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...

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Detalles Bibliográficos
Autores principales: Iliadis, Alexandros, Anastassiou, Dimitris, Wang, Xiaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
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

Internet

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

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