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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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Pubblicato in:Sci Rep
Autori principali: Fischer-Hwang, Irena, Ochoa, Idoia, Weissman, Tsachy, Hernaez, Mikel
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2019
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6803637/
https://ncbi.nlm.nih.gov/pubmed/31636330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-51418-z
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