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An integrated toolkit for accurate prediction and analysis of cis-regulatory motifs at a genome scale

机译:用于在基因组规模上准确预测和分析顺式调控基序的集成工具包

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Motivation: We present an integrated toolkit, BoBro2.0, for prediction and analysis of cis-regulatory motifs. This toolkit can (i) reliably identify statistically significant cis-regulatory motifs at a genome scale; (ii) accurately scan for all motif instances of a query motif in specified genomic regions using a novel method for P-value estimation; (iii) provide highly reliable comparisons and clustering of identified motifs, which takes into consideration the weak signals from the flanking regions of the motifs; and (iv) analyze co-occurring motifs in the regulatory regions. Results: We have carried out systematic comparisons between motif predictions using BoBro2.0 and the MEME package. The comparison results on Escherichia coli K12 genome and the human genome show that BoBro2.0 can identify the statistically significant motifs at a genome scale more efficiently, identify motif instances more accurately and get more reliable motif clusters than MEME. In addition, BoBro2.0 provides correlational analyses among the identified motifs to facilitate the inference of joint regulation relationships of transcription factors.
机译:动机:我们提供了一个集成工具包BoBro2.0,用于预测和分析顺式调控基序。该工具包可以(i)在基因组规模上可靠地识别具有统计学意义的顺式调控基序; (ii)使用一种新颖的P值估计方法,准确扫描指定基因组区域中查询主题的所有主题实例; (iii)提供高度可靠的比较和已识别主题的聚类,其中考虑了来自主题两侧区域的微弱信号; (iv)分析调节区域中的共现基序。结果:我们已经使用BoBro2.0和MEME软件包对模体预测进行了系统的比较。在大肠杆菌K12基因组和人类基因组上的比较结果表明,与MEME相比,BoBro2.0可以更有效地在基因组规模上识别具有统计学意义的基序,更准确地识别基序实例,并获得更可靠的基序簇。此外,BoBro2.0还提供了已识别基序之间的相关分析,以帮助推断转录因子的联合调控关系。

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