HaploView

HaploView performs haplotype analysis and linkage disequilibrium calculation to characterize haplotype structure and visualize LD patterns from primary genotype datasets for genetic association and population studies.


Key Features:

  • Linkage Disequilibrium (LD) Analysis: Computes linkage disequilibrium statistics to identify non-random associations between genetic variants.
  • Population Haplotype Characterization: Characterizes haplotype patterns across populations using primary genotype data to reveal genetic diversity and structure.
  • Visualization and Plotting: Generates visualizations of LD matrices and haplotype patterns and supports plotting of analysis results.
  • Integration with PLINK Results: Supports visualization and plotting of results produced by PLINK for whole-genome association studies.
  • Primary Genotype Data Processing: Processes primary genotype data and computes necessary statistics for analysis of large genomic datasets.

Scientific Applications:

  • Genetic Association Studies: Enables detection and localization of disease-associated variants through LD and haplotype analyses.
  • Population Genetics: Supports analysis of genetic diversity and population structure by characterizing haplotype distributions.
  • Variant Prioritization and Translational Research: Assists fine-mapping and variant interpretation workflows to inform translational and personalized medicine research.

Methodology:

Processes primary genotype data to compute linkage disequilibrium statistics, characterize haplotype patterns, and generate visualizations; plots can be generated from PLINK outputs and computations are performed by underlying computational algorithms for large genomic datasets.

Topics

Collections

Details

License:
MIT
Tool Type:
workflow
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java
Added:
8/20/2017
Last Updated:
11/25/2024

Operations

Publications

Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2004;21(2):263-265. doi:10.1093/bioinformatics/bth457. PMID:15297300.

Documentation