Louis Kessler’s Behold Blog The Behold User Forum
Entries, Comments and Posts
272.
My Whole Genome Sequencing. The VCF File - Blog comment by teepean - 19 Mar 2019
vanlaargen: Could you share your adjusted 23andMe_V3_hg19_ref.tab.gz, please?
273.
Small Segment Matches - Blog entry by lkessler - 19 Mar 2019
Blaine Bettinger posted a poll on his Genetic Genealogy Tips and Techniques Facebook group about 7 hours ago. It is a closed group, but if you are a member you can see the poll here. In four hours, the poll got almost 800 responses and over 350 comments. Blaine asked people to go to GEDmatch Genesis and ...
274.
Inferred Segment Matches - Blog comment by jbissett - 7 Mar 2019
Well Louis, you've apparently done it again. I've been surprised that DMT doesn't get the notoriety it deserves. I look forward to version 3.0. Joe
275.
Inferred Segment Matches - Blog entry by lkessler - 7 Mar 2019
When we match our DNA to other people to find common ancestors, we are comparing segments of DNA that match the other people. That’s only logical, isn’t it. Well, interestingly enough, there’s a technique that will help you determine which ancestors your DNA comes from by using non-matches. Actually, you ...
276.
MyHeritage New AutoClustering Feature is now Live - Blog entry by lkessler - 1 Mar 2019
Another new feature announced during #RootsTech is the MyHeritage DNA integration of Evert-Jan Blom’s AutoClustering method. MyHeritage has become the first major DNA service to offer clustering. MyHeritage’s blog post Introducing AutoClusters for DNA Matches was posted yesterday and describes their new ...
277.
DNA meets Trees at AncestryDNA and MyHeritage DNA - Blog entry by lkessler - 27 Feb 2019
Today’s the first day of #RootsTech. This is the day that many of the genealogy companies announce new features on their site. So it is not ironic at all that today, both AncestryDNA and MyHeritage DNA announced a new feature that matches up your tree with the trees of your DNA matches and shows you the ...
278.
My Whole Genome Sequencing. The VCF File - Blog comment by lkessler - 12 Feb 2019
Interesting. You got over 100,000 more usable SNPs from your combined file than I did. That's a lot. I wonder why.
And thanks for your link to Krahn's program. I'm a Windows guy, but his template will be of interest to me. I'll likely be custom programming my own extract once I get my BAM file.
Yes, Dante ...
279.
My Whole Genome Sequencing. The VCF File - Blog comment by vanlaargen - 10 Feb 2019
"It originally did not accept my VCF from Dante. I contacted Wilhelm and the reason was that Dante did not include RSID values. Wilhelm made the change and sent me a beta of the program for me to try. It now created the raw data file, and correctly did steps 1a, 1b, and 2, above. But he, like GEDmatch, also ...
280.
My Whole Genome Sequencing. The VCF File - Blog entry by lkessler - 6 Feb 2019
I received my results from my Dante Labs Whole Genome test last week. I purchased the test last August when I was able to get it for $399 USD. There were two health reports that I requested that are written in ancient Latin as far as my understanding of them goes. Then there were the VCF files which I was more ...
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Chess and Artificial Intelligence: The Future Changed Today - Blog comment by 12345qaz - 20 Mar 2019