## ----include=FALSE------------------------------------------------------------ library(MCseqReplic) ## ----data--------------------------------------------------------------------- exdata <- read.table(text=" a a b b a a b b b b a a a c c b b b a c b b a c ") weights=rep(1, nrow(exdata)) s.exdata <- TraMineR::seqdef(exdata, weights = weights, id=paste("id",1:nrow(exdata), sep="")) ## ----repdata------------------------------------------------------------------ ## 3 altered sequence datasets set.seed(3) (altseq.list <- MCseqReplicate(s.exdata, J=1, R=3, include.obs=TRUE)) ## ----repdiss------------------------------------------------------------------ (dist.list <- MCdisslist(altseq.list, method="LCS")) ## ----------------------------------------------------------------------------- MCpj(Emean=1.05, pzero=.5) ## ----MCseqdistSE-------------------------------------------------------------- (MCdistSE <- MCseqdistSE(dist.list)) ## ----MCratios----------------------------------------------------------------- MCratios(MCdistSE) ## ----MCdisscorr--------------------------------------------------------------- MCdisscorr(dist.list) ## ----repcompdiss-dissassoc---------------------------------------------------- sex <- c("f","f","f","m","m","m") assoc.list <- lapply(dist.list, TraMineR::dissassoc, group=sex) assoc.list[[1]] ## ----repcompdiss-dissCompare, message=FALSE----------------------------------- library(TraMineRextras) ## for function dissCompare comp.list <- suppressMessages(lapply(dist.list, TraMineRextras::dissCompare, group=sex, squared=FALSE, s=0)) comp.list[[1]] ## ----compgrp-stat-table------------------------------------------------------- comptab <- MCcompgrp(dist.list, group=sex, dissassoc.args=list(R=1000), dissCompare.args=list(squared=FALSE)) round(comptab,3) ## ----compgrp-summary---------------------------------------------------------- summary(comptab[-nrow(comptab),]) ## ----clusqual----------------------------------------------------------------- clqual <- MCclustqual(dist.list, clustmeth="ward.D", ncluster=4, verbose=FALSE) round(clqual$qual.tab[[2]],3) ## ----qual.max----------------------------------------------------------------- clqual ## ----qual.mfreq--------------------------------------------------------------- clqual$max.freq ## ----plotCQI, out.width="70%", fig.width=6, fig.height=4---------------------- ggplotMCcqi(clqual, cqi="PBC") ## ----clusters3---------------------------------------------------------------- clust.list <- lapply(dist.list, WeightedCluster::wcKMedoids, k=3, cluster.only=TRUE) clust.list ## ----clustcomp, echo=TRUE, warning=FALSE, message=FALSE----------------------- (res <- MCclustcomp(clust.list, AMI=TRUE)) ## ----MCmdscorr, message=FALSE------------------------------------------------- MCmdscorr(dist.list, verbose=FALSE, core=1) ## ----MCmds-scores, out.width="70%", fig.width=8, fig.height=7----------------- MCmdsboth <- MCmdscorr(dist.list, what="both") MCmds <- MCmdsboth[[2]] nset <- length(MCmds) title <- paste0("MC",1:nset) if (attr(dist.list,"obs")) title[nset] <- "Obs" layout(matrix(c(1:4,rep(5,4)),nrow=2,byrow=TRUE), heights = c(.75,.25)) for (i in 1:length(altseq.list)) { seqIplot(altseq.list[[i]],sortv=MCmds[[i]], with.legend=FALSE, ylab=NA, yaxis=FALSE, main=title[i]) } seqlegend(altseq.list[[1]],ncol=3, cex=1.5 ) ## ----2mdsfactors-------------------------------------------------------------- mds2.list <- lapply(dist.list, cmdscale, k=2) mds2.list[[1]]