The NHS Genomic Medicine Service has precipitated a sharp increase in the volume and diversity of referrals for cancer-gene sequencing.
The cancer test directory informs a list of essential and investigational genes which can be targeted to maximize clinical insight.
Dr Patrick Tarpey presents an overview of large NGS panel screening from a clinical perspective, illuminating the value of permissive analysis and the necessity for a singular DSS solution to enable rapid exploration of all variant classes in a myriad of different cancer types.
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