MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data

Summary: Detailed analyses of the population-genetic nature of copy number variations (CNVs) and the linkage disequilibrium between CNV and single nucleotide polymorphism (SNP) loci from high-throughput experimental data require a computational tool to accurately infer alleles of CNVs and haplotypes...

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Detalles Bibliográficos
Autores principales: Kato, Mamoru, Nakamura, Yusuke, Tsunoda, Tatsuhiko
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Applications Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638261/
https://www.ncbi.nlm.nih.gov/pubmed/18492685
http://dx.doi.org/10.1093/bioinformatics/btn242

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638261/
https://www.ncbi.nlm.nih.gov/pubmed/18492685
http://dx.doi.org/10.1093/bioinformatics/btn242

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