Evidence map›Paper›PMID 22950368›Full record

ArticleGenome biology2012

Modeling gene expression using chromatin features in various cellular contexts.

Xianjun Dong, Melissa C Greven, Anshul Kundaje, Sarah Djebali, James B Brown, Chao Cheng, Thomas R Gingeras, Mark Gerstein, Roderic Guigó, Ewan Birney and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 143 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
143citing papers in PubMed, 1 pooled it
13.0field-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

143 citing papers in PubMed, 1 synthesis or guideline pooled it, 295 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. GECSI: Large-scale chromatin state imputation from gene expression.bioRxiv : the preprint server for biology · 2025
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  5. Towards universal modeling of transcript isoform expression levels.bioRxiv : the preprint server for biology · 2025
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  15. Summary of ChIP-Seq Methods and Description of an Optimized ChIP-Seq Protocol.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Long-read genome assemblies reveal aZoological research · 2023
    Article
  20. Article

83 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

11 authors at 8 institutions in 3 countries.

Xianjun DongProgram in Bioinformatics and Integrative Biology, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Melissa C Greven
Anshul Kundaje
Sarah Djebali
James B Brown
Chao Cheng
Thomas R Gingeras
Mark Gerstein
Roderic Guigó
Ewan Birney
Zhiping Weng
University of Massachusetts Chan Medical School · USCentre for Genomic Regulation · ESCold Spring Harbor Laboratory · USEuropean Bioinformatics Institute · GBStanford University · USUniversity of California, Berkeley · USWhitney Museum of American Art · USYale University · US

Funding

EDAC: ENCODE Data Analysis CenterU01HG004695 · NHGRI · EUROPEAN MOLECULAR BIOLOGY LABORATORY · PI BIRNEY, EWAN · 2008 to 2012
$6.4M
Nonparametric methods for functional and translational genomicsK99HG006698 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BROWN, JAMES BENTLEY · 2012 to 2013
$206k
NHGRI NIH HHS K99 HG006698NHGRI NIH HHS U01 HG004695
6 · The paper itself

Abstract

backgroundPrevious work has demonstrated that chromatin feature levels correlate with gene expression. The ENCODE project enables us to further explore this relationship using an unprecedented volume of data. Expression levels from more than 100,000 promoters were measured using a variety of high-throughput techniques applied to RNA extracted by different protocols from different cellular compartments of several human cell lines. ENCODE also generated the genome-wide mapping of eleven histone marks, one histone variant, and DNase I hypersensitivity sites in seven cell lines.

resultsWe built a novel quantitative model to study the relationship between chromatin features and expression levels. Our study not only confirms that the general relationships found in previous studies hold across various cell lines, but also makes new suggestions about the relationship between chromatin features and gene expression levels. We found that expression status and expression levels can be predicted by different groups of chromatin features, both with high accuracy. We also found that expression levels measured by CAGE are better predicted than by RNA-PET or RNA-Seq, and different categories of chromatin features are the most predictive of expression for different RNA measurement methods. Additionally, PolyA+ RNA is overall more predictable than PolyA- RNA among different cell compartments, and PolyA+ cytosolic RNA measured with RNA-Seq is more predictable than PolyA+ nuclear RNA, while the opposite is true for PolyA- RNA.

conclusionsOur study provides new insights into transcriptional regulation by analyzing chromatin features in different cellular contexts.

Indexed as

Genome, HumanModels, GeneticModels, StatisticalTranscription, GeneticChromatinHistonesHumansOrgan SpecificityPoly ARNA, MessengerChromatinHistonesPoly ARNA, Messenger

Identifiers

PMID22950368
PMCPMC3491397
OpenAlexW2142205294

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.