Cargando…
Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data
BACKGROUND: Genomic deletions and duplications are important in the pathogenesis of diseases, such as cancer and mental retardation, and have recently been shown to occur frequently in unaffected individuals as polymorphisms. Affymetrix GeneChip whole genome sampling analysis (WGSA) combined with 10...
Autores principales: | Baross, Ágnes, Delaney, Allen D, Li, H Irene, Nayar, Tarun, Flibotte, Stephane, Qian, Hong, Chan, Susanna Y, Asano, Jennifer, Ally, Adrian, Cao, Manqiu, Birch, Patricia, Brown-John, Mabel, Fernandes, Nicole, Go, Anne, Kennedy, Giulia, Langlois, Sylvie, Eydoux, Patrice, Friedman, JM, Marra, Marco A |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148068/ https://www.ncbi.nlm.nih.gov/pubmed/17910767 http://dx.doi.org/10.1186/1471-2105-8-368 |
Ejemplares similares
-
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization
por: Friedman, JM, et al.
Publicado: (2009) -
Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation
por: Tucker, Tracy, et al.
Publicado: (2011) -
Experimental analysis of oligonucleotide microarray design criteria to detect deletions by comparative genomic hybridization
por: Flibotte, Stephane, et al.
Publicado: (2008) -
Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays
por: Auer, Herbert, et al.
Publicado: (2007) -
Transcript copy number estimation using a mouse whole-genome oligonucleotide microarray
por: Carter, Mark G, et al.
Publicado: (2005)