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Dnascope module and subworkflow in Sarek #1193
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…t-valling with Dnascope
…alling with Sentieon Dnascope
…plotyper_joint_germline
…nd genotype_tbi. (Needed for output csv-file.)
Can you check the merge conflicts? |
… Sentieon/haplotyper/joint_germline
LGTM |
Can you sync and update CHANGELOG |
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process { | ||
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// TO-DO: duplicate!! |
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do we need an issue for this todo?
joint_mutect2 = false // if true, enables patient-wise multi-sample somatic variant calling | ||
only_paired_variant_calling = false // if true, skips germline variant calling for normal-paired sample | ||
sentieon_dnascope_emit_mode = "variant" // default value for Sentieon dnascope | ||
sentieon_dnascope_model = "https://s3.amazonaws.com/sentieon-release/other/SentieonDNAscopeModel1.1.model" |
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was this the s3 thing you guys mentioned or is this something new?
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Yeah, I believe Maxime is working on getting that file into igenomes.
Great work, sorry I only got to review it now. Do you have a chance to add it to the subway map/overview image? |
Oh, I totally forgot about that, Rike. I'm afraid I don't know how to use those graphics programs for updating the diagrams. Perhaps you or @maxulysse could update the diagrams? |
Sure. It's an alternative to haplotyper, right? When would you choose which? |
Yes, it is an alternative to Sentieon's haplotyper, but where as Sentieon's haplotyper was designed to give the same results at GATK's haplotypercaller - but faster, Sentieon's dnascope improves both "speed and accuracy, and it can perform structural variant calling in addition to calling SNPs and small indels." |
ok so in the plot should move it inbetween SNps/indels and svs then |
I was thinking more of the sbway map. Anyways I'll make a proposal in the coming days and send it your way |
Implementation of DNAscope. #405
PR checklist
nf-core lint
).nextflow run . -profile 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).