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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. 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)
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Version 1 (earliest) Created 19th Aug 2021 at 00:14 by Tracy Chew
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  Sadsad, R., & Chew, T. (2021). Somatic-ShortV @ NCI-Gadi. WorkflowHub. https://doi.org/10.48546/WORKFLOWHUB.WORKFLOW.148.1
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Created: 19th Aug 2021 at 00:14
Last updated: 25th Jul 2025 at 03:06
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 https://orcid.org/0000-0003-2488-953X
 https://orcid.org/0000-0003-2488-953X
