Evidence map›Paper›PMID 29986088›Full record

ArticleNucleic acids research2018

A deep recurrent neural network discovers complex biological rules to decipher RNA protein-coding potential.

Steven T Hill, Rachael Kuintzle, Amy Teegarden, Erich Merrill, Padideh Danaee, David A Hendrix

Abstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

  1. Article
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  6. Review
  7. Article
  8. Interpretation of RNA Universe and Coding Potential Using IntRNA.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  9. Review
  10. Review
  11. Article
  12. Machine learning approaches enable the discovery of therapeutics across domains.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  13. Article
  14. Deciphering 3'UTR Mediated Gene Regulation Using Interpretable Deep Representation Learning.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  15. Review
  16. Big data and deep learning for RNA biology.Experimental & molecular medicine · 2024
    Review
  17. ntEmbd: Deep learning embedding for nucleotide sequences.bioRxiv : the preprint server for biology · 2024
    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

6 authors.

Steven T HillSchool of Electrical Engineering and Computer Science, Oregon State University, 1148 Kelley Engineering Center, Corvallis, OR 97331, USA.
Rachael KuintzleDepartment of Biochemistry and Biophysics, Oregon State University, 2011 Ag & Life Sciences Bldg, Corvallis, OR 97331, USA.
Amy TeegardenDepartment of Biochemistry and Biophysics, Oregon State University, 2011 Ag & Life Sciences Bldg, Corvallis, OR 97331, USA.
Erich MerrillSchool of Electrical Engineering and Computer Science, Oregon State University, 1148 Kelley Engineering Center, Corvallis, OR 97331, USA.
Padideh DanaeeSchool of Electrical Engineering and Computer Science, Oregon State University, 1148 Kelley Engineering Center, Corvallis, OR 97331, USA.
David A HendrixSchool of Electrical Engineering and Computer Science, Oregon State University, 1148 Kelley Engineering Center, Corvallis, OR 97331, USA.

Funding

Circadian regulation of neuroprotective genes during agingR21AG052950 · NIA · OREGON STATE UNIVERSITY · PI GIEBULTOWICZ, JADWIGA M, HENDRIX, DAVID ANTHONY · 2016 to 2017
$395k
NIA NIH HHS R21 AG052950
6 · The paper itself

Abstract

The current deluge of newly identified RNA transcripts presents a singular opportunity for improved assessment of coding potential, a cornerstone of genome annotation, and for machine-driven discovery of biological knowledge. While traditional, feature-based methods for RNA classification are limited by current scientific knowledge, deep learning methods can independently discover complex biological rules in the data de novo. We trained a gated recurrent neural network (RNN) on human messenger RNA (mRNA) and long noncoding RNA (lncRNA) sequences. Our model, mRNA RNN (mRNN), surpasses state-of-the-art methods at predicting protein-coding potential despite being trained with less data and with no prior concept of what features define mRNAs. To understand what mRNN learned, we probed the network and uncovered several context-sensitive codons highly predictive of coding potential. Our results suggest that gated RNNs can learn complex and long-range patterns in full-length human transcripts, making them ideal for performing a wide range of difficult classification tasks and, most importantly, for harvesting new biological insights from the rising flood of sequencing data.

Indexed as

Neural Networks, ComputerBase SequenceComputational BiologyHumansMachine LearningOpen Reading FramesProtein BiosynthesisReproducibility of ResultsRNA, Long NoncodingRNA, MessengerSequence Analysis, RNARNA, Long NoncodingRNA, Messenger

Identifiers

PMID29986088
PMCPMC6144860

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.