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Beyond the Variants: Mutational Patterns in Next-Generation Sequencing Data for Cancer Precision Medicine

Massively parallel sequencing, also referred to as “next-generation sequencing” (NGS) provides not only information about simple, single nucleotide alterations, but it can also provide information on complex variations, such as insertions and deletions, copy number alterations, and structural varian...

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Detaylı Bibliyografya
Yayımlandı:Front Cell Dev Biol
Asıl Yazarlar: Parilla, Megan, Ritterhouse, Lauren L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7248322/
https://ncbi.nlm.nih.gov/pubmed/32509788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.00370
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