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Description: The Sulston Project - Making the knowledge commons for interpreting cancer genomic variants more effective
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The Sulston Project Making the Knowledge Commons for Interpreting Cancer Genomic Variants More Effective
High-speed and low-cost sequencing, combined with intense clinical interest, have led to widespread use of multi-gene testing for inherited variants conferring risk of cancer. Millions of genetic tests for inherited risk of cancer have been administered since commercial testing of BRCA1/2 variants began in 1996, and yet new variants continue to be found. Determining a variant’s clinical significance can be a challenge. As hereditary cancer testing panels have transitioned to sequencing dozens of genes, rath
More about our project and how we’re improving the knowledge commons
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