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 functions of the human genome. Replacing more cumbersome, low resolution techniques for human genome analysis, such as karyotyping and microarrays, 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.
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Overview
Overview
The field of cancer research is reaping the rewards of these technological innovations, providing deeper scientific knowledge into the genomic causes and implications of cancer, and allowing the identification of novel disease biomarkers that may support patient care through improved diagnostics, prognostics, and treatment decisions.
