Evidence map›Paper›PMID 28542379›Full record

ArticlePloS one2017

Disease-related gene module detection based on a multi-label propagation clustering algorithm.

Xue Jiang, Han Zhang, Xiongwen Quan, Zhandong Liu, Yanbin Yin

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Data Processing and Analysis in Mass Spectrometry-Based Metabolomics.Methods in molecular biology (Clifton, N.J.) · 2023
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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

5 authors.

Xue JiangCollege of Computer and Control Engineering, Nankai University, Tianjin 300350, China.
Han ZhangCollege of Computer and Control Engineering, Nankai University, Tianjin 300350, China.
Xiongwen QuanCollege of Computer and Control Engineering, Nankai University, Tianjin 300350, China.ORCID http://orcid.org/0000-0003-4138-4365
Zhandong LiuDepartment of Pediatrics-Neurology, Baylor College of Medicine, Houston, TX 77030, United States of America.
Yanbin YinDepartment of Biological Sciences, Northern Illinois University, DeKalb, IL 60115, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detecting disease-related gene modules by analyzing gene expression data is of great significance. It is helpful for exploratory analysis of the interaction mechanisms of genes under complex disease phenotypes. The multi-label propagation algorithm (MLPA) has been widely used in module detection for its fast and easy implementation. The accuracy of MLPA greatly depends on the connections between nodes, and most existing research focuses on measuring the similarity between nodes. However, MLPA does not perform well with loose connections between disease-related genes. Moreover, the biological significance of modules obtained by MLPA has not been demonstrated. To solve these problems, we designed a double label propagation clustering algorithm (DLPCA) based on MLPA to study Huntington's disease. In DLPCA, in addition to category labels, we introduced pathogenic labels to supervise the process of multi-label propagation clustering. The pathogenic labels contain pathogenic information about disease genes and the hierarchical structure of gene expression data. Experimental results demonstrated the superior performance of DLPCA compared with other conventional gene-clustering algorithms.

Indexed as

AlgorithmsDisease Models, AnimalGene Regulatory NetworksAnimalsCluster AnalysisComputational BiologyGene Expression ProfilingGenetic MarkersHumansHuntington DiseaseMiceModels, TheoreticalGenetic Markers

Identifiers

PMID28542379
PMCPMC5438150

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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.