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A Parameterized Algorithm for Predicting Transcription Factor Binding Sites

机译:一种预测转录因子绑定站点的参数化算法

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In this paper, we study the Transcription Factor Binding Sites (TFBS) prediction problem in bioinformatics. We develop a novel parameterized approach that can efficiently explore the space of all possible locations of TFBSs in a set of homologous sequences with high accuracy. The exploration is performed by an ensemble of a few Hidden Markov Models (HMM), where the size of the ensemble is the parameter of the algorithm. The ensemble is initially constructed through the local alignments between two sequences that have the lowest similarity value in the sequence set, the parameters of each HMM in the ensemble are revised when the remaining sequences in the set are scanned through by it one by one. A list of possible TFBSs are generated when all sequences in the set have been processed by the ensemble. Testing results showed that this approach can accurately handle the cases where a single sequence may contain multiple binding sites and thus has advantages over most of the existing approaches when a sequence may contain multiple binding sites.
机译:在本文中,我们研究生物信息学中的转录因子结合位点(TFBS)预测问题。我们开发了一种新颖的参数化方法,可以高精度地高精度地探索一组同源序列中所有可能位置的所有可能位置的空间。探索由一些隐藏的马尔可夫模型(HMM)的集合来执行,其中集合的大小是算法的参数。最初通过在序列集中具有最低相似性值的两个序列之间的局部对齐构成集合,当通过它一个接一个地扫描集合中的剩余序列时,在集合中的每个HMM中的参数被修改。当集合已处理集中的所有序列时,会生成可能的TFBS列表。测试结果表明,这种方法可以准确地处理单个序列可以含有多个结合位点的情况,因此当序列可能含有多个绑定站点时,具有大多数现有方法的优点。

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