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Statistical detection of cooperative transcription factors with similarity adjustment

机译:具有相似性调节的合作转录因子的统计检测

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摘要

>Motivation: Statistical assessment of cis-regulatory modules (CRMs) is a crucial task in computational biology. Usually, one concludes from exceptional co-occurrences of DNA motifs that the corresponding transcription factors (TFs) are cooperative. However, similar DNA motifs tend to co-occur in random sequences due to high probability of overlapping occurrences. Therefore, it is important to consider similarity of DNA motifs in the statistical assessment.>Results: Based on previous work, we propose to adjust the window size for co-occurrence detection. Using the derived approximation, one obtains different window sizes for different sets of DNA motifs depending on their similarities. This ensures that the probability of co-occurrences in random sequences are equal. Applying the approach to selected similar and dissimilar DNA motifs from human TFs shows the necessity of adjustment and confirms the accuracy of the approximation by comparison to simulated data. Furthermore, it becomes clear that approaches ignoring similarities strongly underestimate P-values for cooperativity of TFs with similar DNA motifs. In addition, the approach is extended to deal with overlapping windows. We derive Chen–Stein error bounds for the approximation. Comparing the error bounds for similar and dissimilar DNA motifs shows that the approximation for similar DNA motifs yields large bounds. Hence, one has to be careful using overlapping windows. Based on the error bounds, one can precompute the approximation errors and select an appropriate overlap scheme before running the analysis.>Availability: Software to perform the calculation for pairs of position frequency matrices (PFMs) is available at as well as C++ source code for downloading.>Contact:
机译:>动机:对顺式调节模块(CRM)的统计评估是计算生物学中的关键任务。通常,从DNA基序的异常同时出现可以得出结论,相应的转录因子(TF)是协同的。但是,由于发生重叠的可能性很高,相似的DNA基序倾向于随机出现在随机序列中。因此,在统计评估中考虑DNA基序的相似性很重要。>结果:在先前的工作基础上,我们建议调整窗口大小以进行共现检测。使用推导的近似值,可以根据不同的DNA基序集获得相似的窗口大小。这确保了随机序列中同时出现的概率相等。将这种方法应用于人类TF中选定的相似和不相似的DNA图案表明了调整的必要性,并通过与模拟数据进行比较证实了逼近的准确性。此外,很明显,忽略相似性的方法大大低估了具有相似DNA基序的TF协同作用的P值。另外,该方法被扩展为处理重叠的窗口。我们得出近似的Chen-Stein误差范围。比较相似和不相似的DNA基序的错误界限显示,相似的DNA基序的近似值会产生较大的界限。因此,必须小心使用重叠的窗口。根据误差范围,可以在运行分析之前预先计算近似误差并选择适当的重叠方案。>可用性:可在以下位置获得用于对位置频率矩阵(PFM)进行计算的软件:以及用于下载的C ++源代码。>联系方式:

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