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Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection
Despite declining sequencing costs, few methods are available for cost-effective single-nucleotide polymorphism (SNP), insertion/deletion (INDEL) and copy number variation (CNV) discovery in a single assay. Commercially available methods require a high investment to a specific region and are only co...
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| Formato: | Artigo |
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| Idioma: | en |
| Publicado em: |
Oxford University Press
2014
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4041413/ https://ncbi.nlm.nih.gov/pubmed/24682816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gku218 |
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