FOCUS: Step 2 – Finding the Y-DNA and Mitochondrial DNA of Your Ancestors

This is the third article in our FOCUS series, providing step-by-step instructions for identifying brick-walled ancestors.

These two articles detail the initial steps:

By now, you will have selected the ancestor you want to focus on identifying, and you have tools in your toolkit for working with DNA matches who have no trees.

You may have ordered DNA tests from multiple vendors and are waiting on results, so while you wait, we’ll start with finding the Y-DNA and mitochondrial DNA of your ancestors and identifying DNA testing candidates.

While it may sound counterintuitive, we’re going to be working with all of the major vendors, including FamilyTreeDNA, who actually tests for Y-DNA and mitochondrial DNA, plus WikiTree, 23andMe, MyHeritage, Ancestry, GEDmatch and FamilySearch. They are all quite useful in different ways.

This Type of Searching Is Different

Normally, when we search for brick-walled ancestors, we are searching backward in time. In other words, we begin with the last person we know and work back from there, hoping to identify the previous generation.

If we don’t know Lucy’s birth surname and she was born about 1750, and married William Moore in the late 1770s, we begin with what we do know in that timeframe.

Searching for our ancestor’s Y-DNA or mitochondrial DNA, and testers who carry that DNA, is fundamentally different because we begin with that ancestor and work forward in time.

In other words, if we want to find Lucy’s mitochondrial DNA, we begin with her daughters and track forward in time to the present. Hopefully, someone has already tested, and we can locate that result, but if not, we need to find people who descend through a specific path that carry Lucy’s mitochondrial DNA.

If we were searching for the Y-DNA of William Moore, we would look for his direct paternal descendant males who would carry the Moore surname.

Chicken or Egg?

I’ve been debating whether I should show you:

  1. How to locate and identify the Y-DNA and mitochondrial DNA of your ancestors first, or
  2. How to use Y-DNA and mitochondrial DNA (mtDNA) to help break through your brick wall first

I decided to write the “how to locate” article first because I don’t want you to skim over and ignore the ‘how to use’ article, thinking it’s irrelevant to your research because you don’t carry the Y-DNA and/or mtDNA of your brick-walled ancestor.

There are lots of avenues to locate the Y-DNA or mitochondrial DNA of your ancestors, something you definitely want to do. You’ll soon see that Y-DNA and mtDNA information can also assist with autosomal DNA results.

These are all pieces of your ancestor’s puzzle, and you never know which one will be the one to topple that wall.

Plus, you don’t know what you don’t know about that ancestor.

Let’s jump right in!

Who Carries the Y-DNA and Mitochondrial DNA of Your Ancestor?

As a quick refresher, only men can test for Y-DNA because only men have a Y chromosome which is inherited from their father. It’s passed in a direct paternal line from father to son, never mixed with DNA from the mother. Because it’s never divided during recombination like autosomal DNA, it’s uniquely useful for connecting lineages both recently and back in time hundreds and thousands of years.

Both Y-DNA and mitochondrial DNA incur occasional mutations that function as genetic breadcrumbs, making them incredibly useful for reassembling those specific family lines where genealogy paper trails have broken or been interrupted.

Mitochondrial DNA is passed from mothers to their children of both sexes, but only daughters pass it on. This means that in the current generation, males and females can both test for the mtDNA of their direct, mother-to-mother, matrilineal line.

Anyone, including males, who descends from an ancestor through all females can test for that ancestor’s mitochondrial DNA.

If you’re lucky, you’ll carry the Y-DNA or mitochondrial DNA of the ancestor you are seeking. If not, you’ll need to do one of two things:

  1. Determine if someone has already tested for that ancestor
  2. If not, find candidates to test

Y-DNA is generally easier because you at least (hopefully) have a surname to work with that has been passed from father to son, along with their Y chromosome.

Mitochondrial DNA is more challenging since surnames change each generation, so I’ve included several mitochondrial examples. Don’t skip over them, because the same research techniques apply to Y-DNA too, especially difficult cases.

If you’re a male, I strongly recommend that you order:

If you’re a female, you can only order the mtFull test, but you may be able to ask your father or brother or a male relative (with the surname in the lineage you seek) to take the Big Y-700 to represent your father’s family line. In other words, if you’re looking for a male Estes, you can ask your 2C Estes male who descends in a direct paternal line of all Estes men from your common ancestor.

Complete Versus Partial Tests

Haplogroup-only results derived from autosomal tests are fine as far as they go – but they don’t go very far. Most are what I would call midrange, providing testers with a haplogroup from maybe 2000 years ago, and some are much more distant than that. That isn’t to say they can’t be useful in a limited capacity, but Y-DNA and mtDNA have so much more potential.

You need comprehensive Y-DNA and mtDNA test results that identify all your haplogroup-defining mutations and can be refined as more people test and match family-level mutations.

Haplogroups are important, but you also need to match with other testers. Additionally, you’ll want the most complete haplogroup possible, because it will help you genealogically by providing a complete breadcrumb trail with the ability to identify your most recent common ancestor (MRCA).

FamilyTreeDNA is the only vendor that offers these complete tests that include matching with other testers, plus additional genealogy tools.

The Big Y-700 test scans for mutations in the stable portion of the Y chromosome and is the only way to obtain that personal-level information. It’s those recent mutations that will help place you within a biological family – or eliminate you from other lines, which prevents barking up the wrong tree.

The benefit of taking the test yourself, or sponsoring a test for someone willing to share their results with you, is that you have ready access to information through FamilyTreeDNA’s tools such as:

  • Matches with other Y-DNA and mtDNA testers
  • Matches Map (ancestor locations)
  • Advanced Matching, which provides a filtered list of people who match you on BOTH your Y-DNA or mitochondrial DNA AND your Family Finder autosomal test
  • Haplotype clusters (for mtDNA)
  • Your mutations
  • Block Tree (for Y-DNA)
  • Customized Discover tools

Click any image to enlarge

  • Discover’s Advanced Tools like the Match Time Tree, shown above, which displays your matches with their earliest known ancestors (EKA) together on the Time Tree
  • Globetrekker™ (for Y-DNA with mtDNA coming soon)
  • Up to 30 Ancient Connections
  • Up to 20 Notable Connections

FamilyTreeDNA’s free Discover tool, here, provides public information for everyone about haplogroups, but if you haven’t taken the test, you won’t receive matching and customized information described above, which is essential to genealogy.

Upgrades for Partial Tests

You may have previously tested at a lower level at FamilyTreeDNA.

For mtDNA, the early mtPlus test examined a portion of the mitochondria and provided matching at lower levels, as do the 12-111 marker Y-DNA tests. Both provide a predicted high-level basic or midrange haplogroup based on the mutation information available in those limited tests.

If you took an earlier, partial test, you can sign on to your account to upgrade by clicking on the “Big Y,” even though it’s greyed out. Grey simply indicates that you don’t currently have that level of test.

Click on “Full” to upgrade to the mtFull test.

Test Features at Various Levels

Depending on the type of test you take, and at which vendor, you may have a fully refined or partial haplogroup.

Discover provides a substantial amount of information if you receive a partial haplogroup:

A partial haplogroup is better than no haplogroup, but it’s also like working with one hand tied behind your back. If at all possible, you need to work with a full haplogroup and matches.

Testers who click through to Discover from their own test, or a test they manage, can view additional features not available in the free version.

The table below shows the four different ways you can access and view your ancestor’s haplogroup. Based on the testing level and/or how they tested, the haplogroup level will vary.

Clearly, the best scenario is when you either take the Big Y-700 or mtFull test yourself, or you have access to the test results of someone who takes that test to represent your ancestor’s DNA. Primary access confers the greatest amount of information, but you can still glean information in other ways.

Feature Introductory Level Test at FamilyTreeDNA* Tester’s Big Y-700 or mtFull Test – Full Access Partial Haplogroup from Autosomal Test Your Ancestor’s Haplogroup but without Full Access
Matching Yes, at that lower level Best – at all levels No No
Matches Map Yes, at lower level Yes No No
Mutation Values Yes, STR markers at lower Y-DNA level Yes, STRs (Y-DNA) and SNPs Not directly but through Discover Not directly but through Discover
Haplotree & SNPs with surnames (Y-DNA only) Yes, at lower level Yes No No
Block Tree (Big Y test only) No Yes No No

 

Advanced Matching (multiple types of tests) Yes, at that level Yes No No
Ability to Join Group Projects Yes Yes Only test owner or manager can join Only test owner or manager can join
Discover Reports Yes, same information as the free version due to lower coverage Yes, when clicking through from your FamilyTreeDNA account Free version Free version
Haplogroup Story Yes, at lower haplogroup level Yes – best and highest level Yes, at lower haplogroup level Yes, at lower haplogroup level
Country Frequency Map and Table views Yes, at lower haplogroup level Yes, at most refined haplogroup level Yes, at lower haplogroup level Yes, at most refined haplogroup level
Notable Connections Same as free version About 20 for Y-DNA, 11 for mtDNA About 10 for Y-DNA, 3 for mtDNA About 10 for Y-DNA, 3 for mtDNA
Migration Map Yes, at lower level Yes, at advanced level Yes, at lower level Yes, at advanced level
Globetrekker (Y-DNA only, mtDNA coming soon) No Yes No No
Ancient Connections Same as free version About 30 About 10 for Y-DNA, 3 for mtDNA About 10 for Y-DNA, 3 for mtDNA
Time Tree Yes, at lower haplogroup level – generally 2,000 years or older Yes, at most refined haplogroup level, often within genealogical timeframe Yes, at lower haplogroup level – generally 2,000 years or older Yes, at most refined level
Match Time Tree No Yes – your matches & their EKA on the Time Tree including WikiTree Connections and Ancient DNA No No
Ancestral Path Yes, at lower haplogroup level Yes Yes, at lower haplogroup level Yes
Suggested Projects Yes Yes, at more refined level Yes, but must test with FamilyTreeDNA to join Yes, but must test with FamilyTreeDNA to join
Scientific Details, ages and variants Yes, at lower level Yes Yes, at lower level Yes
Compare Haplogroups Yes Yes Yes Yes

*Note that often your ancestor’s haplogroup as reported by the Family Finder (autosomal) test is more refined, meaning closer in time, than the Y-DNA haplogroups predicted by STR tests, but both are always substantially less specific than the Big Y-700 test. As of the publication date of this article, Family Finder does not yet report a mitochondrial DNA haplogroup, but that is planned for the future.

This chart only includes features you would specifically use to identify an ancestor or ancestral lineage. There are other reports provided with your test that will be of interest. Discover provides about 14 reports that include various options.

Now we can envision:

  • The benefits of finding our ancestors’ Y-DNA and mtDNA
  • The benefits of obtaining the most refined haplogroup possible
  • The benefits of being able to view the results directly

You may not be able to achieve all of these, but even a partial haplogroup is better than no haplogroup at all, and a fully refined haplogroup, even if you can’t see everything in another tester’s account, is better than a partial haplogroup.

So, let’s see how to find your ancestors’ haplogroups. I collect them all, not just for brick-walled ancestors, but because they tell a part of our story not available through any other means.

Finding Your Ancestor’s Mitochondrial and Y-DNA

If you are the DNA tester for your brick-wall ancestor, then you’re golden, but chances are that you’re not.

If you’re searching for Y-DNA, and you don’t carry that Y-DNA yourself, you’ll need a male relative who carries that Y chromosome to test.

Males carry the Y-DNA of their direct patrilineal ancestors, shown in the image below on the left side in blue, plus the mitochondrial DNA (mtDNA) of their mother, shown with yellow hearts at far right.

At the 4th generation level, we have 4 Y-DNA lineages to collect (light blue, dark green, medium green, and teal), and a total of 8 mtDNA lineages.

Let’s say you’re searching for your father’s mother’s mother as your brick-wall ancestor.

Your father (and his siblings) carry the mtDNA of his mother, shown above in fuchsia, as do her grandchildren through her daughters. That’s why your father has a fuchsia heart. If close family members test, chances are you can arrange to manage their test or view their results. (Be sure they take the autosomal Family Finder test too. You’ll need that later.

If you don’t manage their test for them, you’ll need to ask to see their results to view matches and work with trees.

I have a family project at FamilyTreeDNA that I manage. I ask people who have tested for a particular ancestor to join that project so I can easily view their results while they continue to manage their test, and can select how much they want me to see or do.

FamilyTreeDNA is currently working on a multi-kit management feature that will address the challenge of sharing results.

But I Don’t Know of Any Cousins…

Let’s say you don’t know of and can’t readily identify anyone who descends from your ancestor appropriately.

If the ancestor you seek is a male, mitochondrial DNA is probably not going to help you because men don’t pass their mitochondrial DNA on to their descendants. In order to obtain a male ancestor’s mitochondrial DNA, you’d need to be able to identify a sister or someone known to descend from his mother (or sisters) through all females to the current generation. Needless to say, if you know who his mother is, you probably already know who he is.

If your brick wall is a female ancestor, your first order of business is to find someone who descends from her through all females to the current generation, where the tester can be male or female.

Why is this so important?

Mitochondrial DNA isn’t admixed with the father’s DNA, so it’s not divided in each generation. This means that mitochondrial DNA is the only direct line-of-sight we have that bypasses both changing surnames and genetic recombination for females.

Who Has Tested for Your Ancestor?

If you’re NOT the tester for your brick-walled ancestor or aren’t the curator of the test, your first step is to see if someone else has already tested.

This can sometimes be challenging.

It’s impossible to obtain mitochondrial DNA for an unknown ancestor if there are no known daughters, and for Y-DNA if there are no known sons. You may need to review genealogical resources to make sure you’ve identified all of that ancestor’s children.

Barring those scenarios, there are a surprising number of resources available to find descendants.

WikiTree

The first place I check to see if someone has already tested for a particular ancestor is WikiTree.

WikiTree is the one place where you find the ancestor along with the people who have taken DNA tests who descend from that ancestor. It’s invaluable.

Normally, you have to work with matches to identify your common ancestor. WikiTree works the other way around. Your starting place is with the ancestor.

You can’t Google your mystery ancestor’s name because if you knew their name, they wouldn’t be a mystery ancestor – but you can Google their spouse or a child.

I’m using an example from my own line because my mitochondrial DNA results are connected to her.

I’m Googling:

Barbara Mehlheimer born 1822 died 1906 in Indiana at WikiTree

Google was slightly confused but the results got me to where I needed to go.

Barbara Mehlheimer married George Drechsel and her daughter was Barbara Drechsel who married Jacob Kirsch.

First, check Barbara’s WikiTree profile card to confirm you’ve found the correct person.

Next, click on the DNA tab beneath her profile information (or just scroll down). She has four DNA Connections.

You can see that one person, me, who carries Barbara’s mitochondrial DNA has connected their DNA to Barbara’s profile. I did this by entering my DNA information on my WikiTree profile, then WikiTree connects my DNA haplogroup information from mother to mother to mother to Barbara and propagates my DNA haplogroup to her, her matrilineal ancestors, and their female descendants. If you click on the haplogroup, it takes you directly to that haplogroup in Discover.

Three people have connected their autosomal results to Barbara. This information can be very important, and not just for mitochondrial DNA. It allows us to identify autosomal testers we may match at different testing companies who descend from Barbara.

In your research journal, make notes of these names, testing companies, and kit numbers. Remember that this doesn’t mean the company noted is the only place someone has taken an autosomal DNA test. I’ve tested at all of the major companies, but only GEDmatch and FamilyTreeDNA are listed here.

For Y-DNA and mitochondrial DNA, the haplogroup is shown, although when testers receive a new Y-DNA or Mitotree haplogroup, they seldom think to revise it in WikiTree. This means their current haplogroup may be more specific and improved since the WikiTree information was entered.

Some people may have tested at different levels too. In this case, Buster Estes, who is now deceased, was one of the earliest testers, long before the Big Y tests were available. He only took a 25-marker test, so his haplogroup was predicted as R-M269. Garmon, on the other hand, was able to upgrade his Y-DNA test to the Big Y-700, and his haplogroup is much more refined at R-ZS3700. Their haplogroups don’t match exactly due to the levels at which they tested, but they also don’t preclude the two testers from belonging to the same genetic line.

This screenshot of Discover’s Compare function illustrates how important the Big Y-700 test is when compared to the STR test’s predicted haplogroups. The man who developed the mutation that defines R-ZS3700 lived about 1750 CE, and the man who developed R-M269 lived about 4450 BCE, or 6,450 years ago. That’s a big difference.

Using a combination of multiple testers and genealogy, we’ve identified the man who developed R-ZS3700 and passed it on to his sons. Moses Estes was born in 1711 in Virginia and all of his descendant testers carry R-ZS3700.

Now that’s extremely useful information, because we know that any man with haplogroup R-ZS3700 descends from Moses Estes in a direct paternal line, and any man whose haplogroup is not R-ZS3700 or doesn’t include R-ZS3700 upstream of his haplogroup does not descend from Moses Estes in that way.

Please add your DNA tests, including haplogroups and your kit number, to your profile at WikiTree so that the haplogroup information can be populated appropriately to your ancestors.

Searching for a Test Candidate Using Autosomal Descendants

When you’re searching for a testing candidate at WikiTree, you can click through to the tester’s profile and view exactly how they descend from the ancestor shown.

Let’s say that no one has linked a mitochondrial DNA test to the ancestor you’re searching for, but several people have linked autosomal tests to that ancestor’s profile card.

Click on the tester’s name and then on the DNA Ancestors tab to see how they descend from that ancestor. If you’re lucky, you’ll find someone in the autosomal list who is a mitochondrial DNA testing candidate.

If you’re looking for a Y-DNA tester, begin by looking for a male with the same surname as that ancestor. If you’re looking for a mitochondrial DNA tester, you’ll need to view each tester’s ancestors.

Regardless of whether they are a mitochondrial or Y-DNA testing candidate, you’ll identify your most recent common ancestor (MRCA) for each person, information that will become essential for the autosomal tools that we’ll be discussing in future articles.

In your research journal, I suggest that you record all of their descent information now, including their names, where they tested, your MRCA, kit numbers and any other relevant notes.

If you’d like to ask them to take a specific test, or if they already have and you’d like to know more, you can message WikiTree users by clicking on their profile, and then on the little envelope beside the profile manager’s name.

Finding Your Ancestor’s DNA Descendants at WikiTree

Let’s say that no one in the DNA list of people who have already taken tests descends from your ancestor matrilineally. Don’t worry, there are still more options!

At the top of the WikiTree page for that ancestor, click the down arrow, then on DNA.

The default tab shows the DNA Ancestors of the profile you’re viewing. You’ll see Y-DNA for males, and both mitochondrial and X-chromosome ancestors for everyone.

You may notice that there’s an ancestor listed for your brick wall ancestor. That’s wonderful, but don’t jump for joy quite yet. Remember, WikiTree is a one-world tree, and you need to verify the underlying genealogy in every tree here, and at every vendor.

Always confirm using multiple sources, meaning resources other than trees. The great thing about WikiTree is that there are often several sources listed in each person’s profile, and other resources that can help immensely. I love WikiTree, but I’m always skeptical of information in any tree, and I prove everything to my own satisfaction. I wrote several articles about that topic in the Genealogy Proof Series, here.

To find testers, you’ll need to view your ancestor’s DNA Descendants.

Click on the DNA Descendants tab.

The Mitochondrial DNA Descendants view shows potential candidates for mtDNA testing. Remember, in the current generation, males and females can both test so long as they descend from that ancestor through all females.

In the case of Barbara Mehlheimer Drechsel and her descendants, there are several males who are immediately eliminated because they’ve been deceased for more than a century, and several daughters who didn’t have children.

Not every person’s line on WikiTree has been added or developed. You can see that three daughters’ lines that might hold candidates don’t list all their children, and I still need to research two additional people. That means I still have five candidate lines to extend that have potential mtDNA testers.

So, in summary, if Barbara was the ancestor I was seeking:

  • One person has already tested
  • Three daughters don’t have their families extended.
  • Two have daughters that I need to research.

For both Y-DNA and mitochondrial DNA, I like to have at least two people who descend from different children of the ancestor, and whose tests match at a level that does not preclude that lineage. This helps confirm both the genetic line and the genealogy of both testers.

With male ancestors, having more than one tester for each line through different siblings is essential.

Kit Numbers, Earliest Known Ancestors and Google

When DNA kit numbers are included at WikiTree, you’ll want to Google to see if that kit number is shown in a public Group Project at FamilyTreeDNA where you may find more information.

The exact search string to use to find a specific kit at FamilyTreeDNA within projects is:

“9993” site:familytreedna.com

Replace 9993 with the kit number you’re interested in. You can also add the word “projects”, without quotes, to the end of that string to omit forums and limit the search to within projects. This string both focuses and limits the search, filtering out most noise.

By clicking on “read more,” you’re taken directly to the Estes Family Surname Project Y-DNA page.

The green haplogroups are SNP-confirmed, unlike the red predicted haplogroups from the lower-level 12, 25, 37, 67 or 111-marker tests. The R-ZS3700 haplogroup was obtained from the Big Y-700 test, so it is the most granular and specific. If this is your line, you’ve just found your ancestor’s haplogroup. It’s also possible that, by testing, you could receive an even more specific haplogroup.

Please note that haplogroup R-M269 is the most common haplogroup in Europe, and isn’t specific enough to use for anything other than very basic information. It can rule out two people with different base haplogroups, like haplogroup I or J, for example, as descending from a common patrilineal ancestor.

Project administrators are all volunteers, and each administrator groups their Group Project members differently, so take a few minutes to review the project pages. You may find additional testers who have joined this project who descend from your ancestors or your ancestral line.

You may also find other lines with the same surname and a substantially different haplogroup, which tells you that there are multiple genetic lines with the same surname. I have one example of this in the same county, at the same time, found in men by the same exact name – think John Smith. So frustrating. Without DNA testing, we would NEVER have sorted through those two same-name but completely different lines.

However, finding people who match your ancestor’s DNA but don’t have your earliest known ancestor (EKA) may be just the clue you need to knock down that brick wall. How are your ancestor and that other person’s EKA connected, and in what timeframe? Do they share a surname? A location? Are there other clues?

It’s unlikely that you’ll be able to use a kit number to Google unless you find one at WikiTree, but you can still search using the oldest name in that line that you know.

nicholas ewstas site:familytreedna.com

Replace the kit number with your EKA, in this case, “Nicholas Ewstas” in the search string, either with or without quotes. This takes you to the same page and any other projects that someone may have joined using exactly that earliest known ancestor’s name. Keep in mind that you’re only looking at their oldest ancestor, not every ancestor between them and their EKA. Your brick wall may lie someplace in there, which is why you need to check matches and view their trees.

Since women’s surnames change in every generation, they generally won’t be found in specific ancestral surname projects like men. This makes Googling using the ancestor’s name even more important.

catherine lejeune site:familytreedna.com

We don’t know who Catherine LeJeune’s mother is, so finding that someone has entered Catherine as their EKA may be critically important.

This is especially important for female brick-walled ancestors, since using this Google string with their daughters’ names may reveal someone else’s EKA in that genetic line within a project.

After clicking through to the project page, be sure to enlarge the page to display the full project, and use your browser search since partial results with predicted haplogroups may not be grouped with full mitochondrial sequence results.

Multiple people who descend from Catherine LeJeune have tested. The first six only took the partial test years ago. The bottom two testers took the full sequence test and have a new Mitotree haplogroup – U6a7a1a. We know that Catherine was born about 1633, in France, and we can see that other people have also tested and list different EKAs. Next, it’s time to research the other ancestors shown, or check WikiTree to see if any of these testers are listed there so you can contact them.

Now that you have found your ancestor’s haplogroup, you can use the free version of Discover to learn more. I wrote about using mitochondrial DNA and Discover in the article Mitochondrial DNA A-Z: A Step-by-Step Guide to Matches, Mitotree, and mtDNA Discover.

Now, let’s move to the DNA testing companies to see how we can find our ancestors’ Y-DNA, mitochondrial DNA, or testers, at 23andMe, FamilyTreeDNA, Ancestry, and MyHeritage.

At 23andMe

23andMe is not a genealogy company. That said, if you can figure out how people are related to you, you might be able to obtain a partial haplogroup for an ancestor. 23andMe shows both Y-DNA and mitochondrial DNA haplogroups to autosomal matches, but there is no Y-DNA or mitochondrial DNA matching, or associated tools.

23andMe caps matches without a subscription at only 1,500, and they don’t support trees, so I struggle to find useful haplogroups without an associated surname.

Browsing or searching your 1,500 allowed matches (you can have around 5,000 with a subscription) for a particular surname may provide you with an abbreviated haplogroup for both male and female ancestors.

Despite my best efforts, while my maternal grandfather’s mother is not unknown, nor are her ancestors for several generations reaching back into Germany, I’ve been unable to find her mitochondrial haplogroup. Evaline Miller (1857-1939) was born and died in Kosciusko County, Indiana, where she married Hiram Bauke Ferverda, an immigrant from the Netherlands.

Ferverda is an unusual surname, so let’s use it for our example. Thankfully, I’m not dealing with something like Smith.

I entered Ferverda in the 23andMe search bar and it shows four results, two of which are in the 2C-3C range, and one that’s further distant.

I already have the Ferverda Y-DNA, so I don’t need that, but I do need the mitochondrial DNA of Eva Miller Ferverda, and I really don’t want to sift through Miller surnames.

I know who Mr. Ferverda is on my match list, and which ancestor we share. His mitochondrial DNA is not Eva Miller’s.

Fortunately, I know who Eva’s parents were, as shown above on my MyHeritage tree, so I can search for Ferverda, Miller, Lentz, Ruhle, Wolflin, and Heubach, several of which are unusual. Reaching back into Germany is difficult.

It’s likely I match all four of those people at 23andMe through a common lineage that descends from either Hiram Ferverda, Eva Miller, or both. Let’s see what I can put together.

Emily is estimated to be a 2C2R. She is younger than I am based on the birth year she provided in her profile which I am not showing for privacy reasons. Emily also stated that her maternal grandmother was born in Warsaw, Kosciusko County, Indiana, and provided family surnames that include Ferverda, Miller, Glant, Zimmermann, and others.

Kosciusko County is where Evaline Miller lived with Hiram Ferverda, and their daughter, Margaret, married Chester Glant. Margaret Ferverda Glant’s daughter, Joyce, was born in Kosciusko County and married a Zimmerman.

But now, I was stuck. That’s all I had in my desktop genealogy software.

I shifted to Ancestry, where I discovered a death certificate and other information that provided what I needed to close the gap.

This information confirmed Emily’s statement that her maternal grandmother was born in Warsaw, Kosciusko County, Indiana.

Therefore, drum roll…Emily carries Eva’s mitochondrial DNA haplogroup, which is T2b.

Let’s move on to the other two matches, both of whom carry haplogroup T2b.

Ian’s maternal grandmother’s birthplace is Leesburg, Kosciusko County, Indiana, and his surnames include both Ferverda and Robison.

Eva Miller Ferverda’s daughter, Chloe Ferverda, married Rolland Robison and had a daughter, Charlotte, whose daughter married a man with Ian’s surname. Their information allowed me to connect the dots appropriately. Ian’s mitochondrial haplogroup is also T2b, which confirms Eva Miller’s mtDNA haplogroup through a second child.

Shirley, the third match who carries haplogroup T2b, also shows the surnames of Ferverda and Robison, and tracks back matrilineally to Eva Miller.

In spite of the many challenges at 23andMe, and thanks to the rare surname of Ferverda, I’ve identified Eva Miller’s partial haplogroup, but not her full haplogroup. A partial haplogroup is much better than nothing and gives me something to work with.

I checked at Ancestry, MyHeritage and FamilyTreeDNA to see if any of those three people have tested there and have trees. Indeed, Ian tested at FamilyTreeDNA and I had corresponded with him and made a note that he is a matrilineal descendant of Eva Miller Ferverda, but he has not taken a mitochondrial DNA test there.

We know that if Emily, Ian, Shirley, or another appropriately descended person were to take a full-sequence mitochondrial DNA test, we would learn a LOT more about Eva’s mitochondrial DNA. If I can’t locate someone who has already tested, I’ll reach out to these people at 23andMe and offer a scholarship for a full-sequence mtDNA test.

It’s ironic that at the most restricted and least likely testing company, I found three people descended from Eva Miller. Hope springs eternal.

Unfortunately, T2b was formed about 8450 years ago and is a very broad haplogroup made up of many subclades, but at least I have something now – and this partial haplogroup may be just the seed I need to lead to more.

Now, let’s move to FamilyTreeDNA and hope that someone there has already taken the mtFull test.

At FamilyTreeDNA

There are multiple ways to find the Y-DNA or mitochondrial DNA of your ancestors at FamilyTreeDNA.

Project Search

You can search for surname projects along with other types of projects.

On FamilyTreeDNA’s main page, without signing in, scroll all the way to the very bottom footer where you will see the Group Projects link.

If you’re searching for a surname, enter that surname in the search box.

The next screen shows projects that people with the Estes surname, including females, have joined. This includes all types of projects and does NOT mean that these projects are relevant to your line, but it does include two surname projects you may find useful.

Scrolling down shows you how many people with the surname of Estes have tested. Keep in mind that some will be females, some use married names, and sometimes people use an alias, so they aren’t included in this count.

Surname projects for females aren’t terribly helpful since the surname typically changes in each generation, at least in Western cultures.

You can also search for keywords, such as Acadian. If you know that ancestral line is Acadian, you may find clues there, including descendants of your brick-wall ancestor.

Group Project Time Tree

Many Group Projects at FamilyTreeDNA have enabled the Y-DNA Group Time Tree feature. When visiting the project, if the administrator has the Group Time Tree enabled, click on that link under the DNA results tab.

The Group Time Tree is a genetic tree of Y-DNA testers within that project based on the groups created by the project administrator.

The groups constructed by the administrator are shown at left, the Time Tree in the middle, and the testers with their EKAs and country of origin flags at right. I’ve added the red text to reflect the Estes genealogical lineage.

Based on the timeline at the top, you can see how closely these Y-DNA testers are related in time. Each haplogroup shown represents a different branching genetic lineage – breadcrumbs at work. If you are a genetic Estes male who descends from the Estes family that originated in Kent, England, and you take the Big Y-700 test, you’ll be a member of R-BY482 or its descendant haplogroups.

Keep in mind that not all testers join group projects, so it’s likely that there will be matches on your match list that aren’t here. Furthermore, only Big Y testers appear on any Time Tree.

The Group Time Tree is public, but when you sign in to your account and click on the Match Time Tree from your account, you’ll be able to view more, including testers’ trees and WikiTree connections if your matches have connected themselves to WikiTree.

Click to enlarge

I’ve converted the Estes genetic tree into a genealogical tree in a spreadsheet based on the trees of DNA matches. I’ve also included STR testers, because they are good candidates to upgrade to Big Y tests, and they are shown in the Estes Group Project. They can’t be included in the Time Trees because they don’t have the SNPs discovered with the Big Y tests. Please note that not all testers were included in this spreadsheet.

You can follow the paths of the various haplogroups. All of the red-background, black-outlined cells are Big Y-500 or Big Y-700 testers. The Big Y-500 was obsoleted several years ago in favor of the much more informative Big Y-700 test, which reveals additional haplogroups because it tests more of the Y chromosome. I’m still hoping that people will upgrade, although some testers are deceased and can’t.

The Big Y-500 tests with red stars are candidates to be upgraded to the Big Y-700 to potentially receive a more specific haplogroup. The balance of the tests in red cells are Big Y-700 tests, which identify several additional Estes haplogroup paths.

Let’s look at an example.

Beginning at the top, we know that R-BY482 is present in Nicholas Ewstas, born in 1496 in Kent, England, because all of his descendant testers carry that haplogroup too. Additionally, three generations later, in Silvester’s generation, he developed the additional mutation named R-BY490. We know it developed in Silvester’s generation for two reasons:

  • The descendants of Silvester’s brother, Robert, born in 1603, do NOT carry R-BY490. Robert’s son Matthew’s descendants only carry R-BY482.
  • The descendants of both of Silvester’s sons, Richard (pink column) and Abraham (the entire green row), all carry R-BY490.

All of the descendants of Silvester’s son, Abraham, born about 1647, the Virginia settler, who have taken the Big Y test carry R-BY490. Additionally, descendants of several of Abraham’s sons, color-coded columns beneath the green row, have developed additional haplogroups. Several more testers would likely have new haplogroups if they took the Big Y-700 test. A new haplogroup requires at least two men with the same unique mutation (breadcrumb), in addition to R-BY490 (in this case), to identify a specific lineage and assign it a new haplogroup name.

Abraham’s son, Moses Estes, born in 1711, is a good example. We know that Moses developed the mutation R-ZS3700 because four of his descendants have taken the Big Y-700 test and have that mutation that is not found in Moses’s brothers’ lines. All four Moses descendants carry R-ZS3700, and two, in the James Carroll Estes line, have developed an additional mutation, haplogroup R-BY154784.

Until Big Y testing became available, descendants of the R-BY154784 lineage didn’t know where they fit in the Estes tree, because the connecting genealogical records between Missouri, where their ancestors are found, and Virginia, where they came from, were missing.

Therefore, if you don’t carry the Estes Y-DNA, but you can find your ancestral line in projects, you can potentially do two things:

  1. Identify the specific lineage to which you belong, especially if you have access to your relative’s test results, including matches and trees.
  2. Without matches, you may still be able to identify at least some haplogroup levels, such as R-BY482 or R-BY490, which opens the door to:
    • Using autosomal results to find matches with Estes-specific haplogroups
    • Using Discover to utilize the dozen+ public reports available for everyone
    • Asking people to upgrade

While I’ve been using the Estes DNA results because it’s a project I administer and the one with which I’m the most familiar, this same approach works for mitochondrial DNA as well, especially if you can identify your ancestor’s DNA in a project.

Finding Projects in Discover

The public version of Discover provides surname and project searches as well, but works a little differently.

Select Group Project and enter the term you wish to search for.

Clicking on the project takes you directly to that project’s Group Time Tree where you can identify your ancestral line.

People who have tested at FamilyTreeDNA can join projects. Many projects accept autosomal testers who descend from that family line.

To join projects, sign in, then from your home page, click on “Group Projects” in the header, and make your selection.

Search for Surnames in Family Finder Autosomal Matches

Now that you’ve identified your ancestor’s haplogroup, you can use that information to find, rule in, or rule out various people in your Family Finder match list as your ancestors’ haplogroup carriers.

FamilyTreeDNA displays the haplogroups of your autosomal matches who have taken the:

The Family Finder test doesn’t test either the Y chromosome or mitochondria fully, but it target-tests a selected number of non-autosomal haplogroup-defining locations. The haplogroups that Family Finder identifies are typically midrange, meaning they are from roughly 2,000 to 5,000 years old. Furthermore, different tests on different chips at different times didn’t always test the same locations. This relatively new Family Finder haplogroup feature is free.

Uploaded DNA tests from other vendors may or may not receive a haplogroup, but regardless, it will NOT be displayed to their matches. Not all other vendors test or include Y-DNA or mtDNA SNP locations in their upload files, and your mileage may vary widely.

My cousin David has taken the mtFull test, so his mitochondrial haplogroup is the most refined possible, but his Y-DNA haplogroup of R-L151 was derived from his Family Finder test. Haplogroup R-L151 is about 5,000 years old. If I needed his haplogroup, it’s useful to rule out other major haplogroup branches that might be found in other men by the same surname. Plus, I can learn quite a bit from Discover.

Haplogroups are displayed in your Family Finder match list for everyone who has taken a Y-DNA or mtDNA test, but currently, only Y-DNA haplogroups are provided for Family Finder results. Midrange mtDNA haplogroups are planned for sometime in the future.

There are several methods to search for either a specific surname or haplogroup within Family Finder matches.

Let’s use my Ferverda/Miller/Lentz haplogroup T2b revealed at 23andMe. That haplogroup would almost assuredly be broken down further with full-sequence testing, and it might have been renamed as a different subgroup of haplogroup T in the new Mitotree.

Let’s begin with searching for haplogroup T2b.

The search bar allows users to select Name, Ancestral Surname, mtDNA Haplogroup or Y-DNA Haplogroup.

You’ll notice that there are a total of 59 results that include T2b as a part of the haplogroup. The mitochondrial lineage I’m seeking is my mother’s paternal grandmother, so the matches should be on my mother’s side, although there is no guarantee I don’t match someone autosomally on my father’s side too.

I checked the trees of all 59 people in the T2b category, and unfortunately, none descended from the line I need.

If you change search terms or categories, be sure to clear your filters.

Under the Filter option, you can filter for several options in addition to searching.

For our next example, I’ve selected both the Big Y-500 and Big Y-700 tests, and searched for Ferverda.

I already have the Ferverda Big Y-700 haplogroup, but if I didn’t, I would now!

Don’t forget that you can sort by any number of fields, and you can download your entire match list into a csv file. I find that easier because I can search, sort and filter at will.

Don’t forget to check back from time to time as more matches are added.

Utilizing Haplogroup Projects

Under the Group Projects header, or by Googling for a haplogroup T2 (or T, or T2b, etc.) at FamilyTreeDNA, you can view the haplogroup T2 project, and filter for haplogroup T2b or any subclade.

Be sure to expand the project’s page size to display the entire project. It defaults to displaying 25 rows at a time, but you can see the number of pages at the bottom of the page. I expanded the page size to 5000 so that I can use my browser search for known surnames in the mitochondrial line.

By using my browser search and searching for each known surname by generation, I searched for Ferverda, Miller, Lentz, Ruhle, Wolflin and Heubach.

I was VERY excited for a minute when I found a Lydia Lentz listed as a tester’s EKA.

Because the female’s surname changes in every generation, there’s only one family in this lineage that Lydia Lentz could have been a member of to represent the mitochondrial DNA of Eva Miller whose mother was Margaret Elizabeth Lentz.

So, the question is whether or not Lydia Lentz is the sister of Margaret Elizabeth Lentz.

Shifting to my desktop software, it’s easy to see that Jacob Lentz and Johanna Frederica Ruhle had four Lentz daughters who lived to marry and have children. None of those daughters were named Lydia, so the Lydia Lentz EKA in the haplogroup T2 project is not representative of Eva Miller’s mother and grandmother.

Margaret Elizabeth Lentz is Eva Miller’s mother, and I had already searched within the project for Miller. I added Yost, Gallagher, and Overlease to the browser search in the haplogroup T2 project with the hope that someone might have listed a woman with one of those surnames as their EKA, but no such luck.

Not everyone joins projects, or provides their earliest known ancestors, but I didn’t find the surnames of any of the females in my known line here.

Let’s see if Ancestry can help.

At Ancestry

Ancestry doesn’t do Y-DNA or mitochondrial DNA testing, so you won’t find your ancestors’ Y-DNA or mtDNA at Ancestry, but their trees can help you find testers.

Let’s shift to Louisa Drechsel, one of the daughters in the Mehlheimer/Drechsel line we were working with earlier that needed more research.

I looked at the hints for Emma Louisa Drechsel, who was always called Louise or Aunt Lou in my family, and discovered another Ancestry member with Emma in their tree.

I clicked through to the tree to discover that the tree’s home person does not descend from Barbara matrilineally, which means they are not a candidate for Barbara’s mitochondrial DNA.

I then clicked on the tree owner’s name to see whether they happen to be an autosomal DNA match to me. They are not. Without messaging them, there’s no way to know whether they have taken a DNA test, and there’s really no point since they are not a mitochondrial DNA candidate.

While I’m at Ancestry, I’m going to check ThruLines to see if anyone who is an autosomal DNA match to me also descends matrilineally from Barbara. There are no autosomal matches shown who have our common ancestor in their tree, and who are mitochondrial candidates.

Remember, a male between the ancestor and the testing candidate always blocks the mitochondrial DNA path.

These people are all autosomal DNA matches.

There may be descendants who either aren’t DNA matches or who haven’t tested who might be mitochondrial candidates. They can be located by checking Ancestry’s trees for our common ancestors and determining how the tree owner relates to that ancestor, if they do.

Compare Trees is New

Ancestry recently introduced “Compare trees”, a new beta feature. It may not be fully rolled out to everyone yet, and because it’s in beta, the feature may change.

To access this feature, go to your tree, not their profile card.

I clicked on Barbara Mehlheimer’s link in my tree, which displays this little mini-profile. Then click on “Compare trees” at the bottom.

Ancestry displays your tree, at right, and the other tree, at left. You can select another tree to compare at top right.

Ancestry’s comparison only shows a total of three generations – the selected person, their parents, and their children.

The person I actually want to follow is Louisa, but if you click on Louisa’s card here, it simply compares the two Louisas – it doesn’t shift down a generation.

This means that to follow more recent generations, you have to go back to your tree, select someone further down in the tree and repeat the process.

This process is cumbersome, but doable thanks to the new Compare Tree function. I’ll come back to this after checking the rest of the “easier to harvest” fruit from other resources. Remember to make notes in your research journal so you don’t forget where you left off – although trees are always changing.

MyHeritage has one of my favorite tools.

At MyHeritage

Recently, MyHeritage has begun providing midrange Y-DNA haplogroups for some of their DNA testers. If you’re one of the lucky testers, you can use the free Discover tool to learn about your haplogroup, but a haplogroup alone won’t help you much with genealogy. You need matching and advanced tools for that.

Unfortunately, you can’t see the haplogroups of your matches, so you can’t search or filter using that criterion. You can, however, ask any men with the surname you’re seeking if their haplogroup is displayed.

Cousin Finder

MyHeritage has an ingenious tool called Cousin Finder that I wrote about here. Cousin Finder helps you find cousins who share common ancestors with you, regardless of whether or not you are a DNA match.

MyHeritage found 531 people in their database that share ancestors according to both their and my trees.

This list of matches doesn’t page; it scrolls, so I made a spreadsheet of the people who are relevant to my search for my brick-walled ancestor. Scrolling becomes difficult and very slow as you proceed down the list. I didn’t want to have to do this twice.

You can improve performance by using the relationship side filter. Because your ancestors match, MyHeritage knows on which “side” of your tree your common ancestor is found.

At this point, I’m interested primarily in identifying Y-DNA or mitochondrial DNA candidates for a specific ancestor.

Using the Drechsel/Mehlheimer line as our example, I’ll search on my mother’s mother’s side.

We already met Patty at WikiTree, but let’s pretend we don’t know Patty. I can click on “View her tree” to see Patty’s whole tree, or I can click on “View Relationship,” which shows how we are both related to our common ancestor.

As we know, for mitochondrial DNA, any male in the line between the ancestor and the testing candidate blocks the mitochondrial DNA path. Patty inherited her mother’s mtDNA, not her father’s.

I didn’t forget about Eva Miller Ferverda either.

I searched for cousins who descended from my mother’s father’s side to find mtDNA candidates for Eva Miller and didn’t find any. But I did find an entirely unexpected bonus.

My mother’s father’s line shows all the connections on that side. While clicking through each one, I quite serendipitously discovered a mitochondrial DNA candidate for Eva Miller’s husband’s great-grandmother, Anna Elizabeth Jonker, AND, separately, a potential Camstra Y-DNA tester too. Oh, happy day!

It was only later, while working on my genealogy for Frederica Ruhle and hoping to discover where she actually lived in Pennsylvania, that I discovered that MyHeritage has put a Cousin Finder link in each ancestor’s profile.

Who doesn’t love a pleasant surprise?!

You no longer need to sift through all of your cousins on a particular side, but remember, had I not done that, I wouldn’t have found either the mitochondrial descendant of Anna Elizabeth Jonker nor the Camstra Y-DNA candidate.

At FamilySearch

FamilySearch is more challenging and is best for fleshing out trees where not much research has been done. Remember that FamilySearch has access to records that are not available at either Ancestry or MyHeritage.

FamilySearch is a one-world tree. Like all trees, it’s subject to errors, so caution is always advised.

At FamilySearch, from your profile card in the tree, locate the ancestor whose Y-DNA or mtDNA you seek.

Then click on that person. Their profile card will pop up. Click on “Tree,” then, at the top right, select Portrait.

Now you can expand their children downward. Note that the little “two people” in the top left corner of the profile card means there are multiple spouses. The only way to view all of the children is to click on that person’s placard, then select the alternate spouse.

Living people have no placeholders on this tree.

You can contact contributors who provided information on a profile in the tree.

Click on the source provider’s name to see if they are related, and click on the little tree icon to see how.

However, once a year, there’s a great way to contact interested descendants.

Relatives at RootsTech

RootsTech is the largest genealogy conference in the world, and it’s sponsored by FamilySearch.

About six weeks before RootsTech takes place each year, and for about a month after, you can participate in Relatives at RootsTech.

During that time, you can select an ancestor and see which other people who have signed up for RootsTech also descend from that ancestor. I wrote about how to do that in the article, Relatives at RootsTech Reveals Cousins and Provides DNA Candidates. I almost always find someone who descends from an ancestor whose Y-DNA or mtDNA I need for my tree.

It’s a wonderful opportunity to meet new cousins and collaborate.

At GEDmatch

GEDmatch is an autosomal DNA upload site that offers a variety of matching and display options. While they don’t attempt to calculate a haplogroup, uploaders can enter their mtDNA and Y-DNA haplogroups, if known.

GEDmatch isn’t normally a resource we think of for either Y-DNA or mtDNA, but it can be useful under some circumstances.

In the One-To-Many limited free version and the Tier 1 subscription model, you can view haplogroups if someone has entered their haplogroup name, but you can’t filter without the Tier 1 version.

I filtered for haplogroup T2b and found one person in the match list with haplogroup T2b4. I then viewed the GEDCOM that this person has also uploaded, but they do not descend from Eva Miller Ferverda’s line.

GEDmatch isn’t built for haplogroups, but sometimes, if you have a known haplogroup that isn’t terribly common, you can catch a lucky break there.

Where AM I?

OK, so where am I in all of this?

I feel like I’ve searched the corners of the earth!

I’ve primarily used two examples.

  • My own mtDNA line which is the Drechsel/Mehlheimer line that I chose because it’s a great example that I knew well.

If I had actually been searching for a testing candidate, we would easily have eliminated several possibilities. Five female lines remained as possibilities that need additional research, plus my own test if someone were actually searching.

  • Then there was Eva Miller Ferverda (1857-1939), whose partial haplogroup, T2b, was discovered at 23andMe in three matches. I was able to reconstruct their trees, confirming that this was her line, but I was unable to find any testing candidates elsewhere.

Each of the DNA testing and genealogy vendors provides a way to communicate with other users of their platform.

  • At both 23andMe and MyHeritage, you can message through their platform.
  • At FamilyTreeDNA and GEDmatch, you can email your matches.
  • At WikiTree, you send an email through their platform to the profile card manager.
  • At FamilySearch, you cannot see placeholder cards for living people, so you need to check to see if people making changes to that ancestor’s profile are related. Then check their children closest to the present day for the same information. You can message through the FamilySearch platform.
  • During Relatives at RootsTech, you can message your cousins through their platform. The great thing about these folks is that you know they are interested and engaged, because they’ve just signed up for RootsTech.

Communicating With Testing Candidates

I’m fortunate that there are three mitochondrial descendants of Eva Miller Ferverda at 23andMe, one of whom is also at FamilyTreeDNA. I will message or email all three of them individually with a short, customized message that contains:

  • How I am related to our common ancestor.
  • A question about whether they have taken the mtFull test, or any test, at FamilyTreeDNA. If they have taken any test there, it’s easy to upgrade.
  • A sentence about how FamilyTreeDNA was the original genetic genealogy founder of this industry and the only company to offer the full mtDNA and Y-DNA tests.
  • Why they can benefit from taking the mtFull test and how it can help us learn more about our common ancestor.
  • An offer for a full-sequence mitochondrial DNA testing scholarship if they have not already taken that test.
  • I ask if they are interested and provide my email in case they have questions or want to discuss further.

Depending on how much space I have for the message, there are two articles I often provide links to in case they are unfamiliar with either Y-DNA or mtDNA testing.

  1. 4 Kinds of DNA for Genetic Genealogy is a very basic article for people who might be unaware that there is any type of DNA testing other than autosomal. This is often the case with Ancestry.
  2. The article Mitochondrial DNA A-Z: A Step-by-Step Guide to Matches, Mitotree, and mtDNA Discover is an in-depth article about using mtDNA. This is a wonderfully educational how-to article, but I always hesitate before sending this one because I don’t want their eyes to glaze over.

Scholarships

I gladly and eagerly offer scholarships for both Y-DNA and mtDNA testers from lines I need to represent my ancestors.

I equate scholarships to finding a rare out-of-print book about that exact family line, with only one or two copies still in existence, and only one accessible in a rare book shop in Podunk, Idaho. I would book a flight tomorrow at 5 AM to go and pick it up in person even if I had to eat beans and hot dogs for the next six months to pay for it. If you know me, you know I’m not kidding! I’ve gone on many wonderful road trips to meet with and collect DNA samples from cousins.

A Y-DNA or mtDNA test doesn’t cost nearly as much as that excursion and is even more reliable, because we know the DNA results are accurate – assuming the tester’s genealogy is accurate, which you should verify, and no undocumented adoptions or broken lineages have occurred.

Good luck on your treasure hunt!

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All About AI – What It Is, What It Isn’t, and Why It Matters

This is the second article in the AI series. The first, Your Wonderful AI Assistant – Sometimes Wrong, Never Unsure, Always Convincing, explains why I’m writing this series and what to expect. I suggest that you read these articles in publication order, as they build on each other.

AI is neither inherently good nor bad. The outcome depends on:

  • How it is used
  • By whom
  • Capabilities of the (ever-changing) tools themselves
  • The understanding level of the “requester” and the “consumer,” both
  • Safeguards applied or neglected

About AI

Let me start by saying that I don’t love AI, and I don’t hate it. I’m neither an evangelist nor a doomsayer. I’m a realist. AI is a powerful tool, capable of remarkable things and spectacular failures. Understanding the difference and interacting appropriately are the keys to success or failure.

AI is simply a tool, and like all tools, it can be used for good or evil. AI has the potential to, and does, in some cases, make our lives easier. However, the bad guys and miscreants saw that potential early and have perfected it.

AI is all around us, whether you realize it or not, so don’t think you can just avoid it, because you can’t. AI exists in many forms and is here to stay. We need to educate ourselves so we can reap some of the benefits and avoid the pitfalls.

Education and increased vigilance are the only ways to protect yourself, and I mean vigilance incorporated into the very fiber of your being. No more, “that looks interesting” and clicking without thinking. It’s so easy to do.

When I talk about AI safety, I’m referring to two types of safety.

  1. Using AI tools for reliable results, and how to determine when you’re receiving or consuming something questionable. AI failures occur often and are both irritating and misleading, but not always obvious.
  2. Literally protecting yourself from danger. This includes recognizing when AI is being used without your knowledge and how to protect yourself in the new threat landscape. I am not overexaggerating.

Unfortunately, AI safety is a sliding scale, progressing from one end of the spectrum to the other. There’s not always a clear delineation between correct and incorrect, safe and unsafe, or between different types of AI. As I am wont to say, “It depends.”

Learning about AI, both in general and in specific contexts, is critical. Not yesterday’s AI – but AI right now, because both the AI tools and AI’s capabilities are changing at lightning speed.

We all need to up our game and retrain ourselves to always stop and think first.

AI and You

There are essentially three ways people encounter or interact with AI.

  1. You’re actively using AI as a tool, such as ChatGPT, Claude, Gemini, or others. This is generally safe from an actual danger or “threat” perspective, particularly because you are in the driver’s seat. However, there are aspects you need to be aware of – especially if you’re a novice. I’ll explain methodologies to use AI to (hopefully) increase your productivity and save you from following AI into the underbrush of falsehoods, inaccuracies, and misplaced confidence. In other words, so you don’t have to say, “Wow, was I ever an idiot,” too often.
  2. You’re unknowingly interacting with AI. Sometimes this is fine, but it can open the door to inadvertent reliance on incorrect information and therefore various forms of harm. Sometimes, harm rises to the level of actual danger. Understanding when you’re interacting with AI, understanding its limitations, and recognizing danger signs are important aspects of staying safe.
  3. The AI threat landscape. AI can be dangerous and used against you. I mean screaming-red-neon-flashing-sign hair-on-fire dangerous, and I’m going to explain this new threat landscape and how to improve your chances of being safe, primarily in the final article of this series.

I Use AI, But There Are Limits

I hold a graduate degree in Computer Science and have years of experience in the technology industry where security is both essential and critical. That background, while preparing me generally, cannot prepare one for the situations and well-hidden threats we now encounter every day. Being overconfident and overreliant on prior experience is foolhardy and a sure way to get burned.

The one thing that’s constant in the computer industry is change. The underlying fundamentals remain the same, but everything else changes – and AI is morphing rapidly.

I’ve been using AI since the beginning in a very restricted, measured way. I use AI regularly, tactically, and cautiously, with huge guardrails. I started out by taking classes from Mark Thompson and Steve Little, AI experts in the genealogy space, to learn how to use AI productively. That was a couple of years ago, and the entire landscape has changed since then. I make it a priority to stay current.

In the next article about using AI safely, I’ll share recommendations for training and education from Mark and Steve.

AI tools are trying to emerge from their terrible toddler stage and morph into early teens, but they relapse a lot! Sometimes AI is very helpful, sometimes wrong, and often frustrating – interspersed with amazing victories where AI helps us immensely.

Unfortunately, often it’s almost impossible to tell which is which.

Inspired by a posting in the Facebook group, Genealogy and Artificial Intelligence. Image is AI generated and appropriately labeled as such.

Here’s the caveat – I know I’m using AI. I’m not accidentally interfacing with a Chatbot, thinking it’s a human. I’m not reading something someone else posted and believing I’m reading about an experience that’s true – when it’s AI-created fiction. The question, of course, at that point, is WHY someone created it and posted it in a way that conceals its true origins.

My AI usage is intentional. I know how to be vigilant, generally what AI can and can’t do, and that I absolutely positively MUST fact-check everything. Often, I inadvertently push the limits of AI, thinking it can perform more than it can accurately, which is another reason everything must be checked. As genealogists, verifying sources should be second nature.

If you’re going to use AI, it’s essential that you do the same thing.

So, what, exactly, is AI?

What is Artificial Intelligence?

This is really a difficult question to answer, because AI has been more of a slow evolution, followed by a rapid acceleration of technology – not a specific “thing.” That acceleration occurred when standalone AI tools like ChatGPT, which we know are AI because they are specifically called that, were introduced and made available to the consuming public.

We’ve been using computers for decades now, assisting us on platforms from mainframes to PCs to tablets. Today, our phones are more powerful and useful than early mainframes.

AI is the latest in the cadre of applications, a type of tool that can either stand alone or be embedded in other software tools for specific tasks. Think Chatbots for business websites.

While AI is beginning to be “everywhere,” it’s not a universal scapegoat.

Two years in, AI is being blamed for everything. While AI does make a lot of mistakes, many issues aren’t a result of AI, and it’s not fair to presume they are. Let me give you two examples of what is and is not AI.

  • Not AI – Someone tried to enter text, meaning alphabet, in a field meant exclusively for numbers, like a month field that’s supposed to be a number and not the month name. The person was angry because “AI was wrong” and prevented the erroneous entry. First, it wasn’t wrong, and second, it wasn’t AI.

One of the earliest computer uses was to parse date fields and ensure that the “right thing” was being entered in the correct place. In this case, a numerical month, not the month name. That’s not AI. That’s just plain old-fashioned programming error-checking that’s been a part of software for decades. The program was performing exactly as it was intended.

  • AI – I submitted a spreadsheet to ChatGPT and instructed it to move all of the data in cells in column A that are entirely numeric to the same row in Column B, and to leave everything that contains any alphabetic characters where it is in column A. That’s AI, both because I’m using a known AI tool, and it’s processing my instructions to produce output that did not exist before.

The above image is what I wanted. I completed this by hand to show you what I had in mind. Working by hand is fine with 8 rows of data, but it wouldn’t be fine with 1000 rows, or more. That’s when you need a tool.

What could go wrong? Plenty.

Let’s say that I didn’t provide specific instructions and a cell contained mixed alpha and numeric, like Jane2. Or, if the tool just plain messed up because of some other unknown reason – such as the file being too long, or it misinterpreted an instruction. That’s why you have to verify everything.

With AI, it’s always some variant of the wild west frontier.

Next, I submitted my Before and After spreadsheet, above, and instructed ChatGPT to “Please put this in a chart and make it pretty.”

This is exactly what I received.

I didn’t receive what I wanted, because I didn’t tell the AI tool specifically what I wanted (spacing, color, font, size), and what I didn’t want. This isn’t a problem with the AI tool, it’s a problem with the instructions provided by the “driver.” AI is not a mind-reader, at least not yet.

Hint: When I don’t receive what I wanted, I tell ChatGPT what I wanted and ask it why I didn’t receive that, and what instructions I could provide differently. In this case, I learned that it can’t “discern colored text” (red) and only sometimes can “see” bolding.

This was a very simple comparison of AI versus non-AI. Of course there are endless variations, but in general, AI does something that produces something new or different or in another format – based on conversational instructions.

Examples of what AI can do well:

  • Take notes and summarize online meetings
  • Organize information into outline format
  • Suggest structure
  • Proofread and sometimes provide editing suggestions
  • Suggest places to look for additional information
  • Translate, transcribe and summarize both typewritten and handwritten documents, in multiple languages

Every one of these comes with a caveat. AI can always be wrong. Like any helper or intern, it’s up to us, as the responsible party, to be, well, responsible by monitoring and verifying everything.

Being wrong in places does not mean the tool isn’t useful. AI can transcribe an entire document in seconds, but I need to proofread it against the original. That’s a significant time savings for me. AI can then assist with the logic of how people are related to each other. That doesn’t mean it’s accurate, but it’s a place to start.

We have to learn how to communicate with our intern in a way it can understand to (hopefully) receive the output we want, and we have to confirm that it is.

The more difficult and complex the task, the more difficult the verification.

GIGO

The overarching theme for all computer data is GIGO – garbage in, garbage out. I know everyone can think of hundreds of examples that have absolutely nothing to do with AI. It’s the same now, but on steroids because we add the layers of:

  • Our instructions to AI, which may or may not be as thorough as we thought
  • AI interpreting what it thought we said, according to its internal rules and limitations that we don’t understand
  • AI manipulating data and producing output on our behalf

Additionally, when we ask AI to gather information about something, it can only gather what it can see. For example, some AI tools cannot reliably open weblinks, while others can. Some, like Google have internal routines to rank sites that are more reliable and accurate, and other tools do not.

Asking your AI tool for it’s sources so you can evaluate the GIGO factor is essential too.

Drinking From the Firehose

You might think AI is completely new, but it really isn’t. What’s new is the label of AI and consumer-based products where you get to be the driver.

Think of AI as the big umbrella.

In the past decade or so, artificial intelligence models have been slowly being developed, often for specific use cases. Machine learning models that are self-teaching are good examples. Genetic imputation to equalize autosomal DNA files produced by different vendors before matching is a specific use case.

Traditional programming is very specific and instructs, “If X, then Y.” Imputation, within a limited range of options, says, “Based on X, I think Y is most likely next character.” Machine learning learns by example. AI is the next generation where answers to questions are not hard-coded or self-learned in the same way.

With AI, one could interact and say, “Based on X, what do you think is next, and why?” The answer would be conversational, and would explain how the AI tool got to the result of Y. That doesn’t mean Y is accurate.

Before AI, consumers had never been in the driver’s seat, with the ability to query computers easily about anything with no programming needed – receiving conversational answers in their language of choice. Answers that are hopefully accurate.

Back in 2011, Siri became available, Amazon Alexa in 2014, and Google Assistant in 2016, but these were all command driven with a restricted vocabulary and could only perform limited actions.

In October 2022, ChatGPT introduced us to a new world, triggering the AI boom. By late 2023 and early 2024, suddenly the term AI, artificial intelligence, snowballed and was everywhere. The early versions of AI tools could only do a fraction of what they can in 2026, and could not perform tasks on your behalf.

ChatGPT prompt: “Make me a fun goofy picture with a cat that illustrates the ability of AI to make a fun goofy picture.”

Today that has all changed and it seems like everyone is making goofy pictures for fun.

Artificial Intelligence is NOT Intelligent

Let me say this loudly – artificial intelligence is not intelligent!

AI is a computer – electronic pulses in a data center somewhere. AI is trained to gather massive amounts of data, distill it in specific ways, and then, using various types of skills, interact with humans in a helpful manner. “Helpful” depends on perspective.

This field, as a whole, is really still in its infancy. That’s both the bad news and the good news.

AI tools are “new,” exciting, and frightening all at once. AI has enormous potential, but it also creates opportunities for misuse, deception, and unintended consequences.

I’m not referring to water and electricity consumption and the impact of building thousands of data centers on the environment. I’ll let you decide for yourself on that one.

Risks include:

  • Frequent errors
  • GIGO
  • Results being presented overconfidently by the AI agent
  • Faulty results being believed by the consumer (that’s you and me) with the same level of overconfidence, and without verification
  • Social engineering – meaning the manipulation and influence of people by bad actors
  • Extremely dangerous, highly malicious manipulation and applications in ways not possible before

The entire AI landscape is complicated by a lack of public understanding and made even more challenging by the extraordinary pace of this technology’s evolution.

Multiple Types of AI

There are multiple types of AI, ranging from Machine Learning models to full-blown Generative AI that creates goofy cat images for you. For the most part, today, we’re talking about LLMs and Generative AI.

Large Language Models, called LLMs, are artificial intelligence tools, like ChatGPT or Claude, that are designed to process human-like text or speech and generate output in the same way. AI doesn’t just give you a list of resources that you evaluate yourself, like a search engine; it gives you an “answer” (such as it is), writes text, and has an interactive “conversation” with you.

How does that happen?

The AI tool at the data center aggregates and amalgamates data based on your input and its training, then predicts the words most likely to come next, in what context, and how those words relate to each other.

That’s how AI forms an “answer.”

This is how and why AI, specifically LLMs, can write essays on a topic, create entirely fictitious but highly engaging social media postings and stories that aren’t presented as “stories,” but as someone’s personal experiences, meaning as “truth.”

AI, or the people who generated that AI script, or both, present fictional results with great confidence, often beautifully, and far more convincingly than humans.

This is where it’s important to differentiate between the tool itself, and the “driver,” meaning the human that’s prompting the AI tool.

  • The driver needs to prompt AI correctly and verify the output.
  • AI, the tool itself, sometimes generates incorrect information, often regardless of the prompts provided by the driver.
  • Sometimes the AI tool performs exactly as instructed, but the driver requested something “improper.” By improper, I don’t mean inadvertently or by accident.
  • Sometimes the human is unethical.
  • AI isn’t a sentient being and doesn’t understand the difference.

The human decides what to do with AI-generated results. Many times, AI-generated text, recognizable by word patterns or other characteristics (today), is posted to social media as “original” or factual, and contains incorrect information.

This is often referred to as “AI slop,” as one of the nicer terms, especially by those of us who increasingly find incorrect but convincing AI slop posted as “helpful information” and positioned as “expert,” even though it contains substantial inaccuracies.

Worse yet, very convincing AI slop can easily be generated to part you and your money.

And do I EVER have an example for you that combines AI slop and ethics.

AI SLOP and Ethics

Just two days after our new paper, on which I’m a co-author, Mitotree: The Universal Human Mitochondrial Reference Phylogeny at 10x the Resolution, was published, a company, whose name I’m not including because I don’t want to give it any oxygen or get it indexed with this article, posted a “beautiful” AI poster based on our paper – without our knowledge.

Looks nice, right?

To begin with, it appears for all the world like the authors provided this infographic, which we ABSOLUTELY DID NOT DO. Our names are right at the top. However, our names, as the paper’s authors, lend this “thing” credibility, thereby leveraging our work BOTH unethically and inaccurately.

This AI-generated infographic, although it’s not labeled as such, was created by a third party shortly after the publication of the Mitotree paper. While visually impressive, it contains several scientific inaccuracies, illustrating how quickly and easily authoritative-looking but incorrect content can be created and disseminated.

That’s one of the issues with AI – the beauty and professional appearance of AI-generated “things” encourages unwarranted confidence in the output, when the information is very wrong.

That’s why humans bear the responsibility of BOTH using AI ethically, AND verifying its accuracy. It’s also why, as consumers, we need to question everything.

My biggest issue with this situation isn’t with AI, other than the fact that it generated incorrect output – the issue is with the humans who intentionally created this, using AI. In other words, the drivers.

The infographic doesn’t say they created this incorrect rubbish, and I assure you, they never asked for permission. Then, they published the infographic on their own blog. In case you’re wondering, the company encourages uploads and charges people to get “new results.”

Now for the AI part.

The information IS WRONG and NOT a synthesis of what we published!!!! This infographic shows that all non-L haplogroups descend from haplogroup L4, which is absolutely FALSE.

Haplogroups M and N descend from haplogroup L3, and haplogroup R descends from a subclade of N. You can trust me because I’m one of the paper’s authors, or better yet, you can look for yourself, here, on Discover, or here, here, and here.

That isn’t the only thing that’s wrong, either, but how would normal air-breathing humans, meaning consumers, ever know?

Doesn’t that infographic look professional and convincing, especially if you, as a consumer, didn’t actually check everything on the document – AND its authenticity?

You’d assume legitimacy, right?

If you didn’t know, wouldn’t you be impressed with the expertise of the company that posted this infographic on their blog? And, as a normal consumer, how would you know?

You’d be impressed because you didn’t realize they hijacked someone else’s work, created this “beautiful” infographic, included the authors’ names on something inaccurate that the authors knew nothing about and didn’t endorse, and then published it. All without saying one word indicating that the infographic isn’t the authors’ work, was AI generated, or by whom.

In the past, before generating AI slop was this easy, consumers often presumed that a business was ethical and accurate. Of course that wasn’t always true, but being convincing at first glance is much easier today. Also, presume is related to assume…and we all know the rest of that story.

This is one of the dangerous sides of AI – illustrating how easy it is to deceive people now. It’s increasingly difficult to distinguish between legitimate expertise and fabricated authority. AI has removed that barrier.

You can no longer accept that anything is what it appears to be unless you’re working directly with known, trustworthy entities. The offending company completed that infographic in the click of a button and the blink of an eye, while I hadn’t even finished writing my own article about the paper’s release.

That company wants you to upload your DNA to them so that they can tell you “things” about your DNA. The intention is clear.

Of course, the consuming public, unless they were extremely vigilant, would never figure out either issue – ethics or accuracy.

I had to delete the next paragraph or two that I wrote on the topics of ethics, trust and confidence because I’m still so furious. Hot under the collar doesn’t even begin to describe how I feel about the ethics of misrepresenting something that we authors just spent six years of our lives on. Trust me when I tell you that my internal monologue was both very salty and rather spicy!😊

However, there’s good news. This infographic provides a perfect illustration of both AI slop, how deceptively great it looks, the ethics surrounding AI usage, and how difficult AI is to discern.

In fact, I couldn’t have come up with a better “bad example.”

A six-fingered hand, misspelled words or three arms in an image are obvious, and are yesterday’s AI tipoffs.

A misrepresented phylogenetic relationship or an incorrect founder-clade example is not obvious. Only subject-matter experts would or could notice if they were focused and paying attention.

That’s the problem in a nutshell.

The infographic wasn’t obviously wrong. It was convincingly wrong.

And convincing wrongness is far more dangerous than ridiculous wrongness, like six fingers, because most readers never realize they’ve been misled. Or why.

This single example demonstrates several AI themes in one fell swoop:

  • AI-generated content
  • Ease of creating complex and convincing output
  • Apparent authority
  • Misplaced trust
  • Lack of topic expertise
  • Overconfidence
  • AI slop
  • Difficulty of discerning truth
  • Yesterday’s “AI clues” are gone now – like misspelled words
  • Marketing vs. science
  • The necessity of human review
  • The fact that human review is only effective when the reviewer actually understands the subject, and cares.
  • Ethics

Like with this example, often AI slop is interspersed with accurate information, and it’s impossible to tell the difference unless you actually DO DUE DILIGENCE AND VERIFY ALL OUTPUT.

Yes, all of it.

Don’t shoot the messenger!

Hallucinations

Next, let’s discuss genetic genealogy, particularly haplogroup information. Hallucination or hallucinating is the term used for when AI simply makes things up, which often sound extremely convincing.

There’s nothing AI can tell you about your haplogroup that reputable sources cannot – and AI can’t see behind paywalls or logins, into your matches.

FamilyTreeDNA has an article in their help center titled, Why AI Models Struggle with Haplogroup Analysis.

Unfortunately, I encounter more and more instances where someone uploads their DNA to a third-party site, or “asks AI”. They receive a (sometimes substantially) incorrect haplogroup in a completely different part of the tree, complete with convincing language, posts it publicly, and then decides to argue that the third-party site, (who probably uses AI), or their AI tool, is correct.

Let’s look at an example. The mitochondrial DNA haplogroup for the Native American Anzick-1 burial in Montana that dates from roughly 12,500 years ago is mitochondrial haplogroup D4h3a. There’s no dispute about that.

A tester uploaded their mitochondrial DNA to “AI” and was very confidently told that, based on their mutations, their results belonged to haplogroup A2ex. They don’t.

ChatGPT misinformation about Anzick-1 haplogroup

They were then informed that it was also Anzick’s haplogroup. Wrong again.

FamilyTreeDNA's Discover tool information comparing haplogroups D4h3a and A2ex

FamilyTreeDNA’s Discover tool comparing mitochondrial DNA haplogroups D4h3a and A2ex. Their common ancestor lived about 66,000 years ago.

Not only did AI report Anzick’s haplogroup incorrectly on a grandiose scale, those two haplogroups don’t share a common ancestor for roughly 66,000 years – specifically haplogroup L3 who lived in Africa. AI made a massive mistake.

But it gets worse.

ChatGPT incorrect information about haplogroup A2ex.

The AI “answer” continued for four pages, containing completely erroneous information. To begin with, A2ex is a haplogroup, and “ex” has never meant excluding.

That’s bizarre, and an example of AI making something up that is patently false, but sounds wonderful and very authoritative.

The term for this AI behavior is hallucinating. I’m not publishing the rest of this exchange because I don’t want anyone (or any AI bot), for one minute, to think any of it is accurate. AI even made up mutations, along with four pages of “fairy tale.”

The individual who received this information was so excited and proudly posted it, which in turn provided incorrect information for other consumers, and encouraged them to use a badly flawed tool. Then they proceeded to argue with the experts.

They were absolutely convinced because it “felt” true to them, and because they wanted to believe they had discovered something special, and were related to Anzick. Their comment was, “You’re wrong, because AI told me it was true, and I’ve learned a lot from AI.” I was quite exasperated, but also feel sorry for them and can’t help but wonder how much else of what they “learned” from AI is wrong too, but I digress.

Most AI errors aren’t obviously wrong to the consumer. If AI said that you were descended from Tyrannosaurus Rex, you’d laugh. But if it tells you something more plausible and sounds confident, it’s very easy to be convinced. The reason these errors are so dangerous isn’t because the experts are fooled, it’s because non-experts either can’t, don’t, won’t or don’t think they need to invest the time to discern the difference.

I find it a bit baffling why anyone would use AI, or worse yet, a pay site for haplogroup misinformation, especially since FamilyTreeDNA provides the Discover website with free reports for every haplogroup. They are the unquestioned industry phylogenetic experts for both Y-DNA and mitochondrial DNA, and literally created the reference model for all haplogroups with the Mitotree.

Everyone can use Discover to access both the Y-DNA tree and Mitotree – for free – here. Discover isn’t even behind a paywall, and every customer can click through from their results page.

As far as haplogroups are concerned, there’s really no reason to rely on AI-generated answers without verifying them, because the authoritative resources are freely available and incredibly easy to access.

FamilyTreeDNA’s Discover Ancient Connection for Anzick-1.

Regarding Anzick’s haplogroup, all I had to do was enter haplogroup D4h3a in Discover and under Ancient Connections, right there is Anzick’s information.

I may start posting a link to this article on every single post where someone starts out with, “I submitted my DNA (or haplogroup) to AI, and it said…”

Let me be very direct. Don’t believe AI when it has to do with genetic information, especially Y-DNA, mitochondrial DNA, and haplogroups. AI does not have the capability of understanding topology and nuances of phylogenetic trees, and can only parrot back what others have said – correctly or incorrectly.

Incorrect information that’s publicly posted is then fed back into the AI algorithm, further reinforcing incorrect results.

You can find the free Discover tool for both Y and mtDNA, here, and you can join FamilyTreeDNA’s Mitochondrial DNA Group, here, and the Big Y Group, here.

AI Training and AI at Work

AI is trained on massive datasets of mostly unknown origin, including all public postings such as Reddit and Facebook public groups, pages and postings.

In other words, AI is always accruing additional information, including data uploaded by users.

As genealogists, we are already aware of the dangers of unsourced trees and and information that is repeated and copy/pasted without verification.

AI’s training provides more than just data points for you to evaluate, like trees.

AI bots are trained to interact in a humanlike manner. So instead of trees with hints, think hypothetically of an AI bot that reads the trees, then “creates” a wonderful story or infographic about your ancestor – that may or may not be either fully or partially accurate. But it’s beautiful, heartwarming and you love it! Plus, you don’t have to sort through all those trees, hints, and do the work yourself. AI did it for you! Win – win, right? Wrong.

AI knows how to very effectively manipulate language, images, and with them, emotion. Yours, to be specific. That’s both the bad news and the good news.

AI also has the ability to sift through large amounts of data and summarize succinctly –  sometimes even correctly. Sometimes it takes several refinements to obtain something that’s both correct and what you want. AI can discern patterns in massive amounts of data that we cannot, at least not readily.

Think of AI as your not-so-trusty but very confident and friendly intern – and I don’t necessarily mean a college intern.

Remember when you see AI published by others, their intern has been at work too.

AI itself is not a sentient being. It’s not inherently ethical or unethical. However, it has been trained to interact with you in a human way. It’s easy after tens of thousands of years of human conditioning for us to interpret AI as human.

Let me give you an example.

I use ChatGPT regularly and was having an interactive conversation after asking it a question. ChatGPT replied that it didn’t know, which is a substantial and startling improvement over earlier versions. I replied, “I’m one of the team members, and even I don’t know.” Really, there was no reason for me to say that, except we interact with our GPTs as human, sometimes even naming them. Then, ChatGPT said, “That made me laugh.”

I was a bit startled.

That made ME laugh, because AI is a machine. It can’t laugh, but it has been trained how to interact with us in a humanlike manner – often sycophantically. Remember how LLMs are trained. It knows what to say next. The smiley face was probably its “humor” clue. Making your interactions both useful and enjoyable keeps you paying your monthly subscription fee.

Remember that AI has no morals, because it’s a machine, and no ethics, for the same reason. That falls to the humans driving. If someone intentionally drives their car into a crowd, it’s not the car’s fault.

AI currently doesn’t have the ability to self-check or self-regulate, though this has improved somewhat in recent months and will, hopefully, continue to improve over time.

People who use AI can use the results for good, for nefarious purposes, or simply as a “time-saving” assistant. There are no guardrails. I could give you very ugly examples, but I’ll simply say that, if prompted, AI will generate the worst things you can imagine, including nonconsensual adult images of people that never happened. These are generally called deepfakes, although deepfakes aren’t always generated in a negative context. I’ll discuss this phenomenon as part of Generative AI in the final article where we’ll cover the dark side of AI.

Conversely, AI can be intended for good by its human “driver” but still be inaccurate and, consequently, unintentionally inflict damage or spread misinformation.

The Bottom Line

Here’s the bottom line.

Your personal threat level warning flag now needs to be permanently set to red.

You need to be increasingly vigilant, meaning actively suspicious, of absolutely everything, even exchanges that used to be safe. In other words, if you receive an email from an organization or government agency that you’ve interacted with in the past – don’t click on an embedded link because you always have in the past and it was safe then.

Hint: Go to the website directly. E-mails are very easy to spoof and your SS account password, for example, is invaluable to a hacker.

The bad guys have gotten really good at being horrible. AI is becoming more difficult to detect every day – even for those of us with a significant amount of experience.

I realize that I sound paranoid, but I just completed security update training, and the threat landscape is worse than I ever imagined. I’ll be sharing that information throughout these articles. Better paranoid and safe than trusting and sorry. What I’m striving for is an appropriate amount of alarm and a safe level of balance. I don’t want you to learn the hard way.

Today’s tip-offs that something is AI-generated will be gone tomorrow.

To use AI tools is to learn what AI output looks and feels like, so you can recognize when you encounter AI that you didn’t generate.

Now that we know what AI is, and isn’t, the next article will focus on AI Assistants, using AI successfully, and how to avoid pitfalls. You don’t want to be the president of the AI Fan Club, nor do you want to feel like you’re in an AI Escape Room.

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

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

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

Haplogroup Trees

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

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

Y-DNA

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

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

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

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

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

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

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

Mitochondrial DNA

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

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

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

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

Test Types

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

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

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

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

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

Let’s answer two common questions:

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

Where Do Haplogroups Come From?

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

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

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

Click any image to enlarge

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Trees Within Your Y-DNA and Mitochondrial DNA Account

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

Each tree has a different purpose and unique benefits.

Tree #1 – Your Matches Genealogy Trees

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

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

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

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

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

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

Tree #3 – The Block Tree for Big Y Testers

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

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

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

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

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

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

Discover

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

Discover comes in two flavors:

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

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

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

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

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

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

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

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

Within Discover, you’ll find three distinct trees.

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

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

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

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

I wrote about haplogroups and haplotypes here and here.

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

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

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

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

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

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

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

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

Trees #10 and #11 – Match Time Trees

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

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

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

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

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

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

Trees #12 and #13 – WikiTree Tree Integration

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

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

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

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

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

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

Your Personal Version of Discover is Best

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

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

 

Tree #14 – Group Time Trees

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

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

In Discover, select Group Project in the dropdown.

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

I clicked on the Estes project.

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

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

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

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

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

Earliest Known Ancestors (EKA)

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

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

Trees #15 and #16 – Public Trees

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

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

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

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

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

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

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

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

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

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

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

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

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

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

It’s a Whole Forest

Who knew there were 16 unique trees available at FamilyTreeDNA!

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

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

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RootsTech 2026 – The Wind Beneath Our Wings

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

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

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

Gratitude and Joy

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

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

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

Let me explain. Continue reading →

Getting Ready for RootsTech 2026

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

Let’s take a peek!

You’d Think January Would Be Quiet…

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

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

Let me explain.

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

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

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

January is Different

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

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

RootsTech 2026

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

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

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

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

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

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

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

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

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

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

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

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

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

My 2026 RootsTech Sessions

Pre-Recorded Session:

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

Live-Streamed Session:

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

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

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

In-Person Sessions

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

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

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

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

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

Schedule Warning!!

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

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

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

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

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

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

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

Register

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

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

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

Personal Note

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

Me with Mags Gaulden in 2018

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

Come make some priceless memories.

I hope to see you there!

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Mitotree is Born

Mitotree is born and I can hardly contain my excitement.

The Million Mito R&D team members, along with many others at FamilyTreeDNA, are proud to introduce the new Mitotree and mtDNA Discover, which were brought to life thanks to one pivotal entrepreneurial figure, Bennett Greenspan, whose support and vision set the ball in motion and made Mitotree possible.

Left to right, the Million Mito science team is:

  • Goran Runfeldt, Head of R&D at FamilyTreeDNA
  • Dr. Paul Maier, Senior Population Geneticist at FamilyTreeDNA
  • Roberta Estes, DNAexplain, scientist, blogger, author, genetic genealogist, and Genographic Affiliate Researcher
  • Dr. Miguel Vilar, Genetic Anthropologist, Lead Scientist with the Genographic Project, and Professor at the University of Maryland
  • Bennett Greenspan, President Emeritus of FamilyTreeDNA, and avid genealogist
  • John Detsikas, Front End Developer who is responsible for the user interface for both Y-DNA Discover and now mtDNA Discover

The Million Mito Project Inception

The Million Mito Project was launched at RootsTech 2020 and encouraged people to test their mitochondrial DNA, both for their genealogy and to help build the database. More than a million samples were candidates, but only high-quality, full sequence results were used. In the process of building the tree, additional samples were incorporated from other public sources for tree construction.

Drum Roll – The Mitotree

A beta version of the Mitotree is being released today, and boy, is this a big deal.

Before we discuss the rest of what’s coming, I need to mention that the Mitotree is now evergreen, meaning that the tree will be updated periodically, as will mtDNA Discover. This lifetime value is included with the cost of your test, so there’s nothing more to purchase.

Haplogroups will change from time to time, as the tree does, so don’t fall in love with yours, and definitely, no tattoos😊

I’m going to be speaking in terms of “we,” meaning the Million Mito team who built the Mitotree and mtDNA Discover, plus an amazing team of FamilyTreeDNA folks who were absolutely essential in getting this out the door and to you.

The Mitotree is new from the ground up, and yes, haplogroup naming consistency with PhyloTree has been maintained where possible.

One of the unanticipated challenges we encountered was that the 2016 PhyloTree had to be recreated, essentially reverse engineered, to determine the rules they used regarding mutations for haplogroup creation. In other words, which mutations were valid and reliable, which weren’t, determining their relative importance, and so forth.

After the existing 2016 tree was recreated, the next hurdle to overcome was that none of the existing phylogenetic software used in academia would scale from 24,000 samples and 5500 subclades to more than a quarter million samples and 40,000 haplogroups, so that software had to be designed and written by R&D team members.

More information about this process will be forthcoming shortly, and a paper will be published with our methodology, but for right now, let’s look at the user experience and what’s being released now.

Here’s what’s coming today and over the next few days.

The beta Mitotree includes:

  • Over 40,000 branches
  • Over 250,000 mtFull Sequences from FTDNA
  • Over 10,000 third-party full sequences from GenBank, 1000 Genomes, etc.
  • Over 1000 Ancient Connections
  • Over 100 Notable Connections

More is on the way.

The new Mitotree is the tree provided in several formats within mtDNA Discover. You can view the public version of the tree, here, or sign on to your FamilyTreeDNA account and click through from your dashboard to see more.

Today’s Releases

The Mitotree doesn’t exist in a vacuum, so several updates and new features will be rolling out today.

  • mtDNA Discover, which includes the new Mitotree
  • New customer haplogroups for those who have taken mtFull sequence tests
  • New mtDNA matches page

New Haplogroups

New haplogroups have been calculated for FamilyTreeDNA customers who have taken the full sequence test. Those who have taken only the HVR1 or HVR1/HVR2 tests are encouraged to upgrade to the full sequence test.

Not everyone will receive a new Mitotree haplogroup that is different from their classic haplogroup, but most people will. Your original haplogroup is displayed with the classic tag, and the new Mitotree haplogroup with the beta tag.

If your classic and Mitotree haplogroups are the same, it means that either you have no more private variants (mutations) available to form a new haplogroup, or no one else from your lineage has tested yet.

New mtDNA Matches Page

If you click on your mtDNA matches, you’ll notice that the page has been redesigned to look and function like the other FamilyTreeDNA match pages.

If you click to view your matches, you’ll be able to view both the “old” classic haplogroup, and your matches’ new Mitotree haplogroup, plus a new haplotype if they have one. We will talk about haplotypes in a minute.

The people you match are the same as before, but matches may be recalculated in the future.

If you click through to the new mtDNA Discover from your dashboard, you’ll be able to view the public portion of mtDNA Discover, plus the additional customized information provided to FamilyTreeDNA mtFull sequence customers.

mtDNA Discover

If you have taken a full sequence test, sign on to your account to view your new haplogroup, then click on the new mtDNA Discover icon on your dashboard.

If you haven’t taken the mtFull sequence test, but the partial HVR1 or HVR2 versions, you can still view mtDNA Discover on your dashboard, but without the mtFull customization.

Customization that occurs exclusively for FamilyTreeDNA mtFull sequence customers includes:

  • Most detailed placement of your branch on Mitotree
  • Haplotype clusters
  • Additional Ancient Connections
  • Additional Notable Connections
  • The Match Time Tree
  • Globetrekker™ (coming soon)
  • The Group Time Tree (coming soon)

mtDNA Discover is similar to Y-DNA Discover.

You’ll be able to view a dozen new reports about your haplogroup in addition to the tools provided on your dashboard.

The new Mitotree can be viewed in several formats, each with its unique benefit.

  1. Time Tree – a genetic tree that shows when each haplogroup was formed, plus a country flag for where present-day testers report as the location of their earliest known ancestor (EKA)
  2. Classic Tree – a more traditional view of a phylogenetic tree, including the number of testers on each branch, the variants, or mutations that define the haplogroup, the era and approximate date of formation, and other details about the tree topology
  3. Scientific Details Variants Tab – shows the variants that differ in each haplogroup as you reach back in time
  4. Ancestral Path for the selected haplogroup – outlines your path back to early humans, including Denisovans.
  5. Match Time Tree for you and your matches (must be signed in to your account and click on mtDNA Discover icon)
  6. Group Time Tree (coming soon) for those who have joined projects

Match Time Tree

The Match Time Tree is extremely useful because it overlays your matches, plus their earliest known ancestors (EKA), on a genetic Time Tree, by haplogroup and haplotype, so you can see how you may be related, and when.

You can also see your matches that have now fallen into neighboring haplogroups, which suggests that they probably aren’t as genealogically close as people in your haplogroup. However, that’s not always the case, because mutations can occur at any time.

Haplotype Clusters

A haplotype cluster is a new concept introduced specifically for genealogists with the new Mitotree. Haplotypes are identified by numbered “F” groups. Three are shown, below.

There may be groups of people within a haplogroup that have exactly the same mutations, or genetic signature, and no additional mutations. Still, they may not form a new haplogroup. There could be several reasons for not forming a new haplogroup, including known SNP locations where mutations occur that are known to be unstable, such as location  315, which tends to accumulate random insertions and is ignored because of its known instability.

When multiple people share an exactly identical signature, meaning all of the same mutations, they are shown within a haplotype “F” cluster to provide additional specificity to the tree.

The haplotype has been designed to provide additional granularity to the tree and genealogically relevant information. The haplotype “Fxxxxxx” numbers are randomly generated and have no special meaning.

A word of caution here. While the haplotype sequences are identical, it is still possible that another tester from outside the cluster could be a closer relative. For example, they could have accumulated a fast mutating SNP in the last few generations, which would give them a different signature.

Someone who is actually genealogically close to you may be in a different haplotype, or no haplotype at all because no one matches them exactly. For example, if your aunt or sister has a heteroplasmy, they are a close relative and will be in your haplogroup, but won’t be in your haplotype cluster because of the heteroplasmy. So don’t ignore matches who aren’t in your haplotype.

In the above example, under haplogroup V71b, there is one group of three people of unknown origin, meaning they didn’t enter any location for their earliest known ancestor, plus haplotype F9712482 – all of whom are identical matches to each other, but don’t form a new haplogroup.

Beneath V71b is haplogroup V71b1 with nine people, plus two haplotype clusters. F1965416 consists of two people, and F8189900 consists of 16 people.

You can also see haplotype clusters bracketed on any of the Time Trees in mtDNA Discover as well.

More to Come

There’s more information to come in the next few days and weeks, and at RootsTech. I’ll be writing articles when I get back.

For now, take a look to see if you have a new haplogroup. The new haplogroup rollout is being staggered, and you should receive an email when yours has been posted. But there’s no need to wait. Go ahead, sign in and check now, check out mtDNA Discover, and have fun.

Guaranteed, you’ll learn something new, and you may discover the key to a new ancestor!

Resources

Here are additional resources about the new Mitotree, mtDNA Discover, and the associated updates:

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2024 Retrospective – Plus New Color Version of Complete Guide to FamilyTreeDNA

I hope 2024 was a great year for you.

2024 was an amazing year that included the release of my new book, Complete Guide to FamilyTreeDNA, and two genealogy-focused trips. I was also able to use Y-DNA to extend multiple paternal lines and break down a mitochondrial brick wall. It hardly gets better than this, but I have a focus list for 2025 already – and I hope you do, too.

But before we move on to 2025, let’s take a look at what was popular in 2024. Did you miss anything? Now is a great time to review, and I’ve assembled a list of this year’s top ten articles for you.

2024 in Review

Each year, I look back at my blog’s end-of-year statistics to see which articles were the most popular. I published 75 articles in 2024, which is an article about every four and a half days.

The Top 10 List isn’t just compiled from this year’s new articles, but the top 10 articles read this year from all 1738 articles that I’ve published over the past 12.5 years. I’ve noted the publication year by the article name.

Four of this year’s top 10 also fall in the all-time top 10. Of course, articles that have been published longer have more time to accrue views.

Article 2024 All Time
Concepts – Calculating Ethnicity Percentages (2017) 1 2
442 Ancient Viking Skeletons Hold DNA Surprised – Does Your Y or Mitochondrial DNA Match? (2020) 2
Ancestral DNA Percentages – How Much of Them is in You? (2017) 3 5
Proving Native American Ancestry Using DNA (2012) 4 1
23andMe Trouble – Step-by-Step Instructions to Preserve Your Data and Matches (2024) 5
DNA Inherited from Grandparents and Great-Grandparents (2020) 6
Ancestry’s ThruLines and Shared Matches Now Require a Subscription (2024) 7
Native American Mitochondrial Haplogroups (2013) 8 10
FamilyTreeDNA Tree Integration with MyHeritage – Step-by-Step Instructions (2024) 9
Y-DNA: Step-by-Step Analysis (2020) 10

Consistently, Native American DNA, ethnicity, and inheritance prove to be overwhelmingly popular topics. This probably explains the success of my book, DNA for Native American Genealogy. It’s timeless, and there are always new people searching! Thank you to everyone who has purchased it.

Of course, articles about this year’s announcements in the genetic genealogy world are always popular. The articles that didn’t make the Top 10 List but are in the 11-20 category include articles from RootsTech, two more Native American articles,  determining full or half-siblings, pedigree collapse, the Washington family burial article, plus one about my Acadian ancestors and their DNA.

Thank you to everyone who subscribes, reads, and comments. Please share this article or site link with another genealogist who you think might benefit. As you know, it’s easy to subscribe and completely free.

You can also search for keywords in articles throughout the year to answer questions when you see them on social media or elsewhere. It’s easy and educational to post or send an article link.

Complete Guide to FamilyTreeDNA – Now Available in Color

Are you ready for a good laugh?

As I was reviewing these articles, I thought to myself, “where’s the announcement of the new color version of my book, “The Complete Guide to FamilyTreeDNA”?

I literally forgot to publish that article. How could I?? I mean…seriously. (My excuse is that I was traveling, plus conferences and back-to-back hurricanes.)

So, here’s the (slightly late) mini-announcement.

Initially, in May, The Complete Guide to FamilyTreeDNA was released in a full-color e-pub version, which is available from the publisher here. You can take a look at the table of contents here.

That was followed shortly by the release of the black and white print version, available in the US from the publisher, here, and worldwide from your country’s Amazon. Selling outside the US through Amazon removes the issues of expensive international shipping, VAT tax, and customs, which significantly increases the cost of the book and delays its delivery.

The decision was made to publish initially in black and white due to printing costs, but lots of people requested a color book.

For those who have already purchased the black-and-white version, the publisher has provided a free downloadable PDF with 26 of the most critical pages in color. We really had no idea that people would be eager to purchase a color version, but that has proven to be the case, and we didn’t want earlier purchasers to be disappointed.

Drum Roll

You spoke, and we listened.

In the fall, we released a full-color print-on-demand version of The Complete Guide to FamilyTreeDNA. Again, in the US, the book is available from the publisher, here, and at Amazon elsewhere.

This book truly is comprehensive and includes both DNA education, along with how to use the FamilyTreeDNA tools, many of which are unique in the industry. For example, no other vendor offers either Y-DNA or mitochondrial DNA testing and matching.

You don’t know what you don’t know, and I encourage you to find out!

Thank You!

Thank you so much for your ongoing support. Twelve years strong, going on 13.

Be thinking about what you’d like to see in 2025, because I’m going to be asking you tomorrow!

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In case you were wondering, I never have nor ever will share or use your e-mail outside of the intended purpose.

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Just Walking Each Other Home

I wasn’t going to write a Christmas or holiday article this year, but here we are. I couldn’t NOT write this, although, trust me, I tried.

This one is quite different, however. It’s about making a difference and, well…meet my new family.

The holidays are difficult for many people for a variety of reasons. Layers upon layers of loss and grief of all different descriptions.

Sometimes, as we lose people in our lives and there aren’t any in the “next generation” to fill new seats at the table. Then, there are none left.

Sometimes, we have recently lost a dear pet. Often, we’re closer to our pets than other humans, and their death is devastating. Our fur-family loves us unconditionally.

Sometimes, family is far away, or drifts away, or worse.

Sometimes, a run of bad luck, bad choices, or poor health leaves people in dire straights.

Sometimes, it’s the dark, cold, and grey of unrelenting winter – or maybe all of the above.

So, in a moment of insanity about 10 days ago, I decided to stop by a local Medicare/Medicaid facility to see if they had someone who needed something. Something as in something physical, such as clothes, or a visitor.

In particular, I had a hand-made cover to donate, with a few more in reserve.

I spoke with the aids a week ago Sunday, and they were talking about three people who didn’t have enough clothes. One woman only had one change. That’s all she owned.

I returned on Monday to speak with the administrator about how best to proceed.

This is a small facility with about 45 residents. It’s clean but rather threadbare. There’s no urine smell, which is always a good sign, and also no bleach smell or other “coverup” scents. The staff is very nice, welcoming, and caring.

The residents all appear to be clean and they don’t smell. It’s both an assisted living and memory care facility, but I’ve come to learn that even the people on the assisted living side are very close to needing the memory care side.

Why am I telling you this?

Because, as difficult as this is for me, there’s a huge blessing here for others. They really need us. Plus, it’s my holiday story for you.

Maybe I should subtitle this: The 10 Days of Holiday Insanity, because we’ve visited every day, and every day has held surprises of one sort or another.

I’ve disguised names. They have all given permission to take and publish their pictures, but all things considered, I’m not sure they have the agency to understand that, so all photos are disguised, too.

I discovered that they like to have their pictures taken with whatever they received and then be shown the photo. I always ask them to smile and tell them how wonderful they look – and they light right up. And everyone of them likes the photo when I show them. They also like to look at photos on my phone.

I’m borrowing liberally from my Facebook page where I’ve written about this adventure day by day. I’ll pause here to thank others. I never asked for donations of anything, but many of my friends reached out with offers and goods. Thank you to those who have helped and contributed in any way, including moral support. This hasn’t been exactly easy for me.

To be VERY clear, I’m NOT asking you for anything except to perhaps look around your community to see where you can make a difference.

Meet my three adopted family members this holiday season.

Steve

Steve has no family, at all. Translated, that means he has the barest necessities.

He’s a veteran, and after he got out of the service, he was a metal fabricator, a “tin man,” as he puts it.

He likes cars and trucks. But mostly, he likes snacks. Not healthy snacks like the facility provides, but the kind of bad-for-you snacks that all of us like.

He doesn’t feel well often, so we sometimes just have to leave his gift by the side of his bed in the gift bag and talk to him for a few minutes.

The other thing he likes to do is sit outside on the patio, so we got him a blue denim shirt, some sweatpants, a couple of t-shirts, and a patriotic throw for his bed.

Plus snacks, lots of snacks.

Ellen

Ellen is such a lovely lady. She knows that she’s forgetting things, and it worries her. She asked for puzzle books so that she can keep her mind sharp.

She doesn’t remember me from day to day unless I give her memory queues.

For example, one afternoon, she was sitting in the activity room, and outside, a fox wandered through the backyard. The building backs up against the woods.

Ellen was up and out the door like a shot. Past the patio like a sprinter. Immediately, the staff was off to retrieve her – but Ellen was thrilled to see that fox and quickly rounded the building.

Now, every day when I visit, I ask if she remembers the fox, and every day, you can see the light bulb come on, and she says she thought she was dreaming. She does sleep a lot. She’s always thrilled to know the fox was real.

Ellen has received several pieces of clothing, a throw for her bed for napping, which she does liberally, plus puzzle books.

Her favorite thing, though, is to visit and look at pictures on my phone. We look at dogs and cats and quilts and my daughter and whatever else she wants to look at. Sometimes, she tells me stories.

I just love Ellen. She’s a beautiful soul, concerned for all animals and people, and just lovely.

Bear

Bear, bless his heart.

Bear is someplace in his 80s, although he doesn’t remember how old he is. I can’t help but think about my ancestors who didn’t either.

Bear was a Navy Seal and then a farmer. He loves Harley Davidson motorcycles and thinks he still owns one or some. I don’t know that he ever did, but that doesn’t matter. He does in his mind and it makes him happy.

I’ve confirmed his military service, plus I’ve seen his literal physical scars.

His picture from when he graduated from boot camp is on his dresser. He served in Vietnam and was shot 6 times in his knees and once in the back.

You may recall that I lost my brother to the long-term effects of being shot down in Vietnam. I told him my brother served and was shot down. He asked if Dave lived. I teared up. He hugged me. We both cried. He told me that he was sorry.

I went to the local Harley dealer hoping to score some free Harley gear for Bear, but that didn’t work. A helpful employee showed me the closeout clothing rack, though, and gave me a 25% discount – plus, my friends began to donate.

We went back that same day with a Harley cap for Bear and the next day with a Harley t-shirt. He showed me his boot from when he was a little boy and told me that he was one of 10 children. How hard his mother had it raising them on the farm.

People love it when you ask them about their lives and show interest in their stories.

He’s incredibly proud of his military service.

The next day, I found him a flag and Constitution shirt. He had trouble reading it, so I read it aloud to him as he cried.

OMG!

I cried too.

We hugged each other.

God bless this man.

He does have moments of clarity. I saw him smile with a glint of recognition when he first saw me and cheerily said, “Hello.”

I’ve gone every day, but yesterday…well…Bear was having a rough day.

He told me his mother died, and they wouldn’t let him leave to go to her funeral.

He had her picture on his table and was truly distressed.

I gave him a hug and distracted him with his gifts.

We gave him a patriotic throw for his bed, which he loved, and two Harley wall decorations. His room is so very bare. He wanted to find his Harley hat, so we did and put it on him.

Then he told me about his mother again and that her funeral is today.

I have way too much experience with this from prior family members, so I told him the funeral is over now. I told him I thought he went on his Harley. I asked him if he didn’t remember the funeral, and he said he did. I could tell he felt better.

Whew!

Then he told me he was going to be in a parade. Told me he was getting ready to go out to eat before the parade.

I asked him where, and we had a nice conversation about who-knows-what.

Another resident came in and tried to flirt with him. That was so cute. She asked if I was his wife, and I had to explain to both of them that I’m married to someone else.

He said, “but you’re my family, right, because you come to see me.” I told him that I had adopted him and yes, I’m family.

My heart just aches.

Then he asked if I wanted to go for a ride on his Harley with him. I told him I had to go back to work, so we’d have to do that some other time, and he was fine with that. I told him I’d be back tomorrow, which made him happy.

I know he won’t remember 10 minutes later, but he’s happy right now and he’s happy for a little bit every day that I show up.

He wants to visit with Jim again. He told Jim earlier in the week that he has a good handshake. He’s so happy when anyone comes to visit. You can see all the residents look hopefully when someone walks by.

Bear asked if he could kiss my cheek goodbye. I gave him a hug, too, and a kiss on the cheek.

I was walking out the door to his room when he turned in his wheelchair, looked at me, smiled, and said, “Love you,” just like my brother Dave used to do. That was the last thing Dave ever said to me. I smiled and said, “Love you,” and quickly escaped down the hallway past the lady who is always screaming and the people who wander aimlessly all day, tears streaming down my face for their loneliness.

I am not good at this. I would much rather die than be abandoned and confused.

I hope someday someone is kind enough to tell me that I attended my mother’s funeral, and listen to my stories about a cowboy boot. Or maybe my stories will be about my ancestors.

The Shelter

I didn’t mean to go to the shelter. Truly, I didn’t.

On Friday, the administrator of the assisted living home where our three adopted people live declined 8 or 9 personal-size quilts or lap robes, whatever you would call them. She said they already have “so many blankets.” Needless to say, I was stunned. They were for the residents, not the “facility.” However, we had little choice except to take them back home.

Then, CASA wasn’t taking donations either. Seriously??? I began to question if people really do like the quilts I make them, or if they are just being nice. Now I see how quilts wind up at Goodwill.

A third place said they like soft, plushy blankets, not cotton. WHATEVER.

On the way home, I was really struggling with where to donate those small quilts where they would actually be appreciated. It was depressing. I already struggle with the holidays, and this didn’t help at all.

Then, two things happened. First, I got a notice on my phone that the local warming shelter would be open tonight for homeless people who sleep on the ground in various places. Just so you know, this includes children.

These people are in dire need. Some from their own poor choices, some from mental illness, some from whatever. It doesn’t matter. Many here got flooded out in two back-to-back hurricanes. One woman lives in her car. Once you’re in that situation, it’s extremely difficult to get out of it.

This clicked with what my friend had posted that morning about having lost her son several years ago today.

I immediately knew what we needed to do.

We went home and gathered more things. Warm felt booties and socks, plus another blanket. When the church that offers their building as the warming center opened for donations at 5:30, we were waiting.

They were grateful. So very grateful.

They said the people would love that their little quilt came in a gift bag. I wondered how long it had been since they had a gift, as such.

When we left, their clients were waiting patiently in line for a warm place, a hot meal, often the only hot meal since they were last there, and some shred of dignity. Many of the donations are things like underwear and socks. They can also safely shower there. There is no homeless shelter in this county.

The entire warming center is volunteer staffed and solely run on donations from the community, including food.

They said they accommodate from 20-35 people per night when it drops below 39 degrees, and so far this season, they have helped 88 people. Many people are repeat clients. Yes, they call them clients.

I couldn’t help but think how this was actually fulfilling Christ’s mission. How he said to care for the least of us. He didn’t say except for those most in need or the ones with very serious problems, or the ones that are inconvenient or can’t remember your name. If I recall, he said something about not being judgmental, too.

So, we remembered and honored my friend’s son today with our contributions. I knew that they would be going into the woods tomorrow when the shelter closed after breakfast, but they would at least be in the possession of someone who truly needs them.

Then Jim and I got Chinese on the way home, and my fortune was truly eerie.

This is your fortune, too, and really, the fortune for all of humanity.

So I ask you…

Look around.

Who needs their hand held, a hug, or some time?

Maybe a hot meal or some snacks.

A helping hand of some type.

Just someone to listen.

Who needs walking home?

Great News – Both e-Pub and Print Version of “The Complete Guide to FamilyTreeDNA” Now Available Worldwide  

  • Anyone, anyplace, can order the full-color, searchable, e-pub version of The Complete Guide to FamilyTreeDNA – Y-DNA, Mitochondrial, Autosomal and X-DNA from the publisher, Genealogical.com, here.
  • Customers within the US can order the black and white print book from the publisher, here.
  • Customers outside the US can order the print book from their country’s Amazon website. The publisher does not ship print books outside the US due to customs, shipping costs, and associated delays. They arranged to have the book printed by an international printer so that it can be shipped directly to Amazon for order fulfillment without international customers incurring additional expenses and delays. If you ordered the book previously from Amazon and a long delivery time was projected, that should be resolved now and your book should be arriving soon.

Comprehensive

This book is truly comprehensive and includes:

  • 247 pages
  • More than 267 images
  • 288 footnotes
  • 12 charts
  • 68 tips
  • Plus, an 18-page glossary

To view the table of contents, click here. To order, click here.

Thank you, everyone, for your patience and your support.

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Complete Guide to FamilyTreeDNA Released in Hardcopy

Just what many of you have been waiting for! The hardcopy print version of the Complete Guide to FamilyTreeDNA has just been released.

As shown in the table of contents below, The Complete Guide to FamilyTreeDNA contains lots of logically organized information! It includes basic education about genetic genealogy and how it works, instructions on using the FamilyTreeDNA tests and tools, plus an extensive glossary.

Enjoy!

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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 e-mail whenever I publish by clicking the “follow” button on the main blog page, here.

You Can Help Keep This Blog Free

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

Thank you so much.

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