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Remove merge_haplotypecaller_filtered #605
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FriederikeHanssen
requested changes
Jun 24, 2022
subworkflows/nf-core/gatk4/single_sample_germline_variant_calling/main.nf
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Co-authored-by: FriederikeHanssen <Friederike.hanssen@qbic.uni-tuebingen.de>
FriederikeHanssen
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maxulysse
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maxulysse
June 29, 2022 08:35
maxulysse
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Jun 30, 2022
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LGTM
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Edited by @FriederikeHanssen : This PR changes the behavior of the Haplotypecaller single sample mode to not parallelize via scatter/gather. The reason being that often FilterVariantTranches fails on smaller regions (even for WGS) if no SNP is present in this particular one. Instead all regions are run together to avoid this kind of behavior.
PR checklist
scrape_software_versions.py
nf-core lint .
).nextflow run . -profile test,docker
).docs/usage.md
is updated.docs/output.md
is updated.CHANGELOG.md
is updated.README.md
is updated (including new tool citations and authors/contributors).