a versatile tool for detecting copy number changes from exome-seq data

High speed p-value computation for regulatory SNP detection using Motif information

Config files used to define parameters specific to compute environments at different Institutions

Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing

DoWhy is a Python library for causal inference that supports explicit modeling and testing of causal assumptions. DoWhy is based on a unified language for causal inference, combining causal graphic…

An R package for inferring the subclonal architecture of tumors