Motif discovery and transcription factor binding sites before and after the next-generation sequencing era

101Citations
Citations of this article
304Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Motif discovery has been one of the most widely studied problems in bioinformatics ever since genomic and protein sequences have been available. In particular, its application to the de novo prediction of putative over-represented transcription factor binding sites in nucleotide sequences has been, and still is, one of the most challenging flavors of the problem. Recently, novel experimental techniques like chromatin immunoprecipitation (ChIP) have been introduced, permitting the genome-wide identification of protein-DNA interactions. ChIP, applied to transcription factors and coupled with genome tiling arrays (ChIP on Chip) or next-generation sequencing technologies (ChIP-Seq) has opened new avenues in research, as well as posed new challenges to bioinformaticians developing algorithms and methods for motif discovery. © The Author(s) 2012. Published by Oxford University Press.

Cite

CITATION STYLE

APA

Zambelli, F., Pesole, G., & Pavesi, G. (2013). Motif discovery and transcription factor binding sites before and after the next-generation sequencing era. Briefings in Bioinformatics, 14(2), 225–237. https://doi.org/10.1093/bib/bbs016

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free