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Understanding the Basics of NGS: From Mechanism to Variant Calling
Identifying disease-causing mutations in DNA has long been the goal of genetic medicine. In the last decade, the toolkit for discovering DNA variants has undergone rapid evolution: mutations that were historically discovered by analog approaches like Sanger sequencing and multiplex ligation-dependen...
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| Izdano u: | Curr Genet Med Rep |
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| Glavni autori: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer US
2015
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4633438/ https://ncbi.nlm.nih.gov/pubmed/26566462 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40142-015-0076-8 |
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