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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Bibliographic Details
Main Authors: Iliadis, Alexandros, Anastassiou, Dimitris, Wang, Xiaodong
Format: Artigo
Language:Inglês
Published: BioMed Central 2014
Subjects:
Research
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4017783/
https://ncbi.nlm.nih.gov/pubmed/24868199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1687-4153-2014-7
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