Comment on DNAddy

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rockSlayer@lemmy.blahaj.zone ⁨2⁩ ⁨weeks⁩ ago

Well it varies depending on what the file is meant for. Usually there’s columns like chromosome, variant position, reference nucleotide, observed nucleotide, type of variation, codon sequence, gene name, etc.

There’s also columns that result from various analyses. In the file I’ve been working on lately, there are columns such as variant impact, level of confidence, pathogenicity, clinical significance, etc.

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