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Andrew Hesse
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Advancements in next-generation sequencing, variant-calling software, and mutation enrichment are facilitating the detection of rare genetic variants. In doing so, these methods have enabled identification of somatic disease, and more specifically cancer, representing as little as 0.01% of bulk genetic material. This improved sensitivity reduces fa... Read More»
Andrew Hesse, Christopher Chen and Honey V. Reddi
Review Article: Adv Mol Diag 2016, 1: 101
DOI: 10.4172/2572-5645.1000101
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