Where Did My Mitochondrial DNA Haplogroup Come From?

Mother’s Day is approaching, so I’m writing articles about mitochondrial DNA inspired by the most common questions in the Mitochondrial DNA for Genealogy Facebook group. I’ll be adding these articles to the Mitochondrial DNA Resource page, here.

FamilyTreeDNA has already started their Mother’s Day sale where both the mitochondrial DNA test and Family Finder are both on sale. Take a look.

I can’t believe how much the prices have dropped over the years – as the technology has improved. I took the full sequence mitochondrial DNA test when it was first offered and I think it was something like $800, as was the first autosomal test I ordered lo those many years ago.

Today, these tests are $139 and $59, respectively, and are critical tools for everyone’s genealogy.

Where Did My Mitochondrial DNA Haplogroup Come From?

This is one of the most common questions about mitochondrial DNA. Everyone wants to know something about their haplogroup.

The answer is multi-faceted and depends on the question you’re actually trying to answer.

There are really two flavors of this question:

  • Where did my ancestors come from in a genealogical timeframe?
  • Where did my ancestors come from before I can find them in genealogical records?

Clearly, the timeframes involved vary to some extent, because when records end varies for each ancestral line. Generally speaking, genealogy records don’t extend back beyond 500 years or so. Whenever your genealogy records end, that’s where your haplogroup and match information becomes critically important to your research.

Fortunately, we have tools to answer both types of questions which actually form a continuum.

Some answers rely on having taken a mitochondrial DNA test at FamilyTreeDNA and some don’t.

  • We’ll discuss finding haplogroup information for people who have taken a (preferably full sequence) mitochondrial DNA test at FamilyTreeDNA.
  • We’ll discuss how people who have obtained their haplogroups through autosomal testing at other vendors can find information.
  • We’ll talk about finding haplogroup information when other family members have tested who carry the mitochondrial DNA of ancestors that you do not.

Tools exist for each of these situations.

Genealogical Timeframe

If you’re trying to answer the question of where other people who carry your haplogroup are found in the world, that question can be further subdivided:

  • Where are the earliest known matrilineal ancestors of my mitochondrial DNA matches located?
  • Where are other mitochondrial DNA testers who carry my haplogroup, even if I don’t match them, found in the world?

Let’s start at FamilyTreeDNA and then move to public resources.

FamilyTreeDNA

Mitochondrial DNA Tests

FamilyTreeDNA provides a great deal of information for people who have taken a mitochondrial DNA test. We’ll step through each tab on a tester’s personal page that’s relevant to haplogroups.

To find the location of your matches’ most distant ancestors, you need to have taken the mitochondrial DNA test at FamilyTreeDNA in order to obtain results and matches. I know this might seem like an obvious statement, but you’d be surprised how many people don’t realize that there are separate tests for Y and mitochondrial DNA.

Your most detailed, and therefore most accurate and specific results will result from taking the Full Sequence test, called the mtFull test and sometimes abbreviated as FMS (full mitochondrial sequence.)

Taking a full sequence test means you’ve tested all three different regions of the mitochondria, HVR1, HVR2, and the Coding Region. Don’t worry about those details. Today, the Full Sequence test is the only test you can order, but people who tested earlier could order a partial test. Those people can easily upgrade today.

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You can see, in the upper right-hand corner of the mitochondrial section of my personal page, above, that I’ve taken both tests. The “Plus” test is the HVR1 and HVR2 portion of the test.

If you haven’t taken any mitochondrial DNA test, then the mitochondrial section doesn’t show on your personal page.

If your Plus and Full buttons are both greyed out, that means you took the HVR1 level test only, and you can click on either button to upgrade.

If your “Full” button is greyed out, that means you haven’t tested at that level and you can click on the Full button to upgrade.

Entering Ancestor Information is Important

Genealogy is a collaborative sport and entering information about our ancestors is important – both for our own genealogy and for other testers too.

Your matches may or may not enter their ancestor’s information in all three locations where it can be useful:

  • Earliest Known Ancestor (found under the dropdown beneath your name in the upper right-hand corner of your personal page, then “Account Settings,” then “Genealogy,” then “Earliest Known Ancestors”)
  • Matches Map (found on your Y or mtDNA personal page tab or “Update Location” on Earliest Known Ancestors tab)
  • Uploading or creating a tree (found under myTree at the very top of your personal page)

Please enter your information by following the notes above, or you can follow the step-by-step instructions, here. You’ll be glad you did.

Your Haplogroup

You’ll find your haplogroup name under the Badges section of your personal page as well as at the top of the mtDNA section.

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The mtDNA section at FamilyTreeDNA has five tabs that each provides different pieces of the puzzle of where your ancestors, and therefore your haplogroups, came from.

Checking all of these tabs in the mtDNA section of your results is critical to gather every piece of evidence provided by your matches and the scientists as well. Let’s take a look at each one and what they reveal about your haplogroup.

Let’s start with your matches.

Matches

On the matches page, you’ll only be matched with people who carry the same haplogroup – or at least the same base haplogroup.

The haplogroup level of your matches depends on the level of test they have taken. In other words, if your match has only taken the HVR1 level test, and they only have a base haplogroup of J, then you’ll only see them, and their haplogroup J, on your HVR1 match page. If they have tested at a higher level and you match them at the HVR1 level, you’ll see the most specific haplogroup possible as determined by the level they tested.

The (default) match page shows your matches at the highest-level test you have tested. In my case, that’s the “HVR1, HVR2, Coding Region” because I’ve taken the full sequence test which tests the entire mitochondria.

At the full sequence level match page, I’ll only see people who match me on the same extended haplogroup. In my case, that’s J1c2f.

Viewing your matches’ Earliest Known Ancestor shows where their ancestors were located, which provides clues as to where your common haplogroup was found in the world at that time. Based on those results, the geographic distribution, what you know about your own ancestors, and how far back in time, your matches’ information may be an important clue about your own ancestry.

Generally, the closer your matches, meaning the fewer mutations difference, the closer in time you share a common ancestor. I say “generally,” because mutations don’t happen on a time schedule and can happen in any generation.

The number of mutations is shown in the column “Genetic Distance.” Genetic Distance is the number of mutations difference between you and your match. So a 3 in the GD column means 3 mutations difference. A GD of 0 is an exact match. At the HVR1 and HVR2 levels, no genetic distance is provided because only exact matches are shown at those levels.

The little blue pedigree icons on the Matches page indicate people who have created or uploaded trees. You’ll definitely want to take a look at those. Sometimes you’ll discover that your matches have added more generations in their tree than is shown in the Earliest Known Ancestor field.

Is Taking the Full Sequence Test Important?

Why is taking the full sequence test important? Looking at my HVR1 matches, below, provides the perfect example.

This shows my first four HVR1-only matches. In other words, these people match me on a small subset of my mitochondrial DNA. About 1000 locations of the total 16,569 are tested in the HVR1 region. You can see that utilizing the HVR1 region, only, the people I match exactly in that region have different extended, or full haplogroups, assigned when taking the full sequence test.

Crystal and Katherine have both taken the full sequence test as indicated by FMS (full mitochondrial sequence,) and they are both haplogroup J1c2f, but Peter is haplogroup J1c2g – a different haplogroup.

Peter is shown as an exact match to me at the HVR1 level, but he has a different full haplogroup, so he won’t be shown as a match at the HVR1/HVR2/Coding Region (full sequence) level.

Crystal and Katherine will match me at the full sequence level if we have three or fewer mutations difference in total.

Susan has only tested to the HVR1 level, so she can only be assigned to haplogroup J from those 1000 locations. That tells us that (at least) one of mutations that defines haplogroup J resides in the HVR1 region.

At the HVR1 matching level, I’ll be matched with everyone I match exactly so long as they are in haplogroup J, the common denominator haplogroup of everyone at that level.

If Susan were to test at the full sequence level, she would obtain a full haplogroup and I might continue to match her at the full sequence level if she is haplogroup J1c2f and matches me with three or fewer mutations difference. At the full sequence level, I’ll only match people who match my haplogroup exactly and match at a genetic distance of 0, 1, 2 or 3.

Now, let’s look at the Ancestral Origins tab.

Ancestral Origins

The Ancestral Origins tab is organized by Country within match level. In the example above, I’ve shown exact matches or GD=0.

The match total on the Ancestral Origins tab shows the number of people whose ancestors were from various locations – as entered by the testers.

The most common places for my full sequence exact matches are in Norway and Sweden. That’s interesting because my ancestor was found in Germany in the 1600s.

There is also a comments column, to the right, not shown here, which may hold additional information of interest such as “Ashkenazi” or “Sicily” or “Canary Islands.”

The Country Total column is interesting too because it tells you how many people are in the database who have indicated that location as ancestral. The Match Percentage column is pretty much irrelevant unless your haplogroup is extremely rare.

Matches Map

The matches map falls into the “picture is worth 1000 words category.”

This is the map of the earliest known matrilineal ancestor locations of my full sequence matches.

My ancestor is the white pin in Germany. Red=exact match, orange=1 mutation difference, yellow=2 mutations difference. I have no GD=3 matches showing.

By clicking on any pin, you can see additional information about the ancestor of the tester.

You can also select an option on the map to view lower testing levels, such as my HVR1 matches shown below.

While some people are tempted to ignore the HVR1 or HVR2 Matches Maps, I don’t.

If the question you’re trying to answer is where your haplogroup came from, viewing the map of where people are located who may match you more distantly in time is useful. While we know for sure that some of these people have different full haplogroups, we also know that they are all members of haplogroup J plus some subclade. Therefore, these matches shared a common haplogroup J ancestor.

J subgroups are clearly European but some are found in Anatolia, the path out of Africa to Europe, although that could be a function of back-migration.

When looking at match maps, keep two things in mind:

  • The information is provided by testers. It’s possible for them to misunderstand what is meant by providing the information for their earliest known “direct maternal ancestor.” I can’t tell you how many male names I’ve seen here. Clearly, the tester misunderstood the purpose and what was being asked – because men don’t pass mitochondrial DNA to their offspring. Check the pins for surnames that seem to fit the pin location, and that pins have been accurately placed.
  • Testing bias. In other words, lots of people have tested in the US as compared to Europe, and probably more people in the UK than say, Turkey. Testing is still illegal in France.

Haplogroup Origins

While the Ancestral Origins tab is organized by the locations of your matches ancestors, the Haplogroup Origins tab is focused on your haplogroup by match level only.

In many cases, the numbers will match your Ancestral Origins exactly, but for other test levels, the numbers will be different.

For example, at the HVR1/HVR2 level, I can easily see at a glance the locations where my haplogroup is found, and the number of my matches in those various locations.

This page is reflective of where the haplogroup itself is found, according to your matches.

There may be other people with the same haplogroup that you don’t match and won’t be reflected on this page.  We’ll see them either in projects or on the Public Mitochondrial Tree in following sections.

Migration Map

The migration map tab shows the path between Mitochondrial Eve who lived in African about 145,000 years ago and your haplogroup today. For haplogroups J, Eve’s descendant left African and traveled through the Middle East and on into Southwest Asia before turning left and migrating throughout Europe.

Clearly, the vast majority of this migration occurred before genealogy, but not all, or you wouldn’t be here today.

Thousands of my ancestors brought my mitochondrial DNA from Africa through Anatolia, through Europe, to Scandinavia, and back to Germany – then on to the US where it continued being passed on for five more generations before reaching me.

Additional Features – Other Tools

On your personal page, scroll down below your Mitochondrial DNA results area and you’ll see Public Haplotrees under the Other Tools tab.

This tree is available to FamilyTreeDNA customers as well as the public.

Public Mitochondrial DNA Haplotree

The public mitochondrial haplotree provided by FamilyTreeDNA includes location information and is available to everyone, customer or not, for free. Please note that only full sequence results were used to construct this tree, so partial results, meaning haplogroups of people who tested at the HVR1/2 levels only, are not included because the haplogroup cannot be refined at that level.

If you’ve received a haplogroup from a different test at another vendor, you can use this public tool to obtain location information. FamilyTreeDNA has the single largest repository of mitochondrial tests in the world, having tested customers for 21 years, and they have made this tree with location information available for everyone.

If you are a customer, you can sign in and access this tree from your account, above.

If you access the haplotree in this manner, be sure to select the mtDNA tree, not the Y DNA tree which is the default.

Or you can simply access the mtDNA the same way as the public, below.

Go to the main FamilyTreeDNA page by clicking here.

On the main page, scroll to the very bottom – yes, just keep scrolling.

At the very bottom, in the footer, you’ll see “Community.” (Hint, if you don’t see Community at the very bottom of this page, you’re probably signed in to your account.)

Click on “mtDNA Haplotree.”

Next, you’ll see the beginning, or root, of the mitochondrial DNA tree, with the RSRS at the top of the page. The tree structure and haplogroups are defined at Phylotree Build 17, here. All of the main daughter haplogroups, such as “J,” are displayed beneath or you can select them across the top.

Enter the haplogroup name in the “Branch Name” field in the upper right. For me, that’s J1c2f.

I don’t match all of the J1c2f people in the database, because there more total country designations shown here (82) than I have full sequence matches with locations provided (50 from my Ancestral Origins page.)

If you click on the three dots at right, you’ll see a Country Report which provides details for this haplogroup and downstream haplogroups, if there are any. I wrote about that, in detail, here.

There are no “J1c2f plus a daughter” haplogroups defined today, so there is nothing listed downstream.

However, that’s not always the case. There may be a downstream clade that you’re not a member of, meaning you don’t carry that haplogroup-defining mutation.

Or, you may have tested someplace that provides you with a partial haplogroup, so you don’t know if you have a subclade or not. You can still glean useful information from partial haplogroups.

Partial Haplogroups From Autosomal Tests

There’s nothing “wrong” with partial haplogroups. It’s nice to know at least some history about your matrilineal ancestry. What you don’t receive, of course, aside from matching, is more recent, genealogical, information.

Both 23andMe and LivingDNA provide autosomal customers with partial mitochondrial haplogroups. Both of these vendors tend to be accurate as far as they go, as opposed to other vendors, who shall remain unnamed, that are often inaccurate.

Autosomal tests don’t specifically test the mitochondrial DNA directly like a full sequence mitochondrial DNA test does, but they do use “probes” that scan specific haplogroup defining locations. Of course, each of the autosomal chips has a finite number of locations and every location that is used for either mitochondrial or Y DNA haplogroups is a space the vendors can’t use for autosomal locations.

Therefore, customers receive partial haplogroups.

In my case, I’ve received J1c at LivingDNA and J1c2 at 23andMe.

Both vendors provide basic information about your haplogroup, along with migration maps. Wikipedia also provides basic haplogroup information. Google is your friend – “mitochondrial haplogroup J Wikipedia.”

DNA Projects

Most haplogroups have a DNA project at FamilyTreeDNA. Note that these projects are administered by volunteers, so your mileage will vary in terms of participant grouping, along with whether or not results or maps are displayed. You can just google for “mitochondrial haplogroup J DNA project at FamilyTreeDNA” and you’ll find the project or perhaps multiple projects to select from. Some haplogroups have a main “J” project and perhaps a subproject, like “J1c,” for example.

You can join the project, either from this page if you’ve tested at FamilyTreeDNA, or from your personal page via the “myProjects” tab at the top of your personal page.

If you’re looking for public haplogroup information, click on “DNA Results.”

If the Haplogroup J DNA testers have joined this project, authorized displaying their results in projects, and provided ancestor information, you will be able to see that on the “Results” page. Projects are often grouped by haplogroup subgroup. Please note that the default page display size is 25, so scroll to the bottom to see how many pages are in the project. Multiply that number times 25 (182 pages total X 25 = 4550) and change the page display size to that number (4550, in this case.)

One of the most useful tools for haplogroup discovery is the project map which offers the same subgroups as the project groupings.

You can select “All” on the dropdown to display the locations of the earliest known ancestors of everyone in this haplogroup project, or you can select a subclade. This map is displaying haplogroup J1c2 as an example of my partial haplogroup.

The Public Mitochondrial Tree and Partial Haplogroups

To find more comprehensive information for partial haplogroups, I can use the free mitochondrial tree at FamilyTreeDNA. While projects only reflect information for people who have joined those particular projects, the tree provides more comprehensive information.

Anyone with a partial haplogroup can still learn a great deal. Like with any haplogroup, you can view where tester’s ancestors lived in the world.

In this case, it doesn’t matter whether I’m looking at partial haplogroups J1c or J1c2, there are many subgroups that I could potentially belong to.

In fact, haplogroup J1c has subclades through J1c17, so there are pages and pages of haplogroup subclade candidates.

Does a Full Haplogroup Really Matter?

How much difference can there be? Is J1c or J1c2 good enough? Good questions.

It depends – on what you want to know.

  • For general interest, perhaps.
  • For genealogy, no.

Genealogists need the most granular results possible to obtain the most information possible. You don’t know what you don’t know. But how much might that be, aside from full sequence matches?

There’s a significant difference in the country details of haplogroup J1c, J1c2 and J1c2f. I created a chart of the top 10 locations, and how many people’s ancestors are found there for J1c, J1c2, and J1c2f.

Wow, that’s a big difference.

How accurately do J1c and J1c2 results reflect the locations in my full J1c2f haplogroup? I color-coded the results and removed the locations from J1c and J1c2 that are not reflected in J1c2f.

As it turns out, the 5 most frequent locations in J1c and the top 3 locations in J1c2 aren’t even in the top 10 of J1c2f. Obtaining a full haplogroup is important.

Current and Past Populations

It’s worth noting that where a current population is found is not always indicative of where an ancestral population was found.

Of course, with genealogy, we can look back a few generations by seeing where the ancestors of our close and distant matches were found.

My earliest known ancestor is found in a marriage record in 1647 in Wirbenz, Germany when she was 26 years old. However, the majority of my exact mitochondrial DNA matches are not found in Germany, or even in Europe, but in Scandinavia. I’m sure there’s a story there to be told, possibly related to the Thirty Years’ War which began in 1618 and devastated Germany. The early German records where she lived were destroyed.

Even in the abbreviated genealogical timeframe where records and surnames exist, as compared to the history of mankind and womankind, we can see examples of population migration and shift with weather, warfare, and opportunity.

We can’t peer further back in time, at least not without ancient DNA, except by a combination of general history, haplogroup inference, and noting where branching from our mother clade occurred.

We know that people move. Sometimes populations were small and the entire population moved to a new location.

Sometimes, the entire population didn’t move, the but descendants of the migrating group survived to take DNA tests, while the population remaining in the original location has no present-day descendants.

Sometimes descendants of both groups survived.

Of course, throughout history, mutations continued to occur in all lines, forming new genetic branches – haplogroups.

Thank goodness they did, because mutations, or lack thereof, are incredibly important clues to genealogy as well as being our breadcrumbs back into the mists of distant time. Those haplogroup-defining mutations are the umbilical cord that allows us to connect with those distant ancestors.

These tools, especially used together, are the best way to answer the question, “Where did my Mitochondrial DNA Haplogroup Come From?”

Where did your haplogroup come from?

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Books

Genealogy Research

Misleading 23andMe Paternal Haplogroup Emails For Females

I received an email for a 23andMe kit that I manage stating “Your Paternal Haplogroup Report is waiting for you.” Really? Cool!!!

Only problem is that the tester is a female – and females don’t have a paternal haplogroup available because females don’t have Y DNA.

Clearly, this is just not possible.

Three things crossed my mind:

  1. Erroneous email, as in “oops.” Some marketing person is going to be in a heap of trouble.
  2. Incompetence following the sale of the company. There have been other recent changes that caused me to wonder, although some were reversed.
  3. Bait and switch. Surely not. 23andMe has never been like that, so this is a distant third.

I knew for an absolute fact, beyond any doubt that this close family member is female.

I also realize that any female who receives this email would excitedly check their Paternal Haplogroup report – thinking that maybe, just maybe, some new scientific discovery had been made so they CAN actually see a paternal haplogroup from their own DNA test.

Time to see what’s going on.

I Signed In

I signed in and saw an unopened Paternal Haplogroup report under “Next Reports” at the top of the main page.

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I checked another female kit that I manage, plus my own. The same thing appeared on both of those accounts too.

This e-mail was clearly not an “oops” email inadvertently sent to a female group of testers. It has to be something else.

Sure enough, on the Ancestry tab, if I scroll down, I see these two placards.

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Maternal Haplogroup, which everyone has, and Paternal Haplogroup, which only males have. Did 23andMe make some kind of mistake? I clicked on the “View Your Report” button for Paternal Haplogroup. It took me to the same page the Paternal Haplogroup link on my main page did.

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My heart just sank.

Sure enough, it’s a pitch to test another family member, a father or brother. 23andMe explains that no, the female tester really doesn’t have a paternal haplogroup.

So, it IS bait and switch, the least likely scenario I expected. I’m really disappointed. I never thought I’d see the day 23andMe would adopt this type of disingenuous marketing technique.

Why Does This Bother Me So Much?

In general, acquisitions make people uneasy, and 23andMe was acquired in February.

We don’t know what to expect of the new owners, or the direction they will take a company. In this case, the company involved, 23andMe, not only has my DNA, they provide information about my health as part of my test.

Consumers need to be able to have confidence that the information 23andMe provides is accurate. We need to be able to trust them, to believe what they tell us about our DNA results without having to wonder if there is something more, or less, in this case, to the story. In other words, that there’s no ulterior motive in their message.

I grew up on a farm and my old farmer Dad used to tell me that “if someone will lie to you about one thing, they will lie to you about anything.”

I would have NO PROBLEM whatsoever with 23andMe sending an email telling females how to obtain a paternal haplogroup for their paternal line.

There’s a significant difference, though, between that and telling female testers that their “Paternal Haplogroup report is waiting for you,” when it’s very clearly not. The email says the report “includes insights about your DNA,” which it clearly does not, because there is no report. 23andMe knows this. That email says “View Report” twice, with links. It’s not a mistake. It’s a hook, using my own DNA as bait, and I’m the fish.

This tactic is misleading, at best. In my opinion, it’s an unethical and dishonest attempt to manipulate unwary or naïve customers. And truthfully, I’m shocked. I never expected behavior like this from 23andMe. It seems so out-of-character about what I thought I understood about Ann Wojcicki. In this 2015 interview in PLOS Genetics, she said, “I think that for our mission, it’s really important that people trust the company.” What happened?

If I WAS inclined to test another family member, given this deceptive bait and switch sales tactic, I assuredly wouldn’t. Telling me I “have” something only to discover I don’t in an attempt to sell me that same “something” is just not a technique I would have expected 23andMe to embrace.

Come on 23andMe, you are, or were, better than this. ☹

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Books

Genealogy Research

Haplogroup Matching: What It Does (and Doesn’t) Mean

“Our haplogroups (sort of) match, so that means we’re related, right?”

Well, maybe.

It depends.

Great Question

This is an oft-asked great question. Of course, the answer varies depending on the context of the question and what is meant by “related.” A haplogroup match may or may not be a valid match for genealogy. A “match” or a “not match” can mean different things.

The questions people often ask include:

  • Does a haplogroup have to match exactly in order for another person to either be considered a match to you?
  • If they don’t match exactly, can they still be considered as a possible match?
  • Conversely, can we rule someone out as a match on a specific genealogical line based on haplogroup alone?

These questions often arise in relation to DNA testing at Family Tree DNA, sometimes when people are trying to compare results to people who have haplogroup estimates, either at FamilyTreeDNA or from testing elsewhere.

In other words, if one person is haplogroup J and someone else is J1, either at the same vendor or at another, what does that tell us? This question pertains to both Y DNA and mitochondrial DNA tests no matter where you’ve tested.

Family Tree DNA offers different levels of Y DNA testing. Interpreting those match results can sometimes be confusing. The same is true for mitochondrial DNA, especially if your matches have not taken the full mitochondrial sequence (mtFull) test.

You might be comparing apples and oranges, or you might be comparing a whole orange (detailed test) with a few slices (haplogroup estimate.) How can you know, and how can you make sense of the results?

If you’re comparing a haplogroup between sources, such as a partial haplogroup determined by testing through a company like 23andMe or LivingDNA to complete tests taken at FamilyTreeDNA, the answer can be less than straightforward.

I discussed the difference between autosomal-based haplogroup assignments and actual testing of both Y DNA and mitochondrial DNA which result in haplogroup assignments, here. In a nutshell, both LivingDNA and 23andMe provide a high-level (base) haplogroup estimates based on a few specific probes when you purchase an autosomal test, but that’s not the same as deeper testing of the Y chromosome or mitochondrial DNA.

The answer to whether your haplogroup has to match is both “yes”, and “no.” Don’t you hate it when this happens?

Let’s look at different situations. But to begin with, there is at least one common answer.

Yes, Your Base Haplogroup Must Match

To even begin to look further for a common ancestor on either your Y DNA line (direct patrilineal) or direct mitochondrial matrilineal line (your mother’s mother’s mother’s line on up the tree), your base haplogroup much match.

In other words, you and your matches must all be in the same base haplogroup. Haplogroups are defined by the presence of specific combinations of mutations which are called SNPs (single nucleotide polymorphisms) in the Y DNA.

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All of these men on the Y DNA matches page are a branch of haplogroup R as shown under the Y-DNA Haplogroup column. There are more matches on down the page (not shown here) with more and different haplogroups. However, you’ll notice that all matches are a subset of haplogroup R, the base haplogroup.

The same is true for mitochondrial DNA haplogroups. You can see in this example that people who have not tested at the FMS (full mitochondrial sequence) level have a less specific haplogroup. The entire mitochondria must be tested in order to obtain a full haplogroup, such as J1c2f, as opposed to haplogroup J.

The Y DNA Terminal SNP Might Not Match

For Y DNA testers, when looking at your matches, even to close relatives, you may not have the same exact haplogroup because:

  • Some people may have tested at different levels
  • Some people in recent generations may have developed a SNP specific to their line.

In other words, haplogroups, testing level, and known genealogy all need to be considered, especially when the haplogroups are “close to each other” on the tree.

For Y DNA, FamilyTreeDNA:

  • Provides all testers with base haplogroup estimates based on STR tests, meaning 12-111 marker panels. These are very accurate estimates, but are also very high level.
  • Offers or has offered in the past both individual SNP tests and SNP packs or bundles that test individual SNPs indicating their presence or absence. This confirms a SNP or haplogroup, but only to that particular level.
  • Offers the Big Y-700 test, along with upgrades to previous Big Y test levels. There have been 3 versions of the Big Y test over time. The Big Y reads the entire gold standard region of the Y chromosome, reporting the known (named) SNP mutations customers do and don’t have. Additionally, the test reports any unnamed SNPs which are considered private variants until multiple men on the same branch of the Y DNA tree test with the same mutation. At that point, the mutation is named and becomes a haplogroup.

That’s why the answer is “no,” your haplogroup does not have to match exactly for you to actually be a match to each other.

A father and son could test, with one having an estimated haplogroup of R-M269 and the other taking the Big Y-700 resulting in a very different Terminal SNP, quite distant on the tree. Conversely, both men could take the Big Y and the son could have a different terminal SNP than the father because a mutation occurred between them. An autosomal DNA test would confirm that they are in fact, father and son.

However, a father and son who test and are placed in different base haplogroups – one in haplogroup I, and the other in haplogroup R, for example, has a very different situation. Their autosomal test would likely confirm that they are not father and son.

Having said this about paternity, especially if haplogroups are estimated and specific Y DNA SNP testing has not been done, don’t have a premature freak-out moment. Look at autosomal DNA, assuming you DO want to know. Y DNA alone should never be used to infer paternity without autosomal testing.

Let’s look at some examples.

Matches and Haplogroups

In the example shown above, you can see that several people have taken the Big Y test, so their SNP will be shown on further down the haplotree than those testers who have not. These are a leaf, not a branch.

You can see by looking at the Terminal SNP column, at far right, that people who have either taken the Big Y, or had any positive SNP test will have a value in the Terminal SNP column.

Anyone who has NOT taken the Big Y or taken a SNP test will have their base haplogroup estimated based on their STR tests. In this case, that estimate is R-M269. People with estimated haplogroups will not show anything in the Terminal SNP column.

It’s possible that if all of these men took the Big Y test that at least some would share the same Terminal SNP, and others might be closely related, only a branch or so different on the tree.

These men in this example are all descendants of Robert Estes born in England in 1555. All have Estes surnames, except for one man who is seeking the identity of his paternal line.

Let’s Look at the Tree

Our tester in the screenshot is haplogroup R-ZS3700 and matches men in the following haplogroups:

  • R-M269
  • R-L21
  • R-BY490
  • R-BY154784

There are a few additional haplogroups not shown because they are further down on his match list, so let’s just work with these for now.

After determining that these men are on the same branch of the Y tree, haplogroup R, the real question is how closely they are related and how close or far distant their terminal SNPs are located. More distance means the common ancestor is further back in time.

However, looks can be deceiving, especially if not everyone has tested to the same level.

The haplogroup furthest up in the tree, meaning the oldest, is R-M269, followed by the man who took the single SNP test for R-L21. Notice that R-M269 has more than 15,000 branches, so while this haplogroup could be used to rule out a match, R-M269 alone isn’t useful to determine genealogical matching.

There are a lot of branches between R-L21 and the next haplogroup on the tree.

Finally, here we go. Our tester is haplogroup R-ZS3700 that has one descendant branch. R-ZS3700 is a branch of R-BY490 that has 2 branches.

R-BY154784 is the last SNP on this branch of the tree. Our tester matches this man too.

Another way of viewing these matches is on the Block Tree provided for Big Y testers.

In this view, you can see that the Estes men all match back to about 18 “SNP generations” ago according to the legend at left, but they don’t match men further back in time who have taken the Big Y test.

Notice the up-arrow where haplogroups R-L21 and R-M269 are shown across the top of the display.

If you click on R-L21, you’ll see that that it appears about 61 SNP generations back in time.

Haplogroup R-M269 appears even further back in time, about 174 SNP generations.

The only reason you will match someone at either the R-L21 or R-M269 level is because you both descend from a common long-ago ancestral branch, hundreds to thousands of years in the past. You and they would both need to take either the Big Y-700 test for Y DNA, or the full sequence mitochondrial DNA test in order to determine your full haplogroup and see your list of matches based on those full sequences.

Public Trees

You can view FamilyTreeDNA‘s extensive public Y DNA tree by haplogroup, here.

You can view their public mitochondrial DNA tree by haplogroup, here.

And the Answer Is…

As you can see, there is no single answer to the question of haplogroup relationships. The answer is also partly defined by the context in which the question is asked.

  1. For two men to be “related” on the Y DNA patrilineal line, yes, minimally, the base haplogroup does have to match. Base haplogroups are defined by the leading letter, like “R” in the examples above.
  2. “Related” based on base haplogroup only can be hundreds or thousands of years back in time, but additional testing can resolve that question.
  3. “Related” can mean before the advent of surnames. However, a match to a man with the same surname suggests a common ancestor with that surname in the past several hundred years. That match could, however, be much closer in time.
  4. For two men to be closely related, assuming they have taken the same version of Big Y test, their haplogroup branches need to be fairly closely adjacent on the haplotree. FamilyTreeDNA will be introducing haplogroup aging soon, meaning SNP/haplogroup branch dates on their haplotree. At that time, the “distance” between men will be easier to understand.
  5. You can exclude a genealogical relationship on the direct paternal line if the two men involved have a different base haplogroup. This question often occurs when people are trying to understand if they “might match” with someone whose haplogroup has been estimated.
  6. This holds true as well for mitochondrial DNA haplogroups and matching.

And there you have it, six answers about what haplogroup matching does and does not mean.

The bottom line is that haplogroups can be a great starting point and you can sometimes eliminate people as potential matches.

However, to confirm genealogical matches, you’ll always need more granular testing that includes actual Y DNA or mitochondrial DNA matching based on marker mutation results, not just haplogroups.

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Genetic Genealogy at 20 Years: Where Have We Been, Where Are We Going and What’s Important?

Not only have we put 2020 in the rear-view mirror, thankfully, we’re at the 20-year, two-decade milestone. The point at which genetics was first added to the toolbox of genealogists.

It seems both like yesterday and forever ago. And yes, I’ve been here the whole time,  as a spectator, researcher, and active participant.

Let’s put this in perspective. On New Year’s Eve, right at midnight, in 2005, I was able to score kit number 50,000 at Family Tree DNA. I remember this because it seemed like such a bizarre thing to be doing at midnight on New Year’s Eve. But hey, we genealogists are what we are.

I knew that momentous kit number which seemed just HUGE at the time was on the threshold of being sold, because I had inadvertently purchased kit 49,997 a few minutes earlier.

Somehow kit 50,000 seemed like such a huge milestone, a landmark – so I quickly bought kits, 49,998, 49,999, and then…would I get it…YES…kit 50,000. Score!

That meant that in the 5 years FamilyTreeDNA had been in business, they had sold on an average of 10,000 kits per year, or 27 kits a day. Today, that’s a rounding error. Then it was momentous!

In reality, the sales were ramping up quickly, because very few kits were sold in 2000, and roughly 20,000 kits had been sold in 2005 alone. I know this because I purchased kit 28,429 during the holiday sale a year earlier.

Of course, I had no idea who I’d test with that momentous New Year’s Eve Y DNA kit, but I assuredly would find someone. A few months later, I embarked on a road trip to visit an elderly family member with that kit in tow. Thank goodness I did, and they agreed and swabbed on the spot, because they are gone today and with them, the story of the Y line and autosomal DNA of their branch.

In the past two decades, almost an entire generation has slipped away, and with them, an entire genealogical library held in their DNA.

Today, more than 40 million people have tested with the four major DNA testing companies, although we don’t know exactly how many.

Lots of people have had more time to focus on genealogy in 2020, so let’s take a look at what’s important? What’s going on and what matters beyond this month or year?

How has this industry changed in the last two decades, and where it is going?

Reflection

This seems like a good point to reflect a bit.

Professor Dan Bradley reflecting on early genetic research techniques in his lab at the Smurfit Institute of Genetics at Trinity College in Dublin. Photo by Roberta Estes

In the beginning – twenty years ago, there were two companies who stuck their toes in the consumer DNA testing water – Oxford Ancestors and Family Tree DNA. About the same time, Sorenson Genomics and GeneTree were also entering that space, although Sorenson was a nonprofit. Today, of those, only FamilyTreeDNA remains, having adapted with the changing times – adding more products, testing, and sophistication.

Bryan Sykes who founded Oxford Ancestors announced in 2018 that he was retiring to live abroad and subsequently passed away in 2020. The website still exists, but the company has announced that they have ceased sales and the database will remain open until Sept 30, 2021.

James Sorenson died in 2008 and the assets of Sorenson Molecular Genealogy Foundation, including the Sorenson database, were sold to Ancestry in 2012. Eventually, Ancestry removed the public database in 2015.

Ancestry dabbled in Y and mtDNA for a while, too, destroying that database in 2014.

Other companies, too many to remember or mention, have come and gone as well. Some of the various company names have been recycled or purchased, but aren’t the same companies today.

In the DNA space, it was keep up, change, die or be sold. Of course, there was the small matter of being able to sell enough DNA kits to make enough money to stay in business at all. DNA processing equipment and a lab are expensive. Not just the equipment, but also the expertise.

The Next Wave

As time moved forward, new players entered the landscape, comprising the “Big 4” testing companies that constitute the ponds where genealogists fish today.

23andMe was the first to introduce autosomal DNA testing and matching. Their goal and focus was always medical genetics, but they recognized the potential in genealogists before anyone else, and we flocked to purchase tests.

Ancestry settled on autosomal only and relies on the size of their database, a large body of genealogy subscribers, and a widespread “feel-good” marketing campaign to sell DNA kits as the gateway to “discover who you are.”

FamilyTreeDNA did and still does offer all 3 kinds of tests. Over the years, they have enhanced both the Y DNA and mitochondrial product offerings significantly and are still known as “the science company.” They are the only company to offer the full range of Y DNA tests, including their flagship Big Y-700, full sequence mitochondrial testing along with matching for both products. Their autosomal product is called Family Finder.

MyHeritage entered the DNA testing space a few years after the others as the dark horse that few expected to be successful – but they fooled everyone. They have acquired companies and partnered along the way which allowed them to add customers (Promethease) and tools (such as AutoCluster by Genetic Affairs), boosting their number of users. Of course, MyHeritage also offers users a records research subscription service that you can try for free.

In summary:

One of the wonderful things that happened was that some vendors began to accept compatible raw DNA autosomal data transfer files from other vendors. Today, FamilyTreeDNA, MyHeritage, and GEDmatch DO accept transfer files, while Ancestry and 23andMe do not.

The transfers and matching are free, but there are either minimal unlock or subscription plans for advanced features.

There are other testing companies, some with niche markets and others not so reputable. For this article, I’m focusing on the primary DNA testing companies that are useful for genealogy and mainstream companion third-party tools that complement and enhance those services.

The Single Biggest Change

As I look back, the single biggest change is that genetic genealogy evolved from the pariah of genealogy where DNA discussion was banned from the (now defunct) Rootsweb lists and summarily deleted for the first few years after introduction. I know, that’s hard to believe today.

Why, you ask?

Reasons varied from “just because” to “DNA is cheating” and then morphed into “because DNA might do terrible things like, maybe, suggest that a person really wasn’t related to an ancestor in a lineage society.”

Bottom line – fear and misunderstanding. Change is exceedingly difficult for humans, and DNA definitely moved the genealogy cheese.

From that awkward beginning, genetic genealogy organically became a “thing,” a specific application of genealogy. There was paper-trail traditional genealogy and then the genetic aspect. Today, for almost everyone, genealogy is “just another tool” in the genealogist’s toolbox, although it does require focused learning, just like any other tool.

DNA isn’t separate anymore, but is now an integral part of the genealogical whole. Having said that, DNA can’t solve all problems or answer all questions, but neither can traditional paper-trail genealogy. Together, each makes the other stronger and solves mysteries that neither can resolve alone.

Synergy.

I fully believe that we have still only scratched the surface of what’s possible.

Inheritance

As we talk about the various types of DNA testing and tools, here’s a quick graphic to remind you of how the different types of DNA are inherited.

  • Y DNA is inherited paternally for males only and informs us of the direct patrilineal (surname) line.
  • Mitochondrial DNA is inherited by everyone from their mothers and informs us of the mother’s matrilineal (mother’s mother’s mother’s) line.
  • Autosomal DNA can be inherited from potentially any ancestor in random but somewhat predictable amounts through both parents. The further back in time, the less identifiable DNA you’ll inherit from any specific ancestor. I wrote about that, here.

What’s Hot and What’s Not

Where should we be focused today and where is this industry going? What tools and articles popped up in 2020 to help further our genealogy addiction? I already published the most popular articles of 2020, here.

This industry started two decades ago with testing a few Y DNA and mitochondrial DNA markers, and we were utterly thrilled at the time. Both tests have advanced significantly and the prices have dropped like a stone. My first mitochondrial DNA test that tested only 400 locations cost more than $800 – back then.

Y DNA and mitochondrial DNA are still critically important to genetic genealogy. Both play unique roles and provide information that cannot be obtained through autosomal DNA testing. Today, relative to Y DNA and mitochondrial DNA, the biggest challenge, ironically, is educating newer genealogists about their potential who have never heard about anything other than autosomal, often ethnicity, testing.

We have to educate in order to overcome the cacophony of “don’t bother because you don’t get as many matches.”

That’s like saying “don’t use the right size wrench because the last one didn’t fit and it’s a bother to reach into the toolbox.” Not to mention that if everyone tested, there would be a lot more matches, but I digress.

If you don’t use the right tool, and all of the tools at your disposal, you’re not going to get the best result possible.

The genealogical proof standard, the gold standard for genealogy research, calls for “a reasonably exhaustive search,” and if you haven’t at least considered if or how Y
DNA
and mitochondrial DNA along with autosomal testing can or might help, then your search is not yet exhaustive.

I attempt to obtain the Y and mitochondrial DNA of every ancestral line. In the article, Search Techniques for Y and Mitochondrial DNA Test Candidates, I described several methodologies to find appropriate testing candidates.

Y DNA – 20 Years and Still Critically Important

Y DNA tracks the Y chromosome for males via the patrilineal (surname) line, providing matching and historical migration information.

We started 20 years ago testing 10 STR markers. Today, we begin at 37 markers, can upgrade to 67 or 111, but the preferred test is the Big Y which provides results for 700+ STR markers plus results from the entire gold standard region of the Y chromosome in order to provide the most refined results. This allows genealogists to use STR markers and SNP results together for various aspects of genealogy.

I created a Y DNA resource page, here, in order to provide a repository for Y DNA information and updates in one place. I would encourage anyone who can to order or upgrade to the Big Y-700 test which provides critical lineage information in addition to and beyond traditional STR testing. Additionally, the Big Y-700 test helps build the Y DNA haplotree which is growing by leaps and bounds.

More new SNPs are found and named EVERY SINGLE DAY today at FamilyTreeDNA than were named in the first several years combined. The 2006 SNP tree listed a grand total of 459 SNPs that defined the Y DNA tree at that time, according to the ISOGG Y DNA SNP tree. Goran Rundfeldt, head of R&D at FamilyTreeDNA posted this today:

2020 was an awful year in so many ways, but it was an unprecedented year for human paternal phylogenetic tree reconstruction. The FTDNA Haplotree or Great Tree of Mankind now includes:

37,534 branches with 12,696 added since 2019 – 51% growth!
defined by
349,097 SNPs with 131,820 added since 2019 – 61% growth!

In just one year, 207,536 SNPs were discovered and assigned FT SNP names. These SNPs will help define new branches and refine existing ones in the future.

The tree is constructed based on high coverage chromosome Y sequences from:
– More than 52,500 Big Y results
– Almost 4,000 NGS results from present-day anonymous men that participated in academic studies

Plus an additional 3,000 ancient DNA results from archaeological remains, of mixed quality and Y chromosome coverage at FamilyTreeDNA.

Wow, just wow.

These three new articles in 2020 will get you started on your Y DNA journey!

Mitochondrial DNA – Matrilineal Line of Humankind is Being Rewritten

The original Oxford Ancestor’s mitochondrial DNA test tested 400 locations. The original Family Tree DNA test tested around 1000 locations. Today, the full sequence mitochondrial DNA test is standard, testing the entire 16,569 locations of the mitochondria.

Mitochondrial DNA tracks your mother’s direct maternal, or matrilineal line. I’ve created a mitochondrial DNA resource page, here that includes easy step-by-step instructions for after you receive your results.

New articles in 2020 included the introduction of The Million Mito Project. 2021 should see the first results – including a paper currently in the works.

The Million Mito Project is rewriting the haplotree of womankind. The current haplotree has expanded substantially since the first handful of haplogroups thanks to thousands upon thousands of testers, but there is so much more information that can be extracted today.

Y and Mitochondrial Resources

If you don’t know of someone in your family to test for Y DNA or mitochondrial DNA for a specific ancestral line, you can always turn to the Y DNA projects at Family Tree DNA by searching here.

The search provides you with a list of projects available for a specific surname along with how many customers with that surname have tested. Looking at the individual Y DNA projects will show the earliest known ancestor of the surname line.

Another resource, WikiTree lists people who have tested for the Y DNA, mitochondrial DNA and autosomal DNA lines of specific ancestors.

Click on images to enlarge

On the left side, my maternal great-grandmother’s profile card, and on the right, my paternal great-great-grandfather. You can see that someone has tested for the mitochondrial DNA of Nora (OK, so it’s me) and the Y DNA of John Estes (definitely not me.)

MitoYDNA, a nonprofit volunteer organization created a comparison tool to replace Ysearch and Mitosearch when they bit the dust thanks to GDPR.

MitoYDNA accepts uploads from different sources and allows uploaders to not only match to each other, but to view the STR values for Y DNA and the mutation locations for the HVR1 and HVR2 regions of mitochondrial DNA. Mags Gaulden, one of the founders, explains in her article, What sets mitoYDNA apart from other DNA Databases?.

If you’ve tested at nonstandard companies, not realizing that they didn’t provide matching, or if you’ve tested at a company like Sorenson, Ancestry, and now Oxford Ancestors that is going out of business, uploading your results to mitoYDNA is a way to preserve your investment. PS – I still recommend testing at FamilyTreeDNA in order to receive detailed results and compare in their large database.

CentiMorgans – The Word of Two Decades

The world of autosomal DNA turns on the centimorgan (cM) measure. What is a centimorgan, exactly? I wrote about that unit of measure in the article Concepts – CentiMorgans, SNPs and Pickin’ Crab.

Fortunately, new tools and techniques make using cMs much easier. The Shared cM Project was updated this year, and the results incorporated into a wonderfully easy tool used to determine potential relationships at DNAPainter based on the number of shared centiMorgans.

Match quality and potential relationships are determined by the number of shared cMs, and the chromosome browser is the best tool to use for those comparisons.

Chromosome Browser – Genetics Tool to View Chromosome Matches

Chromosome browsers allow testers to view their matching cMs of DNA with other testers positioned on their own chromosomes.

My two cousins’ DNA where they match me on chromosomes 1-4, is shown above in blue and red at Family Tree DNA. It’s important to know where you match cousins, because if you match multiple cousins on the same segment, from the same side of your family (maternal or paternal), that’s suggestive of a common ancestor, with a few caveats.

Some people feel that a chromosome browser is an advanced tool, but I think it’s simply standard fare – kind of like driving a car. You need to learn how to drive initially, but after that, you don’t even think about it – you just get in and go. Here’s help learning how to drive that chromosome browser.

Triangulation – Science Plus Group DNA Matching Confirms Genealogy

The next logical step after learning to use a chromosome browser is triangulation. If fact, you’re seeing triangulation above, but don’t even realize it.

The purpose of genetic genealogy is to gather evidence to “prove” ancestral connections to either people or specific ancestors. In autosomal DNA, triangulation occurs when:

  • You match at least two other people (not close relatives)
  • On the same reasonably sized segment of DNA (generally 7 cM or greater)
  • And you can assign that segment to a common ancestor

The same two cousins are shown above, with triangulated segments bracketed at MyHeritage. I’ve identified the common ancestor with those cousins that those matching DNA segments descend from.

MyHeritage’s triangulation tool confirms by bracketing that these cousins also match each other on the same segment, which is the definition of triangulation.

I’ve written a lot about triangulation recently.

If you’d prefer a video, I recorded a “Top Tips” Facebook LIVE with MyHeritage.

Why is Ancestry missing from this list of triangulation articles? Ancestry does not offer a chromosome browser or segment information. Therefore, you can’t triangulate at Ancestry. You can, however, transfer your Ancestry DNA raw data file to either FamilyTreeDNA, MyHeritage, or GEDmatch, all three of which offer triangulation.

Step by step download/upload transfer instructions are found in this article:

Clustering Matches and Correlating Trees

Based on what we’ve seen over the past few years, we can no longer depend on the major vendors to provide all of the tools that genealogists want and need.

Of course, I would encourage you to stay with mainstream products being used by a significant number of community power users. As with anything, there is always someone out there that’s less than honorable.

2020 saw a lot of innovation and new tools introduced. Maybe that’s one good thing resulting from people being cooped up at home.

Third-party tools are making a huge difference in the world of genetic genealogy. My favorites are Genetic Affairs, their AutoCluster tool shown above, DNAPainter and DNAGedcom.

These articles should get you started with clustering.

If you like video resources, here’s a MyHeritage Facebook LIVE that I recorded about how to use AutoClusters:

I created a compiled resource article for your convenience, here:

I have not tried a newer tool, YourDNAFamily, that focuses only on 23andMe results although the creator has been a member of the genetic genealogy community for a long time.

Painting DNA Makes Chromosome Browsers and Triangulation Easy

DNAPainter takes the next step, providing a repository for all of your painted segments. In other words, DNAPainter is both a solution and a methodology for mass triangulation across all of your chromosomes.

Here’s a small group of people who match me on the same maternal segment of chromosome 1, including those two cousins in the chromosome browser and triangulation sections, above. We know that this segment descends from Philip Jacob Miller and his wife because we’ve been able to identify that couple as the most distant ancestor intersection in all of our trees.

It’s very helpful that DNAPainter has added the functionality of painting all of the maternal and paternal bucketed matches from Family Tree DNA.

All you need to do is to link your known matches to your tree in the proper place at FamilyTreeDNA, then they do the rest by using those DNA matches to indicate which of the rest of your matches are maternal and paternal. Instructions, here. You can then export the file and use it at DNAPainter to paint all of those matches on the correct maternal or paternal chromosomes.

Here’s an article providing all of the DNAPainter Instructions and Resources.

DNA Matches Plus Trees Enhance Genealogy

Of course, utilizing DNA matching plus finding common ancestors in trees is one of the primary purposes of genetic genealogy – right?

Vendors have linked the steps of matching DNA with matching ancestors in trees.

Genetic Affairs take this a step further. If you don’t have an ancestor in your tree, but your matches have common ancestors with each other, Genetic Affairs assembles those trees to provide you with those hints. Of course, that common ancestor might not be relevant to your genealogy, but it just might be too!

click to enlarge

This tree does not include me, but two of my matches descend from a common ancestor and that common ancestor between them might be a clue as to why I match both of them.

Ethnicity Continues to be Popular – But Is No Shortcut to Genealogy

Ethnicity is always popular. People want to “do their DNA” and find out where they come from. I understand. I really do. Who doesn’t just want an answer?

Of course, it’s not that simple, but that doesn’t mean it’s not disappointing to people who test for that purpose with high expectations. Hopefully, ethnicity will pique their curiosity and encourage engagement.

All four major vendors rolled out updated ethnicity results or related tools in 2020.

The future for ethnicity, I believe, will be held in integrated tools that allow us to use ethnicity results for genealogy, including being able to paint our ethnicity on our chromosomes as well as perform segment matching by ethnicity.

For example, if I carry an African segment on chromosome 1 from my father, and I match one person from my mother’s side and one from my father’s side on that same segment – one or the other of those people should also have that segment identified as African. That information would inform me as to which match is paternal and which is maternal

Not only that, this feature would help immensely tracking ancestors back in time and identifying their origins.

Will we ever get there? I don’t know. I’m not sure ethnicity is or can be accurate enough. We’ll see.

Transition to Digital and Online

Sometimes the future drags us kicking and screaming from the present.

With the imposed isolation of 2020, conferences quickly moved to an online presence. The genealogy community has all pulled together to make this work. The joke is that 2020’s most used phrase is “can you hear me?” I can vouch for that.

Of course while the year 2020 is over, the problem isn’t and is extending at least through the first half of 2021 and possibly longer. Conferences are planned months, up to a year, in advance and they can’t turn on a dime, so don’t even begin to expect in-person conferences until either late in 2021 or more likely, 2022 if all goes well this year.

I expect the future will eventually return to in-person conferences, but not entirely.

Finding ways to be more inclusive allows people who don’t want to or can’t travel or join in-person to participate.

I’ve recorded several sessions this year, mostly for 2021. Trust me, these could be a comedy, mostly of errors😊

I participated in four MyHeritage Facebook LIVE sessions in 2020 along with some other amazing speakers. This is what “live” events look like today!

Screenshot courtesy MyHeritage

A few days ago, I asked MyHeritage for a list of their LIVE sessions in 2020 and was shocked to learn that there were more than 90 in English, all free, and you can watch them anytime. Here’s the MyHeritage list.

By the way, every single one of the speakers is a volunteer, so say a big thank you to the speakers who make this possible, and to MyHeritage for the resources to make this free for everyone. If you’ve ever tried to coordinate anything like this, it’s anything but easy.

Additonally, I’ve created two Webinars this year for Legacy Family Tree Webinars.

Geoff Rasmussen put together the list of their top webinars for 2020, and I was pleased to see that I made the top 10! I’m sure there are MANY MORE you’d be interested in watching. Personally, I’m going to watch #6 yet today! Also, #9 and #22. You can always watch new webinars for free for a few days, and you can subscribe to watch all webinars, here.

The 2021 list of webinar speakers has been announced here, and while I’m not allowed to talk about something really fun that’s upcoming, let’s just say you definitely have something to look forward to in the springtime!

Also, don’t forget to register for RootsTech Connect which is entirely online and completely free, February 25-27, here.

Thank you to Penny Walters for creating this lovely graphic.

There are literally hundreds of speakers providing sessions in many languages for viewers around the world. I’ve heard the stats, but we can’t share them yet. Let me just say that you will be SHOCKED at the magnitude and reach of this conference. I’m talking dumbstruck!

During one of our zoom calls, one of the organizers says it feels like we’re constructing the plane as we’re flying, and I can confirm his observation – but we are getting it done – together! All hands on deck.

I’ll be presenting an advanced session about triangulation as well as a mini-session in the FamilySearch DNA Resource Center about finding your mother’s ancestors. I’ll share more information as it’s released and I can.

Companies and Owners Come & Go

You probably didn’t even notice some of these 2020 changes. Aside from the death of Bryan Sykes (RIP Bryan,) the big news and the even bigger unknown is the acquisition of Ancestry by Blackstone. Recently the CEO, Margo Georgiadis announced that she was stepping down. The Ancestry Board of Directors has announced an external search for a new CEO. All I can say is that very high on the priority list should be someone who IS a genealogist and who understands how DNA applies to genealogy.

Other changes included:

In the future, as genealogy and DNA testing becomes ever more popular and even more of a commodity, company sales and acquisitions will become more commonplace.

Some Companies Reduced Services and Cut Staff

I understand this too, but it’s painful. The layoffs occurred before Covid, so they didn’t result from Covid-related sales reductions. Let’s hope we see renewed investment after the Covid mess is over.

In a move that may or may not be related to an attempt to cut costs, Ancestry removed 6 and 7 cM matches from their users, freeing up processing resources, hardware, and storage requirements and thereby reducing costs.

I’m not going to beat this dead horse, because Ancestry is clearly not going to move on this issue, nor on that of the much-requested chromosome browser.

Later in the year, 23andMe also removed matches and other features, although, to their credit, they have restored at least part of this functionality and have provided ethnicity updates to V3 and V4 kits which wasn’t initially planned.

It’s also worth noting that early in 2020, 23andMe laid off 100 people as sales declined. Since that time, 23andMe has increasingly pushed consumers to pay to retest on their V5 chip.

About the same time, Ancestry also cut their workforce by about 6%, or about 100 people, also citing a slowdown in the consumer testing market. Ancestry also added a health product.

I’m not sure if we’ve reached market saturation or are simply seeing a leveling off. I wrote about that in DNA Testing Sales Decline: Reason and Reasons.

Of course, the pandemic economy where many people are either unemployed or insecure about their future isn’t helping.

The various companies need some product diversity to survive downturns. 23andMe is focused on medical research with partners who pay 23andMe for the DNA data of customers who opt-in, as does Ancestry.

Both Ancestry and MyHeritage provide subscription services for genealogy records.

FamilyTreeDNA is part of a larger company, GenebyGene whose genetics labs do processing for other companies and medical facilities.

A huge thank you to both MyHeritage and FamilyTreeDNA for NOT reducing services to customers in 2020.

Scientific Research Still Critical & Pushes Frontiers

Now that DNA testing has become a commodity, it’s easy to lose track of the fact that DNA testing is still a scientific endeavor that requires research to continue to move forward.

I’m still passionate about research after 20 years – maybe even more so now because there’s so much promise.

Research bleeds over into the consumer marketplace where products are improved and new features created allowing us to better track and understand our ancestors through their DNA that we and our family members inherit.

Here are a few of the research articles I published in 2020. You might notice a theme here – ancient DNA. What we can learn now due to new processing techniques is absolutely amazing. Labs can share files and information, providing the ability to “reprocess” the data, not the DNA itself, as more information and expertise becomes available.

Of course, in addition to this research, the Million Mito Project team is hard at work rewriting the tree of womankind.

If you’d like to participate, all you need to do is to either purchase a full sequence mitochondrial DNA kit at FamilyTreeDNA, or upgrade to the full sequence if you tested at a lower level previously.

Predictions

Predictions are risky business, but let me give it a shot.

Looking back a year, Covid wasn’t on the radar.

Looking back 5 years, neither Genetic Affairs nor DNAPainter were yet on the scene. DNAAdoption had just been formed in 2014 and DNAGedcom which was born out of DNAAdoption didn’t yet exist.

In other words, the most popular tools today didn’t exist yet.

GEDmatch, founded in 2010 by genealogists for genealogists was 5 years old, but was sold in December 2019 to Verogen.

We were begging Ancestry for a chromosome browser, and while we’ve pretty much given up beating them, because the horse is dead and they can sell DNA kits through ads focused elsewhere, that doesn’t mean genealogists still don’t need/want chromosome and segment based tools. Why, you’d think that Ancestry really doesn’t want us to break through those brick walls. That would be very bizarre, because every brick wall that falls reveals two more ancestors that need to be researched and spurs a frantic flurry of midnight searching. If you’re laughing right now, you know exactly what I mean!

Of course, if Ancestry provided a chromosome browser, it would cost development money for no additional revenue and their customer service reps would have to be able to support it. So from Ancestry’s perspective, there’s no good reason to provide us with that tool when they can sell kits without it. (Sigh.)

I’m not surprised by the management shift at Ancestry, and I wouldn’t be surprised to see several big players go public in the next decade, if not the next five years.

As companies increase in value, the number of private individuals who could afford to purchase the company decreases quickly, leaving private corporations as the only potential buyers, or becoming publicly held. Sometimes, that’s a good thing because investment dollars are infused into new product development.

What we desperately need, and I predict will happen one way or another is a marriage of individual tools and functions that exist separately today, with a dash of innovation. We need tools that will move beyond confirming existing ancestors – and will be able to identify ancestors through our DNA – out beyond each and every brick wall.

If a tester’s DNA matches to multiple people in a group descended from a particular previously unknown couple, and the timing and geography fits as well, that provides genealogical researchers with the hint they need to begin excavating the traditional records, looking for a connection.

In fact, this is exactly what happened with mitochondrial DNA – twice now. A match and a great deal of digging by one extremely persistent cousin resulting in identifying potential parents for a brick-wall ancestor. Autosomal DNA then confirmed that my DNA matched with 59 other individuals who descend from that couple through multiple children.

BUT, we couldn’t confirm those ancestors using autosomal DNA UNTIL WE HAD THE NAMES of the couple. DNA has the potential to reveal those names!

I wrote about that in Mitochondrial DNA Bulldozes Brick Wall and will be discussing it further in my RootsTech presentation.

The Challenge

We have most of the individual technology pieces today to get this done. Of course, the combined technological solution would require significant computing resources and processing power – just at the same time that vendors are desperately trying to pare costs to a minimum.

Some vendors simply aren’t interested, as I’ve already noted.

However, the winner, other than us genealogists, of course, will be the vendor who can either devise solutions or partner with others to create the right mix of tools that will combine matching, triangulation, and trees of your matches to each other, even if you don’t’ share a common ancestor.

We need to follow the DNA past the current end of the branch of our tree.

Each triangulated segment has an individual history that will lead not just to known ancestors, but to their unknown ancestors as well. We have reached critical mass in terms of how many people have tested – and more success would encourage more and more people to test.

There is a genetic path over every single brick wall in our genealogy.

Yes, I know that’s a bold statement. It’s not future Jetson’s flying-cars stuff. It’s doable – but it’s a matter of commitment, investment money, and finding a way to recoup that investment.

I don’t think it’s possible for the one-time purchase of a $39-$99 DNA test, especially when it’s not a loss-leader for something else like a records or data subscription (MyHeritage and Ancestry) or a medical research partnership (Ancestry and 23andMe.)

We’re performing these analysis processes manually and piecemeal today. It’s extremely inefficient and labor-intensive – which is why it often fails. People give up. And the process is painful, even when it does succeed.

This process has also been made increasingly difficult when some vendors block tools that help genealogists by downloading match and ancestral tree information. Before Ancestry closed access, I was creating theories based on common ancestors in my matches trees that weren’t in mine – then testing those theories both genetically (clusters, AutoTrees and ThruLines) and also by digging into traditional records to search for the genetic connection.

For example, I’m desperate to identify the parents of my James Lee Clarkson/Claxton, so I sorted my spreadsheet by surname and began evaluating everyone who had a Clarkson/Claxton in their tree in the 1700s in Virginia or North Carolina. But I can’t do that anymore now, either with a third-party tool or directly at Ancestry. Twenty million DNA kits sold for a minimum of $79 equals more than 1.5 billion dollars. Obviously, the issue here is not a lack of funds.

Including Y and mitochondrial DNA resources in our genetic toolbox not only confirms accuracy but also provides additional hints and clues.

Sometimes we start with Y DNA or mitochondrial DNA, and wind up using autosomal and sometimes the reverse. These are not competing products. It’s not either/or – it’s *and*.

Personally, I don’t expect the vendors to provide this game-changing complex functionality for free. I would be glad to pay for a subscription for top-of-the-line innovation and tools. In what other industry do consumers expect to pay for an item once and receive constant life-long innovations and upgrades? That doesn’t happen with software, phones nor with automobiles. I want vendors to be profitable so that they can invest in new tools that leverage the power of computing for genealogists to solve currently unsolvable problems.

Every single end-of-line ancestor in your tree represents a brick wall you need to overcome.

If you compare the cost of books, library visits, courthouse trips, and other research endeavors that often produce exactly nothing, these types of genetic tools would be both a godsend and an incredible value.

That’s it.

That’s the challenge, a gauntlet of sorts.

Who’s going to pick it up?

I can’t answer that question, but I can say that 23andMe can’t do this without supporting extensive trees, and Ancestry has shown absolutely no inclination to support segment data. You can’t achieve this goal without segment information or without trees.

Among the current players, that leaves two DNA testing companies and a few top-notch third parties as candidates – although – as the past has proven, the future is uncertain, fluid, and everchanging.

It will be interesting to see what I’m writing at the end of 2025, or maybe even at the end of 2021.

Stay tuned.

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Genealogy Research

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Y DNA Resources and Repository

I’ve created a Y DNA resource page with the information in this article, here, as a permanent location where you can find Y DNA information in one place – including:

  • Step-by-step guides about how to utilize Y DNA for your genealogy
  • Educational articles and links to the latest webinars
  • Articles about the science behind Y DNA
  • Ancient DNA
  • Success stories

Please feel free to share this resource or any of the links to individual articles with friends, genealogy groups, or on social media.

If you haven’t already taken a Y DNA test, and you’re a male (only males have a Y chromosome,) you can order one here. If you also purchase the Family Finder, autosomal test, those results can be used to search together.

What is Y DNA?

Y DNA is passed directly from fathers to their sons, as illustrated by the blue arrow, above. Daughters do not inherit the Y chromosome. The Y chromosome is what makes males, male.

Every son receives a Y chromosome from his father, who received it from his father, and so forth, on up the direct patrilineal line.

Comparatively, mitochondrial DNA, the pink arrow, is received by both sexes of children from the mother through the direct matrilineal line.

Autosomal DNA, the green arrow, is a combination of randomly inherited DNA from many ancestors that is inherited by both sexes of children from both parents. This article explains a bit more.

Y DNA has Unique Properties

The Y chromosome is never admixed with DNA from the mother, so the Y chromosome that the son receives is identical to the father’s Y chromosome except for occasional minor mutations that take place every few generations.

This lack of mixture with the mother’s DNA plus the occasional mutation is what makes the Y chromosome similar enough to match against other men from the same ancestors for hundreds or thousands of years back in time, and different enough to be useful for genealogy. The mutations can be tracked within extended families.

In western cultures, the Y chromosome path of inheritance is usually the same as the surname, which means that the Y chromosome is uniquely positioned to identify the direct biological patrilineal lineage of males.

Two different types of Y DNA tests can be ordered that work together to refine Y DNA results and connect testers to other men with common ancestors.

FamilyTreeDNA provides STR tests with their 37, 67 and 111 marker test panels, and comprehensive STR plus SNP testing with their Big Y-700 test.

click to enlarge

STR markers are used for genealogy matching, while SNP markers work with STR markers to refine genealogy further, plus provide a detailed haplogroup.

Think of a haplogroup as a genetic clan that tells you which genetic family group you belong to – both today and historically, before the advent of surnames.

This article, What is a Haplogroup? explains the basic concept of how haplogroups are determined.

In addition to the Y DNA test itself, Family Tree DNA provides matching to other testers in their database plus a group of comprehensive tools, shown on the dashboard above, to help testers utilize their results to their fullest potential.

You can order or upgrade a Y DNA test, here. If you also purchase the Family Finder, autosomal test, those results can be used to search together.

Step-by-Step – Using Your Y DNA Results

Let’s take a look at all of the features, functions, and tools that are available on your FamilyTreeDNA personal page.

What do those words mean? Here you go!

Come along while I step through evaluating Big Y test results.

Big Y Testing and Results

Why would you want to take a Big Y test and how can it help you?

While the Big Y-500 has been superseded by the Big Y-700 test today, you will still be interested in some of the underlying technology. STR matching still works the same way.

The Big Y-500 provided more than 500 STR markers and the Big Y-700 provides more than 700 – both significantly more than the 111 panel. The only way to receive these additional markers is by purchasing the Big Y test.

I have to tell you – I was skeptical when the Big Y-700 was introduced as the next step above the Big Y-500. I almost didn’t upgrade any kits – but I’m so very glad that I did. I’m not skeptical anymore.

This Y DNA tree rocks. A new visual format with your matches listed on their branches. Take a look!

Educational Articles

I’ve been writing about DNA for years and have selected several articles that you may find useful.

What kinds of information are available if you take a Y DNA test, and how can you use it for genealogy?

What if your father isn’t available to take a DNA test? How can you determine who else to test that will reveal your father’s Y DNA information?

Family Tree DNA shows the difference in the number of mutations between two men as “genetic distance.” Learn what that means and how it’s figured in this article.

Of course, there were changes right after I published the original Genetic Distance article. The only guarantees in life are death, taxes, and that something will change immediately after you publish.

Sometimes when we take DNA tests, or others do, we discover the unexpected. That’s always a possibility. Here’s the story of my brother who wasn’t my biological brother. If you’d like to read more about Dave’s story, type “Dear Dave” into the search box on my blog. Read the articles in publication order, and not without a box of Kleenex.

Often, what surprise matches mean is that you need to dig further.

The words paternal and patrilineal aren’t the same thing. Paternal refers to the paternal half of your family, where patrilineal is the direct father to father line.

Just because you don’t have any surname matches doesn’t necessarily mean it’s because of what you’re thinking.

Short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs) aren’t the same thing and are used differently in genealogy.

Piecing together your ancestor’s Y DNA from descendants.

Haplogroups are something like our pedigree charts.

What does it mean when you have a zero for a marker value?

There’s more than one way to break down that brick wall. Here’s how I figured out which of 4 sons was my ancestor.

Just because you match the right line autosomally doesn’t mean it’s because you descend from the male child you think is your ancestor. Females gave their surnames to children born outside of a legal marriage which can lead to massive confusion. This is absolutely why you need to test the Y DNA of every single ancestral line.

When the direct patrilineal line isn’t the line you’re expecting.

You can now tell by looking at the flags on the haplotree where other people’s ancestral lines on your branch are from. This is especially useful if you’ve taken the Big Y test and can tell you if you’re hunting in the right location.

If you’re just now testing or tested in 2018 or after, you don’t need to read this article unless you’re interested in the improvements to the Big Y test over the years.

2019 was a banner year for discovery. 2020 was even more so, keeping up an amazing pace. I need to write a 2020 update article.

What is a terminal SNP? Hint – it’s not fatal😊

How the TIP calculator works and how to best interpret the results. Note that this tool is due for an update that incorporates more markers and SNP results too.

You can view the location of the Y DNA and mitochondrial DNA ancestors of people whose ethnicity you match.

Tools and Techniques

This free public tree is amazing, showing locations of each haplogroup and totals by haplogroup and country, including downstream branches.

Need to search for and find Y DNA candidates when you don’t know anyone from that line? Here’s how.

Yes, it’s still possible to resolve this issue using autosomal DNA. Non-matching Y DNA isn’t the end of the road, just a fork.

Science Meets Genealogy – Including Ancient DNA

Haplogroup C was an unexpected find in the Americas and reaches into South America.

Haplogroup C is found in several North American tribes.

Haplogroup C is found as far east as Nova Scotia.

Test by test, we made progress.

New testers, new branches. The research continues.

The discovery of haplogroup A00 was truly amazing when it occurred – the base of the phylotree in Africa.

The press release about the discovery of haplogroup A00.

In 2018, a living branch of A00 was discovered in Africa, and in 2020, an ancient DNA branch.

Did you know that haplogroups weren’t always known by their SNP names?

This brought the total of SNPs discovered by Family Tree DNA in mid-2018 to 153,000. I should contact the Research Center to see how many they have named at the end of 2020.

An academic paper split ancient haplogroup D, but then the phylogenetic research team at FamilyTreeDNA split it twice more! This might not sound exciting until you realize this redefines what we know about early man, in Africa and as he emerged from Africa.

Ancient DNA splits haplogroup P after analyzing the remains of two Jehai people from West Malaysia.

For years I doubted Kennewick Man’s DNA would ever be sequenced, but it finally was. Kennewick Man’s mitochondrial DNA haplogroup is X2a and his Y DNA was confirmed to Q-M3 in 2015.

Compare your own DNA to Vikings!

Twenty-seven Icelandic Viking skeletons tell a very interesting story.

Irish ancestors? Check your DNA and see if you match.

Ancestors from Hungary or Italy? Take a look. These remains have matches to people in various places throughout Europe.

The Y DNA story is no place near finished. Dr. Miguel Vilar, former Lead Scientist for National Geographic’s Genographic Project provides additional analysis and adds a theory.

Webinars

Y DNA Webinar at Legacy Family Tree Webinars – a 90-minute webinar for those who prefer watching to learn! It’s not free, but you can subscribe here.

Success Stories and Genealogy Discoveries

Almost everyone has their own Y DNA story of discovery. Because the Y DNA follows the surname line, Y DNA testing often helps push those lines back a generation, or two, or four. When STR markers fail to be enough, we can turn to the Big Y-700 test which provides SNP markers down to the very tip of the leaves in the Y DNA tree. Often, but not always, family-defining SNP branches will occur which are much more stable and reliable than STR mutations – although SNPs and STRs should be used together.

Methodologies to find ancestral lines to test, or maybe descendants who have already tested.

DNA testing reveals an unexpected mystery several hundred years old.

When I write each of my “52 Ancestor” stories, I include genetic information, for the ancestor and their descendants, when I can. Jacob was special because, in addition to being able to identify his autosomal DNA, his Y DNA matches the ancient DNA of the Yamnaya people. You can read about his Y DNA story in Jakob Lenz (1748-1821), Vinedresser.

Please feel free to add your success stories in the comments.

What About You?

You never know what you’re going to discover when you test your Y DNA. If you’re a female, you’ll need to find a male that descends from the line you want to test via all males to take the Y DNA test on your behalf. Of course, if you want to test your father’s line, your father, or a brother through that father, or your uncle, your father’s brother, would be good candidates.

What will you be able to discover? Who will the earliest known ancestor with that same surname be among your matches? Will you be able to break down a long-standing brick wall? You’ll never know if you don’t test.

You can click here to upgrade an existing test or order a Y DNA test.

Share the Love

You can always forward these articles to friends or share by posting links on social media. Who do you know that might be interested?

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Genealogy Research

Books

New Discoveries Shed Light on Out of Africa Theory, and Beyond

For many years, the accepted out-of-Africa Y DNA tree branches and calibration, meaning when that exit occurred, have focused on the exit of a single African lineage, CT-M168 which then, after leaving Africa, was believed to have split into three distinct branches:

  • C-M130 – exclusively non-African
  • DE-M145
  • FT-M89 – exclusively non-African (became F-M89)

Not long after, DE split into:

  • D-M174 – exclusively non-African
  • E-M96 – largely African

Obviously, if CT-M168 exited Africa and then branched into the other branches after its exit, either some branches had to have migrated back to Africa, or, there was something we didn’t know.

Turns out, there were multiple “somethings” we didn’t know.

D Divides – Thanks to Men in Nigeria

In August 2019, the paper A Rare Deep-Rooting D0 African Y-Chromosomal Haplogroup and Its Implications for the Expansion of Modern Humans Out of Africa was authored by Haber et al.

I wrote about the haplogroup D split in the article Exciting New Y DNA Haplogroup D Discoveries. 

Haber et al Paper

Abstract from the Haber paper:

Present-day humans outside Africa descend mainly from a single expansion out ∼50,000-70,000 years ago, but many details of this expansion remain unclear, including the history of the male-specific Y chromosome at this time. Here, we reinvestigate a rare deep-rooting African Y-chromosomal lineage by sequencing the whole genomes of three Nigerian men described in 2003 as carrying haplogroup DE* Y chromosomes, and analyzing them in the context of a calibrated worldwide Y-chromosomal phylogeny. We confirm that these three chromosomes do represent a deep-rooting DE lineage, branching close to the DE bifurcation, but place them on the D branch as an outgroup to all other known D chromosomes, and designate the new lineage D0. We consider three models for the expansion of Y lineages out of Africa ∼50,000-100,000 years ago, incorporating migration back to Africa where necessary to explain present-day Y-lineage distributions. Considering both the Y-chromosomal phylogenetic structure incorporating the D0 lineage, and published evidence for modern humans outside Africa, the most favored model involves an origin of the DE lineage within Africa with D0 and E remaining there, and migration out of the three lineages (C, D, and FT) that now form the vast majority of non-African Y chromosomes. The exit took place 50,300-81,000 years ago (latest date for FT lineage expansion outside Africa – earliest date for the D/D0 lineage split inside Africa), and most likely 50,300-59,400 years ago (considering Neanderthal admixture). This work resolves a long-running debate about Y-chromosomal out-of-Africa/back-to-Africa migrations, and provides insights into the out-of-Africa expansion more generally.

In 2003, five Nigerian men were sequenced yielding haplogroup DE, but the sequencing technology since that time has improved dramatically. In 2019, those early samples were resequenced by Haber and analyzed in combination with information not available in 2003.

Resequencing yielded a new ancient clade, branching from the DE lineage close to the divergence of the D and E split. The lineage formed by the Nigerian sample was named D0 (D zero) by the authors to avoid needing to rename the downstream branches. It should be noted that the authors used the older letter-number-letter naming method coined as “nomenclature by lineage” from the first YCC paper, rather than the SNP naming method called “Nomenclature by mutation,” aks shorthand – hence their concern about renaming branches. Having said that, typically the base branch names are retained for reference, regardless, and D0 is clearly a base haplogroup.

The Nigerian samples were narrowed from 5 to 3 quality samples. Those three samples had been collected from unrelated men in different villages from different cultures who spoke different languages. Their Y DNA estimated date of convergence, meaning their most recent common ancestor (MRCA,) is about 2500 years ago.

The results of full genome sequencing are far more robust today and the theories about the exit of mankind from Africa are informed by Neanderthal genomic information. All people worldwide have about 2% Neanderthal genome, but African peoples do not – other than the North African region where back-migration has occurred.

This split in the tree increases the early lineages from 4 to 5 with DE now including the following three branches:

  • D0 – exclusively African (became D2-FT75)
  • E – mainly African
  • D – exclusively non-African (became D1-M174)

Out of Africa Theories

The three out of Africa theories proposed by Haber are illustrated below with Figure 2 from their paper. Please note that dates are estimates and different calculation methodologies produce different date ranges.

click to enlarge

Haber et al put forth the above three theories in their paper.

You’ll note that:

  • Option B shows haplogroup CT exiting Africa as was originally believed, but with D0 and E back-migrating, and E-M35 eventually leaving again, with other E haplogroups remaining.
  • Option C shows CT splitting in Africa with C, DE and FT exiting Africa about the same time, with D0 and E back migrating and E-M35 leaving again.
  • Option D shows CT and DE both splitting in Africa, with only C, D and FT exiting out of Africa initially, together, in one single event, with E-M35 following later.

Option D, of the above options, is the most parsimonious model, meaning the fewest amount of complex items needs to occur and is, therefore, most likely to have actually happened. Option D does not include or require any back-migration to occur and accommodates all of the haplogroups found exclusively in Africa along with those found only outside of Africa.

Dr. Miguel Vilar, anthropologist and former Lead Scientist for National Geographic’s Genographic Project provides the following comment about Option D and introduces Option E.

  • Option E – Haplogroup CT splits into two branches CF and DE within Africa, then haplogroups D and E split followed by CF and D leaving Africa. However, this requires C and F to split after D and E have already split, which is not the current calculated sequence of events. This sequence would constitute a new Option E scenario, where haplogroups CF and D (or pre-D1) leave Africa, with E following later.

Neanderthal

It turns out that the sequencing of the Neanderthal genome appears to be the tie-breaker between scenarios B, C, and D.

All non-Africans carry about 2% Neanderthal in their genomes, worldwide. This means that the Neanderthal had to have interbred with the migrants who left Africa before they dispersed widely. They carried that Neanderthal DNA with them as they dispersed throughout the world, indicating that the entire population that existed at that time, shortly after the exit from Africa, and survived, was intermixed between the two populations.

African peoples do not carry Neanderthal admixture. Therefore, had there been back-migration of haplogroups D0 and E, African peoples would also carry some Neanderthal, and they do not which effectively removes the options of B and C.

To date, scenario D, which also includes other archaeological evidence, is the best fit between the three Haber models, plus Dr. Vilar’s Option E. The Haber paper is short and a good read.

Y Haplotree Updates

FamilyTreeDNA included the changes to haplogroup D, incorporating their own findings.

Michael Sager, the phylogeneticist at Family Tree DNA who is responsible for the Y DNA tree gave a great presentation in early 2020 at Genetic Genealogy Ireland, which you can view here.

The latest tree at Family Tree DNA looks like this, with haplogroup D split into Asian and African lineages.

New Haplogroup F Lineages

So where did the haplogroup F lineage go after having left Africa? New discoveries at FamilyTreeDNA provide some clues.

Before the new haplogroup F branches were added, the haplogroup F tree looked like this. There were known basal F lineages, but FamilyTreeDNA did not have any Big Y testers that belonged to those branches of haplogroup F and were not at that time making use of NGS results from academic studies to define tree branches.

Since then, among the thousands of new Big Y test results, a few haplogroup F lineages have been identified.

click to enlarge

The view of the Y DNA tree at FamilyTreeDNA shows the locations of the various test results. Please note that people in the F-M89 haplogroup may simply have not tested beyond that level today, and would benefit from the Big Y test.

The Y tree now includes the new branch F-F15527 (F1) with four immediate subclades with samples from Indonesia, Malaysia, Vietnam, and the southern border of China, as shown on this map.

What Does This Mean???

Goran Runfeldt, the head of Research and Development at Family Tree DNA says:

Finding F1 exclusively in Southeast Asia is significant because it represents the first split of haplogroup F.

Additionally, it gives some clues about where haplogroup F was before it split between F1 and GHIJK, which represents all the haplogroups F through T.

It is also significant that they all belong to different branches, four immediate subclades of F1, dated to circa 48,000 years ago. This shows a rapid expansion where several lineages quickly diverged then and survived for tens of thousands of years until present day. It is very likely that we will discover other ancient lineages in this part of the tree as more people from this part of the world take a high coverage Y-DNA test.

Michael Sager adds:

We have many distinct lineages close to the root of F (F1a, F1b, F1c, F1d, G, H, IJK.) All of these (and more) arose within a couple thousand years. All of these descendants in conjunction provide excellent support for the theory that F was long out of Africa. We did not have that clear support for haplogroup D as we had a ~20ky bottleneck to account for as well as Ds closest relative, E, being in Africa.

I asked Dr. Vilar for his opinion about the expansion of haplogroup F.

The discovery of new F1 lineages in Southeast Asia suggests that there was both a rapid and a broad expansion of paternal lineages across Eurasia some 55,000 years ago. Rapid because we see F lineages in China and Southeast Asia shortly after modern humans leave Africa some 60,000 years ago.

The pattern in haplogroup F is similar to that of its “cousin lineages” in haplogroup C, which likely moved through South Asia to Southeast Asia and even Australia shortly after its exodus from Africa.

Unlike F, haplogroup C is also found in Central Asia and the Americas, so the two paths may not have been exactly the same.

However, the range of F was also broad, since it gave rise to an older son (GHIJK) years earlier, and much further west. GHIJK likely arose in western Asia, where descendants G, H, and IJ were all born in the following millennia.

Acknowledgments

Thank you to the following individuals for their review of and input to this article:

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Genealogy Research

Books

DNA Tidbit #5: What’s Your Goal?

You probably see this all the time on social media:

“I just got my DNA results. Now what?”

No further information is given.

The answer is, “What is your goal?”

Why did they test and what are they hoping to learn?

DNA Tidbit Challenge: Define goals for answering genealogy questions, allowing you to focus your efforts.

Your DNA testing goal depends on a number of factors including:

  • What test you took, meaning Y DNA, mitochondrial or autosomal.
  • Where you tested and the tools they offer.
  • What you’re hoping to achieve. In other words, why did you test in the first place?

For a short article about the difference between Y, mitochondrial, and autosomal DNA, please click here.

For more seasoned genealogists, we may have taken all the tests and answered many questions already, but still, our research needs to be guided by goals.

I regularly check my matches. I still think I may have had a half-sibling that is yet to be located. After I confirm that no, I don’t have any new close matches, I then look at the rest, making notes where appropriate.

Recently, late one night, I thought to myself, “why am I doing this?” Endlessly scrolling through new matches and randomly seeing if I can figure out where they fit or which ancestor we share.

But why?

Originally, I had two broad goals.

  • I wanted to find Y line males in each line and other males from the same supposed line to confirm that indeed the ancestral line is what the paper trail had identified.
  • To confirm that I am indeed descended from the ancestral lines I think I am, meaning no NPEs. As a genealogist, the only thing I’d hate worse than discovering that I’ve been researching the wrong line for all these years is to keep doing so.

Given that I’ve confirmed my connection to ancestors on most lines back several generations now, what are my goals?

Broad and Deep

I’ve realized over the years that goals are both broad and deep.

Broad goals are as I described above, in essence, spanning the entire tree.

My broad goals have changed a bit over time. I’ve located and tested descendants of many Y lines, but I’m still working on a few. I’ve confirmed most of my lineage back several generations by matching the DNA from other children of the same ancestor and using tools like triangulation and DNAPainter to confirm the segment is actually from the ancestral couple I think it is.

I’ve added the goal of breaking down brick walls.

This means that I need to look deep instead of broad.

Deep means that I need to focus on and formulate a plan for each line.

Looking Deep

I’ve identified three specific deep goals and put together a plan with action steps to achieve those goals.

  • Deep Goal #1 – Collecting and Using Y and Mitochondrial DNA

I like to “collect” the Y DNA and mitochondrial DNA results/haplogroups of my ancestors for different reasons. First, I’ve discovered surprises in where their DNA originated. For both Y DNA and mitochondrial DNA, you can identify their continent of origin as well as confirm ancestors or break down brick walls for that one specific line through matches and other tools at Family Tree DNA.

Looking at my tree, my closest ancestor whose Y DNA or mtDNA I don’t have is my great-grandmother, Evaline Miller (1857-1939) who had 4 daughters who all had daughters. You wouldn’t think it would be this difficult to find someone who descends to current through all daughters.

How do I go about achieving this goal? What are some alternatives?

  • Track and ask family members, if possible.
  • Find descendants using MyHeritage, Ancestry and Geneanet (especially in Europe) trees. Bonus – they may also have photos or information that I don’t, especially since this isn’t a distant ancestor.

click to enlarge

Ancestry’s ThruLines shows your matches by ancestor, so long as the connection can be made through trees. Unfortunately, in this case, no one descends correctly for mitochondrial DNA, meaning through all females to the current generation which can be male. BUT, they might have an aunt or uncle who does, so it’s certainly worth making a contact attempt.

  • I can also use WikiTree to see if someone has already tested in her line. Unfortunately, no.

However, I don’t know the profile manager so maybe I should click and see how we might be related. You never know and the answer is no if you don’t ask😊

Deep Goal #2 – Confirming a Specific Ancestor

I want to confirm that a specific ancestor is my ancestor, or as close as I can get.

What do I mean by that?

In the first couple of close generations, using autosomal DNA, we can confirm ancestral lines and parentage. We can confirm our parents and our grandparents, but further back in that, we have to use a combination of our tree and other tools to confirm our paper genealogy.

For example, as we move further back in time, we can’t confirm that one particular son was the father as opposed to his brother. In closer generations, autosomal DNA might help, but not beyond the first couple of generations. Second cousins always match autosomally, but beyond that, not so much.

Using Y DNA, if we can find a suitable candidate, I can confirm that my Estes ancestor actually does descend through the Estes line indicated by my paper trail.

I need to find someone in my line either to test or who has already tested, of course.

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If they do test and share their match information with me, and others from that same line have tested, I can see their earliest known ancestors on their Y DNA match page.

If someone from that line has already tested and has joined a surname project, you can see their results on the public project page if they have authorized public project display.

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This is also one way of determining whether or not your line has already tested, especially if you have no Y DNA matches to the expected surname and ancestor. If others have tested from that ancestor, and you don’t match them, there’s a mystery to be unraveled.

To see if projects exist for your surnames, you can click here and scroll down to the search box, below.

Please note that if someone else in your family takes the Y DNA test, that doesn’t guarantee that you descend from that ancestor too unless that person is a reasonably close relative and you match them autosomally in the expected way.

Confirmation of a specific ancestor requires two things without Y DNA testing:

  • Sharing autosomal matches, and preferably triangulated segments, with others who descend from that ancestor (or ancestral couple) through another child.
  • Eliminating other common ancestors.

Of course, Ancestry’s ThruLines are useful for this purpose as are MyHeritage’s Theories of Family Relativity, but that only works if people have linked their DNA results to a tree.

My favorite tool for ancestor confirmation is DNAPainter where you can paint your segments from FamilyTreeDNA, 23andMe, MyHeritage and GEDmatch, either individually or in bulk. You can’t use Ancestry DNA information for this purpose, but you can transfer your Ancestry DNA file to those other vendors (except 23andMe) for free, and search for matches without retesting. (Step-by-step transfer instructions are found here.)

Here’s an example of a group of my matches from various companies painted on one of my chromosomes at DNAPainter. You can read all about how to use DNAPainter, here.

I identify every match that I can and paint those segments to that ancestor. Ancestors are identified by color that I’ve assigned.

In this case, I have identified several people who descend from ancestors through my paternal grandmother’s side going back four generations. We have a total of 12 descendants of the couple Henry Bolton and Nancy Mann (burgundy), even though initially I can only identify some people back to either my grandparents (mustard color) or my grandmother’s parents (grey) or her grandparents (blue). The fact that several people descend from Henry and Nancy, through multiple children, confirms this segment back to that couple. Of course, we don’t know which person of that couple until we find people matching from upstream ancestors.

What about that purple person? I don’t know how they match to me – meaning through which ancestor based on genealogy. However, I know for sure at least part of that matching segment, the burgundy portion, is through Henry Bolton and Nancy Mann, or their ancestors.

Deep Goal #3 – Breaking Down a Brick Wall

Of course, the nature of your brick wall may vary, but I’ll use the example of not being able to find the parents of an ancestral couple.

In the above example, I mentioned that each segment goes back to a couple. Clearly, in the next generation, that segment either comes from either the father or mother, or parts from both perhaps. In this case, that oldest burgundy segment originated with either Henry Bolton or Nancy Mann.

In other words, in the next generation upstream, that segment can be assigned to another couple.

Even if we don’t know who that couple is, it’s still their DNA and other people may have inherited that very same segment.

What we need to know is if the people who share that segment with us and each other also have people in their trees in common with each other that we don’t have in our trees.

Does that make sense? I’m looking for commonality between other testers in their trees that might allow me to connect back another generation.

That common couple in their trees may be the key to unlocking the next generation.

Caveat – please note that people they have in common that we don’t may also be wives of their ancestors downstream of our common ancestor. Just keep that in mind.

Let’s shift away from that Bolton example and look at another way to identify clusters of people and common ancestors.

In order to identify clusters of people who match me and each other, I utilize Genetic Affairs autocluster, or the AutoCluster features incorporated into MyHeritage or the Tier 1 “Clusters” option at GEDmatch.

Based on the ancestors of people in this red cluster that I CAN identify, I know it’s a Crumley cluster. The wife of my William Crumley (1767/8 – 1837/40) has never been identified. I looked at the trees of the people in this cluster that I don’t know and can’t identify a common ancestor, and I discovered at least two people have a Babb family in their tree.

Babb was a near neighbor to William Crumley’s family, but I’ve also noticed that Babb married into this line downstream another 3 generations in Iowa. These families migrated from Frederick County, VA to Greene County, TN and on, together – so I’ll need to be very careful. However, I can’t help but wonder if my William’s wife was a Babb.

I need to see if any of my other matches have Babb as a common name. Now, I can search for Babb at any of the testing vendors to see what, if anything, I can discover.

Genetic Affairs has a combined AutoCluster and AutoTree/AutoPedigree function that compares and combines the trees of cluster members for you, here.

Goals Summary

Now, it’s your turn.

  • What are your genealogy goals that DNA can assist with?
  • Are those goals broad or deep?
  • What kind of DNA test can answer or help answer those questions?
  • What tools and research techniques fit the quandary at hand?

I suggest that you look at each ancestor, and in particular each end-of-line ancestor thinking about where you can focus to obtain answers and reveal new ancestors.

Happy ancestor hunting!

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Genealogy Research

Books

Holiday DNA Sales Have Started Early

Wow – the sales started early this year! I understand that Black Friday has morphed into the month of November. I’m good with that!

I’m not really surprised because many people are spending more time at home and let’s face it, genealogy is a great at-home activity. I’m glad the sales are starting earlier and running longer because it encourages more people to become engaged.

Genealogy can even help you produce holiday gifts for others in a myriad of ways. Not just purchasing DNA kits for yourself and family members but creating stories or giving them a book you’ve created with photos of grandma and grandpa’s life, perchance.

Of course, DNA is a HUGE part of genealogy. Even if you’re not going to be able to see Uncle Joe this Thanksgiving, you can certainly have a fun Zoom session and document him swabbing or spitting for his DNA test! Make memories, one way or another

Let’s see what the vendors are offering. Then, be sure to read to the end for a surprise.

FamilyTreeDNA – Early Bird Holiday Sale

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FamilyTreeDNA has more products to offer than any of the other vendors with autosomal, Y DNA and mitochondrial DNA tests, each offering something unique.

Y DNA focuses only on your direct patrilineal (surname) line if you are a male. Mitochondrial DNA follows your matrilineal (mother’s mother’s mother’s) line for both sexes. The Family Finder autosomal test traces all ancestral lines. You can read a quick article about these different tests and how they work in this article:

The Family Finder test uses matches to known family members like parents, aunts, uncles and cousins to assign other matches who match both you and your family member to either maternal or paternal sides of your tree.

You can also use Genetic Affairs AutoCluster, AutoTree and AutoPedigree tools at FamilyTreeDNA to get even more mileage out of your DNA tests.

If you were an early tester with Y and mitochondrial DNA, you can upgrade now to a more robust test to receive more granular results.

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Have you noticed the ancient DNA articles I’ve been writing recently?

Your most refined haplogroup revealed only in the Big Y-700 or mitochondrial mtFull Sequence test allows you to compare your haplogroup with ancient samples most effectively. I promise you, there will be more articles upcoming! These are just pure joy, connecting back in time.

The FamilyTreeDNA sale ends November 24th. Please click here to order or upgrade.

MyHeritage

MyHeritageDNA includes lots of features that other vendors don’t have, such as integrated AutoClusters and Theories of Family Relativity (TOFR) which connects you and your matches through a network of common records and trees. TOFR is surprisingly accurate, either pointing the way to or identifying common ancestors.

I wrote about how to use these and other included tools to unravel your genealogy in this recent article, with a free companion webinar:

Additionally, MyHeritage has a strong focus in Europe that includes lots of European testers – perfect for people whose ancestors are emigrants from another country.

MyHeritageDNA is on sale now for $49, a $30 savings, plus free shipping if you purchase two or more kits. Please click here to order.

This sale ends November 25th.

Ancestry

Best known for their large database, AncestryDNA offers ThruLines which takes advantage of their database size to suggest common ancestors for you and your matches based on multiple trees. I wrote about ThruLines in this article:

The AncestryDNA test is on sale now for $59, a $40 savings, with free US shipping. Please click here to order.

Sale ends November 23rd.

23andMe

23andMe is best known in the genealogy community for the accuracy of their Ancestry Composition, known as ethnicity results, which they paint on your chromosomes.

23andMe also creates a “genetic tree” between you and your closest matches based on who does and who does not match each other, and how they match each other. I wrote about genetic trees and subsequently, how they solved one mystery in these two articles.

While the genetic tree technology isn’t perfected yet, it’s certainly the direction of the future and can provide insight into how you and others are related and where to look for them in your actual genealogy tree.

The 23andMe Ancestry only test is available for a 10% reduction in price at $88.95. Please click here to order.

Of course, 23andMe also offers a health product that includes the ancestry product.

The 23andMe Health + Ancestry test is available for $99, a saving of 50%. Please click here to order.

These sale prices end November 26th.

Surprise!!!

I have an early holiday gift for you too.

Beginning later this week, I’m publishing the first article in a new interactive series aptly named…drum roll…“DNA Tidbits.”

Indeed, there is fruit-of-the-vine to be harvested and that’s exactly what we are going to do – in small steps! Tidbits.

Just like everything else on this blog, it’s completely free of course and we are going to have lots of FUN!

Let me give you a hint – you’ll probably want to have test results at all of these companies because the Tidbits will be bouncing around a bit – so if you need to buy something, please click on the links below.

Thank you and I can’t wait to get started!

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Genealogy Research

Books

Free Y DNA Webinar at Legacy Family Tree Webinars

I just finished recording a new, updated Y DNA webinar, “Wringing Every Drop out of Y DNA” for Legacy Family Tree Webinars and it’s available for viewing now.

This webinar is packed full of information about Y DNA testing. We discuss the difference between STR markers, SNPs and the Big Y test. Of course, the goal is to use these tests in the most advantageous way for genealogy, so I walk you through each step. There’s so much available that sometimes people miss critical pieces!

FamilyTreeDNA provides a wide variety of tools for each tester in addition to advanced matching which combines Y DNA along with the Family Finder autosomal test. Seeing who you match on both tests can help identify your most recent common ancestor! You can order or upgrade to either or both tests, here.

During this 90 minute webinar, I covered several topics.

There’s also a syllabus that includes additional resources.

At the end, I summarized all the information and show you what I’ve done with my own tree, illustrating how useful this type of testing can be, even for women.

No, women can’t test directly, but we can certainly recruit appropriate men for each line or utilize projects to see if our lines have already tested. I provide tips and hints about how to successfully accomplish that too.

Free for a Limited Time

Who doesn’t love FREE???

The “Squeezing Every Drop out of Y DNA” webinar is free to watch right now, and will remain free through Wednesday, October 14, 2020. On the main Legacy Family Tree Webinar page, here, just scroll down to the “Webinar Library – New” area to see everything that’s new and free.

If you’re a Legacy Farmily Tree Webinar member, all webinars are included with your membership, of course. I love the great selection of topics, with more webinars being added by people you know every week. This is the perfect time to sign up, with fall having arrived in all its golden glory and people spending more time at home right now.

More than 4000 viewers have enjoyed this webinar since yesterday, and I think you will too. Let’s hope lots of people order Y DNA tests so everyone has more matches! You just never know who’s going to be the right match to break down those brick walls or extend your line back a few generations or across the pond, perhaps.

You can view this webinar after October 14th as part of a $49.95 annual membership. If you’d like to join, click here and use the discount code ydna10 through October 13th.

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Disclosure

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

Thank you so much.

DNA Purchases and Free Transfers

Genealogy Products and Services

Genealogy Research

Search Techniques for Y and Mitochondrial DNA Test Candidates

I utilize DNA matches in various ways, some of which are a little unusual. In many cases, I mine autosomal DNA matches to search for people whose Y and mitochondrial DNA can provide descendants, including me and them, with additional insights into our common ancestors.

Y and mitochondrial DNA connects testers to their ancestors in ways that autosomal cannot. It’s a different type of DNA, not combined with the DNA of the other parent, so it’s not diluted and halved in each generation like autosomal DNA. Y and mitochondrial lines each descend from only one ancestral line, rich in historical information, with the ability to reach far back in time along with the ability to connect testers recently.

You First

The very first thing you can do to further your own research is to test yourself in three ways:

  • Autosomal DNA – Test at all 4 primary testing vendors, meaning FamilyTreeDNA, MyHeritage, Ancestry and 23andMe. The reason for testing at (or transferring to) multiple vendors is because they each have a unique focus and tools. Perhaps more importantly, they each have different people in their databases. Each testing company has benefits. FamilyTreeDNA has people who tested as long as 20 years ago and are no longer available for testing. MyHeritage has many European testers and you’ll find matches there that you won’t find elsewhere if your ancestors came from Europe. Ancestry has the largest database, but fewer advanced tools.
  • Full Sequence Mitochondrial DNA Available at FamilyTreeDNA, this test allows focus solely on your matrilineal line, meaning your mother’s mother’s mother’s line directly without confusion introduced by DNA from other lines.
  • Y DNA – For males only, also available at FamilyTreeDNA, provides focus on the direct patrilineal, or surname, line.

Obviously, if you haven’t upgraded your own Y and mitochondrial DNA tests to the highest level possible, the first thing you can do is to test or upgrade to the highest level where you receive the most refined amount of information.

(There’s a sale at FamilyTreeDNA right now, lasting until August 31, 2020, so it’s a great time to upgrade or order Y and mitochondrial. Check it out here.)

Different Kinds of DNA Serve Different Genealogical Purposes

Let’s look, briefly at how the various types of DNA tests benefit genealogy. Autosomal tests that you and family members can take will help you find other family members to test for specific Y and mitochondrial DNA lines.

Remember that you can test family members in addition to yourself, so if you’re a female, you may want to recruit your father or an uncle or brother to represent your patrilineal line DNA. If you’d like to read a brief article about the different types of DNA and their benefits, 4 Kinds of DNA for Genetic Genealogy is a good resource.

Y and Mito Pedigree.png

In this image, you can see that if you’re a male you can test for both your Y (blue-square) and mitochondrial DNA (red-circle) ancestral lines. If you’re a female, you can test only your mitochondrial DNA because females don’t have a Y chromosome. Both males and females, of course, can test (green) autosomal DNA which reveals a different type of connection to all of your ancestral lines, but with autosomal, you have to figure out which people match you on which lines.

Y and mitochondrial DNA provides you with a different type of information about laser-focused specific lines that you can’t obtain through autosomal testing, and reaches back in time far beyond the curtain when surnames were adopted.

personal pedigree

You personally can only test for the red-circle mitochondrial DNA line, and perhaps the blue-square Y DNA line if you’re a male. Unless you find family members to test for the Y and mitochondrial DNA of your ancestors, you’re leaving valuable information unresearched. That means all those colored boxes and squares that aren’t blue or red.

I’ve solved MANY brick walls using both Y and mitochondrial DNA, often in conjunction with autosomal.

Let’s take a look at each type of DNA testing a little more in-depth, so that you understand how each one works and why they are important to genealogy.

The Specifics

Y DNA – Y DNA descends through the direct male paternal line and is inherited by men only. You match against other Y DNA testers, hopefully finding surname links.

The Big Y test and upgrade at FamilyTreeDNA provides testers with all 111 traditional STR markers, plus another 589+ STRs available only in the Big Y test, plus a scan of the balance of the rest of the Y chromosome that is useful for genealogy. SNP results are increasingly being used for genealogy, in addition to STRs.

SNPs group men into genetic lineages and STRs help with defining and refining the closest generations when matching to each other. Often, the benefits of these two tests overlap, which is why I recommend that males test to the Big Y-700 level which provides 700+ STR markers plus all SNPs with mutations that define ancestral lineages.

Y DNA haplogroups, derived from SNPs, reveal the geographic part of the world where the lineage originated, such as Europe, the Americas, Asia and Africa, as well as a migration path across the continents based on where SNPs are and were historically found. Ancient DNA samples are being added to the database.

If you or a family member took an earlier Y DNA test, you can upgrade to the Big Y-700 today which provides you with matching for both the STR markers and separately, SNP markers, along with other genealogical tools.

You can order or upgrade your Y DNA here. Don’t forget family members accounts you may control. They may agree to have their kit upgraded too.

To upgrade, sign in to your account, and click on your desired upgrade level under Y DNA testing.

ymt y upgrade.png

Then click on upgrades.

ymt upgrade.png

I wrote about Y DNA in these recent articles:

I have more Y DNA articles planned for the future.

You can search for additional articles by going to the main page of this blog and enter “Y DNA” into the search box for additional articles already published.

Many features such as the matches maps, haplogroup origins and ancestral origins pages are the same for Y DNA results as mitochondrial DNA results. You can view mitochondrial articles here.

Mitochondrial DNA (mtDNA) – Mitochondrail DNA descends through the direct matrilineal line to both sexes of children. Everyone has mitochondrial DNA and it is inherited matrilineally by you from your mother, from her mother, from her mother, etc.

The FMS or full mitochondrial sequence DNA test tests the entire mitochondria that provides information about your direct matrilineal line. Family Tree DNA provides matching, which can sometimes lead to genealogical breakthroughs such as when I identified Lydia Brown, the mother of my Phoebe Crumley and then a couple years later, her mother, Phoebe Cole – via mitochondrial DNA. Those discoveries led us to her mother, Mary Mercy Kent, via genealogy records. All we needed was to punch our way through that initial brick wall – and mitochondrial DNA was our battering ram.

Additionally, you’ll receive a full haplogroup designation which allows you to look back in time before the advent of surnames and identifies the location where your ancestral line came from. For those seeking confirmation of Native American heritage, Y and mitochondrial DNA provides unquestionable proof and doesn’t wash out in time as autosomal DNA does.

Mitochondrial DNA includes haplogroups, matching and other genealogical tools.

You can order or upgrade you or a family member’s mitochondrial DNA here.

To upgrade, sign in to your account, and click on the desired upgrade level.

ymt mt upgrade

Then click on Upgrade if you’re upgrading or Add On if you’re ordering a new product for yourself.

ymt add ons upgrades.png

I wrote several mitochondrial DNA articles and compiled them into a summary article for your convenience.

Autosomal DNA – With autosomal DNA testing, you test once and there’s not an upgrade unless the vendor changes DNA testing platforms, which is rare. Each of the four vendors compares your DNA with all other people who’ve taken that test, or transferred from other companies. They match you with descendants from all of your ancestral lines. While the Y and mtDNA tests look back deeply in time as well as recently on one specific line, the autosomal tests are broad but not deep, spanning all ancestral lines, but limited to approximately 10 generations.

Each autosomal vendor has unique benefits and focus as well as shortcomings. I’ve listed the major points for each vendor relative to searching for Y and mitochondrial
DNA testing candidates. It’s important to understand the advantages of each vendor because it will help you understand the testers you are most likely to find in each database and may help focus your search.

FamilyTreeDNA’s Family Finder

  • Because FamilyTreeDNA archives customer’s DNA for 25 years, many people who tested Y or mitochondrial DNA 20 years ago and are now deceased upgraded to autosomal tests when they became available, or have been upgraded by family members since. These early testers often reach back another generation or so into the past to people born a century ago.
  • Advanced autosomal matching integrates with Y and mitochondrial DNA along with surname and other projects
  • Phased Family Matching provides the ability to link family members that match you to your tree which allows Family Tree DNA to group matches as paternal or maternal by utilizing matching segments to the same side of your family
  • Genetic Affairs, a third-party tool available for testers, builds common trees by reading the trees of your matches and comparing their trees with your own to identify common ancestors.
  • Genetic Affairs builds trees and pedigrees of your matches by searching for common ancestors in your MATCHES trees, even if you have no tree or don’t share those ancestors in your tree. This functionality includes Y and mitochondrial DNA if you have tested. This facilitates discovery of common ancestors of the people who you match, which may well lead you to ancestral discoveries as well.
  • Genetic Affairs offers clustering of your shared matches.
  • DNA file transfers are accepted from other vendors, free, with a $19 one time fee to unlock advanced tools.
  • Family Tree DNA has tested people worldwide, with a few location exceptions, since inception in the year 2000.
  • No direct triangulation, but Phased Family Matching provides maternal and paternal side triangulation when matches can be grouped into maternal and paternal sides.
  • Matches and segment match information are available for download.
  • The great thing about the advanced matching tool at Family Tree DNA is that it facilitates searching for people who match you on different kinds of tests, so it helps determine the potential closeness or distance of Y and mitochondrial relationships.

MyHeritage

Ancestry

  • Ancestry has the largest database, but did not begin testing until 2012 and did not test widely outside of the US/UK for some time. They now sell tests in 34 countries. Their testers are primarily focused in the US, Canada, England, Scotland, Ireland, and diaspora, with some overlap into Europe.
  • Ancestry offers ThruLines, a tool that connects testers whose DNA matches with common ancestors in their trees.
  • Ancestry does not provide a chromosome browser, a tool provided by the other three primary testing companies, nor do they provide triangulation or matching segment location information necessary to confirm that you match on the same segment with other people.
  • Ancestry has issued cease and desist orders to third party tools that perform functions such as clustering, autotrees, autopedigrees or downloading of matches. Ancestry does not provide these types of features for their users.
  • Ancestry does not accept transfers, so if you want to be in Ancestry’s database, you must test with Ancestry.
  • No Y or mitochondrial DNA testing available.
  • Match list is not available for download.

23andMe

  • The primary focus of 23andMe has always been health testing, so many people who test at 23andMe are not interested in genealogy.
  • 23andMe tests are sold in about 50 countries, but not worldwide.
  • 23andMe provides a chromosome browser, triangulation, segment information and a beta genetically constructed tree for close matches.
  • 23andMe does NOT support a genealogical tree either uploaded or created on their site, making tree comparisons impossible.
  • Genetic Affairs AutoCluster works at 23andMe, but AutoTree and AutoPedigree do not because 23andMe does not support trees.
  • 23andMe does make match files available for downloading.
  • No Y or mitochondrial DNA full testing or matching, but basic haplogroups are provided.
  • 23andMe caps matches at 2000, less any matches that have opted out of matching. My matches currently number 1770.
  • 23andMe does not accept transfers from other vendors, so if you want to be in their database, you must test with 23andMe.

Reaching Out to Find Testers

Unfortunately, we only carry the mitochondrial DNA of our mother and only men carry the Y DNA of their father. That means if we want to obtain that DNA information about our other family lines, we have to find people who descend appropriately from the ancestor in question and test that person.

I’ll share with you how I search for people who descend from each ancestor. After finding that person, I explain the situation, why the different kinds of tests are important, and offer a testing scholarship for the Y or mtDNA test at Family Tree DNA if they have not already taken that test. If they’ve tested their autosomal DNA elsewhere. I also explain that they can transfer their autosomal DNA file for free too and will receive new matches.

Here’s an article with links to upload/download instructions for each testing company. Feel free to share.

Each DNA testing company has different features, but you can use all of the companies to find people descended in the appropriate way from each ancestor. It’s easier if you know how to utilize each vendor’s tools to optimize your chances of success. I’m going to step you through the search process with hints and tips for each vendor.

Finding Y DNA and Mitochondrial DNA Candidates at FamilyTreeDNA

Because FamilyTreeDNA tests for both Y and mitochondrial DNA and has for 20 years, you stand a better chance of finding a candidate there who may have already tested, so that’s where I always begin.

Y DNA

Let’s say, for example, that I need to find a male descendant of my Ferverda line in order to ask them to test for Y DNA. The person can be descended from either a close relative, if I know of one, or a more distant relative that I don’t know, but need to find through searching other ways.

Search for Surnames and Projects at Family Tree DNA

First, search the FamilyTreeDNA website for your goal surname among existing testers, and then the appropriate surname project to see if your line has already tested.

ymt ferverda

On the main page, here, scroll down to until you see the prompt, above, and enter the surname. Be sure to consider alternate spellings too.

ymt ferverda search.png

In this case, I see that there is a Ferverda surname project with 18 people, and scrolling on down, that 4 people with this specific surname have tested.

ymt results.png

However, searching for an alternate spelling, the way it’s spelled in the Netherlands, I find that another 10 people have tested.

ymt ferwerda

Of course, some may be females, but they probably know males by that surname.

First, I’m going to check the Ferverda DNA project to see if a Ferverda male from my line has tested, and if so, to what level.

Click on the project link in the search results to see the DNA Project.

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Note two things. First, the administrator’s name, as you may need this later. If you click on their name, their email address is displayed.

Second, click on DNA Results and select Y DNA if you’re presented with a choice. If the project has a public facing page, and most do, you’ll see something like the following information.

ymt project

Hey look, it’s my lucky day, given that both of these men descend from my ancestor. I happen to know that they have both taken the Big Y test, because I’m the project administrator, but you won’t know that. One way to get an idea is if they have less than the full 111 markers showing, they probably haven’t taken the Big Y, because a 111 upgrade is included in the Big Y test today.

You have three options at this point to contact one of these men:

  • See if the people are on your own autosomal DNA match list, or the match lists of kits from that family that you manage. If so, you can view their email address and contact them. If you haven’t yet tested autosomally, meaning the Family Finder test, at Family Tree DNA, you can transfer autosomal tests from elsewhere, for free, which means you will be viewing matches within hours or a couple days. Otherwise, you can order a Family Finder test, of course.
  • If the person with the Ferverda or Ferwerda surname is not on your Family Finder match list, reach out to the project administrator with a note to the person you want to contact and ask the administrator to forward your email to the project member.
  • If the administrator doesn’t answer, contact Family Tree DNA support and make the same request.

Checking Family Finder, one of those people is on my match list and I’m pretty sure it’s the right person, because when I click on his profile, not only does the haplogroup match the DNA project, but so does the ancestor.

ymt ferverda profile.png

Searching Family Finder

If there isn’t a DNA project match you can identify as your direct line ancestor, you can search your Family Finder matches for the surname to find a male with that surname. If your match has a tree, see if your ancestor or ancestral line is showing, then note whether they have taken a Y DNA test. They may have taken a Y test, but have not joined a project or not entered any “earliest known ancestor.” You can see which tests they’ve taken by looking at the little tabs above their profile on their tree, or on their profile card.

ymt ferverda tree

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Regardless, you’re now in touch with a potential contact.

Don’t dismiss females with that surname, or people who show that surname in their ancestral surname list. Women with the surname you’re looking for may have husbands, fathers, brothers or uncles who descend from the line you are seeking.

ymt search field.png

Utilize Genetic Affairs

My ace in the hole at FamilyTreeDNA is the Genetic Affairs AutoTree and AutoPedigree function.

Genetic Affairs is a third-party tool that you can use to assist with analysis of your matches at FamilyTreeDNA.

ymt genetic affairs

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At Genetic Affairs, selecting AutoTree generates trees where common ancestors of you and your matches, or your matches to each other, are displayed.

Your goal is to identify people descended from a common ancestor either directly paternally through all males for Y DNA or through all females to the current generation, which can be males, for mitochondrial DNA.

This article provides step-by-step instructions for the Genetic Affairs AutoTree and AutoPedigree functions.

Mitochondrial DNA

Mitochondrial DNA lineages are a bit more challenging because the surname changes every generation and DNA projects are unlikely to help.

The AutoTree/AutoPedigree report through Genetic Affairs serves the same purpose for mitochondrial DNA – building trees that intersect with a common ancestor. I generally drop the “minimum size of the largest DNA segment shared with the match” to 7 cM for this report. My goal running this report for this purpose isn’t to analyze autosomal DNA, but to find testing candidates based on how my matches descend from a specific ancestor, so I want to include as many matches as possible.

Family Finder Can Refine Y and mtDNA Information

In some cases, a Family Finder test can refine a potential relationship between two people who match on either Y DNA or mitochondrial. Additionally, you may want to encourage, or gift, specific matches with an upgrade to see if they continue to match you at higher testing levels.

Let’s say that two men match closely on a Y DNA test, but you’d like to know how far back the common ancestor lived.

ymt y matches.png

In this instance, you can see that the second match has taken a BIg Y and a Family Finder test, but the exact match (genetic distance of 0) has not. If the first individual cannot provide much genealogy, having them take a Family Finder test would help at least rule out a relationship through second cousins and would give you at least some idea how far back in time your common ancestor may have lived. If you do match on Family Finder, you receive an estimate of your relationship and can check the match level possibilities using the DNAPainter Shared cM Tool. If they upgrade to the Big Y-700 test, you may be able to differentiate your line from theirs, or confirm when and where a split occurred – or that there is no split.

This same autosomal testing scenario works for mitochondrial DNA.

For people who have taken both tests, Family Finder plus either Y or mitochondrial DNA, the Advanced Matching menu allows you to select combinations of tests and projects to query.

ymt advanced

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Finding Y and Mitochondrial DNA Candidates at MyHeritage

MyHeritage provides a wonderful tool called Theories of Family Relativity (TOFR) which finds common ancestors between you and your DNA matches, even if the ancestor is not in both trees, so long as a path exists between the two testers’ trees using other trees or research documents, such as census records. Of course, you’ll need to verify accuracy.

ymt tofr.png

At MyHeritage, select DNA Matches, then “Has Theory of Family Relativity.”

ymt mh ferverda

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You can see that I have 65 matches with a Theory of Family Relativity. Additionally, I can then search by surname.

ymt mh ferverda tree.png

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If I am looking for a Ferverda Y DNA candidate, I’ve found one thanks to this TOFR.

If you don’t find a tree where your match descends from your ancestor in the desired way, you can also widen the search by de-selecting Theories of Family Relativity and instead selecting SmartMatchs or shared surname combined with the name of your ancestor. There are many search and filter combinations available.

Let’s look at a mitochondrial DNA example where I’m searching for a descendant of Elizabeth Speaks who married Samuel Clarkson/Claxton.

ymt smartmatches

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In this case, I have one SmartMatch, which means that someone by the name of Elizabeth Speaks is found in my matches tree. I need to look to see if it’s the RIGHT Elizabeth Speaks and if my match descends through all females to the current generation. If so, I’ve found my mitochondrial DNA candidate and I can leave them a message.

You can also view SmartMatches (without a DNA match) from your own tree.

I can go to that person in my tree, click on their profile, and see how many SmartMatches I have. Clicking on 13 SmartMatches allows me to view those matches and I can click through to the connected trees.

ymt mt speaks.png

I can also click on “research this person” to discover more.

If you’re still not successful, don’t give up quite yet, because you can search in the records for trees that shows the person whom you seek. A SmartMatch is only created if the system thinks it’s the same person in both trees. Computers are far from perfect.

ymt mh trees

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Narrow the search as much as possible to make it easier to find the right individual, and then view the trees for descent in the proper manner.

Another wonderful tool at MyHeritage is the Genetic Affairs AutoCluster tool, built-in for MyHeritage users.

ymt mh cluster.png

The above cluster shows that one person carries the surname of Elizabeth’s husband. Viewing the accompanying spreadsheet for the AutoCluster run reveals that indeed, I’ve already identified a couple of matches as descendants of the desired ancestral couple. The spreadsheet shows links to their trees, my notes and more.

ymt cluster ss

Clusters show you where to look. Without the cluster, I had only identified two people as descendants of this ancestral couple. I found several more candidates to evaluate and two mitochondrial candidates are found in this cluster.

Finding Y and Mitochondrial DNA Candidates at 23andMe

23andMe is a little more tricky because they don’t support either uploaded or created user trees which makes finding descendants of a particular ancestor quite challenging.

However, 23andMe attempts to create a tree of your closer relatives genetically. which you can find under “DNA Relatives,” under the Ancestry tab, then “Family Tree” at the top.

I’ve added the names of my ancestors when I can figure out who the match is. Please note that this “created tree” is seldom exactly accurate, but there are often enough hints that you’ll be able to piece together at least some of the rest.

Here’s part of my “created” tree at 23andMe. I’m at far right.

ymt23 tree.png

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If you’re a genealogist, your eyes are going to glaze over about now, because the “people” aren’t in the correct locations – with maternal and paternal sides of the tree swapped. Also, please note, the locations in which they place people are estimates AND 23andMe does NOT take into account or provide for half-relationships.

That said, you can still obtain candidates for Y and mitochondrial DNA testing.

In this case, I’m searching for a mitochondrial DNA candidate for Evaline Miller, my grandfather’s mother or a Y DNA candidate for the Ferverda line.

I can tell by the surname of the male match, Ferverda, that he probably descends through a son, making him a Y DNA candidate.

Both Cheryl and Laura are possible mitochondrial DNA candidates for Evaline Miller, based on this tree, depending of course on how they actually do descend.

I can contact all of my matches, but in the event that they don’t answer, I’m not entirely out of luck. If I can determine EXACTLY how the match descends, and they descend appropriately for mitochondrial DNA, I can view the match to see at least a partial haplogroup. Since 23andMe only uses relatively close matches when constructing your tree, I’m relatively likely to recognize the names of the testers and may have them in my genealogy program.

By clicking on the Ferverda male, I can see that his Y haplogroup is I-Z58. That’s not nearly as refined as the Y DNA information at Family Tree DNA, but it’s something if I have nothing else and he doesn’t answer my query that would include the offer of a Y DNA test at Family Tree DNA.

ymt 23 hap

You can search at 23andMe by surname, but unless your match has entered their ancestral surnames and you recognize surnames that fit together, without a tree, unless your match answers your query, it’s very difficult to determine how you connect.

ymt 23 search.png

You can also view “Relatives in Common,” hoping to recognize someone you know as a common match.

ymt relatives in common

Please note that 23andMe does allow testers to enter a link to a tree, but few do.

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It’s worth checking, and be sure to enter your own tree link location.

Finding Y and Mitochondrial DNA Candidates at Ancestry

Ancestry’s ThruLines provides an excellent tool to find both Y and mitochondrial DNA participants.

Ancestry organizes their ThruLines by ancestor.

ymt thrulines

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Select your desired Ancestor, someone whose DNA you seek. Clearly, Y DNA candidates are very easy because you simply choose any male ancestor in the correct line with the surname and look for a male match with the appropriate surname.

In this case, I’m selecting Martha Ruth Dodson, because I need her mitochondrial DNA.

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By clicking on her “card” I then see my matches assigned to her ThruLine.

Ymt ancestry thruline

Obviously, for mitochondrial DNA, I’m looking for someone descended through all females, so Martha’s daughter, Elizabeth Estes’s son Robert won’t work, but her daughter, Louisa Vannoy, at left is the perfect candidate. Thankfully, my cousin whom I match, at bottom left is descended through all females to the current generation, which can be male or female, so is a mitochondrial DNA candidate.

Finding Y and Mitochondrial DNA Candidates in Trees in General

I’ve utilized the combination of trees and DNA matches at FamilyTreeDNA through Genetic Affairs, Ancestry and MyHeritage, but you can also simply search for people who descend from the same ancestor based on their tree alone at the vendors who support trees as part of genealogical records. This includes both Ancestry and MyHeritage but also sites like Geneanet which is becoming increasingly popular, especially in Europe. (I have not worked extensively with Geneanet yet but plan to take it for a test drive soon.)

My reason for utilizing DNA matches+trees first is that the person has already been introduced to the concept that DNA can help with genealogy, and has obviously embraced DNA testing at least once. Not only that, with the assist of a Theory of Family Relativity, ThruLine or genetic Affairs automation tools, it’s much easier to find appropriate candidates.

Finding Y and Mitochondrial DNA Candidates at WikiTree

If you reach beyond DNA testing companies, WikiTree provides a valuable feature which allows people to specify that they descend from a particular ancestor, and if they have DNA tested, how they descend – including Y DNA, mitochondrial DNA and autosomal.

Here’s an example on the profile of John Y. Estes at WikiTree, one of my Estes ancestors.

ymt wiki.png

If someone descends appropriately for either Y or mitochondrial DNA line, and has taken that test, their information is listed.

In this case, there are two Y DNA testers and two autosomal, but no mitochondrial DNA which would have descended from John’s mother, of course.

You can click on the little green arrow icon to see how any DNA tested person descends from the ancestor whose profile you are accessing.

ymt wiki compare

Of course, the same surname for males is a good indication that the man in question is descended from that paternal line, but check to be sure, because some males took their mother’s surname for various reasons.

Here’s my line-of-descent from John Y. Estes. I can click on anyone else whose DNA information is listed as well to see how they descend from John. If they descend from John through all females, then they obviously descend from his wife though all females too which means they are a mitochondrial DNA candidate for her.

ymt wiki relationship.png

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Clicking on autosomal testers may reveal someone appropriately descended from the ancestor in question.

You can then click on any ancestor shown to view their profile, and any DNA tested descendants.

By clicking on name of the descendant whose DNA test you are interested in, you’ll be able to view their profile. Look for the Collaboration section where you can send them a private message that will be delivered by email from WikiTree.

ymt collaborate

Finding Y and Mitochondrial DNA Candidates at GedMatch

One final avenue to find Y and mitochondrial DNA candidates is through GedMatch, It’s probably the least useful option, though, because the major vendors all have some sort of tree function, except for 23andMe, and for some reason, many people have not uploaded GEDCOM files (trees) to GEDmatch.

Therefore, if you can find someone on GedMatch that tested elsewhere perhaps, such as LivingDNA who also provides a base haplogroup, or 23andMe, and they uploaded a GEDCOM file (tree) to GedMatch, you can utilize the GEDmatch “Find common ancestors” automated tree-matching functionality.

gedmatch mrca matches

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GEDmatch produces a list of your matches with common ancestors in their trees, allowing you to select the appropriate ancestor or lineage.

I wrote step-by-step instructions in the article, GEDmatch Introduces Automated Tree Matching.

Additionally, GEDmatch includes the Genetic Affairs AutoCluster tool in their Tier1 subscription offering,

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Gedmatch users who know their Y and mitochondrial haplogroup can enter that information in their profile and it will be reflected on the autosomal match list.

ymt gedmatch hap

Summary Chart

In summary, each testing vendor has a different focus and unique tools that can be used to search for Y and mitochondrial DNA candidates. Additionally, two other resources, WikiTree and GEDmatch, although not DNA testing vendors, can lead to discovering Y and mtDNA candidates as well.

I’ve created a quick-reference chart.

  Family Tree DNA MyHeritage Ancestry 23andMe Wikitree GEDmatch
Y DNA Test Yes No No No, partial haplogroup provided No test, listed by ancestor No, user entered
mtDNA Test Yes No No No, partial haplogroup provided No test, listed by ancestor No, user entered
DNA Projects Yes No No No Some Some
Strengths other than mentioned categories 20 year worldwide customer base, phased family matching European focus, SmartMatches, wide variety of filters Largest autosomal database Genetic tree beta DNA by ancestor May include users not found elsewhere who tested outside the major companies
Drawbacks No direct triangulation or tree matching No Genetic Affairs AutoTree or AutoPedigree Can’t download matches, no triangulation, clusters, AutoTree, or AutoPedigree No trees, 2000 match limit “One tree” may be incorrect Few trees, no AutoTree or AutoPedigree
Clustering Genetic Affairs Included in advanced tools No, prohibited Genetic Affairs N/A Included in Tier1
Genetic Affairs AutoTree & AutoPedigree Yes No No No, no tree support N/A No
Tree matching between users No, through Genetic Affairs Theories of Family Relativity ThruLines No Not directly MRCA common ancestors in Tier1

Now it’s your turn. Which Y and mitochondrial DNA lines can you find today?

Happy Hunting!

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