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Germline-ShortV @ NCI-Gadi is an implementation of the BROAD Institute's best practice workflow for germline short variant discovery. This implementation is optimised for the National Compute Infrastucture's Gadi HPC, utilising scatter-gather parallelism to enable use of multiple nodes with high CPU or memory efficiency. This workflow requires sample BAM files, which can be generated using the Fastq-to-bam @ NCI-Gadi pipeline. Germline-ShortV can be applied to model and non-model organisms (including non-diploid organisms).
Infrastructure_deployment_metadata: Gadi (NCI)
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Version 1 (earliest) Created 17th Aug 2021 at 05:35 by Tracy Chew
Added/updated 2 files
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  Sadsad, R., Samaha, G., & Chew, T. (2021). Germline-ShortV @ NCI-Gadi. WorkflowHub. https://doi.org/10.48546/WORKFLOWHUB.WORKFLOW.143.1
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Created: 17th Aug 2021 at 05:35
Last updated: 25th Jul 2025 at 03:04
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  Genomics, DNA mutation, Whole genome sequencing, Population genomics, Genetic variation, DNA polymorphism
  
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 https://orcid.org/0000-0003-2488-953X
 https://orcid.org/0000-0003-2488-953X



