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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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| Publicat a: | Biomed Rep |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2017
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| Matèries: | |
| Accés en línia: | 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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