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Chemical effects in biological systems--data dictionary (CEBS-DD): a compendium of terms for the capture and integration of biological study design description, conventional phenotypes, and 'omics data

Toxicol Sci. 2005 Dec;88(2):585-601. doi: 10.1093/toxsci/kfi315. Epub 2005 Sep 8.

Abstract

A critical component in the design of the Chemical Effects in Biological Systems (CEBS) Knowledgebase is a strategy to capture toxicogenomics study protocols and the toxicity endpoint data (clinical pathology and histopathology). A Study is generally an experiment carried out during a period of time for the purpose of obtaining data, and the Study Design Description captures the methods, timing, and organization of the Study. The CEBS Data Dictionary (CEBS-DD) has been designed to define and organize terms in an attempt to standardize nomenclature needed to describe a toxicogenomics Study in a structured yet intuitive format and provide a flexible means to describe a Study as conceptualized by the investigator. The CEBS-DD will organize and annotate information from a variety of sources, thereby facilitating the capture and display of toxicogenomics data in biological context in CEBS, i.e., associating molecular events detected in highly-parallel data with the toxicology/pathology phenotype as observed in the individual Study Subjects and linked to the experimental treatments. The CEBS-DD has been developed with a focus on acute toxicity studies, but with a design that will permit it to be extended to other areas of toxicology and biology with the addition of domain-specific terms. To illustrate the utility of the CEBS-DD, we present an example of integrating data from two proteomics and transcriptomics studies of the response to acute acetaminophen toxicity (A. N. Heinloth et al., 2004, Toxicol. Sci. 80, 193-202).

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetaminophen / toxicity
  • Administration, Oral
  • Animals
  • Biomedical Research*
  • Database Management Systems*
  • Databases, Factual*
  • Dose-Response Relationship, Drug
  • Proteomics
  • Research Design*
  • Systems Biology / methods*
  • Terminology as Topic*
  • Toxicity Tests
  • Toxicogenetics

Substances

  • Acetaminophen