Evidence map›Paper›PMID 19286833›Full record

ArticleBioinformatics (Oxford, England)2009

Statistical detection of cooperative transcription factors with similarity adjustment.

Utz J Pape, Holger Klein, Martin Vingron

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Structure-aided prediction of mammalian transcription factor complexes in conserved non-coding elements.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2013
    Article
  3. Article
  4. Article
  5. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Utz J PapeComputational Molecular Biology, Max Planck Institute for Molecular Genetics, Ihnestr. 73 and Mathematics and Computer Science, Free University of Berlin, Takustr. 9, 14195 Berlin, Germany. utz.pape@molgen.mpg.de
Holger Klein
Martin Vingron

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationStatistical assessment of cis-regulatory modules (CRMs) is a crucial task in computational biology. Usually, one concludes from exceptional co-occurrences of DNA motifs that the corresponding transcription factors (TFs) are cooperative. However, similar DNA motifs tend to co-occur in random sequences due to high probability of overlapping occurrences. Therefore, it is important to consider similarity of DNA motifs in the statistical assessment.

resultsBased on previous work, we propose to adjust the window size for co-occurrence detection. Using the derived approximation, one obtains different window sizes for different sets of DNA motifs depending on their similarities. This ensures that the probability of co-occurrences in random sequences are equal. Applying the approach to selected similar and dissimilar DNA motifs from human TFs shows the necessity of adjustment and confirms the accuracy of the approximation by comparison to simulated data. Furthermore, it becomes clear that approaches ignoring similarities strongly underestimate P-values for cooperativity of TFs with similar DNA motifs. In addition, the approach is extended to deal with overlapping windows. We derive Chen-Stein error bounds for the approximation. Comparing the error bounds for similar and dissimilar DNA motifs shows that the approximation for similar DNA motifs yields large bounds. Hence, one has to be careful using overlapping windows. Based on the error bounds, one can precompute the approximation errors and select an appropriate overlap scheme before running the analysis. AVAILABILITY: Software to perform the calculation for pairs of position frequency matrices (PFMs) is available at http://mosta.molgen.mpg.de as well as C++ source code for downloading.

Indexed as

AlgorithmsSequence Analysis, DNAComputational BiologyDNASequence AlignmentTranscription FactorsDNATranscription Factors

Identifiers

PMID19286833
PMCPMC2722994

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.