Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
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Updated
Jan 27, 2020 - Nextflow
Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Nextflow pipeline for analysis of direct RNA Nanopore reads
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Detect germline or somatic variants from normal or tumour/normal whole-genome, whole exome, or targeted sequencing with high performance computing.
Create required reference genome index files for WGS data analysis
Course for ROPES summer school, May 2023
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