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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fujita, Shiro, Masago, Katsuhiro, Okuda, Chiyuki, Hata, Akito, Kaji, Reiko, Katakami, Nobuyuki, Hirata, Yukio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492560/
https://www.ncbi.nlm.nih.gov/pubmed/28685054
http://dx.doi.org/10.3892/br.2017.911

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492560/
https://www.ncbi.nlm.nih.gov/pubmed/28685054
http://dx.doi.org/10.3892/br.2017.911

Ejemplares similares