Evidence map›Paper›PMID 21414987›Full record

ArticleBioinformatics (Oxford, England)2011

COSINE: COndition-SpecIfic sub-NEtwork identification using a global optimization method.

Haisu Ma, Eric E Schadt, Lee M Kaplan, Hongyu Zhao

Abstract readComparative Study
In one paragraph

Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

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3 · Its place in the literature

Who cites it

54 citing papers in PubMed.

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  14. Predicting Protein Functions Based on Differential Co-expression and Neighborhood Analysis.Journal of computational biology : a journal of computational molecular cell biology · 2021
    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.

Haisu MaProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06511, USA.
Eric E Schadt
Lee M Kaplan
Hongyu Zhao

Funding

STATISTICAL METHODS TO MAP GENES FOR COMPLEX TRAITSR01GM059507 · NIGMS · YALE UNIVERSITY · PI ZHAO, HONGYU · 1999 to 2013
$3.6M
NIGMS NIH HHS GM59507NIGMS NIH HHS R01 GM059507
6 · The paper itself

Abstract

motivationThe identification of condition specific sub-networks from gene expression profiles has important biological applications, ranging from the selection of disease-related biomarkers to the discovery of pathway alterations across different phenotypes. Although many methods exist for extracting these sub-networks, very few existing approaches simultaneously consider both the differential expression of individual genes and the differential correlation of gene pairs, losing potentially valuable information in the data.

resultsIn this article, we propose a new method, COSINE (COndition SpecIfic sub-NEtwork), which employs a scoring function that jointly measures the condition-specific changes of both 'nodes' (individual genes) and 'edges' (gene-gene co-expression). It uses the genetic algorithm to search for the single optimal sub-network which maximizes the scoring function. We applied COSINE to both simulated datasets with various differential expression patterns, and three real datasets, one prostate cancer dataset, a second one from the across-tissue comparison of morbidly obese patients and the other from the across-population comparison of the HapMap samples. Compared with previous methods, COSINE is more powerful in identifying truly significant sub-networks of appropriate size and meaningful biological relevance. AVAILABILITY: The R code is available as the COSINE package on CRAN: http://cran.r-project.org/web/packages/COSINE/index.html.

Indexed as

AlgorithmsGene Regulatory NetworksComputational BiologyGene Expression ProfilingHapMap ProjectHumans

Identifiers

PMID21414987
PMCPMC3138081

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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.