Haplotypecaller fix + single sample germline VC#557
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maxulysse merged 27 commits intonf-core:devfrom Jun 16, 2022
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maxulysse
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Jun 9, 2022
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@nf-core-bot fix linting |
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The test data is just no working for the single sample workflow. I always get: Reverse enigneering the modules test, the vcf used there was run through genotypegvcf, which is not happening in this part of the workflow |
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Alright, I don't know how to get the tests to work, last try is using the tumor reads for it. I have tested it on 17 real targeted datasets now, and it works fine. |
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PR checklist
scrape_software_versions.pynf-core lint .).nextflow run . -profile test,docker).docs/usage.mdis updated.docs/output.mdis updated.CHANGELOG.mdis updated.README.mdis updated (including new tool citations and authors/contributors).