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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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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2011
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3041647/ https://ncbi.nlm.nih.gov/pubmed/21269491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8794-4-14 |
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