Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
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Updated
Nov 18, 2024 - Nextflow
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Nextflow bioinformatics pipeline for large-scale analysis of Multiple Myeloma genomes
A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
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