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Add option to restrict analysis to specific contigs #644
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In long-reads I imagine this strategy would not call translocations with one good breakpoint in an interesting gene on 1-22, X, Y and the other breakpoint mapping to a few different places (including unplaced contigs). Would this be an issue here? |
Hi Felix! We have added the option to restrict the analysis to chromosomes only because alignments to unplaced contigs can be messy, leading to less reliable results. We want to minimize any potential errors from those alignments. |
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Could you add to the usage documentation?
Otherwise it looks good to me. I'd lean towards using a BED-file rather than a regions string, but both work.
Makes sense to not deal with such variants at all, thanks for clarifying! |
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👍
Co-authored-by: Anders Jemt <[email protected]>
Co-authored-by: Anders Jemt <[email protected]>
PR checklist
nf-core lint
).nextflow run . -profile test,docker --outdir <OUTDIR>
).nextflow run . -profile test_one_sample,docker --outdir <OUTDIR>
).nextflow run . -profile debug,test,docker --outdir <OUTDIR>
).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).