| abf.normal | Calculate approximate Bayes factor (ABF) for normal prior. |
| abf.t | Calculate approximate Bayes factor (ABF) for t distribution... |
| abf.Wakefield | Calculate approximate Bayes factor (ABF) using method of... |
| agtstats | Hypertension association statistics for SNPs near the AGT... |
| align.snpdata.coding | Update genotype coding when there are coded allele... |
| allelesAB | Paste together (vectors of) A and B alleles after sorting... |
| bp.scores | Genetic risk scores for blood pressure. |
| cad.scores | Genetic risk scores for coronary artery disease risk |
| coeff.extract | Coefficient extractor for fitted models. |
| combine.moments2 | Builds a matrix of second moments for a set of individuals,... |
| contrasting.rainbow | Rainbow of colours permuted to maximise contrast. |
| est.moments2 | Estimate regression coefficients using quadratic... |
| fitmix | Fit finite mixture of univariate Gaussian densities to data. |
| fitmix.plot | Plot empirical density and components and total density for... |
| fitmix.r2 | For finite mixture of univariate Gaussian densities, computes... |
| fitmix.simulate | Simulate from finite mixture of univariate Gaussian... |
| gls.approx.logistic | Calculate weights and transformed phenotype so that one... |
| grs.filter.Qrs | Filter SNPs for inclusion in genetic risk score using... |
| grs.make.scores | Make genetic risk scores from individual-level data. |
| grs.onesnp.apply | Convenience tool to fit a series of single-SNP models. |
| grs.plot | Diagnostic plot for genetic risk score calculation from... |
| grs.summary | Genetic risk score calculation from summary statistics. |
| gtx-package | Genetics ToolboX |
| gtx.params | Parameter format for multi-SNP analyses |
| hapmap.read.haplotypes | Read hapmap haplotypes. |
| hapmap.snpdata | Extract individual level snp/haplotype data from HapMap |
| height.scores | Genetic risk score for height. |
| lipid.cad.scores | Genetic risk scores for serum lipid levels and coronary... |
| lipid.scores | Genetic risk scores for serum lipid levels |
| liver.scores | Genetic risk scores for liver enzyme traits. |
| lm.moments2 | Fit normal linear model using pre-built matrix of second... |
| magic.scores | Genetic risk scores for glucose/insulin traits. |
| make.moments2 | Build matrix of second moments from subject-specific data. |
| mincover | Compute minimum size of cover of overlapping intervals. |
| moments2 | Class for summary statistic matrix of second moments. |
| mthfrex | Simulated example finemapping genotype and phenotype data. |
| multimatch | Match with multiple matching possible. |
| multipheno.T2 | Multi-phenotype test for association |
| ncp | Compute non-centrality parameter of chi squared distribution. |
| parse.snps | Parse text representation of a SNP embedded in flanking... |
| read.snpdata.impute | Read genotype dosages in the format output by IMPUTE. |
| read.snpdata.mach | Read genotype dosages in the format output by MACH |
| read.snpdata.minimac | Read genotype dosages in the format output by minimac |
| read.snpdata.plink | Read genotype dosages in the format output by PLINK. |
| remap.q2t | Remap coordinates from BLAT query sequence to BLAT target... |
| sanitise.whitespace | Remove leading and trailing spaces; convert double spaces to... |
| snpdata | Class for SNP genotype and phenotype data. |
| snphwe | Exact test of Hardy-Weinberg. |
| snphweCounts | Exact test of Hardy-Weinberg. |
| snps.BRCA1 | Genotyping array annotation for SNPs near the BRCA1 gene. |
| stepdown.moments2 | Stepwise downward model selection using summary statistic... |
| stepup.moments2 | Stepwise upward model selection using summary statistic... |
| t2dex | Simulated example genotype and longitudinal phenotype data. |
| t2d.scores | Genetic risk scores for type 2 diabetes risk. |
| test.subsample | Test approximation used in genetic risk score analyses. |
