Evidence map›Paper›PMID 30302823›Full record

ArticleGenetic epidemiology2018

Overlapping clustering of gene expression data using penalized weighted normalized cut.

Sebastian J Teran Hidalgo, Tingyu Zhu, Mengyun Wu, Shuangge Ma

Abstract read
In one paragraph

Article in Genetic epidemiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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  3. 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.

Sebastian J Teran HidalgoDepartment of Biostatistics, Yale University, New Haven, Connecticut.
Tingyu ZhuDepartment of Statistics, Xiamen University, Xiamen, China.
Mengyun WuDepartment of Biostatistics, Yale University, New Haven, Connecticut.
Shuangge MaDepartment of Biostatistics, Yale University, New Haven, Connecticut.ORCID 0000-0001-9001-4999

Funding

Novel methods for identifying genetic interactions in cancer prognosisR01CA204120 · NCI · YALE UNIVERSITY · PI Shuangge Ma · 2016 to 2026
$3.5M
Assisted Network-based Analysis of Cancer Gene Expression StudiesR03CA216017 · NCI · YALE UNIVERSITY · PI MA, SHUANGGE · 2017 to 2018
$168k
NCI NIH HHS R01 CA204120NCI NIH HHS R03 CA216017NIH HHS CA204120NIH HHS CA216017
6 · The paper itself

Abstract

Clustering has been widely conducted in the analysis of gene expression data. For complex diseases, it has played an important role in identifying unknown functions of genes, serving as the basis of other analysis, and others. A common limitation of most existing clustering approaches is to assume that genes are separated into disjoint clusters. As genes often have multiple functions and thus can belong to more than one functional cluster, the disjoint clustering results can be unsatisfactory. In addition, due to the small sample sizes of genetic profiling studies and other factors, there may not be sufficient evidence to confirm the specific functions of some genes and cluster them definitively into disjoint clusters. In this study, we develop an effective overlapping clustering approach, which takes account into the multiplicity of gene functions and lack of certainty in practical analysis. A penalized weighted normalized cut (PWNCut) criterion is proposed based on the NCut technique and an

Indexed as

AlgorithmsGene Expression RegulationBreast NeoplasmsCluster AnalysisComputer SimulationFemaleGene Expression ProfilingGene OntologyHumansModels, Geneticgene expression dataNCutoverlapping clusteringpenalization

Identifiers

PMID30302823
PMCPMC6239939

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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.