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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 18th Aug 2021 at 00:14 by Tracy Chew
Added/updated 2 files
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Cali Willet
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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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Views: 3522 Downloads: 342
Created: 18th Aug 2021 at 00:14
Last updated: 9th Sep 2021 at 02:33
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