This repository is currently in development but will contain the code used for the analysis detailed in the manuscript:
Structural variants at the BRCA1/2 loci are a common source of homologous repair deficiency in high grade serous ovarian carcinoma
- Commands used for primary processing of the WGS and RNAseq data
- Code used to implement the HRDetect model published by Davies et al1 and instructions for use
- Notebooks detailing downstream analysis described in the paper
Ailith Ewing
Alison Meynert
Graeme Grimes
1. [https://www.nature.com/articles/nm.4292]↩