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Haplotypecaller fix + single sample germline VC #557
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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 |
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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LGTM
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).