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A classification model for distinguishing copy number variants from cancer-related alterations
BACKGROUND: Both somatic copy number alterations (CNAs) and germline copy number variants (CNVs) that are prevalent in healthy individuals can appear as recurrent changes in comparative genomic hybridization (CGH) analyses of tumors. In order to identify important cancer genes CNAs and CNVs must be...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2010
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2897829/ https://ncbi.nlm.nih.gov/pubmed/20525196 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-297 |
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