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Warning Newer version of the nf-core template is available. Your pipeline is using an old version of the nf-core template: 3.2.0. For more documentation on how to update your pipeline, please see the nf-core documentation and Synchronisation documentation. |
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| // https://github.com/nf-core/modules/tree/master/subworkflows | ||
| // You can also ask for help via your pull request or on the #subworkflows channel on the nf-core Slack workspace: | ||
| // https://nf-co.re/join | ||
| // TODO nf-core: A subworkflow SHOULD import at least two modules |
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Is this true here? We don't really need more than one in this case, but it seems logical to have this as a subworkflow.
(The Y-DNA stuff will definitely offer making a reference genome that can be used by Yleaf as part of a subworkflow.)
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Importing one one module is fine 👍
I agree that a SWF makes more sense.
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| if (params.run_mtdna_haplogroup) { | ||
| if (!params.run_genotyping) { | ||
| error "Cannot run mtDNA haplogroup classification (--run_mtdna_haplogroup) without running genotyping (--run_genotyping). VCF files are required as input." |
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So there used to be a vcf2genome in eager2 that output a consensus fasta. Is that still a thing? Because haplogrep3 also works with mtDNA sequences aligned to rCRS or RSRS.
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no. vcf2genome is discontinued and will not be supported in eager 3.* .
Consensus sequence calling will be added soon™ ( #1142 ).
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manual_tests.md
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…roblem with collection/name not working
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Whoops rebase disaster... See #1148 for proper commits |
Work in progress - adding mtDNA haplogroup classification
Haplogrep3 integration
--treeneeds to be passed in fromhaplogrep3_tree_id[... 1h50m passes]
PR checklist
nf-core pipelines lint).nextflow run . -profile test,docker --outdir <OUTDIR>).nextflow run . -profile debug,test,docker --outdir <OUTDIR>).docs/usage.mdis updated.docs/output.mdis updated.CHANGELOG.mdis updated.README.mdis updated (including new tool citations and authors/contributors).