A carregar...
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...
Na minha lista:
| Publicado no: | Biomed Rep |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2017
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|