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2_GTS.R
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2_GTS.R
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# Long-term selection in layers (GTS)
# Ivan Pocrnic
# Clean
rm(list = ls())
# Load packages
library("AlphaSimR")
library("tidyverse")
# Load fje
source("../functions.R")
# Set WD
args = commandArgs(trailingOnly=TRUE)
if (length(args) < 1) {
stop("Must provide replicate number [1] and number of sires [2] !!!")
}
rep = args[1]
noSires = as.numeric(args[2])
scenarioMain = paste("Additive", noSires, sep="_")
scenarioName = paste("Rep_", rep, "_Additive_GS", sep="")
dire = paste("../../data",scenarioMain,scenarioName, sep = "/")
unlink(dire, recursive = TRUE)
dir.create(path = dire, recursive = TRUE, showWarnings = FALSE)
setwd(dir = dire)
noDams=1080
# Create blupf90 parameter files and bash scripts
prepare_par()
# For the sake of comparison, use the same Burn-in as for the Standard scenario
bdirname = paste("Rep_", rep, "_Additive", sep="")
bdir = paste("..",bdirname, "burnin.RData", sep = "/")
load(bdir)
# Parents in the 1st gen of selection are from the last generation of burn-in
GSStartMales = StartMalesBurnin
GSStartFemales = StartFemalesBurnin
# Year is the last year of the burn-in
year = year_burnin
# Separately keep selected/genotyped dams to use for the 1st gen of GS
# Those dams are the same as dams in the PG from the last gen (for the 1st gen of selection)
damg= vector("list",30)
damg[[6]] = StartFemalesBurnin
for(gen in 6:15){
Program = "Genomic"
cat("Working on the round:",Program, ":", gen,"\n")
year = year + 1
# Mate initial sires and dams:
p_start = selectCross(pop=c(GSStartMales,GSStartFemales), nFemale = noDams, nMale = noSires, nCrosses = noDams, nProgeny = 20)
# Selected first 4 M & 9 F hatched per mating (per full-sib family):
p2m = selectWithinFam(p_start,nInd = 4, famType = "B", sex = "M", use = "rand")
p2f = selectWithinFam(p_start,nInd = 9, famType = "B", sex = "F", use = "rand")
# Prepare genotypes I:
# Each time select all relevant genotypes (ugly code now!)
# Also need if/else due to transition phase from burnin to genomics
if(gen > 6){
# Selected dams from the G-4 keep genotypes:
run_prepareGENO(damg[[gen-1]])
# Selected sires from the G-4 keep genotypes:
run_prepareGENO(p2ms)
# Selected dams from the G-3 keep genotypes:
run_prepareGENO(p2fs)
# Selected sires from the G-3 keep genotypes:
run_prepareGENO(p3ms)
# Selected dams from the G-2 keep genotypes:
run_prepareGENO(p3fs)
# Selected sires from the G-2 keep genotypes:
run_prepareGENO(p4ms)
# Selected dams from the G-1 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(GSStartMales)
# All male candidates from this generation get genotypes:
run_prepareGENO(p2m)
} else {
# Selected dams from the G-1 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(GSStartMales)
# All male candidates from this generation get genotypes:
run_prepareGENO(p2m)
}
candidatesgroup = 1
RecSys = RecSysMale(RecSys, p2m)
RecSys = RecSysFemale(RecSys, p2f)
OldDir = getwd()
Dir = paste("GBlup", Program, gen, candidatesgroup, sep = "_")
unlink(paste(OldDir,Dir, sep = "/"), recursive = TRUE)
dir.create(path = Dir, showWarnings = FALSE)
setwd(dir = Dir)
# Prepare pedigree and datafile for blupf90
# Removes phenotypes that are not really available at given timepoint
run_prepare(RecSys)
# Run blupf90, and update GEBV in recording system
RecSys = run_gblup(RecSys)
setwd(dir = OldDir)
# Clean marker files from the last round of selection:
unlink("mrk*")
unlink("markeri*")
# Set EBV for selection candidates:
p2m@ebv = as.matrix(RecSys[RecSys$IId %in% p2m@id, c("EbvT1", "EbvT2","EbvT3")])
p2f@ebv = as.matrix(RecSys[RecSys$IId %in% p2f@id, c("EbvT1", "EbvT2","EbvT3")])
# Summarize Selection Candidates from Batch 1
CSumm = PullSumm(CSumm,p2m,"M")
CSumm = PullSumm(CSumm,p2f,"F")
CSummTogether = PullSummTogether(CSummTogether, c(p2m,p2f))
# Select next generations F & M based on ebv:
# Select males:
p2ms = selectInd(p2m, noSires, use = "ebv", sex = "M", trait=selIndex, b=iweight)
# Mate young selected males with selected females (From Previous Generation)
# Those females were already selected in previous generation and saved as damg[[gen]]
p33=selectCross(pop=c(p2ms,damg[[gen]]), nFemale = noDams, nMale = noSires, nCrosses = noDams, nProgeny = 20)
# Selected first 4 M & 9 F hatched per mating (per full-sib family):
p3m = selectWithinFam(p33,nInd = 4, famType = "B", sex = "M", use = "rand")
p3f = selectWithinFam(p33,nInd = 9, famType = "B", sex = "F", use = "rand")
# Prepare genotypes II:
# Each time select all relevant genotypes (ugly code now!)
# Also need if/else due to transition phase from burnin to genomics
if(gen > 6){
# Selected dams from the G-4 keep genotypes:
run_prepareGENO(p2fs)
# Selected sires from the G-4 keep genotypes:
run_prepareGENO(p3ms)
# Selected dams from the G-3 keep genotypes:
run_prepareGENO(p3fs)
# Selected sires from the G-3 keep genotypes:
run_prepareGENO(p4ms)
# Selected dams from the G-2 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-2 keep genotypes:
run_prepareGENO(GSStartMales)
# Selected dams from the G-1 keep genotypes:
run_prepareGENO(damg[[gen]])
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(p2ms)
# All male candidates from this generation get genotypes:
run_prepareGENO(p3m)
} else {
# Selected dams from the G-2 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-2 keep genotypes:
run_prepareGENO(GSStartMales)
# Selected dams from the G-1 keep genotypes:
# run_prepareGENO(damg[[gen]])
# In first gen of GS these are the same as GSStartFemales
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(p2ms)
# All male candidates from this generation get genotypes:
run_prepareGENO(p3m)
}
candidatesgroup = 2
RecSys = RecSysMale(RecSys, p3m)
RecSys = RecSysFemale(RecSys, p3f)
OldDir = getwd()
Dir = paste("GBlup", Program, gen, candidatesgroup, sep = "_")
unlink(paste(OldDir,Dir, sep = "/"), recursive = TRUE)
dir.create(path = Dir, showWarnings = FALSE)
setwd(dir = Dir)
# Prepare pedigree and datafile for blupf90
# Removes phenotypes that are not really available at given timepoint
run_prepare(RecSys)
# Run blupf90, and update GEBV in recording system
RecSys = run_gblup(RecSys)
setwd(dir = OldDir)
# Clean marker files from the last round of selection:
unlink("mrk*")
unlink("markeri*")
# Set EBV for selection candidates:
p3m@ebv = as.matrix(RecSys[RecSys$IId %in% p3m@id, c("EbvT1", "EbvT2","EbvT3")])
p3f@ebv = as.matrix(RecSys[RecSys$IId %in% p3f@id, c("EbvT1", "EbvT2","EbvT3")])
# Summarize Selection Candidates from Batch 1
CSumm = PullSumm(CSumm,p3m,"M")
CSumm = PullSumm(CSumm,p3f,"F")
CSummTogether = PullSummTogether(CSummTogether, c(p3m,p3f))
# Select males:
p3ms = selectInd(p3m, noSires, use = "ebv", sex = "M", trait=selIndex, b=iweight)
# Select females:
p2fs = selectInd(p2f, noDams, use = "ebv", sex = "F", trait=selIndex, b=iweight)
# Actually EBV of these females was already estimated previously.
# Q3:
year = year + 1
# Mate young selected males with selected females (From Previous Generation)
p44=selectCross(pop=c(p3ms,p2fs), nFemale = noDams, nMale = noSires, nCrosses = noDams, nProgeny = 20)
# Selected first 4 M & 9 F hatched per mating (per full-sib family):
p4m = selectWithinFam(p44,nInd = 4, famType = "B", sex = "M", use = "rand")
p4f = selectWithinFam(p44,nInd = 9, famType = "B", sex = "F", use = "rand")
# Prepare genotypes III:
# Each time select all relevant genotypes (ugly code now!)
# Also need if/else due to transition phase from burnin to genomics
if(gen > 6){
# Selected dams from the G-4 keep genotypes:
run_prepareGENO(p3fs)
# Selected sires from the G-4 keep genotypes:
run_prepareGENO(p4ms)
# Selected dams from the G-3 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-3 keep genotypes:
run_prepareGENO(GSStartMales)
# Selected dams from the G-2 keep genotypes:
run_prepareGENO(damg[[gen]])
# Selected sires from the G-2 keep genotypes:
run_prepareGENO(p2ms)
# Selected dams from the G-1 keep genotypes:
run_prepareGENO(p2fs)
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(p3ms)
# All male candidates from this generation get genotypes:
run_prepareGENO(p4m)
} else {
# Selected dams from the G-3 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-3 keep genotypes:
run_prepareGENO(GSStartMales)
# Selected dams from the G-2 keep genotypes:
# run_prepareGENO(damg[[gen]])
# In first gen of GS these are the same as GSStartFemales
# Selected sires from the G-2 keep genotypes:
run_prepareGENO(p2ms)
# Selected dams from the G-1 keep genotypes:
run_prepareGENO(p2fs)
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(p3ms)
# All male candidates from this generation get genotypes:
run_prepareGENO(p4m)
}
# Third batch of selection candidates:
candidatesgroup = 3
# Generate records:
RecSys = RecSysMale(RecSys, p4m)
RecSys = RecSysFemale(RecSys, p4f)
OldDir = getwd()
Dir = paste("GBlup", Program, gen, candidatesgroup, sep = "_")
unlink(paste(OldDir,Dir, sep = "/"), recursive = TRUE)
dir.create(path = Dir, showWarnings = FALSE)
setwd(dir = Dir)
#getwd()
# Prepare pedigree and datafile for blupf90
# Removes phenotypes that are not really available at given timepoint
run_prepare(RecSys)
# Run blupf90, and update GEBV in recording system
RecSys = run_gblup(RecSys)
setwd(dir = OldDir)
# Clean marker files from the last round of selection:
unlink("mrk*")
unlink("markeri*")
# Set EBV for selection candidates:
p4m@ebv = as.matrix(RecSys[RecSys$IId %in% p4m@id, c("EbvT1", "EbvT2","EbvT3")])
p4f@ebv = as.matrix(RecSys[RecSys$IId %in% p4f@id, c("EbvT1", "EbvT2","EbvT3")])
# Summarize Selection Candidates from Batch 1
CSumm = PullSumm(CSumm,p4m,"M")
CSumm = PullSumm(CSumm,p4f,"F")
CSummTogether = PullSummTogether(CSummTogether, c(p4m,p4f))
# Select males:
p4ms = selectInd(p4m, noSires, use = "ebv", sex = "M", trait=selIndex, b=iweight)
# Select females:
p3fs = selectInd(p3f, noDams, use = "ebv", sex = "F", trait=selIndex, b=iweight)
# Actually EBV of these females was already estimated previously.
# Mate young selected males with selected females (From Previous Generation)
p55=selectCross(pop=c(p4ms,p3fs), nFemale = noDams, nMale = noSires, nCrosses = noDams, nProgeny = 20)
# Selected first 4 M & 9 F hatched per mating (per full-sib family):
p5m = selectWithinFam(p55,nInd = 4, famType = "B", sex = "M", use = "rand")
p5f = selectWithinFam(p55,nInd = 9, famType = "B", sex = "F", use = "rand")
# Prepare genotypes IV:
# Each time select all relevant genotypes (ugly code now!)
# Also need if/else due to transition phase from burnin to genomics
if(gen > 6){
# Selected dams from the G-4 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-4 keep genotypes:
run_prepareGENO(GSStartMales)
# Selected dams from the G-3 keep genotypes:
run_prepareGENO(damg[[gen]])
# Selected sires from the G-3 keep genotypes:
run_prepareGENO(p2ms)
# Selected dams from the G-2 keep genotypes:
run_prepareGENO(p2fs)
# Selected sires from the G-2 keep genotypes:
run_prepareGENO(p3ms)
# Selected dams from the G-1 keep genotypes:
run_prepareGENO(p3fs)
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(p4ms)
# All male candidates from this generation get genotypes:
run_prepareGENO(p5m)
} else {
# Selected dams from the G-4 keep genotypes:
run_prepareGENO(GSStartFemales)
# Selected sires from the G-4 keep genotypes:
run_prepareGENO(GSStartMales)
# Selected dams from the G-3 keep genotypes:
# run_prepareGENO(damg[[gen]])
# In first gen of GS these are the same as GSStartFemales
# Selected sires from the G-3 keep genotypes:
run_prepareGENO(p2ms)
# Selected dams from the G-2 keep genotypes:
run_prepareGENO(p2fs)
# Selected sires from the G-2 keep genotypes:
run_prepareGENO(p3ms)
# Selected dams from the G-1 keep genotypes:
run_prepareGENO(p3fs)
# Selected sires from the G-1 keep genotypes:
run_prepareGENO(p4ms)
# All male candidates from this generation get genotypes:
run_prepareGENO(p5m)
}
candidatesgroup = 4
RecSys = RecSysMale(RecSys, p5m)
RecSys = RecSysFemale(RecSys, p5f)
OldDir = getwd()
Dir = paste("GBlup", Program, gen, candidatesgroup, sep = "_")
unlink(paste(OldDir,Dir, sep = "/"), recursive = TRUE)
dir.create(path = Dir, showWarnings = FALSE)
setwd(dir = Dir)
#getwd()
# Prepare pedigree and datafile for blupf90
# Removes phenotypes that are not really available at given timepoint
run_prepare(RecSys)
# Run blupf90, and update GEBV in recording system
RecSys = run_gblup(RecSys)
setwd(dir = OldDir)
# Clean marker files from the last round of selection:
unlink("mrk*")
unlink("markeri*")
# Set EBV for selection candidates:
p5m@ebv = as.matrix(RecSys[RecSys$IId %in% p5m@id, c("EbvT1", "EbvT2","EbvT3")])
p5f@ebv = as.matrix(RecSys[RecSys$IId %in% p5f@id, c("EbvT1", "EbvT2","EbvT3")])
# Summarize Selection Candidates from Batch 1
CSumm = PullSumm(CSumm,p5m,"M")
CSumm = PullSumm(CSumm,p5f,"F")
CSummTogether = PullSummTogether(CSummTogether, c(p5m,p5f))
# This are initial parents for the next ronud:
# Select males:
GSStartMales = selectInd(p5m, noSires, use = "ebv", sex = "M", trait=selIndex, b=iweight)
# Select females:
GSStartFemales = selectInd(p4f, noDams, use = "ebv", sex = "F", trait=selIndex, b=iweight)
# Actually EBV of these females was already estimated previously.
# These are actualy selected in Q1 next year after they got T2 Phenotype
# But same as before, we pretend as we already have their EBV
# Select females:
p5fs = selectInd(p5f, noDams, use = "ebv", sex = "F", trait=selIndex, b=iweight)
damg[[gen+1]] = p5fs
}
save.image("results.RData")