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Nature Biotechnology  22, 1268 - 1274 (2004)
Published online: 6 October 2004; | doi:10.1038/nbt1015

The challenges of modeling mammalian biocomplexity

Jeremy K Nicholson1, Elaine Holmes1, John C Lindon1 & Ian D Wilson2

1  Biological Chemistry, Biomedical Sciences Division, Imperial College London, Sir Alexander Fleming Building, South Kensington, London SW7 2AZ, UK.

2  Dept. of Drug Metabolism and Pharmacokinetics, AstraZeneca Pharmaceuticals, Mereside, Alderley Park, Macclesfield, Cheshire SK10 4TG, UK.

Correspondence should be addressed to Jeremy K Nicholson j.nicholson@imperial.ac.uk
Understanding the relationships between human genetic factors, the risks of developing major diseases and the molecular basis of drug efficacy and toxicity is a fundamental problem in modern biology. Predicting biological outcomes on the basis of genomic data is a major challenge because of the interactions of specific genetic profiles with numerous environmental factors that may conditionally influence disease risks in a nonlinear fashion. 'Global' systems biology attempts to integrate multivariate biological information to better understand the interaction of genes with the environment. The measurement and modeling of such diverse information sets is difficult at the analytical and bioinformatic modeling levels. Highly complex animals such as humans can be considered 'superorganisms' with an internal ecosystem of diverse symbiotic microbiota and parasites that have interactive metabolic processes. We now need novel approaches to measure and model metabolic compartments in interacting cell types and genomes that are connected by cometabolic processes in symbiotic mammalian systems.

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Nature Biotechnology
ISSN: 1087-0156
EISSN: 1546-1696
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