This is Part 3 of a multi-part series.
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.
This series focuses on answering the questions of identity through autosomal testing, in particular, for minority ancestry. By minority, I mean any small, elusive amount of any type of ancestry you are seeking to discover in your heritage. In my case, that’s both Native American and African.
This segment, Part 3, focuses on using pedigree charts to gauge expected results, how autosomal ethnic groups are determined and how fragmented minority admixture mapping is different from other techniques. This leads us into Part 4 which shows the various results from different testing companies and how they differ.
Part 5 features third party analysis tools and Part 6 begins the analyses of the data that parts 3, 4 and 5 provide.
Let’s hope that with all of this information, we can answer at least part of the question: Who am I? Who am I really?
A lot of who I am has to do with who my ancestors were, where they lived, what they did, choices they made. Did they fight in the American or French Revolution? On which side? Were they Native? Were they African? Were they slaves? So, who were they?
One of the reasons I began with genetic genealogy more than a decade ago was to confirm or disprove the persistent family history of Native American heritage that I had been unable to resolve using only traditional genealogy tools. I have made inroads with that, in unexpected ways and places, because of and in addition to genetic genealogy. Genetic genealogy and traditional genealogy go hand in hand.
It’s difficult tracking down each line to perform mitochondrial or Yline DNA tests. Sometimes, it’s beyond difficult and it’s impossible. Lines die out, people refuse to test or you simply can’t find the right people. We need other tools.
Enter autosomal genetics. From the beginning, early in genetic genealogy, we had the CODIS type forensic and paternity type tests. I reviewed the results of those early tests relative to my pedigree chart in a paper I wrote, Revealing American Indian and Minority Heritage Using Y-line, Mitochondrial, Autosomal and X Chromosomal Testing Data Combined with Pedigree Analysis published in JoGG in the Fall 2010 Issue. We’ve come a long way since then.
In that article, I dissected my pedigree chart to determine how much of different types of ancestry I carried and how that compared with the testing that had been performed at that time.
Using the end of line ancestors pedigree analysis method described in the paper, which determines the percentage of ethnicity that each end-of-line ancestor contributed to me, my origins totals were as follows:
Geographic Origin Chart
(1) The ethnic heritage of several lines could probably be inferred by surname or ethnicity of marriage partner. However, I have avoided the temptation to make inferences within the United States, as the Native or African ancestry may well lie with one of these ancestors. These are in fact the perfect candidates and to eliminate them from consideration by inferring origins would be a disservice.
In broader categories, and combining those that are similar, we find:
This is a useful exercize, not just for minority admixture, but to help evaluate the results you receive from the various testing companies. For example, you might notice that there is no Scandinavian showing in my pedigree chart, which makes Ancestry’s 80% British and 12% Scandinavian suspect right off the bat. It also makes results as high as 25% Native American reported in one of the earlier tests impossible. This pedigree analysis tool helps you understand what is reasonable to expect in terms of ethnicity breakdown.
Now that we know what the majority ancestry looks like and any minority ancestry that we are aware of, let’s take a look at the various types of autosomal testing available.
Tests and Population Markers
In the paper, I reviewed the older results from companies using either CODIS or proprietary markers. These low resolution tests are out of date now (although many are still being sold) and have been replaced by the much more thorough wide spectrum tests using chip based technology, allowing hundreds of thousands of DNA locations to be tested and evaluated. Of course, the word evaluated is the loose cannon in that sentence, because the quality of the evaluation is key here. And the evaluation is dependent upon accurate and widespread data bases to compare DNA results against to determine which populations have higher and lower frequencies of specific alleles (markers) occurring in their populations.
For example, let’s compare a population in Siberia that shows 100% of a specific marker value, let’s say a value of 10 at marker location ZZZ. Now let’s compare that result to a population from Africa at that same marker location, but with a value never found in Siberia, let’s say a value of 7. Each of thousands of markers are evaluated this way, creating patterns. Now, you have a tester who doesn’t know where their ancestors are from, whose results at marker location ZZZ have a value of 10. Would you say they are more likely to have ancestry in Siberia or Africa?
This participant’s marker results for ZZZ go in the “very strongly Siberia” bucket. Of course, other markers they carry might indicate Africa, or Europe, or elsewhere, because we are a Heinz 57 mix of all of our ancestors. But this is, in essence, how our ethnicity is determined by autosomal DNA testing. Needless to say, you can be a lot more accurate with thousands of markers than with the 15 or 21 CODIS markers, or even the 300+ in some of the proprietary tests.
Using autosomal results to determine ethnicity is called BGA testing, or Biogeographical Ancestry testing. It has been used for years to determine percentages of ethnicity. So, how is what I’m doing different and what makes it unique and new to genetic genealogy?
1. Traditional BGA testing deals in percentages of ethnicity, meaning generally 1% or more. Small amounts are difficult to track in the best of circumstances. When dealing with small amounts of admixture, not all tests will be able to identify the minority ethnicity in question. We’re using these tests, plus additional BGA chromosomal painting tools combined with some spreadsheet comparison techniques to cross that 1% threshold.
2. The prevailing winds in this industry have been that anything smaller than 1% was undetectable, and that any amount of admixture less than 7cM, 5cM or 3.5cM (depending on the source) was usless. While this is relatively accurate (but not always) when determining a genealogical relationship within the past few generations, it’s not true when looking beyond the accepted 6 to 7 generation threshold where the 1% ethnicity issue comes into play. At that point, we know we can’t identify the minority ancestor genealogically, so we have to identify them by their membership in a minority population group. I am using a variety of tools and techniques to reach across that threshold.
3. Instead of using these various tools to try to establish a genealogical relationship with another tester (such as we share a common great-grandfather), I am using these tools to attempt to identify which line or lines carry minority admixture. If you already know who in your family tree contributes that admixture, you don’t need this technique. If you are looking to confirm minority admixture below 1%, searching for the minority admixture contributing line, or trying to figure out which of your known ancestors contributed minority admixture, then this technique is for you.
Typically these tools have been used to track segments from known ancestors, like a Jewish grandmother, for example. These segments are large and evident. That’s not the case with small amounts of minority admixture. Using several BGA tools together helps to eliminate the possibility of one tool picking up on these small segments and another one missing it. We are bringing all of the resources from various camps together to bear on the situation. This is the ultimate form of recycling, using the shreds that were left on the cutting room floor and deemed to be usless when in actuality, they are diamonds in the rough. We’re reassembling them and looking at them from a different perspective. It’s a new kind of quilting!
A New Name
As I’ve worked through this process, it seems that Minority Admixture Mapping best suits what we are doing, so MAP it is. It makes sense and you can say it.
I still want to know who I am, so in Part 4, we begin our data analysis by looking at the autosomal ethnicity results of the various testing companies and how they compare.
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