Abstract
BackgroundDNA copy number aberration (CNA) is very important in the pathogenesis of tumors and other diseases. For example, CNAs may result in suppression of anti-oncogenes and activation of oncogenes, which would cause certain types of cancers. High density single nucleotide polymorphism (SNP) array data is widely used for the CNA detection. However, it is nontrivial to detect the CNA automatically because the signals obtained from high density SNP arrays often have low signal-to-noise ratio (SNR), which might be caused by whole genome amplification, mixtures of normal and tumor cells, experimental noise or other technical limitations. With the reduction in SNR, many false CNA regions are often detected and the true CNA regions are missed. Thus, more sophisticated statistical models are needed to make the CNAs detection, using the low SNR signals, more robust and reliable.ResultsThis paper presents a conditional random pattern (CRP) model for CNA detection where much contextual cues are explored to suppress the noise and improve CNA detection accuracy. Both simulated and the real data are used to evaluate the proposed model, and the validation results show that the CRP model is more robust and reliable in the presence of noise for CNA detection using high density SNP array data, compared to a number of widely used software packages.ConclusionsThe proposed conditional random pattern (CRP) model could effectively detect the CNA regions in the presence of noise.
Highlights
DNA copy number aberration (CNA) is very important in the pathogenesis of tumors and other diseases
It is nontrivial to detect the CNA automatically because the signals obtained from high density single nucleotide polymorphism (SNP) arrays often have low signal-to-noise ratio (SNR) values, which may be caused by whole genome amplification, mixture of normal and tumor cells, experimental noise and other technical limitations
More sophisticated statistical models are needed urgently to make the CNAs detection robust and reliable using the signals with low SNR, a number of software packages have been developed for the BioMed Central bution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited
Summary
DNA copy number aberration (CNA) is very important in the pathogenesis of tumors and other diseases. It is nontrivial to detect the CNA automatically because the signals obtained from high density SNP arrays often have low signal-to-noise ratio (SNR), which might be caused by whole genome amplification, mixtures of normal and tumor cells, experimental noise or other technical limitations. Detection of copy number aberrations (CNA) using single nucleotide polymorphism (SNP) array data or Array comparative genomic hybridization (CGH) data is becoming important in disease pathogenesis analysis [16]. It is nontrivial to detect the CNA automatically because the signals obtained from high density SNP arrays often have low SNR values, which may be caused by whole genome amplification, mixture of normal and tumor cells, experimental noise and other technical limitations. More sophisticated statistical models are needed urgently to make the CNAs detection robust and reliable using the signals with low SNR, a number of software packages have been developed for the BioMed Central bution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited
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