Passing Messages between Biological Networks to Refine Predicted Interactions

被引:145
作者
Glass, Kimberly [1 ,2 ]
Huttenhower, Curtis [2 ]
Quackenbush, John [1 ,2 ]
Yuan, Guo-Cheng [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
基金
美国国家科学基金会;
关键词
GENE-EXPRESSION DATA; TRANSCRIPTIONAL NETWORKS; GENOMIC DATA; CHIP-CHIP; INFERENCE; INTEGRATION; DISCOVERY; MODULES; PHASE; RECONSTRUCTION;
D O I
10.1371/journal.pone.0064832
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Regulatory network reconstruction is a fundamental problem in computational biology. There are significant limitations to such reconstruction using individual datasets, and increasingly people attempt to construct networks using multiple, independent datasets obtained from complementary sources, but methods for this integration are lacking. We developed PANDA (Passing Attributes between Networks for Data Assimilation), a message-passing model using multiple sources of information to predict regulatory relationships, and used it to integrate protein-protein interaction, gene expression, and sequence motif data to reconstruct genome-wide, condition-specific regulatory networks in yeast as a model. The resulting networks were not only more accurate than those produced using individual data sets and other existing methods, but they also captured information regarding specific biological mechanisms and pathways that were missed using other methodologies. PANDA is scalable to higher eukaryotes, applicable to specific tissue or cell type data and conceptually generalizable to include a variety of regulatory, interaction, expression, and other genome-scale data. An implementation of the PANDA algorithm is available at www.sourceforge.net/projects/panda-net.
引用
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页数:14
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