Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Biomed Rep |
|---|---|
| Prif Awduron: | , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
D.A. Spandidos
2017
|
| Pynciau: | |
| Mynediad Ar-lein: | 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 |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|