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Implement GATK-gCNV tool for CNV detection #415
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Hi @egenomics! Correct me if I am wrong, but this looks like a feature we already implemented in release 1.1.0. Relevant PR here #362. |
Closing this issue for now, but feel free to open it back up if you think this feature is lacking. 😄 |
In release 2.2.0, seems like the outputs from GATK CNV segment calls are not merged in a family-based VCF first: container: 'quay.io/biocontainers/mulled-v2-c8daa8f9d69d3c5a1a4ff08283a166c18edb0000:511069f65a53621c5503e5cfee319aa3c735abfa-0'###BASH output Content in .command.sh may give insight on why the output fam_1_sv.vcf.gz is empty: cat <<-END_VERSIONS > versions.yml Note that in the line with "sample3_gatkcnv_segments_refiltered.vcf.gz:null fam_1_cnvnator.vcf.gz:null", two files were labelled as null, potentially due to array overflow of unexpected number of input VCF files. |
@ramprasadn Should the GATK SV workflow include a SVDB merge step as well (Similar to line 39 of the cnvnator workflow https://github.com/nf-core/raredisease/blob/fa61a657257a14a6433e3d751c577ab4c9d2eda4/subworkflows/local/variant_calling/call_sv_cnvnator.nf)? |
Tracked in issue #634 |
Description of feature
Hi,
It would be awesome if GATK-gCNV new tool for CNV detection in WES, targeted panels and WGS could be implemented in the pipeline.
The original paper is here: https://www.nature.com/articles/s41588-023-01449-0
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