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Might one want to run several variant-callers but only skip the variant-filter for some of them? Like
nextflow run nf-core/sarek <usual stuff> --tools haplotypecaller,sentieon_haplotyper --skip_tools haplotypecaller_filter
With a cmd like that the variant-filter could only be applied to the vcf from the GATK haplotypecaller and NOT to the vcf from the Sentieon Haplotyper. Do we need that kind of flexibility?
Description of feature
No need to have three (or more) params for skipping the variant-filtering.
Replace the "options"
haplotypecaller_filter
,haplotyper_filter
anddnascope_filter
for--skip_tools
withvariant_filter
https://nfcore.slack.com/archives/C02MDBZAYJK/p1694010751853099
Also, add variant-filtering for mutect2.
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