TY - GEN
T1 - A Collective NMF method for detecting protein functional module from multiple data sources
AU - Zhang, Yuan
AU - Du, Nan
AU - Ge, Liang
AU - Jia, Kebin
AU - Zhang, Aidong
PY - 2012
Y1 - 2012
N2 - Detecting functional modules from protein-protein interaction (PPI) networks is an active research area with many practical applications. However, there is always a critical concern on the false PPI interactions which are derived from the high-throughput experiments and the unsatisfactory results obtained from single PPI network with severe information insufficiency. To address this problem, we propose a Collective Non-negative Matrix Factorization (CoNMF) based soft clustering method which efficiently integrates information of gene ontology (GO), gene expression data and PPI networks. In our method, the three data sources are formed into two graphs with similarity adjacency matrices and these graphs are approximated by a matrix factorization with their common factor which provides the straightforward interpretation of clustering results. Extensive experiments show that we can improve the module detection performance by integrating multiple biological data sources and that CoNMF yields superior results compared to other multiple data sources fusion methods by identifying a larger number of more precise protein modules with actual biological meaning and certain degree of overlapping.
AB - Detecting functional modules from protein-protein interaction (PPI) networks is an active research area with many practical applications. However, there is always a critical concern on the false PPI interactions which are derived from the high-throughput experiments and the unsatisfactory results obtained from single PPI network with severe information insufficiency. To address this problem, we propose a Collective Non-negative Matrix Factorization (CoNMF) based soft clustering method which efficiently integrates information of gene ontology (GO), gene expression data and PPI networks. In our method, the three data sources are formed into two graphs with similarity adjacency matrices and these graphs are approximated by a matrix factorization with their common factor which provides the straightforward interpretation of clustering results. Extensive experiments show that we can improve the module detection performance by integrating multiple biological data sources and that CoNMF yields superior results compared to other multiple data sources fusion methods by identifying a larger number of more precise protein modules with actual biological meaning and certain degree of overlapping.
KW - Algorithm
UR - https://www.scopus.com/pages/publications/84869478245
U2 - 10.1145/2382936.2383053
DO - 10.1145/2382936.2383053
M3 - Conference contribution
AN - SCOPUS:84869478245
SN - 9781450316705
T3 - 2012 ACM Conference on Bioinformatics, Computational Biology and Biomedicine, BCB 2012
SP - 655
EP - 660
BT - 2012 ACM Conference on Bioinformatics, Computational Biology and Biomedicine, BCB 2012
T2 - 2012 ACM Conference on Bioinformatics, Computational Biology and Biomedicine, BCB 2012
Y2 - 7 October 2012 through 10 October 2012
ER -