Evidence map›Paper›PMID 23090257›Full record

ReviewNature reviews. Genetics2012

ChIP-seq and beyond: new and improved methodologies to detect and characterize protein-DNA interactions.

Terrence S Furey

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 394 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
394citing papers in PubMed, 3 pooled it
27.4field-weighted citation impact, top 1% of its field
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

394 citing papers in PubMed, 3 syntheses or guidelines pooled it, 862 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Inferring Gene Regulatory Networks in Stem Cells: Methods and Applications.Methods in molecular biology (Clifton, N.J.) · 2027
    Review
  5. Decoding chromosome organization using proximity labeling and long-read sequencing.Journal of genetics and genomics = Yi chuan xue bao · 2026
    Article
  6. Article
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  11. Functional Genomics Studies of Psychiatric Disorders in Individuals of Latin American Populations: A Scoping Review.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2026
    Article
  12. Probing transcription factor subsets in gene regulatory networks.Algorithms for molecular biology : AMB · 2026
    Article
  13. Review
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  20. A rapid test for protein-DNA interactions.Nucleic acids research · 2026
    Article

334 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

1 author at 1 institution in 1 country.

Terrence S FureyDepartment of Genetics, Carolina Center for Genome Sciences, Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, 120 Mason Farm Road, CB#7264, Chapel Hill, North Carolina 27599, USA. tsfurey@email.unc.edu
University of North Carolina at Chapel Hill · US

Funding

Comprehensive Identification of Active Functional Elements in Human ChromatinU54HG004563 · NHGRI · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E · 2007 to 2011
$9.7M
Validation of prognostic and pathway signatures in lethal prostate cancerU01CA157703 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GLEAVE, MARTIN EDWIN, HALABI, SUSAN · 2011 to 2015
$2.5M
Identifying disease-related functional regulatory variants in open chromatinR21DA027040 · NIDA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOHLKE, KAREN L. · 2009 to 2010
$936k
NCI NIH HHS U01 CA157703NHGRI NIH HHS U54 HG004563NHGRI NIH HHS U54‑HG004563NIDA NIH HHS R21 DA027040NIDA NIH HHS R21‑DA027040
6 · The paper itself

Abstract

Chromatin immunoprecipitation experiments followed by sequencing (ChIP-seq) detect protein-DNA binding events and chemical modifications of histone proteins. Challenges in the standard ChIP-seq protocol have motivated recent enhancements in this approach, such as reducing the number of cells that are required and increasing the resolution. Complementary experimental approaches - for example, DNaseI hypersensitive site mapping and analysis of chromatin interactions that are mediated by particular proteins - provide additional information about DNA-binding proteins and their function. These data are now being used to identify variability in the functions of DNA-binding proteins across genomes and individuals. In this Review, I describe the latest advances in methods to detect and functionally characterize DNA-bound proteins.

Indexed as

AnimalsBinding SitesChromatinChromatin ImmunoprecipitationDNADNA-Binding ProteinsDNA FootprintingHistonesHumansProtein BindingSequence Analysis, DNASequence Tagged SitesChromatinDNADNA-Binding ProteinsHistones

Identifiers

PMID23090257
PMCPMC3591838
OpenAlexW2092988184

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.