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Denoising of Aligned Genomic Data

Noise in genomic sequencing data is known to have effects on various stages of genomic data analysis pipelines. Variant identification is an important step of many of these pipelines, and is increasingly being used in clinical settings to aid medical practices. We propose a denoising method, dubbed...

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Detalles Bibliográficos
Autores principales: Fischer-Hwang, Irena, Ochoa, Idoia, Weissman, Tsachy, Hernaez, Mikel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803637/
https://www.ncbi.nlm.nih.gov/pubmed/31636330
http://dx.doi.org/10.1038/s41598-019-51418-z