Evidence map›Paper›PMID 29070071›Full record

ArticleGenome biology2017

McEnhancer: predicting gene expression via semi-supervised assignment of enhancers to target genes.

Dina Hafez, Aslihan Karabacak, Sabrina Krueger, Yih-Chii Hwang, Li-San Wang, Robert P Zinzen, Uwe Ohler

Abstract read
In one paragraph

Article in Genome biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Leveraging Machine Learning for Predicting Circadian Transcription in mRNAs and lncRNAs.Proceedings. IEEE International Conference on Bioinformatics and Biomedicine · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Interpreting machine learning models to investigate circadian regulation and facilitate exploration of clock function.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Understanding 3D genome organization by multidisciplinary methods.Nature reviews. Molecular cell biology · 2021
    Review
  13. Article
  14. Article
  15. Chromatin accessibility profiling methods.Nature reviews. Methods primers · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Computational Biology Solutions to Identify Enhancers-target Gene Pairs.Computational and structural biotechnology journal · 2019
    Review
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

7 authors.

Dina HafezDepartment of Computer Science, Duke University, Durham, 27708, NC, USA.
Aslihan KarabacakBerlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine, Berlin, 13125, Germany.
Sabrina KruegerBerlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine, Berlin, 13125, Germany.
Yih-Chii HwangGenomics and Computational Biology Graduate Program, University of Pennsylvania, Philadelphia, 19104, PA, USA.
Li-San WangGenomics and Computational Biology Graduate Program, University of Pennsylvania, Philadelphia, 19104, PA, USA.
Robert P ZinzenBerlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine, Berlin, 13125, Germany. Robert.Zinzen@mdc-berlin.de.
Uwe OhlerDepartment of Computer Science, Duke University, Durham, 27708, NC, USA. Uwe.Ohler@mdc-berlin.de.

Funding

THE NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITEU24AG041689 · NIA · UNIVERSITY OF PENNSYLVANIA · PI LI-SAN WANG · 2012 to 2026
$42.3M
UPenn ADCC Biomarker CoreP30AG010124 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DETRE, JOHN A · 1991 to 2020
$35.1M
Computational genome-wide RNA profiling using next-generation sequencingR01GM099962 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI WANG, LI-SAN · 2012 to 2016
$1.5M
NIA NIH HHS P30 AG010124NIA NIH HHS U24 AG041689NIGMS NIH HHS R01 GM099962
6 · The paper itself

Abstract

Transcriptional enhancers regulate spatio-temporal gene expression. While genomic assays can identify putative enhancers en masse, assigning target genes is a complex challenge. We devised a machine learning approach, McEnhancer, which links target genes to putative enhancers via a semi-supervised learning algorithm that predicts gene expression patterns based on enriched sequence features. Predicted expression patterns were 73-98% accurate, predicted assignments showed strong Hi-C interaction enrichment, enhancer-associated histone modifications were evident, and known functional motifs were recovered. Our model provides a general framework to link globally identified enhancers to targets and contributes to deciphering the regulatory genome.

Indexed as

Enhancer Elements, GeneticGene Expression Regulation, DevelopmentalMachine LearningAnimalsDeoxyribonuclease IDrosophila melanogasterEmbryonic DevelopmentGenes, ReporterHistone CodeNucleotide MotifsPromoter Regions, GeneticSequence Analysis, DNATranscription FactorsDeoxyribonuclease ITranscription FactorsDrosophila melanogasterEnhancer to target gene assignmentGene expressionGene regulationInterpolated Markov modelMachine learningSemi-supervised model

Identifiers

PMID29070071
PMCPMC5657048

What OpenQuestion holds

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LicenceCC BY
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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.