Limits...
Network and data integration for biomarker signature discovery via network smoothed T-statistics.

Cun Y, Fröhlich H - PLoS ONE (2013)

Bottom Line: We here propose a technique that integrates network information as well as different kinds of experimental data (here exemplified by mRNA and miRNA expression) into one classifier.Moreover, obtained gene lists can be clearly associated to biological knowledge, such as known disease genes and KEGG pathways.We demonstrate that our data integration strategy can improve classification performance compared to using a single data source only.

View Article: PubMed Central - PubMed

Affiliation: Algorithmic Bioinformatics, Bonn-Aachen International Center for IT, Bonn, Germany.

ABSTRACT
Predictive, stable and interpretable gene signatures are generally seen as an important step towards a better personalized medicine. During the last decade various methods have been proposed for that purpose. However, one important obstacle for making gene signatures a standard tool in clinics is the typical low reproducibility of signatures combined with the difficulty to achieve a clear biological interpretation. For that purpose in the last years there has been a growing interest in approaches that try to integrate information from molecular interaction networks. We here propose a technique that integrates network information as well as different kinds of experimental data (here exemplified by mRNA and miRNA expression) into one classifier. This is done by smoothing t-statistics of individual genes or miRNAs over the structure of a combined protein-protein interaction (PPI) and miRNA-target gene network. A permutation test is conducted to select features in a highly consistent manner, and subsequently a Support Vector Machine (SVM) classifier is trained. Compared to several other competing methods our algorithm reveals an overall better prediction performance for early versus late disease relapse and a higher signature stability. Moreover, obtained gene lists can be clearly associated to biological knowledge, such as known disease genes and KEGG pathways. We demonstrate that our data integration strategy can improve classification performance compared to using a single data source only. Our method, called stSVM, is available in R-package netClass on CRAN (http://cran.r-project.org).

Show MeSH

Related in: MedlinePlus

Sub-graph of disease related module identified by stSVM (MSKCC prostate cancer).The shown sub-graph consists of consistently selected genes in the interactome of the AR. For better visualization edges between neighbors of the AR are omitted. Red: cancer related genes; yellow: prostate cancer related genes.
© Copyright Policy
Related In: Results  -  Collection


getmorefigures.php?uid=PMC3760887&req=5

pone-0073074-g005: Sub-graph of disease related module identified by stSVM (MSKCC prostate cancer).The shown sub-graph consists of consistently selected genes in the interactome of the AR. For better visualization edges between neighbors of the AR are omitted. Red: cancer related genes; yellow: prostate cancer related genes.

Mentions: For both, ovarian and prostate cancer, network modules were highly enriched for known disease genes ( for prostate cancer in MSKCC prostate cancer case, for ovarian cancer in ovarian cancer case) according to FunDO. Figure 5 and Figure 6 visualize sub-networks of these modules centered at the AR (MSKCC prostate cancer) and BRCA1 (ovarian cancer), respectively.


Network and data integration for biomarker signature discovery via network smoothed T-statistics.

Cun Y, Fröhlich H - PLoS ONE (2013)

Sub-graph of disease related module identified by stSVM (MSKCC prostate cancer).The shown sub-graph consists of consistently selected genes in the interactome of the AR. For better visualization edges between neighbors of the AR are omitted. Red: cancer related genes; yellow: prostate cancer related genes.
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC3760887&req=5

pone-0073074-g005: Sub-graph of disease related module identified by stSVM (MSKCC prostate cancer).The shown sub-graph consists of consistently selected genes in the interactome of the AR. For better visualization edges between neighbors of the AR are omitted. Red: cancer related genes; yellow: prostate cancer related genes.
Mentions: For both, ovarian and prostate cancer, network modules were highly enriched for known disease genes ( for prostate cancer in MSKCC prostate cancer case, for ovarian cancer in ovarian cancer case) according to FunDO. Figure 5 and Figure 6 visualize sub-networks of these modules centered at the AR (MSKCC prostate cancer) and BRCA1 (ovarian cancer), respectively.

Bottom Line: We here propose a technique that integrates network information as well as different kinds of experimental data (here exemplified by mRNA and miRNA expression) into one classifier.Moreover, obtained gene lists can be clearly associated to biological knowledge, such as known disease genes and KEGG pathways.We demonstrate that our data integration strategy can improve classification performance compared to using a single data source only.

View Article: PubMed Central - PubMed

Affiliation: Algorithmic Bioinformatics, Bonn-Aachen International Center for IT, Bonn, Germany.

ABSTRACT
Predictive, stable and interpretable gene signatures are generally seen as an important step towards a better personalized medicine. During the last decade various methods have been proposed for that purpose. However, one important obstacle for making gene signatures a standard tool in clinics is the typical low reproducibility of signatures combined with the difficulty to achieve a clear biological interpretation. For that purpose in the last years there has been a growing interest in approaches that try to integrate information from molecular interaction networks. We here propose a technique that integrates network information as well as different kinds of experimental data (here exemplified by mRNA and miRNA expression) into one classifier. This is done by smoothing t-statistics of individual genes or miRNAs over the structure of a combined protein-protein interaction (PPI) and miRNA-target gene network. A permutation test is conducted to select features in a highly consistent manner, and subsequently a Support Vector Machine (SVM) classifier is trained. Compared to several other competing methods our algorithm reveals an overall better prediction performance for early versus late disease relapse and a higher signature stability. Moreover, obtained gene lists can be clearly associated to biological knowledge, such as known disease genes and KEGG pathways. We demonstrate that our data integration strategy can improve classification performance compared to using a single data source only. Our method, called stSVM, is available in R-package netClass on CRAN (http://cran.r-project.org).

Show MeSH
Related in: MedlinePlus