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Pscan:在共调控或共表达基因的序列中寻找过度富集的转录因子结合位点基序。

Pscan: finding over-represented transcription factor binding site motifs in sequences from co-regulated or co-expressed genes.

作者信息

Zambelli Federico, Pesole Graziano, Pavesi Giulio

机构信息

Dipartimento di Scienze Biomolecolari e Biotecnologie, University of Milan, Milan, Italy.

出版信息

Nucleic Acids Res. 2009 Jul;37(Web Server issue):W247-52. doi: 10.1093/nar/gkp464. Epub 2009 May 31.

Abstract

The first step in gene expression, transcription, is modulated by the interaction of transcription factors with their corresponding binding sites on the DNA sequence. Pscan is a software tool that scans a set of sequences (e.g. promoters) from co-regulated or co-expressed genes with motifs describing the binding specificity of known transcription factors and assesses which motifs are significantly over- or under-represented, providing thus hints on which transcription factors could be common regulators of the genes studied, together with the location of their candidate binding sites in the sequences. Pscan does not resort to comparisons with orthologous sequences and experimental results show that it compares favorably to other tools for the same task in terms of false positive predictions and computation time. The website is free and open to all users and there is no login requirement. Address: http://www.beaconlab.it/pscan.

摘要

基因表达的第一步即转录,是由转录因子与其在DNA序列上相应的结合位点之间的相互作用所调控的。Pscan是一种软件工具,它用描述已知转录因子结合特异性的基序来扫描一组来自共调控或共表达基因的序列(如启动子),并评估哪些基序显著富集或缺失,从而提示哪些转录因子可能是所研究基因的共同调控因子,以及它们在序列中的候选结合位点位置。Pscan并不依赖于与直系同源序列的比较,实验结果表明,在错误阳性预测和计算时间方面,它与执行相同任务的其他工具相比具有优势。该网站免费向所有用户开放,无需登录。网址:http://www.beaconlab.it/pscan

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d5f/2703934/37cf956625dc/gkp464f1.jpg

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