Research Object Crate for Somatic-ShortV @ NCI-Gadi

Original URL: https://workflowhub.eu/workflows/148/ro_crate?version=1

Somatic-ShortV @ NCI-Gadi is a variant calling pipeline that calls somatic short variants (SNPs and indels) from tumour and matched normal BAM files following [GATK's Best Practice Workflow](https://gatk.broadinstitute.org/hc/en-us/articles/360035894731-Somatic-short-variant-discovery-SNVs-Indels-). This workflow is designed for the National Computational Infrastructure's (NCI) Gadi supercompter, leveraging multiple nodes on NCI Gadi to run all stages of the workflow in parallel. Infrastructure\_deployment\_metadata: Gadi (NCI)

Author
Tracy Chew, Rosemarie Sadsad, Cali Willet
License
GPL-3.0

Contents

Main Workflow: Somatic-ShortV @ NCI-Gadi
Size: 20568 bytes
Main Workflow Diagram: 94503907-ebb0cc80-024a-11eb-800c-41854b1f041c.png
Size: 246369 bytes