ngs-pipeline
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Pipeline for Somatic Variant Calling with WES and WGS data
Thank you so much for sharing this pipeline! I would like to re-use this to build a pipeline to call crispr off target effects. Unfortunately this repository lacks a License...
https://github.com/brentp/somalier
It currently has the same values as the WES file. Figure out better resource levels for WGS
Right now the pipeline requires sample type be specified as `normal` or `tumor` - the upper case versions cause an error. Call `tolower()` on the `units` data frame in `common.smk`...
Software like SomaticSniper and VarScan perform the same job as Mutect2. Utilizing many different callers can catch variants that one caller may miss. Results from each caller would be aggregated...