Evidence map›Paper›PMID 41675247›Full record

ArticleQuantitative biology (Beijing, China)2023

DeepRCI: predicting RNA-chromatin interactions via deep learning with multi-omics data.

Yuanpeng Xiong, Xuan He, Dan Zhao, Tao Jiang, Jianyang Zeng

Abstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Yuanpeng XiongDepartment of Computer Science and Technology Tsinghua University Beijing 100084 China.
Xuan HeInstitute for Interdisciplinary Information Sciences Tsinghua University Beijing 100084 China.
Dan ZhaoInstitute for Interdisciplinary Information Sciences Tsinghua University Beijing 100084 China.
Tao JiangDepartment of Computer Science and Technology Tsinghua University Beijing 100084 China.
Jianyang ZengInstitute for Interdisciplinary Information Sciences Tsinghua University Beijing 100084 China.

Funding

RNA Regulatory Networks in Neuronal Cell Type Diversity and FunctionR01NS125018 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Chaolin Zhang · 2022 to 2026
$3.0M
NINDS NIH HHS R01 NS125018
6 · The paper itself

Abstract

Chromatin-associated RNA (caRNA) acts as a ubiquitous epigenetic layer in eukaryotes, and has been reported to be essential in various biological processes. Here, we propose a highly interpretable computational framework, named DeepRCI, to identify the interactions between various types of RNAs and chromatin. DeepRCI can serve as a useful tool for characterizing RNA-chromatin interactions and studying the underlying gene regulatory code. Background: Chromatin-associated RNA (caRNA) acts as a ubiquitous epigenetic layer in eukaryotes, and has been reported to be essential in various biological processes, including gene transcription, chromatin remodeling and cellular differentiation. Recently, numerous experimental techniques have been developed to characterize genome-wide RNA-chromatin interactions to understand their underlying biological functions. However, these experimental methods are generally expensive, time-consuming, and limited in identifying all potential sites, while most of the existing computational methods are restricted to detecting only specific types of RNAs interacting with chromatin. Methods: Here, we propose a highly interpretable computational framework, named DeepRCI, to identify the interactions between various types of RNAs and chromatin. In this framework, we introduce a novel deep learning component called variformer and integrate multi-omics data to capture intrinsic genomic features at both RNA and DNA levels. Results: Extensive experiments demonstrate that DeepRCI can detect RNA-chromatin interactions more accurately when compared to the state-of-the-art baseline prediction methods. Furthermore, the sequence features extracted by DeepRCI can be well matched to known critical gene regulatory components, indicating that our model can provide useful biological insights into understanding the underlying mechanisms of RNA-chromatin interactions. In addition, based on the prediction results, we further delineate the relationships between RNA-chromatin interactions and cellular functions, including gene expression and the modulation of cell states. Conclusions: In summary, DeepRCI can serve as a useful tool for characterizing RNA-chromatin interactions and studying the underlying gene regulatory code.

Indexed as

deep learningmulti‐omics dataRNA‐chromatin

Identifiers

PMID41675247
PMCPMC12807194

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.