Evidence map›Paper›PMID 25933378›Full record

ArticlePloS one2015

A hybrid approach of gene sets and single genes for the prediction of survival risks with gene expression data.

Junhee Seok, Ronald W Davis, Wenzhong Xiao

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 1 paper.

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

What it found

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2 · The registry

The trial behind it

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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

1 citing paper in PubMed.

  1. 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.

Junhee SeokSchool of Electrical Engineering, Korea University, Seoul 136-713, Republic of Korea.
Ronald W DavisStanford Genome Technology Center, Palo Alto, California, United States of America.
Wenzhong XiaoStanford Genome Technology Center, Palo Alto, California, United States of America; Massachusetts General Hospital and Shriners Hospital for Children, Boston, Massachusetts, United States of America.

Funding

WHOLE YEAST GENOME TRANSCRIPTIONAL AND FUNCTIONAL GENE MAPS--A FEASIBILITY STUDYP01HG000205 · NHGRI · STANFORD UNIVERSITY · PI DAVIS, RONALD WAYNE, HOWE, ROGER THOMAS · 1990 to 2016
$120.9M
Inflammation and the Response to InjuryU54GM062119 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI TOMPKINS, RONALD GARY · 2001 to 2010
$78.6M
Bedside Genomics in Severe TraumaR01GM101401 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI TOMPKINS, RONALD GARY, XIAO, WENZHONG · 2012 to 2013
$826k
NHGRI NIH HHS P01 HG000205NHGRI NIH HHS P01-HG00205NIGMS NIH HHS R01 GM101401NIGMS NIH HHS R01-GM101401NIGMS NIH HHS U54 GM062119NIGMS NIH HHS U54-GM62119
6 · The paper itself

Abstract

Accumulated biological knowledge is often encoded as gene sets, collections of genes associated with similar biological functions or pathways. The use of gene sets in the analyses of high-throughput gene expression data has been intensively studied and applied in clinical research. However, the main interest remains in finding modules of biological knowledge, or corresponding gene sets, significantly associated with disease conditions. Risk prediction from censored survival times using gene sets hasn't been well studied. In this work, we propose a hybrid method that uses both single gene and gene set information together to predict patient survival risks from gene expression profiles. In the proposed method, gene sets provide context-level information that is poorly reflected by single genes. Complementarily, single genes help to supplement incomplete information of gene sets due to our imperfect biomedical knowledge. Through the tests over multiple data sets of cancer and trauma injury, the proposed method showed robust and improved performance compared with the conventional approaches with only single genes or gene sets solely. Additionally, we examined the prediction result in the trauma injury data, and showed that the modules of biological knowledge used in the prediction by the proposed method were highly interpretable in biology. A wide range of survival prediction problems in clinical genomics is expected to benefit from the use of biological knowledge.

Indexed as

Databases, GeneticGene Expression RegulationComputational BiologyGenesHumansRisk FactorsSurvival AnalysisWounds and Injuries

Identifiers

PMID25933378
PMCPMC4416884

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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.