Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Why do you think that https://github.com/nf-core/rnaseq is a good alternative to sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Why do you think that https://github.com/nf-core/rnaseq is a good alternative to sarek