require(tidyverse)
require(rlang)
#library(gplots)
#library(LDheatmap)
library(genetics)
library(ape)
library(EMMREML)
library(compiler) #this library is already installed in R
library("scatterplot3d")
source("/home/alice/Github/CDBNgenomics/data-raw/GAPIT-example/GAPIT_functions.R")
source("/home/alice/Github/CDBNgenomics/data-raw/GAPIT-example/EMMA_functions.R")
## Use GAPIT to run GWAS on the BLUPs for each phenotype
#Step 1: Import and format phenotypic data; create phenotype directory
projectdir <- "/home/alice/Github/CDBNgenomics/data-raw/GAPIT-example/"
setwd(projectdir)
gapit_phe_asreml <- read.table(file = "/home/alice/Github/CDBNgenomics/data-raw/GAPIT-example/kinBLUP_phenotypedOnly_GAPIT_PC0_2019-02-27.txt", head = TRUE)
# Run GAPIT on this LbY
myGAPIT <- GAPIT(
Y = gapit_phe_asreml,
PCA.total = 0,
model = "CMLM",
file.GD="Numerical_format_GD_CDBN_001_359_pedigree_fillin_chr",
file.Ext.GD="txt",
file.GM="Numerical_format_GM_CDBN_001_359_pedigree_fillin_chr",
file.Ext.GM="txt",
file.from = 1,
file.to = 11,
file.path = "/home/alice/Github/CDBNgenomics/data-raw/GAPIT_Numerical_format_files/"
)
# other options for GAPIT:
# Model.selection = TRUE
# SNP.fraction = 0.4
# args(GAPIT) # see function arguments: default for model is "MLM"
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