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首页> 外文期刊>BMC Medical Genomics >A novel SNP analysis method to detect copy number alterations with an unbiased reference signal directly from tumor samples
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A novel SNP analysis method to detect copy number alterations with an unbiased reference signal directly from tumor samples

机译:直接从肿瘤样品中以无偏参考信号检测拷贝数变化的新型SNP分析方法

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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 technology have improved detection of copy number alterations, the increase in the number of measured signals, noise from array probes, variations in signal-to-noise ratio across batches and disparity across laboratories leads to significant limitations for the accurate identification of CNA regions when comparing tumor and normal samples. Methods To address these limitations, we designed a novel "Virtual Normal" algorithm (VN), which allowed for construction of an unbiased reference signal directly from test samples within an experiment using any publicly available normal reference set as a baseline thus eliminating the need for an in-lab normal reference set. Results The algorithm was tested using an optimal, paired tumorormal data set as well as previously uncharacterized pediatric malignant gliomas for which a normal reference set was not available. Using Affymetrix 250K Sty microarrays, we demonstrated improved signal-to-noise ratio and detected significant copy number alterations using the VN algorithm that were validated by independent PCR analysis of the target CNA regions. Conclusions We developed and validated an algorithm to provide a virtual normal reference signal directly from tumor samples and minimize noise in the derivation of the raw CN signal. The algorithm reduces the variability of assays performed across different reagent and array batches, methods of sample preservation, multiple personnel, and among different laboratories. This approach may be valuable when matched normal samples are unavailable or the paired normal specimens have been subjected to variations in methods of preservation.
机译:背景技术癌症中的基因组不稳定会导致异常的基因组拷贝数改变(CNA),这是肿瘤发生的基础机制。使用微阵列和其他技术,通过将肿瘤样品CN与正常参考样品CN进行比较来检测肿瘤CNA。尽管微阵列技术的进步改善了对拷贝数变化的检测,但测量信号数量的增加,阵列探针产生的噪声,批次间信噪比的变化以及实验室间的差异导致对准确鉴定DNA的重大限制。比较肿瘤样本和正常样本时的CNA区域。方法为了解决这些局限性,我们设计了一种新颖的“虚拟正常”算法(VN),该算法可使用任何公开可用的正常参考集作为基准,直接从实验中的测试样品中构建无偏参考信号,从而消除了对实验室内正常参考集。结果使用最佳配对肿瘤/正常数据集以及以前没有特征的儿科恶性神经胶质瘤(没有正常参考集)对算法进行了测试。使用Affymetrix 250K Sty微阵列,我们展示了改进的信噪比,并使用VN算法检测到显着的拷贝数变化,这些变化已通过对目标CNA区的独立PCR分析进行了验证。结论我们开发并验证了一种算法,可以直接从肿瘤样本中提供虚拟的正常参考信号,并最大程度地减少原始CN信号的噪声。该算法减少了在不同试剂和阵列批次,样品保存方法,多名人员以及不同实验室之间进行的测定的可变性。当无法获得匹配的正常样本或配对的正常样本的保存方法有所不同时,这种方法可能会很有价值。

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