Evidence map›Paper›PMID 28193886›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Improved regulatory element prediction based on tissue-specific local epigenomic signatures.

Yupeng He, David U Gorkin, Diane E Dickel, Joseph R Nery, Rosa G Castanon, Ah Young Lee, Yin Shen, Axel Visel, Len A Pennacchio, Bing Ren and 1 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Mapping Chromatin Occupancy ofbioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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.

Yupeng HeGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
David U GorkinLudwig Institute for Cancer Research, University of California, San Diego, La Jolla, CA 92093.
Diane E DickelLawrence Berkeley National Laboratory, Berkeley, CA 94720.
Joseph R NeryGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Rosa G CastanonGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Ah Young LeeLudwig Institute for Cancer Research, University of California, San Diego, La Jolla, CA 92093.
Yin ShenInstitute for Human Genetics, University of California, San Francisco, CA 94143.
Axel ViselLawrence Berkeley National Laboratory, Berkeley, CA 94720.
Len A PennacchioLawrence Berkeley National Laboratory, Berkeley, CA 94720.
Bing RenLudwig Institute for Cancer Research, University of California, San Diego, La Jolla, CA 92093.
Joseph R EckerGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037; ecker@salk.edu.

Funding

UCSD/SDSU IRACDAK12GM068524 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TREJO, JOANN · 2003 to 2025
$24.4M
Center for Mammalian Regulatory GenomicsU54HG006997 · NHGRI · LUDWIG INSTITUTE FOR CANCER RES LTD · PI REN, BING · 2012 to 2016
$14.3M
Epigenetic Alterations of the Developing Brain in Animal Models of SchizophreniaR01MH094670 · NIMH · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI BEHRENS, M MARGARITA, ECKER, JOSEPH R · 2011 to 2015
$3.6M
Epigenomic mapping approaches for cell-type classification in the brainU01MH105985 · NIMH · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI BEHRENS, M MARGARITA, ECKER, JOSEPH R · 2014 to 2016
$3.3M
Howard Hughes Medical InstituteNHGRI NIH HHS U54 HG006997NIGMS NIH HHS K12 GM068524NIMH NIH HHS R01 MH094670NIMH NIH HHS U01 MH105985
6 · The paper itself

Abstract

Accurate enhancer identification is critical for understanding the spatiotemporal transcriptional regulation during development as well as the functional impact of disease-related noncoding genetic variants. Computational methods have been developed to predict the genomic locations of active enhancers based on histone modifications, but the accuracy and resolution of these methods remain limited. Here, we present an algorithm, regulatory element prediction based on tissue-specific local epigenetic marks (REPTILE), which integrates histone modification and whole-genome cytosine DNA methylation profiles to identify the precise location of enhancers. We tested the ability of REPTILE to identify enhancers previously validated in reporter assays. Compared with existing methods, REPTILE shows consistently superior performance across diverse cell and tissue types, and the enhancer locations are significantly more refined. We show that, by incorporating base-resolution methylation data, REPTILE greatly improves upon current methods for annotation of enhancers across a variety of cell and tissue types. REPTILE is available at https://github.com/yupenghe/REPTILE/.

Indexed as

AlgorithmsComputational BiologyDNA MethylationEnhancer Elements, GeneticEpigenesis, GeneticEpigenomicsGene Expression RegulationGenomicsHistone CodeHistonesHumansTranscription, GeneticHistonesbioinformaticsDNA methylationenhancer predictionepigeneticsgene regulation

Identifiers

PMID28193886
PMCPMC5338528

What OpenQuestion holds

Textmetadata
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.