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I would like to genotype variants detected with Mutect2. The variants were identified from targeted sequencing of high coverage (> 500x). Do you have any parameters to recommend for running graphtyper genotype with high coverage data? I tried --no_filter_on_coverage parameter but I am curious if you have any other suggestion,
Thank you in advance for your time!
The text was updated successfully, but these errors were encountered:
Hello,
I would like to genotype variants detected with
Mutect2
. The variants were identified from targeted sequencing of high coverage (> 500x). Do you have any parameters to recommend for runninggraphtyper genotype
with high coverage data? I tried--no_filter_on_coverage
parameter but I am curious if you have any other suggestion,Thank you in advance for your time!
The text was updated successfully, but these errors were encountered: