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Where Do I Come From: James Shoemaker

Saturday, November 16, 2013

Where Do I Come From: James Shoemaker

Real People's DNA Stories

Bible Studies, DNA Tests, Mother's Nursing-Home Confessions Lead to New Life

NOVEMBER 16, 2013 — Until he took an autosomal ancestry test, James T. Shoemaker had little concept of his heritage. He assumed he was just an average white European American like his Appalachian neighbors.

Although raised in a Pentecostal Church, Shoemaker always felt a strong pull toward Jewish culture. So last year he went to his doctor and asked for a DNA test. "I wanted to see if there were any Jewish lines in my ancestry," he said.

He ended up taking a DNA Fingerprint Plus, a complete analysis of one's genetic ancestry that includes ethnic markers and megapopulation admixture matches.

Fast forward from that first eye-opener and today the 53-year-old Waynesboro, Pa. resident is halfway through a conversion process to Judaism at B'nai Abraham, a Reform congregation in Hagerstown, Md., where he is being mentored by youngish Rabbi Ari Plost.

"I got all three ancestral markers for Jewish I, II and III," Shoemaker recalls, “so I went to see my mother, Jacqueline Rose, at the nursing home in Hagerstown, and she admitted, ‘Well, yeah, my parents, uh, they were both Jewish."

It was the first he had heard of it. “Mom never said a word about having Jewish ancestors. It turned my life around.”

The fact that he got a "double dose" of Jewish alleles in his marker results confirmed the truth of his mother's admission that both she and his father came from Jewish families.

Shoemaker next took a Premium Male DNA Ancestry Test to determine whether his father's Y chromosome line was perhaps Jewish. The results were delivered to him in mid-November.

His particular haplotype did indeed match several other Jewish men, including those with the surnames Brown, Hendrix, Shepard, Getz, Phillips, Lewetag and Sequeira. "The subject’s specific male haplotype (surname line) probably came from Southwest Germany or the Low Lands, to judge from the modal matches and patterns of distribution," according to the report.

As for the surname itself, the Surname History section (included in every Premium Male report, cost $325.00), had some valuable clues for Shoemaker's genealogy.

"Shoemaker is probably a translation of the Dutch or German equivalent Schuhmacher or Shumacher meaning "shoemaker." It is noted as a Jewish family name in Southwest Germany and the Saarland in France, including Lörrach in Baden (Lars Menk, A Dictionary of German Jewish Surnames, Bergenfield: Avotaynu, 2005, pp. 673-74). It could also come from Schuster, a more common Jewish German surname (p. 675)."

A Mason since 1990, and flirting at one time with Messianic Judaism, Shoemaker feels as though his earlier attempts to connect with his Jewish heritage were blind and unguided without the hard testimony of DNA. "All these things I've been interested in with my studies and religious life now fall into place," he said. "I'm finding out why."

What lies in the future? This Pesach, Shoemaker will have an official bar mitzvah, complete with ritual bath and reading from the Torah. He then plans to attend Hebrew Union College in Cincinnati. "What I am really looking forward to," he says, "is making aliyah to the Land of Israel."

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Native Americans Have Deep Ancestry in Europe: Yes, It's Official

Wednesday, October 30, 2013

Shocking, Long Overdue Revision to American Indian Genetics

By Donald N. Yates

The ecstatic waters . . .

Through their ancestral patterns dance.

—William Butler Yeats, "News for the Delphic Oracle"

We've been saying it all along but it looks as though geneticists may be forced by new findings in ancient DNA to admit that early Siberian people and present-day Native Americans both have strong roots in Europe, only secondarily in Asia. The nuclear genetic bomb was dropped by Danish geneticist Eske Willerslev at a conference on "First Americans Archeology," held October 16-19, 2013, at Santa Fe, N.M. The city that gave birth to the original atom bomb hosted a glittering roster of speakers in a venue better known for its turquoise jewelry, fry bread and avante garde art, including big draws Achilli, Adovasio, Dillehay, Gonzalez and Schurr.

The paradigm-shifting conference program will be commemorated with a book Paleoamerican Odyssey ($56) to be published by Texas A&M Press later this year.

Leaked reports in the news media focused on Willerslev's paper, "Genetics as a Means for Understanding Early Peopling of the Americas," which concerned the genetic sequencing of two ancient Siberians' bones discovered in the 1920s and now in the Hermitage Museum in St Petersburg. Analysis of a bone in one of the arms of a boy found near the village of Mal'ta close to Lake Baikal yielded the oldest complete genome of a modern human sequenced to date.

Of the 24,000 year-old skeleton that was Exhibit A, Willerslev was quoted in The Siberian Times, as saying, "His DNA shows close ties to those of today's Native Americans. Yet he apparently descended not from East Asians, but from people who had lived in Europe or western Asia." He added, "The finding suggests that about a third of the ancestry of today's Native Americans can be traced to 'western Eurasia.'"

The 4-year-old boy, who died 24,000 years ago in a homeland previously assumed to account for all the Indians who crossed a theoretical Bering land-bridge and founded the First Americans, had a male Y-chromosomal haplogroup of R1b, the most common lineage in modern Europe, and a female mitochondrial lineage of U, the dominant prototype in pre-historic Europe. As it happens, I am the same combination, R1b for male and U for female, as are innumerable others in our in-house study on Cherokee DNA, published, lo, some five years ago.

Whereas previous "peopling of the Americas" stuff has clung to and recycled haplogroup studies (sex-lines), the new shock research relies on autosomal DNA, total genomic contributions from all ancestral lines, not just male-only, not just female-only descent. The title of a blog from Eurogenes rightly emphasizes this:  "Surprising aDNA [autosomal] results from Paleolithic Siberia (including Y DNA R)."  

When we introduced the 18-Marker Ethnic Panel as an enhancement for our main autosomal product, DNA Fingerprint Plus, lo, again, these five years now and counting, we presented a map of prehistoric human migrations showing without any equivocation that "Native Americans," even as Cavalli-Sforza demonstrated two decades ago, were closer in genetic distance to Europeans than Asians. In fact, we claimed, on the basis of autosomal DNA, that having Native American I or Native American II was a result discrete and separate from East Asian, since Native Americans obtained frequencies of its occurrence as high as 80% and Asians were on the polar opposite of the scale, at the bottom for carrying it. Other methods frequently confused Native American and East Asian to the point of invalidity, particularly those products claiming to arrive at racial or ethnic percentages.

The moral is that autosomal DNA trumps Y chromosome and mitochondrial evidence, and only ancient autosomal DNA can truly explain modern DNA. Even one of the most antipathetic students of American Indian DNA, Theodore G. Schurr, seems to rethinking the rigid definitions that have built careers and won tenure for geneticists and anthropologists for decades. For the fanatics who have been toeing the party line on haplogroup Q, as set down by Schurr's company, Family Tree DNA, and its followers, we note the following statement of recantation or at least qualification, taken from the Santa Fe program:

"Tracing Human Movements across Siberia and into the Americas: New

Insights from Mitochondrial DNA and Y-Chromosome Data."

In this paper, I present genetic data from native Siberian and indigenous

populations of North America that help to address questions

about the process and timing of the peopling of the Americas. These

new genetic data indicate that Eskimoan- and Athapaskan-speaking

populations are genetically distinct from one another, as well as each

to Amerindian groups, and that the formation of these circumarctic

populations was the result of two population expansions that occurred

after the initial expansion of settlement of the Americas. Our high-resolution

analysis of Y chromosome haplogroup Q has also reshaped the

organization of this lineage, making connections between New World

and Old World populations more apparent and demonstrating that

southern Altaians and Native Americans share a recent common ancestor.

The data also make clear that Y-chromosomal diversity among the

first Native Americans was greater than previously recognized. Overall,

these results greatly enhance our understanding of the peopling of

Siberia and the Americas from both mtDNA and Y-chromosome

perspectives.

"Genetic genealogy" has become a fashionable buzzword, but to my knowledge few research studies or blogs and hardly any commercial tests authentically combine the two concepts. According to genealogy, I myself am about one-quarter Choctaw-Cherokee and three-quarters European. But genetics says my mitochondrial line (U2e) is Eurasian, even though I have traced it to a Cherokee woman who married the Indian trader Enoch Jordan about 1790 in north Georgia.  Estimates from other "genetic genealogy" companies for my Native American ancestry, and I've taken them all, range from 0% (23&me) to 8% (Family Tree DNA, AncestryByDNA). 

DNA Consultants, the company I founded in 2003, does not give percentages of ancestry by policy, but half my top matches in our autosomal analysis are Native American, and North Asian/Siberian is No. 1 in my megapopulation result, followed by Central Asian and Native American (and only distantly by Northern European). On an autosomal approach, if not haplogroup basis, my genes are Native American, which is how I self-identify. If I were to be pulled over for being a brown person in the state of Arizona, where I currently reside, and Sheriff Joe ran my DNA profile numbers through the system he would find that I am 15 times more likely to be North Asian than Northern European, and twice as likely to be American Indian than East Asian, European American or Iberian American (Hispanic).

Read the whole analysis of my personal genetics, with actual reports from various companies, in the Cherokee Results pages on the DNA Consultants website. You may also find an extended study showing what autosomal DNA can do at:

Reconstructing Your Ancestry and Parentage (blog post, March 14, 2012)

If and when geneticists get serious about identifying the European sources of the American Indian gene pool, and hopefully they will round up not just one suspect (Denmark?), I would like for those who get paid and promoted to study us to please consider the following points:

—First New Cherokee Data Published in More Than Ten Years (announcement, August 1, 2012) - in-house study described numerous instances of U, findings published in Donald Yates' Old World Roots of the Cherokee.

—Stephen C. Jett, who taught geography at The Ohio State University 1963-1964 and then at the University of California, Davis, serving thrice as Geography chair and becoming emeritus in 2000, current editor of Pre-Columbiana, has frequently pointed out that just because Native American haplogroups match Siberian haplogroups doesn't mean the population of either Native America or Siberia was the same in remote history as today. He considered this a big fallacy of Big Science.

—Constantine Rafinesque, whose History of the American Indians was the first and most comprehensive treatment of the subject, believed all the early settlers of the Americas came "through the Atlantic," and only beginning about 1000 BCE did the Iztacans and Oguzians (Central Asian Turkic peoples) arrive. See our blog:  American Indian and Turkic People Share Deep Ancestry (June 6, 2012).

—Canadian environmentalist Farley Mowat, the author of thirty-seven books, has constantly challenged the conventional knowledge that Vikings were the first Europeans to reach North America. In The Farfarers he describes the Alban people of Old Europe as visitors and colonists from the time when walrus hunters discovered the sea routes to the West before the Bronze Age. America's original name of the White (or Beautiful) Land is mentioned by Rafinesque and in Hindu, Greek, Egyptian, Mesopotamian, Arabic, Algonquian Indian, Irish, Norse and Chinese accounts.  See "An Interview with Farley Mowat" on YouTube.

—Cyclone Covey of Wake Forest University, among other historians, has noted that Clovis Culture appears fully formed without any antecedents in America, with the most perfect examples of Clovis points traced in a cline of occurence in archeological sites to the Atlantic Coast.

—The earliest Americans clearly practiced the same Mother Goddess religion elaborately documented in the east Mediterranean and Old Europe by Marija Gimbutas. Their ideas of matriarchy or gylany (in Riana Eisler's coinage) did not come from Asia. See Archeologist of the Goddess (webpage) and "Syncretism, Not Animism" (PPT), a presentation given at the Sandy, Utah conference, March 29, 2011.

—When customers of DNA Consultants with various degrees of Native American admixture have their European population matches analyzed, a frequent top result is Finland or Finno-Ugric or Uralic. This "false match" could be explained by shared ancestry between the present-day Finns (where U is the modal haplogroup) and ancestors of Native Americans coming from Europe. Consider taking the EURO DNA test ($99).

—John L. Sorenson and Carl L. Johannessen in World Trade and Biological Exchanges before 1492 (2009) document several plants that originated in the Eastern Hemisphere (not Asia) and traveled early by human hand to the Americas. For instance, Cannabis sativa (marijuana) moved from Western Asia or Europe to Peru by 100 CE, and mugwort (Artemisia vulgaris) was brought to Mexico from across the Atlantic Ocean by 1500 BCE. Both grow in profusion in Europe and temperate parts of Central Asia. Goosefoot (an important Ohio Valley Moundbuilder staple), cotton, coconuts, bananas, turmeric and North American myrtle likely took the same route. In the opposite direction, Mexican agave spread to the Mediterranean world by 300 BCE.

Archeologists described the recent news from Santa Fe as jaw-dropping. We expect that when the definitive report on the Siberian boy's 24,000 year-old genome appears in the journal Nature, where it is at press, their hair may fall out. At any rate, the European origins of Indians is going to be a game changer not only in genetics, but anthropology, archeology, government and, perhaps most significantly, in the self-awareness of millions of Americans who count Native Americans among their ancestors.

 
























Our standard world migration map had the story right years ago.


Comments

Don Danielson commented on 30-Oct-2013 05:36 PM

I can add no data, only my applause. There are, truly, more similarities among people than differences.

James Stritzel commented on 11-Nov-2013 03:03 PM

CONGRATULATIONS!! For vindication of what you and DNA Consultants have been in the forefront of for years. Still will be fierce resistance but the light of your leadership is starting to shine and grow in the ‘Official Establishment’.

I remember and still have a book from the early 1990’s “Giving Voice to Bear” by David Rockwell. In it he wrote of the similarity of how Bear is depicted/revered/hunted around the sub-Arctic. Briefly wrote about a circumpolar subarctic culture. That has stuck with me 20+ years.

Here with Eske Willerley’s “….genetic bombshell….” is validation of what must have been pre-Columbian peopling of Americas other than the orthodox version.

Thanks so much for your dedication, determination and achievements in the DNA Field.

Jim Stritzel

Anonymous commented on 14-Nov-2013 09:18 PM

I have a lot of Siberian DNA as well as a lot of Greek and Iranian DNA, but come from Black Sea area/Georgia. But look European. MtDNA is H1b. Mom's dad's Y chromo is R1b. We were supposed to have come from the Caucasus in ancestral times. Lots of redheads in the family. Curious.

Bill Hucks commented on 20-Nov-2013 05:15 PM

This is one of many articles I've read on the Siberian boy. You mention that his Ydna is R1b, however it is not mentioned in any other articles. I'm very curious to know if R1b has indeed, been confirmed. --That was reported in the full version of the scientific paper.


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Autosomal Testing Revalidated

Sunday, September 15, 2013

Autosomal Ancestry Tests: More Confirmation of Their Stability

By Teresa Panther-Yates

How fast does the molecular clock tick? Americans, especially, like most everything fast. We don’t think too much about the word slow. But two scientists have changed our minds about that. As often happens in science, two research teams independently reached the same groundbreaking results. The breakthrough in the present case concerns the mutation rate of DNA and has profound implications for human evolution as well as for autosomal DNA ancestry analysis.

What is the DNA mutation rate? This is the rate at which a genetic marker mutates or changes over time. James X Sun et al in the recent article in Nature Genetics, “A Direct Characterization of Human Mutation Based on Microsatellites,” and A. Kong et al in the recent article, “Rate of de novo Mutations and the Importance of Father’s Age to Disease Risk,” in Nature both made an important, recent discovery. The speed of mutation in DNA is slower and more stable than previously thought. They discovered this how? By the magic of math.

How can math help us discover our ancestry? DNA is stable. Because it is so stable, we can calculate our way all the way back to when we swung in the trees and threw guavas at gorillas. (Even early man was in the trees longer than previously thought according to Charles Choi in his recent article in Science, “Early Human ‘Lucy’ Swung from the Trees.”) And these calculations lead us to the stories of our ancestors.

What does this mean concerning autosomal DNA ancestry tests? They have even more scientific validity. Second-generation DNA ancestry testing is based on these very genetic markers, and that is confirmation that the alleles on your DNA that are examined using a statistical basis have been relatively unchanged for the past 20,000 years. That’s about twice the length of what we call world history, hence a meaningful enough time frame for valid inferences about population patterns and ancestry of individuals.

These common and not-so-common markers that everyone has are behind the method making it possible for anyone to take an autosomal ancestry test. Autosomal or non-sex-linked markers change at a much slower rate than the Y chromosome, for instance, which seems to be highly changeable, depending on the father’s age (Kong 201). The Y chromosome is a marker only males have. It is used for other types of tests: male, haplotype, sex-linked DNA tests. Only males can take these tests, and it only provides information about that one male line.

Who knows what our DNA has yet to tell us? Or what DNA tests there will be in the future. This is an exciting new field. But what you can know now with a true and thorough autosomal DNA test is more than most realize is possible. The DNA Fingerprint Test is a simple test anyone can take that gives you a comprehensive snapshot of your cumulative ancestry.

Above:  Sample laboratory readout of a DNA profile or fingerprint.

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Where Do I Come From: Shawn

Monday, July 22, 2013

Where Do I Come from:  Shawn

Real People's DNA Stories

Ethnicity Beyond European Migration

By Shawn

My journey into DNA testing began with my desire to expand on my known heritage, while clarifying debated Jewish ancestry.  What I have found in return is that my ancestral paper trail only uncovers a small portion of the blood that runs through my veins.  My DNA Consultants results, for the most part were quite surprising.  My European matches were fairly consistent with my country origins on paper and surrounding areas.  The major surprise, however, was that my number one European match was Romani/Gypsy and my number 10 match was Czech Republic.... 

Things became much more interesting with my World Population Matches.  My scores (in order) were Romani/Gypsy, Middle Eastern, African, Iberian, Central European, African-American, Jewish, Mediterranean European, European American and Eastern European.  I also came up with Native American admixture to top it off.  These results are causing me to believe that there may be a line or more of family lineages that I have yet to tap into. 

Looking back on things now, I have received comments from others concerning my phenotype such as "I'm not sure what you are,” "You don't look Irish" and "You must have some Black ancestry."  Some have even just assumed I was Hispanic or Caucasian.  Interestingly enough, almost all acknowledge that they see my Italian/Spanish phenotype, while a few also see slight Native American.   

While my results provided insight into how diverse my blood really is, they also put an end to an age-old family debate as to our Jewish ethnicity.  One of my relatives from a few generations past would passionately defend her position that our family line was indeed Jewish, while another family member would vigorously put forth his position that we were not Jewish.  He would try to prove our non-Jewishness any time he could.  I also had another family member along that same family line say that he almost did not get hired for a job because the hirer thought he was Jewish.  I always believed these accounts, especially since as young as I can remember I have found this side of my family (Italian and German) to phenotypically look Italian and/or Jewish.  

So where does all this leave me now?  My results show my blood is much more than simply Italian, French, Irish and German.  They confirm family testimony of Spanish/Portuguese/Iberian and Jewish ancestry.  Perhaps more interestingly, my results leave me re-assessing my ethnicity or multi-ethnic heritage, end years of family verbal passages or debates and leave me with intriguing new ancestries that are waiting to be discovered. 

Comments

Maria OConnor commented on 23-Jul-2013 12:42 AM

Shawn: Countries frontiers are artificial. For example, there are people of celtic heritage in northern Spain, northern Portugal, all over Ireland, all over England, all over Scotland, all over Wales, Southern Germany, northern France, Northern Italy, etc. All of them, even considering the come from different places have the same celtic DNA. So, if you have an ancestor from Spain or Portugal, could be of celtic origen, or mediterranean origen.
If a person has jewish sefardi dna, it could be originated from Southern Spain, Southern Portugal, North Africa, Middle East, etc.
Also, in South America there are great numbers of people of European ancestry, including non hispanic non portugue ancestry, like Irish, German, Italians, etc.
Is quite complicated, due to ancient and new migrations.


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Where Do I Come From: Monica Sanowar

Friday, July 12, 2013

Where Do I Come From

Real People's DNA Stories

A Red-Hot Tale from the Nation's Capital

By Monica R. Sanowar

  

I took my first test with Family Tree in 2006. This test showed my mtDNA as L3e2b2 and it went like this:

52% West African

39% European

9% EAST ASIAN

0% Native American

I could not believe the East Asian part, and I shrugged it off and thought—that has to be Native American.

So, fast forward—I took another test with Ancestry.com. This was autosomal and showed:

48% - West African

44% - European

8% - UNKNOWN

How can you be UNKNOWN?

Neither of these tests really breaks down what country your people may have originated from. So then I tried 23&me, their autosomal offering.

49% - West African

48.3% European - Central - Northern - Non-specific

and the leftovers were .7 EAST ASIAN & NATIVE (although the NA box did not turn red)

and 1.4% UNSPECIFIED

I knew from family history that NA was on both sides of my fence. I also was aware that I had four of the traits Melungeon people have. I have the ridge in the back of my head that you can lay your finger in; I have ridges on the teeth and I can make the clicking sound on the shovel teeth; I have the Asian eyefold, and the very high arches. Can't get my foot inside of a boot and if I do, I can't get it off.  I was amazed that I got my results in less than two weeks!

Finally, I tried DNA Consultants. Its test was the very first that didn't show "UNKNOWN" or non-specific. Everything was accounted for, although I did find a few shocks. No one told me about Sephardic Jews or the Portuguese. At last, a test verified my Native roots with valid matches to tribes or nations and confirmed Native American autosomal markers—from both parents, as I had been told.

I got into Native culture back in 1983 when I started to go to powwows. I finally felt at home. I enjoyed seeing people that looked like me, mixed. My great-great-great grandmother was listed on the FREE NEGRO LIST where it asked How Freed? And it was written BORN FREE. Then came a description— a light-skinned black, with long straight black hair and a small scar on her hand. Below is a picture of her daughter, Alethea Preston Pinn. Alethea's father was a white man named Allen Preston. Alethea had seven children with James E. Colvin, who was white, and all

of their children were put on Walter Plecker's list of "mongrels" not allowed to vote or go to school. That was 1943. Not that long ago.

So, I got a second cousin to take the test with 23&me who comes directly from

Sarah Pinn (the alleged light-skinned black woman). My cousin's haplogroup came in A2N - Native American.

I know that some things may show and some not, but DNA Consultants' test knocked the EAST ASIAN right off the page. I've learned a lot of different things with DNA testing, but DNA Consultants' is the best one I have seen and is well worth the money. 

I love it when these geneticists and genealogists out there decide what you do or do not have in your family tree, especially the Indian part of the tree.  As if this just could not have happened . . . .  I am proud of all of it.  I can just about hang up a flag from everywhere.   

I can't praise the DNA Fingerprint Plus enough and wish I'd known about it years ago. I really appreciate all of the knowledge and insight Dr. Yates has about genealogy and history that I was totally unaware of. I actually spoke to him on the phone at length and he truly made my day. I highly recommend DNA Consultants' service to people who are looking for the truth about their genealogy.

And speaking of spicy mixtures, check out my hot sauces at Sun Pony. They've got secret, all-natural ingredients just like the family!

Alethea Preston Pinn, my great-great-grandmother on my paternal side.

My mother, Mary Wood.

My great-aunt Lenora Wood.

 

Elizabeth Colvin, a granddaughter of Alethea Preston Pinn. "Contrary to the belief and convictions of many people, long hair really does exist in my family," says Monica Sanowar. "It isn't a made-up fantasy and this was long before hairweaves.  My cousin's hair was down to her calves." 

Guest blog author Monica Sanowar is the founder of Sun Pony Distributors Inc., makers of a line of all-natural, wholesome condiments and energy supplements found in stores up and down the East Coast. Her first hot sauce was Yellow Thunder and her Native name is Sundancer. SunPony's D.C. Redbone Hot Sauce is the official hot sauce of the Anacostia Indians, D.C.'s little known indigenous people, who were first recorded by Capt. John Smith in 1608.  Sanowar lives in Washington, D.C., not far from the Anacostia's village site, now a national historical landmark. Watch grassdancer Rusty Gillette in a video about D.C. Redbone. 
Comments

Phyllis Starnes commented on 12-Jul-2013 04:42 PM

Monica Sanowar,

I had the pleasure of analyzing your personal DNA profile and preparing your report.

I am pleased that our detailed report validated your known ancestry.

Thank you for sharing your experience with DNA Consultants.

Phyllis Starnes
Assistant Investigator
DNA Consultants


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DNA Frontiersman: Jim Bentley

Saturday, January 26, 2013

Behind the Numbers:  Jim Bentley


Jim Bentley, DNA Frontiersman

 

(Part Three of a Series)

We interviewed  one of Chromosomal Labs Bode Technology’s senior staff members, Director of Sales and Marketing Jim Bentley, to get his perspective on industry changes over the past thirty-five-plus years.

 

 

Jim Bentley.

 

 

When did you first get interested in DNA?

JB: I’ll have to preface my answer with a few remarks on “the early days.” When I graduated from Arizona State University in the 1970s, DNA testing as we know it, was not really a field that was in existence. There was not a lot going on. The little work I did with chromosomes was using electron microscopy. I worked in the biochemistry department, however and performed hundreds of assays using poly-acrylamide gel electrophoresis, mainly for separation of proteins. This technique, although improved and streamlined remains in use today for DNA-STR separation. The field we’re in today where we can determine a person’s profile and compare it with others for forensics  for relationships, ancestry, missing persons, adoptions and the like, that technology hadn’t been developed yet. It wasn’t quite as easy as it is today.

Tell us more about the evolution of DNA testing.

 

JB: It basically began with blood groups and types. The first paternity test was done in a court case with Charlie Chaplin in the 1940s. He was excluded as the father, but the court said he could go ahead and pay child support anyway—probably, because he could afford it. Since that time, scientists started moving past groups and types into some other techniques. Human Leukocyte Testing (HLA), DQ-Alpha, and Restriction Enzyme STR testing (RFLP) are examples of the evolution of DNA testing.

The big breakthrough came when Dr. Alec Jeffreys at the University of Leicester discovered STR testing in England the late 1980s. He used STR profiling on the Colin Pitchfork case. Colin Pitchfork became the first criminal convicted on the basis of DNA evidence and as a result of a mass DNA screening operation. He was charged with raping and murdering two teenage girls. Since that time the forensic community has really refined the techniques to perform STR testing. They’ve made it simpler and more accurate. It’s really moved exponentially in the last twenty years. Today competent biologists and chemists can produce excellent results, every time.  Dr. Jeffreys has been knighted for his contributions.

So what got you involved?

JB:  I came out of college as a chemist, one interested in the medical field. I started out working in clinical chemistry and toxicology. The work we did with DNA was extremely limited and very costly. But I did stick with a career in clinical chemistry. Within four years after graduating from school I was managing a clinical laboratory in Houston, Texas called National Health Laboratories. It was a laboratory of about one hundred scientists and support staff. After mergers, acquisitions and such, that company remains as Lab Corp. (It performs more than 1 million tests on more than 370,000 specimens each day.)

What opportunities for professional growth did you have over the years?

JB: Through taking a lot of continuing education coursework, I became proficient and qualified as a general supervisor in clinical chemistry, toxicology, hematology, parasitology, microbiology, serology—everything except for tissue work like histology and cytology, which was done by certified medical experts in those specialties. My interests kept me in touch with the staff pathologists, however, as well as all the rest of the laboratory. Though my present-day field did not exist at the time I graduated, by staying current I was able to benefit from the changes and be part of an emerging valuable service provided not only to the medical community but also to the forensic one, and the general population at large.

 

What are some famous cases you’ve been involved with . . . that you can talk about?

 

JB:  Actually, that’s my problem. We’ve been involved in a number of high-profile cases, but we’re not allowed to talk about any of them. Most have been on the forensic side, serial killer trials in Arizona, also in California, some that made the news in Florida . . Texas . . .Georgia.

Were you involved in catching the Grim Sleeper?

JB:  Actually, that’s an ongoing case in Los Angeles we are familiar with, but we didn’t do the work on it, so we can talk about that one. The importance of the Grim Sleeper case has to do with familial testing and autosomal DNA. It was termed the Grim Sleeper case because there were a number of homicides that took place beginning in the mid-1980s, all with the same basic MO [modus operandi], and then the murderer went underground for fourteen years. The victims were typically prostitutes shot with a firearm. In 2010, a suspect, Lonnie David Franklin Jr., 57, was arrested and charged with multiple counts of murder. He has not yet been convicted, nor the evidence against him tested in court.

How was DNA used to catch him?

 

JB: So here were a number of cold cases, but they were being tracked, and the law enforcement authorities in Los Angeles continued to monitor progress. The sole survivor of one of the Grim Sleeper’s attacks furnished a description of him as a black man in his 30s, along with other details. According to her story in the press, he lured her into an orange Ford Pinto, shot her in the chest with a pistol, took Polaroid’s and raped her, leaving her for dead. In 2008, the body count was thirteen, and a $500,000 reward was put out for “America’s Most Wanted.”

It became the first use in California, and one of the first three cases in the United States, of the use of familial DNA searching, that is, using the FBI’s CODIS database to match one family member’s profile with a suspect’s profile. The LA police were able to provide a close partial match to  Franklin’s crime scene profile with that of his son, whose CODIS markers were on file for a minor crime. They then set up a kind of mini-sting operation at a pizza parlor in Buena Park, where they knew the family liked to eat. Undercover detectives masqueraded as waiters and busboys. When the family left, they whisked away an unfinished pizza slice. The crust yielded DNA which police linked on a more solid basis to Lonnie Franklin. It was the first high-profile case in which a family member’s DNA had been used to catch a criminal. The ACLU and others had been critical of familial searching on grounds of privacy, and there is still a lot of debate over familiar searching because it might open up the search and include those who hadn’t committed any crime.

Did this help produce new commercial products like the “cousin finders”?

 

Only a few states are doing familial searching, and they are pretty guarded about it. It’s hard for me to make a connection. Certainly, these developments have been concentrated in the past three or four years, but the use of this technique is spreading.

Are people legitimately suspicious about DNA databases?

 

JB: Fears surface from time to time. There have been claims that keep popping up that someone’s going to take everything that’s in the database and use it to determine genetic deficiencies that could lead to medical issues down the road. Once it was speculated that if such  information was released, insurance companies would begin denying people coverage based on their profiles.

This is the mother of conspiracy theories, isn’t it?

 

JB:  It really is. For the most part—not for everyone—the vast majority of the markers we are using are in the “junk DNA” area. That is, they don’t by themselves “do” anything or give you genetic information on the face of things. There may be one or two markers that possibly could be construed as yielding some medical information—such as a trisomy at vWA or TPOX [a CODIS locus]. But by and large, you are not going to be able to do any medical diagnostics with the markers we run. Usually trisomies such as Down’s syndrome would be physically expressed and not hidden. It’s a little different with SNP panels [single nucleotide polymorphisms] such as those run by 23&me. With a high number of those, it’s entirely possible to predict medical predisposition. That’s what they base their business on.

Let’s talk some more about the CODIS database.

JB:  It’s important to realize that even law enforcement doesn’t provide much access to the CODIS [Combined DNA Identification System] databank. That’s something I have to give the FBI credit for. They have developed a system that is secure. It’s the DNA administrator at each facility who has undergone FBI training and uploads the data under very strict rules, and they are notified of any “hits” that involve them, but otherwise there is very little access, and the use of the database is very even across the country. There are not a large number of portals that can be used to access the CODIS database. There are several hundred law enforcement laboratories that are running profiles across the country, and the database is best thought about on three different levels:  LDIS, SDIS and NDIS, local, state and national versions. Between our labs in Phoenix and Virginia, we’ve tested over a million profiles for entry into CODIS. That’s about one-tenth of the entire number. I can tell you there is tight security. Hundreds of thousands of investigations have been aided by a DNA hit (we don’t like to say “match” so much, because statistically nothing is 100%) generating a lead.

How did you get bitten by the genealogy bug?

JB: I’ve always been fascinated with ancestry. I think it came about because my father took an interest in discovering our family’s roots and had to do so at the time by traveling to Salt Lake City, Utah, and poring over whatever records he could find there about our fathers, and great-grandfathers, and great-great-grandfathers, and so forth. He had tintypes of some of the relatives. We had various pieces of the puzzle. My father pretty much consolidated everything back to William Bentley, who settled in Rhode Island in the early 1700s and had come from Bedfordshire, England. He put together a book for family use. He glorified a few of them and left a few out that weren’t ready for glorification. For the sensitivity of some of the relatives, he left a few details out, but it was a pretty solid piece of work. For me, it kind of fostered this interest in ancestry and its importance. Certainly, when I started at Chromosomal Labs • Bode Technology, we started looking at the various tools that could be used. Our history, to be sure, is passed down from generation to generation. Initially, we were using mitochondrial DNA, Y-SNP’s and Y-STRs and then autosomal STRs to determine how we’re connected to general and specific individuals back to the Revolutionary War days and how you are linked with the world population, what your roots were. I have a particular Y haplogroup of G2a, which is not one of the more common ones.

Hmm . . . you and Joseph Stalin.

JB:  [Laughs]. Is that what his haplogroup was? Uh-oh! He was one of the worst. Well, I got interested in G2a and hooked up with about 50 other Bentleys and we identified our founder  patriarch haplotype. I get emails from them on a regular basis. The other thing we tried to find out was what in the world were all these G2a’s doing in England. I don’t know. But one of the things I find in the literature most often was that the Sarmatians were horsemen that gave the Romans a pretty rough time. Eventually, they were decimated. The Romans took their remaining cavalry and pressed them into service for 12 to 13 years or longer. Some were dispatched to Hadrian’s Wall. Now do I know for a hundred percent certainty that’s where I came from? No, but its fun to regard that as a hypothetical personal history.

You have a Scythian gene, don’t you?

 

JB:  Yes, I do according to the analysis DNA Consultants did for my autosomal ancestry. The work Dr. Yates has done on the rare alleles supports a lot of the stuff the family has been putting together for years and years.  I was very pleased to get my Rare Genes from History report back showing I had the Scythian gene. That seems to go along with the Sarmatian theory about the Bentleys.

How do you see the industry changing over the next few years?

 

JB:  I can speak best about changes I am seeing in the field. They’re getting closer to having rapid DNA testing on a chip. This gives flexibility to those who want to use DNA as “point of use” testing. The FBI this past year came out at the Promega conference and said that within the next two years they would like to see wide adoption of “point of use” testing. The IntegenX prototype allows you to put your swab into a cartridge, insert it into the instrument on the fly and get your STR results in a few hours. Previously, Rapid DNA testing was not only time-consuming and lab-bound but it was very expensive. It cost several hundred dollars in reagents alone. As the technology improves to allow 2 hour testing in our lab or on a chip, reagent and personnel time continue to drop,  Now, the FBI would like to see point of use testing in every booking station in the country. At the last show, I also saw an instrument from Illumina that would run Y-STRs, mtDNA and autosomal DNA profiles simultaneously on one sample. Another change that is coming is we will see an expanded profile becoming the standard, perhaps something similar to the GlobalFiler kit from Life Technologies with its 24 loci. With the new technology you can increase the speed for amplifying the specimen by five times and achieve nine times the discriminating power or resolution.

Any final remarks?

 

JB: The DNA testing field is on the threshold of even greater accolades of appreciation both from the scientific community and the public. If DNA wasn’t even in anyone’s mind twenty years ago, soon it will be part of everyone’s daily lives.

 
























Sir Alec Jeffreys, inventor of DNA fingerprinting, and Jim Bentley at forensics meeting.




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Elizabeth Hirschman, Modern Pioneer

Friday, December 07, 2012
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Behind the Numbers:  Elizabeth Hirschman

  (Part Two of a Series)

We interviewed Rutgers marketing professor Elizabeth Caldwell Hirschman, author of several books and articles incorporating DNA in her research, to hear her personal story in our continuing series about the people behind the scenes in the field of DNA testing.

 

Elizabeth Hirschman with MBA students at Rutgers in December 2009.


When did you first get interested in DNA?

ECH: I got interested in DNA testing around 2000 when I discovered I was Melungeon after reading Brent Kennedy's 1994 book. Brent suggested several different ancestries that possibly contributed to the Melungeon population and I wanted to find out which of these were correct and which ones I had. I already suspected Jewish ancestry because of the naming patterns in my family over the past 300 years, as well as some of their habits --e.g., not eating pork, getting married in a home instead of a church, cleaning house on Friday afternoon, no eggs with blood spots, washing all meat, etc. We also had some genetic anomalies -- shovel teeth (sinodonty), palatal tori and large rear cranial extensions, as well as polydactylism.

Tell us more.

 

ECH:  Over the course of the past decade I have been found to have Native American, Spanish, Ashkenazi Jewish, African, Mediterranean and Gypsy/Northwestern India ancestry. My Dad turned out to have substantial Gypsy and African ancestry. He and I share a large cranial rear extension that I believe likely comes from the African ancestry -- the photos I have seen of the !Kung Bushmen look just like our head shapes. My Mom has Native American and/or Sino-Siberian ancestry. She also possessed the Asian teeth and palatal tori found in this group.

You've written several books and articles with Donald Yates; how did that come about?

ECH:  We shared ancestry from the Coopers, a prominent pioneer family in Daniel Boone’s time. In 2000, I wrote him out of the blue when he was a professor in Georgia and introduced myself and asked if possibly the Coopers were Jewish. We began to correspond by email. I told him I was sure one of the reasons I was working so hard to figure out the Melungeon story was because I had to figure out who I am. “Up until last year,”  I remember telling him, “I thought I was Scotch-Irish, English , white and Presbyterian.” It was a big transition to Sephardic, brown and Jewish. It turned out that we were distant cousins and had numerous links in our Melungeon ancestry.

What was a typical publication?

ECH: One article was called “Suddenly Melungeon! Reconstructing Consumer Identity Across the Color Line.” This was published by Routledge in 2007 in a handbook on consumer culture theory edited by Russell Belk.  

 

How did the Jewish findings play out?

 

ECH:  On a personal level, both Don and I, as well as his wife Teresa, returned to Judaism, he and Teresa in Savannah and I in New Jersey. On a professional level, we started the Melungeon Surname DNA Project, which focused on Scottish clan and Melungeon surnames (i.e., male or Y chromosome lines), and later included Native American mitochondrial DNA.  Initially, many people in the genetic genealogy community were frustrated that the incoming Jewish DNA results were not originating in the Middle East, as they had strongly believed and hoped, but were showing a lot of Khazar, Central Asian, Eastern European and Western European/Spanish/French input.

Can you elaborate?

ECH:  Critics were not happy that DNA was proving a wider and more inclusive picture of the Jewish people. Where Don and I have performed a service, I believe, is by just following the DNA trail and accepting new findings (e.g., the Gypsy/Roma) when they come in, instead of clinging to an a priori theory/belief/wish, for instance, the claim of a Middle Eastern origin for the majority of Jews.

What tests have you ordered from DNA Consultants?

 

ECH: I ordered every test as they became available over the years, first the Y chromosome and mitochondrial or male-line and female-line tests and later the autosomal or DNA fingerprint tests that analyze your total ancestry.  I helped organize the first autosomal Melungeon study by contributing samples from my mother and brother and obtaining samples from well-known Melungeons like Brent Kennedy and his brother Richard. Increasingly, our testing took on the aspect of a family group study. For instance, I was able by comparing multiple results from relatives to reconstruct my father’s ancestry quite satisfactorily, even though he died many years ago. I took the Rare Genes from History for all available family members. There is a streak of the Thuya Gene and First Peoples Gene in all of us, as well as the Sinti Gene (which is Gypsy), while my brother Dick got our father’s Khoisan Gene, which is African. Incidentally, it has the same source as the !Kung people and head shape I mentioned before.

If you had H. G. Wells' time machine where would you go?

 

ECH: I would love to be able to visit my ancestors and see what they looked like, where they lived, how they lived and learn how they got to Appalachia from such disparate parts of the world. I wish I could talk with them. My project now is to visit all the places they are known to have come from and see what the architecture, climate, food, and people are like. That is about as close to "meeting" them as I will be able to get. So far, I’ve traveled to Scotland, Ireland, Wales, England, Spain, Tunisia and Morocco on the trail of my Sephardic Jewish ancestors. I am trying to get to the Silk Road to see Central Asia, Turkey and Northwest India in the near future.

Professor Hirschman has published over 200 journal articles and academic papers in marketing, consumer behavior, sociology, psychology and semiotics. She is past President of the Association for Consumer Research and American Marketing Association-Academic Division. Professor Hirschman was named one of the Most Cited Researchers in Economics and Business by the Institute for Scientific Information in 2009; this recognition is given to the top .5% of scholars in a given field.  


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Behind the Numbers: Phyllis Starnes

Tuesday, November 20, 2012

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Phyllis Starnes:  Designer Genes


We interviewed Phyllis E. Starnes, assistant investigator, to find out what fascinates her about the field of DNA testing. Her story is the first in a series titled "Behind the Numbers" about the workers behind the scenes in our industry, from lab technicians to statisticians.

 

Interviewer:  How did you first get interested in DNA?

PES:  I went to the Melungeon Union in Kingsport [Tennessee, in 2002]. Beth Hirschman had her “stalk,” a diagram of her Melungeon family tree with all the names in her genealogy, many of which were also my surnames. I heard Dr. Yates speak at that meeting. They had their lines all pinpointed, thanks to DNA studies.

Interviewer:  What was your next step after that?

PES:  I came home and did a lot of genealogy research on the computer.

Interviewer: And then?

PES:  The first year DNA Consultants opened for business, which was 10 years ago, I ordered a Y chromosome test for my husband Billy. Other companies were offering the same product, but DNA Consultants was the only one to give you a full analysis and customized explanation of things. Then I ordered my own mitochondrial DNA test.

Interviewer:  Any surprises?

PES:  Billy’s top matches for his male line, the Starnes surname line, were Macedonia and Albania. My mitochondrial mutations matched Native Americans. I became the first of the “Anomalous Cherokees” whose female lineages didn’t fit in the traditional scheme of “Indians out of Asia.” In fact, my Hypervariable Region 2 mutations matched only one other sample in the world, and that was Dr. Yates, who is Cherokee in his direct female line.

Interviewer:  What did your husband and the rest of your family think?

PES:  Some were excited, as I was, but most were just not interested. My kids thought the strong Native American matches were very interesting.

Interviewer:  What other family members did you test?

PES:  As soon as autosomal testing arrived, with the DNA Fingerprint Test, I did Billy and myself, of course, Julia, Kiely and Holli (our three daughters), our granddaughter Keely, my Dad’s sister and Mother’s sister, an uncle and his wife, a niece and a cousin.

Interviewer:  What did you find out?

PES:  Within the immediate family, it was obvious who got which ancestry and trait from whom, and how they all resonated. One of the big surprises was my father’s side, which proved to have quite a bit of Native American and Iberian. The “First Peoples” gene came from his side and passed on down through our girls. On my mother’s side, 11 out of 20 matches was India.

Interviewer:   India!?

PES:  Yes, it appears we were finally seeing the extensive Romani/Gypsy heritage in her family. People had always told me I was like a Gypsy, from my clothes and jewelry to my attitude and outlook. When Billy was in the Navy, I told him one day, ‘I’m tired of being a Gypsy.’ I said I wanted to settle down in one place.

Interviewer:  Did you settle down?

PES:  Yes, we’ve lived in a small town in East Tennessee for almost 40 years. We moved here in 1973.

Interviewer:  Any other surprises in your DNA?

PES:  If you were to chart our geographical matches, both in terms of autosomal DNA as well as the female and male lines, it would surround the Mediterranean. That’s where Familial Mediterranean Fever comes in.

Interviewer:  Who has FMF in your family?

PES:  Billy, myself, Julia, Holli and a cousin. I’m sure others have it but it has not been diagnosed and they may call it instead fibromyalgia. Brent Kennedy [author of a book on Melungeons and their genetics] is a cousin many times over.

Interviewer:  What do you enjoy about your job?

PES:  It’s like a holiday every day. With customers coming out of North Carolina or East Tennessee, I see a lot of the same matches and genealogy I have personally encountered in my own experience with DNA testing. I recognize a lot of genetic cousins.

Interviewer:  When did you first hear the word “Melungeon”?

PES:  I grew up in Southwest Virginia in the little town where the Stony Creek Church is located. The church minutes contain the first written instance of the word. The register is all of mine and Billy’s ancestors, and part of Beth’s [Elizabeth Hirschman, author of books on Melungeons].

Interviewer:  What do you see in the future of DNA testing?

PES:  I think we’ve only glimpsed the tip of the iceberg so far, even though it’s been 10 years. We’ll continue to have new knowledge, new products. I highly recommend our customized approach.

Interviewer:  Any parting shots?

PES:  I’ve worked in sales all my life—jewelry management and design, my own interior decorating shop, running my own hair salon—but I have found something to be truly excited about in DNA. Funny I couldn’t get this excited about selling diamonds! If you think about it, your genes are the ultimate design for living.



Donald Yates and Elizabeth Hirschman speaking at Fourth Melungeon Union, Kingsport, Tenn., in June 2002. Hirschman, a professor at Rutgers University, went on to publish Melungeons: The Last Lost Tribe in America. Yates, a professor at Georgia Southern University at the time, founded a service for evaluating DNA reports that became DNA Consultants. The two authors have collaborated on a number of books and articles, including Jews and Muslims in British Colonial America. 












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Rare Genes from Ancient DNA

Wednesday, October 17, 2012
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Authentic sequences from the ancient human past are a rarity in the world of DNA testing. But when a team of archeologists put the mummies of King Tut and his immediate family on the operating table in 2010, they were successful in deriving almost complete DNA profiles for the boy king and others in the Amarna dynasty that ruled Egypt more than three thousand years ago. Now three of the DNA signatures of Egyptian pharoahs from that famous forensic study by Zahi Hawass and the Supreme Council of Antiquities in Cairo--plus others newly discovered--are available as part of a commercial direct-to-the-consumer autosomal DNA testing panel.

In October 2012, DNA Consultants launched its Rare Genes from History Report. Based on a customer's DNA fingerprint or autosomal profile, the additional analysis sells for $289. It compares your laboratory results with 26 rare alleles or ancestry markers whose trail has been traced through world history and evolving population changes by the company's statisticians. 

Take the Thuya Gene, for instance. Like most of the other Rare Genes from History, it has an African origin in deep time. But it experienced its greatest expansion in ancient Egypt, where it was carried by the queens of Upper and Lower Egypt and High Priestesses of the temples. It was reported in the profile of Queen Thuya's mummy, and we can see that she passed it to her children, grandchildren and descendants. King Tut was a great-grandson and has it, according to the new forensic evidence.

Today, as many as one-fourth of all people on earth would test positive for the Thuya Gene. It is twice as common in Somalia as outside Africa and is found in 40% of Muslim Egyptians.

That's not so rare after all, but unsurprising. Egyptian civilization lasted for three thousand years and sowed the seed of its peoples and ideas throughout the world. We can imagine that Autosomal Thuya started out in East Africa about 100,000 years ago, and that her descendants were prominent in the first out-of-Africa group as well as in the Middle Easterners who helped spread agriculture, animal husbandry, religion and settled town life to Europe. 

The spirit of Thuya lives on in 27% of Jews who have been tested in academic studies. Extrapolating to world population figures, that's nearly 400,000 people, about evenly divided between the United States and Israel.

See also "Prelaunch of New Autosomal Products" (August 26, 2012)
"Rare Genes from History" (webpage)
"Rare Genes from History Panel Now Available for $289.00"

The classic DNA study by the Supreme Council of Antiquities in Cairo, Egypt is: Hawass Z, Gad YZ, Ismail S, et al. Ancestry and Pathology in King Tutankhamun's Family. JAMA. 2010;303(7):638-647. The feat by scientists has also been featured on Discovery Channel

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What is a Megapopulation?

Monday, April 09, 2012

The dictionary defines "megapopulation" as a very large one, from the Greek suffix mega, the same element as in "megabyte." In statistics, a population is the whole field from which you choose a sample or representative segment. Thus, to test American Hispanic/Latinos you might draw a sample of 400 people from a predefined population of everyone with a Hispanic surname in a telephone book.

How reliable and valid your sample is depends on methodology. By combining populations you can study a metapopulation (all related populations, for instance North and South American Latin or Iberian populations) or megapopulation (all populations with Iberian ancestry in the world).

Going from the small to the large, we  have then:

Individual

Sample
Population
Metapopulation
Megapopulation
Universe

In a census, the sample and population coincide; everyone is counted.

In population statistics, this hierarchy might look like this:

John Doe
Arizona Hispanic study (n=104, that is 104 persons in the sample)
U.S. Hispanics
North American Hispanic
Iberian American
Iberian or Part-Iberians in the World

At DNA Consultants, megapopulations are the broadest ethnic category calculated and reported to you. (We look at metapopulations, too, but only as a control measure.) Our database coverage is described below.

Megapopulation Names

and number of populations included

 

African 17

African American 28

American Indian 24

Australoid 3

Austronesian 6

Central Asian 39

Central European 13

East Asian 39

East European 8

European American 24

Iberian 32

Iberian American 61

Jewish 3

Mediterranean European 20

Melungeon 1

Middle Eastern 36

North Asian 3

Northern European 15

Romani 4

South Asian 35

Southeast Asian 12

 

 

Beyond Megapopulations (and percentage of total populations) These categories correspond roughly to what people used to think of as "race," a now-discredited notion. They are continent-specific, with African and Caucasian extended to North and South American African and European populations.

 

African   45     11%  

 

Amerind   24    6%

 

Austral 9    2%

 

Asian  67    17%

 

Caucasian  255    64%

 

 

 

Another Calculation We created these totals to see what kind of white versus non-white coverage the database has.

 

White  255  64%

Non-White  145   36%

Total 400 Populations

And that's all you need to know about megapopulations! But in case you're still confused here are some useful links:

Metapopulation in Wikipedia

Autosomal DNA Based Populations in atDNA 4.0 (DNA Consultants)
405 Populations with links to further information in many cases

What Everyone Always Wanted: Our New Megapopulations Report

30-Nov-2011
After a lot of hard work, DNA Consultants has introduced "bottom l... (more)

New Megapopulations: The Bottom Line
17-Nov-2011
Work by our head of statistics over the summer has made it possible to... (more)

Population Pages Are Coming!
09-Apr-2012
Have you ever wanted to know more about the populations you match? May... (more)



Comments

Charlene commented on 13-Apr-2012 01:03 PM

Glad to see the DNA Newsletter is still coming out. Have been missing it and looking for it to appear. Always some interesting things in it. Was pleased with the items I ordered from you a few months ago. Many thanks. Charlene

Arcpoint Labs of Overland Park commented on 16-Apr-2012 03:12 PM

Great site! Bookmarking it now!


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