Published August 11, 2026
| Version 4.0.69
Software
Open
github.com/broadinstitute/long-read-pipelines/SRWholeGenome_Simplified
Authors/Creators
Description
This workflow performs single-sample variant calling on Illumina reads from one or more flow cells containing replicates of the same sample. The workflow merges multiple samples into a single BAM prior to variant calling.
Files
github.com-broadinstitute-long-read-pipelines-SRWholeGenome_Simplified_4.0.69.zip
Files
(57.4 kB)
| Name | Size | Download all |
|---|---|---|
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md5:58f7876eda778423d1708fdc7d33ef35
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57.4 kB | Preview Download |
Additional details
Related works
- Is identical to
- https://dockstore.org/aliases/workflow-versions/10.5281-zenodo.21891789 (URL)
- https://dockstore.org/workflows/github.com/broadinstitute/long-read-pipelines/SRWholeGenome_Simplified:4.0.69 (URL)
- https://dockstore.org/api/ga4gh/trs/v2/tools/%23workflow%2Fgithub.com%2Fbroadinstitute%2Flong-read-pipelines%2FSRWholeGenome_Simplified/versions/4.0.69/PLAIN-WDL/descriptor/SRWholeGenome_Simplified.wdl (URL)