Somatic-ShortV-nf
main @ 495dafb

Workflow Type: Nextflow
Work-in-progress

This is a Nextflow implementaion of the GATK Somatic Short Variant Calling workflow. This workflow can be used to discover somatic short variants (SNVs and indels) from tumour and matched normal BAM files following GATK's Best Practices Workflow. The workflowis currently optimised to run efficiently and at scale on the National Compute Infrastructure, Gadi.

Version History

main @ 495dafb (earliest) Created 20th Dec 2023 at 01:12 by Georgina Samaha

Build skeleton template


Frozen main 495dafb
help Creators and Submitter
Citation
Deshpande, N., Chew, T., Willet, C., & Samaha, G. (2023). Somatic-ShortV-nf. WorkflowHub. https://doi.org/10.48546/WORKFLOWHUB.WORKFLOW.691.1
Activity

Views: 1167   Downloads: 256

Created: 20th Dec 2023 at 01:12

Last updated: 20th Dec 2023 at 01:16

help Attributions

None

Total size: 46 KB
Powered by
(v.1.16.0-main)
Copyright © 2008 - 2024 The University of Manchester and HITS gGmbH