Abstract

BackgroundAlthough biomedical information is growing rapidly, it is difficult to find and retrieve validated data especially for rare hereditary diseases. There is an increased need for services capable of integrating and validating information as well as proving it in a logically organized structure. A XML-based language enables creation of open source databases for storage, maintenance and delivery for different platforms.MethodsHere we present a new data model called fact file and an XML-based specification Inherited Disease Markup Language (IDML), that were developed to facilitate disease information integration, storage and exchange. The data model was applied to primary immunodeficiencies, but it can be used for any hereditary disease. Fact files integrate biomedical, genetic and clinical information related to hereditary diseases.ResultsIDML and fact files were used to build a comprehensive Web and WAP accessible knowledge base ImmunoDeficiency Resource (IDR) available at . A fact file is a user oriented user interface, which serves as a starting point to explore information on hereditary diseases.ConclusionThe IDML enables the seamless integration and presentation of genetic and disease information resources in the Internet. IDML can be used to build information services for all kinds of inherited diseases. The open source specification and related programs are available at .

Highlights

  • Biomedical information is growing rapidly, it is difficult to find and retrieve validated data especially for rare hereditary diseases

  • We present a new data model called fact file, which integrates biomedical information related to hereditary diseases into a Web and WAP accessible knowledge base

  • The disease information is stored in Inherited Disease Markup Language (IDML)-based fact files, which form the central repository for data retrieval of ImmunoDeficiency Resource (IDR) service [23,24,29] available at http://bioinf.uta.fi/idr/

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Summary

Introduction

Biomedical information is growing rapidly, it is difficult to find and retrieve validated data especially for rare hereditary diseases. The completion of the draft sequence of the human genome [2,3] and advances in molecular biology provide new opportunities to increase our understanding of the role of genetic factors in human health and disease [1]. The number of identified genetic diseases has increased exponentially [4]. The new knowledge can be applied to the prevention, diagnosis and treatment of diseases. This far, the knowledge of genetics has had a large role in the health care of only a (page number not for citation purposes)

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