Published March 2, 2026
| Version SlideSeq_v3.6.5
Software
Open
github.com/broadinstitute/warp/mt_coverage_merge
Authors/Creators
Description
This workflow builds a combined mtDNA MatrixTable from per-sample VCFs, imputes hom-ref coverage from a coverage DB, and outputs annotated (full and filtered) callsets.
Files
github.com-broadinstitute-warp-mt_coverage_merge_SlideSeq_v3.6.5.zip
Files
(10.0 kB)
| Name | Size | Download all |
|---|---|---|
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md5:97face09bc872285b8301f7e2a1a89bb
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10.0 kB | Preview Download |
Additional details
Related works
- Is identical to
- https://dockstore.org/aliases/workflow-versions/10.5281-zenodo.18840851 (URL)
- https://dockstore.org/workflows/github.com/broadinstitute/warp/mt_coverage_merge:SlideSeq_v3.6.5 (URL)
- https://dockstore.org/api/ga4gh/trs/v2/tools/%23workflow%2Fgithub.com%2Fbroadinstitute%2Fwarp%2Fmt_coverage_merge/versions/SlideSeq_v3.6.5/PLAIN-WDL/descriptor/mt_coverage_merge.wdl (URL)