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NEW YORK (GenomeWeb) – Women with cancer who are found to have pathogenic genetic variants may receive care that does not reflect what current evidence-based practice guidelines indicate they should receive, according to an analysis performed by Stanford University's Allison Kurian and her colleagues.

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Jan
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Sophia Genetics

This webinar will discuss how Moffitt Cancer Center has implemented a new capture-based application to accurately assess myeloid malignancies by detecting complex variants in challenging genes in a single experiment.  

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Feb
26
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Feb
27
Sponsored by
Stilla

Since the publication of the “The Digital MIQE Guidelines: Minimum Information for Publication of Quantitative Digital PCR Experiments” (dMIQE) in 2013, there has been a large expansion of the applications of dPCR such as single nucleotide variations (SNVs) and copy number variations (CNVs) measurements associated with disease diagnostics.