Evaluation of copy number variation detection for a SNP array platform

BACKGROUND: Copy Number Variations (CNVs) are usually inferred from Single Nucleotide Polymorphism (SNP) arrays by use of some software packages based on given algorithms. However, there is no clear understanding of the performance of these software packages; it is therefore difficult to select one...

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Detalles Bibliográficos
Autores principales: Zhang, Xin, Du, Renqian, Li, Shilin, Zhang, Feng, Jin, Li, Wang, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015297/
https://www.ncbi.nlm.nih.gov/pubmed/24555668
http://dx.doi.org/10.1186/1471-2105-15-50

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015297/
https://www.ncbi.nlm.nih.gov/pubmed/24555668
http://dx.doi.org/10.1186/1471-2105-15-50

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