Evidence map›Paper›PMID 20056654›Full record

ArticleNucleic acids research2010

On the detection and refinement of transcription factor binding sites using ChIP-Seq data.

Ming Hu, Jindan Yu, Jeremy M G Taylor, Arul M Chinnaiyan, Zhaohui S Qin

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing 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

64 citing papers in PubMed.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. Review
  8. Set cover-based methods for motif selection.Bioinformatics (Oxford, England) · 2020
    Article
  9. Article
  10. Article
  11. FisherMP: fully parallel algorithm for detecting combinatorial motifs from large ChIP-seq datasets.DNA research : an international journal for rapid publication of reports on genes and genomes · 2019
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

4 more citing papers are in PubMed but not listed here.

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

5 authors.

Ming HuCenter for Statistical Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA.
Jindan Yu
Jeremy M G Taylor
Arul M Chinnaiyan
Zhaohui S Qin

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
VACCINIA PSA FOR ANDROGEN-MODULATED POST-SURGICAL RECURRENCE OF PROSTATE CANCERP50CA069568 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COONEY, KATHLEEN A · 1995 to 2013
$31.3M
Epitomic Biomarkers of Prostate CancerU01CA111275 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, RUBIN, MARK A. · 2004 to 2015
$6.8M
Model-Based Methods for Analyzing ChIP Sequencing DataR01HG005119 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI QIN, ZHAOHUI · 2009 to 2012
$1.2M
Statistical Methods for the Analysis of Microarray DataR01GM072007 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GHOSH, DEBASHIS · 2004 to 2008
$1.1M
The Role of beta-adrenergic Signaling in Prostate CancerK99CA129565 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YU, JINDAN · 2008 to 2009
$310k
Howard Hughes Medical InstituteNCI NIH HHS K99 CA129565NCI NIH HHS K99CA129565NCI NIH HHS P30 CA046592NCI NIH HHS P30CA46592NCI NIH HHS P30CA69568NCI NIH HHS P50 CA069568NCI NIH HHS U01 CA111275NCI NIH HHS U01CA111275NHGRI NIH HHS R01 HG005119NHGRI NIH HHS R01HG005119NIGMS NIH HHS R01 GM072007NIGMS NIH HHS R01GM72007Wellcome Trust
6 · The paper itself

Abstract

Coupling chromatin immunoprecipitation (ChIP) with recently developed massively parallel sequencing technologies has enabled genome-wide detection of protein-DNA interactions with unprecedented sensitivity and specificity. This new technology, ChIP-Seq, presents opportunities for in-depth analysis of transcription regulation. In this study, we explore the value of using ChIP-Seq data to better detect and refine transcription factor binding sites (TFBS). We introduce a novel computational algorithm named Hybrid Motif Sampler (HMS), specifically designed for TFBS motif discovery in ChIP-Seq data. We propose a Bayesian model that incorporates sequencing depth information to aid motif identification. Our model also allows intra-motif dependency to describe more accurately the underlying motif pattern. Our algorithm combines stochastic sampling and deterministic 'greedy' search steps into a novel hybrid iterative scheme. This combination accelerates the computation process. Simulation studies demonstrate favorable performance of HMS compared to other existing methods. When applying HMS to real ChIP-Seq datasets, we find that (i) the accuracy of existing TFBS motif patterns can be significantly improved; and (ii) there is significant intra-motif dependency inside all the TFBS motifs we tested; modeling these dependencies further improves the accuracy of these TFBS motif patterns. These findings may offer new biological insights into the mechanisms of transcription factor regulation.

Indexed as

AlgorithmsSequence Analysis, DNAAmino Acid MotifsBayes TheoremBinding SitesChromatin ImmunoprecipitationComputational BiologyComputer SimulationTranscription FactorsTranscription Factors

Identifiers

PMID20056654
PMCPMC2853110

What OpenQuestion holds

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Registered trials

None linked

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.