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The idea here is to transform each variant to a sequence from the user-defined x nucleotides before the variant to the user-defined z nucleotides after the variant. The user may ask for the reference or the mutant sequence
I am not aware of tool which can do this but there are tools which generate consensus sequence like bcftools consensus which has a way to generate a consensus sequence from a target region of the reference. vcf-consensus has similar behavior
The text was updated successfully, but these errors were encountered:
The idea here is to transform each variant to a sequence from the user-defined x nucleotides before the variant to the user-defined z nucleotides after the variant. The user may ask for the reference or the mutant sequence
I am not aware of tool which can do this but there are tools which generate consensus sequence like bcftools consensus which has a way to generate a consensus sequence from a target region of the reference. vcf-consensus has similar behavior
The text was updated successfully, but these errors were encountered: