Systems biology data analysis methodology in pharmacogenomics
- PMID: 21919609
- PMCID: PMC3482399
- DOI: 10.2217/pgs.11.76
Systems biology data analysis methodology in pharmacogenomics
Abstract
Pharmacogenetics aims to elucidate the genetic factors underlying the individual's response to pharmacotherapy. Coupled with the recent (and ongoing) progress in high-throughput genotyping, sequencing and other genomic technologies, pharmacogenetics is rapidly transforming into pharmacogenomics, while pursuing the primary goals of identifying and studying the genetic contribution to drug therapy response and adverse effects, and existing drug characterization and new drug discovery. Accomplishment of both of these goals hinges on gaining a better understanding of the underlying biological systems; however, reverse-engineering biological system models from the massive datasets generated by the large-scale genetic epidemiology studies presents a formidable data analysis challenge. In this article, we review the recent progress made in developing such data analysis methodology within the paradigm of systems biology research that broadly aims to gain a 'holistic', or 'mechanistic' understanding of biological systems by attempting to capture the entirety of interactions between the components (genetic and otherwise) of the system.
Conflict of interest statement
The authors have no other relevant affiliations or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
No writing assistance was utilized in the production of this manuscript.
References
Bibliography
-
- Motsinger-Reif AA, Jorgenson E, Relling MV, et al. Genome-wide association studies in pharmacogenomics: successes and lessons. Pharmacogenet Genomics. 2010 doi: 10.1097/FPC.0b013e32833d7b45. Epub ahead of print. Comprehensive review of genome-wide association study pros and cons in the pharmacogenomics context. - DOI - PMC - PubMed
Websites
-
- Heckerman DA. Tutorial on learning with Bayesian networks Technical report MSR-TR-95–06, Microsoft research. 1995 http://research.microsoft.com/en-us/um/people/heckerman/tutorial.pdf Detailed introduction to BN modeling.
-
- Friedman N, Nachman I, Pe’er D. Learning Bayesian network structure from massive datasets: The “sparse candidate” algorithm. Proc. Fifteenth Conference on Uncertainty in Artificial Intelligence. UAI ’99; 1999. pp. 196–205. www.cs.huji.ac.il/~nirf/Papers/FPN1.pdf.
-
- GraphViz (Graph Visualization) software. www.graphviz.org.
-
- Ariadne Pathway Studio pathway analysis software. www.ariadnegenomics.com/products/ pathway-studio.
-
- KEGG Pathway Database. www.genome.jp/kegg/pathway.html.
Publication types
MeSH terms
Grants and funding
- RC2 HL102419/HL/NHLBI NIH HHS/United States
- 5RC2HL102419/HL/NHLBI NIH HHS/United States
- U01 GM074492/GM/NIGMS NIH HHS/United States
- 5R01HL083498/HL/NHLBI NIH HHS/United States
- R01 HL072810/HL/NHLBI NIH HHS/United States
- R01 HL083498/HL/NHLBI NIH HHS/United States
- U01 HG004402/HG/NHGRI NIH HHS/United States
- R03 LM009738/LM/NLM NIH HHS/United States
- 5R03LM009738/LM/NLM NIH HHS/United States
- 5P50GM065509/GM/NIGMS NIH HHS/United States
- 5R01HL084099/HL/NHLBI NIH HHS/United States
- 2U01GM074492/GM/NIGMS NIH HHS/United States
- R01 HL084099/HL/NHLBI NIH HHS/United States
- 5R01HL072810/HL/NHLBI NIH HHS/United States
- R01 AI085014/AI/NIAID NIH HHS/United States
- 1R01AI085014/AI/NIAID NIH HHS/United States
- 3U01HG004402/HG/NHGRI NIH HHS/United States
- 5R01HL086694/HL/NHLBI NIH HHS/United States
- P50 GM065509/GM/NIGMS NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical