ArticleBioinformatics (Oxford, England)2009
M are better than one: an ensemble-based motif finder and its application to regulatory element prediction.
Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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5 citing papers in PubMed, 24 citations in OpenAlex.
- Identification of large disjoint motifs in biological networks.BMC bioinformatics · 2016Article
- LASAGNA: a novel algorithm for transcription factor binding site alignment.BMC bioinformatics · 2013Article
- Searching for transcription factor binding sites in vector spaces.BMC bioinformatics · 2012Article
- PROSPER: an integrated feature-based tool for predicting protease substrate cleavage sites.PloS one · 2012Article
- Mechanisms and evolution of control logic in prokaryotic transcriptional regulation.Microbiology and molecular biology reviews : MMBR · 2009Review
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3 authors at 1 institution in 1 country.
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Abstract
motivationIdentifying regulatory elements in genomic sequences is a key component in understanding the control of gene expression. Computationally, this problem is often addressed by motif discovery, where the goal is to find a set of mutually similar subsequences within a collection of input sequences. Though motif discovery is widely studied and many approaches to it have been suggested, it remains a challenging and as yet unresolved problem.
resultsWe introduce SAMF (Solution-Aggregating Motif Finder), a novel approach for motif discovery. SAMF is based on a Markov Random Field formulation, and its key idea is to uncover and aggregate multiple statistically significant solutions to the given motif finding problem. In contrast to many earlier methods, SAMF does not require prior estimates on the number of motif instances present in the data, is not limited by motif length, and allows motifs to overlap. Though SAMF is broadly applicable, these features make it particularly well suited for addressing the challenges of prokaryotic regulatory element detection. We test SAMF's ability to find transcription factor binding sites in an Escherichia coli dataset and show that it outperforms previous methods. Additionally, we uncover a number of previously unidentified binding sites in this data, and provide evidence that they correspond to actual regulatory elements. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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