Φορτώνει......
Comparison of methods to detect copy number alterations in cancer using simulated and real genotyping data
BACKGROUND: The detection of genomic copy number alterations (CNA) in cancer based on SNP arrays requires methods that take into account tumour specific factors such as normal cell contamination and tumour heterogeneity. A number of tools have been recently developed but their performance needs yet...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2012
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3472297/ https://ncbi.nlm.nih.gov/pubmed/22870940 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-13-192 |
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