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On Estimation of Allele Frequencies via Next-Generation DNA Resequencing with Barcoding
Next Generation Sequencing (NGS) has revolutionized biomedical research in recent years. It is now commonly used to identify rare variants through re-sequencing individual genomes. Due to the cost of NGS, researchers have considered pooling samples as a cost-effective alternative to individual seque...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3666873/ https://ncbi.nlm.nih.gov/pubmed/23730349 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12561-013-9084-y |
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