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by beaugunderson
987 days ago
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23andMe uses a SNP array, or SNP chip, to look at SNPs (single-nucleotide polymorphisms, or more generally, single nucleotides that vary within a population). Basically what it gives you is a diff against a reference genome. So yes, while not a full genome sequence you can still get a VCF file out of it, impute sites that are not on the chip, use it for genealogy analysis, look at someone's disease carrier status, genetic disease likelihood, etc. |
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