Evidence map›Paper›PMID 35664803›Full record

ArticleNAR genomics and bioinformatics2022

tRForest: a novel random forest-based algorithm for tRNA-derived fragment target prediction.

Rohan Parikh, Briana Wilson, Laine Marrah, Zhangli Su, Shekhar Saha, Pankaj Kumar, Fenix Huang, Anindya Dutta

Open access · goldAbstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 3'-tRF-CysFunctional & integrative genomics · 2023
    Article
  5. Review
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.

Rohan ParikhDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22901, USA.
Briana WilsonDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22901, USA.
Laine MarrahDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22901, USA.
Zhangli SuDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22901, USA.
Shekhar SahaDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22901, USA.
Pankaj KumarDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22901, USA.
Fenix HuangBiocomplexity Institute, University of Virginia, Charlottesville, VA 22901, USA.
Anindya DuttaDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22901, USA.ORCID https://orcid.org/0000-0002-3559-2574
University of Virginia · USUniversity of Alabama at Birmingham · USBiocom · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Mechanism of action of an lncRNA for directing muscle differentiationR01AR067712 · NIAMS · UNIVERSITY OF VIRGINIA · PI DUTTA, ANINDYA · 2016 to 2020
$1.7M
Involvement of Noncanonical Short RNAs in Gene Repression through the RNA-Induced-Silencing ComplexR01GM146756 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DUTTA, ANINDYA · 2022 to 2025
$1.3M
The role of small RNA modifications in gliomaK99CA259526 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SU, ZHANGLI · 2022 to 2023
$221k
Stability of a novel family of short noncoding RNAs, tRFs: Effect on oncogenesisF30CA254134 · NCI · UNIVERSITY OF VIRGINIA · PI WILSON, BRIANA · 2020 to 2022
$120k
NCI NIH HHS F30 CA254134NCI NIH HHS K99 CA259526NCI NIH HHS P30 CA044579NIAMS NIH HHS R01 AR067712NIGMS NIH HHS R01 GM146756
6 · The paper itself

Abstract

tRNA fragments (tRFs) are small RNAs comparable to the size and function of miRNAs. tRFs are generally Dicer independent, are found associated with Ago, and can repress expression of genes post-transcriptionally. Given that this expands the repertoire of small RNAs capable of post-transcriptional gene expression, it is important to predict tRF targets with confidence. Some attempts have been made to predict tRF targets, but are limited in the scope of tRF classes used in prediction or limited in feature selection. We hypothesized that established miRNA target prediction features applied to tRFs through a random forest machine learning algorithm will immensely improve tRF target prediction. Using this approach, we show significant improvements in tRF target prediction for all classes of tRFs and validate our predictions in two independent cell lines. Finally, Gene Ontology analysis suggests that among the tRFs conserved between mice and humans, the predicted targets are enriched significantly in neuronal function, and we show this specifically for tRF-3009a. These improvements to tRF target prediction further our understanding of tRF function broadly across species and provide avenues for testing novel roles for tRFs in biology. We have created a publicly available website for the targets of tRFs predicted by tRForest.

Identifiers

PMID35664803
PMCPMC9155213
OpenAlexW4281682125

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.