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Similarity Analysis between Transcription Factor Binding Sites by Bayesian Hypothesis Test

机译:贝叶斯假设检验分析转录因子结合位点之间的相似性

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摘要

Transcription factor binding sites (TFBS) in promoter sequences of higher eu-karyotes are commonly modeled using position frequency matrices (PFM). The ability to compare PFMs representing binding sites is especially important for de novo sequence motif discovery, where it is desirable to compare putative matrices to one another and to known matrices. We propose to identify and group similar profiles using Bayesian hypothesis test between PFMs, describing a column-by-column method for PFM similarity quantification based on Bayes factor and posterior probability of null model that aligned columns are independent and identically distributed observation from the same multinomial distribution. We group TFBS frequency matrices from less redundant JASPAR into matrix families by cluster analysis according to Bayes factors and posterior probability of similar PFMs. Clusters of highly similar matrices are identified. We further compare the performance of this method to Pearson £ test on simulated data. The proposed method is very simple, easily implemented and outperforms the other method in our test. Taking Pearson product moment correlation coefficient as an objective criterion of the performance, results indicate that Bayesian test performs better than the classical methods on average.
机译:通常使用位置频率矩阵(PFM)来模拟高等真核生物的启动子序列中的转录因子结合位点(TFBS)。比较代表结合位点的PFM的能力对于从头序列基序发现特别重要,在这种情况下,希望将推定的矩阵相互比较以及与已知的矩阵进行比较。我们建议使用PFM之间的贝叶斯假设检验来识别相似的轮廓并将其分组,描述一种基于Bayes因子和空模型的后验概率的逐列方法进行PFM相似性量化,即对齐的列是独立的且来自相同多项式的分布均匀的观测值分配。我们根据贝叶斯因素和类似PFM的后验概率,通过聚类分析将TFBS频率矩阵从冗余度较低的JASPAR划分为矩阵族。确定高度相似的矩阵簇。我们进一步将该方法的性能与模拟数据上的Pearson£测试进行比较。所提出的方法非常简单,易于实现,并且在我们的测试中优于其他方法。以皮尔逊乘积矩相关系数作为性能的客观标准,结果表明贝叶斯测试的平均性能优于经典方法。

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