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I'm afraid I've gotten myself quite confused around the use of --common_variants.
Is this option only compatible when --known_genotypes are NOT provided, or can it also be used with --known_genotypes?
My understanding is that if --known_genotypes are provided, then
a) there's no need to call variants de novo using freebayes. Instead, it will [optionally] remap, then skip the freebayes step, and rely on the provided VCF for variant information.
b) Since it will use the variants in the provided known_genotypes VCF, this is incompatible with a common_variants file.
In this sense, --common_variants can only be used if NOT using --known_genotypes (ie a genotype reference VCF)
Are these assumptions correct?
The text was updated successfully, but these errors were encountered:
Hi,
I'm afraid I've gotten myself quite confused around the use of
--common_variants
.Is this option only compatible when
--known_genotypes
are NOT provided, or can it also be used with--known_genotypes
?My understanding is that if
--known_genotypes
are provided, thena) there's no need to call variants de novo using freebayes. Instead, it will [optionally] remap, then skip the
freebayes
step, and rely on the provided VCF for variant information.b) Since it will use the variants in the provided known_genotypes VCF, this is incompatible with a
common_variants
file.In this sense,
--common_variants
can only be used if NOT using--known_genotypes
(ie a genotype reference VCF)Are these assumptions correct?
The text was updated successfully, but these errors were encountered: