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首页> 外文期刊>British Journal of Cancer >Balancing false positives and false negatives for the detection of differential expression in malignancies
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Balancing false positives and false negatives for the detection of differential expression in malignancies

机译:平衡假阳性和假阴性以检测恶性肿瘤中的差异表达

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A basic problem of microarray data analysis is to identify genes whose expression is affected by the distinction between malignancies with different properties. These genes are said to be differentially expressed. Differential expression can be detected by selecting the genes with P-values (derived using an appropriate hypothesis test) below a certain rejection level. This selection, however, is not possible without accepting some false positives and negatives since the two sets of P-values, associated with the genes whose expression is and is not affected by the distinction between the different malignancies, overlap. We describe a procedure for the study of differential expression in microarray data based on receiver-operating characteristic curves. This approach can be useful to select a rejection level that balances the number of false positives and negatives and to assess the degree of overlap between the two sets of P-values. Since this degree of overlap characterises the balance that can be reached between the number of false positives and negatives, this quantity can be seen as a quality measure of microarray data with respect to the detection of differential expression. As an example, we apply our method to data sets studying acute leukaemia.
机译:微阵列数据分析的基本问题是鉴定其表达受具有不同特性的恶性肿瘤之间的区别影响的基因。据说这些基因是差异表达的。可以通过选择P值(使用适当的假设检验得出)低于特定排斥水平的基因来检测差异表达。但是,如果不接受一些假阳性和阴性,就不可能进行这种选择,因为与表达受不同恶性肿瘤区别影响且不受其影响的基因相关的两组P值重叠。我们描述了一种基于接收者操作特征曲线研究微阵列数据中差异表达的程序。该方法对于选择平衡假阳性和阴性数的拒绝水平以及评估两组P值之间的重叠程度很有用。由于这种重叠程度表征了假阳性和阴性数量之间可以达到的平衡,因此该数量可以看作是微阵列数据相对于差异表达检测的质量度量。例如,我们将我们的方法应用于研究急性白血病的数据集。

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