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You really just uploaded a limited patch file against a much larger project, and the results wouldn't compile or do anything interesting.

Technically, it's just a limited set of variants-- if you really want to open source your DNA, please get a whole genome sequence (it's about $5-10K right now) and upload the BAM files to PGP. That is more valuable, scientifically speaking, than just a variant file because there is a lot of data reduction going from the full readset to a variants file. In particular, we don't know if they called your positions correctly, we don't know much about your genomic rearrangements (indels etc) because this is a 23&Me microarray (you didn't get their exome or WGS product, right?) and those are really limited in their utility.