Evidence map›Paper›PMID 27307613›Full record

ArticleBioinformatics (Oxford, England)2016

A network-driven approach for genome-wide association mapping.

Seunghak Lee, Soonho Kong, Eric P Xing

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Ensembles of Lasso Screening Rules.IEEE transactions on pattern analysis and machine intelligence · 2018
    Article
  6. Article
  7. Article
  8. 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

3 authors.

Seunghak LeeSchool of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Soonho KongSchool of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Eric P XingSchool of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.

Funding

NIDA Center of Excellence OF Computational Drug Abuse Research (CDAR)P30DA035778 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAHAR, IVET, XIE, XIANG-QUN · 2014 to 2018
$5.4M
Linking Genetics, Genomics and Phenomics to Better Understand Asthma SeverityRC2HL101487 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BLEECKER, EUGENE ROLAND, KAMINSKI, NAFTALI · 2009 to 2010
$3.5M
Genome-Transcription-Phenome-Wide Association: a new paradigm for association stuR01GM087694 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI WU, WEI, XING, ERIC P · 2009 to 2014
$2.5M
Time/Space-Varying Networks of Molecular Interactions: A New Paradigm for StudyinR01GM093156 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI XING, ERIC P · 2010 to 2014
$2.2M
Toward PanOmic and Personalized Association Study of Complex Diseases - A New Statistical and Computational Paradigm for Personalized MedicineR01GM114311 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI WENZEL, SALLY E, WU, WEI · 2015 to 2018
$2.2M
ARRA NIH HHSNHLBI NIH HHS RC2 HL101487NIDA NIH HHS P30 DA035778NIGMS NIH HHS R01 GM087694NIGMS NIH HHS R01 GM093156NIGMS NIH HHS R01 GM114311
6 · The paper itself

Abstract

motivationIt remains a challenge to detect associations between genotypes and phenotypes because of insufficient sample sizes and complex underlying mechanisms involved in associations. Fortunately, it is becoming more feasible to obtain gene expression data in addition to genotypes and phenotypes, giving us new opportunities to detect true genotype-phenotype associations while unveiling their association mechanisms.

resultsIn this article, we propose a novel method, NETAM, that accurately detects associations between SNPs and phenotypes, as well as gene traits involved in such associations. We take a network-driven approach: NETAM first constructs an association network, where nodes represent SNPs, gene traits or phenotypes, and edges represent the strength of association between two nodes. NETAM assigns a score to each path from an SNP to a phenotype, and then identifies significant paths based on the scores. In our simulation study, we show that NETAM finds significantly more phenotype-associated SNPs than traditional genotype-phenotype association analysis under false positive control, taking advantage of gene expression data. Furthermore, we applied NETAM on late-onset Alzheimer's disease data and identified 477 significant path associations, among which we analyzed paths related to beta-amyloid, estrogen, and nicotine pathways. We also provide hypothetical biological pathways to explain our findings. AVAILABILITY AND IMPLEMENTATION: Software is available at http://www.sailing.cs.cmu.edu/ CONTACT: : epxing@cs.cmu.edu.

Indexed as

Genome-Wide Association StudyChromosome MappingGenetic Association StudiesGenotypePhenotypePolymorphism, Single Nucleotide

Identifiers

PMID27307613
PMCPMC4908354

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LicenceCC BY-NC
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Registered trials

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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.