Accelerating cancer research through comprehensive genomic analysis

The rapid advancement of sequencing technologies over the last two decades has delivered unprecedented insights into the structure and function of the human genome. Researchers can now use high-throughput sequencing technologies for routine analysis of human genome samples to uncover causative variations for a range of diseases and disorders — at nucleotide resolution. The field of cancer research is reaping the rewards of this, providing deeper scientific knowledge into the genomic causes and implications of cancer, allowing identification of novel disease biomarkers that may advance patient care. Read this White Paper to learn more about how the unique attributes of...