A comparison of genomic copy number calls by Partek Genomics Suite, Genotyping Console and Birdsuite algorithms to quantitative PCR

BACKGROUND: Copy number variants are >1 kb genomic amplifications or deletions that can be identified using array platforms. However, arrays produce substantial background noise that contributes to high false discovery rates of variants. We hypothesized that quantitative PCR could finitely determ...

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Detalles Bibliográficos
Autores principales: Grayson, Britney L, Aune, Thomas M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084167/
https://www.ncbi.nlm.nih.gov/pubmed/21489293
http://dx.doi.org/10.1186/1756-0381-4-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084167/
https://www.ncbi.nlm.nih.gov/pubmed/21489293
http://dx.doi.org/10.1186/1756-0381-4-8

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