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.
'#
#' Analyze allele frequency of a single marker
#'
#' Analyze allele frequency of a single marker
#' @param population Population list
#' @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 chromosome Number of the chromosome of the relevant SNP
#' @param snp Number of the relevant SNP
#' @param snp.name Name of the SNP to analyze
#' @examples
#' data(ex_pop)
#' analyze.population(ex_pop, snp=1, chromosome=1, gen=1:5)
#' @return Frequency of AA/AB/BB in selected gen/database/cohorts
#' @export
analyze.population <- function(population, chromosome = NULL, snp=NULL, snp.name=NULL, database=NULL, gen=NULL, cohorts=NULL){
if(length(snp.name)==1){
n.snp <- which(population$info$snp.name == snp.name)
} else{
p.snp <- sum(population$info$length[0:(chromosome-1)]) + population$info$position[[chromosome]][snp]
n.snp <- sum(population$info$snp[0:(chromosome-1)]) + snp
}
groups <- sum(nrow(database), length(gen), length(cohorts))
state <- matrix(0, nrow=3, ncol = groups)
col <- 1
if(length(gen)>0){
for(index in 1:length(gen)){
genos <- get.geno(population, gen = gen[index])[n.snp,]
state[,col] <- c(sum(genos==0), sum(genos==1), sum(genos==2))
col <- col + 1
}
}
if(length(database)>0){
for(index in 1:nrow(database)){
genos <- get.geno(population, database = database[index,,drop=FALSE])[n.snp,]
state[,col] <- c(sum(genos==0), sum(genos==1), sum(genos==2))
col <- col + 1
}
}
if(length(cohorts)>0){
for(index in 1:length(cohorts)){
genos <- get.geno(population, cohorts = cohorts[index])[n.snp,]
state[,col] <- c(sum(genos==0), sum(genos==1), sum(genos==2))
col <- col + 1
}
}
datatime <- c(gen, database[,1], as.numeric(population$info$cohorts[cohorts,2]))
state.prob <- t(t(state)/colSums(state))
maxp <- max(state.prob)
graphics::plot(datatime ,state.prob[1,],xlim=c(min(datatime),max(datatime)),ylim=c(0,maxp),type="l",xlab="generation", ylab="frequency", lwd=3,
main="")
graphics::lines(datatime ,state.prob[2,],lty=2, lwd=3)
graphics::lines(datatime ,state.prob[3,],lty=3, lwd=3)
graphics::points(datatime ,state.prob[1,], pch = 0)
graphics::points(datatime ,state.prob[2,], pch = 1)
graphics::points(datatime ,state.prob[3,], pch = 2)
graphics::legend("topleft",legend = c("AA","AB","BB"),lty=c(1,2,3), lwd=c(3,3,3), pch=c(0,1,2))
return(state)
}
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