Hey all
Just trying to find a way to call around 100,000 single-point positions from BAM files calling both mismatches from the reference genome and also homozygous to the reference.
I can't call every variant in WGS data(and then filter) as the file size for every individual will be huge
Ideas ??
Cheers
Josh
Just trying to find a way to call around 100,000 single-point positions from BAM files calling both mismatches from the reference genome and also homozygous to the reference.
I can't call every variant in WGS data(and then filter) as the file size for every individual will be huge
Ideas ??
Cheers
Josh
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