Association Viewer
Association Viewer visualizes SNPs and genomic annotations to contextualize genome-wide association study (GWAS) results and related genetic variation.
Key Features:
- Genomic context visualization: Displays SNPs and other genetic variants alongside gene annotations, linkage disequilibrium (LD) plots, and user-supplied datasets within genomic regions.
- Data integration: Retrieves gene annotations from Ensembl and LD data from HapMap for use in analyses.
- Custom data import: Accepts user tracks in BED and WIG file formats to incorporate custom datasets.
- Efficient data handling: Implements on-the-fly downloading of supplementary data with local caching to reduce redundant retrieval.
- Track operations: Supports aggregation and intersection of multiple data tracks for comparative analyses across regions.
- Scalability: Handles very large-scale genomic datasets for high-throughput genetic studies.
- Cross-platform compatibility: Implemented in Java and reported to run on Microsoft Windows XP, MacOSX, and GNU/Linux.
Scientific Applications:
- GWAS interpretation: Visualizes association signals to aid identification of candidate genes and interpretation of genomic architecture underlying trait associations.
- Genomic research: Enables detailed examination of genetic variation for applications in functional genomics, population genetics, and evolutionary biology.
- Custom data analysis: Integrates user-provided tracks to support hypothesis-driven exploration and analysis of specific datasets.
Methodology:
Implemented in Java; retrieves Ensembl gene annotations and HapMap LD data, imports BED and WIG files, implements on-the-fly data download with local caching, and supports aggregation or intersection of multiple data tracks.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Java
- Added:
- 12/6/2017
- Last Updated:
- 11/24/2024
Operations
Publications
Martin O, Valsesia A, Telenti A, Xenarios I, Stevenson BJ. AssociationViewer: a scalable and integrated software tool for visualization of large-scale variation data in genomic context. Bioinformatics. 2009;25(5):662-663. doi:10.1093/bioinformatics/btp017. PMID:19168913. PMCID:PMC2647839.