用于检测DNA调控位点的微妙基序发现

M. Comin, L. Parida
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引用次数: 9

摘要

我们解决了检测共识母题的问题,这些母题发生在多个序列的微妙变化中。这些通常是DNA序列中的功能域,如转录结合因子或其他调节位点。这个问题的普遍性一直被认为是困难的,各种基准数据可以作为不同计算方法的试金石。我们提出了一种以无监督组合模式发现为中心的方法。参数是通过对共识母题进行仔细的统计分析来选择的。该方法在基准数据上工作得很好,并且足够通用,可以扩展到共识基元中的变化包括索引(以及突变)的场景。我们还介绍了在人类DNA序列中检测转录结合因子的一些结果。可用性:该系统将在www.research.ibm.com/computationalgenomics上提供。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subtle Motif Discovery for Detection of DNA Regulatory Sites
We address the problem of detecting consensus motifs, that occur with subtle variations, across multiple sequences. These are usually functional domains in DNA sequences such as transcriptional binding factors or other regulatory sites. The problem in its generality has been considered difficult and various benchmark data serve as the litmus test for different computational methods. We present a method centered around unsupervised combinatorial pattern discovery. The parameters are chosen using a careful statistical analysis of consensus motifs. This method works well on the benchmark data and is general enough to be extended to a scenario where the variation in the consensus motif includes indels (along with mutations). We also present some results on detection of transcription binding factors in human DNA sequences. Availability: The system will be made available at www.research.ibm.com/computationalgenomics.
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