Single nucleotide variant sequencing errors in whole exome sequencing using the Ion Proton System

Errors in sequencing are a major obstacle in the interpretation of next-generation sequencing (NGS) results. In the present study, sequencing errors identified from analysis of single nucleotide variants (SNVs) identified during exome sequencing of human germline DNA were studied using the Thermo Fi...

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Publicado en:Biomed Rep
Main Authors: Fujita, Shiro, Masago, Katsuhiro, Okuda, Chiyuki, Hata, Akito, Kaji, Reiko, Katakami, Nobuyuki, Hirata, Yukio
Formato: Artigo
Idioma:Inglês
Publicado: D.A. Spandidos 2017
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Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5492560/
https://ncbi.nlm.nih.gov/pubmed/28685054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/br.2017.911
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