FOCUS – A New Series Focused on Breaking Down Brick Walls

When I teach about genetic genealogy, people often ask, “What’s next? How can I break down my brick wall?” Sometimes I can reply that a Y-DNA test or mitochondrial DNA will help them under specific circumstances. But more often than not, what they really need is a precise, step-by-step methodology that includes autosomal DNA and utilizes multiple tools and techniques across vendors.

Even after people have taken Y-DNA and/or mitochondrial DNA tests PLUS autosomal tests at the major vendors, we still need a methodology to work with combinations of those results. Often, the answers we need aren’t just sitting there like a pretty rock, waiting to be picked up and admired, but depend on us using the results and matches as tools to help focus our search in the right direction.

It’s more like a scavenger hunt than a single discovery.

Focus

Sometimes I feel like a fish out of water – flip-flopping from ancestor to ancestor, match to match and hint to hint, hoping that the magic bullet will fall into my lap, but that almost never happens.

By this point in my research, I’ve perused all the easy records and many of the not-so-easy ones. If you don’t have a surname, or you don’t have a first name, or worse yet, you don’t have either, how is one supposed to search for records?

The good news is that you still carry at least one record in your own body and/or the bodies of your relatives. The DNA of your ancestors.

This is where we’re going to focus our efforts – hence FOCUS, the name of this new series.

Everyone is going to select their closest, or one of their closest, brick-walled ancestors, and we’re going to use several methods and tools to focus on identifying that ancestor.

Prepare

Before I publish the next article in the series, there are a few things that I’d like you to think about and do in preparation.

  • First, there’s no guarantee that you’ll break through your brick wall during this series. You might, and you also might not. You stand a much better chance of breaking through that brick wall if you focus and follow these steps than if you don’t.

Keep in mind that even negative evidence is evidence, and just because you don’t break through right away doesn’t mean you won’t. New people test everyday and new records become available too. If nothing else, your ancestor will have more meat on their bones, and you’ll have a process to build upon.

  • Second, if your brick wall is very close in time, meaning parents or grandparents, you’ll want the already-written “In Search Of Unknown Family” series, which you can find, here.
  • Third, you’ll need to keep a research journal or log by ancestor, family or location, which will also include your other related ancestors. For example, if you’re looking for Lucy whose surname you don’t know, but you know that she married William Moore, then your research journal will apply to William Moore too, and other people including their children and either spouse’s parents and siblings, whether that was your intention or not. The neighbors are probably relevant as well.

That “it takes a village” saying is particularly relevant here. People didn’t tend to move to the next location alone, and often their community consisted of their cousins and relatives – who are also your relatives, and hold clues to the identity of your ancestor. When I’m extracting records for the Moore surname in Halifax County, VA, for example, I extract everything for that and similarly spelled surnames, not just one particular person, so I don’t have to replow that field.

Tracking and Recording Your Research

If you don’t already have a research journal methodology, I would suggest a spreadsheet.

Here’s a screenshot of two rows in my “Halifax County” spreadsheet where I’ve recorded separate rows for each person in every record. Note that I started this spreadsheet years ago and omitted some columns that I later wished I had included, like the access date.

You’ll want to record:

  • Item number beginning with 1. In the example above, the item number is 6, and it’s 6 for every person in that record. Each person in this transaction gets their own separate row, with the same item number. The next record I extracted would be item 7.
  • Access date (date you found and retrieved the record)
  • Last name
  • First name
  • State (add a column for country if multiple countries are relevant for this family)
  • County
  • Town, township or city
  • Geographic places like road or creek names (these can be VERY important)
  • Year, month and day that the record occurred
  • Record repository or source (including a link if applicable – you may want to add a separate column for the link)
  • Record type (deed, will, tax list, etc.)
  • Role of individual (buyer, seller, witness, etc.)
  • Names of additional people in the record (I retain the same item number and other information, changing the name of the person, their role and sometimes an associated comment)
  • Transcribed text of the record itself
  • Comment, which can include things like the name of an image, something about what you were searching for when you found the record, links, or anything else relevant

You will want to be able to sort and filter this spreadsheet when you are finished. Hint – be sure your date fields and formats are sortable in the way you wish. I normally use filters instead of the sort feature.

The goal isn’t just to record your findings, but to make this spreadsheet as useful as possible to make discoveries that are only available by comparing and incorporating multiple records.

For example, let’s say that you’re extracting all of the Moore records in a Halifax County, VA deed book, and you want to know how many times the surname Henderson is found in the Moore deeds or in conjunction with the Moore family. Is there a pattern? You won’t recognize a pattern from any ONE record, but you may eventually wonder if the Henderson’s are related to the Moore family, and if so, how.

You’ll also want to record nonproductive or negative evidence. For example, let’s say you searched the Halifax County Plea Book for William Moore (including More and Mohr) and found no occurrences. That’s important, because otherwise you‘ll eventually search again, so enter that as a record item.

Note that with the full text search feature introduced by FamilySearch a couple of years ago, if you extracted records from a book that did NOT include every-name indexing including property lines, creek names and witnesses – you’ll want to redo that search using the full text feature at FamilySearch. There’s often LOTS of valuable information buried in records that won’t be found if you’re only viewing records indexed by buyer and seller, for example.

Your To-Do List Before the Series Begins

The In Search Of Unknown Family Series introduces important concepts, so reading that series is your first assignment in preparation for the upcoming FOCUS articles.

Test Your DNA With the Major Vendors

It’s important to test with the major vendors. Each vendor has matches and tools that the others don’t, and we need to identify and work with as many relevant matches as possible.

If you have NOT taken an autosomal DNA test at the first three following vendors, order these tests now so you have results to work with.

  1. AncestryDNA
  2. FamilyTreeDNA – Purchase a Family Finder test or upgrade an earlier Family Finder test to the new Family Finder NGS test. You should upgrade if you uploaded your autosomal DNA file from another vendor at any time, or tested at FamilyTreeDNA directly before March of 2026. The upgrade is only $29.
  3. MyHeritage DNA
  4. A fourth vendor, 23andMe, is optional, but testing there certainly won’t hurt.

23andMe Sidebar

I have an issue with 23andMe’s policy of forcing customers to repurchase a DNA test at $199 PLUS a subscription at $149 for the first year, renewable at $69 per year, in order to obtain any of their latest tools. This happened around the time of their data breach and subsequent bankruptcy.

I would feel much better about the situation as a whole if a new owner had taken the wheel, but the original owner resigned from the 23andMe board, formed another corporation, and was allowed to buy 23andMe out of the bankruptcy that occurred on her watch.

Furthermore, 23andMe does not support genealogy trees, nor do they have Y-DNA or mitochondrial DNA testing and matching, or research records.

I have (begrudgingly) ordered an upgrade for my own 23andMe test in order to include accurate information in these articles, but I won’t be focusing on 23andMe specifically aside from any unique feature. You can apply the same concepts and techniques to results at 23andMe where possible.

Test Your Relatives

If you have close upstream relatives, such as parents, grandparents, aunts, uncles, and cousins who also descend from your brick-walled ancestor, please ask them to test too.

I explain what I’m trying to achieve, why their test is important, and offer scholarships to sweeten the pie. I view purchasing their DNA tests in the same way I view purchasing a rare research book that I KNOW includes my ancestors but it not available anyplace else.

Your shared matches are extremely important and may provide that brick-wall-breaker. Perhaps even more importantly, they will have relevant matches that you don’t.

So how do you know who to test? You certainly want to test everyone relevant, without wasting money.

Let’s look at this example where Lucy is the brick-walled ancestor I’m seeking to identify. Her children (labeled siblings) and grandchildren (1C) are all deceased, but second cousins (2C), Rhonda, Charles and Sally are all available to test. Test each of them because they will all have some different segments of DNA from Lucy that the others don’t have.

Lazarus is also a second cousin, but he’s deceased. However, William, my father (in this example, not my real pedigree), and his sister, Jane are both available to test.

You ALWAYS want to test both of your parents and every available grandparent or direct ancestor. In this example, I’ll only inherit some portion of Lucy’s DNA that my father has, but Jane, my aunt, will carry segments of Lucy’s DNA that my father didn’t inherit from Lazarus. Jane’s matches on those segments that neither my father nor I have may be just what we need to identify Lucy.

If Lazarus has other children not shown in this example, we certainly want to test them too.

If the relevant parent has tested, you don’t need to test any of their children. However, if the parent hasn’t tested, absolutely test as many of their children or descendants as possible.

In this case, Rhonda, Jane, Charles and Sally have all tested, so I don’t need to test their children. Their children can only have as much of Lucy’s DNA as their parents had.

However, if any of them had been deceased, then I should test as many of their children as I can to “gather up” as much of Lucy’s DNA as possible.

If any of the people upstream of the bold red people have other children, those children or their descendants would be testing candidates too. Ideally, you want as many descendant testers as possible to increase your chances of identifying that ancestor.

Selecting Your Brick-Wall Ancestor

I want you to be successful, so you’re going to select your closest brick-walled ancestor within certain parameters. If you have multiple brick-walled ancestors at the at the same genealogical distance, you’ll choose one to focus on.

Why your closest brick-walled ancestor? If your brick wall is 5 generations back from you, and they are 5 generations back from your DNA match as well, that means you’re dealing with a 4th cousin match.

This also means that ancestor’s DNA has been divided a total of 10 times – five times on the path of descent to you, and five times on the path of descent to your match.

A 4th cousin match is likely to be in the 35 cM range. You can view the matching ranges for various relationships at DNAPainter, here.

The entire 4th cousin (4C) matching range is 0-139 cM. You won’t match all of your 4th cousins and are likely to match only 50-70% of your 4th cousins.

That said, the average person has between 1,500 and 4,000 4th cousins. At the 4th cousin level, you have 32 ancestors, so only between 46 and125 4th cousins will descend from any given ancestor, and of those, only a few will have taken a DNA test. The more children that ancestor had that lived to marry and have children of their own, the better your chances of more matches.

The Selection Process

I’m going to be stepping through the ancestor selection process with you, discussing who is and isn’t a good candidate, and why. I’m also going to be using this same methodology to (hopefully) identify one of my own mystery ancestors too.

I have no brick walls closer than 4th cousins. If I did, I’d choose the closest brick wall. You should too in order to have the best chance of solving this puzzle. The further back in time, the more difficult the solve will be.

In my tree, I have four mystery ancestors at the 5X great-grandparent level on my father’s side, and one on my mother’s side.

Those will be the four ancestors I consider selecting. And no, before you do it, I don’t recommend working on all four of them at the same time. Remember, the purpose is to FOCUS.

  • Select an ancestor as close generationally as possible, because it’s more likely that both you and other people will carry at least some of their DNA, and the same segment(s) of DNA. Matches closer in time generally carry more total DNA in common, which means better matching and more shared matches.
  • Given that the majority of testers are from the US, and assuming you are from the US too, I don’t recommend selecting an ancestor from another country unless you are very comfortable with that language and working with those records. Generally, there will be fewer people who have tested from other countries. If you are going to work with an ancestor from another country, be sure you are in both the MyHeritage and FamilyTreeDNA databases.

My mother’s entire paternal line is either Dutch or German Brethren, and her Dutch ancestors only immigrated in the mid 1800s, so have few descendants in the databases.

My closest brick wall on her paternal line is Traut Enterlein, a German man who was named in an out-of-wedlock baptism for his daughter in Germany in 1823. He is not found in any other records in that part of Germany, so actually identifying “who he is”, even with a name, would be extremely difficult, and I have nothing to “anchor to” here.  He is eliminated as a candidate because he’s found in a country where I don’t speak the language, where fewer people have taken DNA tests, and we’ve already spent a substantial amount of time trying to identify him in the records.

Brick-walled ancestors on Mom’s maternal side are two generations further back in time. Half are German and the other half are a combination of English and Acadian.

  • Avoid both endogamy and pedigree collapse, if possible. I don’t recommend a line with baked-in challenges that will make DNA more difficult.

Acadians are heavily endogamous and often suffer from pedigree collapse since there were so few founding families in the mid-1600s. The same goes for Brethren families who immigrated in the early 1700s. Those lines are too far back generationally anyway, so they have already been eliminated, but if they weren’t, I’d eliminate them because of heavy endogamy and pedigree collapse, both, not to mention record loss.

My father’s side has much better candidates.

  • Try to select an ancestor where you have some familiarity with the location, the culture, and the records. If you have printed resources at the ready, possibly ones that are not online, that’s a plus.
  • When you’re trying to decide between ancestors, select one whose spouse you are sure of, and who has children you can document. Do you know important things about them like their religion, where they lived during specific times, and who their neighbors were? If not, take some time now to brush up on what you do know about their spouse and children.
  • Check back at all of the records vendors and resources, including Ancestry, MyHeritage, WikiTree, and FamilySearch, to see if anything new is easily available for either your brick-wall candidate or their spouse.
  • I do NOT recommend selecting an ancestral couple, neither of whom you can identify, unless you’re “lucky” enough to have no other brick-walled ancestors to choose from. It’s possible to solve this “double-blind” couple, but it’s substantially more difficult because you have no same-generation anchor.

My Candidates

I’m selecting one of my brick walls and hope to solve it during this process. Let’s run through the decision-making process so you’ll understand some of the considerations and why they weigh as factors. I wish I didn’t have so many choices, and I’d like to solve them all, but my best chance is to work on one at a time.

Most candidates are women because their birth surnames tend to easily become lost after they marry, and with their surname, their parents are lost too. Given how little we know, we have to presume (dangerous word), at least for now, that your missing female ancestor was the mother of all of their husband’s children, unless we know or subsequently prove otherwise.

Let’s review my candidates.

  1. Lucy was born about 1754, probably in Virginia, and died in 1832 in Halifax County, VA. She married William Moore between 1772 and 1774, who may or may not have been a circuit-riding minister at that time. She is found under her own name on the 1830 census, there’s an 1826 chancery suit, and I know who her children and neighbors are, so she might be a good candidate. One vote against selecting Lucy is that I don’t know where she was born, nor do I know where they were married, although there’s a very strong possibility that it took place in Halifax County. The fact that he was a circuit-rider means he could have met her anyplace. If they were married in Halifax County, their families could have been allied before arriving there. William Moore’s family came from Prince Edward County about 1770, and we know who his parents were. One good thing is that Lucy is a fairly uncommon name, but there are multiple William Moores in Halifax County, and there are two other Lucy Moores. One is her daughter, and one is her daughter-in-law. The fact that Lucy and William Moore had 12 known children, with at least 8 who married, means there is a good chance of matching at least some descendants. Unfortunately, I don’t have her mitochondrial DNA, which removes one possible tool unless I can find a tester.
  2. Jane, born about 1760 in an unknown location, but probably Virginia, was the wife of Lazarus Dodson. They moved across multiple frontiers into what would become early Tennessee, an area that sustained substantial record loss. Jane died between 1830 and 1840. There’s a lot of uncertainty about Jane’s life. She probably had at least 8 children, and we know something about six of them. Given that we already have a better candidate with Lucy, I’ll eliminate Jane for now.
  3. William Crumley’s wife, whose name I don’t know, was born around 1765 or 1770, possibly in Virginia. She was married to William Crumley around 1786 or 1787, probably in Frederick County, VA, or nearby. I do have her mitochondrial DNA and we know the family was Quaker which are both benefits. I’ve been working with a cousin who has delved deeply into Quaker records, and I have some records from a trip to the FamilySearch Library in Salt Lake City that I have not yet processed. She and William had at least 10 children who married, and I know quite a bit about them. She would probably be an excellent choice. For lack of another name, I’ve been calling her H2a1, her legacy mitochondrial haplogroup before Mitotree, but she has a much more complete haplogroup now. She would be a good candidate, and I REALLY want to identify her.
  4. Mary, wife of John Harrold (by various spellings), was born about 1750, possibly in Ireland, although it would be unusual for a first-generation Irish immigrant to end up deep in the Appalachian frontier. Mary died in 1826 in Wilkes County, NC. We know nothing about John’s background, other than he served in the Revolutionary War, in Virginia. He may have been living in Botetourt County, although we don’t know for sure, and there are multiple men by that name. Mary had at least 7 children, six of whom were married. We do not have her mitochondrial DNA. Given that we know so little about John, and we have better candidates with both Lucy, William Moore’s wife, and William Crumley’s wife, I’m eliminating Mary for now.
  5. Isabel, the wife of Michael McDowell – another couple from Wilkes County, NC. Their daughter married the son of Mary and John Harrold. Isabel was probably born about 1750, someplace in Virginia. We don’t know where they were married, but it could have been in Franklin County, VA. They lived in Wilkes County for several decades before moving on to Claiborne County, TN. We know very little about Michael’s early life, other than his Revolutionary War service, although I’ve written about him four times as additional information dribbles out. They had at least 8 children, and a deposition after Michael’s death tells us where they moved and settled, which is a very big plus. We know her first name thanks to a 1793 deed. Isabel is a reasonable candidate, but I eliminated her after comparison to the other candidates, in part because of multiple frontier moves with few records and no known point of origin.
  6. Elizabeth, wife of Andrew McKee, was born about 1767, possibly someplace in Virginia. They were in Washington Co., VA by 1789, although we don’t know where either originated. They may have married before they moved to Washington County, where we find several records. They had 14 children. Twelve are known to have married, and the other two probably did as well. We know who their neighbors were. We also have Elizabeth’s mitochondrial DNA. Unfortunately, we know nothing about Andrew McKee’s family or where he was from. However, Elizabeth is a strong candidate because so many records exist in Washington County, they had a large number of children, and many continued to live in Washington County or nearby, making them easier to track.
  7. If I didn’t already have good candidates, there’s one more ancestor I’d consider, even though James Lee Claxton/Clarkson is a generation further back in my tree, born about 1775, and his unknown parents are the brick walls. I know I just told you NOT to do this, so I won’t either, but the reason I might have considered his parents, or more specifically his father, as a strong candidate is because we have several Y-DNA matches, including Big-Y testers, and we know the ancestors of his matches came from NC. We also have many autosomal testers and matches, which would help immensely, and there’s a Clarkson/Claxton DNA Surname Project. A contiguous surname is a HUGE benefit not available with female ancestors, and I just feel that I’m SO CLOSE to solving this mystery. For now, James’s parents are eliminated because they are two generations further back in time than our other candidates, we know nothing about either of them, except Y-DNA results, and we have better candidates for this exercise.

After evaluation, I still have two candidates in the running – Lucy, wife of William Moore, and H2a1, William Crumley’s wife. I haven’t decided for sure yet, but right now, William Crumley’s wife is leading because I have an amazing collaborator along with some unprocessed records that may hold important information. I know there probably aren’t any smoking guns there, but when combined with DNA, we may well ignite that gunpowder.

FOCUS

Are you ready to focus?

Let’s get our ducks in a row.

  • Order any DNA tests you need to order for yourself and relatives now.
  • Select your ancestor.
  • Prepare your research journal by reviewing which records you’ve already researched and record what you have.
  • Refamiliarize yourself. Take a look at those results again with fresh eyes. It helps when reviewing match results to be able to view surnames in your matches trees and recall that you’ve seen that name before, and where.
  • Check to see if any new records or resources are now available.

Who do you want to find?

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The New Family Finder NGS Test Results, Comparison, and Preparation

This article is focused on two things.

  1. Comparison of my new NGS and the earlier Family Finder tests
  2. How to prepare for yours if you’ve ordered the upgrade

I compared my results from my older Family Finder test with my new NGS Family Finder test results. As an early beta tester, I have two separate tests, a strategy that is not recommended because it causes duplicate matches for people within the database. Additionally, multiple kits for one person doubles the results and could skew future ethnicity research for myOrigins.

Therefore, FamilyTreeDNA has announced very attractively priced upgrades at $29 for both:

  • People who have taken Family Finder test directly at FamilyTreeDNA
  • People who have uploaded their DNA files into Family Finder from other companies

After seeing my comparison, you may want to compare your own results when they arrive, so I’ve documented that process. Warning: this took between 4 and five days because I was working with a spreadsheet with more than 15,000 rows, and I had to write scripts to perform multiple functions. It was NOT fun and I do not recommend it.

Personally, had I known then what I know now about how reliable the new NGS test is, I wouldn’t have bothered with the comparison. However, I would have downloaded my original match list for posterity, just in case.

If you purchase an upgrade to the new NGS Family Finder, your new test results will replace your older Family Finder test results, but will preserve important account features such as linked matches, any notes you have taken, and more. That’s another reason to upgrade rather than order a separate new test. They’ve done the heavy lifting, not to mention that you’ll save about $50 when compared to the price of a new test.

Why is the New NGS Family Finder Test Better?

The new NGS test holds immense promise for the future. This includes better matching, beginning now. Essentially, FamilyTreeDNA is skating to where the puck is going to be (hockey analogy) and preparing for future tools. That future is not far away!

An amazing new set of tools is goaled for release around the end of the year. And I do mean amazing. They are being beta-tested internally now.

Dave Vance spoke about the new Family Finder NGS test at the ECGGC conference in late August, which you can view through the end of 2026 if you register for the virtual  conference, here, and watch the recorded sessions. You’re looking for the DNA Academy on Saturday evening. I can’t share specific preview slides with you as they are noted in his presentation as “not for distribution,” so my pen is capped for now.

All I can say is that after seeing what’s in store, people were literally throwing their billfold at the folks at the FamilyTreeDNA booth – and I do mean literally. “Here – take my money, please!” as the billfold went sailing. We all had a good laugh, but he was serious.

One presenter (not me, just in case you are wondering) left her credit card and a list of tests to upgrade while she was presenting.

They ran out of swab kits at the conference shortly after Dave’s presentation about what the future holds.

Additionally, you will also be treated to THE absolute best presentation I’ve ever seen about what NGS testing is, how it works, and how it compares to traditional tests, low-pass whole-genome tests, and medical-grade whole-genome tests.

You’ll be a passenger on the Genome Valley train, so climb aboard!

So, without spilling any beans, what’s so great about the NGS test?

To begin with, the older Family Finder tests won’t be able to provide everything the new NGS test will be able to offer – and those completely new tools are in active development today.

Why?

The NGS test targets over 280 million base pairs, up from the currently available 700,000.

That’s more than 400 TIMES the coverage.

This increases coverage in the human genome from about .02% to about 9%.

To quote FamilyTreeDNA, “This change allows us to deliver more precise autosomal results today while creating a strong foundation for future reports and tools.”

You can read the FamilyTreeDNA FAQ here.

Before we move on to the comparison, let’s talk for a minute about test types and uploads from other vendors.

Tests and Uploads

All new Family Finder tests purchased at FamilyTreeDNA since March 2, 2026 have been tested using Next Generation Sequencing (NGS), so the following matrix does not apply to those tests. Those tests don’t need to be upgraded.

If you sign on to your account, on the Family Ancestry dashboard, and see that your NGS button is grey, then you have not upgraded. Click on that grey button to read more and to upgrade. Right now the upgrade is $29, but I don’t know if that is a promotional price or permanent.

If you tested at FamilyTreeDNA prior to March 2, 2026, or uploaded a DNA file from another vendor, your test will fall into one of the following upgrade path categories.

Tested at FamilyTreeDNA before March 2, 2026 Uploaded and purchased the Unlock Uploaded but did not purchase the Unlock
Upgrade Path Can use sample stored in lab if enough DNA remains* If you purchased any other type of test at FamilyTreeDNA, they will use DNA stored in the lab if enough remains. Otherwise, you will be sent swabs. If you purchased any other type of test at FamilyTreeDNA, they will use DNA stored in the lab if enough remains. Otherwise, you will be sent swabs.
New Swabs* If needed, they will notify you Yes, if needed, will notify or send swabs if you have not taken a direct test at FamilyTreeDNA Yes, if needed, will notify or send swabs if you have not taken a direct test at FamilyTreeDNA
NGS Results Will replace existing results Will replace existing results Will replace existing results

*You will be notified if enough DNA does not remain, and you will be sent new swabs. Be sure your address is current.

One of the reasons the NGS test performs better, even with existing matches from earlier tests, is because less imputation is involved. Let’s talk for a minute about imputation and how it works.

The Concept of Imputation

Most vendors change chips internally from time to time, and FamilyTreeDNA is no different. The difference this time is that the new NGS test covers exponentially more DNA than any earlier test, and all earlier tests combined. This means more than 400 times greater coverage, which in turn means less imputation is needed to compensate for the inevitable no-reads and to be compatible with files that tested different DNA locations.

Imputation is also used when comparing DNA files between vendors who don’t test the same locations.

Click to enlarge any image

Here’s an illustration of the concept of how imputation works.

All of the FamilyTreeDNA chip versions over the years have included about 700,000 locations, as have most other vendors. But the locations tested are not universally the same.

In our simplified concept example, FamilyTreeDNA’s tested “locations” are shown with blue cells.

The total of 20 squares shows the maximum amount of DNA tested by any of the three vendors shown, combined.

Green Vendor 1 in our illustration tests the same amount of DNA that FamilyTreeDNA tests, 12 squares, but some locations are the same and some are different. Of the 12 colored squares for both vendors, seven are the same locations, and five are not. The locations that are the same can be compared directly, but the locations that are different have to undergo special handling called imputation.

Looking at any location in our DNA, one of four nucleotides, or letters, can be present: T, A, C or G on each strand of our chromosomes, although we are only looking at one strand in our example.

Using a very simplified model of imputation, think of imputation as “filling in the blanks” using clues from surrounding letters – kind of like a crossword puzzle.

When two vendors’ data doesn’t overlap, imputation is used to fill in the blanks, as accurately as possible, for the missing data.

Using a word analogy, for vendors one and two only, we see that blue location three has no Family Finder data, where green Vendor 1 does, and the same with location five. If blue locations two and four are C and T, and three has to make a word, then there are few options. In this case, let’s say it’s cat, and location five is imputed to an A too.

Now moving to green Vendor 1, their locations two and five need to be imputed. Moving away from the word analogy, let’s look to the human genome, and let’s say that most of the time, location two is a C if location one and three are Gs. So green location two is imputed to C.

If there’s not enough quality surrounding data, imputation can’t be performed reliably. Hence, location six is still in limbo here.

You can see that in our scenario, location three is the only mismatch, out of three imputed locations. Does location three mismatch because imputation was wrong? We don’t know. Do locations two and five match because imputation was wrong? We don’t know.

All things considered, imputation is based on the science of probability, and is usually relatively reliable, but it’s still not the same as comparing actual data. The more locations that have to be imputed, and the longer the stretch, the greater the possibility of error. Every vendor implements imputation differently too. Even vendors who don’t and have never accepted uploads still use imputation internally to equalize their own legacy files from earlier test versions.

Stepping back once again to compare the four vendors, you’ll notice that pink Vendor 3 only tested half as much DNA as the blue Family Finder test and green Vendor 1, and again, not all of the same locations. That’s exactly what happened with one of the vendors last December – they dropped the number of DNA locations tested to about 400,000 from about 700,000. In our example, you can see how much would have to be imputed. Locations 11, 15, 19 and 20 can’t be imputed for the pink vendor’s file because there’s no surrounding DNA. Location 17 can’t be imputed for the green vendor for the same reason.

When vendors impute to match multiple versions of other vendors’ uploaded files, it can quickly become messy.

The answer, of course, is a “supertest,” which tests all of the locations that overlap everyone, including that vendor’s own earlier tests.

Welcome to Family Finder NGS, shown in orange at the bottom of our example comparison.

As you can see, the orange NGS test covers all of the locations tested by all of the other tests.

NGS is targeted testing for a specific set of locations that are known to undergo mutations in the human genome and provides extremely high-quality results. Imputation for the NGS file is rarely necessary, although imputation for the other vendors’ and earlier file versions is still required for them to match to each other.

This is exactly why the upgrade is recommended, and why there’s no benefit to retaining your old test. The NGS test tests far more data and provides much more reliable matching.

NGS is the great equalizer.

NGS Test Comparison Process

I took my NGS test during the initial R&D development and testing phase, so my original Family Finder test was not upgraded. This afforded me the opportunity to compare the two results.

I downloaded the match files for both of my tests, the original Family Finder and the new NGS Family Finder test, color-coded the background of the cells, not the text inside the cells, and dropped them into a single combined spreadsheet.

It doesn’t matter what colors you choose, but be sure you can easily see the difference. I used apricot for the original Family Finder test matches and light purple for the new NGS test.

As we walk through these results together, you’ll notice that I continue to refer to them by color. In part, that’s so I can maintain my own sanity as I compare results. When I write these types of articles, I have to check and recheck results.

When the same person showed as a match to both tests (meaning they had both an apricot and purple row), I calculated the difference in matching amounts of DNA (cMs) between the match’s results on both tests. I added several calculation columns, which are not shown above.

I’ll tell you, this was not a trivial exercise. It was painful and I really don’t recommend it.

Let’s take a look at the results.

Total Matches

I have some matches with the new NGS test that I do not have with the legacy Family Finder, and I have some matches on the older test that are no longer present on the NGS test.

  Old Family Finder (apricot) NGS Family Finder (purple) Difference
Total Matches 9014 7719 1,295
Maternal 1665 Not linked
Paternal 3783 Not linked
X-Matches 2198 1849 349

I have not yet linked the same matches in my NGS test, so I can’t compare the number of maternal and paternal matches. Fortunately, when you upgrade an existing test, FamilyTreeDNA preserves your linked matches, so you won’t need to relink.

Relationship Estimates

  Old Family Finder (apricot) NGS Family Finder (purple)
1st-2nd cousins, Great/Half Uncle/Aunt/Niece/Nephew, Great-Grandparent/Grandchild 6 6
1st-3rd cousin 1 1
2nd-3rd cousin 5 4
2nd-4th cousin 127 132
3rd-5th cousin 1937 1900
4th to remote 6938 5676
Total 9014 7719

The closest relationships remained the same. One 2nd-3rd cousin moved to the 2nd-4th cousin range by losing 10 cM, 194 cM to 184 cM, but they were apparently on the threshold anyway. That match is actually my second cousin, so both ranges are accurate. It was also a transfer kit, so they did not test at FamilyTreeDNA. This revised match is probably the difference between actual reads and imputed reads in some regions, meaning the match is now more accurate.

275 matches had a predicted relationship change, but not uniformly in one direction, and no one moved more than one category in either direction. This all makes sense.

Match Differences

  Number
Matches found in both the apricot and purple spreadsheets 7,352
Unique (comparable) matches in both spreadsheets 7,174
Matches in original Family Finder apricot only 1,681
Matches in NGS purple only 400

A total of 7,352 matches appear in both spreadsheets, meaning the apricot and purple names matched exactly.

Unfortunately, some people had multiple tests, so I couldn’t always compare apples to apples because they appear three times or more on the combined spreadsheet, and I don’t know which of their kits are which.

If someone with the same exact name had more than one match for either or both tests, I did not compare them because their matching amounts were different, and I didn’t know which one(s) my old test matched, versus which one(s) my new test matched. Usually, one was an upload and one was a test at FamilyTreeDNA, but not always. I excluded those 178 match rows from the analysis.

Therefore, 7,174 matches could be directly compared.

There were 1,681 people who match ONLY on the old Family Finder test, and 400 that match only on the new NGS test. And yes, I downloaded the match files at the same time on the same day, so this comparison was controlled for any time difference.

cM Differences

  Number
Largest apricot match not in purple (NGS) list 26.3 cM
Largest purple (NGS) match not in apricot list 27.63 cM
Largest difference 69.86 cM NGS kit more
NGS detected greater over 10 cMs 19
NGS detected less over 10 cM 7
Total NGS greater 2,924
Total NGS less 3,040
No change 1,090

The largest value difference where a match appeared in the original apricot Family Finder test, and not in the purple NGS test, was 26.3 cMs.

The largest value difference where a match appeared in the NGS purple Family Finder test, and not in the apricot original Family Finder test was 27.63 cMs.

The largest difference between the two tests was 69.86 cMs larger detected by the NGS test. This match was a known second cousin whose matching cMs went from 373.06 to 442.92, but the longest block only increased a negligible amount from 87.47 to 87.69.

The next largest difference was with a 1C1R with a 41.56 cMs difference, also with the NGS-detected value being larger.

In all cases where the number of differing cMs was 16 or greater, the NGS had detected more.

There were very few tests that differed more than 10 cMs. In 19 cases, the NGS test detected a greater difference of 10 cMs or higher, meaning if the original test value was 100 cMs, in the NGS test, it was 110 cMs or greater.

In 7 cases the NGS test detected a smaller difference of 10 cMs or more, meaning that if the original test value was 100 cMs, in the NGS test, it was 90 cMs or smaller.

Out of the 7,174 tests being compared, 19 tests with greater than a 10 cM variation isn’t very many, around 0.26%.

In total, 1,090 matches had no change at all, while 2,924 NGS matches had more matching DNA detected, and 3,160 matches had less.

All but 287 of those differences were less than 5 cMs, and 6778 were less than 1 cM. In other words, literally not worth counting.

myOrigins Ethnicity

We all know to expect changes in our ethnicity from time to time at all vendors. The NGS test is exciting because it covers a much larger portion of our genome. As more people test, the reference library also becomes larger, which means that the ethnicity predictions can and will become more refined too

myOrigins Old Family Finder (apricot) NGS Family Finder (purple)
Central Europe 57% 52%
England, Wales, Scotland 28% 33%
Ireland 15% 14%
Magyar <1% <2%
AmerIndian Andes and Caribbean <1 (see below) N/A
AmerIndian North America <1% (chr 1 & 13) <1 (chr 1 & 2)
Anatolia, Armenia, Mesopotamia, North Africa <1 (chr 13) <1% (chr 10)

None of my major categories changed, but the amounts attributed to each category changed somewhat.

Trace regions, which are less than 1%, shifted some as well, as did their chromosome locations.

For me, this is particularly interesting, because I paint my ethnicity segments at DNAPainter in order to overlay my Native American segments over the matches with whom I’ve identified common ancestors.

Those segments, matches, and ancestors, taken together, help identify the source of the Native American segments.

My Native segment on chromosome one stayed essentially the same, but the Native segment on chromosome 13 is not present on the new NGS test. However, a new Native American segment is now shown on chromosome 2 in the same location that 23andMe also shows a Native American segment.

Chromosome one has already been proven to a Native American ancestor on my mother’s side, but I have hit a brick wall on the chromosome 13 segment. Now, I’ve painted the Native Segment on chromosome 2 and it aligns with the same ancestral line as my Native American segment on chromosome 1.

My Middle Eastern/North African segment still exists, but the location has changed. This segment was adjacent to my Native American segment on chromosome 13 before, on my father’s side, which suggested a history of enslavement. I thought I knew which ancestral line they both descend from, but now I need to review my matches and reconsider.

Unfortunately, my parents are both deceased and there’s no DNA available, so I cannot upgrade their tests or purchase new ones for them. No aunts or uncles are available either. In this case, cousin matches and their associated genealogy on those segments become critically important.

Native American and African American segments are often the best, and sometimes the only hints we have to find and identify those ancestors.

Preparing for Your NGS Results

To be very clear, you don’t necessarily need to compare or prepare, BUT, if you order an upgrade to an existing test, your old match list will be replaced with the new one. Your old match list will not be preserved unless you do it.

What may change?

  • Your ethnicity results will probably change somewhat
  • You will have matches you did not have before
  • Some existing matches, especially at low matching levels, will no longer be there
  • The amount of DNA you share with some people will change

Important: Any notes you have recorded on your matches and any matches that you have linked will be preserved and carried over to your new results when your new test is complete.

If you want to preserve your matches from your earlier test, or your myOrigins results, you’ll need to download your match list, and either download or take screenshots of your ethnicity information.

Ability to Download Tested at FamilyTreeDNA before March 2, 2026 Uploaded and purchased the Unlock Uploaded but did not purchase the Unlock
myOrigins Can download Can download Cannot download
Chromosome Painter (ethnicity) Can download Can download Cannot download
Match list with segment and other information Can download Can download Cannot download
Raw data file Can download Cannot download* Cannot download*

*On tests you uploaded, you don’t need to download the raw data file because you already have it from the originating vendor.

What information is included in your Match List download file?

  • Match name
  • Relationship Range
  • Shared Data cMs
  • Longest Block cMs
  • Linked Relationship (if you linked them in your tree) – this feature is what allows FamilyTreeDNA to assign your matches maternally, paternally or to both sides using triangulation
  • Ancestral Surnames that they’ve entered
  • Y-DNA Haplogroup if applicable
  • mtDNA Haplogroup if applicable
  • Notes
  • Paternal/Maternal or Both side(s) match (if you’ve linked people and this match can be assigned using triangulation. (This is why it’s important to link as many people as possible to their place in your tree.)
  • X-Match cMs
  • Autosomal Transfer yes/no

If you match the same person on the NGS test, this information is preserved for that match.

Where to Download

You must have 2FA (Two-Factor Authentication) enabled for all downloads.

The files you may want to download are found on your dashboard in two locations.

  • Family Finder Matches
  • Chromosome Painter (ethnicity)

Family Finder Matches Download

To download your list of matches with their complete information, click on Family Finder Matches on the dashboard, then on “Export CSV.”

This download provides all the fields mentioned above, whereas the Chromosome Browser segment download provides only your matching segment data, without the additional information.

Download MyOrigins Ethnicity Segment Data

To download your myOrigins ethnicity segments, click on Chromosome Painter on your dashboard, then on “Download Segments.” You can also view or copy those segments by viewing the Detailed Segments tab.

I paint these segments at DNAPainter so that I can correlate my ethnicity regions with my ancestors’ segments.

To assign segments accurately, it helps immensely to have at least one parent’s DNA results too, and preferably both.

You may also want to take a screenshot of your myOrigins map. Note the left-side scroll bar when you’re taking screenshots.

What’s Next?

What else can you do at FamilyTreeDNA to benefit your genealogy?

  • If you haven’t already, upload a GEDCOM file or create a tree at MyHeritage, and link your Family Finder test to your results.
  • Link your individual matches to their place in your tree. This allows FamilyTreeDNA to use segments triangulated with linked matches to assign other matches to either the maternal or paternal side of your tree, or both.
  • Add your line to WikiTree. It’s easy. Begin with yourself and add ancestors until you connect with someone who is already in WikiTree. For me, it was the grandparent level.
  • Add your WikiTree link to your FamilyTreeDNA account under the gear in the upper right-hand corner, then Genealogy, then Family Tree. This gives your matches an easy way to identify common ancestors by using WikiTree’s Find Relationships feature, and provides two types of tree resources for you and your matches – MyHeritage and WikiTree.
  • Make sure your Earliest Known Ancestor information is correct and up-to-date with your most recent research, including a specific map location. You’ll find that under the gear too, then Genealogy, then Earliest Known Ancestors.
  • Add your surname list to your profile under the gear, Genealogy, Surnames tab.
  • Use the Matrix tool at FamilyTreeDNA to see how much DNA your shared matches share with each other.
  • Y-DNA – If you’re a male, test your Y-DNA, which is your father’s direct paternal line. The Big Y-700 test provides you with matches and the most detailed information possible.
  • mtDNA – Everyone can take a mitochondrial DNA test, which shows matches and provides information about your mother’s direct matrilineal line.
  • Use Advanced Matching, found under Additional Tests and Tools on your dashboard page, near the bottom, which allows you to select from multiple tests to see who matches you on both types of tests. For example, those who match you on both your full sequence mtDNA test and your Family Finder test.
  • Join projects relevant to your family surname, geography or broader interests. You’ll find Group Projects in the top banner of your dashboard page after signing in.
  • Utilize the Discover tools for both Y-DNA and mitochondrial DNA results.

Check your matches often to see who is new and what might have changed as people upgrade to the new NGS test and more people test.

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