Efficient variant-call data storage and retrieval library using the TileDB storage library.
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Updated
May 18, 2024 - C++
Efficient variant-call data storage and retrieval library using the TileDB storage library.
📊 Identify cell types and pathways affected by genetic risk loci.
Use reference genetic map to interpolate genetic position for a query set of variants
Compute imputed variant exclusion lists based on https://doi.org/10.1002%2Fgepi.21603
A Bayesian grouped mixture of regressions model capable of estimating SNP marker effect sizes for multiple outcomes simultaneously
Scalable Implementation of generalized mixed models using GDS files in Phenome-Wide Association Studies
Code and Tutorials for Running the MArginal ePIstasis Test (MAPIT)
Visual Machine Learning of Genome-Phenome Associations
A flexible tool for the multi-resolution localization of causal variants across the genome, accounting for population structure.
Rare variant test software for next generation sequencing data
Estimation of Maternal, Imprinting and interaction effects using Multinomial modelling
GWAS third-level epistatic search tool for cluster architectures
Tool for integrative gene-based association analysis using GWAS summary stats
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