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Inferring combined CNV/SNP haplotypes from genotype data
Motivation: Copy number variations (CNVs) are increasingly recognized as an substantial source of individual genetic variation, and hence there is a growing interest in investigating the evolutionary history of CNVs as well as their impact on complex disease susceptibility. CNV/SNP haplotypes are cr...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2913665/ https://ncbi.nlm.nih.gov/pubmed/20406911 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq157 |
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