"BaseSpace Variant Interpreter"

Interpreting structural variation in cancer genomes

A user story from the Genomics England 100,000 Genomes Project cancer programme1 By Jawahar Swaminathan, Ph.D., Program Manager – Population Genomics Illumina and Genomics England announced a Bioinformatics and Clinical Interpretation partnership (BCIP) in 2016 to “develop a platform and knowledge base that can be used to improve and automate genome interpretation.” In 2017, following […]