Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data

In addition to single-nucleotide polymorphisms (SNP), copy number variation (CNV) is a major component of human genetic diversity. Among many whole-genome analysis platforms, SNP arrays have been commonly used for genomewide CNV discovery. Recently, a number of CNV defining algorithms from SNP genot...

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Detalles Bibliográficos
Autores principales: Kim, Soon-Young, Kim, Ji-Hong, Chung, Yeun-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492655/
https://www.ncbi.nlm.nih.gov/pubmed/23166530
http://dx.doi.org/10.5808/GI.2012.10.3.194

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492655/
https://www.ncbi.nlm.nih.gov/pubmed/23166530
http://dx.doi.org/10.5808/GI.2012.10.3.194

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