As molecular knowledge of cancer continually evolves, comprehensive genomic profiling (CGP) is ushering in a new era in cancer care.
With a single CGP test, pathologists and providers can interrogate hundreds of genes, using less tissue and increasing the probability of detecting actionable findings. Yet, one of the most difficult challenges of implementing CGP in-house is the downstream variant analysis and interpretation. One CGP panel can yield thousands of genetic variants. Analyzing these variants and effectively managing the data can be incredibly time-consuming and complex.
In this webinar from DNAnexus, speakers discuss how DNAnexus and Qiagen Digital Insights are partnering to develop an agnostic, end-to-end workflow for comprehensive genomic profiling that goes from FASTQ to final report within minutes.
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