Evidence map›Paper›PMID 37294799›Full record

ArticleBioinformatics (Oxford, England)2023

DeepITEH: a deep learning framework for identifying tissue-specific eRNAs from the human genome.

Tianjiao Zhang, Liangyu Li, Hailong Sun, Guohua Wang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Tianjiao ZhangCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.ORCID 0000-0001-9807-8620
Liangyu LiCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.ORCID 0009-0004-0594-5625
Hailong SunCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.
Guohua WangCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.ORCID 0000-0001-7381-2374

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationEnhancers are vital cis-regulatory elements that regulate gene expression. Enhancer RNAs (eRNAs), a type of long noncoding RNAs, are transcribed from enhancer regions in the genome. The tissue-specific expression of eRNAs is crucial in the regulation of gene expression and cancer development. The methods that identify eRNAs based solely on genomic sequence data have high error rates because they do not account for tissue specificity. Specific histone modifications associated with eRNAs offer valuable information for their identification. However, identification of eRNAs using histone modification data requires the use of both RNA-seq and histone modification data. Unfortunately, many public datasets contain only one of these components, which impedes the accurate identification of eRNAs.

resultsWe introduce DeepITEH, a deep learning framework that leverages RNA-seq data and histone modification data from multiple samples of the same tissue to enhance the accuracy of identifying eRNAs. Specifically, deepITEH initially categorizes eRNAs into two classes, namely, regularly expressed eRNAs and accidental eRNAs, using histone modification data from multiple samples of the same tissue. Thereafter, it integrates both sequence and histone modification features to identify eRNAs in specific tissues. To evaluate the performance of DeepITEH, we compared it with four existing state-of-the-art enhancer prediction methods, SeqPose, iEnhancer-RD, LSTMAtt, and FRL, on four normal tissues and four cancer tissues. Remarkably, seven of these tissues demonstrated a substantially improved specific eRNA prediction performance with DeepITEH, when compared with other methods. Our findings suggest that DeepITEH can effectively predict potential eRNAs on the human genome, providing insights for studying the eRNA function in cancer. AVAILABILITY AND IMPLEMENTATION: The source code and dataset of DeepITEH have been uploaded to https://github.com/lyli1013/DeepITEH.

Indexed as

Deep LearningRNA, Long NoncodingEnhancer Elements, GeneticGenome, HumanHistonesHumansTranscription, GeneticHistonesRNA, Long Noncoding

Identifiers

PMID37294799
PMCPMC10281860

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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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.