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CardioGenBase: A Literature Based Multi-Omics Database for Major Cardiovascular Diseases
Alexandar V1, Pradeep G Nayar2, R Murugesan1
1Faculty of Allied Health Sciences, Chettinad Academy of Research and Education, Kelambakkam 603 103, Tamil Nadu, India.
CardioGenBase is a new online database that consolidates gene-disease associations for major cardiovascular diseases (CVDs). This resource aids researchers in understanding CVD genetic factors and developing new diagnostic and therapeutic strategies.
Area of Science:
- Genetics and Genomics
- Cardiovascular Research
- Bioinformatics
Background:
- Cardiovascular diseases (CVDs) are a leading cause of global morbidity and mortality.
- Genetic and epigenetic factors significantly contribute to CVD development.
- Existing multi-omics data for CVDs lack comprehensive integration, hindering mechanistic understanding.
Purpose of the Study:
- To develop a centralized, literature-based online database for cardiovascular disease (CVD) gene-disease associations.
- To provide a comprehensive resource for understanding the genetic underpinnings of major CVDs.
- To support advanced research in CVD pathophysiology and genetics.
Main Methods:
- Developed CardioGenBase, a literature-based database, by extracting gene-disease associations from PubMed and MEDLINE.
- Compiled data on approximately 1,500 cardiovascular disease genes from over 24,000 research articles.
- Integrated diverse data types including gene-disease evidence, ontology, pathways, SNPs, protein interactions, and expression data.
Main Results:
- CardioGenBase covers major cardiovascular diseases: cerebrovascular, coronary artery disease (CAD), hypertensive heart disease, inflammatory heart disease, ischemic heart disease, and rheumatic heart disease.
- The database includes detailed information for ~1,500 CVD genes.
- Includes integrated tools for gene-disease association and gene expression analysis, with visual aids.
Conclusions:
- CardioGenBase is the first comprehensive database offering gene-disease associations for major cardiovascular diseases in a single portal.
- It serves as a vital resource for genome-wide association studies, genetic, epigenetic, and pharmacological research in CVDs.
- Facilitates novel methodologies for understanding CVD pathophysiology and advancing personalized medicine.
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