CardioGenBase: A Literature Based Multi-Omics Database for Major Cardiovascular Diseases

PLoS One. 2015 Dec 1;10(12):e0143188. doi: 10.1371/journal.pone.0143188. eCollection 2015.

Abstract

Cardiovascular diseases (CVDs) account for high morbidity and mortality worldwide. Both, genetic and epigenetic factors are involved in the enumeration of various cardiovascular diseases. In recent years, a vast amount of multi-omics data are accumulated in the field of cardiovascular research, yet the understanding of key mechanistic aspects of CVDs remain uncovered. Hence, a comprehensive online resource tool is required to comprehend previous research findings and to draw novel methodology for understanding disease pathophysiology. Here, we have developed a literature-based database, CardioGenBase, collecting gene-disease association from Pubmed and MEDLINE. The database covers major cardiovascular diseases such as cerebrovascular disease, coronary artery disease (CAD), hypertensive heart disease, inflammatory heart disease, ischemic heart disease and rheumatic heart disease. It contains ~1,500 cardiovascular disease genes from ~2,4000 research articles. For each gene, literature evidence, ontology, pathways, single nucleotide polymorphism, protein-protein interaction network, normal gene expression, protein expressions in various body fluids and tissues are provided. In addition, tools like gene-disease association finder and gene expression finder are made available for the users with figures, tables, maps and venn diagram to fit their needs. To our knowledge, CardioGenBase is the only database to provide gene-disease association for above mentioned major cardiovascular diseases in a single portal. CardioGenBase is a vital online resource to support genome-wide analysis, genetic, epigenetic and pharmacological studies.

MeSH terms

  • Biological Availability
  • Cardiovascular Diseases / drug therapy
  • Cardiovascular Diseases / genetics*
  • Chromosomes, Human / genetics
  • Databases, Genetic*
  • Gene Ontology
  • Humans
  • MEDLINE
  • Polymorphism, Single Nucleotide
  • Protein Interaction Maps
  • Transcriptome

Grants and funding

The authors have no support or funding to report.