Nothing
findSexGroups.func <- function(linkageGroupList, strandStateMatrix, callThreshold=0.2)
{
createTable <- function(group, allStrands)
{
groupStrands <- allStrands[group,, drop=FALSE]
tables <- sapply(1:ncol(groupStrands),
function(y) sapply(c(paste(c(1,2,3), collapse="|"), 2),
function(x) length(grep(x, groupStrands[,y]))))
tabTots <- apply(tables, 1, sum)
tabTots <- tabTots[2]/tabTots[1]
}
LGconsensus <- data.frame(do.call(rbind, lapply(linkageGroupList, createTable, strandStateMatrix)))
LGconsensus <- LGconsensus[order(LGconsensus),1, drop=FALSE]
LGconsensus <- rownames(LGconsensus[which(LGconsensus[,1] <= callThreshold), ,drop=FALSE])
if(length(LGconsensus) == 0)
{
warning('NO SEX LINKAGE GROUPS FOUND.')
return(linkageGroupList)
}else{
LGNames <- replace(names(linkageGroupList), names(linkageGroupList) == LGconsensus, paste("sex", LGconsensus, sep='_'))
names(linkageGroupList) <- LGNames
return(linkageGroupList)
}
}
####################################################################################################
#' Bar plot all linkage groups, with the true chromosomes of contigs coloured.
#' @param linkageGroupList a LinkageGroupList object as generated by clusterContigs
#' @param strandStateMatrix a StrandStateMatrix object as generated by preprocessStrandTable
#' @param callThreshold a value between 0 and 1 to threshold the proportion of libraries in which scaffolds are heterozygous (ie
#' unlikely to be a monosome sex chromosome). Default value is 0.2
#'
#' @return the same LinkageGroupList entered into the function, but with potential sex chromosomes highlighted in the name attribute
#'
#' @aliases findSexGroups
#' @export
####################################################################################################
setMethod('findSexGroups',
signature = signature(linkageGroupList = 'LinkageGroupList', strandStateMatrix='StrandStateMatrix'),
definition = findSexGroups.func
)
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