Nothing
'#
Authors
Torsten Pook, torsten.pook@uni-goettingen.de
Copyright (C) 2017 -- 2020 Torsten Pook
This program is free software; you can redistribute it and/or
modify it under the terms of the GNU General Public License
as published by the Free Software Foundation; either version 3
of the License, or (at your option) any later version.
This program is distributed in the hope that it will be useful,
but WITHOUT ANY WARRANTY; without even the implied warranty of
MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
GNU General Public License for more details.
You should have received a copy of the GNU General Public License
along with this program; if not, write to the Free Software
Foundation, Inc., 59 Temple Place - Suite 330, Boston, MA 02111-1307, USA.
'#
#' Generate plink-file (pedmap)
#'
#' Generate a ped and map file (PLINK format) for selected groups and chromosome
#' @param population Population list
#' @param path Location to save pedmap-file
#' @param database Groups of individuals to consider for the export
#' @param gen Quick-insert for database (vector of all generations to export)
#' @param cohorts Quick-insert for database (vector of names of cohorts to export)
#' @param non.genotyped.as.missing Set to TRUE to replaced non-genotyped entries with "./."
#' @param use.id Set to TRUE to use MoBPS ids instead of Sex_Nr_Gen based names
#' @examples
#' data(ex_pop)
#' \donttest{
#' file_path <- tempdir()
#' get.pedmap(path=file_path, ex_pop, gen=2)
#' file.remove(paste0(file_path, ".ped"))
#' file.remove(paste0(file_path, ".map"))
#' }
#' @return Ped and map-file for in gen/database/cohorts selected individuals
#' @export
get.pedmap <- function(population, path=NULL, database=NULL, gen=NULL, cohorts=NULL, non.genotyped.as.missing=FALSE,
use.id=FALSE){
haplo <- get.haplo(population, database=database, gen=gen, cohorts=cohorts, export.alleles=FALSE)
# haplo <- get.haplo(population, gen=1)
if(length(path)==0){
path <- "population"
}
chr.nr <- sum(population$info$snp)
start <- 1
for(index in 1:length(population$info$snp)){
if(population$info$snp[index]>0){
chr.nr[start:(start+population$info$snp[index]-1)] <- index
start <- start + population$info$snp[index]
}
}
mapfile <- cbind(chr.nr, population$info$snp.name, 0 ,population$info$bp)
mapfile[is.na(mapfile)] <- 0
haplo1 <- t(haplo[,(1:(ncol(haplo)/2))*2-1])
haplo2 <- t(haplo[,(1:(ncol(haplo)/2))*2])
if(non.genotyped.as.missing){
is_genotyped <- t(get.genotyped.snp(population, gen=gen, database = database, cohorts=cohorts))
if(sum(!is_genotyped)>0){
haplo1[!is_genotyped] <- "N"
haplo2[!is_genotyped] <- "N"
}
}
ped <- cbind(haplo1, haplo2)
ped <- ped[,c(0,ncol(haplo1))+ rep(1:ncol(haplo1), each=2)]
ped[ped==0] <- "A"
ped[ped==1] <- "C"
family.base <- get.database(population, gen=gen, database=database, cohorts=cohorts)
n.animals <- sum(family.base[,4]-family.base[,3]+1)
family <- sex.s <- numeric(n.animals)
tillnow <- 1
for(index in 1:nrow(family.base)){
if(diff(family.base[index,3:4])>=0){
family[tillnow:(tillnow+diff(family.base[index,3:4]))] <- index
sex.s[tillnow:(tillnow+diff(family.base[index,3:4]))] <- family.base[index,2]
tillnow <- tillnow + diff(family.base[index,3:4]) +1
}
}
pedi <- get.pedigree(population, database = family.base, id=use.id)
pedfile <- cbind(family, pedi[,1],pedi[,2],pedi[,3],sex.s,0,ped)
pedname <- paste0(path,".ped")
utils::write.table(file=pedname, pedfile, col.names = FALSE, row.names = FALSE, quote=FALSE)
mapname <- paste0(path,".map")
utils::write.table(file=mapname, mapfile, col.names = FALSE, row.names = FALSE, quote=FALSE)
}
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