--- title: "GEVACO Introduction" author: | | Sydney Manning | Department of Pharmacotherapy | University of North Texas Health Science Center -- Fort Worth date: "Dec 8, 2021" output: pdf_document vignette: > %\VignetteIndexEntry{GEVACO Introduction} %\VignetteEngine{knitr::rmarkdown} %\VignetteEncoding{UTF-8} --- ````{r setup, include = FALSE} knitr::opts_chunk$set( collapse = TRUE, comment = "#>" ) ```` ````{r, results="hide", warning=FALSE, message=FALSE} library(GEVACO) # load the library ```` ## Data requirements At minimum to run this analysis you need a file storing genotype information and a covariate/trait file. The covariate/trait file should be text based and can have as many columns/covariates as desired, but the first few must be in a specific order. * Column 1: Phenotype * Column 2: Environmental factor * Columns 3+: Additional covariates ````{r} data(cov_example) # read in the example covariate data head(cov_example) # view the format of the covariate file ```` If you have PLINK bed files or files in other format, you will need to convert the genotypes to a genotype matrix and filter it for your SNPs of interest. We chose to filter our dataframe by finding the location of all SNPs meeting our desired threshold of minor allele frequency. ````{r} data(geno_example) # read in the example genomic file # we included the first 20 SNPs to meet our criteria, each column head(geno_example) # is a different SNP ```` ## Performing the screening test Using the filtered genomic data, all that's left is to input it with the covariate information into the final function. The default number of simulation iterations is 1E5, and the default number of knots is 7. ````{r} results <- GxEscreen(dat=cov_example, geno=geno_example, nsim = 1e5, K=7) # run the screen # view the first few results: these are the p.values for each SNP in the final head(results) # genomic file ```` The final output is a vector containing the p-value of each SNP used in the simulation.