Evidence map›Paper›PMID 25486472›Full record

ReviewCell cycle (Georgetown, Tex.)2014

Role of ChIP-seq in the discovery of transcription factor binding sites, differential gene regulation mechanism, epigenetic marks and beyond.

Rasika Mundade, Hatice Gulcin Ozer, Han Wei, Lakshmi Prabhu, Tao Lu

Abstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing 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

85 citing papers in PubMed.

  1. Article
  2. UnlockingNAR genomics and bioinformatics · 2026
    Article
  3. Article
  4. Review
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  15. Article
  16. A review of post-GWAS studies in schizophrenia.Translational psychiatry · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. Article

25 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.

Rasika Mundadea Department of Pharmacology and Toxicology ; Indiana University School of Medicine ; Indianapolis , IN USA.
Hatice Gulcin Ozer
Han Wei
Lakshmi Prabhu
Tao Lu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many biologically significant processes, such as cell differentiation and cell cycle progression, gene transcription and DNA replication, chromosome stability and epigenetic silencing etc. depend on the crucial interactions between cellular proteins and DNA. Chromatin immunoprecipitation (ChIP) is an important experimental technique for studying interactions between specific proteins and DNA in the cell and determining their localization on a specific genomic locus. In recent years, the combination of ChIP with second generation DNA-sequencing technology (ChIP-seq) allows precise genomic functional assay. This review addresses the important applications of ChIP-seq with an emphasis on its role in genome-wide mapping of transcription factor binding sites, the revelation of underlying molecular mechanisms of differential gene regulation that are governed by specific transcription factors, and the identification of epigenetic marks. Furthermore, we also describe the ChIP-seq data analysis workflow and a perspective for the exciting potential advancement of ChIP-seq technology in the future.

Indexed as

Epigenesis, GeneticGene Expression ProfilingSequence Analysis, DNABinding SitesChromatin ImmunoprecipitationHistonesHumansTranscription FactorsHistonesTranscription Factorsandrogen receptor; BWAARBurrows-Wheeler aligner; C. elegansCaenorhabditis elegans; ChIPChIP-seq processing pipeline; STATChIP sequencing; DNAchromatinchromatin immunoprecipitation; CRschromatin regulators; ChIP-seqc-Jun NH2-terminal kinase; Kdeoxyribonuclease; EMSAdeoxyribonucleic acid; DNaseelectrophoresis mobility shift assay; ENCODEencyclopedia of DNA elements; FDRfalse discovery rate; GRglucocorticoid receptor; HDAChaematopoietic stem progenitor cells; HMhigh throughputhigh throughput ChIP; IL-βhistone deacetylase; HEKhistone modification; HTChIPhuman embryonic kidney; HSPCsimmunoprecipitationinterferon; JNKinterleukin β; IFNlysine; MACSmodel-based analysis of ChIP-seq; MEMEModel Organism ENCyclopedia Of DNA Elements; NF-κBmultiple Em for motif elicitation; modENCODEnuclear factor κB; PCRpolymerase chain reaction; RNAribonucleic acid; R-ChIProbotic ChIP; SNPsequencingshort oligonucleotide alignment program; SPPsignal transducers and activators of transcription; SUMOsingle nucleotide polymorphism; SOAPsmall ubiquitin-like modifier; TFstranscription factor binding sites; TSStranscription factors; TFBStranscription start site; UCSCultraviolet.University of California Santa Cruz; UV

Identifiers

PMID25486472
PMCPMC4614920

What OpenQuestion holds

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LicenceCC BY-NC
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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.