Evidence map›Paper›PMID 24829448›Full record

ArticleNucleic acids research2014

ToppMiR: ranking microRNAs and their mRNA targets based on biological functions and context.

Chao Wu, Eric E Bardes, Anil G Jegga, Bruce J Aronow

Abstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Role of microRNA-25 in high glucose cultured Müller glia.International journal of ophthalmology · 2021
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Bioinformatic tools for microRNA dissection.Nucleic acids research · 2016
    Review
  10. Article
  11. 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

4 authors.

Chao WuDepartment of Computer Science, University of Cincinnati, Cincinnati, OH 45221, USA Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Eric E BardesDivision of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Anil G JeggaDepartment of Computer Science, University of Cincinnati, Cincinnati, OH 45221, USA Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA Department of Pediatrics, University of Cincinnati, Cincinnati, OH 45221, USA.
Bruce J AronowDepartment of Computer Science, University of Cincinnati, Cincinnati, OH 45221, USA Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA Department of Pediatrics, University of Cincinnati, Cincinnati, OH 45221, USA bruce.aronow@cchmc.org.

Funding

Progenitor Cell Biology Consortium Administrative Coordinating CenterU01HL099997 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI TERRIN, MICHAEL L · 2009 to 2015
$29.9M
Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2012 to 2014
$9.9M
GUDMAP- Database and WebsiteU01DK092983 · NIDDK · UNIVERSITY OF EDINBURGH · PI BALDOCK, RICHARD ALAN · 2011 to 2016
$3.2M
Global Gene Expression Atlas of Craniofacial Development (Research Project)U01DE020049 · NIDCR · CINCINNATI CHILDRENS HOSP MED CTR · PI POTTER, S. STEVEN · 2009 to 2013
$1.4M
NCATS NIH HHS UL1 TR000077NCATS NIH HHS UL1 TR000077-04NHLBI NIH HHS U01HL099997NIDCR NIH HHS U01-DE20049NIDDK NIH HHS 3U01DK092983-01S1NIDDK NIH HHS P30 DK078392
6 · The paper itself

Abstract

Identifying functionally significant microRNAs (miRs) and their correspondingly most important messenger RNA targets (mRNAs) in specific biological contexts is a critical task to improve our understanding of molecular mechanisms underlying organismal development, physiology and disease. However, current miR-mRNA target prediction platforms rank miR targets based on estimated strength of physical interactions and lack the ability to rank interactants as a function of their potential to impact a given biological system. To address this, we have developed ToppMiR (http://toppmir.cchmc.org), a web-based analytical workbench that allows miRs and mRNAs to be co-analyzed via biologically centered approaches in which gene function associated annotations are used to train a machine learning-based analysis engine. ToppMiR learns about biological contexts based on gene associated information from expression data or from a user-specified set of genes that relate to context-relevant knowledge or hypotheses. Within the biological framework established by the genes in the training set, its associated information content is then used to calculate a features association matrix composed of biological functions, protein interactions and other features. This scoring matrix is then used to jointly rank both the test/candidate miRs and mRNAs. Results of these analyses are provided as downloadable tables or network file formats usable in Cytoscape.

Indexed as

SoftwareGene Expression ProfilingGene Regulatory NetworksInternetMicroRNAsRNA, MessengerMicroRNAsRNA, Messenger

Identifiers

PMID24829448
PMCPMC4086116

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.