Big News! Probable Native American Haplogroup Breakthrough

We are on the verge of another new and very exciting discovery, but we need funding to finish the research.  Let me tell you about what’s going on and maybe you’ll decide to be a part of this new discovery by making a contribution.

It’s not everyday that someone gets the opportunity to make a significant contribution to scientific discovery.  But you have that opportunity today.

I believe a new Native American haplogroup has been discovered.  We have strong evidence, but we need to finish testing on a group of people for the final proof.  People whose DNA results qualify for testing have been notified, and several are ready and willing to have their results upgraded, but don’t have the funding.  I’ve funded some, and I’ve used contributed funds I’ve squirreled away from past donations, and now I’m reaching out in the hopes that together we can collaboratively make this happen.

Most of you know that I’m a long time researcher in both the genetic genealogy and Native American fields, particularly where they intersect.  I’ve being involved with genetic genealogy since the beginning and am tri-racial myself, descended from multiple Native ancestors and tribes.  I write the Personal DNA Reports for Family Tree DNA, own www.dnaexplain.com and write the free blogs, www.dna-explained.com and www.nativeheritageproject.com.   You can verify anything in this article directly with Bennett Greenspan, the President of Family Tree DNA at bcg@familytreedna.com.  In fact, Bennett is both aware and supportive of this DNA testing endeavor and has offered reduced test pricing for a short time to facilitate this discovery process.

By the way, this is not the first time this has happened.  I was also involved with a similar discovery in December 2010.  You can read about that discovery at this link.  http://dna-explained.com/2012/09/11/lenny-trujillo-the-journey-of-you/

Ok, now that you know who I am and why I care, let me tell you about the discovery.

Discovery of a New Native American Haplogroup

To date, only 5 female Native American base haplogroups, or clans, have been discovered.   A, B, C, D and X.  Within these haplogroups are subgroups, and not all subgroups in each haplogroup are Native American.  Some are Asian and European.  In fact, in haplogroup A, which is the haplogroup being studied in this project, only subgroup A2 has been confirmed to be Native American – until now.

Recently, I was working with a client’s DNA, writing a Personal DNA Report, and I realized, based on her information and that of some of the people she matched, that a subgroup of haplogroup A4 is also very likely Native American.

For Native American history, this is a big discovery.  But we need more information.  We need to proof.  How can we do that?

Advanced Testing

We need to test people in haplogroup A who are predicted to fall into this new Native American haplogroup at the full sequence level.  Mitochondrial DNA testing falls into three levels.  The highest level, the full sequence level is the one that tests the entire mitochondria and is required to obtain a full haplogroup assignment.  In other words, if you don’t test the full sequence, you’ll know that you are haplogroup A, but you’ll never know if you are A2, A4 or A10 for that matter.

Of people who have tested only at the lower levels, we have identified a small group of people who we believe will test to be haplogroup A4 or a subgroup based on some specific mutations.  Bennett Greenspan has offered discount testing for the upgraded test through July 5th.

Some people have been able to pay for their own upgrade, but not all, and I certainly don’t want the lack of funds to impede the discovery and proof of a new haplogroup.  This is akin to raising the history of this group of Native people from the dead, from the dust where some of our history and people have been lost until now.

We need several hundred dollars in total.  If everyone that we’d like to test participates, it will cost more than $2000.  You can contribute directly to the haplogroup A4 mtDNA project at Family Tree DNA and the funds will be used directly for this testing.  Every little bit helps – no amount is too small.  You can contribute in memory of someone, anonymously, or however you wish.

http://www.familytreedna.com/group-general-fund-contribution.aspx?g=mtDNA-A4a

In a few months, we’ll let you know the outcome of this testing and what we discover, right here.  I can hardly wait!

Thank you in advance for your support.

Roberta Estes

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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 Services

Genealogy Research

Triangulation for Autosomal DNA

In our last article, Triangulation for Y DNA, we covered triangulation for the Y chromosome, how it works, and how it can help a genetic genealogist.

In this article, we’re going to cover triangulation for autosomal DNA.

Triangulation for autosomal DNA is kind of a chicken and egg thing.  The goal is to associate and identify specific DNA segments to specific ancestors.  The easiest way to do this, or to begin the process, is with known relatives.  This gets you started identifying “family segments.”  From that point, you can use the known family segments, along with some common sense tools, to identify other people that are related through those common ancestors.  Through those matches with other people, you can continue to break down your DNA into more and more granular family lines.  This is easiest to visualize thinking about your 4 grandparents.

Triangulation is easiest if you have parents or grandparents living, and you can test them.  Yes, all of them.  Their DNA will give your immediate pointers when you have matches to which side of the family you share with your matches.  If you can test your 4 grandparents, you immediately know which of those 4 lines someone who matches you descends through, because they will also match one, and hopefully only one, of your 4 grandparents.  However, for some of us, testing even one parents is simply not possible, so first, let’s look at some examples of triangulation without your parents DNA results.

I’m fortunate that one of my cousins has given a lot of focus to our Vannoy line.  Vannoy was the surname of my great-grandmother, Elizabeth Vannoy (1846-1918) who married Lazarus Estes (1845-1919).  The Vannoy line has a mystery we’ve been trying to solve for decades now called, “Who Was Elijah Vannoy’s Father?”.  Elijah was Elizabeth’s grandfather.  Your family probably has a similar mystery, and these tools hold the potential to answer those questions.  They also have the potential to introduce more questions.  But then again, isn’t that the way of genealogy?  For every ancestor we find, we get two more questions.

Several of the Vannoy cousins are interested in solving this mystery as well, so they have taken the autosomal Family Finder test at Family Tree DNA.

We know how they are related, and the men have all been proven to be Vannoy via Y-line testing.  By doing this, we’ve assured no undocumented adoptions, also known as NPEs (NonParental Events) in the Vannoy line.

We expect our cousins to match, and indeed they do.  This is my test result showing my three cousins who match me.

In my family mystery, “Who Was Elijah Vannoy’s Father?”, there are 4 candidates, all brothers who lived in Wilkes County, NC in the late 1700s.  Elijah was born in 1786.  We have the wives surnames.  Hickerson is our primary candidate surname, so I wanted to see everyone who matches me on my match list who also shows the Hickerson surname.  I enter that surname in the “ancestral surname” box, and click on “run report.”  The matches returned will all carry the Hickerson surname, which you can see by scrolling for the highlighted names. Turns out, it was only my Vannoy cousins – today – but tomorrow might be different.

Vannoy match 1

Now for the triangulation tool.

I want to see if these three people share common DNA not just with me, but with each other.  If we all share a common segment of DNA, then that confirms a common ancestor and attributes the DNA at that address on that chromosome to that specific ancestral family.  This is the fundamental concept on which triangulation is based.

In my case, the known ancestral family is Vannoy, not Hickerson, at least not yet, so let’s look at the Vannoy cousins as compared to me.

vannoy match 2

Each of the participants results are color coded.  On the page below, you can see that each matching segment of the chromosomes is colored.  It turns out that all of us share a fairly large segment on Chromosome 15.  So now we can attribute that segment to Elijah Vannoy, our oldest proven ancestor in that line.  You can also see some areas where one or two of my cousins match my DNA, but not all of us.  Those can also be attributed to Elijah Vannoy’s line since we share no other (known) common ancestors.

vannoy match 3

This cousin match is simple because the men share the same surname, but if this was 3 women with different surnames, the matching would still work.  The challenge of course would be to find the common ancestor.  In this case, if all 3 women had Elijah Vannoy in their tree, we could still tell that this segment of Chromosome 15 was attributed to the Vannoy family because they all matched me and matched each other as well on the same DNA segment.

Eliminating False Matches

Now let’s move to the “what ifs.”  When my kids were young, I just hated sentences that started with “what if.”

What if I have a fourth match, Jane, with unknown ancestry who matches me on these segments, but does not match any of my cousins?

To determine this you would also have to look at your cousin’s matches or ask Jane if she also matches those cousins.  Remember that half of your DNA is that of your mother and the other half is that of your father.  You will have people that match you, and potentially on the same segments as your known relatives match you, but are not related to both you and your relatives.  This means they are matching you on the other half of your DNA.  In this case, if Jane didn’t match my Vannoy cousins too on that same segment of chromosome 15, then we would know that Jane’s match would be from my mother’s side.

To illustrate this point, let’s move to my results at 23andMe.

Let’s use Family Inheritance Advanced to see an example of two people who match me on the same segment, but are from opposite sides of my family.  My cousins Stacy and Cheryl are from Dad’s and Mom’s side of the family, respectively.  We know they don’t share common ancestry, but look, they both match me on four of the same segments.

cheryl stacy match

How is this possible, you ask.  Remember, I have two halves of each chromosome, one from Mom and one from Dad.  It just so happens that Cheryl and Stacy both match me on the same segment, but they are actually matching two different sides of my chromosome.  For this reason, these are called HIRs, or Half Identical Regions.

Now let’s prove this to the doubting Thomas’s out there.

cheryl stacy match 2

Here is the comparison of Cheryl and Stacy directly to each other.  They do have one small matching segment, 6 cM, so on the small side.  But they don’t match each other on any of the segments where I match both of them.

If they did match each other and me on the same locations, it would mean that we three have common ancestry.

The fact that they match each other on one segment could also mean they have distant common ancestry, which could be from one of our common lines or a line that I don’t share with them, or it could mean they have an identical by state (IBS) segment, meaning they come from a common population someplace hundreds to thousands of years ago.

The real message here is that you can never, ever, assume.  We all know about assume, and if you do, it will.  In this case, assuming would have been easy if you didn’t delve into the big picture, because both of these family lines contain Millers from Ohio living in close proximity in the 1800s.  However these Miller lines have been proven not to be the same lines (via Yline testing) and therefore, any assumptions would have been incorrect, despite the suggestive location and in-common names. Furthermore, cousin Stacy’s Miller line married into her line after our common ancestor, so is not blood related to me.  But conclusions are easy to jump to, especially for excited or inexperienced genetic genealogists.  It’s tempting even for those of us who are fairly seasoned now, but after you’ve been burned a few times, you do learn some modicum of restraint!

So, what’s next?

Color your Chromosomes

In my article, “The Autosomal Me – the Holy Grail – Identifying Native Genealogy Lines,” I described in detail the process of downloading your DNA information from either 23andMe or Family Tree DNA and then utilizing that information in a spreadsheet to look at matches – not 3 or 4 matches at a time, but chromosome by chromosome.

In my case, I was fortunate to have my mother’s DNA results at Family Tree DNA before she passed away, and I was equally as fortunate that they were still viable for the Family Finder test.  Believe me, I held my breath.

Because I have her results, I can tell immediately if my matches are from her side or from my father’s side.  If the person matches both Mom and me, then it’s from her side.  See how easy triangulation is.

Let’s take a look at Chromosome 15 with all of those Vannoy matches on my spreadsheet and see what kind of information we can glean.

vannoy table 1

On my master spreadsheet, my Mother’s matches have been copied in and are color coded, but since none of these people match Mother, I have eliminated that aspect here to avoid unnecessary confusion.

The people identified as “Dad” mean that I know they are genealogically related on my father’s side.  People who match Mother genetically are labeled Mom.  There aren’t any on this segment of chromosome 15, in our example above.  The blank cells in that column, by inference, match Dad’s DNA, since they don’t match Mom.  When I confirm genealogically how we’re related, I’ll enter “Dad” in that column, but not until then.

I’d like to comment on information gleaned from the spreadsheet.  Every DNA segment has a story to tell.

Cousin Estes

First, Cousin Estes, with yellow highlighting, is one of my closest Estes relatives.  He is a third cousin on the Estes side and also descends from Lazarus Estes and Elizabeth Vannoy.  He matches me on the segment from 26 (million) to 58 (million). My Vannoy group of matches, shaded green, extend from 33 to 58, so this tells me that the area from 26 to 33 where I match Cousin Estes, and not any Vannoys, is probably from an Estes ancestor, and not the Vannoy line.

Unfortunately, I don’t have any other matches on this segment, so I can’t figure out which line it comes from, just yet.

The green areas are common between me, cousin Estes and the Vannoy cousins.  If we could find a Hickerson match on these same segments, we could then solve the family mystery AND attribute part of this DNA to the Hickerson line.  But so far, no dice.  This is why it’s important to continue to look and to reach out to people you match, especially those who don’t enter their family surnames or post a GEDCOM file.  The answer may be waiting for you.

The Insanity Factor

The pink segment labeled Cousin Younger is making me insane, so let me share some insanity with you.

The Younger line descends through the Estes line, significantly upstream. The Y DNA of Marcus Younger, who had 1 son who had 1 son, does not match the expected Younger DNA line in Halifax County, Va.  Cousin Younger’s only solid Y match also doesn’t match his expected family line, so we’re fish out of water on the Y-line.  Two undocumented adoption cases that match each other, but no one else.  Great, just great.  These are the things genetic genealogy nightmares are made of.

Mary Younger, daughter of Marcus Younger, married George Estes who fought in the Revolutionary War.  Their son John R. Estes married Nancy Ann Moore in Halifax County and they settled in Claiborne County, TN about 1820 where the Vannoy family is found as well, having migrated from Wilkes Co., NC.  John Y. Estes, son of John R. Estes had son Lazarus Estes who married Elizabeth Vannoy.  Here’s the generational progression:

  1. Marcus Younger – wife unknown, Y DNA doesn’t match Younger line
  2. Mary Younger married George Estes, Halifax Co., VA
  3. John R. Estes married Nancy Ann Moore, moved to Claiborne Co, TN
  4. John Y. Estes married Rutha Dodson
  5. Lazarus Estes married Elizabeth Vannoy
  6. George Estes married Ollie Bolton
  7. My father, William Sterling Estes

And of course, there’s a monkey-wrench, so let’s throw it in.  Marcus Younger’s grandson, ancestor of Cousin Younger, married a Moore woman in Halifax County, VA.  We believe we know who her parents are, but we’re not positive.  If they are who we believe, Y-line DNA tests say the 2 Moore families, living within sight of each other, aren’t the same Moore line….but they interact closely and my Moore line doesn’t match any Moores upstream anyplace.  So, we have another unknown ingredient in the soup.

So, from me, Marcus Younger is 7 generations upstream.  I should carry about 1.5% of his DNA.  I was pleased to see that my Younger cousin and I matched.

However, and this is a BIG however, the Vannoy line should not be related to the Younger line.  We know that both of these cousins are matching on my father’s side, not just because of the genealogy, but because neither matches my mother.  But they are somehow related, as Cousin Younger is matching the Vannoy group big as life on chromosome 15.  Could this be an IBS (identical by state) segment?  Yes, it’s small – but I’m not comfortable relegating it to IBS because it’s genealogically “inconvenient,” at least not yet.

So, something may well be wrong, amiss or unknown in the genealogy, either in Tennessee, which is doubtful as we have that fairly solidly nailed down, especially in recent generations, or in Virginia where there is at least one known disconnect and possibly two taking into consideration the Moore monkeywrench.  Still, the Vannoy family was not living in the same state as the Younger family and came from New Jersey to North Carolina, not from Virginia.  Maybe the connection is in one of the unknown wives lines.

So, you can see my reason for being perplexed.  One thing is sure.  DNA doesn’t lie.  It’s up to us to figure out the message it is conveying and which ancestor it is from.

Powerful Tools

I hope you can see what a powerful tool we have at our disposal.  Of course, it can reveal who your ancestors are, along with some surprises.  I don’t mind the surprises.  I view them as gifts from the ancestors.  It’s those crazy-making half-surprises that bother me.  I swear, the ancestors have a sense of humor.

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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 Services

Genealogy Research

Triangulation for Y DNA

Based on the number of questions I’m receive about triangulation, it’s time to write an article.

There are two kinds of triangulation that we use in genetic genealogy.  One type is for the Y chromosome and it’s to determine the original values of the DNA of the common ancestor.  The second type of triangulation is for autosomal DNA and it’s to determine if you share a common ancestor with someone and what the DNA of that ancestor looked like.

This article is about the first type, for Y DNA.

Why would you want to use triangulation?

Sometimes in order to know if a particular line has descended from an ancestor, you need to know what that ancestor’s Y DNA marker values were.

For example, if you have an ancestor born in the 1600s, and he had two sons whose descendants tested today, each line could have 4 mutations each, or 6, which could put the matching software over the threshold – meaning they might not be reported as matches.  We have this situation in one of the Estes lines that seems to be particularly prone to mutate.

Family Tree DNA has set up match thresholds.  For someone to be listed as your match, they need to have no more than the following total number of mutations difference from your results.

Markers in Panel Tested Maximum Number of Mutations Allowed

12

0 unless in a common project, then 1

25

2

37

4

67

7

111

10

So you can see that if you have a high number of mutations in the first panel or two, you might not show as a match.

But if you know what the original ancestors Y-line DNA looks like, then it’s easy to tell that they really are matches and that both lines have simply had several mutations.

It’s much more accurate to compare everyone to the original ancestor instead of trying to compare them to each other.

Let’s take a look at the Estes project by way of example.

Abraham Estes, the progenitor of the Southern Estes line was born in 1647 in Nonington, Kent, England.  He immigrated to Virginia in 1683 and began begetting shortly thereafter.  His wife was Barbara, and although the internet is full of family trees that say her last name is Brock, there is not one shred of evidence to support that.  In any case, Abraham and Barbara had a total of 8 sons who lived and the sons had about 42 sons, so we have a good number of Estes families throughout the US today, mostly descending from Abraham.  There is also a northern line founded by Abraham’s cousin, Richard Estes although they don’t have nearly as many descendants.

triangulation Y dna

This chart shows the results of DNA testing through 7 different Estes lines, 6 of which are Abraham’s sons and one of which is a descendant of the Northern line.

The green row at the top is Abraham’s reconstructed DNA, and now, everyone in the project gets compared to Abraham on my spreadsheet.

It’s easy to see how this is done.  For each marker, beginning with 393, we determine what the normal value is for the family.  For marker 393, all lines carry a value of 13.  One line, John through Elisha, shows a mutation to a value of 14 which would signal a line marker mutation for this particular line.  This is quite useful, because when we see someone who carries a value of 14 at this location, especially in conjunction with any other line marker mutations that might exist in that line, like a value of 11 at marker 391, we know where to look genealogically to find the tester’s place in the family.  Line marker mutations are great guideposts.

So, marker by marker, I’ve reconstructed Abraham, shown at the top in green.

Marker Frequency

You might wonder why the value of 25 at 390 is red and underscored and 12 at 391 is bolded, red and underscored.

One of the things I do for each of my family lines, and for clients who order Personalized DNA Reports, is to determine which of their markers carry rare values.  In this case, the value of 25 at 390 is found in only 16% of haplogroup R1b1a2.  The value of 12 at 391 is found in only 4% of the haplogroup R1b1a2 population.  My threshold for rare markers is less than 25% and for very rare, 6% or less.  Bold red indicates very rare, red indicates rare and the underscore is present so that people printing in black and white can see the difference

Why and how does this make a difference?  In a situation where you’re trying to decide if someone really does match the Estes line, this information can be a big help.

The last kit on the chart does carry the Estes surname, but does not match the Estes line genetically.  This is obvious by looking at all the yellow squares, which are mismatches to Abraham, but let’s say that this person tested at 12 markers and he matched the Estes DNA on all of our rare markers, but mismatches a couple on the more common markers.  This is more likely a true Estes match than if they mismatch us on all of our rare markers.  The Estes rare markers combined create a type of family genetic fingerprint.  This is particularly important for adoptees.

And yes, to answer the next question, a Marker Frequency Table can be purchased separately for those who want their marker frequencies through 111 markers, but don’t want a Personalized DNA Report, by purchasing a Quick Consult.  A marker frequency table looks like this but extended, of course, through all of your markers:

Frequency table

Now, we know what the original Abraham Estes’s DNA looked like.  We also know which of our markers are unique.  This can also help us when comparing to other surnames we may be related to before the advent of surnames.  There is family history to be gleaned from those matches as well.

And lastly, because we also have cousin Richard’s DNA signature, we can use that information to reconstruct the common ancestor of Abraham Estes and Richard Estes, which is the grandfather of both men, Robert Estes, born 1555 in Ringwould, Kent, England.  Not bad for genetic technology, reaching back more than 450 years in time and telling us what our ancestor’s DNA looked like, and all without even reaching for a shovel.

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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 Services

Genealogy Research

The Warrior Gene

warrior 1

In sports, business or your personal life, how you respond to stress and aggression may be in your genes, or at least partly so.  Let’s take a look at a great documentary and the science behind it.

Human behavior is complex and influenced by our genes, our environment, and our circumstances. One of the most provocative and often controversial of genetic variants has been dubbed the “Warrior Gene.”

Studies have linked the “Warrior Gene” to increased risk-taking and to retaliatory behavior. Men with the “Warrior Gene” are not necessarily more aggressive, but they are more likely to respond aggressively to perceived conflict.

On December 14, 2010, National Geographic Channel’s Explorer: “Born to Rage?” documentary investigated the discovery behind a single “warrior gene” directly associated with violent behavior.

warrior 2

With bullying and violent crime making headlines, this controversial finding stirs up the nature-versus-nurture debate. Now, former Grammy-winning rocker, author and radio/television broadcaster Henry Rollins goes in search of carriers from diverse, sometimes violent backgrounds who agree to be tested for the genetic mutation. Who has the warrior gene? And are all violent people carriers? The results turn assumptions upside down.

warrior 3

A rock band front man. A bullet-scarred Harley rider. A former gang member from East L.A. Even a Buddhist monk with a far-from-peaceful past. Which one carries the gene associated with violence? An extraordinary discovery suggests that some men are born with impulsive, aggressive behavior … but it’s not always who you think.

It’s a hotly debated topic: nature versus nurture. Many experts believe our upbringing and environment are the primary influences on our behavior, but how much are we predisposed by our DNA? The discovery of a single gene variation affecting only men, which appears to play a crucial role in managing anger, argues that nature may have a far bigger influence on behavior. It’s this low-functioning, shortened gene linked to violent behavior that has become known as the “warrior gene,” and one-third of the male population has it.

One of those men, who describes himself as “fairly furious all the time” and agrees to be tested for the gene with a simple cheek swab, is Henry Rollins — a former poster boy of youthful rebellion and the American punk scene.  Some of his tattoos are too provocative and socially offensive to show. 

warrior 4

In this special Explorer episode, he dives into his own history of rage and searches out others with aggressive behavior from a range of different backgrounds. “If you can think of a stove, and the pilot light is always on, always ready to light all four burners, that is me, all the time,” he says. “I’m always ready to go there.”

Follow Rollins as he meets with former foot soldiers in one of the most violent street gangs in East Los Angeles; fighters in the ultraviolent sport of mixed martial arts, and Harley Davidson bikers. He’ll also talk to a Navy SEAL veteran and Buddhist monks whose lives weren’t always so tranquil.

After learning more about the warrior gene, many of the men believe they have it, which could offer an explanation of their past behavior. Their sentiment mimics Rollins as he says, “If I find out that I have the warrior gene, that would be interesting. If I find out I don’t, I must say, I would feel a bit of disappointment.” As the anticipation builds, be there when they receive the surprising outcome of the test.

Explorer VII: Inside the Warrior Gene NGCUS Episode Code: 4833

Then, Explorer takes a look at the original study — on one family with generations of men displaying patterns of extreme physical aggression — that led Dutch geneticist Dr. Han Brunner to the revolutionary discovery of this rare genetic dysfunction. We’ll also take a look at new revelations that warrior gene carriers are significantly more likely to punish when provoked. In one study attempting to demonstrate this, subjects are given permission to administer punishment to their partner (who was secretly instructed to make a nuisance of himself), with unexpected results.

For any man questioning his inner warrior, a simple cheek swab test is available at Family Tree DNA.

So wanna know who, in the documentary, had the warrior gene?  Well, hint….it wasn’t the biker…although his lady assured him he would always be her warrior.  But I’m not going to tell you who does have it.  All I’ll say is that you’ll be amazed at the outcome.  The link to watch the video is below.  Enjoy!

http://topdocumentaryfilms.com/born-rage-inside-warrior-gene/

The Science

Let’s take a look at the actual science behind this most interesting and controversial mutation.

The Warrior Gene is a variant of the gene MAO-A on the X chromosome and is one of many genes that play a part in our behavioral responses. The “Warrior Gene” variant reduces function in the MAOA gene. Because men have one copy of the X-chromosome, a variant that reduces the function of this gene has more of an influence on them. Women, having two X-chromosomes, are more likely to have at least one normally functioning gene copy, and scientists have not studied variants in women as extensively.

Recent studies have linked the Warrior Gene to increased risk-taking and aggressive behavior. Whether in sports, business, or other activities, scientists found that individuals with the Warrior Gene variant were more likely to be combative than those with the normal MAO-A gene. However, human behavior is complex and influenced by many factors, including genetics and our environment. Individuals with the Warrior Gene are not necessarily more aggressive, but according to scientific studies, are more likely to be aggressive than those without the Warrior Gene variant.

This test is available for both men and women, however, there is limited research about the Warrior Gene variant amongst females. Additional details about the Warrior Gene genetic variant of MAO-A can be found in the paper titled “A functional polymorphism in the monoamine oxidase A gene promoter” by Sabol et al, 1998.

When testing for the Warrior Gene, we are looking for an absence of MAOA (monoamine oxidase A) on the X chromosomes. Based on how many times we see the repeat of a certain pattern on the X or Xs we can tell if the MAOA is present or absent (depleted). Three repeats of the pattern indicates that the X chromosome is deficient of MAOA and therefore you have the Warrior Gene. If we see 3.5, 4 or 5 repeats of the pattern, MAOA is present and this is a normal variant of the gene on your X chromosome.

warrior 6However, women have 2 X chromosomes where men have 1 X and 1 Y. As mentioned above, the gene is carried on the X chromosome, so women can either have it 1) not at all, 2) on only 1 X (therefore making them a carrier), or 3) on both Xs (exhibiting the trait).

Looking at results, with one X-chromosome, men with the “Warrior Gene” will show a value of 3. Other men will have normal variants: 3.5, 4, 4.5 or 5. With two X-chromosomes, women will have two results. For example, a woman might have 3 and 3, 3 and 5, or 4.5 and 5.

This first example is of a female with one copy of the normal variant and one copy of the Warrior Gene indicated by a value of 3.

warrior 7

In the second example, shown below, this female has the Warrior Gene trait, because she carries the Warrior Gene depletion, shown as a value of 3, on both of her chromosomes, the one contributed to her by her father and the one contributed to her by her mother.  This also tells us that her father has the Warrior Gene, since he carries only the X chromosome contributed by his mother, which he gave to his daughter.  It also tells us that her mother was either a carrier, if she had only the one copy she gave to her daughter, or had the Warrior Gene herself is she carried two copies.

warrior 8

A male’s results would have only one result listed.  If he has a value of 3, he had the Warrior Gene.  Any other value is NOT indicative of the Warrior Gene.

Happiness Gene in Women

In an unexpected turn of events, in August 2012, another study in the journal Progress in Neuro-Psychopharmacology & Biological Psychiatry indicates that while this gene may express as aggression in men, it may be the happiness gene in women.  Even women with only one copy of the gene were shown to be happier than women who carry no copies. A study of 193 women and 152 men evaluated their happiness level and women who carried this mutation on one or both X chromosomes rated themselves as significantly happier than women who did not carry this trait.  There was no difference in the male participants.

http://www.livescience.com/22789-gene-linked-to-happiness-in-women.html

Caveat

Among the many advances and discoveries of modern DNA and genetics are ‘scientific’ oddities. These genetic wonders make it into popular culture and sometimes develop a life there that far outpaces their academic worth.  But they are interesting. These factoids are best used as ‘cocktail party conversation’ starters or maybe a good way to tease Uncle Leo at the family picnic. Family Tree DNA, where you can find out if you have the Warrior Gene, portrays it to their customers as just that, a novelty.

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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 Services

Genealogy Research

Supreme Court Decision – Genes Can’t Be Patented

In a victory for consumers, patients, researchers and women, the Supreme Court today returned a decision that human genes cannot be patented.

Their decision states that DNA ”is a product of nature and not patent eligible merely because it has been isolated.”

This case was a result of a suit against Myriad Genetics, a company that was granted patents for isolating two human genes, known as BRCA1 and BRCA2, both of which are well known breast cancer genes, recently brought to light by Angelina Jolie’s decision to have preventative mastectomys after both the gene and related breast cancer were found to be prevalent in her family.  Shortly after that decision and surgery, Jolie’s aunt died of breast cancer.

While companies cannot patent the genes themselves, they can develop treatments and hopefully, cures, and those can be patented.  Synthetic genes created are also eligible for patents.  Myriad wasn’t the only company to do this.  The government has issued patents to over 4000 genes to both companies and universities.

The patenting of genes made it impossible for other competing companies who could test for the gene technically to do so.  In other words, it artificially created a sole supplier situation where only one company could provide the test for that gene, and therefore could set the price wherever they wanted.  Jolie revealed that the cost of screening for those two genes alone was $3000, a cost prohibitive to many women.  However, the actual cost of the testing is significantly less.  I was wondering just how much less, then the answer arrived in my inbox.

I know that Gene by Gene, through its division, DNA Traits has the capability to offer this test and has been selling it internationally since 2012.  Bennett Greenspan, president of Gene by Gene has discussed this with me privately, and how terribly it pained him not to be able to do this testing to help people within the US.  Bennett shared some pretty profound thoughts about the unfair situation this created.

I was just getting ready to call Bennett, when less than 6 hours after the Supreme Court decision, I received an e-mail from Gene by Gene, which contained the answer – $995.  So the actual cost to the American consumer is only about one third to one quarter of what they were being charged as a result of the patent.

Today’s Supreme Court decision is truly a victory for patients, consumers, researchers, women and all US citizens.  Below is the content of the e-mail I received from Gene by Gene announcing the ability for DNATraits to sell the BRCA test in the US.

dnatraits brca

In effort to increase access to potentially lifesaving BRCA1 and BRCA2 tests, DNATraits can now offer tests for $995, a fraction of the cost of similar tests prior to the court decision

HOUSTON — Jun. 13, 2013 – Thanks to today’s U.S. Supreme Court decision opening the door to greater access to genetic medicine by American patients and their health care providers, testing for genes specifically linked to breast, ovarian and other cancers will now be more widely available and at a lower cost than ever before.

DNATraits, a division of Houston-based genomics and genetics testing company Gene By Gene, Ltd., announced today that it will offer testing for the BRCA1 and BRCA2 genes in the United States for $995.  Prior to today’s unanimous Supreme Court ruling, when exorbitant licensing fees kept DNATraits and others from offering BRCA gene tests in the United States, the cost for such tests was around $4,000.

“We’re pleased to make this important testing more widely available and accessible in the United States,” said Gene By Gene President Bennett Greenspan.  “Our highly automated CLIA-registered lab and efficient processes enable us to make genetic and genomic testing more affordable and accessible to more individuals, in the U.S. and worldwide.  And that’s our company’s mission, in a nutshell.”

The company’s announcement about the tests, which gained national attention when actress Angelina Jolie courageously revealed in May that being a BRCA1 carrier was among the factors in her decision to have a preventive double mastectomy, comes after today’s Supreme Court ruling in “Association For Molecular Pathology v. Myriad Genetics.”

“We commend the Supreme Court for opening the door to greater technological innovation and access to genetic tools that promise to save and improve the quality of human lives in the United States,” Greenspan added.  “It’s critical that as an industry we are able to continue to engage in healthy competition to drive down the costs of these tests – because as more individuals have access to and undergo them, the more information we’ll have about many serious diseases that eventually may lead to cures.”

DNATraits has processed testing for the BRCA1 and BRCA2 genes for individuals living outside the U.S. since 2012.  Those genes are processed using traditional Sanger DNA sequencing, which is considered the gold standard for DNA analysis, at the company’s Genomic Research Center in Houston, a CLIA-registered lab which has processed more than 5 million discrete DNA tests from more than 700,000 individuals and organizations globally.

In addition to the BRCA gene tests, DNATraits offers a pre-natal array that covers 111 population specific diseases, as well as other not population-specific diseases, like Duchene Muscular Dystrophy.

Customer Inquiries

Individuals interested in learning more about either the BRCA1 or BRCA2 tests should ask their doctors for more information.  They and their health care providers can also visit the company’s website, www.dnatraits.com, or call (713) 868-1438 for more information.

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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 Services

Genealogy Research

The Autosomal Me Summary and Links

“The Autosomal Me” is a 9 part series published between February 6, 2013 and May 31, 2013.  They are a bit dated now, but the concepts are still rock solid.

Here are all of the links in one place.

Part 1 was “The Autosomal Me – Unraveling Minority Admixture” and Part 2 was “The Autosomal Me – The Ancestors Speak.”  Part 1 discussed the technique we are going to use to unravel minority ancestry, and why it works.  Part two gave an example of the power of fragmented chromosomal mapping and the beauty of the results.

Part 3, “The Autosomal Me – Who Am I?,” reviewed using our pedigree charts to gauge expected results and how autosomal results are put into population buckets.

Part 4, “The Autosomal Me – Testing Company Results,” shows what to expect from all of the major testing companies, past and present, along with Dr. Doug McDonald’s analysis.

In Part 5, “The Autosomal Me – Rooting Around in the Weeds Using Third Party Tools,” we looked at 5 different third party tools and what they can tell us about our minority admixture that is not reported by the major testing companies because the segments are too small and fragmented.

In Part 6, “The Autosomal Me – DNA Analysis – Splitting Up” we began the analysis part of the data we’ve been gathering.   We looked at how to determine whether minority admixture on specific chromosomes came from which parent.

Part 7, “The Autosomal Me – Start, Stop, Go – Identifying Native Chromosomal Segments” took a deeper dive and focused on the two chromosomes with proven Native heritage and began by comparing those chromosome segments using the 4 GedMatch admixture tools.

Part 8, “The Autosomal Me – Extracting Data Segments and Clustering,” we  extract all of the Native and Blended Asian segments in all 22 chromosomes, but only used chromosomes 1 and 2 for illustration purposes.  We then clustered the resulting data to look for trends, grouping clusters by either the Strong Native criteria or the Blended Asian criteria.

The final segment, Part 9, “The Autosomal Me – The Holy Grail – Identifying Native Genealogy Lines,” utilized all of the chromosomal information we’ve gathered in the earlier steps.  We apply that information to our matches and determine which of our lines are the most likely to have Native Ancestry.  This, of course, fulfills the goal of using DNA information to identify small amounts of minority admixture.

In summary, this series has been quite interesting and indeed, it did achieve the goals initially set forth.  However, it was very manually intensive and took far longer than anticipated, partly due to circumstances beyond my control, like software updates and vendor changes.  A second reason that it took longer than expected was due to the sheer amount of work involved in the various steps, particularly steps 8 and 9.  In addition, because Minority Admixture Mapping (MAP) is developmental, I had to try several different approaches to determine which one, or ones, worked best.  Despite the immense amount of work, I would describe this approach certainly as useful and successful.  In fact, I don’t know how else I would have ever eliminated some genealogical lines as candidates for Native heritage and focused on others without the combination of MAP’s new techniques combined with both old and new tools provided by others.

Having said that, I would suggest that this technique, because of the intensive manual effort required, is only for the very committed genetic genealogist – the warrior, so to speak.  It also will not work well with only a few matches.  I would suggest that you would need at least 200 or 300 matches, preferably more, which is typical of someone with colonial American heritage.  If that is you, and you are desperate to find your minority admixed lines….then this type of project may be for you.  Please thoroughly read all 9 articles before beginning.

Many of the techniques in the various steps can be utilized individually, without completing the entire MAP process.  For example, comparing vendor and third party results, using the GedMatch admixture tools and the chromosome comparisons for percentages of ethnicity all provide useful information in their own right, outside of the full MAP process.

Bon voyage on your journey of discovery to find “The Autosomal You”!  Your ancestors are the pot of gold at the end of that rainbow.

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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 Services

Genealogy Research

The Autosomal Me – The Holy Grail – Identifying Native Genealogy Lines

holy grail

Sangreal – the Holy Grail.  We are finally here, Part 9 and the final article in our series.  The entire purpose of The Autosomal Me series has been to use our DNA and the clues it holds to identify minority admixture, in this case, Native American, and by identifying those Native segments, and building chromosomal clusters, to identify the family lines that contributed that Native admixture.  Articles 1-8 in the series set the stage, explained the process and walked us through the preparatory steps.  In this last article, we apply all of the ingredients, fasten the lid, shake and see what we come up with.  Let’s take a minute and look at the steps that got us to this point.

Part 1 was “The Autosomal Me – Unraveling Minority Admixture” and Part 2 was “The Autosomal Me – The Ancestors Speak.”  Part 1 discussed the technique we are going to use to unravel minority ancestry, and why it works.  Part two gave an example of the power of fragmented chromosomal mapping and the beauty of the results.

Part 3, “The Autosomal Me – Who Am I?,” reviewed using our pedigree charts to gauge expected results and how autosomal results are put into population buckets.

Part 4, “The Autosomal Me – Testing Company Results,” shows what to expect from all of the major testing companies, past and present, along with Dr. Doug McDonald’s analysis.

In Part 5, “The Autosomal Me – Rooting Around in the Weeds Using Third Party Tools,” we looked at 5 different third party tools and what they can tell us about our minority admixture that is not reported by the major testing companies because the segments are too small and fragmented.

In Part 6, “The Autosomal Me – DNA Analysis – Splitting Up” we began the analysis part of the data we’ve been gathering.   We looked at how to determine whether minority admixture on specific chromosomes came from which parent.

Part 7, “The Autosomal Me – Start, Stop, Go – Identifying Native Chromosomal Segments” took a deeper dive and focused on the two chromosomes with proven Native heritage and began by comparing those chromosome segments using the 4 GedMatch admixture tools.

Part 8, “The Autosomal Me – Extracting Data Segments and Clustering,” we  extract all of the Native and Blended Asian segments in all 22 chromosomes, but only used chromosomes 1 and 2 for illustration purposes.  We then clustered the resulting data to look for trends, grouping clusters by either the Strong Native criteria or the Blended Asian criteria.

In this final segment, Part 9, we will be applying the chromosomal information we’ve gathered to our matches and determine which of our lines are the most likely to have Native Ancestry.  This, of course, has been the goal all along.  So, drum roll…..here we go.

In Part 8, we ended by entering the start and stop locations of both Strong Native and Blended Asian clusters into a table to facilitate easy data entry into the chromosome match spreadsheet downloaded from either 23andMe or Family Tree DNA.  If you downloaded it previously, you might want to download it again if you haven’t modified it, or download new matches since you last downloaded the spreadsheet and add them to the master copy.

My goal is to determine which matches and clusters indicate Native ancestry, and how to correlate those matches to lineage.  In other words, which family lines in my family were Native or carry Native heritage someplace.

The good news is that my mother’s line has proven Native heritage, so we can use her line as proof of concept.  My father’s family has so many unidentified wives, marginalized families and family secrets that the Native line could be almost any of them, or all of them!  Let’s see how that tree shakes out.

Finding Matches

So let’s look at a quick example of how this would work.  Let’s say I have a match, John, on chromosome 4 in an area where my mother has no Native admixture, but I do.  Therefore, since John does not match my mother, then the match came from my father and if we can identify other people who also match both John and I in that same region on that chromosome, they too have Native ancestry.  Let’s say that we all also share a common ancestor.  It stands to reason at that point, that the common ancestor between us indicates the Native line, because we all match on the Native segment and have the same ancestor.  Obviously, this would help immensely in identifying Native families and at least giving pointers in which direction to look.  This is a “best case’ example.  Some situations, especially where both parents contribute Native heritage to the same chromosome, won’t be this straightforward.

Based on our findings, the maximum range and minimum (least common denominator or “In Common” range is as follows for the strongest Native segments on chromosomes 1 and 2.

  Chromosome 1 Chromosome 2
Largest   Range 162,500,000   – 180,000,000 79,000,000   – 105,000,000
Smallest   Range 165,658,091   – 171,000,000 90,000,000   – 103,145,425

At GedMatch

At GedMatch, I used a comparison tool to see who matched me on chromosome 1.  Only 2 people outside of immediate family members matched, and both from Family Tree DNA.  Both matched me on the critical Native segments between about 165-180mg.  I was excited.  I went to Family Tree DNA and checked to see if these two people also matched my mother, which would confirm the Native connection, but neither did, indicating of course that these two people matched me on my father’s side.  That too is valuable information, but it didn’t help identify any common Native heritage with my mother on chromosome 1.  It did, however, eliminate them as possibilities which is valuable information as well.

DNAGedcom

I used a new tool, DNAGedcom, compliments of Rob Warthen who has created a website, DNA Tools, at www.dnagedcom.com.  This wonderful tool allows you to download all of your autosomal matches at Family Tree DNA and 23andMe along with their chromosomal segment matches.  Since my mother’s DNA has only been tested at Family Tree DNA, I’m limiting the download to those results for now, because what I need is to find the people who match both she and I on the critical segments of chromosome 1 or 2.

Working with the Download Spreadsheet

It was disappointing to discover that my mother and I had no common matches that fell into this range on chromosome 1, but chromosome 2 was another matter.  Please note that I have redacted match surnames for privacy.

step 9 table 1

The spreadsheet above shows the comparison of my matches (pink) and Mother’s (white).  The Native segment of chromosome 2 where I match Mother is shaded mustard.  I shaded the chromosome segments that fell into the “common match” range in green.  Of those matches, there is only one person who matches both Mother and I, Emma.  The next step, of course, is to contact Emma and see if we can discover our common ancestor, because whoever it is, that is the Native line.  As you might imagine, I am chomping at the bit.

There are no segments of chromosome 2 that are unquestionably isolated to my father’s line.

Kicking it up a Notch

Are you wondering about now how something that started out looking so simple got so complex?  Well, I am too, you’re not alone.  But we’ve come this far, so let’s go that final leg in this journey.  My mom always used to say there was no point in doing something at all if you weren’t going to do it right.  Sigh….OK Mom.

The easiest way to facilitate a chromosome by chromosome comparison with all of your matches and your Strong Native and Blended Asian segments is to enter all of these segment groups into the match spreadsheet.  If you’re groaning and your eyes glaze over right after you do one big ole eye roll, I understand.

But let’s take a look at how this helps us.

On the excerpt from my spreadsheet below, for a segment of chromosome 5, I have labeled the people and how they match to me.  The ones labeled “Mom” in the last column are labeled that way because these people match both Mom and I.  The ones labeled “Dad” are labeled that way because I know that person is related on my father’s side.

Using the information from the tables created in Step 8, I entered the beginning and end of all matching segment clusters into my spreadsheet.  You can see these entries on lines 7, 8, 22, 23 and 24.  You then proceed to colorize your matches based on the entry for either Mom or Dad – in other words the blue row or the purple row, line 7, 22 or 24.  In this example, actually, line 5 Rex, based on the coloration, should have been half blue and half purple, but we’ll discuss his case in a minute.

The you can then sort either by match name or by chromosome to view data in both ways.  Let’s look at an example of how this works.

Legend:

  • White Rows:  Mother’s matches.  When Mother and I both match an individual, you’ll see the same matches for me in pink.  This double match indicates that the match is to Mother’s side and not Father’s side.
  • Pink Rows:  My matches.
  • Purple “Mom” labels in last column:  The individual matches both me and Mom.  This is a genetic match.
  • Teal “Dad” labels in last column: Genealogically proven to be from my father’s side.  This is a genealogical, not a genetic label, since I don’t have Dad’s DNA and can only infer these genetically when they don’t also match Mother.
  • Dark Pink Rows labeled “Me Amerind Only” are Strong Native or Blended Asian segments from Chromosome Table that I have entered.  My segments must come from one of my parents, so I’ve either colored them purple, if the match is someone who matches Mother and I both, or teal, if they don’t match both Mom and I, so by inference they come from my father’s line.
  • Dark Purple Rows labeled “Mom Amerind Only” are Mom’s segments from the Chromosome Table.
  • Dark Teal Rows labeled “Dad Amerind Only” are inferred segments belonging to my father based on the fact that Mother and I don’t share them.

Inferred Relationships

This is a good place to talk for just a minute about inferred relationships in this context.  Inference gets somewhat tenuous or weak.  The inferred matches on my father’s side began with the Native segments in the admix tools.  Some inferences are very strong, where Mother has no Native at all in that region.  For example, Mom has European and I have Native American.  No question, this had to come from my father.  But other cases are much less straightforward.

In many cases, categorization may be the issue.  Mom has West Asian for example and I have Siberian or Beringian.  Is this a categorization issue or is this a real genetic difference, meaning that my Siberian/Beringian is actually Native and came from my father’s side?

Other cases of confusion arise from segment misreads, etc.  I’ve actually intentionally included a situation like this below, so we can discuss it.  Like all things, some amount of common sense has to enter the picture, and known relationships will also weigh heavily in the equation.  How known family members match on other chromosome segments is important too.  Do you see a pattern or is this match a one-time occurrence?  Patterns are important.

Keep in mind that these entries only reflect STRONG Asian or Native signals, not all signals.  So even if Mother doesn’t have a strong signal, it doesn’t mean that she doesn’t have ANY signal in that region.  In some cases, start and stop segments for Mom and Dad overlapped due to very long segments on some matches.  In this case, we have to rely on the fact that we do have Mother’s actual DNA and assume that if they aren’t also a match to Mother, that what we are seeing is actually Dad’s lines, although this may not in actuality always be true.  Why?  Because we are dealing with segments below the matching threshold limit at both Family Tree DNA and 23andMe, and both of my parents carry Native heritage.  We can also have crossed a transitional boundary where the DNA that is being matched switches from Mom’s side to Dad’s side.

Ugh, you say, now that’s getting messy.  Yes, it is, and it has complicated this process immensely.

The Nitty-Gritty Data Itself

step 9 table 2

Taking a look at this portion of chromosome 5, we have lots going on in this cluster.  Most segments will just be boring pink and white (meaning no Native), but this segment is very busy.  Mom and I match on a small segment from 52,000,000 to 53,000,000.  Indeed, this is a very short segment when compared to the entire chromosome, but it is strongly Native.  We both also match Rex, our known cousin.  I’ve noted him with yellow in the table. Please note that Mom’s white matches are never shaded.  I am focused on determining where my own segments originate, so coloring Mother’s too was only confusing.  Yes, I did try it.

You can see that Mother actually shares all or any part of her segment with only me and Rex.  This simplifies matters, actually.  However, also note that I carry a larger segment in this region than does Mother, so either we have a categorization issue, a misread, or my father also contributed.  So, a conundrum.  This very probably implies that my father also carried Native DNA in this region.

Let’s see what Rex’s DNA looks like on this same segment of chromosome 5, from 52-53 using Eurogenes.  In the graph below, my chromosome is the top bar, Rex’s the middle and the bottom bar shows common DNA with the black nonmatching.  Yellow is Native American, red is South Asian, putty is Siberian, lime green is Mediterranean, teal is North Europe, orange is Caucus.

Step 9 item 3

This same comparison is shown to Mother’s DNA (top row) below.

step 9 item 4

It’s interesting that while Mother doesn’t have a lot of yellow (Native), she does have it throughout the same segment where Rex’s occurs, from about 52 through 53.5.

Does this actually point to a Native ancestor in the common line between Rex, Mom and I, which is the Swiss/German Johann Michael Miller line which does include an unidentified wife stateside, or does this simply indicate a common ancient population long ago in Asia?  It’s hard to say and is deserving of more research.  I feel that it is most likely Native because of the actual yellow, Native segment. If this was an Asian/European artifact, it would be much less likely to carry the actual yellow segment.

Is Rex also genealogically related to my father?  As I’ve worked through this process with all of my chromosomes and matches, I’ve really come to question if one of my father’s dead ends is also an ancestral line of my mother’s.

The key to making sense of these results is clusters.

Clusters vs Singleton Outliers

The work we’ve already done, especially in Step 8, clusters the actual DNA matching segments.  We’ve now entered that information into the spreadsheet and colored the segments of those who match.  What’s next?

The key is to look for people with clusters.  Many matches will have one segment, of say, 10 that match, colored.  Unless this is part of a large chromosome cluster, it’s probably simply an outlier.  Part of a large chromosome cluster would be like the large Strong Native segments on chromosome 1 or 2, for example.  How do we tell if this is a valid match or just an outlier?

Sort the spreadsheet by match name.  Take a look at all of the segments.

The example we’ll use is that of my cousin, Rex.  If you recall, he matches both me and Mother, is a known first cousin twice removed to me, (genetically equal to a second cousin), and is descended from the Miller line.

In this example, I also colored Mother’s segments because I wanted to see which segments that I did not receive from her were also Native. You can see that there are many segments where we all match and several of those are Native.  These also match to other Miller descendants as well, so are strongly indicative of a Native connection someplace in our common line.

If we were only to see one Native segment, we would simply disregard this as an outlier situation.  But that’s not the case.  We see a cluster of matches on various segments, we match other cousins from the same line on these segments, and reverting back to the original comparison admixture tools verifies these matches are Native for Rex, Mom and me.

step 9 item 5

Hmmmm…..what is Dad’s blue segment color doing in there?  Remember I said that we are only dealing with strong match segments?  Well, Mom didn’t have a strong segment at that location and so we inferred that Dad did.  But we know positively that this match does come from Mother’s side.  I also mentioned that I’ve come to wonder if my Mom and Dad share a common line.  It’s the Miller line that’s in question.  One of Johann Michael Miller’s children, Lodowick, moved from Pennsylvania to Augusta County, Virginia in the 1700s and his line became Appalachian, winding up in many of the same counties as my father’s family.  I’m going to treat this as simply an anomaly for now, but it actually could be, in this case, an small indication that these lines might be related.  It also might be a weak “Mom” match, or irrelevant.  I see other “double entries” like this in other Miller cousins as well.

What is the pink row on chromosome 12?  When I grouped the Strong Native and Asian Clusters, sometimes I had a strong grouping, and Mom had some.  The way I determined Dad’s inferred share was to subtract what Mom had in those segments from mine.  In a few cases, Mom didn’t have enough segments to be considered a cluster but she had enough to prevent Dad from being considered a cluster either, so those are simply pink, me with no segment coloring for Mom or Dad.

Let’s say I carry Strong Native/Mixed Asian at the following 8 locations:

10, 12, 14, 16, 18, 20, 22, 24

This meets the criteria for 8 of 15 ethno-geographic locations (in the admix tools) within a 2.5 cM distance of each other, so this cluster would be included in the Mixed Asian for me.  It could also be a Strong Native cluster if it was found in 3 of 4 individual tools.  Regardless of how, it has been included.

Let’s now say that Mom carries Native/Mixed Asian at 10, 12 and 14, but not elsewhere in this cluster.

Mom’s 3 does not qualify her for the 8/15 and it only leaves Dad with 5 inferred segments, which disqualifies him too.  So in this case, my cluster would be listed, but not attributable directly to either parent.

What this really says is that both of my parents carry some Native/Blended Asian on this segment and we have to use other tools to extrapolate anything further.  The logic steps are the same as for Dad’s blue segment.  We’re going to treat that as an outlier.  If I really need to know, I can go back to the actual admixture tools and see whether Mom or Dad really match me strongly on which segments and how we compare to Rex as well.  In this case, it’s obvious that this is a match to my Mother’s side, so I’m leaving well enough alone.

Let’s see what the matches reveal.

Matches

Referring back to the Nitty Gritty Data spreadsheet, Mom’s match to Phyllis on row 15 confirms an Acadian line.  This is the known line of Mother’s Native ancestry.  This makes sense and they match on Native segments on several other chromosomes as well.  In fact, many of my and Mother’s matches have Acadian ancestry.

My match to row 19, Joy, is a known cousin on my father’s side with common Campbell ancestry.  This line is short however, because our common ancestor, believed to be Charles Campbell died before 1825 in Hawkins County, TN.  He was probably born before 1750, given that his sons were born about 1770 and 1772.  Joy and I descend from those 2 sons.  Charles wife and parents are unknown, as is his wife.

My match to row 20, inferred through my father’s side, is to a Sizemore, a line with genetically proven Native ancestry.  Of course, this needs more research, but it may be a large hint.  I also match with several other people who carry Sizemore ancestors.  This line appears to have originated near the NC/VA border.

I wanted to mention rows 4 and 17.  Using our rules for the spreadsheet, if I match someone and they don’t also match Mother on this segment, I have inferred them to be through my father.  These are two instances that this is probably incorrect.  I do match these people through Mother, but Mother didn’t carry a strong signal on this segment, so it automatically became inferred to Dad.  Remember, I’m only recording the Strong Native or the Blended Asian segments, not all segments.  However, I left the inferred teal so that you can see what kinds of judgment calls you’ll have to make.  This also illustrates that while Mom’s genetic matches are solid, Dad’s inferred matches are less so and sometimes require interpretation.  The proper thing to do in this instance would be to refer back to the original admixture tools themselves for clarification.

Let’s see what that shows.

step 9 item 6

Using HarrappaWorld, the most pronounced segment is at about 52.  Teal is American.  You can see that Mother has only a very small trace between 53 and 54, almost negligible.  Mother’s admixture at location 52 is two segments of purple, brown and cinnamon which translate to Southwest Asian (lt purple), Mediterranean (dk purple), Caucasian (brown) and Balock (cinnamon), from Pakistan.

Checking Dodecad shows pretty much the same thing, except Mother’s background there is South Asian, which could be the same thing as Caucus and Pakistan, just different categorizations.

In this case, it looks like the admixture is not a categorization issue, but likely did come from my father.  Each segment will really be a case by case call, with only the strongest segments across all tools being the most reliable.

It’s times like this that we have to remember that we have two halves of each chromosome and they carry vastly different information from each of our parents.  Determining which is which is not always easy.  If in doubt, disregard that segment.

Raw Numbers

So, what, really did I figure out after all of this?

First, let’s look at some numbers.

I was working with a total of 292 people who had at least one chromosomal segment that matched me with a Strong Native or Blended Asian segment.  Of those, 59 also matched Mom’s DNA.  Of those, 18 had segments that matched only Mom.  This means that some of them had segments that also matched my father.  Keep in mind, again, that we are only using “strong matches” which involves inferring Dad’s segments and that referring back to the original tools can always clarify the situation.  There seems to be some specific areas that are hotspots for Native ancestry where it appears that both of my parents passed Native ancestry to me.

Many of my and my mother’s 59 matches have Acadian ancestry which is not surprising as the Acadians intermarried heavily with the Native population as well as within their own ethnic group.

Several also have Miller Ancestry.  My Miller ancestor is Johann Michael Miller (1692-1771) who immigrated in the colonial period and settled on the Pennsylvania frontier.  His son, Philip Jacob Miller’s (1726-1799) wife was a woman named Magdalena whose last name has been rumored for years to be Rochette, but no trace of a Rochette family has ever been found in the county where they lived, region or Brethren church history…and it’s not for lack of looking.  Several matches point to Native Ancestry in this line.  This also begs the question of whether this is really Native or whether it is really the Asian heritage of the German people.  Further analysis, referring back to the admixture tools, suggests that this is actually Native. It’s also interesting that absolutely none of Mother’s other German or Dutch lines show this type of ancestry.

There is no suggestion of Native ancestry in any of her other lines.  Mother’s results are relatively clean.  Dad’s are anything but.

Dad’s Messy Matches

My father’s side of the family, however, is another story.

I have 233 matches that don’t also match my mother.  There can be some technical issues related to no-calls and such, but by and large, those would not represent many.  So we need to accept that most of my matches are from my Father’s side originating in colonial America.  This line is much “messier” than my mother’s, genealogically speaking.

Of those 233 matches, only 25 can be definitely assigned to my father.  By definitely assigned, I mean the people are my cousins or there is an absolutely solid genealogical match, not a distant match.  Why am I not counting distant matches in this total?  We all know by virtue of the AncestryDNA saga that just because we match family lines and DNA does NOT mean that the DNA match is the genealogical line we think it is.  If you would like to read all about this, please refer to the details in CeCe Moore’s blog where she discussed this phenomenon.  The relevant discussion begins just after the third photo in this article where she shows that 3 of 10 matches at Ancestry where they “identify” the common DNA ancestor are incorrect.  Of course, they never SAY that the common ancestor is the DNA match, but it’s surely inferred by the DNA match and the “leaf” connecting these 2 people to a common ancestor.  It’s only evident to someone who has tested at least one parent and is savvy enough to realize that the individual whose ancestor on Mom’s side that they have highlighted, isn’t a match to Mom too.  Oops.  Mega-oops!!!

However, because we are dealing in our project, on Dad’s side, with inferences, we’re treading on some of the same ground.  Also, because we are dealing with only “strong clustered” segments, not all Native or Asian segments and because it appears that my parents both have Native ancestry.  To make matters worse, they may both have Algonquian, Iroquoian or both.

I have also discovered during this process that several of my matches are actually related to both of my parents.  I told you this got complex.

Of the people who don’t match Mother, 32 of them have chromosomal matches only to my father, so those would be considered reliable matches, as would the closest ones of the 25 that can be identified genealogically as matching Dad.  Many of these 25 are cousins I specifically asked to test, and those people’s results have been indispensable in this process.

In fact, it’s through my close circle of cousins that we have been able to eliminate several lines as having Native ancestry, because it doesn’t’ show as strong and they don’t have it either.

Many of these lines group together when looking at a specific chromosome.  There is line after line and cousin after cousin with highlighted data.

Dad’s Native Ancestors

So what has this told me?  This information strongly suggests that the following lines on my father’s side carry Native heritage.  Note the word “carry.”  All we can say at this point is that it’s in the soup – and we can utilize current matches at our testing company and at GedMatch, genealogy research and future matches to further narrow the branches of the tree.  Many of these families are intermarried and I have tried to group them by marriage group.  Obviously, eventually, their descendants all intermarried because they are all my ancestors on my father’s side.  But multiple matches to other people who carry the Native markers but aren’t related to my other lines are what define these as lines carrying Native heritage someplace.

  • Campbell – Hawkins County, Tn around 1800, missing wife and parents, married into the Dodson family
  • Dodson – Hawkins County, Tn, Virginia – written record of Lazarus Dodson camping with the Cherokee – missing wife, married into the Campbell and Estes family
  • Claxton/Clarkson – Russell Co., Va, Claiborne and Hancock Co., Tn – In NC associated with the known Native Hatcher family.  Possibly a son-in-law.  Missing family entirely.
  • Cook – Russell Co., Va. – daughter married Claxton/Clarkson – missing wives
  • Harrold, Harrell, Herrell – Hancock Co., Tn., Wilkes Co., NC – missing wives
  • McDowell – Hancock Co. Tn, Wilkes Co., NC, Augusta Co., Va – married into the Harrell family, missing wife
  • McNeil, McNiel – Wilkes Co., NC – missing wives, married into the Vannoy family
  • Vannoy – Wilkes County – some wives unaccounted for pre-1800
  • Crumley – Greene County, Tn., Lee Co., Va. – oral history of Native wife, married into the Vannoy family
  • Brown – Greene County, Tn, Montgomery Co., Va – married into the Crumley family, missing wives

While this looks like a long list, the list of families that don’t have any Native ancestry represented is much longer and effectively serves to eliminate all of those lines.  While I don’t have “THE” answer, I certainly know where to focus my research.  Maybe there isn’t the one answer.  Maybe there are multiple answers, in multiple lines.

The Take Away

Is this complex?  Yes!  Is it a lot of work?  You bet it is!  Is everything cast in concrete?  Never!  You can see that by the differences we’ve found in data interpretation, not to mention issues like no-calls (areas that for some reason in the test don’t read) and cross overs where your inheritance switches from your mom’s side to your dad’s side.  Is there any other way to do this?  No, not if your minority admixture is down in that weedy area around 1%.

Is it worth it?  You’ll have to decide.  It guess it depends on how desperately you want to know.

Part of the reason this is difficult is because we are missing tools in critical locations.  It’s an intensively laborious manual process.  In essence, using various tools, one has to figure out the locations of the Native and Asian chromosome segments and then use that information to infer Native matches by a double match (genetic match at DNA company plus match with Strong Native/Blended Asian segment) with the right parent.  It becomes even more complex if neither parent is available for testing, but it is doable although I would think the reliability could drop dramatically.

Tidbits and Trivia

I’ve picked up a number of little interesting tidbits during this process.  These may or may not be helpful to you.  Just kind of file them away until needed:)

  • Matches at testing companies come and go….and sometimes just go.  At Family Tree DNA, I have some matches that must be trembling on the threshold that come and go periodically.  Now you see them, now you don’t.  I lost matches moving from the Affy chip to the Illumina chip and lost additional matches between Build 36 and 37.  Some reappeared, some haven’t.
  • The start and stop boundaries changed for some matches between build 36 and build 37.  I did not go back and readjust, as most of these, in the larger scheme of things, were minor.  Just understand that you are looking for  patterns here that indicate Native heritage, not exact measurements.  This process is a tool, and unfortunately, not a magic wand:)
  • The centromere locations change between builds.  If you have matches near or crossing the middle of the chromosome, called the centromere, there may be breaks in that region.  I enter the centromere start and stop locations in my spreadsheet so that if I notice something odd going on in that region, the centromere addresses are right there to alert me that I’m dealing with that “odd” region.  You can find the centromere addresses in the FAQ at Family Tree DNA for their current build.
  • At 23andMe, when you reach the magic 1000 matches threshold, you start losing matches and the matching criteria is elevated so that you can stay under 1000 matches.  For people with colonial American or Jewish heritage, in other words those with high numbers of matches, this is a problem.
  • Watch for matches that are related to both sides of your family.  If your family lived in colonial America, you’re going to have a lot of matches and many are probably related to each other in ways you aren’t aware of.
  • If your parents are related to each other, this process might simply be too complex and intertwined to provide enough granular data to be useful.
  • Endogamous groups are impossible to sort through as to where, meaning which ancestor, the DNA came from.  This is because the original group founders’ DNA is just getting passed around and around, with little or no new DNA being introduced.  The effect of this on downstream generations relative to genetic genealogy is that matches appear to be more closely related than they are because of the amount of matching DNA they carry.  For my Brethren and my Acadian groups of people, I just list them by the group name, since, as the saying goes, “if you’re related to one Acadian, you’re related to all Acadians.”
  • If you’re going to follow this procedure, save one spreadsheet copy with the Strong Native only and then a second one with both the Strong Native and Blended Asian.  I’m undecided truthfully whether the Mixed Asian adds enough resolution for the extra work it generates.
  • When in question, refer back to the original tools.  The answer will always be found there.
  • Unfortunately, tools change.  You may want to take screen shots.  During this process, FTDNA went from build 36 to 37, match thresholds changed, 23andMe introduced a new user interface (which I find much less intuitive) and GedMatch has made significant changes.  The net-net of this is when you decide to undertake this project, commit to it and do it, start to finish.  Doing this little by little makes you vulnerable to changes that may make your data incompatible midstream – and you may not even realize it.
  • This entire process is intensively manual.  My spreadsheet is over 5500 rows long.  I won’t be doing it again…although I will update my spreadsheet with new matches from time to time.  The hard work is already done.
  • This same technique applies to any minority ancestry, not just Native, although that’s what I’ve been hunting for and one of the most common inquiries I receive.
  • I am hopeful that in the not too distant future many of these steps and processes will be automated by the group of bright developers that contribute to GedMatch or via other tools like DNAGedcom. HINT – HINT!!!

I would like to follow this same process to identify the source of my African heritage, but I’m thinking I’ll wait for the tools to become automated.  The great irony is that it’s very likely in the same lines as my Native ancestors.

If You Want to Test

What does it take to do this for yourself using the tools we have today, as discussed?

If your parents are living, the best gift you can give yourself is to test them, now, while you still can.  My mother has been gone for several years, but her DNA archived at Family Tree DNA was still viable.  This is not always the case.  I was fortunate.  Her DNA is one of the best gifts she gave me.  Not just by inheritance, but by having hers tested.  I thank her every single day, for both!  I could not have written this article without her DNA results.  The gift that keeps on giving.

If you don’t have a parent to test, you can test several other family members who will provide some information, but clearly won’t carry the same amounts of common DNA with you as your parents.  These would include your aunts and uncles, your parents’ siblings and what I’ve referred to as your close cousin circle.  Attempt to test at least someone from each line.  Yes, it gets expensive, but as one of my cousins said, as she took her third or 4th DNA test.  “It’s only money.  This is about family.”

You can also test your own siblings as well to obtain more information that you can use to match up to your family lines. Remember, you only receive half of your parents DNA, and your siblings will received some DNA from your parents that you didn’t.

I don’t have any other siblings to test, but I have tested cousins from several lines which have proven invaluable when trying to discern the sources of certain segments. For example, one of these Native segments fell on a common segment with my cousin Joy.  Therefore, I know it’s from the Campbell line, and because I have the Campbell paternal Y-DNA which is European, I know immediately the Native admixture would have had to be from a wife.

Much of this puzzle is deductive, but we now have the tools, albeit manual, to do this type of work that was previously impossible.  I am somewhat disappointed that I can’t pinpoint the exact family lines, yet, but hopefully as more people test and more matches provide genealogical information, this will improve.

If you want to play in this arena, you need to test at either Family Tree DNA, 23andMe, or both.  Right now, the most cost effective way to achieve this is to purchase a $99 kit from 23andMe, test there, then download your results from 23andMe and upload them to Family Tree DNA for $99.  That way, you are fishing in both pools.  Be aware that less than half of the people who test at either company download results to GedMatch, so your primary match locations are with the testing companies.  GedMatch is auxiliary, but critical for this analysis.  And the newest tool, DNAGedcom is a Godsend.

Also note that transferring your result to Family Tree DNA is NOT the same thing as actually testing there.  Why does this matter?  If you want a future test at Family Tree DNA, who is the premiere genetic genealogy testing company, offering the most variety and “deepest” commercial tests, they archive your DNA for 25 years, but if you transfer results, they don’t have your DNA to archive, so no future products can be ordered.  All I can say is thank Heavens Mom’s DNA was there.

Ancestry.com doesn’t provide any tools such as the chromosome browser or even the basic information of matching segments.  All you get is a little leaf that says you’re related, but the questions of which segment or how are not answerable today at Ancestry and as CeCe’s experience proved, its unreliable.  It’s  possible that you share the same surnames and ancestor, but your genetic connection is not through that family line.  Without tools, there is no way to tell.  Ancestry released raw data files a few weeks ago and very recently, GedMatch has implemented the ability to upload them so that Ancestry participants can now utilize the additional tools at GedMatch.

Although this has been an extraordinarily long and detailed process, I can’t tell you how happy I am to have developed this new technique to add to my toolbox.  My Native and African ancestors have been most elusive.  There are no records, they didn’t write and probably didn’t even speak English, certainly not initially.  The only clues to their existence, prior to DNA, were scant references and family lore.  The only prayer of actually identifying them is though these small segments of our DNA – yep – down in the weeds.  Are there false starts perhaps, and challenges and maybe a few snakes down there?  Yes, for sure, but so is the DNA of your ancestors.

Happy gardening and rooting around in the weeds.  Just think of it as searching for the very best buried treasure!  It’s down there, just waiting to be found.  Keep digging!

I hope you’ve enjoyed this series and that it leads you to your own personal genealogical treasure trove!

treasure chest

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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 Services

Genealogy Research

Picture This

Margaret Herrell, what did you look like?

Margaret died in 1892, but we don’t have a photo of her nor of her second husband Joseph Preston Bolton who died in 1887.  Her son, my great-grandfather, Joseph “Dode” Bolton died in 1920 and we don’t have a picture of him either, or his wife, Margaret Claxton/Clarkson who died just days later in the flu epidemic.  The closest I can get is this photo of Margaret Herrell’s daughter.

Smith-Martin

Pleasant Smith and Surelda Martin (1836-1890) – daughter of my ancestor Margaret Herrell with her first husband, Anson Cook Martin – Hancock County, Tennessee.

Today, there was an article in “abroad in the yard” by Lee Rimmer that discussed an academic paper published in PLOS Genetics this week by Liu et al titled “A Genome-Wide Association Study Identifies 5 Loci Influencing Facial Morphology in Europeans.”

We all know that facial characteristics are genetic.  Identical twins look more alike that fraternal twins, and fraternal twins look more alike that cousins or half-siblings.  But exactly which genes contribute to that structural composition of faces is unknown, or has been until now.  This recent paper identifies 5 genes that influence to some extent the morphology of the face by identifying specific facial landmarks and the genes that influence them.  Researchers expect to find hundreds or thousands more, but many of these may play small roles.

Already people are talking about forensic applications where from a drop of blood, a hair, spit or other body fluids or tissues, one could sequence the DNA, then create a 3D profile or image of the perpetrator of the crime.  Indeed, that is the holy grail of forensic genetics.

And yes, it’s a long way in the future.  However, the very definition of “long way” is certainly open to debate.  We’ve covered genetic ground in the past decade alone that we never thought possible.

This (future) application has other possibilities for genealogists.  We already know how to phase data, to attribute it to one parent or the other.  Using those and other comparative and triangulation tools, we also know how to determine genetic sequences that we share inherited from specific ancestors.  In fact, once that genetic segment is identified as inherited from a particular ancestral line, might it be possible in the future to indeed, reassemble enough of the DNA of that ancestor (by knowing the genes involved and the descendants who carry those genes today) to create an image of that long dead ancestor?

Maybe one day, not terribly far in the future, we’ll be able to submit a list of segments of DNA to a special processing “studio” online, that will in return provide us with what our ancestor looked like, long before the advent of cameras when only the images of royalty were preserved.  And maybe, just maybe, if you tell them the place and time your ancestor was born, and his or her occupation, if you know, you’ll also receive the “photo” of your ancestor dressed in period clothes and hairstyle.

And while it might not be exact, just like this “cleaned up” photo isn’t exact from an  original, shown below, it’s most assuredly better than nothing – and in that image we can certainly see something very similar to our ancestor – and in them we can see ourselves.

Smith-Martin orig

Let’s hope that this big genealogical dream of what today seems impossible happens in our lifetime so that we can complete our family tree by recreating images of ancestors from long ago.  Indeed, how much closer could one feel to an ancestor than to have their image resurrected by the DNA, their DNA, carried by their descendants. And what an incredible crowdsourcing project – it may take a virtual genealogical village.

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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 Services

Genealogy Research

No (DNA) Bullying

No Bullying

There are hardly any hobbies that hold more passion than genealogy.  Once hooked by the bug, most people never retire and one of the things they worry about passing down to their family are their genealogy records – even if the family of today isn’t terribly interested.

So it’s easy to understand the degree of passion and enthusiasm, but sometimes this passion can kind of go astray and it crosses the line from something positive to something not nearly so nice.

Genetic genealogy is the latest tool in the genealogists’ arsenal, but it introduces some new challenges and unfortunately, with the increased number of people testing, we’re seeing some examples of what I consider bullying – for DNA, for identification and for information.

Bullying is unwelcome aggressive behavior that involves repeated threats, physical or electronic contact or a real or perceived imbalance of power.  Generally, the victim feels they can’t make it stop.  This has become especially prevalent in the cyber age.  And bullying is not just about kids.

I’m going to look at 3 types of situations.  It’s easy to see both perspectives, but bullying by any other name is still bullying, even though the bully probably doesn’t see it that way.  Guaranteed, the recipient does.

You’ve Got the DNA I Need

Let’s say that Aunt Gladys is the last person alive in a particular line who can provide DNA to represent that line.  But Aunt Gladys, for whatever reason, doesn’t want to test.  It’s fine to discuss this, to talk about her concerns, and perhaps you can find a solution to address them, like testing anonymously.

But let’s say that Aunt Gladys simply says “no,” end of story.  What then?

Yes, Aunt Gladys carries the information that you need, but it’s HER DNA that needs to be tested, and if she says no, then her decision should be respected, as difficult as it may be and as unreasonable as it may seem.  Maybe Aunt Gladys knows something you don’t – like she is adopted or some other secret that she does not wish to reveal.  Badgering Aunt Gladys from this point forward is going to do nothing other than cause hard feelings and make Aunt Gladys want to avoid you.

You may think you’re “just discussing” but from her perspective, you may be bullying.  Now, it’s OK to beg and cry once, but if you’re slipped into the realm of “if you don’t test, I’ll tell Uncle Harvey that you scratched his car back in 1953,” you’ve stepped over that line.

Won’t Answer E-Mails

I can’t tell you how often I hear this story.  “I match with person XYZ and they won’t share their information.”  Most of the time, they won’t answer e-mails.  And the question follows, of course, as to why they tested in the first place.

These tests have been around for a number of years now.  Many people have died or moved or the purpose of the test was fulfilled and they aren’t interested beyond that.  Think of your Aunt Gladys.  If you did convince her to test, it wouldn’t be for her, but for you and she certainly would not be interested in answering random e-mails.

There could be a number of reasons, depending on the testing company used, that someone might not answer.  In particular, many people test at 23andMe for health reasons.  It doesn’t matter to them if you’re a first cousin or any other relation, they simply aren’t interested or don’t have the answers for you.

It’s alright to send 2 or 3 e-mails to someone.  E-mails do get lost sometimes.  But beyond that, you’ve put yourself into the nuisance category.  But you can be even worse than a nuisance.

I know of one case where someone googled the e-mail of their contact, discovered the person was a doctor, and called them at the office.  That is over the line into cyber-stalking.  If they wanted to answer the e-mail, they would have.  If they don’t want to, their decision needs to be respected.

I Know You Know

This situation can get even uglier.  I’ve heard of two or three situations recently.  One was at Ancestry where someone had a DNA match and their trees matched as well.  At first the contact was cordial, but then it deteriorated into one person insisting that the other person had information they weren’t divulging and from there it deteriorated even further.

This is a hobby.  It’s supposed to be fun.  This is not 7th grade.

Adoptions

However, there are other situations much more volatile and potentially serious. In some cases, often in adoptions, people don’t want contact.  Sometimes it’s the parent and sometimes it’s the adoptee.  But those aren’t the only people involved.  There are sometimes half-siblings that are found or cousins.

For the adoptees and the parents, there are laws in each state that govern the release of their legal paperwork to protect both parties.  Either party can opt out at any time.

But for inadvertently discovered family connections, this isn’t true.  Think of the person who doesn’t know they are adopted, for example, who discovers a half-sibling and through that half sibling their biological mother.  Neither person may welcome or be prepared for this discovery or contact.

Imagine this at the dinner table with the family gathered, “Hey guess what, I got a half-sibling match today on my DNA.  I wonder if that’s some kind of mistake.  How could that be?”

So if you match someone as a half sibling or a cousin, and they don’t want to continue the conversation, be kind and respectful, and leave the door open to them if they change their mind in the future.  Pushing them can only be hurtful and nonproductive.

Dirty Old (and Formerly Young) Men

And then, there’s the case of the family pervert.  Every family seems to have one.  But it’s not always who you think it is.  By the very nature of being a pervert, they hide their actions – and they can be very, very good at it.  Practice makes perfect.

Let’s say that Jane likes genealogy, but she was molested as a child by Cousin Fred.  Some of the family knows about this, and some don’t believe it.  The family was split by this incident, but it was years in the past now.  Jane wants nothing to do with Fred’s side of the family.

(By the way, if you think this doesn’t happen, it does.  About 20% of woman have been raped, 30% of them by family members (incest), many more molested, and children often by relatives or close family friends.  15% of sexual assault victims are under the age of 12.  Many childhood cases are never prosecuted because the children are too young to testify.  Perverts and pedophiles don’t wear t-shirts announcing such or have a “P” tattooed on their forehead.  Often family members find it hard to believe and don’t, regardless of the evidence, casting the victimized child in the position of being a liar and “troublemaker.”  Need convincing?  Think of what Ariel Castro’s family said and how well he hid his dark side and the Boston bombers’ family comments about their innocence in the face of overwhelming evidence to the contrary.)

Jane’s an adult now and DNA tests.  She has a match and discovers that it’s on Fred’s side of the family.  Jane tells the person that she doesn’t want anything to do with that side of the family, has no genealogy information and wants no contact.  The match doesn’t believe Jane and then becomes insistent, then demanding, then accusatory, then threatening.

This is clearly over the line.  Jane said she didn’t want any continued contact.  That should have been the end of the discussion.

But let’s say this one gets worse.  Let’s say that because of this, Cousin Fred wakes up and decides that Jane is interesting again and begins to stalk Jane, and her children……

Does this make you shake in your shoes?  It should.  Criminals not only aren’t always playing with a full deck, but don’t play by any of the same rules as the rest of us.  Cousin Fred might just be very grateful for that information about Jane and view it as a wonderful “opportunity,” provided by his “supportive” family member who has now endangered both Jane and her children.

Who’s Yer Daddy?

In another recent situation, John discovered by DNA testing that he is not the biological child of his father.  He subsequently discovered that his mother was raped by another male, married to another close family member.  When John discovered that information, he promptly lost interest in genealogy altogether.

A year or so later, John matched someone closely who was insistent that he provide them with how he was related to them.  John knew, but he did not feel that it was any of their business and he certainly did not want to explain any of the situation to the perpetrator’s family member, who, by the way, had already mentioned what a good person the perpetrator was.  However, the person continued to harass and badger John until he changed his e-mail address.

I so wanted to ask these people, “What part of “NO” don’t you understand?”

Mama’s Baby, Daddy’s Maybe

In one final example, adoptees often make contact with their birth mother first, and then, if at all, with their birth father.  Sometimes the birth mothers are not cooperative with the (now adult) child about the identity of their father.  Often, this is horribly frustrating to the adoptee.  In at least one case, I know of a birth mother who would never tell, leaving the child an envelope when she died.  The child was just sure the father’s name was in the envelope, but it was not.  I can only imagine that level of disappointment.

Why would someone be so reticent to divulge this information?  The primary reasons seem to be that either the mother doesn’t know due to a variety of circumstances that can range from intoxication to rape, the woman never told the father that she had a baby and placed the child for adoption, the father was abusive and the mother was/is afraid of him/his family, the father was married, or the father was a relative, which means not only might the father still be alive, the mother may still have a relationship of some type with him.  The mother may have lied for years to protect herself, and in doing so, protected the father as well.

Clearly, this situation has a lot of potential to “shift” a lot of lives and not always in positive ways.  One woman didn’t want to make contact with her child other than one time because she had never told her husband of 30 years that she had a child before their marriage.  One woman made contact, but did not want to divulge that the child’s father was her older brother, still alive.  Victims often keep the secrets of their attackers out of misplaced shame and guilt.  Think Oprah here.  Mother may not be simply being stubborn, but acting like the victim she is and trying to preserve whatever shreds of dignity are left to her.  She may also be embarrassed by a lapse in judgment.  One adoptee realized when counting forward from her birth date that she was conceived right at New Years and when she realized that, she figured out that her mother, who drank heavily when she was younger, probably did not know who her father was, and didn’t want to admit that.

As frustrating as this is for the adoptee, the birth mother does have the right not to have her life turned upside down.  Badgering her will only result in losing the potential for a relationship from the current time forward.  Being respectful, understanding and gentle may open the door for future information.

R-E-S-P-E-C-T

I can hear Aretha now.

If you haven’t walked a mile in their moccasins, so to speak, you can’t possibly know the situation of the person on the other end of your request for DNA or information.  Don’t make the mistake of stepping over the line from excitement into bully behavior.

Think of the potential situations the person on the other end may be dealing with.  Ultimately, if they say no, then no it is and no should be enough without an explanation of why.  Generally bullying doesn’t work anyway, because someone who feels like you are threatening them or being too aggressive will clam right up and it will be that proverbial cold day in Hades before they tell you anything.  It’s important to keep communications from sounding like you’re demanding or entitled.  My mother always said “you’ll catch more flies with honey than with vinegar.”  I always found that very irritating, probably because I needed to hear it just then – but regardless – it’s true.

Keep in mind, genetic genealogy is about genealogy.  It’s a hobby.   It’s fun.  If it becomes otherwise and puts people at jeopardy, then we need to take a step back and take a deep breath.

Most people don’t mean to cross the line into bullying.  They just get excited and sometimes desperate.  Hopefully this discussion will help us all be more aware of where the polite line is in communicating with our family members and matches.

If you are the victim of information bullying, cyber-stalking or someone puts you in an uncomfortable situation, there are steps you can take to remedy the situation.  Most bullying sites are directed at adolescents, but the advice still applies.

If you know you don’t want contact initially, then make your accounts anonymous or don’t respond to requests.  If you realize that you don’t want contact after the initial contact, for whatever reason, say so.  After that, do not engage in communications with someone who is attempting to bully you.  If they threaten you or threaten to reveal information or your identity if you don’t give them information or do something, that action falls into the blackmail realm, which a crime.  Complying with a threat to protect yourself or your family generally only results in more of the same.  You are not dealing with a nice person.  At this point, you are way beyond genealogy and your own internal “danger” sign should be flashing bright neon red.

If disengaging does not take care of the problem, save all messages/contacts and contact your attorney who may advise you to contact the police or the FBI if the problem crosses state lines.  Depending on what state you/they live in and exactly what they have done, you may have a variety of options if they won’t stop, especially if they do something that does in fact manage to turn your life upside down and/or a crime is involved, like blackmail.  Of course, this is akin to closing the barn door after the cow leaves.  Hopefully, the person causing the problem is simply an over-zealous genealogist, means you no harm, realizes what they have done or are doing, and will get a grip and compose themselves long before this point.

Bullying of course is not because of DNA or unique to genetic genealogy, but the new products introduce new social situations that we have not previously had tools to discover nor the opportunity to address in quite the same way.

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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.

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Genealogy Services

Genealogy Research

Still Part Redman Deep Inside

Do you have a persistent story of Native American heritage in your family?

Standing Bear, Ponca, 1877Mark Green’s wife did.  Her ancestor Nancy Pittman’s mother was supposed to be a Cherokee Indian.  If your family was from the south, chances are you have some similar story.

Mark tracked her story both through DNA and the Cherokee records.  Her DNA showed 1% Native ancestry, but the records pertaining to the Guion-Miller Roll provided additional information.  It’s most interesting, because although the paperwork having to do with her 1907 application is ambiguous, with the application subsequently denied, the DNA, some 100 years and a few generations later, isn’t.

Here’s Mark’s article about the family story, his research and what he found.  Sometimes a little footwork goes a long way – and there are lots of records available having to do with the Cherokee and 5 Civilized Tribes who were removed to Oklahoma.

http://southerngreens.blogspot.com/2013/04/im-still-part-redman-deep-inside.html

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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 Services

Genealogy Research