TY - JOUR
T1 - Lean Big Data integration in systems biology and systems pharmacology
AU - Ma'ayan, Avi
AU - Rouillard, Andrew D.
AU - Clark, Neil R.
AU - Wang, Zichen
AU - Duan, Qiaonan
AU - Kou, Yan
N1 - Funding Information:
This project was supported by NIH grants R01GM098316, U54CA189201-01, U54HG006097-S1 to A.M. The authors thank Drs. Mario Medvedovic and Stephan Schurer for useful discussions.
Publisher Copyright:
Copyright © 2014 Elsevier Ltd. All rights reserved.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Data sets from recent large-scale projects can be integrated into one unified puzzle that can provide new insights into how drugs and genetic perturbations applied to human cells are linked to whole-organism phenotypes. Data that report how drugs affect the phenotype of human cell lines and how drugs induce changes in gene and protein expression in human cell lines can be combined with knowledge about human disease, side effects induced by drugs, and mouse phenotypes. Such data integration efforts can be achieved through the conversion of data from the various resources into single-node-type networks, gene-set libraries, or multipartite graphs. This approach can lead us to the identification of more relationships between genes, drugs, and phenotypes as well as benchmark computational and experimental methods. Overall, this lean 'Big Data' integration strategy will bring us closer toward the goal of realizing personalized medicine.
AB - Data sets from recent large-scale projects can be integrated into one unified puzzle that can provide new insights into how drugs and genetic perturbations applied to human cells are linked to whole-organism phenotypes. Data that report how drugs affect the phenotype of human cell lines and how drugs induce changes in gene and protein expression in human cell lines can be combined with knowledge about human disease, side effects induced by drugs, and mouse phenotypes. Such data integration efforts can be achieved through the conversion of data from the various resources into single-node-type networks, gene-set libraries, or multipartite graphs. This approach can lead us to the identification of more relationships between genes, drugs, and phenotypes as well as benchmark computational and experimental methods. Overall, this lean 'Big Data' integration strategy will bring us closer toward the goal of realizing personalized medicine.
KW - data integration
KW - network analysis
KW - network pharmacology
KW - side-effect prediction
KW - systems pharmacology
KW - target prediction
UR - http://www.scopus.com/inward/record.url?scp=84961371413&partnerID=8YFLogxK
U2 - 10.1016/j.tips.2014.07.001
DO - 10.1016/j.tips.2014.07.001
M3 - Review article
C2 - 25109570
AN - SCOPUS:84961371413
SN - 0165-6147
VL - 35
SP - 450
EP - 460
JO - Trends in Pharmacological Sciences
JF - Trends in Pharmacological Sciences
IS - 9
ER -