Comprehensive coverage of cardiovascular disease data in the disease portals at the Rat Genome Database

Author:

Wang Shur-Jen1,Laulederkind Stanley J. F.1,Hayman G. Thomas1,Petri Victoria1,Smith Jennifer R.1,Tutaj Marek1,Nigam Rajni1,Dwinell Melinda R.2,Shimoyama Mary1

Affiliation:

1. Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin; and

2. Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin

Abstract

Cardiovascular diseases are complex diseases caused by a combination of genetic and environmental factors. To facilitate progress in complex disease research, the Rat Genome Database (RGD) provides the community with a disease portal where genome objects and biological data related to cardiovascular diseases are systematically organized. The purpose of this study is to present biocuration at RGD, including disease, genetic, and pathway data. The RGD curation team uses controlled vocabularies/ontologies to organize data curated from the published literature or imported from disease and pathway databases. These organized annotations are associated with genes, strains, and quantitative trait loci (QTLs), thus linking functional annotations to genome objects. Screen shots from the web pages are used to demonstrate the organization of annotations at RGD. The human cardiovascular disease genes identified by annotations were grouped according to data sources and their annotation profiles were compared by in-house tools and other enrichment tools available to the public. The analysis results show that the imported cardiovascular disease genes from ClinVar and OMIM are functionally different from the RGD manually curated genes in terms of pathway and Gene Ontology annotations. The inclusion of disease genes from other databases enriches the collection of disease genes not only in quantity but also in quality.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute (NHBLI)

Publisher

American Physiological Society

Subject

Genetics,Physiology

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