gpart
gpart partitions genomes into linkage disequilibrium (LD) units and visualizes LD structure to support analysis of high-density single nucleotide polymorphism (SNP) data from next-generation sequencing (NGS).
Key Features:
- Clustering algorithms: Employs clustering algorithms to define LD blocks or analysis units composed of SNPs.
- Visualization: Produces images that display LD structure together with gene positions for up to 20,000 SNPs in a single figure.
- Computational efficiency: Optimized to process large genome sequencing datasets within time and memory constraints on standard computing environments.
Scientific Applications:
- Genetic linkage and association studies: Identifying haplotype blocks and LD units to inform association mapping of traits and diseases.
- Complex trait gene mapping: Facilitating localization of genes associated with complex traits via LD partitioning.
- Population genetics: Characterizing LD structure to study population-specific patterns of genetic variation.
- Evolutionary biology: Exploring genomic LD patterns to infer evolutionary processes affecting genetic architecture.
Methodology:
Applies clustering algorithms to SNP/genomic data to delineate regions of linkage disequilibrium and visualizes those regions alongside gene positions, with optimizations for efficient processing of large datasets.
Topics
Details
- License:
- MIT
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- R
- Added:
- 8/9/2019
- Last Updated:
- 11/24/2024
Operations
Publications
Kim SA, Brossard M, Roshandel D, Paterson AD, Bull SB, Yoo YJ. gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks. Bioinformatics. 2019;35(21):4419-4421. doi:10.1093/bioinformatics/btz308. PMID:31070701. PMCID:PMC6821423.
PMID: 31070701
PMCID: PMC6821423
Funding: - NRF: NRF-2018R1A2B6008016
- CIHR: MOP-84287, PJT 159463
- Canadian Institutes of Health Research Strategic Training for Advanced Genetic Epidemiology: GET-101831