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A sequential Monte Carlo framework for haplotype inference in CNV/SNP genotype data
Copy number variations (CNVs) are abundant in the human genome. They have been associated with complex traits in genome-wide association studies (GWAS) and expected to continue playing an important role in identifying the etiology of disease phenotypes. As a result of current high throughput whole-g...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017783/ https://www.ncbi.nlm.nih.gov/pubmed/24868199 http://dx.doi.org/10.1186/1687-4153-2014-7 |