Evidence map›Paper›PMID 29036516›Full record

ArticleBiostatistics (Oxford, England)2018

A two-stage approach of gene network analysis for high-dimensional heterogeneous data.

Sangin Lee, Faming Liang, Ling Cai, Guanghua Xiao

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
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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

4 authors.

Sangin LeeDepartment of Information and Statistics, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon 34134, Korea.
Faming LiangDepartment of Biostatistics, University of Florida, FL 32610, USA.
Ling CaiQuantitative Biomedical Research Center, Department of Clinical Sciences, and Children's Research Institute, University of Texas Southwestern Medical Center, 6000 Harry Hines Blvd, Dallas, TX 75390, USA.
Guanghua XiaoQuantitative Biomedical Research Center, Department of Clinical Sciences, Department of Bioinformatics, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 6000 Harry Hines Blvd, Dallas, TX 75390, USA.

Funding

Integrative Analysis to Identify Therapeutic Targets for Lung CancerR01CA172211 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI XIAO, GUANGHUA · 2013 to 2017
$1.6M
Equivalent Partial Correlation Methods for Integrative Genetic Network Analysis R01GM117597 · NIGMS · UNIVERSITY OF FLORIDA · PI LIANG, FAMING · 2015 to 2017
$1.0M
NCI NIH HHS R01 CA172211NIGMS NIH HHS R01 GM117597
6 · The paper itself

Abstract

Gaussian graphical models have been widely used to construct gene regulatory networks from gene expression data. Most existing methods for Gaussian graphical models are designed to model homogeneous data, assuming a single Gaussian distribution. In practice, however, data may consist of gene expression studies with unknown confounding factors, such as study cohort, microarray platforms, experimental batches, which produce heterogeneous data, and hence lead to false positive edges or low detection power in resulting network, due to those unknown factors. To overcome this problem and improve the performance in constructing gene networks, we propose a two-stage approach to construct a gene network from heterogeneous data. The first stage is to perform a clustering analysis in order to assign samples to a few clusters where the samples in each cluster are approximately homogeneous, and the second stage is to conduct an integrative analysis of networks from each cluster. In particular, we first apply a model-based clustering method using the singular value decomposition for high-dimensional data, and then integrate the networks from each cluster using the integrative $\psi$-learning method. The proposed method is based on an equivalent measure of partial correlation coefficients in Gaussian graphical models, which is computed with a reduced conditional set and thus it is useful for high-dimensional data. We compare the proposed two-stage learning approach with some existing methods in various simulation settings, and demonstrate the robustness of the proposed method. Finally, it is applied to integrate multiple gene expression studies of lung adenocarcinoma to identify potential therapeutic targets and treatment biomarkers.

Indexed as

Data Interpretation, StatisticalGene ExpressionGene Regulatory NetworksModels, StatisticalBiostatisticsCluster AnalysisGenomicsHumansLung Neoplasms

Identifiers

PMID29036516
PMCPMC5862270

What OpenQuestion holds

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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.