Materials for short, half-day workshops

All code for the paper

Sample selection for exome sequencing based on dmp/IMPACT sequencing metrics

utilities to make waterfall plots of mutation signature data

Annotates variants in MAF with OncoKB annotation.

10x Genomics Linked-Read Diploid De Novo Assembler

Roslin is a reproducible and reusable workflow for Cancer Genomic Sequencing Analysis

Utility functions for FACETS

neoantigen prediction from WES/WGS

Load, review and adjust facets fits