Louis Kessler’s Behold Blog The Behold User Forum
Blog Comments
112.
WGS Result Files - Blog comment by lkessler - 23 Apr 2019
Kendraz: When I purchased my kit back in August 2018, the hard drive with the BAM and FASTQ files was included free of charge. I did note in November that they started charging $69 extra for the hard drive containing your raw data.
I am purely looking at the short versus long reads for the purpose of ...
113.
Genetic Affairs Clustering at 23andMe - Blog comment by lkessler - 6 Apr 2019
Ah, yes. Evert-Jan: Take a look at Shelley's article.
114.
Comparing Raw Data from 5 DNA Testing Companies - Blog comment by lkessler - 6 Apr 2019
Sullrich: Yes, that’s an excellent example of how the shared SNPs are very dependent on the chip that is used. Thanks for the offer of SNPs. I’d love to see a sample of Living DNA’s raw data from their new chip.
115.
Comparing Raw Data from 5 DNA Testing Companies - Blog comment by sullrich1 - 5 Apr 2019
Hi Louis,
Thanks for the very interesting and informative post. I recently (March 2019) got my autosomal DNA test results from Living DNA. When I compared the number of shared SNPs between Living DNA, FTDNA and Ancestry, I got different percentage of SNPs shared between them than what you found; ~39% and 23% ...
116.
Genetic Affairs Clustering at 23andMe - Blog comment by shelley - 24 Mar 2019
Hi Louis, I've written about it before (and you even commented on my post!). http://twigsofyore.blogspot.com/2018/03/triangulation-is-icing-not-cake.html.
117.
Chess and Artificial Intelligence: The Future Changed Today - Blog comment by 12345qaz - 20 Mar 2019
Totally agree that AI will change our lives in the future. I spent a lot of time studying this issue. Read mostly here: https://www.greenontheinside.net/tag/artificial-intelligence/. Artificial Intelligence is very interesting.
118.
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?
119.
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
120.
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 ...
My Whole Genome Sequencing. The VCF File - Blog comment by blzlovr - 2 May 2019