knitr::opts_chunk$set( collapse = TRUE, comment = "#>" )
library(GAPIT3documentation) knitr::opts_chunk$set(fig.align = "center")
Load example data.
myPhenoFile <- system.file("extdata", "mdp_traits.txt.gz", package = "GAPIT3documentation") myGenoFile <- system.file("extdata", "mdp_genotype_test.hmp.txt.gz", package = "GAPIT3documentation") myPhenotypes <- read.table(myPhenoFile, header = TRUE) myGenotypes <- read.table(myGenoFile, header = FALSE) head(myPhenotypes) myGenotypes[1:4, 1:9]
From GAPIT.R we have the first call to GAPIT.DP.
DP = GAPIT.DP(G=G, GD=GD, GM=GM, KI=KI0, Z=Z, CV=CV, CV.Inheritance = Para$CV.Inheritance, GP = GP, GK = GK, group.from = Para$group.from, group.to = Para$group.to, group.by = Para$group.by, DPP = Para$DPP, FDRcut = Para$FDRcut, kinship.cluster = Para$kinship.cluster, kinship.group = Para$kinship.group, kinship.algorithm = Para$kinship.algorithm, NJtree.group = Para$NJtree.group, NJtree.type = Para$NJtree.type, plot.bin = Para$plot.bin, PCA.col = Para$PCA.col, PCA.3d = Para$PCA.3d, sangwich.top = Para$sangwich.top, sangwich.bottom = Para$sangwich.bottom, LD=Para$LD,bin.from = Para$bin.from, bin.to = Para$bin.to, bin.by = Para$bin.by, inclosure.from = Para$inclosure.from, inclosure.to = Para$inclosure.to, inclosure.by = Para$inclosure.by, SNP.P3D = Para$SNP.P3D, SNP.effect = Para$SNP.effect, SNP.impute = Para$SNP.impute, PCA.total = Para$PCA.total, SNP.fraction = Para$SNP.fraction, seed = Para$seed, BINS = Para$BINS, SNP.test=Para$SNP.test, SNP.MAF= Para$SNP.MAF, FDR.Rate = Para$FDR.Rate, SNP.FDR = Para$SNP.FDR, SNP.permutation = Para$SNP.permutation, opt = Para$opt, SNP.CV = Para$SNP.CV, SNP.robust = Para$SNP.robust, Inter.Plot = Para$Inter.Plot, Inter.type = Para$Inter.type, file.from = Para$file.from, file.to = Para$file.to, file.total= Para$file.total, file.fragment = Para$file.fragment, file.path = Para$file.path, file.G = Para$file.G, file.Ext.G= Para$file.Ext.G, file.GD = Para$file.GD, file.GM = Para$file.GM, file.Ext.GD = Para$file.Ext.GD, file.Ext.GM = Para$file.Ext.GM, ngrid = Para$ngrid, llim = Para$llim, ulim = Para$ulim, esp = Para$esp, Multi_iter = Para$Multi_iter, num_regwas = Para$num_regwas, LD.chromosome = Para$LD.chromosome, LD.location = Para$LD.location, LD.range = Para$LD.range, QC = Para$QC, GTindex = Para$GTindex, cutOff = Para$cutOff, Model.selection = Para$Model.selection, output.numerical = Para$output.numerical, Random.model = Para$Random.model, Create.indicator = Para$Create.indicator, QTN = Para$QTN, QTN.round = Para$QTN.round, QTN.limit = Para$QTN.limit, QTN.update = Para$QTN.update, QTN.method = Para$QTN.method, Major.allele.zero = Para$Major.allele.zero, method.GLM = Para$method.GLM, method.sub = Para$method.sub, method.sub.final = Para$method.sub.final, method.bin = Para$method.bin, bin.size = Para$bin.size, bin.selection = Para$bin.selection, memo = Para$memo, Prior = Para$Prior, ncpus = Para$ncpus, maxLoop = Para$maxLoop, threshold.output = Para$threshold.output, WS = Para$WS, alpha = Para$alpha, maxOut = Para$maxOut, QTN.position = Para$QTN.position, converge = Para$converge, iteration.output = Para$iteration.output, acceleration = Para$acceleration, iteration.method = Para$iteration.method, PCA.View.output = Para$PCA.View.output, output.hapmap = Para$output.hapmap, file.output = Para$file.output, Geno.View.output = Para$Geno.View.output, plot.style = Para$plot.style, SUPER_GD = Para$SUPER_GD, SUPER_GS = Para$SUPER_GS, CG = Para$CG, model = model )
GAPIT.DP calls GAPIT.Genotype
myGenotype <- GAPIT.Genotype(G = G, GD = GD, GM = GM, KI = KI, PCA.total = PCA.total, kinship.algorithm = kinship.algorithm, SNP.fraction = SNP.fraction, SNP.test = FALSE, file.path = file.path, file.from = file.from, file.to = file.to, file.total = file.total, file.fragment = file.fragment, file.G = file.G, file.Ext.G = file.Ext.G, file.GD = file.GD, file.GM = file.GM, file.Ext.GD = file.Ext.GD, file.Ext.GM = file.Ext.GM, SNP.MAF = SNP.MAF, FDR.Rate = FDR.Rate, SNP.FDR = SNP.FDR, SNP.effect = SNP.effect, SNP.impute = SNP.impute, NJtree.group = NJtree.group, NJtree.type = NJtree.type, LD.chromosome = LD.chromosome, LD.location = LD.location, LD.range = LD.range, GP = GP, GK = GK, bin.size = NULL, inclosure.size = NULL, sangwich.top = sangwich.top, sangwich.bottom = sangwich.bottom, GTindex = NULL, file.output = file.output, Create.indicator = Create.indicator, Major.allele.zero = Major.allele.zero, Geno.View.output = Geno.View.output, PCA.col=PCA.col, PCA.3d=PCA.3d )
# library(GAPIT3) #myGAPIT <- GAPIT()
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