We develop community-driven, reusable approaches to process, analyse and aggregate large-scale sequencing data to improve cancer diagnostics and therapeutic choices.

Recent blogposts

We are hiring a Research Software Engineer and a Bioinformatician, closing June 2nd 2019.

We are detecting sites of HPV18 oncovirus integration into the human genome, and investigating the mechanism it facilitated cervical …

Building a panel of unrelated normals to filter somatic variant calls from artefacts and germline leakage.

On expanding the Broad’s Integrative Genomics Viewer (IGV) to read input directly from AWS S3.

We evaluate differences between bwa-mem and minimap2-aligned reads for somatic variant calling.