From the Genetic Genealogist, wishing all my readers a fun and safe summer holiday!Â Don’t forget, family gatherings are a great place to talk about genealogy, or to gather money for a fun and interesting genetic genealogy test!
Two weeks ago, EyeonDNA posted about genetic genealogy testing in the Czech Republic by two companies, Genomac and Forensic DNA Service. A recent article in the Prague Post details the animosity over ethical concerns which exists between these two competitors.
A few days later, Ludvik Urban responded to the article via Rootsweb, and EyeonDNA shared Mr. Urban’s response with her readers. Today, you can read Genomac’s response (from one of the founders, Dr. Marek Minarik) to Mr. Urban’s concerns about the company.
Whew! Luckily, both sides were able to share their side of the story – it makes for some interesting reading!
I have a very lonely surname according to estimates, there are only about 1000 to 2000 Bettingers in the United States. In the 1930 census, the most recent census which is indexed and available to genealogists, there were just 1,300 Bettingers. Therefore, not surprisingly, I was the first Bettinger to experiment with genetic genealogy and had the opportunity to start a Bettinger surname project, which I did. Sadly, however, my project still has just one member. I originally tried to email some potential relatives, but only a few seemed interested, and none decided to take the plunge.
My particular Y-DNA has an interesting story (I think that everyone’s Y-DNA has an interesting story, it’s just that I’ve decided to share mine!). My most distant paternal ancestor came to America in the late 1700’s and had six sons (and 1 daughter who didn’t live long), only 5 of whom passed on their Y-DNA. I am descended from the third son, and I call our line “Branch #3.” For the next three generations of Branch #3, each of my ancestors had two boys, one who passed on Y-DNA to the present, and one that has not. In my grandfather’s generation, he was the only male. He returned to the tradition of having two boys, but only one of those boys (my father) has passed on his Y-DNA. My father, however, decided to buck the trend and have three boys, while I’ve passed on my Y-DNA to my son.
Â Â Â Â Â Â Â Â Â I consider my new friendship with Hsien and other fellow bloggers to be one of the great successes of this blog, and I thank her for the opportunity to share my enthusiasm for genetic genealogy with her readers!
With Friday’s release of a paper in PLoS Genetics, the Genographic Project also released a spreadsheet with the results of over 16,000 mtDNA tests, including HVS-I and SNP results (available here). In addition to sequencing the HVS-I region of mtDNA samples the Project is now testing 22 SNPs. These SNPs were chosen based upon a number of factors, which are discussed in the paper.
“Twenty one SNPs and the 9-bp deletion make up the total of 22 biallelic sites. For simplicity, we will refer to all biallelic sites as SNPs. The number of SNPs tested was gradually increased from ten at inception of the project to the 22 currently used. The ten initial SNPs were 3594, 4580, 5178, 7028, 10400, 10873, 11467, 11719, 12705, and 14766 (numbers refer to the nucleotide position in the mitochondrial genome). The panel was augmented to a total of 20 coding-region SNPs by including the following additional ten SNPs: 4248, 6371, 8994, 10034, 10238, 10550, 12612, 13263, 13368, and 13928. The panel was further augmented by the addition of SNP 2758, to a total of 21 coding-region SNPs and finally by including the 9-bp deletion at position 8280 to a total of 22 coding-region SNPs (Figure 4). Two further changes were made: positions 8994 and 13928 used in some early work were respectively replaced with their phylogenetic equivalents 1243 and 3970. Therefore, the current panel includes the following SNPs, with their respective gene locations shown in brackets : 2758 (16S), 3594 (ND1), 4248 (M), 4580 (ND2), 5178 (ND2), 6371 (COI), 7028 (COI), 8280 (9-bp deletion) (NC7), 8994 (ATPase6), 10034 (G), 10238 (ND3), 10400 (R), 10550 (NDRL), 10873 (ND4), 11467 (ND4), 11719 (ND4), 12612 (ND5), 12705 (ND5), 13263 (ND5), 13368 (ND5), 13928 (ND5), and 14766 (Cytb).”
The Genographic Project is probably the largest genetic genealogy project in the world. For $99, the project will sequence seqments of either your mtDNA or your Y chromosome for addition into their publicly available database. The goal of the project, with ten research centers around the world, is to “map humanity’s genetic journey through the ages,” and to “address anthropological questions on a global scale using genetics as a tool.” There has been a huge response to this project, and they just released their first research paper using the results they have collected to date:
â€œFamily Tree DNA is proud to announce that the first paper resulting from data collected through the Genographic Project has been published today at the PLOS GENETICS.â€œThe Genographic Project Public Participation Mitochondrial DNA Databaseâ€ can be found at http://genetics.plosjournals.org and it will be uploaded to the Family Tree DNA public library as well.
Two fellow genealogists recently nominated me for a “The Thinking Blogger Award.â€My honored thank you to Tim at Genealogy Reviews Online and Randy at Genea-Musings.The rules of this meme are pretty simple:
1.If you get tagged, write a post with links to 5 blogs that make you think;
2.Link to the original post at The Thinking Blog (see above) so that people can easily find the exact origin of the meme, and;
3.Optionally, display the â€œThinking Blogger Awardâ€ graphic.
There is a certain occurrence in genetic genealogy called a Non-Paternal or Non Paternity Event.This is a break in the ancestry of a personâ€™s Y chromosome and surname.A person named â€œSmith,â€ for instance, might have a Y chromosome that is clearly â€œJohnson.â€
A non paternal event can occur when an adopted male takes the surname of his adoptive family, or a male child takes his step-fatherâ€™s surname, or a male child takes his motherâ€™s surname (undoubtedly there are other circumstances as well).
When a break in the Y chromosome is suspected or confirmed, it is possible that the break might have occurred 1,000 years ago, 100 years ago, or with the testeeâ€™s birth.
Two companies recently teamed up to offer their services to families with roots in the African Diaspora.Slave Descendants Freedom Society and Diversity Restoration Solutions are bringing a seminar series to 50 cities in the
â€œThis interactive seminar series is a stepping stone in that it seeks to help African Americans find their self identity, understand the benefits of restoring the core family base, and move forward in leveraging resources as a people,â€ said Sheppard, author of â€œAncestorâ€™s Call,â€ a genealogy and historical accounting of the Grandy family and Moses Grandy, an ancestor whose story was originally told in a rare 1843 slave narrative. â€œItâ€™s important that we lay the foundation for generations coming after us; our children and grandchildren need to know who they are in order to receive their inheritance. This seminar honors the contributions of our ancestors but with an emphasis that this recognition should not occur just during Black History Month, but as a way of life, everyday. Participants will come away with a greater understanding of themselves, an action plan for tracing their family tree and hopefully a stronger appreciation for family and desire to pay it forward in their community.â€A pdf brochure is available.
If you missed Ira Flatow’s interview with Megan Smolenyak on NPR’s Science Friday, you can download the podcast in a number of different formats at NPR.Â The interview is the result of this week’s big announcement that Ancestry.com is teaming up with Sorenson Genomics to offer DNA testing.Â Great job Megan!