Moss enables high sensitivity single-nucleotide variant calling from multiple bulk DNA tumor samples

Intra-tumor heterogeneity renders the identification of somatic single-nucleotide variants (SNVs) a challenging problem. In particular, low-frequency SNVs are hard to distinguish from sequencing artifacts. While the increasing availability of multi-sample tumor DNA sequencing data holds the potentia...

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Detalles Bibliográficos
Autores principales: Zhang, Chuanyi, El-Kebir, Mohammed, Ochoa, Idoia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044184/
https://www.ncbi.nlm.nih.gov/pubmed/33850139
http://dx.doi.org/10.1038/s41467-021-22466-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044184/
https://www.ncbi.nlm.nih.gov/pubmed/33850139
http://dx.doi.org/10.1038/s41467-021-22466-9

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