Evidence map›Paper›PMID 28361698›Full record

ArticleBMC genomics2017

A clustering-based approach for efficient identification of microRNA combinatorial biomarkers.

Yang Yang, Ning Huang, Luning Hao, Wei Kong

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. The Potential Role of miRNAs as New Biomarkers for Osteoporosis.International journal of endocrinology · 2018
    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

4 authors.

Yang YangDepartment of Computer Science and Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, 200240, Shanghai, China. yangyang@cs.sjtu.edu.cn.
Ning HuangDepartment of Computer Science and Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, 200240, Shanghai, China.
Luning HaoDepartment of Computer Science and Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, 200240, Shanghai, China.
Wei KongDepartment of Computer Science and Engineering, Shanghai Maritime University, 1550 Hai Gang Ave., Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) have great potential serving as tumor biomarkers and therapeutic targets. As the rapid development of high-throughput experimental technology, gene expression experiments have become more and more specialized and diversified. The complex data structure has brought great challenge for the identification of biomarkers. In the meantime, current statistical and machine learning methods for detecting biomarkers have the problem of low reliability and biased criteria.

resultsThis study aims to select combinatorial miRNA biomarkers, which have higher sensitivity and specificity than single-gene biomarkers. In order to avoid exhaustive search and redundant information, miRNAs are firstly clustered, then the combinations of representative cluster members are assessed as potential biomarkers. Both the criteria for the partition of clusters and selection of representative members are based on Fisher linear discriminant analysis (FDA). The FDA-based criterion has been demonstrated to be superior to three other criteria in selecting representative members, and also good at refining clusters. In the comparison with eight common feature selection methods, this clustering-based method performs the best with regard to the discriminative ability of selected biomarkers.

conclusionsOur experimental results demonstrate that the clustering-based method can identify microRNA combinatorial biomarkers with high accuracy and efficiency. Our method and data are available to the public upon request.

Indexed as

AlgorithmsBiomarkers, TumorBreast NeoplasmsCluster AnalysisDiscriminant AnalysisFemaleHumansMaleMicroRNAsProstatic NeoplasmsReproducibility of ResultsSensitivity and SpecificityBiomarkers, TumorMicroRNAsBiomarkerClusteringMicroRNA

Identifiers

PMID28361698
PMCPMC5374636

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.