| add_u | Add confounder variables and their instruments | 
| allele_frequency | Estimate allele frequency from SNP | 
| arbitrary_map | Create an arbitrary map | 
| ascertain_samples | Ascertain some proportion of cases and controls from binary... | 
| choose_effects | Get vector of effects that explain some amount of variance | 
| contingency | Obtain 2x2 contingency table from marginal parameters and... | 
| correlated_binomial | Simulate two correlated binomial variables | 
| create_system | Wrapper for simulation pipeline | 
| estimate_system_effects | Estimate the effects of all SNPs on all phenotypes | 
| expected_mse | Calculate expected MSE | 
| expected_se | Expected se given beta, af, n and vy | 
| expected_ssx | Calculate expected SSX | 
| fast_assoc | Get summary statistics in simple linear regression | 
| generate_gwas_params | Generate SNP effects given MAF, h2 and selection | 
| generate_gwas_ss | Modify SNP effects to account for LD | 
| generate_gwas_ss_1 | Create a GWAS summary dataset | 
| generate_ldobj | Generate LD matrix objects from reference panel | 
| get_effs | Get effs for two traits and make dat format | 
| get_ld | Get LD matrix for a specified region from bfile reference... | 
| get_population_allele_frequency | Estimate the allele frequency in population from case/control... | 
| get_regions_from_ldobjdir | Determine regions from LD file | 
| gwas | Perform association of many SNPs against phenotype | 
| gx_to_gp | Translate risk from liability to probability scale | 
| hap_freqs | Estimate haplotype frequencies for two loci | 
| init_parameters | Choose initial parameters for direct effects on X and Y | 
| ldetect | Data frame of independent LD regions | 
| lor_to_rsq | Estimate proportion of variance of liability explained by SNP... | 
| make_geno | Create genotype matrix | 
| make_mvdat | Take several exposures and one outcome and make the data... | 
| make_phen | Simulate variable based on the influences of other variables | 
| merge_exp_out | Organise outputs from 'gwas' into harmonised dat format | 
| pipe | Pipe operator | 
| range01 | Scale variable to have range between 0 and 1 | 
| read_ldobjdir | Read in LD objects into list | 
| recode_dat | Recode data to make every effect on x positive | 
| recode_dat_intercept | Intercept recoding to have every effect on x positive | 
| recode_dat_simple | Simple recoding to have every effect on x positive | 
| risk_cross_plot | Plot liability vs probability disease risk | 
| risk_simulation | Make simulation to compare disease and liability scales | 
| sample_beta | Sample beta values given standard errors | 
| sample_system_effects | Sample the actual effects based on initial parameters | 
| simulate_geno | Simulate genotypes from haplotypes | 
| simulateGP-package | simulateGP: Functions for Simulating Genotype-Phenotype... | 
| simulate_haplotypes | Simulate haplotypes of two loci | 
| simulate_population | Simulate individual level data from initial parameters | 
| stuff | General funcs | 
| summary_set | Wrapper for generating a summary set | 
| test_ldobj | Create test LD object | 
| test_system | Apply MR tests to system | 
| y_to_binary | Convert continuous trait to binary | 
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