem to like the “mystery” and “short story” aspect, and I salt each story with the history of the region and relevant historical events of the timeframe. You might find your ancestors here too, or other helpful information.

Find a way to share about your ancestors!

Do You Have Suggestions for 2026 Topics?

Do you have suggestions or requests for article topics in 2026? If so, please comment on this article and let me know.

Check Out the 2025 List

Here’s the list of the 2025 articles. Did you miss something fun? Enjoy!

  Title Category Date Link
1 Welcome to 2025 – Opportunities and New Genetic Genealogy Articles Welcome, general 1-2-2025 https://dna-explained.com/2025/01/02/welcome-to-2025-opportunities-and-new-genetic-genealogy-articles/
2 Anne Doucet (1713-1791), Oceans, Rivers, and Perseverance – 52 Ancestors #438 52 Ancestors 1-4-2025 https://dna-explained.com/2025/01/04/anne-doucet-1713-1791-oceans-rivers-and-perseverance-52-ancestors-438/
3 Register for RootsTech 2025 Now RootsTech 1-16-2025 https://dna-explained.com/2025/01/16/register-for-rootstech-2025-now/
4 What IS the McNeil Family History, by George Franklin McNeil – 52 Ancestors #439 52 Ancestors 1-19-2025 https://dna-explained.com/2025/01/20/what-is-the-mcneil-family-history-by-george-franklin-mcneil-52-ancestors-439/
5 Jean Garceau dit Tranchemontagne (c1785-1711), Soldier from Saint Marseault – 52 Ancestors #440 52 Ancestors 1-29-2025 https://dna-explained.com/2025/01/29/jean-garceau-dit-tranchemontagne-c1785-1711-soldier-from-saint-marseault-52-ancestors-440/
6 Memories Resurface When the Old Family Home Gets a Facelift Genealogy 2-3-2025 https://dna-explained.com/2025/02/03/memories-resurface-when-the-old-family-home-gets-a-facelift/
7 MyHeritage Introduces Ethnicity v2.5 MyHeritage 2-6-2025 https://dna-explained.com/2025/02/06/myheritage-introduces-ethnicity-v2-5/
8 Relatives at RootsTech Reveals Cousins and Provides DNA Candidates RootsTech, techniques 2-8-2025 https://dna-explained.com/2025/02/08/relatives-at-rootstech-reveals-cousins-and-provides-dna-candidates/
9 FamilyTreeDNA’s New Matrix Shows How Your Matches Are Related to Each Other FamilyTreeDNA 2-12-2025 https://dna-explained.com/2025/02/12/familytreednas-new-matrix-shows-how-your-matches-are-related-to-each-other/
10 René Doucet (c1680-c1731), Lifetime of Incessant Upheaval – 52 Ancestors #441 52 Ancestors 2-15-2024 https://dna-explained.com/2025/02/16/rene-doucet-c1680-c1731-lifetime-of-incessant-upheaval-52-ancestors-441/
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Michel Richard dit Sansoucy (c1630 – 1686/1689), Carefree Acadian – 52 Ancestors #465

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Michel Richard was born about 1630, according to the Acadian census. We know he was born in France, because the first French settlers had not arrived in Acadia by 1630.

What we don’t know is where, or the identity of his parents.

Bona Arsenault, in his 1978 edition of HISTOIRE ET GENEALOGIE DES ACADIENS; 1625-1810, quoted on WikiTree and by Karen Theriot Reader, states that:

Michel Richard dit Sansoucy, born in 1639, originally from the Saintonge [an old province in the west part of France, now largely Charente-Inferieure. Its capital was Saintes]. Michel arrived in Acadia with the expedition of Emmanuel Le Borgne and de Guilbault in 1652 or 1651; he was with sieur de Saint-Mas, representative of Le Borgne. (Footnote cites Bona Arsenault’s own Histoire des Acadiens; and Louis Richard, in the Memoires de la Société Généalogique Canadienne-Francoise, vol. VI, no 1 (Jan 1954).)

Unfortunately, no sources were provided, and we know that the 1639 birth year is incorrect. No evidence has surfaced to confirm this location information, so for now, it remains unproven. As more parish records are transcribed and translated, Michel’s family information may come to light, although Richard is not an uncommon surname in France.

Sansoucy

Michel’s dit name or nickname is interesting. Sansoucy, means carefree, or without cares. It does not seem to be a place name, so it would either be a military nickname or indicative of Michel’s personality.

I like to think of him in this light!

A Brother by the Same Name

Michel probably had a younger brother, by the same name, who also settled in Port Royal, marrying Francoise Boudrot about 1663, and having two children with her before passing away, probably about 1667. Francoise remarried to Etienne Robichaud about 1668.

Francoise’s two children by Richard, Madeleine Richard Robichaud, born about 1664, and Charles Richard dit Cadet Robichaud, born about 1667, were known by the surname of their step-father, Etienne Robichaud. However, Charles used the dit name of “Cadet” signifying “the younger” and Y-DNA testing of several descendants has confirmed that indeed, he is genetically descended from the Richard line, not the Robichaud line.

These Big Y-700 tests from the French Heritage DNA Project show that the Richard and Robichaud men from these genealogy lines descend from the same genetic lineage. The common haplogroup, R-FT137222, formed about 1637, with a range that extends in both directions.

Cadet would indicate that both Richard brothers had the same name – a situation not unheard of and found in other Acadian families too, especially if they are half-siblings. We find this same situation occurring in “our” Michel Richard “dit Sansoucy” line, with two sons being named Alexandre. The older Alexander Richard was born about 1668 to Madeleine (Madelaine) Blanchard, and the younger Alexandre Richard was born about 1686 to second wife, Jeanne Babin.

I think the phrase, “It’s complicated,” could sum up the Richard family.

Port Royal

In the 1671 census, Michel is enumerated with Abraham Dugas on one side, and Charles Melanson on the other. Those two men lived directly across the river from each other.

Here, I’m standing on or near the Melanson land, looking across the Riviere du Port Royal at the Dugas land, at left, which is just west of the fort.

Michel Richard was listed as a 41-year-old laborer, or ploughman, wife Madeleine Blanchard, 28, along with seven children, Rene, 14, Pierre, 10, Catherine, 8, Martin, 6, Alexandre, 3, and twins, Anne and Magdeleine, 5 weeks. They have 15 cattle, 14 sheep, and are farming 14 arpents of land.

Twins, especially twins who both lived, are rare.

The census suggests Michel’s birth in 1630, Madeleine’s in 1643, and their marriage about 1656, so after the initial fall of Acadia in 1654.

Taken together, this tells us that Michel Richard was in Acadia prior to the fall and would have been a witness to and participant in those events.

The 1654 Fall of Acadia

In 1654, Michel would have been about 24 years old. He probably arrived in Acadia as a laborer, craftsman, or perhaps even a soldier. If he arrived with his parents or other family members, other than “Cadet” Richard, there was no trace of them by 1671.

Tensions had been escalating in the North Atlantic between the French, English, and Dutch colonies as extensions of their home countries.

In the summer of 1654, Oliver Cromwell in England was outfitting the English colonists in Boston with ships and soldiers to attack the Dutch in New Netherlands, today’s New York.

By the time they were prepared to attack, Major Robert Sedgwick was informed that the war had been settled, and peace was at hand. The trouble was that Sedgwick was prepared for battle, and had been authorized to take other territories belonging to the French after attacking New Netherlands, if time permitted. Given that he could no longer attack New Netherlands, that’s all the encouragement he needed.

He set out to capture all three Acadian forts: Saint John, Port Royal (now Annapolis Royal, NS), and Pentagouet (now Castine, Maine).

On July 14th, after Fort Saint John surrendered, Sedgwick crossed the Baie Française, now the Bay of Fundy, and attacked Port Royal, which was under the control of Emmanuel Le Borgne. Le Borgne had been at Saint John the day before attacking rival Charles La Tour when Sedgwick arrived there. Le Borgne quickly retreated to Port Royal, which gave him a day to prepare for Sedgwick’s arrival. It wasn’t much time, but better than nothing.

Le Borgne’s men lay in wait and ambushed Sedgwick, killing one and wounding six more. The more experienced professional English soldiers quickly returned fire, ambushed the ambushers, giving them no time to reload, and killed five men. We don’t know if those five men were French soldiers or Acadians.

The French soldiers and Acadians retreated into the fort, where the English laid siege to Port Royal. Knowing that the combined forces of about 200 men in Port Royal stood no chance against the 750 English and colonial soldiers, they surrendered on August 8th.

Le Borgne obtained generous surrender terms, meaning that the Acadians were to remain unharmed, keep their homes and belongings, be allowed to continue to worshiping as Catholics, and the French soldiers were to be transported back to France. Nevertheless, the English captured 113 men, more than 23 cannons, 500 weapons, and more than 50 barrels of gunpowder. In violation of the agreement, the Sedgwick had the Acadians’ livestock slaughtered.

It’s unclear whether all 113 captives were French soldiers, or a mixture of soldiers and Acadians. It’s unlikely that Michel was a French soldier, or he would have been sent back to France at this time, so he must have arrived in a different capacity.

Le Borgne’s own ship had been captured too, laden with a valuable cargo of alcohol. The surrender terms allowed him to keep the ship, AND his alcohol. He, as a French administrator, returned to France, but his sons were allowed to remain in Acadian, and he was allowed to keep his property. These suspiciously generous terms for Le Borgne personally fueled accusations of treason. The fact that Le Borgne had somehow escaped on July 13th from Saint John when the English were attacking, instead of fighting to defend Fort Saint John, furthered those accusations.

Regardless, Acadia was now under English control and would remain so until it was returned to the French in 1667 under the Treaty of Ryswick. In 1670, the transfer was completed, and was followed by the 1671 Acadian census, which provides us with a glimpse of what happened in Acadia between 1654 and 1670.

The next census in Acadia took place seven years later, in 1678.

The 1678 Census

The 1678 census was much less specific than the earlier one. We have the name of the head of household, the wife, the number of children by sex, and how much livestock they owned.

Michel Richard’s neighbors, in order, are shown as:

  • Jean Labat and Renee Gautrot – Labat was a military engineer who was sent to oversee the reconstruction of the fort. He lived in Port Royal, on the waterfront.
  • Rene Landry and Perrine Bourg
  • E(tienne) Pellerin and Jeanne Savoye – the Pellerin family lived in Port Royal and eventually owned Hogg Island.
  • Francois Brossard and Catherine Richard – Michel Richard’s newly married daughter.
  • Michel Richard and Madeleine Blanchard (their names only)
  • Germain Doucet and Marie Landry – lived in Port Royal
  • Michel Richard (no wife’s name, but the balance of his family and livestock are listed). Four boys, five girls, living on 10 arpents of land with 21 cattle.
  • Michael Boudrot at the brook – Michael Boudrot was the neighbor of Abraham Dugas.

This strongly suggests that the couple lived in Port Royal, and not yet upriver.

Additionally, there’s a very interesting note that indicates that Michel had three separate plots of land:

  • Sans Soucy, 29, 1 arpent of high land, bordering at one end of the river, part the other end on the North wood on one side Anthoine Hebert, Denis Godet.
  • 6 arpents at Port Royal, Lyon Rampat? Bordering on Germain then on the meadow and the petite Riviere then on Renee Landry
  • 3 arpents at gros Cap on Claude Terriot, Barnabe Martin at the road then at the river, 260 frontage

What types of information can we extract from this?

  • Michel’s age is not 29, which would place his birth in 1649, an impossibility given his first child’s birth in 1657. He would have been 48 or maybe 49, not 29. Perhaps this was misread or misrecorded.
  • Anthoine Hebert lives upriver beside Daniel LeBlanc at BelleIsle and so does the Godet (Gaudet) family, on the North side of the river.
  • Gros cap, “large cape,” may be the town of Port Royal itself, or the point of land where it sits, given that the Chemin du Cap is the road leading to the south out of Port Royal.
  • Renee Landry lives beside Jean Labat in Port Royal.
  • Germain Doucet lives on the other side of Michel Richard in the 1678 census in Port Royal.
  • We know, based on Nicole Barrieau’s thesis, that Michel Richard’s land was not among that expropriated in 1705 in Port Royal when the new fort was built, so his land was either further east along the waterfront, on the south side of the main road, along the Cape Path, or had already been settled in another way by 1705.

In 1671 and through 1678, based on the neighbors in the census, and the 1678 census notes, we can determine that Michel lived someplace along the waterfront in Port Royal for most of his life. This makes sense, given that we know that he was in Acadia before it fell in 1654.

Acadians in Gray, authored by Steven Cormier, states, in part, that:

First came Michel Richard dit Sansoucy, a young soldier born in the Saintonge region of France in c1630. He appeared at Port-Royal in the early 1650s in the entourage of Emmanuel Le Borgne. When his term of service ended, he remained in the colony, took up farming, obtained two grants of land from Le Borgne “at some ten to fifteen miles from the fort” on the upper Rivière au Dauphin, now the Annapolis River.

I very much wish Mr. Cormier had provided sources for this information.

Researcher Paul LeBlanc, prior to his death, believed that Michel’s dit name was derived from the location of Saintonge, although a male from Saintonge would be known as a “Saintongese.”

One of the pieces of land referenced by Cormier may be the land where Michel Richard’s son, the younger Alexandre Richard, eventually lived, near Bridgetown. Alexandre married Marie Levron about 1711, whose parents lived directly across the River from Port Royal.

Port Royal in 1686

What was Port Royal like in 1686?

We are fortunate that Labat drew a map in 1686 to encourage investment and settlement in Port Royal.

The church and cemetery are shown in this drawing.

The church is shown with the number #2, and above the church, the cemetery is annotated with #4.

The fort where Michel Richard would have served, assuming he did arrive as a soldier with Le Bourg, is shown in ruins, labeled #3, on the water, by the boats.

If Michel lived upriver in 1686, instead of in Port Royal, they lived in the BelleIsle area where 1500 arpents of prime marshland was awarded by a succession of stakeholders over the years.

Madeleine Blanchard Dies

Based on the 1686 census, Madeleine Blanchard died between 1678 and 1683 when Michel Richard remarried to Jeanne Babin. Jeanne was 15 at the time, so born about 1667, and Michel was 52.

In 1667, Michel had 10 living children, ranging in age from 20 down to 3. He needed a wife, even if his new wife was younger than his four eldest children.

In the 1686 census, we find Michel Richard, age 56, Jeanne Babin, 18, with children: Martin, 19, Alexandre, 17, Marie, 12, Cecile, 10, Marguerite, 7, and Michel, 2. Five other children are married. Marguerite was the last child born to Madeleine Blanchard, and Michel, age 2, is Michel’s first child with Jeanne Babin.

In addition to the blended family, they have two guns, 16 cattle, 30 sheep, and eight hogs on 12 arpents of land.

Based on the neighbors, it appears that Michel is probably living upriver by 1686, but that’s anything but certain. The census taker may not have been recording in the order that people lived. He may also have been paddling back and forth across the river.

The 1693 Census

By the 1693 census, Jeanne Babin has remarried to Laurent Doucet, and they have a three-year-old child, suggesting that they married about 1689.

We know that Michel Richard and Jeanne’s second child, Alexandre Richard, was born about 1686, which places Michel’s death sometime between 1686 and 1689.

Michel’s Funeral

Michel died before the Catholic church, which stood beside the fort in Port Royal, was burned in 1690 during another attack by the English.

His funeral would have been held in the church with the priest saying mass. His coffin would have been carried outside, where he was laid to rest in the cemetery in the churchyard, surrounded by his family and fellow Acadians.

Lost beneath the ramparts of the reconstructed fort today, when Michel was buried, a simple little church and adjacent cemetery behind the ramparts served the Acadian population and the French soldiers, all of whom were Catholic.

Michel was laid to rest within view of the garrison where he may have served, and assuredly defended in 1654. All that’s left of his grave today is mist and memories.

Belle-Ile-en-Mer

After the Expulsion of the Acadians in 1755, a decade later, in 1765, a group of 78 refugee Acadian families made their way to the French Island of Belle-Île-en-Mer where each family gave depositions about the origins of their ancestors.

The French were trying to determine how to help settle the refugees and whether they were actually French descendants. Clearly, they were. The French King settled the Acadian families in four regions on the island, providing them with housing and livestock.

The resulting depositions provide a plethora of information about the earliest Acadian ancestors. Of course, a few generations removed, not everything was perfectly accurate.

According to Stephen A. White, Genealogist,Centre d’études acadiennes January 17, 2005:

In four separate depositions, Michel Richard is mentioned by his Sansoucy dit name. He married Madeleine Blanchard at Port Royal, according to Pierre Doucet, the husband of Michel’s great-granddaughter Marie-Blanche Richard. (Doc. inéd., Vol. III, pp. 53-54).

Pierre mistakenly called his wife’s great-grandmother Anne, instead of Madeleine, but the 1671 census shows her true given name (see DGFA-1, pp. 1373-1374).

Three other depositions confirm the French origin of Michel Richard dit Sansoucy, although two of these attribute the given names of René to him and Marie to his wife, one from his great-grandson Pierre Richard (Doc. inéd., Vol. II, p. 191) and the other from Joseph LeBlanc dit Le Maigre, on behalf of his son Joseph, whose wife Angélique Daigre was another great-grandchild of the ancestor (ibid., p. 178).

The last deposition, from Pierre Trahan, whose father-in-law’s first wife was Michel Richard’s daughter, provides no given name for the ancestor and does not mention his spouse at all (ibid., Vol. III, p. 111).

Michel Richard’s Land in Acadia

Alexander Richard, the youngest son of Michel Richard, lived on land upriver, near present-day Bridgetown in 1710, according to the Labat map. This is probably the land granted to his father, Michel, assuming that Steven Cormier is right about Michel being granted land about 15 miles, or so, upriver. It fits that description exactly.

Michel Richard had two sons named Alexandre, the older one by Madeleine Blanchard, and the younger one by Jeanne Babin.

For a long time, I mistakenly assumed that the Alexandre Richard who lived on this land was Michel’s eldest son, Alexandre (c1668-1709), not his youngest, born about 1686. His eldest died in 1709, so it clearly cannot be him living on that land in 1710.

On this reconstructed Acadian map from MapAnnapolis, Alexandre Richard is shown living near present-day Bridgetown. The Gaudet, Petitpas, and Bastarche familes also owned land nearby, settling near Bridgetown and intermarrying.

There’s another possibility to be considered, too.

Based on the 1671 census location of Antoine Babin, this could have been his land before his grandson, the younger Alexandre Richard, farmed it. Antoine died about 1687, leaving 11 children. It’s a stretch to think that his middle daughter, Jeanne, inherited his land, then passed it to her son nearly a quarter century later.

The proximity of the Richard and Babin land to each other is probably more a function of the fact that Michel Richard and Antoine Babin were both granted land, probably by Le Borgne, anout the same time, and may have selected it together. After all, Michel Richard married Antoine’s daughter not long before both men died. Antoine and Michel were about the same age.

Alexandre Richard would have inherited the land from someone. His mother, Jeanne Babin, would have held it after Michel’s death. Her older son, Michel Richard Jr., settled in Beaubassin, so it makes perfect sense for this land to descend to Jeanne Babin, then on to Alexandre, her other son by Michel Richard Sr.. Michel Sr. and Jeanne Babin only had two children.

Perhaps Alexandre’s father, Michel Richard Sr., died before he was able to develop the land, but he was trying to leave something to one of his sons. Maybe specifically the youngest son, whom he knew he would never be able to raise. Michel was 56 when Alexandre was born. For all we know, Michel may have been ill and it’s possible that he died even before Alexandre’s birth.

Of course, the land needed to be dyked and drained for at least three years before it could be farmed, but that could wait until Alexandre was old enough.

I like to think of Michel walking here, selecting the land, imagining his grandchildren playing in the sunshine decades in the future.

This map may be slightly skewed. I used the 1710 original map and landmarks to attempt to locate Alexander’s property more precisely in preparation for a 2024 visit, so let’s see what we have.

Of course, it doesn’t help that some of the geography has been changed in the intervening three centuries. Roads have been laid, rivers have flooded, changing their courses, and, of course, those original maps weren’t 100% accurate.

It was easy to match up both the east bend in the river and the Bridgetown bend, although the Bridgetown bend has changed a bit. I should probably have turned one of these maps upsidedown.

Alexander Richard’s property was probably someplace near or between the two red stars.

Unfortunately, the view from the Harvest Highway and also from 201 is very obscured by trees.

Perhaps the best view of both sides is from the bridge itself.

This is looking south, but keeping in mind that the Acadians specialized in farming reclaimed marshland. The view looking north probably overlooks Alexandre’s fields.

Click to enlarge any image

You can see the river running beneath the bridge on the highway, where that first car is located, just before the sign. The fields between this bridge and the river would have been Alexandre’s.

Alexandre, and possibly Michel before him, would have worked these fields, as seen from the bridge over the Annapolis River.

The fields visible on both the left and right sides of the bridge, on the south side of the river, would probably have been his.

The location of the house and barn today, above the fields, is probably near the same place as it was then.

On the northeast side of the intersection of 101 and 201, there’s a small dirt road that serves one farm and also provides utility road access.

I drove up this road until I reached a fence with a warning sign, and the road began to deteriorate substantially.

This well-manicured field is still farmed.

I can see Alexandre tending the crops and farm animals, remembering his father fondly.

The father he never knew, who died when he was just a toddler.

The father who provided for him, even from the other side of death.

I returned to Highway 201, the road along the south side of the river, and turned towards the east bend.

Based on the river bends and the distance between easily identified landmarks, the Richard land may have been as far east as the red arrow.

These fields are hundreds of years old – drained by Alexander Richard and his neighbors and possibly begun by Michel.

Acadian men worked together on these tasks. Everyone helped everyone.

This model shows Acadian farmland. It takes at least three years after a salt marsh is dyked for the salt to wash out so it can be cultivated, and the dykes must be maintained to keep the fields salt-free.

Notice the stream, which is one of the cornerstone anchor landmarks I used to align this Google map with the 1710 map when searching for Alexandre’s land.

Michel Richard’s Legacy

I drove by, looking towards the river over the reclaimed marshland, thinking about Michel.

Did he ever dream that his descendant would return to find him, some three and a half centuries later? WikiTree, which doesn’t include all of his descendants, shows nearly 200,000. That’s ten times the size of the entire county where Annapolis Royal is located today, half the size of the Halifax, Nova Scotia, metropolitan region and one quarter of the population of all of Nova Scotia. That’s incredible for a humble Acadian farmer.

Everyone wants to leave a legacy. Sansoucy, carefree, is what pops into my mind when I soak in this sun-drenched summertime landscape, picturing Michel walking here.

Indeed, perhaps Michel Richard’s legacy of land enabled his son, Alexandre, to be Sansoucy too.

Perhaps a little of his Sansoucy has been passed down to all of us.

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Ancestry’s ThruLines Has a New Pedigree View

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Update: Ancestry obsoleted this new feature on December 5, 2025.

Ancestry recently updated ThruLines and introduced a new pedigree view.

I’m not sure that everyone has the new view yet, so here’s what to expect.

If you do have the new feature, let’s take a look, because there’s new functionality you may not have discovered.

When I signed in and clicked on ThruLines on the DNA tab, the first thing I saw certainly looked different. Needless to say, I was surprised because I wasn’t expecting anything new.

Click on any image to enlarge

This doesn’t look anything like what we’re used to, but Ancestry provides navigation buttons.

One person mentioned that the new view was so small they couldn’t really see clearly, but by rolling your mouse button up or clicking on the little “+” button in the upper right-hand corner, it’s easy to enlarge.

That said, on this and especially on subsequent screens, I would very much like for there to be less white space at the top, or have a “full screen” option.

You can navigate up your tree by clicking on the little up arrows above the ancestors in the top row.

The Tile Display is Still There

But perhaps more importantly for people who prefer the previous display, it’s actually right there.

Click on the little tile button to switch from the pedigree to the traditional tile view.

It’s easy to toggle back and forth.

Take a look at the new ThruLines layout. If you don’t like it, select the tiled version

Why Do I Like the Pedigree View?

I like the pedigree view because it lets me easily see how people connect with each other. While I’m intimately familiar with the more recent generations, I don’t like the more distant ancestors all being smooshed together in the tile view.

In the pedigree view, I can see how many of my matches descend from each ancestor in the tree format.

Clicking on that number opens the dropdown showing the matches and how they descend from that ancestor.

In these expanded tree views, we really do need a full-screen option. It is challenging to see the entire sequence of descent.

My focus right now is on determining if anyone that I match carries the mitochondrial DNA of my paternal grandmother. On other ancestral lines, I have both the Y-DNA and mtDNA from generations back in time, but not my grandmother. I’m hoping to remedy that.

This layout makes it easy to see that there are many potential candidates for generations upstream. If I find the right person, descended from that ancestor through all females to the current generation, which can be male, I’ll be offering them a DNA testing scholarship for a mitochondrial DNA test at FamilyTreeDNA.

Suggestions for Improving the View

Perhaps Ancestry will provide the option of selecting a default view, so we can select our favorite – tile or pedigree – plus a full-screen option for pedigree view.

Another alternative would be for the pedigree view to be horizontal and extend left to right instead of top to bottom, the same as Ancestry’s traditional trees.

Truthfully, I really like the pedigree format and functionality of the new ThruLines pedigree view, but I greatly prefer the layout of this traditional tree. It’s much easier to see and is expandable without running off the top or bottom of the screen. Maybe Ancestry could combine the best features of both.

Update: A sharp-eyed reader caught that the “Evaluate” feature is now gone, which used to allow you to evaluate other people’s trees that suggested the ThruLines connection. This is really important, and I hope that Ancestry restores it. Genealogists must evaluate everything and weigh the evidence when determining if a connection is accurate.

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