Last updated: 2019-11-21

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Knit directory: IITA_2019GS/

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Objective

Two-stage genomic prediction refers to the following procedure:

Stage 1: Fit a linear mixed model to the data without genomic data. Individuals (e.g. clones / accessions) are modeled as independent and identically distributed (i.i.d.) random effects. The BLUPs for this random effect represent the measurable total genetic values of each individual. All the experimental design variation, e.g. replication and blocking effects have been controlled for in the creation of our new response variable, the BLUPs from the gneotype random effect.

Stage 2: Using a modified version of the BLUPs from step 1 as the response variable, fit a genomic prediction model, which now has reduced size because the number of observations is now the same as the number of individuals.

NOTE: In the animal breeding literature single-step often refers to predictions that combine pedigree and marker information simultaneously. That is not our meaning here.

The code below represents Stage I.

Set-up training datasets

Read in the trial data and group it by trait

rm(list=ls()); gc()
library(tidyverse);library(magrittr)
trials<-readRDS("data/IITA_ExptDesignsDetected_72619.rds")
phenos<-trials %>% 
  unnest(TrialData) %>% 
  select(programName,locationName,studyYear,TrialType,studyName,
         CompleteBlocks,IncompleteBlocks,
         yearInLoc,trialInLocYr,repInTrial,blockInRep,observationUnitDbId,
         germplasmName,FullSampleName,
         Trait,Value,MaxNOHAV,NOHAV,PropHAV,
         TCHARTcovar,CMDcovar) %>% 
  mutate(GID=ifelse(!is.na(FullSampleName),FullSampleName,germplasmName),
         IncompleteBlocks=ifelse(IncompleteBlocks==TRUE,"Yes","No"),
         CompleteBlocks=ifelse(CompleteBlocks==TRUE,"Yes","No")) %>% 
  group_by(Trait) %>% 
  nest(.key = "TrainingData")
rm(trials); gc()

For certain traits, made alternative versions after discussion with IYR.

Curates yield traits based on PropHAV, and CMD severity.

Splits DM according to TCHART, with yellow when >2, else white.

# Set yield traits to missing if <5% or 75% plants harvested (PropHAV)
phenos %<>% 
  bind_rows(
    phenos %>% 
      filter(Trait %in% c("logRTNO","logFYLD","logTOPYLD")) %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(PropHAV) & PropHAV>=0.5)),
             Trait=paste0(Trait,"_propHAVpt5"))
  ) %>% 
  bind_rows(
    phenos %>% 
      filter(Trait %in% c("logRTNO","logFYLD","logTOPYLD")) %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(PropHAV) & PropHAV>=0.75)),
             Trait=paste0(Trait,"_propHAVpt75"))
  ) %>% 
  bind_rows(
    phenos %>% # Or set missing when NOHAV<5
      filter(Trait %in% c("logRTNO","logFYLD","logTOPYLD")) %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(NOHAV) & NOHAV>5)),
             Trait=paste0(Trait,"_nohav5"))
  )
phenos %<>% 
  bind_rows( 
    phenos %>% # Or set missing if CMD severity was>2
      filter(Trait %in% c("logRTNO","logFYLD","logTOPYLD")) %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(CMDcovar) & CMDcovar<=2)),
             Trait=paste0(Trait,"_lowCMD"))
  ) %>% 
  bind_rows(
    phenos %>% # white roots only
      filter(Trait=="DM") %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(TCHARTcovar) & TCHARTcovar<=2)),
             Trait=paste0(Trait,"_white"))
  ) %>% 
  bind_rows(
    phenos %>% # yellow roots only
      filter(Trait=="DM") %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(TCHARTcovar) & TCHARTcovar>2)),
             Trait=paste0(Trait,"_yellow"))
  )

In addition, we wanted to do at list a basic check on the cost/benefit of continuing to use data from earlier than 2012. So for every trait possible, I

  1. All Historical Data Included
  2. IITA data post-2012
phenos %<>% 
  mutate(TrainingData=map(TrainingData,~filter(.,as.numeric(studyYear)>2012)),
         Dataset="2013toPresent") %>% 
  bind_rows(phenos %>% 
              mutate(Dataset="HistoricalDataIncluded") %>% 
              filter(!Trait %in% c("BRNHT1","PLTHT"))) # BRNHT1 and PLTHT lacked "historical" observations
# phenos %>% 
#   mutate(Nobs=map_dbl(TrainingData,~nrow(.))) %>% 
#   select(Trait,Nobs,Dataset) %>% 
#   spread(Dataset,Nobs) %>% 
#   mutate(HowManyHistoricalObs=HistoricalDataIncluded-`2013toPresent`) %>% # %$% summary(HowManyHistoricalObs)
#   arrange(HowManyHistoricalObs)
# Basically, only BRNHT1 and PLTHT lacked "historical" observations

Fit Stage I mixed-model

IID models, get BLUPs from asreml

Set-up the models to be fit for each data chunk

library(furrr) # for parallel processing using purrr functions
options(mc.cores=12)
plan(multiprocess)
library(asreml) # cbsurobbins license as of July 2019
phenos %<>%
  mutate(asFixedFormula="Value ~ yearInLoc",
         asFixedFormula=ifelse(grepl("logRTNO",Trait) | grepl("logFYLD",Trait) | grepl("logTOPYLD",Trait),
                               paste0(asFixedFormula," + PropHAV"),asFixedFormula),
         asRandFormula=paste0("~idv(GID) + idv(trialInLocYr) + at(CompleteBlocks,'Yes'):repInTrial ",
                              "+ at(IncompleteBlocks,'Yes'):blockInRep"))

Fit the models in parallel, keeping only key information to save space

Save for future analysis.

asModelsFit<-phenos %>%
  mutate(fitAS=future_pmap(.,function(asFixedFormula,asRandFormula,TrainingData,...){
    # debugging 
    # -------------
    # asFixedFormula<-phenos$asFixedFormula[[1]]
    # asRandFormula<-phenos$asRandFormula[[1]]
    # TrainingData<-phenos$TrainingData[[1]]
    # -------------
    out<-asreml(as.formula(asFixedFormula),
                random = as.formula(asRandFormula),
                data = TrainingData, maxiter = 40,workspace=400e6)
    ll<-summary(out,all=T)$loglik
    varcomp<-summary(out,all=T)$varcomp
      Vg<-varcomp["GID!GID.var","component"]
      Ve<-varcomp["R!variance","component"]
      H2=Vg/(Vg+Ve)
      blups<-summary(out,all=T)$coef.random %>% 
        as.data.frame %>% 
        rownames_to_column(var = "GID") %>% 
        select(GID,solution,`std error`) %>% 
        filter(grepl("GID",GID)) %>% 
        rename(BLUP=solution) %>% 
        mutate(GID=gsub("GID_","",GID),
               PEV=`std error`^2, # asreml specific
               REL=1-(PEV/Vg), # Reliability 
               drgBLUP=BLUP/REL, # deregressed BLUP
               WT=(1-H2)/((0.1 + (1-REL)/REL)*H2)) # weight for use in Stage 2
      out<-tibble(loglik=ll,Vg,Ve,H2,
                  blups=list(blups),varcomp=list(varcomp))
    return(out) }))
asModelsFit %<>% 
  select(-TrainingData,-asFixedFormula,-asRandFormula) %>% 
  unnest(fitAS)
saveRDS(asModelsFit,file="data/iita_blupsForCrossVal_72619.rds")

Curate field data

Redo set-up of training data chunks. Based on preliminary results, discontinued anlaysis for the yield trait variants.

Curation in this case is just outlier removal based on residuals, followed by refitting of the Stage I mixed-model to get new BLUPs.

rm(list=ls()); gc()
library(tidyverse);library(magrittr)
trials<-readRDS("data/IITA_ExptDesignsDetected_72619.rds")
phenos<-trials %>% 
  unnest(TrialData) %>% 
  dplyr::select(programName,locationName,studyYear,TrialType,studyName,
         CompleteBlocks,IncompleteBlocks,
         yearInLoc,trialInLocYr,repInTrial,blockInRep,observationUnitDbId,
         germplasmName,FullSampleName,
         Trait,Value,MaxNOHAV,NOHAV,PropHAV,
         TCHARTcovar,CMDcovar) %>% 
  mutate(GID=ifelse(!is.na(FullSampleName),FullSampleName,germplasmName),
         IncompleteBlocks=ifelse(IncompleteBlocks==TRUE,"Yes","No"),
         CompleteBlocks=ifelse(CompleteBlocks==TRUE,"Yes","No")) %>% 
  group_by(Trait) %>% 
  nest(.key = "TrainingData")
rm(trials); gc()
phenos %<>%
  bind_rows(
    phenos %>% 
      filter(Trait=="DM") %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(TCHARTcovar) & TCHARTcovar<=2)),
             Trait=paste0(Trait,"_white"))
  ) %>% 
  bind_rows(
    phenos %>% 
      filter(Trait=="DM") %>% 
      mutate(TrainingData=map(TrainingData,~filter(.,!is.na(TCHARTcovar) & TCHARTcovar>2)),
             Trait=paste0(Trait,"_yellow"))
  )
phenos %<>%
  mutate(asFixedFormula="Value ~ yearInLoc",
         asFixedFormula=ifelse(grepl("logRTNO",Trait) | grepl("logFYLD",Trait) | grepl("logTOPYLD",Trait),
                               paste0(asFixedFormula," + PropHAV"),asFixedFormula),
         asRandFormula=paste0("~idv(GID) + idv(trialInLocYr) + at(CompleteBlocks,'Yes'):repInTrial ",
                              "+ at(IncompleteBlocks,'Yes'):blockInRep"))

Function to detect outliers

Refit mixed-models and this time recover studentized residuals and flag outliers as observations with |studentized-residuals|>3.3

fitASmodelsWithOutlierDetect<-function(asFixedFormula,asRandFormula,TrainingData,...){
  # debug function
  # ---------------------------
  # asFixedFormula<-phenos$asFixedFormula[[1]]
  # asRandFormula<-phenos$asRandFormula[[1]]
  # TrainingData<-phenos$TrainingData[[1]]
  #rm(asFixedFormula,asRandFormula,TrainingData); gc()
  # ---------------------------
  out<-asreml(as.formula(asFixedFormula),
              random = as.formula(asRandFormula),
              data = TrainingData, 
              maxiter = 40,workspace=400e6,aom=T)
  stdRes <- out$aom$R[,"stdCondRes"]
  nedf <- out$nedf 
  studRes <- stdRes / sqrt( (nedf - stdRes^2)/(nedf - 1) ) 
  outliers<-which(abs(studRes)>3.3)
  ll<-summary(out,all=T)$loglik
  varcomp<-summary(out,all=T)$varcomp
  vg<-varcomp["GID!GID.var","component"]
  ve<-varcomp["R!variance","component"]
  H2tmp<-vg/(vg+ve)
  blups<-summary(out,all=T)$coef.random %>% 
    as.data.frame %>% 
    rownames_to_column(var = "GID") %>% 
    dplyr::select(GID,solution,`std error`) %>% 
    filter(grepl("GID",GID)) %>% 
    rename(BLUP=solution) %>% 
    mutate(GID=gsub("GID_","",GID),
           PEV=`std error`^2,
           REL=1-(PEV/vg),
           drgBLUP=BLUP/REL,
           WT=(1-H2tmp)/((0.1 + (1-REL)/REL)*H2tmp))
  out<-list(loglik=ll,Vg=vg,Ve=ve,H2=H2tmp,
            blups=list(blups),
            varcomp=list(varcomp),
            Outliers=list(outliers))
  return(out) }

Run two cycles of outlier remval

Fit models with asreml

library(furrr)
options(mc.cores=12); plan(multiprocess)
library(asreml)
asModelsFit<-phenos %>%
      mutate(fitAS=future_pmap(.,fitASmodelsWithOutlierDetect))

Count and remove outliers

asModelsFit %<>% 
      mutate(NoutR1=map_dbl(fitAS,~length(.$Outliers[[1]])))
asModelsFit %<>% 
      mutate(OutliersR1=map(fitAS,~.$Outliers[[1]]))
asModelsFit %<>% 
      mutate(TrainingData=map2(TrainingData,fitAS,function(TrainingData,fitAS){
            outliers2remove<-fitAS$Outliers[[1]]
            out<-TrainingData[-outliers2remove,]
            return(out) }))

Refit models with asreml after removing outliers

asModelsFit %<>%
      mutate(fitAS=future_pmap(.,fitASmodelsWithOutlierDetect))

Repeat for a second cycle of outlier removal

asModelsFit %<>% 
      mutate(NoutR2=map_dbl(fitAS,~length(.$Outliers[[1]])),
             OutliersR2=map(fitAS,~.$Outliers[[1]]),
             TrainingData=map2(TrainingData,fitAS,function(TrainingData,fitAS){
                   outliers2remove<-fitAS$Outliers[[1]]
                   out<-TrainingData[-outliers2remove,]
                   return(out) }),
             fitAS=future_pmap(.,fitASmodelsWithOutlierDetect))

Format and save blups for cross-validation, fit after 2 rounds of outlier removal

asModelsFit %<>%
      dplyr::select(-TrainingData,-asFixedFormula,-asRandFormula) %>% 
      mutate(fitAS=map(fitAS,as_tibble)) %>% 
      unnest(fitAS)
saveRDS(asModelsFit,file="data/iita_blupsForCrossVal_outliersRemoved_73019.rds")

Next step

Stage II: Cross-validation Run 1


sessionInfo()
R version 3.6.1 (2019-07-05)
Platform: x86_64-apple-darwin15.6.0 (64-bit)
Running under: macOS Mojave 10.14.6

Matrix products: default
BLAS:   /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRblas.0.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRlapack.dylib

locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

attached base packages:
[1] stats     graphics  grDevices utils     datasets  methods   base     

loaded via a namespace (and not attached):
 [1] workflowr_1.5.0.9000 Rcpp_1.0.3           rprojroot_1.3-2     
 [4] digest_0.6.22        later_1.0.0          R6_2.4.1            
 [7] backports_1.1.5      git2r_0.26.1         magrittr_1.5        
[10] evaluate_0.14        stringi_1.4.3        rlang_0.4.1         
[13] fs_1.3.1             promises_1.1.0       whisker_0.4         
[16] rmarkdown_1.17       tools_3.6.1          stringr_1.4.0       
[19] glue_1.3.1           httpuv_1.5.2         xfun_0.11           
[22] yaml_2.2.0           compiler_3.6.1       htmltools_0.4.0     
[25] knitr_1.26