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Analyse multiple disease subtypes and build associated gene networks using genome-wide expression profiles

Overview of attention for article published in BMC Genomics, May 2015
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Title
Analyse multiple disease subtypes and build associated gene networks using genome-wide expression profiles
Published in
BMC Genomics, May 2015
DOI 10.1186/1471-2164-16-s5-s3
Pubmed ID
Authors

Sara Aibar, Celia Fontanillo, Conrad Droste, Beatriz Roson-Burgo, Francisco J Campos-Laborie, Jesus M Hernandez-Rivas, Javier De Las Rivas

Abstract

Despite the large increase of transcriptomic studies that look for gene signatures on diseases, there is still a need for integrative approaches that obtain separation of multiple pathological states providing robust selection of gene markers for each disease subtype and information about the possible links or relations between those genes. We present a network-oriented and data-driven bioinformatic approach that searches for association of genes and diseases based on the analysis of genome-wide expression data derived from microarrays or RNA-Seq studies. The approach aims to (i) identify gene sets associated to different pathological states analysed together; (ii) identify a minimum subset within these genes that unequivocally differentiates and classifies the compared disease subtypes; (iii) provide a measurement of the discriminant power of these genes and (iv) identify links between the genes that characterise each of the disease subtypes. This bioinformatic approach is implemented in an R package, named geNetClassifier, available as an open access tool in Bioconductor. To illustrate the performance of the tool, we applied it to two independent datasets: 250 samples from patients with four major leukemia subtypes analysed using expression arrays; another leukemia dataset analysed with RNA-Seq that includes a subtype also present in the previous set. The results show the selection of key deregulated genes recently reported in the literature and assigned to the leukemia subtypes studied. We also show, using these independent datasets, the selection of similar genes in a network built for the same disease subtype. The construction of gene networks related to specific disease subtypes that include parameters such as gene-to-gene association, gene disease specificity and gene discriminant power can be very useful to draw gene-disease maps and to unravel the molecular features that characterize specific pathological states. The application of the bioinformatic tool here presented shows a neat way to achieve such molecular characterization of the diseases using genome-wide expression data.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 37 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Canada 1 3%
Unknown 36 97%

Demographic breakdown

Readers by professional status Count As %
Student > Master 9 24%
Researcher 7 19%
Student > Ph. D. Student 6 16%
Student > Postgraduate 3 8%
Professor 3 8%
Other 5 14%
Unknown 4 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 13 35%
Biochemistry, Genetics and Molecular Biology 7 19%
Medicine and Dentistry 6 16%
Computer Science 3 8%
Immunology and Microbiology 1 3%
Other 3 8%
Unknown 4 11%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 March 2016.
All research outputs
#15,365,885
of 22,858,915 outputs
Outputs from BMC Genomics
#6,694
of 10,662 outputs
Outputs of similar age
#156,620
of 266,695 outputs
Outputs of similar age from BMC Genomics
#181
of 258 outputs
Altmetric has tracked 22,858,915 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 10,662 research outputs from this source. They receive a mean Attention Score of 4.7. This one is in the 29th percentile – i.e., 29% of its peers scored the same or lower than it.
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