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MotifMap: a human genome-wide map of candidate regulatory motif sites

机译:MotifMap:候选调控基序位点的全人类基因组图

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摘要

>Motivation: Achieving a comprehensive map of all the regulatory elements encoded in the human genome is a fundamental challenge of biomedical research. So far, only a small fraction of the regulatory elements have been characterized, and there is great interest in applying computational techniques to systematically discover these elements. Such efforts, however, have been significantly hindered by the overwhelming size of non-coding DNA regions and the statistical variability and complex spatial organizations of mammalian regulatory elements.>Results: Here we combine information from multiple mammalian genomes to derive the first fairly comprehensive map of regulatory elements in the human genome. We develop a procedure for identifying regulatory sites, with high levels of conservation across different species, using a new scoring scheme, the Bayesian branch length score (BBLS). Using BBLS, we predict 1.5 million regulatory sites, corresponding to 380 known regulatory motifs, with an estimated false discovery rate (FDR) of <50%. We demonstrate that the method is particularly effective for 155 motifs, for which 121 056 sites can be mapped with an estimated FDR of <10%. Over 28K SNPs are located in regions overlapping the 1.5 million predicted motif sites, suggesting potential functional implications for these SNPs. We have deposited these elements in a database and created a user-friendly web server for the retrieval, analysis and visualization of these elements. The initial map provides a systematic view of gene regulation in the genome, which will be refined as additional motifs become available.>Availability: >Contact: ; >Supplementary information: are available at Bioinformatics online.
机译:>动机:获得人类基因组中编码的所有调控元件的全面图谱是生物医学研究的一项基本挑战。迄今为止,仅对一小部分的监管要素进行了特征描述,人们非常关注应用计算技术来系统地发现这些要素。但是,由于非编码DNA区域的巨大规模以及哺乳动物调节元件的统计变异性和复杂的空间组织,这些工作受到了严重阻碍。>结果:在这里,我们将来自多个哺乳动物基因组的信息结合在一起得出人类基因组中第一个相当全面的调控元件图。我们使用贝叶斯分支长度评分(BBLS)这一新的评分方案,开发了一种程序,用于识别具有较高保护水平的不同物种的调控位点。使用BBLS,我们可以预测150万个调控位点,对应于380个已知的调控基序,估计的错误发现率(FDR)<50%。我们证明了该方法对于155个图案特别有效,可以针对121个056个位点进行映射,估计FDR <10%。超过28K的SNP位于与150万个预测的基序位点重叠的区域,表明这些SNP具有潜在的功能含义。我们已经将这些元素存储在数据库中,并创建了一个用户友好的Web服务器来检索,分析和可视化这些元素。初始图谱提供了基因组中基因调控的系统视图,将随着其他基序的出现而得到完善。>可用性: >联系方式:; >补充信息:可在线访问生物信息学。

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