R/initialize_vl_cd4_list.R

Defines functions initialize_vl_cd4_list

Documented in initialize_vl_cd4_list

#' @title Title
#'
#' @description Description
#'
#' @param x A number.
#' @param y A number.
#' @return return value here.
#' @details
#' Additional details here
#' @examples
#' example function call here
#' @export
initialize_vl_cd4_list <- function(dat,at)
{
#vl_list saves the viral load of each agent each timestep
#only want to do this for short/small models runs for qaqc steps  
if(dat$param$save_vl_list){
  dat$vl_list<-vector('list',length=dat$param$n_steps)
  #populate vl/cd4 list for timestep 1
  vl_ix <- which(dat$pop$Status==1)
  # Define new sequences to identify viruses with 0, 1, 2, 3, or 4 mutations  
  seq0 <- c(1) #0  mutations
  seq1 <- c(2,3,5,9,17) #1 mutations
  seq2 <- c(4,6,7,10,11,13,18,19,21,25) #2 mutations
  seq3 <- c(8,12,14,15,20,22,23,26,27,29) #3 mutatoins
  seq4 <- c(16,24,28,30,31) #5 mutations
  seq5 <- c(32) #5 mutations

  K65R <-  c(2,4,6,8,10,12,14,16, 2+16,4+16,6+16,8+16,10+16,12+16,14+16,16+16) # TDF resistance
  M184V <- c(3,4,7,8,11,12,15,16, 3+16,4+16,7+16,8+16,11+16,12+16,15+16,16+16)  # 3TC
  K103N <- c(5,6,7,8,13,14,15,16, 5+16,6+16,7+16,8+16,13+16,14+16,15+16,16+16)    # EFV
  K103N_gEFV <- c(13,14,15,16, 13+16,14+16,15+16,16+16) # EFV-high
  M184V_K65R <-  c(4,8,12,16, 4+16,8+16,12+16,16+16)# 3TC high / TDF high
  GenericTDF <- c(17:32)
  GenericEFV <- c(9:16,25:32)

  
  dat$vl_list[[at]] <- cbind(dat$pop$id[vl_ix], #Agent
                        dat$pop$V[vl_ix], #VL
                        dat$pop$CD4[vl_ix],#CD4
                        dat$pop$CD4count[vl_ix]/200, # CD4c
                        at, #Time
                        dat$pop$V_vec[vl_ix,seq0], # Muts0
                        rowSums(dat$pop$V_vec[vl_ix,seq1,drop=F]), # Muts1
                        rowSums(dat$pop$V_vec[vl_ix,seq2,drop=F]), # Muts2
                        rowSums(dat$pop$V_vec[vl_ix,seq3,drop=F]), # Muts3
                        rowSums(dat$pop$V_vec[vl_ix,seq4,drop=F]), # Muts4
                        dat$pop$V_vec[vl_ix,seq5], # Muts5
                        dat$pop$Drug1[vl_ix], #D1
                        dat$pop$Drug2[vl_ix], #D2
                        dat$pop$Drug3[vl_ix], #D3
                        rowSums(dat$pop$I_vec[vl_ix,,drop=F]), #I
                        rowSums(dat$pop$M_vec[vl_ix,,drop=F]), #M
                        rowSums(dat$pop$L_vec[vl_ix,,drop=F]), #L
                        rowSums(dat$pop$V_vec[vl_ix,K65R,drop=F])/dat$pop$V[vl_ix],#K65R
                        rowSums(dat$pop$V_vec[vl_ix,M184V,drop=F])/dat$pop$V[vl_ix], #M184V
                        rowSums(dat$pop$V_vec[vl_ix,K103N,drop=F])/dat$pop$V[vl_ix], #K103N
                        rowSums(dat$pop$V_vec[vl_ix,K103N_gEFV,drop=F])/dat$pop$V[vl_ix], # K103N + generic EFV 
                        rowSums(dat$pop$V_vec[vl_ix,M184V_K65R,drop=F])/dat$pop$V[vl_ix], #M184VK65R
                        rowSums(dat$pop$V_vec[vl_ix,GenericTDF,drop=F])/dat$pop$V[vl_ix],
                        rowSums(dat$pop$V_vec[vl_ix,GenericEFV,drop=F])/dat$pop$V[vl_ix],
                        dat$pop$Drug4[vl_ix]) #D4 (generic 2nd line)

 
}else{dat$vl_list<-NULL}
  
  return(dat)
}
EvoNetHIV/RoleSPVL documentation built on May 17, 2018, 6:41 p.m.