ViVa
ViVa visualizes natural genetic variation from publicly available genome datasets to support analysis of variation at gene, gene-family, and gene-network levels for hypothesis generation and testing.
Key Features:
- Data Accessibility: Leverages publicly available genomic datasets, including the Arabidopsis thaliana 1001 Genomes Project, to enable exploration of natural variation.
- Multi-level Analysis: Enables analysis of variation at the gene, gene-family, and gene-network levels.
- Extensibility: Supports integration with interspecific genetic variation databases such as the 3,000 Rice Genomes Project and ClinVar.
- Pathway- and Network-focused Analysis: Facilitates focused exploration of specific pathways or networks, for example the nuclear auxin signaling pathway.
Scientific Applications:
- Hypothesis Generation and Testing: Facilitates generation and testing of hypotheses by analyzing natural variation to confirm known biology and suggest novel hypotheses.
- Pathway Validation: Applied to well-studied pathways, such as the nuclear auxin signaling pathway in Arabidopsis thaliana, to corroborate existing functional insights.
- Comparative and Cross-species Analysis: Enables comparative studies across species and databases by integrating datasets from projects like the 3,000 Rice Genomes Project and ClinVar.
- Investigation of Less-characterized Gene Families and Networks: Supports discovery-driven analyses of poorly characterized gene families and networks using natural variation data.
Methodology:
Collaborative analyses focusing on specific pathways or networks to explore how natural variation influences biological functions.
Topics
Details
- Added:
- 11/14/2019
- Last Updated:
- 1/11/2021
Operations
Publications
Hamm MO, Moss BL, Leydon AR, Gala HP, Lanctot A, Ramos R, Klaeser H, Lemmex AC, Zahler ML, Nemhauser JL, Wright RC. Accelerating structure‐function mapping using the ViVa webtool to mine natural variation. Plant Direct. 2019;3(7). doi:10.1002/pld3.147. PMID:31372596. PMCID:PMC6658840.
DOI: 10.1002/PLD3.147
PMID: 31372596
PMCID: PMC6658840
Funding: - National Science Foundation: DBI‐1402222, IOS‐1546873