Evidence map›Paper›PMID 33160328›Full record

ArticleBMC bioinformatics2020

Prediction of enhancer-promoter interactions using the cross-cell type information and domain adversarial neural network.

Fang Jing, Shao-Wu Zhang, Shihua Zhang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Machine and Deep Learning Methods for Predicting 3D Genome Organization.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  4. Article
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  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Chromatin Hubs: A biological and computational outlook.Computational and structural biotechnology journal · 2022
    Review
  13. Predicting 3D chromatin interactions from DNA sequence using Deep Learning.Computational and structural biotechnology journal · 2022
    Review
  14. Article
  15. Article
  16. 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

3 authors.

Fang JingKey Laboratory of Information Fusion Technology of Ministry of Education, School of Automation, Northwestern Polytechnical University, 127 West Youyi Road, Xi'an, 710072, Shaanxi, China.
Shao-Wu ZhangKey Laboratory of Information Fusion Technology of Ministry of Education, School of Automation, Northwestern Polytechnical University, 127 West Youyi Road, Xi'an, 710072, Shaanxi, China. zhangsw@nwpu.edu.cn.ORCID http://orcid.org/0000-0003-1305-7447
Shihua ZhangNCMIS, CEMS, RCSDS, Academy of Mathematics and Systems Science, Chinese Academy of Sciences, 55 Zhongguancun East Road, Beijing, 10090, China. zsh@amss.ac.cn.

Funding

CAS Frontier Science Research Key Project for Top Young Scientist QYZDB-SSW-SYS008National Natural Science Foundation of China 11661141019National Natural Science Foundation of China 61621003National Natural Science Foundation of China 61873202National Ten Thousand Talent Program for Young Top-notch Talents, the Key Research Program of the Chinese Academy of Sciences KFZD-SW-219Strategic Priority Research Program of the Chinese Academy of Sciences XDB13040600
6 · The paper itself

Abstract

backgroundEnhancer-promoter interactions (EPIs) play key roles in transcriptional regulation and disease progression. Although several computational methods have been developed to predict such interactions, their performances are not satisfactory when training and testing data from different cell lines. Currently, it is still unclear what extent a across cell line prediction can be made based on sequence-level information.

resultsIn this work, we present a novel Sequence-based method (called SEPT) to predict the enhancer-promoter interactions in new cell line by using the cross-cell information and Transfer learning. SEPT first learns the features of enhancer and promoter from DNA sequences with convolutional neural network (CNN), then designing the gradient reversal layer of transfer learning to reduce the cell line specific features meanwhile retaining the features associated with EPIs. When the locations of enhancers and promoters are provided in new cell line, SEPT can successfully recognize EPIs in this new cell line based on labeled data of other cell lines. The experiment results show that SEPT can effectively learn the latent import EPIs-related features between cell lines and achieves the best prediction performance in terms of AUC (the area under the receiver operating curves).

conclusionsSEPT is an effective method for predicting the EPIs in new cell line. Domain adversarial architecture of transfer learning used in SEPT can learn the latent EPIs shared features among cell lines from all other existing labeled data. It can be expected that SEPT will be of interest to researchers concerned with biological interaction prediction.

Indexed as

Neural Networks, ComputerArea Under CurveCell LineHumansPromoter Regions, GeneticRegulatory Sequences, Nucleic AcidROC CurveCell lineConvolutional neural networkEnhancer–promoter interactionsGradient reversal layerTransfer learning

Identifiers

PMID33160328
PMCPMC7648314

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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.