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Whole genome sequencing data from pedigrees suggests linkage disequilibrium among rare variants created by population admixture
Next-generation sequencing technologies have been designed to discover rare and de novo variants and are an important tool for identifying rare disease variants. Many statistical methods have been developed to test, using next-generation sequencing data, for rare variants that are associated with a...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143626/ https://www.ncbi.nlm.nih.gov/pubmed/25519326 http://dx.doi.org/10.1186/1753-6561-8-S1-S44 |