Evidence map›Paper›PMID 25822417›Full record

ArticlePloS one2015

Module-based association analysis for omics data with network structure.

Zhi Wang, Arnab Maity, Chuhsing Kate Hsiao, Deepak Voora, Rima Kaddurah-Daouk, Jung-Ying Tzeng

Abstract read
In one paragraph

Article in PloS one, 2015. 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. Trial
  2. Article
  3. 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

6 authors.

Zhi WangBioinformatics Research Center, North Carolina State University, Raleigh, North Carolina, 27695, United States of America.
Arnab MaityDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, 27695, United States of America.
Chuhsing Kate HsiaoInstitute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Deepak VooraInstitute for Genome Sciences and Policy, Duke University, Durham, North Carolina, United States of America.
Rima Kaddurah-DaoukDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, North Carolina, United States of America.
Jung-Ying TzengBioinformatics Research Center, North Carolina State University, Raleigh, North Carolina, 27695, United States of America; Department of Statistics, North Carolina State University, Raleigh, North Carolina, 27695, United States of America; Department of Statistics, National Cheng-Kung University, Taiwan, R.O.C.

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Genome-wide Haplotype Association Analysis in Mental DisordersR01MH084022 · NIMH · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TZENG, JUNG-YING · 2009 to 2011
$1.1M
Phase I Clinical Trial Describing the Pharmacogenomics of AspirinRC1GM091083 · NIGMS · DUKE UNIVERSITY · PI GINSBURG, GEOFFREY S · 2009 to 2010
$1000k
Statistical Methods for Analysis of High-Dimensional Gene and Environment DataR00ES017744 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MAITY, ARNAB · 2011 to 2013
$663k
NCI NIH HHS P01 CA142538NIEHS NIH HHS R00 ES017744NIGMS NIH HHS RC1 GM091083NIMH NIH HHS R01 MH084022
6 · The paper itself

Abstract

Module-based analysis (MBA) aims to evaluate the effect of a group of biological elements sharing common features, such as SNPs in the same gene or metabolites in the same pathways, and has become an attractive alternative to traditional single bio-element approaches. Because bio-elements regulate and interact with each other as part of network, incorporating network structure information can more precisely model the biological effects, enhance the ability to detect true associations, and facilitate our understanding of the underlying biological mechanisms. However, most MBA methods ignore the network structure information, which depicts the interaction and regulation relationship among basic functional units in biology system. We construct the connectivity kernel and the topology kernel to capture the relationship among bio-elements in a module, and use a kernel machine framework to evaluate the joint effect of bio-elements. Our proposed kernel machine approach directly incorporates network structure so to enhance the study efficiency; it can assess interactions among modules, account covariates, and is computational efficient. Through simulation studies and real data application, we demonstrate that the proposed network-based methods can have markedly better power than the approaches ignoring network information under a range of scenarios.

Indexed as

AlgorithmsComputational BiologyComputer SimulationGene Regulatory NetworksHumansPolymorphism, Single Nucleotide

Identifiers

PMID25822417
PMCPMC4378989

What OpenQuestion holds

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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.