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[[Rarefy|'''rarefy''']] is a tool to help selecting informative families and individuals from a sample. It takes account pedigree structure and calculates an informative score for each individual to evaluate the potential of carrying trait-influencing rare variants. It has been used for selecting individuals in Minnesota Twins substance abuse whole-genome sequencing project and SardiNia deep sequencing project.
[[Rarefy|'''rarefy''']] is a tool to help selecting informative families and individuals from a sample. It takes account pedigree structure and calculates an informative score for each individual to evaluate the potential of carrying trait-influencing rare variants. It has been used for selecting individuals in Minnesota Twins substance abuse whole-genome sequencing project and SardiNia deep sequencing project.
[[FamRvTest|'''famRvTest''']] is an efficient tool for rare variant association analysis. It handles related individuals and study specific covariates. The tool supports both single variant and gene-level associations. It has been used in eQTL and quantitative traits association analysis in T2Dgenes project.
[[FamRvTest|'''famRvTest''']] is an efficient tool for rare variant association analysis. It handles related individuals and study specific covariates. The tool supports both single variant and gene-level associations with various methods implemented. It has been used in eQTL and quantitative traits association analysis in T2Dgenes project.
[[RAREMETALWORKER|'''raremetalworker''']] is a tool to generate summary statistics for meta-analysis of rare variants using raremetal. It handles both related and unrelated individuals.
[[RAREMETALWORKER|'''raremetalworker''']] is a tool to generate summary statistics for meta-analysis of rare variants using raremetal. It handles both related and unrelated individuals.
[[RAREMETAL|'''raremetal''']] is a tool for meta-analysis of rare variants. It supports both single variant and gene-level tests.
[[RAREMETAL|'''raremetal''']] is a tool for meta-analysis of rare variants. It supports both single variant and gene-level tests.
