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  • Oral presentation
  • Open Access

Toxicological knowledge discovery by mining emerging patterns from toxicity data

  • 1Email author,
  • 2,
  • 2,
  • 2 and
  • 2
Journal of Cheminformatics20135 (Suppl 1) :O9

  • Published:


  • Expert System
  • Toxicology
  • Association Rule
  • Rule Mining
  • Association Rule Mining

Predicting the risk of toxic and environmental effects of chemical compounds is of great importance to all chemical industries [1]. Expert systems have shown success in predicting toxic risk by applying established knowledge of toxicology encoded as a knowledge base of structural alerts and a reasoning model. A disadvantage of expert systems is that developing new structural alerts requires considerable time and effort from domain experts. In order to expedite this process a software tool has been developed that can automatically mine representations of activating features directly from toxicity datasets and present them in an interpretable form.

Our knowledge discovery tool applies emerging pattern (EP) mining [2]: a form of association rule mining [3] that is well known to computer science, but is relatively new to chemistry [4]. The EP mining algorithm accepts any data expressed as a series of binary properties, which is divided into two classes, and extracts patterns of those properties that are frequent within the data and are more frequent in one data class compared to the other. By mining emerging patterns from toxicity datasets, encoded as fingerprints of binary descriptors, the tool generates patterns of features that distinguish toxicants from innocuous compounds. These patterns represent potentially activating features of the toxic compounds that may then be used to define new alerts.

The knowledge discovery tool has been tested using a public dataset of 3489 mutagens and 2981 non-mutagens, encoded as fingerprints of approximately 2000 functional groups and ring descriptors. EPs were produced and grouped into a number of hierarchical families. Six of the EPs that represented distinct chemical classes were selected for manual inspection by a toxicology expert. Relevant literature was analysed to find a mechanistic rationale for the mined features, which resulted in four new structural alerts for in vitro mutagenicity.

Authors’ Affiliations

Information School, The University of Sheffield, Sheffield, S1 4DP, UK
Lhasa Limited, Leeds, LS2 9HD, UK


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© Sherhod et al.; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.