Evidence map›Paper›PMID 25025130›Full record

ArticlePloS one2014

OMIT: dynamic, semi-automated ontology development for the microRNA domain.

Jingshan Huang, Jiangbo Dang, Glen M Borchert, Karen Eilbeck, He Zhang, Min Xiong, Weijian Jiang, Hao Wu, Judith A Blake, Darren A Natale and 1 more

Abstract read
In one paragraph

Article in PloS one, 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. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The development of non-coding RNA ontology.International journal of data mining and bioinformatics
    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

11 authors.

Jingshan HuangSchool of Computing, University of South Alabama, Mobile, Alabama, United States of America.
Jiangbo DangCorporate Technology, Siemens Corporation, Princeton, New Jersey, United States of America.
Glen M BorchertDepartment of Biology, University of South Alabama, Mobile, Alabama, United States of America.
Karen EilbeckSchool of Medicine, University of Utah, Salt Lake City, Utah, United States of America.
He ZhangSchool of Computing, University of South Alabama, Mobile, Alabama, United States of America.
Min XiongSchool of Computing, University of South Alabama, Mobile, Alabama, United States of America.
Weijian JiangSchool of Computing, University of South Alabama, Mobile, Alabama, United States of America.
Hao WuSchool of Computing, University of South Alabama, Mobile, Alabama, United States of America.
Judith A BlakeThe Jackson Laboratory, Bar Harbor, Maine, United States of America.
Darren A NataleGeorgetown University Medical Center, Washington, DC, United States of America.
Ming TanMitchell Cancer Institute, University of South Alabama, Mobile, Alabama, United States of America.

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Glucose metabolism and ErbB2-mediated cancer progressionR01CA149646 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI TAN, MING · 2011 to 2016
$1.4M
OmniSearch: A semantic search tool for discovering microRNAs' critical roles in hU01CA180982 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI HUANG, JINGSHAN · 2014 to 2016
$913k
NCI NIH HHS P30 CA034196NCI NIH HHS R01 CA149646NCI NIH HHS R01-CA149646NCI NIH HHS U01 CA180982
6 · The paper itself

Abstract

As a special class of short non-coding RNAs, microRNAs (a.k.a. miRNAs or miRs) have been reported to perform important roles in various biological processes by regulating respective target genes. However, significant barriers exist during biologists' conventional miR knowledge discovery. Emerging semantic technologies, which are based upon domain ontologies, can render critical assistance to this problem. Our previous research has investigated the construction of a miR ontology, named Ontology for MIcroRNA Target Prediction (OMIT), the very first of its kind that formally encodes miR domain knowledge. Although it is unavoidable to have a manual component contributed by domain experts when building ontologies, many challenges have been identified for a completely manual development process. The most significant issue is that a manual development process is very labor-intensive and thus extremely expensive. Therefore, we propose in this paper an innovative ontology development methodology. Our contributions can be summarized as: (i) We have continued the development and critical improvement of OMIT, solidly based on our previous research outcomes. (ii) We have explored effective and efficient algorithms with which the ontology development can be seamlessly combined with machine intelligence and be accomplished in a semi-automated manner, thus significantly reducing large amounts of human efforts. A set of experiments have been conducted to thoroughly evaluate our proposed methodology.

Indexed as

RNA InterferenceAlgorithmsComputational BiologyGene OntologyHumansMicroRNAsRNA, MessengerMicroRNAsRNA, Messenger

Identifiers

PMID25025130
PMCPMC4099014

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.