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All,
Does anyone know any tool that can summarize the variants in a multi-sample VCF file? I would require a table format summary of variants that shows:
a) #novel
b) #dbSNP
c) dbSNP_%
d) #heterozygous
e) #homozygous
for each sample as columns:
Any suggestion would be useful.
Raj
Does anyone know any tool that can summarize the variants in a multi-sample VCF file? I would require a table format summary of variants that shows:
a) #novel
b) #dbSNP
c) dbSNP_%
d) #heterozygous
e) #homozygous
for each sample as columns:
Any suggestion would be useful.
Raj
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