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Systematic Evaluation of Sanger Validation of NextGen Sequencing Variants
BACKGROUND: Next-generation sequencing (NGS) data are used for both clinical care and clinical research. DNA sequence variants identified using NGS are often returned to patients/participants as part of clinical or research protocols. The current standard of care is to validate NGS variants using Sa...
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| Vydáno v: | Clin Chem |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4878677/ https://ncbi.nlm.nih.gov/pubmed/26847218 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1373/clinchem.2015.249623 |
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