A novel SNP analysis method to detect copy number alterations with an unbiased reference signal directly from tumor samples

BACKGROUND: Genomic instability in cancer leads to abnormal genome copy number alterations (CNA) as a mechanism underlying tumorigenesis. Using microarrays and other technologies, tumor CNA are detected by comparing tumor sample CN to normal reference sample CN. While advances in microarray technolo...

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Detalles Bibliográficos
Autores principales: Lisovich, Alex, Chandran, Uma R, Lyons-Weiler, Maureen A, LaFramboise, William A, Brown, Ashley R, Jakacki, Regina I, Pollack, Ian F, Sobol, Robert W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041647/
https://www.ncbi.nlm.nih.gov/pubmed/21269491
http://dx.doi.org/10.1186/1755-8794-4-14

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041647/
https://www.ncbi.nlm.nih.gov/pubmed/21269491
http://dx.doi.org/10.1186/1755-8794-4-14

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