Using somatic variant richness to mine signals from rare variants in the cancer genome

Sequencing cancer genomes reveals low frequency novel somatic variants without known function. Here, the authors leverage statistical methodology from the fields of computational linguistics and ecology to highlight the potentially important signals harboured by these novel variants that are often d...

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Auteurs principaux: Saptarshi Chakraborty, Arshi Arora, Colin B. Begg, Ronglai Shen
Format: article
Langue:EN
Publié: Nature Portfolio 2019
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Accès en ligne:https://doaj.org/article/2b7877645b70435c97a71442e14a8db7
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