Cargando…
Whole genome DNA copy number changes identified by high density oligonucleotide arrays
Changes in DNA copy number are one of the hallmarks of the genetic instability common to most human cancers. Previous micro-array-based methods have been used to identify chromosomal gains and losses; however, they are unable to genotype alleles at the level of single nucleotide polymorphisms (SNPs)...
Autores principales: | Huang, Jing, Wei, Wen, Zhang, Jane, Liu, Guoying, Bignell, Graham R, Stratton, Michael R, Futreal, P Andrew, Wooster, Richard, Jones, Keith W, Shapero, Michael H |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525261/ https://www.ncbi.nlm.nih.gov/pubmed/15588488 http://dx.doi.org/10.1186/1479-7364-1-4-287 |
Ejemplares similares
-
CARAT: A novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays
por: Huang, Jing, et al.
Publicado: (2006) -
Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes
por: Shen, Fan, et al.
Publicado: (2008) -
Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH
por: Neill, Nicholas J, et al.
Publicado: (2010) -
Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma
por: Wang, Xiaoyu, et al.
Publicado: (2015) -
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data
por: Greenman, Chris D., et al.
Publicado: (2010)