A mixture model for signature discovery from sparse mutation data

Abstract Mutational signatures are key to understanding the processes that shape cancer genomes, yet their analysis requires relatively rich whole-genome or whole-exome mutation data. Recently, orders-of-magnitude sparser gene-panel-sequencing data have become increasingly available in the clinic. T...

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Autores principales: Itay Sason, Yuexi Chen, Mark D.M. Leiserson, Roded Sharan
Formato: article
Lenguaje:EN
Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/1eee8e0e684b4c5797b96c3ffaa77b66
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