Evidence map›Paper›PMID 33319172›Full record

ArticleiScience2020

Revealing Epigenetic Factors of circRNA Expression by Machine Learning in Various Cellular Contexts.

Mengying Zhang, Kang Xu, Limei Fu, Qi Wang, Zhenghong Chang, Haozhe Zou, Yan Zhang, Yongsheng Li

Open access · goldAbstract read
In one paragraph

Article in iScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Optimal design of synthetic circular RNAs.Experimental & molecular medicine · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Navigating the genomic instability mine field of osteosarcoma to better understand implications of non-coding RNAs.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2022
    Article
  10. Review
  11. Article
  12. Review
  13. 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

8 authors at 3 institutions in 1 country.

Mengying ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Kang XuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Limei FuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Qi WangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Zhenghong ChangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Haozhe ZouCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Yan ZhangSchool of Life Science and Technology, Harbin Institute of Technology, Harbin 150001, China.
Yongsheng LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Harbin Medical University · CNHainan Medical University · CNHarbin Institute of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circular RNAs (circRNAs) have been identified as naturally occurring RNAs that are highly represented in the eukaryotic transcriptome. Although a large number of circRNAs have been reported, the underlying regulatory mechanism of circRNAs biogenesis remains largely unknown. Here, we integrated in-depth multi-omics data including epigenome, transcriptome, and non-coding RNA and identified candidate circRNAs in six cellular contexts. Next, circRNAs were divided into two classes (high versus low) with different expression levels. Machine learning models were constructed that predicted circRNA expression levels based on 11 different histone modifications and host gene expression. We found that the models achieve great accuracy in predicting high versus low expressed circRNAs. Furthermore, the expression levels of host genes of circRNAs, H3k36me3, H3k79me2, and H4k20me1 contributed greatly to the classification models in six cellular contexts. In summary, all these results suggest that epigenetic modifications, particularly histone modifications, can effectively predict expression levels of circRNAs.

Indexed as

BioinformaticsOmicsTranscriptomics

Identifiers

PMID33319172
PMCPMC7725743
OpenAlexW3109142067

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.