23andMe and GlaxoSmithKline Partnership Ends, Sparking Additional Layoffs

23andMe has been slimming down. In April, they announced they were cutting about 75 jobs in their therapeutics division, equating to about 9% of their workforce, and now they have cut another 71 employees in response to the end of the five-year GSK partnership.

GenomeWeb reported the earlier and most recent 23andMe layoffs, along with a 6% revenue dip, here. 23andMe is a publicly held company and reported a net loss of $104.6 million.

In 2018, 23andMe partnered with GSK, GlaxoSmithKline, a British drug company, to jointly develop drugs based on the genomic profiles of their customers who choose to participate in this type of research. You may have noticed that 23andMe asks a wide variety of questions that genealogy testing companies typically don’t, and they also report on health and traits.

At the onset of the partnership, GSK made a $300 million equity investment in 23andMe. If you need to cure insomnia, you can read the SEC filing, here.

The original partnership was to last four years and could be extended for an additional 5th year, which it was, landing another 50 million dollars in the 23andMe coffers.

According to the press release by 23andMe and this 2020 blog article, the partnership has been successful, adding more than 40 genetically validated drug discovery programs to the GSK portfolio, making me wonder why the partnership was not extended.

Customers

The 23andMe page for medical professionals states that they have more than 12 million customers worldwide.

23and Me has stated several times that about 80% of their customers opt-in to research, which means that their de-identified DNA sequences are made available to both 23andMe and their selected partners for research purposes.

Accordingly, about 8 million people have opted-in to research.

If you’re doing the math, that means that:

  • 23andMe received $29.17 for each of their 12 million customers

Viewed another way:

  • 23andMe received $43.75 for each of their 8 million customers who are opted-in for research

Attempting to Increase Revenues

In the past several months, 23andMe has attempted to staunch the corporate blood flow by:

Neither of these moves have been well-received by genealogists.

Purchase Price

23andMe sells two types of tests. One is for both health and ancestry, and the second is for ancestry, aka genealogy, only.

  • The 23andMe Health and Ancestry test is currently priced at $229. The yearly membership costs an additional $69, for a total of $298, but the membership is currently free during the first year. That’s a lot for an autosomal test that only buys you up to 5000 matches.
  • The 23andMe ancestry-only test is $119, but comes with restrictions, including the 1500 match limit.

For comparison purposes, this article shows how many matches I have at each vendor.

If you want more than 1500 matches, you MUST PURCHASE the Health and Ancestry test, not the lower-cost genealogy-only test, plus the additional membership.

This is a very difficult pill to swallow (pardon the pun.) None of the other DNA testing companies limit your matches or charge for matching, and their prices right now for their autosomal tests are as follows:

Subscription aka Membership

In order to entice customers into purchasing subscriptions, called memberships, 23andMe allows up to 5000 matches instead of 1500. 23andMe has also limited additional features, taking them away from their original customers and putting them behind the subscription paywall.

In October 2020, when they implemented subscriptions, called memberships, along with these changes, they reduced their customers’ original match limit from 2000 to 1500. Of course, to receive more matches, you could purchase a new test and subscribe. No thank you.

In another attempt to throttle services to earlier customers, there were initially no ethnicity updates for people in October of 2020 who had tested on V2, V3 or V4 chips, although following public outcry, they reversed that position for at least the V3 and V4 customers. No other DNA testing company excludes customers from ethnicity updates. 

One cannot perform other functions, such as sort or filter by haplogroup on their site, unless you purchase the Health and Ancestry test, plus a membership. You can, however, download your matches and sort/filter that way..

What’s Next for 23andMe?

23andMe says they are now actively pursuing new big pharma partners.

I hope they can find their way forward. While I don’t often find relevant matches at 23andMe anymore, and I have an issue with their subscription policy, especially removing features from existing customers, they do have a pool of 12 million-ish people. These matches certainly help many people, especially because their health customers probably won’t have tested elsewhere.

Having said that, I can’t help but wonder how many of those 12 million are the same person multiple times because they’ve had to purchase multiple tests. I’ve purchased three for myself over the years, and I’m not purchasing a fourth – but I digress.

  • 23andMe is still a good site for matching, especially for adoptees or people seeking unknown family members. You can also see how your matches match each other. You just never know where that critical match is going to pop up.
  • 23andMe provides painted ethnicity chromosome segments, along with FamilyTreeDNA. In my opinion, they are the top two vendors for ethnicity accuracy.
  • 23andMe and FamilyTreeDNA both report X-DNA matching, which can be very useful.
  • 23andMe is still the only vendor to construct a genetic tree – and yes – I know it’s not always completely accurate. Still, their tree creation is innovative and automated – based on how you match people and how they match each other. For adoptees and people seeking parents or grandparents, it’s essential because they start with nothing.
  • 23andMe doesn’t allow customers to upload or create a family tree, so you can’t view the family tree of your matches to find a common ancestor. You can include a link to your online family tree in your Enhanced Profile under Settings, but many people never see this, or aren’t genealogists.

Unfortunately, 23andMe is not focused on genealogy – at all. Their focus has always been medicine and health. From their perspective, genealogists are candidates to opt-in for genetic research, but that doesn’t mean genealogists can’t still benefit – even if we don’t opt-in, don’t purchase the more expensive $229 Health and Ancestry test, and don’t purchase their membership.

If you’re interested in more recent relatives, 23andMe is great because the 1500 match limit won’t impact you at all. Closer relatives will cluster at the top of your match list.

If you’re looking for matches that descend from more distant ancestors, you may find it worthwhile to purchase the more expensive test and the membership, at least for one year.

Filtering/Sorting Restriction Workaround 

While there’s no way around the 1500 or 5000 match limit, except that 23andMe won’t roll someone off of your match list if you’ve communicated with them, or tried to, there is a workaround for the restrictive filtering.

I check my matches periodically, sorting by the newest matched relatives. I also download my match list occasionally. I find it easier to review the information in spreadsheet format because I can search for surnames, locations, haplogroups and other information much more easily than online, especially given the restrictive filters.

However, when you download your match list, that information is downloaded as well.

Be sure to record notes on each match at 23andMe when you discover relevant information by clicking on the match and scrolling to the very bottom of the page. Your notes at 23andMe are downloaded onto the spreadsheet along with the rest of their information.

The instructions for downloading your match list, which is NOT the same as downloading your DNA file, are contained in this article. Give it a try!

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Which DNA Test Should I Buy? And Why?

Which DNA test should I buy, and why?

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

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

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

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

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

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

Multiple Questions

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

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

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

Easy Answers First

The answer to #4 is easy.

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

So, yes, John can purchase a test.

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

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

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

Goals

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

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

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

Ethnicity in General

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

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

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

Additionally, each company provides different tools for their customers.

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

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

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

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

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

Let’s Start with Native American

Let’s evaluate the information that John provided.

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

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

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

First, we need to convert generations to 16ths.

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

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

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

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

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

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

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

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

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

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

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

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

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

Would  Ethnicity/Population Tests Show This Much Native?

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

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

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

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

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

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

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

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

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

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

Ethnicity has a lot more to offer than just percentages.

Best Autosomal Tests for Native Ethnicity

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

Click images to enlarge

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

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

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

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

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

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

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

Autosomal and Genealogy

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

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

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

Best Autosomal Test for Matching Other Testers

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

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

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

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

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

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

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

Ancestry does NOT provide any segment information.

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

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

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

Test or Upload

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

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

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

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

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

GEDmatch

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

Other Types of DNA

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

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

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

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

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

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

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

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

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

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

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

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

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

My Recommendation

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

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

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

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

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

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

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

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

Shopping and Research List

Here are the tests and links recommended above:

More Than He Asked

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

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

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

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

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

Which Test Should I Order?

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

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

Enjoy!!!

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Mother’s Day Visitation Two Decades Out

I hope that you are enjoying Mother’s Day, whether you’re the Mom being honored, you’re honoring your mother, or you’re one of the millions who “mother” and love others, one way or another.

I didn’t have time to complete my normal article for today, but I certainly didn’t want to let Mother’s Day pass without acknowledgment.

I didn’t get my article finished because, let’s just say, I’ve been extremely busy with something VERY interesting.

I can’t tell you everything, but I can tell you a little!

Just a couple of days ago, I was able to visit Mom once again in the freezer at FamilyTreeDNA.

Mom’s DNA has been housed there since 2003, when she swabbed for her first DNA test. It’s so hard to believe that was two decades ago. So much has changed.

That stored DNA sample allowed me to upgrade Mom to the Family Finder test in 2012, six years after she passed away.

In 2013, I visited Mom at FamilyTreeDNA in the freezer and realized, as I looked in that little window, that there was more of my mother in that freezer than anywhere else on earth. My DNA is in there too, with her, just sayin’. I won’t be buried beside her in the soil, but I am near her in that freezer every day. Somebody has to keep an eye on her!

In intervening years, FamilyTreeDNA purchased a larger freezer and moved Mom from the earlier location across the room to the larger cryo-preservation cemetery – I mean freezer.

Now, Mom, with a few million of her friends and several thousand of our relatives, is partying it up in there when no one is looking.

Time Capsule

Every time I stare through that window, it’s like peering backward into a time capsule. I wonder, if all the Y-DNA was processed at the Big Y-700 level, how much of the entire Y-DNA phylogenetic tree would we be able to reconstruct?

People often skip testing mitochondrial DNA, passed from mothers to all their children, thinking it won’t be genealogically useful. I assure you, that’s not always the case. Furthermore, if you don’t test, DNA can never be useful. Every single person has mitochondrial DNA, so just imagine how much of the mitochondrial tree would be created if every one of those samples was tested at or upgraded to the full sequence level.

How many dead ends are in that freezer, meaning no living people carry that line anymore? I’m one of those people because I have no grandchildren through my daughter. Mom’s, her mother’s, and my mitochondrial DNA dies with my generation.

Based on my mitochondrial DNA sequence, meaning my mutations, I’ll VERY likely have a new haplogroup when the Million Mito Project rolls out, and even more likely that it will be at least three branches down the tree, closer in time.

What pieces of our human history will be lost if the people in that freezer don’t test their mitochondrial DNA at the full sequence level? The full sequence is needed to construct the mitochondrial tree of all humanity.

How many more matches would we have if everyone in that freezer had a Family Finder test? How many brick walls would fall? How many mysteries would be solved? Would we be able to reconstruct the DNA of our ancestors from their descendants?

What happens if we never open that time capsule, individually and collectively?

“Just Do It”

I had to pinch myself, though. As I stood in that lab, viewing through that window what I considered a sacred and hallowed space for Mom and humanity as well, I was reminded of what Mom said to me not long before she died. In fact, I can hear her frail voice.

“You need to do that.” 

What was “that”?

“That” was transforming her DNA results into a story – her story, her history and genealogy – and how she connected with the story of all humankind. Her “story” revealed her history, our history, even before genealogy, connecting with her soul. She could touch people whose names she would never know, but who contributed their mitochondrial DNA to her. It brought them alive.

I had an entire litany of sensible, level-headed reasons why I could never “do that,” beginning with the fact that I already had a career and owned a business. I had a family, children, and responsibilities – nope – no can do, Mom.

Not to be deterred, Mom gently stopped me in the process of listing all the perfectly logical and valid reasons why that would never work and told me that all of that was just preparing me for what I was “supposed to do,” and I needed to “just do it.” This was nothing like the mother I knew, always conservative in her advice and never wanting me to step out, even a little bit, onto an unstable limb. Let alone leap off the cliff of uncertainty with absolutely no safety net.

What had happened to my mother?

I simply couldn’t make her understand – all those years ago.

Then, my gaze drifts back to the present, and I remember that I’m staring into a freezer, not a time machine. Mom has already had all the tests available today. But many of her frozen neighbors have not.

As I stood, looking into that window, into the past, and perhaps into the future, I was afraid to turn around.

People were standing behind me, filming. I didn’t want anyone to see those tears slipping down my cheeks. After all, I had simply been looking at a window, right? Just a window. Not a cemetery. Not a portal. Not a time machine, no reason for tears – unless you understand the magnitude of what the freezer holds.

I so hoped that those hot tears didn’t entirely ruin my makeup, or that I could at least escape to the restroom to fix it without being noticed.

The Greatest Journey

On the way to the restroom, I saw this framed magazine, a wink and a nod from Mom, I’m sure. Indeed, our DNA is the greatest journey ever told, ever embarked upon, and the story is not yet entirely written. Mom said DNA would change the world as we know it, and she was right.

Mom, I found a way – or maybe fate found me back in 2004. That fateful fork in the road, although I’m not sure I even realized I had slipped onto that road untaken until it was too late to turn back.

Maybe Mom pushed those buttons from the other side, because I’ve been passionately “doing that” one way or another now for almost two decades. And finally, finally, we are going to be able to tell a larger story.

You and me, Mom. Hand in hand with our cousins. All of them – on every continent around the world.

Making history is on the horizon. DNA rocks. Here’s to all the mothers!!!

Thank You

Happy Mother’s Day, Mom. I love and miss you oh so much. And, while I wasn’t at the time, I’m – ahem – so incredibly grateful for the swift kick in the behind called encouragement.

But then, isn’t that the age-old story of motherhood?

Until next time Mom, you behave in there!

_____________________________________________________________

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DNA: In Search Of…Your Grandparents

Are you searching for an unknown relative or trying to unravel and understand unexpected results? Maybe you discovered that one or both of your parents is not your biological parent. Maybe one of your siblings might be a half-sibling instead. Or maybe you suddenly have an unexpected match that looks to be an unknown close relative, possibly a half-sibling. Perhaps there’s a close match you can’t place.

Or, are you searching for the identity of your grandparent or grandparents? If you’re searching for your parent or parents, often identifying your grandparents is a necessary step to narrow the parent-candidates.

I’ve written an entire series of “In Search of Unknown Family” articles, permanently listed together, here. They will step you through the search process and help you understand how to unravel your results. If you’re new, reading these, in order, before proceeding, would be a good idea.

Identifying a Grandparent

I saved this “grandparents” article for later in the series because you will need the tools and techniques I’ve introduced in the earlier articles. Identifying grandparents is often the most challenging of any of the relationships we’ve covered so far. In part because each of those four individuals occupies a different place in your tree, meaning their X, Y-DNA and mitochondrial DNA is carried by different, and not all, descendants. This means we sometimes have to utilize different tools and techniques.

If you’re trying to identify any of your four grandparents, females are sometimes more challenging than males.

Why?

Women don’t have a Y chromosome to test. This can be a double handicap. Female testers can’t test a Y chromosome, and maternal ancestors don’t have a Y chromosome to match.

Of course, every circumstance differs. You may not have a male to test for paternal lines either.

The maternal grandfather can be uniquely challenging, because two types of DNA, Y-DNA and mitochondrial DNA matching are immediately eliminated for all testers.

While I’ve focused on the maternal grandfather in this example, these techniques can be utilized for all four grandparents as well as for parents. At the end, I’ll review other grandparent relationships and additional tools you might be able to utilize for each one.

In addition to autosomal DNA, we can also utilize mitochondrial DNA, Y-DNA and sometimes X DNA in certain situations.

Testing, Tests and Vendors

As you recall, only men have a Y chromosome (blue arrow), so only genetic males can take a Y-DNA test. Men pass their Y chromosome from father to son in each generation. Daughters don’t receive a Y chromosome.

Everyone has their mother’s mitochondrial DNA (pink arrow.) Women pass their mitochondrial DNA to both sexes of their children, but only females pass it on. In the current generation, represented by the son and daughter, above, the mother’s yellow heart-shaped mitochondrial DNA is inherited by both sexes of her children. In the current generation, males and females can both test for their mother’s mitochondrial DNA.

Of course, everyone has autosomal DNA, inherited from all of their ancestral lines through at least the 5th or 6th generation, and often further back in time. Autosomal DNA is divided in half in each generation, as children inherit half of each parents’ autosomal DNA (with the exception of the X chromosome, which males only inherit from their mother.)

The four major vendors, Ancestry, 23andMe, FamilyTreeDNA and MyHeritage sell autosomal DNA tests, but only FamilyTreeDNA sells Y-DNA and mitochondrial DNA tests.

Only 23andMe and FamilyTreeDNA report X matching.

All vendors except Ancestry provide segment location information along with a chromosome browser.

You can read about the vendor’s strengths and weaknesses in the third article, here.

Ordering Y and Mitochondrial DNA Tests

If you’re seeking the identities of grandparents, the children and parents, above, can test for the following types of DNA in addition to autosomal:

Person in Pedigree Y-DNA Mitochondrial
Son His father’s blue star His mother’s pink heart
Daughter None Her mother’s pink heart
Father His father’s blue star His mother’s gold heart
Mother None Her mother’s pink heart

Note that none of the people shown above in the direct pedigree line carry the Y-DNA of the green maternal grandfather. However, if the mother has a full sibling, the green “Male Child,” he will carry the Y-DNA of the maternal grandfather. Just be sure the mother and her brother are full siblings, because otherwise, the brother’s Y-DNA may not have been inherited from your mother’s father. I wrote about full vs half sibling determination, here.

Let’s view this from a slightly different perspective. For each grandparent in the tree, which of the two testers, son or daughter, if either, carry that ancestor’s DNA of the types listed in the columns.

Ancestor in Tree Y-DNA Mitochondrial DNA Autosomal DNA X DNA
Paternal Grandfather Son Neither Son, daughter Neither
Paternal Grandmother Has no Y chromosome None (father has it, doesn’t pass it on to son or daughter) Son, daughter Daughter (son does not receive father’s X chromosome)
Maternal Grandfather Neither Neither Son, daughter Son, daughter (potentially)
Maternal Grandmother Has no Y chromosome Son, daughter Son, daughter Son, daughter (potentially)

Obtaining the Y-DNA and mitochondrial DNA of those grandparents from their descendants will provide hints and may be instrumental in identifying the grandparent.

FamilyTreeDNA

You’ll need to order Y-DNA (males only) and mitochondrial DNA tests separately from autosomal DNA tests. They are three completely different tests.

At FamilyTreeDNA, the autosomal DNA test is called Family Finder to differentiate it from their Y-DNA and mitochondrial DNA tests.

Their autosomal test is called Family Finder whether you order a test from FamilyTreeDNA, or upload your results to their site from another vendor (instructions here.)

I recommend ordering the Big Y-700 Y-DNA test if possible, and if not, the highest resolution Y-DNA test you can afford. The Big Y-700 is the most refined Y-DNA test available, includes multiple tools and places Big Y-700 testers on the Time Tree through the Discover tool, providing relatively precise estimates of when those men shared a common ancestor. If you’ve already purchased a lower-precision Y-DNA test at FamilyTreeDNA, you can easily upgrade.

I wrote about using the Discover tool here. The recently added Group Time Tree draws a genetic Y-DNA tree of Big-Y testers in common projects, showing earliest known ancestors and the date of the most recent common ancestor.

You need to make sure your Family Finder, mitochondrial DNA and Y-DNA (if you’re a male) tests are ordered from the same account at FamilyTreeDNA.

You want all 3 of your tests on the same account (called a kit number) so that you can use the advanced search features that display people who match you on combinations of multiple kinds of tests. For example, if you’re a male, do your Y-DNA matches also match you on the autosomal Family Finder test, and if so, how closely? Advanced matching also provides X matching tools.

X DNA is included in autosomal tests. X DNA has a distinct matching pattern for males and females which makes it uniquely useful for genealogy. I wrote about X DNA matching here.

If you upload your autosomal results to FamilyTreeDNA from another company, you’re only uploading a raw DNA file, not the DNA itself, so FamilyTreeDNA will need to send you a swab kit to test your Y-DNA and mitochondrial DNA. If you upload your autosomal DNA, simply sign in to your kit, purchase the Y-DNA and/or mitochondrial DNA tests and they will send you a swab kit.

If you test directly at FamilyTreeDNA, you can add any test easily by simply signing in and placing an order. They will use your archived DNA from your swab sample, as long as there’s enough left and it’s of sufficient quality.

Fish In All Ponds

The first important thing to do in your grandparent search is to be sure you’re fishing in all ponds. In other words, be sure you’ve tested at all 4 vendors, or uploaded files to FamilyTreeDNA and MyHeritage.

When you upload files to those vendors, be sure to purchase the unlock for their advanced tools, because you’re going to utilize everything possible.

If you have relatively close matches at other vendors, ask if they will upload their files too. The upload is free. Not only will they receive additional matches, and another set of ethnicity results, their results will help you by associating your matches with specific sides of your family.

Why Order Multiple Tests Now Instead of Waiting?

I encourage testers to order their tests at the beginning of their journey, not one at a time. Each new test from a vendor takes about 6-8 weeks from the time you initially order – they send the test, you swab or spit, return it, and they process your DNA. Of course, uploading takes far less time.

If you’re adding elapsed time, two autosomal tests (Ancestry and 23andMe), two uploads (FamilyTreeDNA and MyHeritage,) a Y-DNA and a mitochondrial DNA test, if all purchased serially, one after the other, means you’ll be waiting about 6-8 months.

Do you want to wait 6-8 months? Can you afford to?

Part of that answer has to do with what, exactly, you’re seeking.

A Name or Information?

Are you seeking the name of a person, or are you seeking information about that person? With grandparents, you may be hoping to meet them, and time may be of the essence. Time delayed may not be able to be recovered or regained.

Most people don’t just want to put a name to the person they are seeking – they want to learn about them. You will have different matches at each company. Even after you identify the person you seek, the people you match at each company may have information about them, their photos, know about their life, family, and their ancestors. They may be able and willing to facilitate an introduction if that’s what you seek.

One cousin that I assisted discovered that his father had died just 6 weeks before he made the connection. He was heartsick.

Having data from all vendors simultaneously will allow you to compile that data and work with it together as well as separately. Using your “best” matches at each company, augmented by both Y-DNA and mitochondrial DNA can make MUCH shorter work of this search.

Your Y-DNA, if you’re a male will give you insights into your surname line, and the Big-Y test now comes with estimates of how far in the past you share a common ancestor with other men that have taken the Big-Y test. This can be a HUGE boon to a male trying to figure out his surname line.

Y-DNA and mitochondrial DNA, respectively, will eliminate many people from being your mother or father, or your direct paternal or direct maternal line ancestor. Both provide insights into which population and where that population originated as well. In other words, it provides you lineage-specific information not available elsewhere.

Your Y-DNA and mitochondrial DNA can also provide critically important information about whether that direct line ancestor belonged to an endogamous population, and where they came from.

Strategies

You may be tempted to think that you only need to test at one vendor, or at the vendor with the largest database, but that’s not necessarily true.

Here’s a table of my closest matches at the 4 vendors.

Vendor Closest Maternal Closest Paternal Comments
Ancestry 1C, 1C1R Half 1C, 2C I recognized both of the maternal and neither of the paternal.
23andMe 2C, 2C 1C1R, half-gr-niece Recognized both maternal, one paternal
MyHeritage Mother uploaded, 1C Half-niece, half 1C Recognized both maternal, one paternal
FamilyTreeDNA Mother tested, 1C1R Parent/child, half-gr-niece Recognized all 4

To be clear, I tested my mother at FamilyTreeDNA before she passed away, but if I was an adoptee searching for my mother, that’s the first database she would be in. As her family, we were able to order the Family Finder test from her archived DNA after she had passed away. I then uploaded her DNA file to MyHeritage, but she’ll never be at either 23andMe or Ancestry because they don’t accept uploads and she clearly can’t test.

Additionally, being able to identify maternal matches by viewing shared matches with my mother separates out close matches from my paternal side.

Let’s put this another way, I stand a MUCH BETTER chance of unraveling this mystery with the combined closest matches of all 4 databases instead of the top ones from just one database.

I’m providing analysis methodologies for working with results from all of the vendors together, in case your answer is not immediately obvious. Taking multiple tests facilitates using all of these tools immediately, not months later. Solving the puzzle sooner means you may not miss valuable connection opportunities.

You may also discover that the door slams shut with some people, but another match may be unbelievably helpful. Don’t unnecessarily limit your possibilities.

Here’s the testing and upload strategy I recommend.

What When Ancestry 23andMe MyHeritage FamilyTreeDNA GEDmatch
Order autosomal test Initially Yes Yes Upload Upload Upload
Order Big-Y DNA test if male Initially Yes
Order mitochondrial DNA test Initially Yes
Upload free autosomal file From Ancestry or 23andMe Yes Yes Yes
Unlock Advanced Tools When upload file $29 $19 $9.95 month
Includes X Matching No Yes No Yes Yes
Chromosome Browser, segment location information No Yes Yes Yes Yes

When you upload a DNA file to a vendor site, only upload one file per site, per tester. Otherwise, multiple tests simply glom up everyone’s match list with multiple matches to the same person and can be very confusing.

  • One person took an autosomal test at a company that accepts uploads, forgot about it, uploaded a file from another vendor later, and immediately thought she had found her parent. She had not. She “found” herself.
  • Another person though she had found two sisters, but one person had uploaded their own file from two different vendors.

Multiple vendor sites reveal multiple close matches to different people which increase your opportunity to discover INFORMATION about your family, not just the identity of the person.

Match Ranges

Given that we are searching for an unknown maternal grandfather, your mother may not have had any (known) full siblings. The “best” match would be to a full or half siblings to your parents, or their descendants, depending on how old your grandparents would be.

Let’s take the “worst case” scenario, meaning there are no full siblings AND there are many possible generations between you and the people you may match.

Now, let’s look at DNAPainter’s Shared cM tool.

You’re going to be looking for someone who is either your mother’s half sibling on her father’s side, or who is a full sibling.

If your mother is adopted, it’s possible that she has or had full siblings. If your mother was born circa 1920, it’s likely that you will be matching the next generation, or two, or three.

However, if your mother was born later, you could be matching her siblings directly.

I’m going to assume half siblings for this example, because they are more difficult than full siblings.

Full sibling relationships for your mother’s siblings are listed at right. Your full aunt or uncle at top, then their descendant generations below.

At left, in red, are the half-sibling relationships and the matching amounts.

You can see that if you’re dealing with half 1C3R (half first cousin three times removed,) you may not match.

Therefore, in order to isolate matches, it’s imperative to test every relevant relative possible.

Who’s Relevant for DNA Testing?

Who is relevant to test If you’re attempting to identify your maternal grandfather?

The goal is to be able to assign matches to the most refined ancestor possible. In other words, if you can assign someone to either your grandmother’s line, or your grandfather’s line, that’s better than assigning the person to your grandparents jointly.

Always utilize the tests of the people furthest up the tree, meaning the oldest generations. Their DNA is less-diluted, meaning it has been divided fewer times. Think about who is living and might be willing to test.

You need to be able to divide your matches between your parents, and then between your grandparents on your mother’s side.

  • Test your parents, of course, and any of their known siblings, half or full.
  • If those siblings have passed away, test as many of their children as you can.
  • If any of your grandparents are living, test them
  • If BOTH of your grandparents on the same side aren’t available to test, test any, preferably all, living aunts or uncles.
  • If your maternal grandmother had siblings, test them or their descendants if they are deceased.
  • If your parents are deceased, test your aunts, uncles, full siblings and half-siblings on your mother’s side. (Personally, I’d test all half-siblings, not just maternal.)
  • Half-siblings are particularly valuable because there is no question which “side” your shared DNA came from. They will match people you don’t because they received part of your parent’s DNA that you did not.

Furthermore, shared matches to half-siblings unquestionably identify which parent those matches are through.

Essentially, you’re trying to account for all matches that can be assigned to your grandparents whose identities you know – leaving only people who descend from your unknown maternal grandfather.

Testing your own descendants will not aid your quest. There is no need to test them for this purpose, given that they received half of your DNA.

I wrote about why testing close relatives is important in the article Superpower: Your Aunts’ and Uncles’ DNA is Your DNA Too – Maximize Those Matches!

Create or Upload a Tree

Three of the four major vendors, plus GEDMatch, support and utilize family trees.

You’ll want to either upload or create a tree at each of the vendor sites.

You can either upload a GEDCOM file from your home computer genealogy software, or you can create a tree at one of the vendors, download it, and upload to the others. I described that process at Ancestry, here.

Goal

Your goal is to work with your highest matches first to determine how they are related to you, thereby eliminating matches to known lineages.

Assuming you’re only searching for the identity of one grandparent, it’s beneficial to have done enough of your genealogy on your three known grandparents to be able to assign matches from those lines to those sides.

Step 1 is to check each vendor for close matches that might fall into that category.

The Top 15 at Each Vendor

Your closest several autosomal matches are the most important and insightful. I begin with the top 15 autosomal results at each vendor, initially, which provides me with the best chance of meaningful close relationship discoveries.

Create a Spreadsheet or Chart

I hate to use that S word (spreadsheet), because I don’t want non-technical people to be discouraged. So, I’m going to show you how I set up a spreadsheet and you can simply create a chart or even draw this out on paper if you wish.

I’ve color-coded columns for each of my 4 grandparents. The green column is the target Maternal Grandfather whose identity I’m seeking.

I match our first example; Erik, at 417 cM. Based on various pieces of information, taken together, I’ve determined that I’m Erik’s half 1C1R. His 8 great-grandparent surnames, or the ones he has provided, indicate that I’m related to Eric on my paternal grandfather’s line.

You’ll want to record your closest matches in this fashion.

Let’s look at how to find this information and work with the tools at the individual vendors.

23andMe

Let’s start at 23andMe, because they create a potential genetic tree for you, which may or may not be accurate.

I have two separate tests at 23andMe. One is a V3 and one is a V4 test. I keep one in its pristine state, and I work with the second one. You’ll see two of “me” in the tree, and that’s why.

23andMe makes it easy to see estimated relationships, although they are not always correct. Generally, they are close, and they can be quite valuable.

Click on any image to enlarge

The maternal and paternal “sides” may not be positioned where genealogists are used to seeing them. Remember, 23andMe has no genealogy trees, so they are attempting to construct a genetic tree based on how people are related to you and to each other, with no prior knowledge. They do sometimes have issues with half-relationships, so I’d encourage you to use this tree to isolate people to the three grandparents you know.

In my case, I was able to determine the maternal and paternal sides easily based on known cousins. This is the perfect example of why it’s important to test known relatives from both sides of your family.

My paternal side, at right, in blue, was easy because I recognized my half-sister’s family, and because of known cousins who I recognized from having tested elsewhere. I’ve worked with them for years. The blue stars show people I could identify, mostly second cousins.

My maternal side is at left, in red. Normally, for genealogists, the maternal side is at right, and the paternal at left, so don’t make assumptions, and don’t let this positioning throw you.

I’m pretending I don’t know who my maternal grandfather is. I was able to identify my maternal grandmother’s side based on a known second cousin.

That leaves my target – my maternal grandfather’s line.

All of the matches to the left of the red circle would, by process of elimination, be on my maternal grandfather’s side.

The next step would be to figure out how the 5 people descending from my maternal grandfather’s line are related to each other – through which of their ancestors.

On the DNA Relatives match list, here’s what needs to be checked:

  • Do your matches share surnames with you or your ancestors?
  • Do they show surnames in common with each other?
  • Is there a common location?
  • Birth year which helps you understand their potential generation.
  • Did they list their grandparents’ birthplaces?
  • Did they provide a family tree link?
  • Do they also match each other using the Relatives in Common feature?
  • Do they triangulate, indicated by “DNA Overlap” in Relatives in Common?
  • Who else is on the Relatives in Common list, and what do they have in common with each other?
  • Looking at your Ancestry Composition compared with theirs, what are your shared populations, and are they relevant? If you are both 100% European, then shared populations aren’t useful, but if both people share the same minority ancestry, especially on the same segments, it may indeed be relevant – especially if it can’t be accounted for on the known sides of the family.

Reach out to these people and see what they know about their genealogy, if they have tested elsewhere, and if they have a genealogy tree someplace that you can view.

If they can tell you their grandparents’ names, birth and death dates and locations, you can check public sources like WikiTree, FamilySearch and Geni, or build trees for them. You can also use Newspaper resources, like Newspapers.com, NewspaperArchive and the newspapers at MyHeritage.

I added the top 15 23andMe matches into the spreadsheet I created.

You’ll notice that not many people at 23andMe enter surnames. However, if you can identify individuals from your 3 known lines, you can piggyback the rest by using Relatives in Common in conjunction with the genetic tree placement.

Be sure to check all the people that are connected to the target line in your genetic tree.

You’ll want to harvest your DNA segments to paint at DNAPainter if you don’t solve this mystery with initial reviews at each vendor.

Ancestry

Let’s move to Ancestry next.

At Ancestry, you’ll want to start with your closest matches on your match list.

Ancestry classifies “Close Matches” as anyone 200 cM or greater, which probably won’t reach as far down as the matches we’ll want to include.

Some of the categories in the Shared cM Chart from DNAPainter, above, don’t work based on ages, so I’ve eliminated those. I also know, for example, that someone who could fall in the grandparent/grandchild category (blue star,) in my case, does not, so must be a different relationship.

Second cousins, who share great-grandparents, can be expected to share about 229 cM of DNA on average, or between 41 and 592 cM. First cousins share 866 cM, and half first cousins share 449 cM on average.

I have 13 close matches (over 200 cM), but I’m including my top 15 at each vendor, so I added two more. You can always go back and add more matches if necessary. Just keep in mind that the smaller the match, the greater the probability that it came from increasingly distant generations before your grandparents. Your sweet spot to identify grandparents is between 1C and 2C.

I need to divide my close matches into 4 groups, each one equating to a grandparent. Record this on your spreadsheet.

You can group your matches at Ancestry using colored dots, which means you can sort by those groups.

You can also select a “side” for a match by clicking on “Yes” under the question, “Do you recognize them?”

Initially, you want to determine if this person is related to you on your mother’s or father side, and hopefully, through which grandparent.

Recently, Ancestry added a feature called SideView which allows testers to indicate, based on ethnicity, which side is “parent 1” and which side is “parent 2.” I wrote about that, here.

Make your selection, assuming you can tell which “side” of you descends from which parent based on ethnicity and/or shared matches. How you label “parent 1,” meaning either maternal or paternal, determines how Ancestry assigns your matches, when possible.

Using these tools, which may not be completely accurate, plus shared matches with people you can identify, divide your matches among your three known grandparents, meaning that the people you cannot assign will be placed in the fourth “unknown” column.

On my spreadsheet, I assign all of my closest matches to one of my grandparents. Michael is my first cousin (1C) and we share both maternal grandparents, so he’s not helpful in the division because he can’t be assigned to only one grandparent.

The green maternal grandfather is who I’m attempting to identify.

There are 4 people, highlighted in yellow, who don’t fall into the other three grandparent lines, so they get added to the green column and will be my focus.

I would be inclined to continue adding matches using a process known as the Leeds Method, until I had several people in each category. Looking back at the DNAPainter cM chart, at this point, we don’t have anyone below 200 cM and the matches we need might be below that threshold. The more matches you have to work with, the better.

At Ancestry, you cannot download your matches into a spreadsheet, nor can you work with other clustering tools such as Genetic Affairs, so you’ll have to build out your spreadsheet manually.

Check for the same types of information that I reviewed at 23andMe:

  • Review trees, if your matches have them, minimally recording the surnames of their 8 great-grandparents.
  • Review shared matches, looking for common names in the trees in recent generations.
  • View shared matches with people with whom you have a “Common Ancestor” indication, which means a ThruLine. You won’t have Thrulines with your target grandparent, of course, but Thrulines will allow you to place the match in one of the other columns. I wrote about ThruLines here, here and here.
  • ThruLines sometimes suggests ancestors based on other people’s trees, so be EXCEEDINGLY careful with potential ancestor suggestions. That’s not to say you should discount those suggestions. Just treat them as tree hints that may have been copy/pasted hundreds of times, because that’s what they are.

I make notes on each match so I can easily see the connection by scanning without opening the match.

Now, I have a total of 30 entries on my spreadsheet, 15 from 23and Me and 15 from Ancestry.

Why Not Use Autosclusters?

Even with vendors who allow or provide cluster tools, I don’t use an automated autocluster tool at this point. Autocluster tools often omit your closest matches because your closest matches would be in nearly half of all your clusters, which isn’t exactly informative. However, for this purpose, those are the very matches we need to evaluate.

After identifying groups of people that represent the missing grandparent, using our spreadsheet methodology, autoclusters could be useful to identify common surnames and even to compare the trees of our matches using AutoTree, AutoPedigree and AutoKinship. AutoClusters cannot be utilized at Ancestry, but is available through MyHeritage and at GEDmatch, or through Genetic Affairs for 23andMe and FamilyTreeDNA.

Next, let’s move to FamilyTreeDNA.

FamilyTreeDNA

FamilyTreeDNA is the only vendor that provides Family Matching, also known as “bucketing.” FamilyTreeDNA assigns your matches to either a paternal or maternal bucket, or both, based on triangulated matches with someone you’ve linked to a profile in your tree.

The key to Family Matching is to link known Family Finder matches to their profile cards in your tree.

Clicking on the Family Tree link at the top of your personal page allows you to link your matches to the profile cards of your matches.

FamilyTreeDNA utilizes these linked matches to assign those people, and matches who match you and those people, both, on at least one common segment, to the maternal or paternal tabs on your match list.

Always link as many known people as possible (red stars) which will result in more matches being bucketed and assigned to parents’ sides for you, even if neither parent is available to test.

I wrote about Triangulation in Action at FamilyTreeDNA, here.

You can see at the top of my match list that I have a total of 8000 matches of which 3422 are paternal, 1517 are maternal and 3 match on both sides. Full siblings, their (and my) children and their descendants will always match on both sides. People with endogamy across both parents may have several matches on both sides.

If your relevant parent has tested, always work from their test.

Because we are searching for the maternal grandfather, in this case, we can ignore all tests that are bucketed as paternal matches.

Given that we are searching for my maternal grandfather, I probably have not been able to link as many maternal matches, other than possibly ones from my maternal grandmother. This means that the maternal grandfather’s matches are not bucketed because there are no identified matches to link on that side of my tree.

If you sort by maternal and paternal tabs, you’ll miss people who aren’t bucketed, meaning they have no maternal or paternal icon, so I recommend simply scanning down the list and processing maternal matches and non-bucketed matches.

By being able to confidently ignore paternally bucketed matches and only processing maternal and non-assigned matches, this is equivalent to processing the first 48 total matches. If I were to only look at the first 15 matches, 12 were paternal and only 3 are maternal.

Using bucketing at FamilyTreeDNA is very efficient and saves a lot of work.

Omitting paternal matches also means we are including smaller matches which could potentially be from common ancestors further back in the tree. Or, they could be younger testers. Or simply smaller by the randomness of recombination.

FamilyTreeDNA is a goldmine, with 16 of 20 maternal matches being from the unknown maternal grandfather.

Next, let’s see what’s waiting at MyHeritage.

MyHeritage

MyHeritage is particularly useful if your lineage happens to be from Europe. Of course, if you’re searching for an unknown person, you probably have no idea where they or their ancestors are from. Two of my best matches first appeared at MyHeritage.

Of course, your matches with people who descend from your unknown maternal grandfather won’t have any Theories of Family Relativity, as that tool is based on BOTH a DNA match plus a tree or document match. However, Theories is wonderful to group your matches to your other three grandparents.

MyHeritage provides a great deal of information for each match, including common surnames with your tree. If you recognize the surnames (and shared matches) as paternal or maternal, then you can assign the match. However, the matches you’re most interested in are the highest matches without any surnames in common with you – which likely point to the missing maternal grandfather.

However, those people may, and probably do, have surnames in common with each other.

Of the matches who aren’t attributed to the other three grandparents, the name Ferverda arises again and again. So does Miller, which suggests the grandparent or great-grandparent couple may well be Ferverda/Miller.

Let’s continue working through the process with our spreadsheet and see what we can discover about those surnames.

Our 60 Results

Of the 60 total results, 15 from each vendor, a total of 24 cannot be assigned to other columns through bucketing or shared matches, so are associated with the maternal grandfather. Of course, Michael who descends from both of my maternal grandparents won’t be helpful initially.

Cheryl, Donald and Michael are duplicates at different vendors, but the rest are not.

Of the relevant matches, the majority, 12 are from FamilyTreeDNA, four each are from Ancestry and MyHeritage, and three are from 23andMe.

Of the names provided in the surname fields of matches, in matches’ trees in the first few generations, and the testers’ surnames, Ferverda is repeated 12 times, for 50% of the time. Miller is repeated 9 times, so it’s likely that either of those are the missing grandfather’s surname. Of course, if we had Y-DNA, we’d know the answer to that immediately.

Comparing trees of my matches, we find John Ferverda as the common ancestor between two different matches. John is the son of Hiram Ferverda and Eva Miller who are found in several trees.

That’s a great hint. But is this the breakthrough I need?

What’s Next?

The next step is to look for connections between the maternal grandmother, Edith Lore, who is known in our example, and a Ferverda male. He is probably one of the sons of Hiram Ferverda and Eva Miller. Do they lived in the same area? In close proximity? Do they attend the same church or school? Are they neighbors or live close to the family or some of their relatives? Does she have connections with Ferverda family members? We are narrowing in.

Some of Hiram and Eva’s sons might be able to be eliminated based on age or other factors, or at least be less likely candidates. Any of their children who had moved out of state when the child was conceived would be less likely candidates. Age would be a factor, as would opportunity.

Target testing of the Ferverda sons’ children, or the descendants of their children would (probably) be able to pinpoint which of their sons is more closely related to me (or my mother) than the rest.

In our case, indeed, John Ferverda is the son we are searching for and his descendant, Michael is the highest match on the list. Cheryl and Donald descend from John’s brother, which eliminates him as a candidate. Another tester descends from a third Ferverda son, which eliminates that son as well.

Michael, my actual first cousin with a 755 cM match at one vendor, and 822 cM at a second vendor, is shown by the MyHeritage cM Explainer with an 88% probability that he is my first cousin.

However, when I’m trying to identify the maternal grandfather, which is half of that couple, I need to focus one generation further back in time to eliminate other candidates.

The second and third closest matches are both Donald at 395 cM and Cheryl at 467 cM who also share the same Ferverda/Miller lineage and are the children of my maternal grandfather’s brother.

On the spreadsheet, I need to look at the trees of people who have both Ferverda and Miller, which brought me to both Cheryl and Donald, then Michael, which allowed me to identify John Ferverda, unquestionably, as my grandfather based on the cM match amounts.

Cheryl and Donald, who are confirmed full siblings, and my mother either have to be first cousins, or half siblings. Their match with mother is NOT in the half-sibling range for one sibling, and on the lower edge with the other. Mother also matches Michael as a nephew, not more distantly as she would if he were a first cousin once removed (1C1R) instead of a nephew.

Evaluating these matches combined confirms that my maternal grandfather is indeed John Ferverda.

What About X DNA?

The X chromosome has a unique inheritance path which is sometimes helpful in this circumstance, especially to males.

Women inherit an X chromosome from both parents, but males inherit an X chromosome from ONLY their mother. A male inherits a Y chromosome from his father which is what makes him male. Women inherit two X chromosomes, one from each parent, and no Y, which is what makes them female.

Therefore, if you are a male and are struggling with which side of your tree matches are associated with, the X chromosome may be of help.

Your mother passed her X chromosome to you, which could be:

  • Her entire maternal X, meaning your maternal grandmother’s X chromosome
  • Her entire paternal X, meaning your maternal grandfather’s X chromosome (which descends from his mother)
  • Some combination of your maternal grandmother and maternal grandfather’s chromosomes

One thing we know positively is that a male’s X matches are ALWAYS from their maternal side only, so that should help when dividing a male’s matches maternally or paternally. Note – be aware of potential pedigree collapse, endogamy and identical-by-chance matches if it looks like a male has a X match on his father’s side.

Unfortunately, the X chromosome cannot assist females in the same way, because females inherit an X from both parents. Therefore, they can match people in the same was as a male, but also in additional ways.

  • Females will match their paternal grandmother on her entire X chromosome, and will match one or both of their maternal grandparents on the X chromosome.
  • Females will NEVER match their paternal grandfather’s X chromosome because their father did not inherit an X chromosome from his father.
  • Males will match one or both of their maternal grandparents on their X chromosome.
  • Males will NEVER match their paternal grandparents, because males do not receive an X chromosome from their father.

The usefulness of X DNA matching depends on the inheritance path of both the tester AND their match.

When Can Y-DNA or Mitochondrial DNA Help with Grandparent Identification?

If you recall, I selected the maternal grandfather as the person to seek because no tester carries either the Y-DNA or mitochondrial DNA of their maternal grandfather. In other words, this was the most difficult identification, meaning that any of the other three grandparents would be, or at least could be, easier with the benefit of Y-DNA and/or mitochondrial DNA testing.

In addition to matching, both Y-DNA and mitochondrial DNA will provide testers with location origins, both continental and often much more specific locations based on where other testers and matches are from.

Y-DNA often provides a surname.

Let’s see how these tests, matches and results can assist us.

  • Paternal grandfather – If I was a male descended from John Ferverda paternally, I could have tested both my autosomal DNA PLUS my Y-DNA, which would have immediately revealed the Ferverda surname via Y-DNA. Two Ferverda men are shown in the Ferverda surname DNA project, above.

That revelation would have confirmed the Ferverda surname when combined with the high frequency of Ferverda found among autosomal matches on the spreadsheet.

  • Maternal grandmother – If we were searching for a maternal grandmother, both the male and female sibling testers (as shown in the pedigree chart) would have her mitochondrial DNA which could provide matches to relevant descendants. Mitochondrial DNA at both FamilyTreeDNA and 23andMe could also eliminate anyone who does not match on a common haplogroup, when comparing 23andMe results to 23andMe results, and FamilyTreeDNA to FamilyTreeDNA results at the same level.

At 23andMe, only base level haplogroups are provided, but they are enough to rule out a direct matrilineal line ancestor.

At FamilyTreeDNA, the earlier HVR1 and HVR2 tests provide base level haplogroups, while full sequence testing provides granular, specific haplogroups. Full sequence is the recommended testing level.

  • Paternal grandmother – If we were searching for a paternal grandmother, testers would, of course, need either their father to test his mitochondrial DNA, or for one of his siblings to test which could be used in the same way as described for maternal grandmother matching.

Summary

Successfully identifying a grandparent is dependent on many factors. Before you make that identification, it’s very difficult to know which are more or less important.

For example, if the grandparent is from a part of the world with few testers, you will have far fewer matches, potentially, than other lines from more highly tested regions. In my case, two of my four grandparents’ families, including Ferverda, immigrated in the 1850s, so they had fewer matches than families that have been producing large families in the US for generations.

Endogamy may be a factor.

Family size in past and current generations may be a factor.

Simple luck may be a factor.

Therefore, it’s always wise to test your DNA, and that of your parents and close relatives if possible, and upload to all of the autosomal databases. Then construct an analysis plan based on:

  • How you descend from the grandparent in question, meaning do you carry their X DNA, Y-DNA or mitochondrial DNA.
  • Who else is available to test their autosomal DNA to assist with shared matches and the process of elimination.
  • Who else is available to test for Y-DNA and/or mitochondrial DNA of the ancestor in question.

If you don’t find the answer initially, schedule a revisit of your matches periodically and update your spreadsheet. Sometimes DNA and genealogy is a waiting same.

Just remember, luck always favors the prepared!

Resources

You may find the following resource articles beneficial in addition to the links provided throughout this article.

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cM Explainer™ – New MyHeritage Relationship Prediction Tool

At RootsTech, MyHeritage introduced cM Explainer, a new tool for all of their DNA customers that utilizes both the total matching cMs (centimorgans) plus the ages of the people involved, if provided by the customers, to estimate the relationship possibilities between two matches.

According to the MyHeritage blog article, here:

DNA Matches are characterized by the amount of DNA shared between two individuals, measured using a unit of genetic distance called centimorgans (cM). cM Explainer™ is unique in the way it uses both the centimorgan value as well as the ages of the two individuals (if known) to fine-tune its predictions, making MyHeritage the only major genealogy company to offer relationship prediction at this level of granularity and accuracy.

cM Explainer™ is fully integrated into the MyHeritage platform to shed light on any DNA Match found on MyHeritage, and is also available as a free standalone tool to benefit individuals who have tested with other DNA services.

Using cM Explainer

cM Explainer is automatically implemented for all MyHeritage DNA customers, so there’s nothing to do except utilize the tool in conjunction with the additional DNA tools already provided by MyHeritage.

Just click on DNA Matches if you’re a DNA customer, or under DNA Tools if you want to use the cM Explainer standalone tool.

Let’s look at my matches.

As you can see, two of my matches have provided their ages which appear in their match information.

The new cM Explainer probable relationship is listed as well. In Charlene’s case, she’s predicted to be a half first cousin, and Cheryl is predicted to be either a half first cousin, or a parent’s 1st cousin, which is another way of saying first cousin once removed.

Recall that “once removed” means one side of the descendant tree is one generation longer than the other. Cheryl and my Mom are first cousins (1C) and Cheryl and I are first cousins once removed (1C1R) or, said another way, I’m Cheryl’s first cousin’s daughter.

Probable Relationships

Some matches receive two listed “Probable Relationships,” but everyone can view additional estimates.

Click on the purple “Review DNA Match” button to view detail information.

My match’s segment information is provided, in addition to the possible relationships, in order of most probable first. To see additional information, click on the “show more relationships” link.

Charlene has a total of 5 possible relationships listed, each with its own probability calculated. One of my matches has a total of 8 possible relationships displayed.

Next, you’ll see the diagram of possible relationships.

Don’t forget to click on the “Relationships” dropdown in the upper right corner of the diagram.

You can click on Full relationships, Half relationships, or All Relationships.

I clicked on “all” which displays everything together.

Clicking the “Show probabilities for MRCA” box in the upper left-hand corner adds the probability that you and your match descend from a specific generation, or MRCA (most recent common ancestor.)

The highest or best probable relationship for cousin Charlene is calculated as 51.8% half first cousin.

The other possibilities are less likely. The second most likely is “Parent’s first cousin,” at 24.3%.

Charlene is my first cousin once removed (1C1R,) at the bottom. Stated another way, Charlene is my first cousin’s child, calculated at 4.5%, which should be genetically equivalent to a half first cousin at 51.8%. As you can see in the chart above, there’s VERY large probability difference between those two, which may be because of the expected comparative ages of the people in those positions involved.

Let’s take a minute to look at how half and “removed” relationships work genetically.

Half and “Removed” Relationships

In this example, John was married twice, to Mary and Sue. John had son Jim with Mary, and both daughters, Anna and Bonnie, with Sue. Their descendants took DNA tests.

In this chart, you can see that half-relationships of any kind carry half the average expected shared DNA as the full version of the same relationship. The yellow people, descendants of John and Mary, are half relationships to the green people because John was married to both Mary and Sue, having children with both wives.

The green people descend from full siblings, Anna and Bonnie, the children of Sue.

In the first generation, Jim and Anna are half siblings and share about 25% of their DNA. Anna and Bonnie are full siblings and share about 50% of their DNA. By extension, of course, Jim and Bonnie are half siblings too, sharing approximately 25% of their DNA, but not the exact same DNA as Jim and Anna share.

In the next generation, Jordan and Andrew are half first cousins and share about 6.25% of their DNA, while Andrew and Brad are full first cousins and share about 12.5% of their DNA.

Below the second cousin level, some cousins won’t match each other, but that doesn’t mean they aren’t cousins. It only means they didn’t happen to inherit a common segment of DNA from their common ancestors.

At the fourth-generation level, Jeremy and Abraham are half third cousins and share less than 1% or about 26.56 cM of their DNA, while Abraham and Betty are full third cousins and share about 53.13 cM of their DNA.

That half division of DNA occurred several generations earlier because Jim and Anna are half siblings which means that they only share half as much DNA as full siblings Anna and Bonnie. Of course, each subsequent generation will be a half relationship, and share roughly half as much as the full equivalent of that same relationship.

Once Removed

However, when the generations are offset by one, or once removed (1R,) the DNA is halved again. Looking at the chart again, half third cousins (3C,) Jeremy and Abraham share about 0.39% or about 25.56 cM of their DNA. Abraham and Beverly, who are 3C1R (third cousins once removed) are ALSO expected to share about 25.56 cM, the same amount of their DNA. In this comparison, the halving occurs in the last generation by the generational offset, when comparing Abraham with Beverly.

Of course, Jeremy and Beverly share the smallest percentage of all, because they are Half third cousins once removed, so they would be expected to share only about 13.28 cM of their DNA, assuming they share any at all.

I wrote about the various percentages expected of each relationship level and compiled a comprehensive chart in this article.

Of course, MyHeritage has included the factor of age to attempt to refine the relationship more succinctly.

How Accurate is cM Explainer?

I created a chart of my closest matches who are known, proven relatives.

Results where My Heritage has provided exact, accurate predictions are shown in red.

My first thought when I saw this new tool was that all of the people with whom I shared a Theory of Family Relativity (TOFR), especially relationships I had confirmed (or at least not rejected) would be predicted in cM Explainer to be that same relationship. Well, I was wrong.

Of the 8 matches with whom I have an accurate TOFR, the relationships of 4, or 50%, are correct, but the other 4 are not, so clearly, MyHeritage is not relying on TOFRs for cM Explainer, at least not solely, if at all.

Person Total cM # Segments Actual Relationship TOFR MyHeritage cM Explainer
Michael 822.8 31 1C Y 1C
Alberta 744.2 25 Half niece *1 (2nd on list) Y 1C
Dana 521.8 17 Half 1C1R (not on list) N 1st C dau, half 1C
Charlene 477.5 24 1C1R *2 (4th on list) N Half 1C
Cheryl 477.2 23 Parent’s 1C (2nd on list) N Half 1C, parent’s 1C
David 460.4 17 2C (3rd on list) N Half 1C
Buster 409.9 16 1C1R *3 N Parent’s 1C
Donald 381.7 17 1C1R (3rd on list) N 2C
Kurt 378.9 16 Half great-nephew (not on list) N 2C
Teresa 330.4 13 Half great-nephew (not on list) Y 2C
Shirley 223.3 8 2C1R (2nd on list) Y 2C
Sydney 217.8 10 Half great-nephew (not on list) N 2C dau, 1C dau
Buzz 212.7 9 2C Y 2C
Amos 182.7 8 1C2R (8th on list) N 2C son
Denny 166.9 6 3C (2nd on list) N 2C
Thomas 156.4 7 2C Y 2C
Patty 150.6 9 2C Y 2C
Cathy 102.9 5 3C Y 3C
Carol 87 7 2C1R (2nd on list) N 3C

*1 – Half aunt/uncle is equivalent to half niece/nephew – it’s simply a matter of perspective.

*2 – 1C1R (first cousin once removed) is the same relationship as a first cousin’s child, just said differently.

*3 – Your parent’s first cousin in your first cousin once removed (1C1R.)

In the Actual Relationship column, I’ve indicated the actual relationship, then if the actual relationship is shown on the chart of possibilities provided by MyHeritage, and if so, at which position.

For example, I’ve listed Alberta’s “Actual Relationship” as my half-niece. Additionally, there’s a comment at *1 below the chart. MyHeritage predicted Alberta as my first cousin, but the correct half-niece designation is shown second on the list.

In this case, I’m fairly sure I know exactly why the relationship miscalculation occurred. Alberta’s mother, my half-sister, was born to my father’s first wife. My mother was 22 years younger than my father, so my mother is roughly the same age as my half-sister. I am the same age as my half-sister’s oldest children. Therefore, we have an unusual generational difference where ages might be misleading.

In the second position, MyHeritage estimated Alberta as half-aunt, which is the same as half niece, depending on whose perspective you’re speaking from, so cM Explainer was close. In normal circumstances, 1st Cousin is probably the most likely relationship although having children separated by two decades certainly is not unheard of.

MyHeritage correctly predicted 6 of 19 relationships, for 31.6% accuracy.

The correct relationship was on the relationship list most of the time, but was omitted entirely 4 times. The common factor in the entirely missing relationships is that they are all half-relationships. While they were not all from the same family line, they did all involve long generations, meaning children born over a very long period. That’s not uncommon with half-siblings, and half relationships are notoriously difficult to sort from other candidate relationships. These situations might possibly be considered statistical outliers.

Equivalent Relationships

A half first cousin should be genetically equivalent to a first cousin, once removed, based on the amount of expected DNA for those relationships.

However, in at least one case, these two relationships are calculated with different resulting probabilities. Half first cousin is 41.5%, and 1st cousins child (aka 1C1R or 1st cousin once removed) is 43.8%.

Keep in mind, though that MyHeritage is using the age of the two individuals in their calculations, which could alter the results based on the combination of factors calculated into the probabilities. It’s 85% likely that the match is one of those two relationships.

Your Thoughts?

I’m interested in your thoughts on this new tool. How does it work for you? What about endogamy or pedigree collapse? Do you find it useful? How are you utilizing it in your research?

Shortly, I’ll do a comparison article with other tools to see how the publicly available cM Explainer tool stacks up against the rest.

Thanks to MyHeritage for making this tool free for all to use, here.

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RootsTech 2023 – Truly United

Finally, finally, we were on our way, winging our way across the world from near and far – flying and motoring into snowy Salt Lake City for RootsTech. It seemed like we had been preparing forever, and Murphy visited many of us as gremlins trying to keep us away – but we persevered, and Murphy’s ploy just didn’t work.

Grab a cup of your favorite beverage, because you’re going to RootsTech with me!

I started out very early in dense fog which was a precursor to a nightmare at the airport. We didn’t know that yet, and the sun emerged beautifully as we were on our way.

Utah was blanketed with snow a few days before our arrival. We were hoping for no more snow.

The snow cover made for stunningly beautiful photos from the air.

The Kennecott Copper Mine outside Salt Lake City is three miles wide, nearly a mile deep and looked very interesting and beautiful laced with snow. These terraces are actually roughly 500 miles of dirt road. This used to be a mountain that was 8400 feet in elevation.

During the flight, I read about my ancestor, Stephen Hopkins and couldn’t help but think about how shocked he would have been that I flew across the country some 413 years after he was shipwrecked in Bermuda on the way to Jamestown, eventually lived in Jamestown for 4 years, sailed back to England, remarried, then arrived on the Mayflower in Plymouth Colony.

His ships and mine were very, very different.

FamilySearch Library

Some of us arrived early for research or meetings, or both.

FamilySearch took the opportunity presented during the Covid shutdown to remodel and upgrade the facilities significantly. The new library is both beautiful and super-functional.

The workstations now have three monitors.

There’s a lovely new break room with vending machines, tables, and a fridge.

To put things in perspective, the break room is larger than the preserved pioneer cabin that stands beside the library.

I’m struck by the contrast of the small cabin standing beside the FamilySearch library at left, and museum at right, and just a block away from skyscrapers.

Rather than leave and waste valuable research time, we had a picnic lunch in the break room.

I went to Salt Lake City early to visit the FamilySearch Library and attempt to break down a brick wall. I think I might have done that. We will see.

Other researchers did the same thing, and you can view a special GenFriends episode, here, hosted by Cheryl Hudson Passey, where several of us shared our excitement about our research, discoveries and simply gathering together again.

I was very excited to meet my cousin, Audrey Hill, for the first time in person, at the library. We’ve been collaborating for several months on our John Hill (1737-1805) and Catherine Mitchell (1738-1827) line. She’s already following up on a lead I never did (my bad.) Go Audrey!!

I spent two days perusing book after book after book in the Virginia and Maryland counties where my Dobkins and Johnson ancestors were known to have lived, then moved to the historically adjacent counties.

I was incredibly discouraged, but on the evening of the second day, back at my hotel again, I reviewed all of the library resources and noticed that I had missed one book that was shelved elsewhere.

Glory be, I *think* I’ve found him and his family.

My Peter Johnson line’s Y-DNA matches the Jochimsson (Yocum) line, so I have a LOT of work to do. But now at least I know where to dig!

I needed this entire book, not just a few pages.

Fortunately for me, Jim volunteered to scan the entire book at one of the new book-scanning stations.

I’m SOOO excited.

RootsTech and the FamilySearch library ran golf carts back and forth between the facilities throughout the conference.

Decisions, decisions.

Well, if you can’t decide, just go to the chocolate shop to think things over😊

The Night Before

Preconference events began on Wednesday evening with the media dinner which allows us to understand the layout, when to be someplace, and where that place might be. It also allows provides accurate information to pass on to you.

Of course, many of us have known each other for years. As the first event of RootsTech, after three years of being apart, it felt like one huge family reunion with everyone catching up. So many hugs!!!

And selfies.

It was wonderful to see Marie Cappart again. I’ll never forget walking down the street in Amsterdam with two friends and hearing someone shouting my name from some distance away. I turned around and there was Marie, running toward me, arms outstretched. What are the chances??

The influencers and media were treated to a tour of the show floor after setup was supposed to be complete.

Finishing touches were being put on the Expo Hall and booths. I guess I never realized how large these booths are and that they actually have to be “constructed”.

The next morning, the show would open and thousands of excited genealogists would descend on the Salt Palace for the next three days.

RootsTech Opens

Finally, the Salt Palace, with its legendary signs outside, was ready to receive genealogy guests.

Everyone was so happy to see each other again. My friends, Janna Helstein, Schelly Taladay Dardashti and Daniel Horowitz with MyHeritage photobombing the group. This was the best of several photos because we were all joyfully laughing so hard.

The absolute best part of RootsTech 2023 was seeing people again, in person. Zoom and similar platforms have been sanity-saving for the past three years – but they aren’t people.

Humans are, I think, wired for connection to each other.

I’ve worked “home office” for decades now, but not without regular contact with others.

The classes were great and there was a lot that was wonderful at RootsTech – but hands down, the best part was hugging so many people.

In case you aren’t aware, genealogists are huggers.

If someone were to have followed me around taking photos, there would have been hundreds of hugs. And I don’t mean polite greeting distant hugs. I mean the “OMG I haven’t seen you in a lifetime and everyone was concerned we might never see each other again” holding tight, never-letting-go hugs.

Mags Gaulden and I spotted each other in front of the WikiTree booth, and some kind soul took our picture. I tried to do a nice thing for her and made DNA masks, not remembering that she was allergic to my cat assistants. Thank goodness Mags realized it quickly enough to remove the masks before they had the opposite of the intended effect. I really do not want to be listed in her obituary! “Cause of death: Roberta’s masks.”

Tears streamed down people’s faces as they saw each other, especially that first day. And I don’t mean because of cat hair, either.

There were thousands of selfies joyfully taken. Lots of “blooper” ones too, but just the giddiness of being together again was intoxicating and overshadowed the challenges of the past few years. For a minute, or a few, everyone could just forget about everything else and enjoy our three-day adrenaline high.

And of course, sometimes things change, and many people weren’t there, for a variety of reasons. I missed so many people and there was more than one moment of silence.

Attendance

Here’s the RootsTech Expo Hall from the second floor. It felt like “coming home” after a long absence.

I was standing inside when the doors opened on the first day. People were waiting, but not the mob like past years.

In a Zoom call with RootsTech staff a week or ten days before the conference, they said they had 6000 paid admissions at that time, and a week or so later, they said they were anticipating the same number of attendees as 2020 which was about three times that number.

That number was clearly aspirational, but it didn’t happen.

I’ve been attending RootsTech since 2018, and the actual in-person attendance, based on observation, was lower than it has been since I’ve been attending. Of course, while we may be getting used to Covid, it’s not over and still a significant concern to many. I had my doubts.

Now that I’ve said that about attendance, let me expand. There were over a million registered online for the virtual sessions PLUS the livestreamed sessions that were held in person as well. I don’t know how many more than a million attended, but that number will only grow because those sessions remain available for viewing after RootsTech. In other words, Rootstech sessions have become a library which you can find and enjoy, here.

Clearly, more people in total were reached in 2023 than in 2020.

Questions for Attendees

This year, I had three in-person classes, and no virtual classes. All three were well-attended.

I don’t know how many people attended my sessions, but I know I took about 2000 DNAeXplain ribbons that were passed out to attendees at the exit doors of my classes if they wanted them for their RootsTech badges. I brought home maybe 100.

After everything is set up for the session (thank you Jim,) I always chat with the people in my sessions that show up early. There’s no reason not to have a little fun for everyone.

My first session was at 9:30 the first day, right after the conference opened at 9. I was passing out ribbons personally to people who were early and I saw the confused looks. So I demonstrated what to do with the ribbons with my own badge.

Ribbons on badges are a RootsTech staple, and it’s the only conference I’ve ever attended with that tradition. I realized, based on the confused looks, that we had several first-time attendees.

I was so excited to welcome people at the beginning of my first session, back to in-person genealogy, and that feeling was palpable throughout the room and the conference as a whole.

How Many First-Time Attendees?

When my session started, I asked how many people were attending RootsTech for the first time, and I was very surprised to discover that roughly half the room raised their hands.

Half!!!

That’s HUGE. No wonder there were so many confused looks about the ribbons.

My three sessions, in order, were:

  • DNA for Native American Genealogy: 10 Ways to Find Your Native American Ancestors
  • DNA Journey – Follow Your Ancestors Path
  • Big Y for the Win

I mention this because of the next questions I asked.

Who Has Taken a DNA Test for Genealogy?

In the first session, “DNA for Native American Genealogy,” I asked who had taken a DNA test, and more than half raised their hands, but several had not. Frankly, that surprised me given how long DNA testing has been available now. I talked to people afterwards, and the common thread for those who had not seemed to be:

  • They didn’t know which vendor or which DNA test to take for this purpose.
  • They thought the ancestor was too far back in time and they would not have any Native results. In my session, I talked about testing the older generations and your cousins. Also, that you don’t know what you don’t know. I asked how many people would purchase a book if they thought the answer to that question even MIGHT be inside, and every single person raised their hand.

I also pointed people to the Native section on my blog, to my book, DNA for Native American Genealogy, and to my second blog focused entirely on early Native American records, www.nativeheritageproject.com.

In the second class, “DNA Journey – Follow Your Ancestor’s Path,” probably three fourths of the class had taken a DNA test. That session was really fun. I used several case studies to illustrate how different kinds of DNA have broken down brick walls AND showed me exactly, and I mean literally exactly where my ancestors were from. I used Y-DNA, mitochondrial DNA and autosomal to accomplish this. Who among you DOESN’T want to stand where your ancestors stood?

Yep, we all do.

I think it was in the second class that I asked a question about how many people had taken the three different types of tests, and here’s the breakdown:

  • Who has taken a DNA test? – The majority of the room
  • Who has taken an autosomal test – It looked to be the same number of people as above
  • Who has taken (or sponsored) a Y-DNA test – Maybe 10% of the room
  • Who has taken a mitochondrial DNA test – A scattering of people

As genealogists, we need to do more Y-DNA and mitochondrial DNA testing, because we don’t know what we don’t know and may well be missing.

In the third class, “Big Y for the Win,” which included both Y-DNA STR testing and the Big Y-700, comparing and contrasting the tests, how to use them, and why the Big Y provides significant advantages, most of the people had taken some type of DNA test.

The second question I asked in the Big Y class was how many people had taken or sponsored a Big Y test, and significantly more than half had, which is what I would have expected.

However, given the session topic, I was surprised to learn that few had used the new, free, Discover Tools, or the recently released Group Time Tree. Both were developed and created by FamilyTreeDNA to maximize the usefulness of Y-DNA haplogroups, and they are amazing.

How Many People Have Tested?

As part of the information that I gathered during the conference, Ancestry has tested 23 million people and MyHeritage 6.5 million. I don’t have a current number for FamilyTreeDNA or 23andMe, but the last numbers I heard some months ago were 2 and 5 million, respectively.

There are clearly more (and new) people who are interested in genealogy and are still DNA testing candidates – especially Y-DNA and mitochondrial DNA which have separate inheritance paths, providing additional and unique benefits as compared to autosomal tests.

Keynotes

The keynote sessions were livestreamed, so you can still view them here. Be sure to watch Steve Rockwood’s welcome. He may be the CEO, but he’s an exceptionally caring, inspirational and humble, man.

I attended two of three keynote sessions. Each keynote session actually included three speakers, which was initially confusing.

Steve Rockwood’s message is that “All Means All” – everyone is included. He also thanked and encouraged people to not be further divisive during this difficult time, and instead to choose inclusion.

Steve asked several questions and in answer to his queries, attendees were encouraged to hold up their phones with their flashlight on. As you can see, the entire huge room is filled with light – our light. One at a time. We can all be the light. You can hear Steve’s message for yourself, here.

Another session I enjoyed immensely was Jordin Sparks, the youngest ever American Idol winner. I’ve been in concert venues that were smaller, so it was a real treat to enjoy this inspirational story plus four of her amazing songs.

I really encourage you to watch this video, especially if you love music. Even Jordin’s guitarist was wiping his eyes!

She literally played to a packed house and I don’t think there was a dry eye anyplace.

Jordin has an incredible voice and an inspirational story. Do yourself a favor and listen, here.

MyHeritage Keynote and Announcements

Aaron Godfrey, VP of Marketing with MyHeritage announced new products and initiatives during the keynote on day 2.

The new Photo Dater app, available soon, will estimate when a photo was taken based on clothes, hairstyles and other items in the photo.

Additionally, Aaron announced the cM Explainer, a wonderful new tool which predicts relationship estimates between DNA matches and includes the ages of the testers, among other factors. cM Explainer is incorporated into your DNA matches at MyHeritage in addition to being independently available for free, here.

I’ll be reviewing this new feature in an article, soon.

In another surprise, Aaron announced that MyHeritage has donated another 5000 kits to DNA Quest, for adoptees, here.

MyHeritage also introduced color coding for family trees, here. If you’re a MyHeritage user, this feature is already available for you on your tree, so check it out.

MyHeritage takes the “most new announcements at RootsTech” award with these new features.

Vendor Booth Sessions

Truth be told, I didn’t even get to visit all of the various booths. I meant to, but it just didn’t happen.

At least two vendors offered sessions throughout all three days. There were probably others, but between my three RootsTech sessions, three booth sessions and the book signing, in addition to keynotes, meetings and interviews, I just wasn’t able to attend many booth sessions.

The ones I did attend were wonderful. I focused on DNA, of course. Let’s start with FamilyTreeDNA.

Sherman McRae presented “Unexpected Y-DNA Results” in the FamilyTreeDNA booth where he’s showing how to utilize the Y-DNA Time Tree in the Discover tool, and the Group Time Tree.

You can view Sherman’s main session, Connect the Forefathers, here.

You just never know when a pilgrim is going to show up for your session.

Janine Cloud, an enrolled Cherokee tribal member and manager of Group Projects at FamilyTreeDNA discussed Y-DNA, mitochondrial and autosomal avenues to prove Native ancestors using DNA, using her own Cherokee ancestors as an example.

Dr Paul Maier, Population Geneticist, Goran Runfeldt, Head of Research and Michael Sager, Phylogeneticist answer questions about Y-DNA in the AMA (Ask Me Anything) session.

Paul and Goran also hosted an AMA for mitochondrial DNA as well, an often overlooked but valuable resource.

In addition to the Native American AMA session for FamilyTreeDNA which I gave with Janine, I gave two booth presentations for MyHeritage, “Time Travel with Your Ancestors” and “AutoClusters for the Win,” both of which were recorded meaning you  just might see them in the future.

The Time Travel session utilized the MyHeritage AI tools to see what my ancestors who came from specific regions or cultures might have looked like in that time and place. In the slide above the AI photo of my grandmother is combined with the document and with the Genetic Group that incorporates that part of Germany.

I combined the AI images with MyHeritage records that link those ancestors to a specific location, showing the predicted ethnicity, genetic groups when applicable, and then the actual location – some of which I’ve visited. My ancestor owned that windmill in the Netherlands, above. Combining these tools is so much FUN. My heritage provided the AI photos, records and ethnicity. I’m the one who did the traveling, of course, but in this way, time travel is possible!

I really enjoyed using this story-telling methodology that incorporates all 4 types of genealogy research and clues.

In the AutoClusters for the Win session in the MyHeritage booth, I discussed how I utilized AutoClusters to solve an adoption case in my own family, and how you can use this very powerful tool as well. The methodology I used works equally as well for genealogy mysteries.

In another MyHeritage booth presentation, Janna Helshtein told an amazing and moving story about her grandparents, their escape from the Holocaust, move to Israel, and more – in their own “voices” using MyHeritage’s Deep Story.

We all sat spellbound.

Janna also offers a free guide on how she created and integrated the Deep Story verbiage that her grandparents “spoke.” It was actually quite easy.

There was more to Janna’s story, but I don’t want to spoil it for you.

I believe MyHeritage intends to make their booth sessions available through social media.

Here, Janna and I are celebrating with a quick picnic style lunch after her presentation. She truly knocked it out of the park.

Shifting Attendance

I’m sharing my opinion here, and not anything a RootsTech spokesperson told me.

I was surprised that the in-person attendance was down as much as it was, truthfully. I think in-person was down by either half or maybe even two-thirds. Some decline wouldn’t have surprised me, but this much was sobering.

I was also VERY surprised that roughly half of the attendees were new. And that number could have actually been higher. That’s a good thing, meaning new people are being attracted to genealogy.

These two things, together, suggest the following to me:

  • The passing of time, Covid, and aging-out of some people caused some decline. I know several people who passed away during the past three years, not to mention those whose lives changed dramatically due to their partner’s illness, passing or life circumstances. Several people lost jobs or moved, or both, or are in that process now.
  • Now let’s flip this and say that the virtual and FREE capability for much of RootsTech made the conference accessible and available to many who could not attend in person. For that, I’m very grateful. I have a friend who has been very ill and participated by taking selfies of herself with the livestreamed sessions on her monitor behind her. She posted her photos on social media to be with us. That warmed my heart so much.
  • I think that the reason there were so many new people was because they were able to attend virtually during 2021 and 2022. Essentially this means that while virtual RootsTech was challenging for everyone on the behind-the-scenes production side, to put it mildly, it served to recruit many new genealogists who would not have participated in person had they not previously attended online.

Based on discussions at the media dinner table, and other statements by Steve Rockwood, CEO of FamilySearch, FamilySearch, including RootsTech, is reaching out to young people and to other areas of the world as well.

According to Steve, who, by the way, turns out to be my 11th cousin according to Relatives at RootsTech and the FamilySearch Tree, RootsTech will forever be a blended conference event.

This year, in addition to the local emcee, there were 15 people in other countries hosting in their locations, times and in their native languages.

This year there were 304 virtual classes, 205 in person, and some of those were streamed online as well.

Don’t forget that Relatives at RootsTech is still available through March 31st and you can contact cousins to collaborate. Some may represent Y-DNA or mitochondrial DNA testing lines that you need for matching and to complete your tree.

Vendors

That brings me to the topic of vendors.

Three of the four major DNA vendors were present, meaning Ancestry, FamilyTreeDNA and MyHeritage. 23andMe was absent in 2020 and again this year. Their last DNA innovation was their genetic tree in September of 2019.

Many of the smaller vendors were not in attendance. I had made friends with several of the Mom and Pop vendors and almost none of them were there this year, nor were many of the organizations and smaller companies. I spoke with several people and they said, almost universally, that the cost of the virtual booths over the past two years, the work involved, and the fact that those virtual booths did not generate many sales, not even equal to the amount of the booth rent, had soured the experience.

Not only are conference booths very expensive, so is the invested labor and time. For those of you who don’t know, booth rent is only a part of it. You want carpet? That’s more. A chair? That’s more. Two chairs? More. A trash basket? More. Oh, you need wireless to handle sales? LOTS more.

I’d say that the Expo Hall was only half to one third of the size it had been previously. Mind you, it’s still huge, especially compared to many other conferences, but I missed seeing many of my favorite vendors.

For example, neither Genealogical.com nor Deseret Books were there this year, so there was no bookstore, and neither were many of the fun t-shirt vendors or others that sold jewelry or genealogy-related merchandise.

I hope that FamilySearch will put their creative caps on and perhaps reach out to their vendors, both past and current, and figure out a way to make RootsTech vendors attractive to the online crowd. Perhaps a “search” game where you have to visit vendor booths to find items. Maybe there could be some permanent online stores as well.

There were fewer food vendors too, but in case anyone was wondering, I could still smell cinnamon-almonds throughout the facility😊

I did run into some of my long-time vendor friends.

My friend Jessica Taylor with Legacy Tree Genealogists. I regularly refer people seeking genealogists who understand both genealogy and DNA to Legacy Tree Genealogists.

I don’t need to tell you how much I love DNAPainter and it was great to see Jonny Perl and Patricia Coleman in the DNAPainter booth.

I feel kind of bad because I obviously caught Rob Warthen and Carol Carman by surprise in the East Coast Genetic Genealogy Conference booth, but it’s the only photo I have of their booth.

Last fall’s ECGGC conference was very successful and I’m planning to speak in person this year, in Baltimore, October 6-8, 2023. Save the date. Last year was the first year and it was wonderful.

My Book Signing

FamilyTreeDNA was kind enough to host my book signing for DNA for Native American Genealogy in conjunction with the Native American Ask Me Anything session. Many thanks to Joe Brickey for her help with this event as well.

After the AMA session, which was the final event of Saturday, just before closing, we took a group picture with the FamilyTreeDNA team, or at least the staff members in the booth at that time.

I did learn that perhaps the last thing Saturday might not be the best time for a book signing, because lots of people leave on Friday night. On the other hand, on Saturday, admission to the conference is free, at least to the show floor, with lots of children’s activities and programs for LDS families. Saturday is always very busy in terms of traffic, with sometimes more Saturday visitors than paying conference attendees. It will be interesting to see final RootsTech conference numbers.

The Thank You That Made My Day!!!

One lovely lady, Charis, came up to me after my first session and explained that she saw an ad for RootsTech. She decided she needed to purchase a ticket and attend. She had never heard of me, but she is very focused on documenting her Native ancestry. She sat in the front row in my first session and paid rapt attention. (Speakers do notice, in case you wondered.)

Charis came up to me afterwards and told me that this class alone was worth her registration fee.

She made my day, but I thought to myself that she would attend other sessions that she would find equally as valuable. After all, the conference was just beginning. She found me the next day and repeated what she had said. On day 3, she attended the Ask Me Anything session, arriving early. She said the said the same thing, AGAIN, and I asked if we could take a picture together. As presenters, we take our time, spend our money to attend these conferences, and invest the effort because we want to help people.

People like Charis make this all worthwhile.

Sweetness Personified

I’m sorry, I just can’t resist sharing the sweetest picture series ever.

In 2020, I met my cousin, Heidi Campbell and her baby at RootsTech. Three years later, I saw Heidi again, with a beautiful new addition to the family.

I just can’t tell you how wonderful it was to hold this baby. The last baby I held was Heidi’s little one, three years ago. The look on Heidi’s face is priceless too when he’s reaching for my glasses. He had the biggest smile EVER on his face and he’s booping noses with me. We had so much fun.

My heart just melted into a huge puddle. I so much wish they lived close so I could “grandma.” Thank you, Heidi, for sharing your sunshine with me.

Rolling Up the Sidewalks

On Saturday, literally at one minute after 3 when the conference closed, the workers at the Salt Palace started rolling up the sidewalks, or in this case, the carpets.

It’s a wrap!!!

Afterglow

At the Salt Lake City airport, I ran into two people and had the opportunity to talk to them again and hug goodbye once more. You’d think we would all have had enough of genealogy, but not a chance. More hugs, gratitude for togetherness, and anticipation for next year.

Winging my way home again, having walked about 6 miles each day, according to Fitbit, I was tired, desperately tired, and my everything hurt. However, I was also incredibly fulfilled to have connected again with old friends and met so many new people that I now look forward to seeing again. We are very fortunate to be members of such a wonderful, diverse and universal community.

I couldn’t help but think, as we crossed the winding Mississippi River, how fortunate we are that we have “time travel” in this way. I’m also struck with how many different ways we have to time travel, with Y-DNA and mitochondrial DNA at FamilyTreeDNA, autosomal testing and ethnicity at various vendors, and actual historical records that are becoming ever-more available remotely.

Using artificial intelligence, we can “see” our ancestor’s heritage in our own faces, or, in this case, the face of my grandfather using the MyHeritage AI Time Machine.

Using our DNA, we can identify the parts of those ancestors that we carry today, reaching back in time several generations with autosomal DNA. In addition to autosomal, both Y-DNA and mitochondrial DNA provide close matches and reach back in time, focused on one specific line, providing insights for millennia.

Time travel, truly reimagined.

There are so many ways to discover and connect with our ancestors available to us today. If we don’t carry the DNA of ancestors a few generations upstream, perhaps selected cousins do. We have several tools and databases at our disposal to find testers.

The DNA of our ancestors can and does actually lead us home, to them and, sometimes, exactly where they lived, as I illustrated with several case studies in my presentation, “Follow Your Ancestors Path.” Today, these options are available to everyone.

RootsTech is in the history books for another year, with new friendships made and old ones renewed. Indeed, we were finally reunited with each other, and introduced to cousins we had never met before. We shared tools, methodologies and information to identify our ancestors. We all left fervently hoping to be reunited again next year.

Please enjoy the amazing RootsTech musical finale here.

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Sneak Preview: Introducing the FamilyTreeDNA Group Time Tree

Drum roll please!!!

This is a sneak peek of a new tool being rolled out by FamilyTreeDNA in a VERY EARLY BETA soft launch.

Right now, the only way to view the Group Time Tree is by using the link to my group project, below, then, search for a different project name. I’ll show you, but first, let’s talk about this VERY COOL new tool for Big Y group project results.

The Group Time Tree is a feature that group project administrators and project members have wanted for a VERY long time!

At FamilyTreeDNA, the words “group” and “project” are both used to describe Group Projects which are projects run by volunteer administrators. FamilyTreeDNA customers can join any number of projects to collaborate with other testers who have a common interest.

Four basic types of public group projects exist:

  • Surname Group Projects
  • Haplogroup Group Project
  • Geographic Group Projects which can include other types of special interests
  • Mitochondrial Lineage Group Projects

What Does the Regular Discover Time Tree Do?

The Discover tool that was recently introduced (here) provides a Time Tree view of any specific haplogroup (but no surnames or ancestors) in relation to:

  • Big Y testers (not SNP-only testers and not STR results because they can’t be used for time-to-most-recent-common-ancestor (TMRCA) calculations)
  • Ancient Connections
  • Notable Connections

Using the regular Discover Haplogroup took, here’s an example of the haplogroups of the Estes (and other) men, beginning with the R-BY154784 lineage near the bottom. Time is at the top. The only way you know they are Estes men is because I told you. The Discover tool is haplogroup specific, not surname specific.

What Does the New Group Time Tree Do?

The brand-new Group Time Tree is an extension of the Discover technology, but focused within projects and includes both surnames and earliest known ancestors for people who have opted-in to have their results display in public group projects. This tool only works for group projects that have the public display enabled, and includes only data that the administrator has included. Not all administrators have enabled the display of the “Paternal Ancestor” field, for example.

Now, you can see Big Y group project members:

  • All mapped together on a genetic time tree, or
  • By project subgroups defined by the project administrator

I want to provide a friendly reminder that this is a BETA tool and will be fully rolled out in the not-too-distant future. In the meantime, it’s fun to have a sneak preview!!!

Estes DNA Group Project

Before going further, here are some screen shots of the Estes DNA Group Project for comparison.

I’ve created multiple color-coded groups within the project based on the genealogy and Y-DNA matches of the participants. The teal groups all descend from the Estes line from Kent, England, and match each other. Since not every man with an Estes surname descends from this line, there are also other color-identified groups.

Additionally, in the Estes project, I do not restrict members to males with the Estes surname, so there are several non-Estes men who have joined. Their Y-DNA shows in the project so I have placed them in an “Autosomal – Not Y DNA” group because they are Estes-related autosomally, not through the direct Y-DNA surname line.

I’ve grouped other clusters of Estes-surname males who do not descend from the Kent line into other color-coded groups, which turned out to be extremely beneficial for the new Group Time Tree.

Let’s see how the Estes Project works with the new Group Time Tree.

The Estes Group Time Tree

Here’s the link to the Estes Group Time Tree. I’ll be using the Estes data for this article, then show you how to view other group projects of your choosing from this link. So please read these instructions.

The Group Time Tree shows a genetic family tree of direct paternal lineages on a time scale. It shows how Big Y tested members of Group Projects are related to each other and when their shared ancestors are estimated to have lived.

Click on any image to enlarge

This is the first display I see.

Looking around, I notice the menu.

Select either “All search results” or the group or groups you want to view.

If you compare the groups above on the menu to the project screen shots, you’ll notice that the colors along the left side equate to the colors of the project subgroupings. We have Eastridge, meaning those who are not genetically Estes, then “Estes Autosomal, Not Y DNA,” then a group of teal project groupings who descend from the Estes Kent line.

I clicked on “Select All Search Results” which displayed everyone in the project from all haplogroups. This resulted in the Estes men being scrunched on the right-hand side, below, due to the long timeframe involved, which is not useful.

What is VERY useful is the Paternal Ancestor column which is the earliest known ancestor (EKA) for each tester’s line. Hopefully, this will encourage everyone to enter their EKA and location. You can find instructions, here.

Ok, let’s “De-select all” and just focus on specific groups.

Much better. I can see a much more relevant timeline for the men in the line being researched. The Estes men are no longer scrunched up along the right side because the left-to-right time is much shorter – 1500ish vs 100,000ish years.

The colored dot on the location flag indicates which colored group these men have been assigned to by the project administrator.

It’s very easy to see if two groups (or two men) descend from the same paternal line.

Next, I added the Eastridge group back into the display as an experiment.

The common ancestor between the single Eastridge Big Y tester and the Estes men is back in the Stone Age, about 35,000 BCE.

I do feel compelled to mention that this information can’t necessarily be extrapolated for all Eastridge men, because there are a few men with Eastridge surnames that are actually genetically Estes men. Someplace along the line, the name got changed. This is the perfect example of why every man needs to test their Y-DNA.

You can remove the menu by clicking on Subgroups.

You make the menu re-appear by clicking on Subgroups again.

I LOVE – LOVE – LOVE that I can see the ancestors and the clusters and I didn’t have to do this grouping myself. These men could have been in one big group in the project and the software would have created the clusters for me.

For example, there has been debate for decades about whether or not Moses Estes of South Carolina was descended from Abraham Estes, the immigrant, and if so, through which son.

Based on the Big Y-700 test (the Big Y-500 did not reveal this) and clustering, we know assuredly that Moses Estes of SC:

  • Descended from the Kent line
  • Descended from Abraham who has mutation R-BY490
  • Did NOT descend from Abraham’s son Moses whose descendants have mutation R-ZS3700

I’ve been keeping this project spreadsheet for years now. It’s wonderful to be able to see a genetic tree visualization. The Big Y men are blocked in red.

I’m hopeful that the balance of the men who have NOT yet taken the Big Y-700 will upgrade now because there’s so much more to learn. This is especially true for men who reach a brick wall prior to Abraham. The Big Y-700 test, perhaps combined with STRs, will place them in a lineage.

I’m sure that we would discover new haplogroups among Abraham’s descendants if they would all upgrade. There are more men who have not tested at the Big Y level than those that have.

Display Options

Under display options, you can add Ancient or Notable connections, remove confidence bars, and adjust the tree height.

Discoveries for Administrators

As a project administrator, one thing I discovered is that I might want to regroup within some of my projects to take full advantage of the color coding on the Group Time Tree. If you are a project administrator, you may want to ponder the same.

I also discovered that when I clicked on Country Map, I did not have Project Statistics enabled.

If you make project configuration changes, this report will only be updated weekly, so it’s not immediate.

The country map shows the distribution of all the countries within the project, not specific groups within projects

You can view Country Maps in either map or table format, but remember that if the project is a surname project and includes autosomal testers, the map view will not be representative of the surname itself. This view shows all groups.

Viewing Another Group Project

To view a different group project, simply enter that project name in the search box. For now, this is how you’ll be able to view group projects until this tool is fully rolled out.

I entered the surname “Speak” and was presented with these options.

Obviously, the surname Speak or a variation is found in these projects. Just click to view.

Your Turn

If you have not yet taken or upgraded to the Big Y-700 test, now’s the time. Order or upgrade, here.

If you have already taken the Big Y-700 test, or want to view a project, click on this link, and search for your project of choice.

Have fun!!!

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The Best of 2022

It’s that time of year where we look both backward and forward.

Thank you for your continued readership! Another year under our belts!

I always find it interesting to review the articles you found most interesting this past year.

In total, I published 97 articles in 2022, of which 56 were directly instructional about genetic genealogy. I say “directly instructional,” because, as you know, the 52 Ancestors series of articles are instructional too, but told through the lives of my ancestors. That leaves 41 articles that were either 52 Ancestors articles, or general in nature.

It has been quite a year.

2022 Highlights

In a way, writing these articles serves as a journal for the genetic genealogy community. I never realized that until I began scanning titles a year at a time.

Highlights of 2022 include:

Which articles were your favorites that were published in 2022, and why?

Your Favorites

Often, the topics I select for articles are directly related to your comments, questions and suggestions, especially if I haven’t covered the topic previously, or it needs to be featured again. Things change in this industry, often. That’s a good thing!

However, some articles become forever favorites. Current articles don’t have enough time to amass the number of views accumulated over years for articles published earlier, so recently published articles are often NOT found in the all-time favorites list.

Based on views, what are my readers’ favorites and what do they find most useful?

In the chart below, the 2022 ranking is not just the ranking of articles published in 2022, but the ranking of all articles based on 2022 views alone. Not surprisingly, six of the 15 favorite 2022 articles were published in 2022.

The All-Time Ranking is the ranking for those 2022 favorites IF they fell within the top 15 in the forever ranking, over the entire decade+ that this blog has existed.

Drum roll please!!!

Article Title Publication Date 2022 Ranking All-Time Ranking
Concepts – Calculating Ethnicity Percentages January 2017 1 2
Proving Native American Ancestry Using DNA December 2012 2 1
Ancestral DNA Percentages – How Much of Them in in You? June 2017 3 5
AutoKinship at GEDmatch by Genetic Affairs February 2022 4
442 Ancient Viking Skeletons Hold DNA Surprises – Does Your Y or Mitochondrial DNA Match? Daily Updates Here September 2020 5
The Origins of Zana of Abkhazia July 2021 6
Full or Half Siblings April 2019 7 15
Ancestry Rearranged the Furniture January 2022 8
DNA from 459 Ancient British Isles Burials Reveals Relationships – Does Yours Match? February 2022 9
DNA Inherited from Grandparents and Great-Grandparents January 2020 10
Ancestry Only Shows Shared Matches of 20 cM and Greater – What That Means & Why It Matters May 2022 11
How Much Indian Do I Have in Me??? June 2015 12 8
Top Ten RootsTech 2022 DNA Sessions + All DNA Session Links March 2022 13
FamilyTreeDNA DISCOVER Launches – Including Y DNA Haplogroup Ages June 2022 14
Ancient Ireland’s Y and Mitochondrial DNA – Do You Match??? November 2020 15

2023 Suggestions

I have a few articles already in the works for 2023, including some surprises. I’ll unveil one very soon.

We will be starting out with:

  • Information about RootsTech where I’ll be giving at least 7 presentations, in person, and probably doing a book signing too. Yes, I know, 7 sessions – what was I thinking? I’ve just missed everyone so very much.
  • An article about how accurately Ancestry’s ThruLines predicts Potential Ancestors and a few ways to prove, or disprove, accuracy.
  • The continuation of the “In Search Of” series.

As always, I’m open for 2023 suggestions.

In the comments, let me know what topics you’d like to see.

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Concepts: Your Matches on the Same Segment are NOT Necessarily Related to Each Other

Just because two (or more) people match you on the same segment does NOT mean they are related to each other.

This is a fundamental concept of DNA matching and of using a chromosome browser.

I want to make this concept crystal clear.

This past week, I’ve had two people contact me with the same question that’s based up on a critical misunderstanding, or maybe just lack of understanding.

It’s not intuitive – in fact, it’s counter-intuitive. I understand why they don’t understand.

It seems logical that if two or more people show up as a match to you on the chromosome browser, on the same segment, you’ve hit a home run and all you need to do is to identify their common ancestor who will also be your common ancestor, or at least related. Right?

NOT SO FAST!

Let’s walk through this, step-by-step. Once you “get it,” you’ll never forget it, and you can use this to help other people understand too. Please notice there are lots of links here to other articles I’ve written if you need refreshers or help with terms.

Yay! – I’ve Got Matches

OK, so you’ve just discovered that you have a close match with three people, on the same segment. You’re thrilled! Maybe you’re trying to identify your grandparent, so first or second cousin matches are VERY exciting for you.

They are also close enough matches with large enough segments that you don’t need to worry about false positive matches, meaning identical by chance.

Let’s take a look. I’m using FamilyTreeDNA because that’s where the majority of my family has tested, plus they have a nice chromosome browser and their unique matrix tool.

We have three nice-sized matches to people estimated to be my first or second cousins. I’ve selected all three and compared them in the chromosome browser. The large red match is 87 cM and the blue and teal matches are 39 cM each, and completely within the 87 cM segment, so completely overlapping.

I’ve hit the mother-lode, right?

All I need to do is identify THEIR common ancestor and I’ll surely find mine.

Right???

Nope

Just because they all three match ME on this same segment does NOT mean they all match each other and are from the same side of my family. All three people DO NOT NECESSARILY have the same ancestor. From this information alone, we cannot tell.

I know this seems counterintuitive, especially since you’re seeing them all on MY chromosomes – which are the background pallet.

However, remember that I have two chromosomes. One from my father and one from my mother.

These matches are ALWAYS FROM THE PERSPECTIVE OF THE TESTER.

So, I’m going to see matches in exactly the same location – matches on my mother’s chromosome and matches on my father’s chromosomes – painted on the same segment locations of my chromosome.

Let’s prove that in the simplest of ways.

Mom and Dad

This is my kit, compared with my Dad and Mom.

I only took a screen shot of my first several chromosomes, but you can see that I match both of my parents on the full length of each chromosome – on the same exact segments.

I am the background – the pallet upon which my matches are painted.

First, my father is painted, then my mother – their match to me displayed on my chromosomes.

I assure you, my father and mother are NOT related to each other. I’ll prove it.

I could simply select one parent, then look for the other parent on the shared matches list.

Or, I could use the Matrix tool, especially if I wanted to see if a group of people are related to me and also to each other.

The Matrix

The Matrix tool is available under “See More,” in the Autosomal DNA Results & Tools section.

The Matrix allows you to select 10 or fewer matches to see if they are matches to each other. We already know they are matches to you.

I added my parents into the matrix.

My parents do not match each other, meaning they are not genetically related, because their intersecting cell is not blue.

Next, let’s select those three other people I match and see if they match each other.

Yes indeed, we can see that Cheryl and Donald match each other, but Amos matches NEITHER Cheryl nor Don. Yet, the segments of Cheryl and Donald, who had the 39 cM blue and teal segments on the chromosome browser fall entirely within Amos’s 87 cM segment.

Therefore, if Cheryl and Donald do not match Amos, that means that Cheryl and Donald are from one side of my family, and Amos is from the other. This is absolutely true in this instance because we are comparing the exact same segment on my DNA, so everyone has to match me maternally or paternally, or by chance (IBC.) The segment size alone removes the possibility of IBC.

Each parent gave me one copy of chromosome 4, so everyone who matches me on chromosome 4 must match one or the other parent on that chromosome segment.

I’ve added my parents back into the comparison, at the bottom, with the three matches on chromosome 4. Now you can see that same segment again, and everyone matches me, parents included, of course.

There’s no way to tell the difference whether the blue, red and teal match is on my mother’s or father’s side without additional information.

Again, let’s prove it.

Everybody, Let’s Dance

I added my Mom and Dad back into the matrix.

You can see that Mom and Cheryl and Donald all match each other, plus me of course, by inference because these are my matches.

You can see that Amos and my Dad match each other, and me of course, but not the other people.

Settled

So, we’ve settled that, right.

In my case, I could provide this great example, because I do in fact have parental tests to use for comparison.

You can see when I remove my Dad and Amos that Cheryl and Donald and my Mom all match each other. If I were to remove my Mom, Cheryl and Donald would match each other.

If I remove Mom, Donald and Cheryl, Dad and Amos match each other.

Of course, you may not have either of your parents’ DNA to use as an anchor for matching. You may, in fact, be searching for a parent or close relative.

If you do have “anchor people,” by all means, use them. In fact, upload or create a tree, link your anchor people and as many others as possible to their profiles in your tree at FamilyTreeDNA so your matches will be automatically bucketed, meaning assigned maternally or paternally. FamilyTreeDNA is the only company that offers linking and triangulated bucketing.

But, if you’re searching for your parents or know nothing about your family, you won’t have an anchor point, so what’s next?

What’s Next?

Using a combination of matching, shared matches and the matrix, you can create your own grouping of matches.

My suggestion is to start with your 10 closest matches.

Pull all 10 into the matrix.

Remember, you will match these people across your chromosomes. The only question the matrix answers is “do my matches match each other,” and a “yes” doesn’t’ necessarily mean they match each other on the same line you match either or both of them on.

I’ve noted how each person is related to me.

You can see that there’s a large block of matches on my paternal side. Some are labeled “Father- both.” These people are related both maternally and paternally to my father, because either the families intermarried, or they are descendants of my paternal grandparents.

Three, Donald, Dennis and Cheryl are related on my mother’s side, but it’s worth noting that Dennis doesn’t match Cheryl or Donald. That doesn’t mean he’s not on my mother’s side, it simply means he descends through her maternal line, not the paternal line like Donald and Cheryl. Remember, we’re not comparing people who match on the same chromosome this time – we’re comparing my closest matches across all chromosomes, so it makes sense that my mother’s maternal matches won’t match her paternal matches, but they would both match Mom if she were in the matrix. Clearly they all match me or they would not be in my match list in the first place.

You could also run a Genetic Affairs AutoCluster or AutoTree to cluster your matches for you into groups, although you can’t select specifically which individuals to include, except by upper and lower thresholds.

Regardless of the method you select, you still need to do the homework to figure out the common ancestors, but it’s a lot easier knowing who also match each other.

Circling Back to the Beginning

Now, when you see those two or three or more people all matching you on the same segment on the chromosome browser, you KNOW that you can’t immediately assume they match you and therefore are all related to each other. It’s possible, and even probable that some of them will match you because they match your mother’s chromosome and some will match your father’s chromosome – so they are from different sides of your family.

The Matrix tool shows you, for groups of 10 or less, who also matches each other.

What you are doing by determining if multiple people share common segments and match each other is triangulation. I wrote about triangulation at each company in the articles below:

Unfortunately, Ancestry does not provide a chromosome browser, so triangulation is not possible, but Ancestry does provide shared matching with some caveats. However, some Ancestry customers do upload their DNA file to FamilyTreeDNA, MyHeritage or GEDmatch. You can find step-by-step download/upload instructions for all vendors, here.

Additional Resources

You’ve probably noticed there are lots of links in this article to other articles that I’ve written. You might want to go back and take a look at those if you’re in the process of educating yourself or need help wrapping your head around the “same segment address – two parents – your matches are not created equal” phenomenon.

Here are a couple of additional articles that will help you understand matching on both parents’ sides, and how to get the most out of matching, segments, triangulation and chromosome browsers.

I prepared a triangulation resource summary article, here:

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

Thank you so much.

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Connect Your DNA Test, and Others, to Your Tree

To optimize your DNA tests, each tester needs to take advantage of the features offered by each vendor.

In order to do that, we need to perform the following tasks.

  1. Upload or create a tree (except at 23andMe who does not support trees)
  2. Connect our own test to our own profile card on our tree
  3. Connect other tests we manage to their (or our) tree, depending on the vendor
  4. Connect matches who are known relatives to their profiles on our tree

Each vendor handles these situations differently, so we’ll look at each one of the vendors with step-by-step instructions for handling those situations. We all want to get the most out of the tests we’ve taken!

Plant a Tree

If you have not created or uploaded a tree at each one of the vendors (except 23andMe who does not support genealogy trees), please do so. However, 23andMe does provide for links to your tree elsewhere, so we will review that function.

I manage my “master tree” on my own computer, but I also maintain trees at both Ancestry and MyHeritage where I attach documents and research found at that vendor. I also update my ancestors at WikiTree to be sure other researchers benefit from new discoveries.

I have not uploaded my full tree from my computer anyplace because I have many private notes that are not appropriate for disclosure, not to mention speculative and unproven relationships. I created a pared-down tree at one time to upload to both Ancestry and MyHeritage, and build those trees out from there.

I’m often asked about replacing your tree at the various vendors with an updated tree. If you do that, be aware that you will lose your DNA connections and document links. I do NOT recommend that. I simply maintain multiple trees. I wrote about this in the article, “Genealogy Tree Replacement – Should I or Shouldn’t I?” If you are considering that option, PLEASE read that article first.

RootsMagic, Family Tree Maker, and Legacy Family Tree Software all provide a syncing option with various vendors and FamilySearch, although not every vendor allows access to each of those software companies. I probably should experiment with the syncing option, but given a family member’s terrible experience some years back, I’ve been unwilling to do that. My biggest fear is that I will corrupt the file and not notice it until it’s far too late to revert to a backup.

When you upload or create a tree, make sure deceased and living people are marked as such, and you’ve opted to share your tree. If you don’t, you accidentally have a private tree. Worse yet, you might not realize it. I wrote about that in Quick Tip: Trees, Death Dates and Unintentionally Private Ancestors.

Now, let’s take a look at each vendor.

23andMe

23andMe does not support traditional genealogy trees, but they do provide a location for you to link your tree at another vendor or source.

Under your name at the right side, you’ll see “View Your Profile” under the dropdown.

I’ve not been able to find a generic Ancestry tree link that will allow non-Ancestry subscribers to view my tree, but it’s easy to do at MyHeritage. Simply open your tree at  MyHeritage and just copy the link at the top. Don’t worry, people won’t see anyone living.

If you want to use “one world” types of trees, you can also link to other trees such as FamilySearch or WikiTree, but just remember that you don’t control that content.

You don’t need to connect yourself to your tree at 23andMe, because there is no genealogy tree. However, 23andMe constructs a “genetic tree” for you using your closest matches, based on how you match other people, and how they match each other.

You can view your tree under “Family and Friends,” then “Family Tree.”

I added my ancestors’ names so it’s easy to keep straight. You can do that by simply clicking on the colored circle representing the ancestor, starting with your parents.

If you know that one of your matching relatives is not in exactly the correct tree location, you can click on their circle, and then click on Edit to make modifications.

You may want to add a relative that you can identify but who isn’t connected on the tree that 23andMe constructed.

Looking on the far-right side of the tree, in the lower corner, you’ll see “Add a Relative.” Click there and follow the instructions.

Ancestry

At Ancestry, you need to link your test to “you” in a tree. Your test can only be linked to one person in one tree at a time. You can change this, but you will lose any ThruLines you currently have. They will be regenerated based on the new tree you connect your test to, but based on the tree and other factors, they may not be the same. My recommendation is if you’re going to disconnect yourself and reconnect yourself elsewhere, record everything first.

Alternatively, you can take a second DNA test and simply link that second test to another tree. IMHO, that’s a better alternative. You can leave one in place as your research tree and use the second test to experiment with.

To link your test to your tree, select the “DNA” tab. At far right, you’ll see “Settings.”

You need to tell Ancestry who you are in your tree. Click on “Settings,” then scroll to “Tree Link.”

You can also link other tests you directly manage to their placards in your tree as well.

These links allow Ancestry to form ThruLines using both DNA matches and common ancestors in trees for 7 generations.

On your DNA Match page, Ancestry will ask you if you recognize a match.

If you click on “Yes,” you’ll be asked which side the match is on.

Then you’ll be given a long list of possible relationships in most-likely to least-likely order. Literally, Erik is the last option offered.

Select and confirm.

I’m not positive exactly HOW this helps Ancestry help you, but I suspect it confirms and helps Ancestry perfect ThruLines, relationship predictions, and perhaps even “sides” of ethnicity.

I wrote about Optimizing Your Tree at Ancestry for More Hints and DNA ThruLines.

FamilyTreeDNA

At FamilyTreeDNA, every DNA test kit has its own kit number and associated tree, so you don’t need to tell FamilyTreeDNA who you are if you create a tree from scratch on their site.

FamilyTreeDNA offers a unique family matching feature that sorts your matches into maternal and paternal sides.

In order to take advantage of this, you will need a tree. You can upload a GEDCOM file, although the upload at FamilyTreeDNA does not seem to do well with very large files.

If you don’t have a GEDCOM file on your computer, you can download a tree from either Ancestry or MyHeritage and upload to FamilyTreeDNA.

I wrote about this in the article Download Your Ancestry Tree and Upload it Elsewhere for Added Benefit.

If you upload a tree, you’ll be asked to select the person in the tree that is “you,” meaning the person who tested their DNA.

You’ll want to link known matches to your tree to enable Family Matching, aka bucketing, so that FamilyTreeDNA can divide and assign your matches maternally and paternally.

If you are building your tree at FamilyTreeDNA from scratch, simply click to begin and complete the information on the placards to add your information, then your parents, building out from there. You’ll want to add the ancestral lines to connect with your closest matches on your match list.

Family matching, or bucketing, is enabled by linking known matches to their proper place on your tree. FamilyTreeDNA then evaluates each match, determining if they match a common segment with you and someone you’ve linked. If that match does share a segment with both of you, meaning they triangulate, then that person is assigned either maternally, paternally, or both. I wrote about Triangulation in Action at FamilyTreeDNA, here.

The best people to link are your parents and grandparents, of course, but that’s not always an option. You’ll want to link as many matches as you can.

To link people, either click on the Family Tree tab at the top of the page, or on the “Link on Family Tree” under Relationship Range for individual matches.

Simply click on “Link Matches,” then drag and drop your match to their placard.

Here’s an example of linking parents.

Once someone is linked, the green dot will appear signifying that they are linked, and which type of test. Green is a Family Finder autosomal test, blue means they’ve taken a Y DNA test, and pink is a mitochondrial DNA test.

If your parents aren’t available to test, link every upstream relative that you can identify. By this, I mean that your children and full siblings will match you on both sides, so aren’t helpful for parental-side assignment.

People who have DNA tests from both parents can expect around 80% of their matches to be assigned maternally, paternally, or both.

If you have relatives who have tested at other vendors, you can ask them to upload to FamilyTreeDNA for free matching.

MyHeritage

At MyHeritage, you will connect yourself and any relatives whose tests you manage to your tree.

Under “DNA,” select “Manage DNA kits.”

At the right, you’ll click on the three dots, also known as a hamburger menu (who knew.)

Select Assign (if this is a new test or a transfer) or Re-assign a kit.

Be sure to do this for every kit you manage. I made that mistake and wrote about how I discovered and fixed the problem, here. Kit assignment enables Theories of Family Relativity and other super-helpful features.

I wrote about several things you can do to optimize your chances of receiving Theories of Family Relativity, here.

You can upload DNA kits to MyHeritage from tests taken at other vendors, here.

Fish in All the Ponds

I have provided step-by-step download/upload instructors for all vendors, here. It’s important to fish in all available ponds by making sure you have DNA tests at all four vendors. Then, upload or create trees and complete this bit of housekeeping to increase your chances of catching fish!

_____________________________________________________________

Follow DNAexplain on Facebook, here or follow me on Twitter, here.

Share the Love!

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

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

You Can Help Keep This Blog Free

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

Thank you so much.

DNA Purchases and Free Uploads

Genealogy Products and Services

My Book

Genealogy Books

Genealogy Research