Evidence map›Paper›PMID 22228832›Full record

ArticleNucleic acids research2012

A highly efficient and effective motif discovery method for ChIP-seq/ChIP-chip data using positional information.

Xiaotu Ma, Ashwinikumar Kulkarni, Zhihua Zhang, Zhenyu Xuan, Robert Serfling, Michael Q Zhang

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Article
  2. Bioinformatics Approaches in Noncoding RNAs Research.Experientia supplementum (2012) · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. A survey on deep learning in DNA/RNA motif mining.Briefings in bioinformatics · 2021
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Computational methodology for ChIP-seq analysis.Quantitative biology (Beijing, China) · 2013
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Xiaotu MaDepartment of Molecular and Cell Biology, Center for Systems Biology, University of Texas at Dallas, 800 W. Campbell Road, Richardson, TX 75080, USA.
Ashwinikumar Kulkarni
Zhihua Zhang
Zhenyu Xuan
Robert Serfling
Michael Q Zhang

Funding

PROTEIN CODING GENES IN THE HUMAN GENOMER01HG001696 · NHGRI · UNIVERSITY OF TEXAS DALLAS · PI ZHANG, MICHAEL Q · 1997 to 2010
$5.1M
NHGRI NIH HHS HG001696
6 · The paper itself

Abstract

Identification of DNA motifs from ChIP-seq/ChIP-chip [chromatin immunoprecipitation (ChIP)] data is a powerful method for understanding the transcriptional regulatory network. However, most established methods are designed for small sample sizes and are inefficient for ChIP data. Here we propose a new k-mer occurrence model to reflect the fact that functional DNA k-mers often cluster around ChIP peak summits. With this model, we introduced a new measure to discover functional k-mers. Using simulation, we demonstrated that our method is more robust against noises in ChIP data than available methods. A novel word clustering method is also implemented to group similar k-mers into position weight matrices (PWMs). Our method was applied to a diverse set of ChIP experiments to demonstrate its high sensitivity and specificity. Importantly, our method is much faster than several other methods for large sample sizes. Thus, we have developed an efficient and effective motif discovery method for ChIP experiments.

Indexed as

Chromatin ImmunoprecipitationRegulatory Elements, TranscriptionalSoftwareAlgorithmsAnimalsBinding SitesCCCTC-Binding FactorCluster AnalysisComputer SimulationDrosophila melanogasterEmbryonic Stem CellsGene Regulatory NetworksHigh-Throughput Nucleotide SequencingMiceNucleotide MotifsOligonucleotide Array Sequence AnalysisCCCTC-Binding FactorCtcf protein, mouseRepressor ProteinsTranscription Factors

Identifiers

PMID22228832
PMCPMC3326300

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Registered trials

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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.