A regression model for estimating DNA copy number applied to capture sequencing data
2012
Rigaill, Guillem, G. | Cadot, Sidney | Kluin, Roelof J. C. | Xue, Zheng | Bernards, René | Majewski, Ian J. | Wessels, Lodewyk F. A. | Unité de recherche en génomique végétale (URGV) ; Institut National de la Recherche Agronomique (INRA)-Université d'Évry-Val-d'Essonne (UEVE)-Centre National de la Recherche Scientifique (CNRS) | Netherlands Cancer Institute Antoni van Leeuwenhoek ; Partenaires INRAE | The Cancer Systems Biology Center grant by NWO; NHMRC research [575581]
International audience
Mostrar más [+] Menos [-]Inglés. Motivation: Target enrichment, also referred to as DNA capture, provides an effective way to focus sequencing efforts on a genomic region of interest. Capture data are typically used to detect single-nucleotide variants. It can also be used to detect copy number alterations, which is particularly useful in the context of cancer, where such changes occur frequently. In copy number analysis, it is a common practice to determine log-ratios between test and control samples, but this approach results in a loss of information as it disregards the total coverage or intensity at a locus. Results: We modeled the coverage or intensity of the test sample as a linear function of the control sample. This regression approach is able to deal with regions that are completely deleted, which are problematic for methods that use log-ratios. To demonstrate the utility of our approach, we used capture data to determine copy number for a set of 600 genes in a panel of nine breast cancer cell lines. We found high concordance between our results and those generated using a single-nucleotide polymorphsim genotyping platform. When we compared our results with other log-ratio-based methods, including ExomeCNV, we found that our approach produced better overall correlation with SNP data.
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