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