Evidence map›Paper›PMID 26130578›Full record

ArticleBioinformatics (Oxford, England)2015

Integrating full spectrum of sequence features into predicting functional microRNA-mRNA interactions.

Zixing Wang, Wenlong Xu, Yin Liu

Abstract readEvaluation Study
In one paragraph

Article in Bioinformatics (Oxford, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

3 authors.

Zixing WangDepartment of Neurobiology and Anatomy, University of Texas Health Science Center at Houston and.
Wenlong XuDepartment of Neurobiology and Anatomy, University of Texas Health Science Center at Houston and.
Yin LiuDepartment of Neurobiology and Anatomy, University of Texas Health Science Center at Houston and University of Texas Graduate School of Biomedical Sciences, Houston, Texas, USA.

Funding

Bayesian Methods in Signal Transduction Network AnalysisR01LM010022 · NLM · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LIU, YIN · 2011 to 2014
$901k
6 · The paper itself

Abstract

motivationMicroRNAs (miRNAs) play important roles in general biological processes and diseases pathogenesis. Identifying miRNA target genes is an essential step to fully understand the regulatory effects of miRNAs. Many computational methods based on the sequence complementary rules and the miRNA and mRNA expression profiles have been developed for this purpose. It is noted that there have been many sequence features of miRNA targets available, including the context features of the target sites, the thermodynamic stability and the accessibility energy for miRNA-mRNA interaction. However, most of current computational methods that combine sequence and expression information do not effectively integrate full spectrum of these features; instead, they perceive putative miRNA-mRNA interactions from sequence-based prediction as equally meaningful. Therefore, these sequence features have not been fully utilized for improving miRNA target prediction.

resultsWe propose a novel regularized regression approach that is based on the adaptive Lasso procedure for detecting functional miRNA-mRNA interactions. Our method fully takes into account the gene sequence features and the miRNA and mRNA expression profiles. Given a set of sequence features for each putative miRNA-mRNA interaction and their expression values, our model quantifies the down-regulation effect of each miRNA on its targets while simultaneously estimating the contribution of each sequence feature to predicting functional miRNA-mRNA interactions. By applying our model to the expression datasets from two cancer studies, we have demonstrated our prediction results have achieved better sensitivity and specificity and are more biologically meaningful compared with those based on other methods. AVAILABILITY AND IMPLEMENTATION: The source code is available at: http://nba.uth.tmc.edu/homepage/liu/miRNALasso. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. CONTACT: Yin.Liu@uth.tmc.edu.

Indexed as

Gene Expression ProfilingSequence Analysis, RNADown-RegulationHumansMicroRNAsModels, GeneticNeoplasmsRNA, MessengerSensitivity and SpecificityMicroRNAsRNA, Messenger

Identifiers

PMID26130578
PMCPMC4804770

What OpenQuestion holds

Textmetadata
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.