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plot.MEDseq:
MEDseq_clustnames gains the MAP=FALSE
arg., for use when size=TRUE: this is now used byplot.MEDseq (where soft=FALSE corresponds to
MAP=TRUE) when both SPS &
size are TRUE.TraMineR type y-axis labels now properly
account for all combinations of soft &
weighted,subset is invoked &/or
type="ms", with additional minor fixes to
subset arg.type="ms" can now show noise component’s modal sequence
by setting subset appropriately,MEDseq_clustnames arg. cluster can now
also be passed via ... when SPS=TRUE.TraMineR arg. col.entr to be
passed via ... when type="Ht" or
type="dH".MEDseq_control arg.
tau0:
tau0 can now always be supplied as a vector (previously
allowed only with noise.gate=TRUE).tau0 is supplied as a vector with
noise.gate=TRUE.tau0 != 0.5 (the
implied default) for G=2 models with noise.MEDseq_control gains new init.z option
"soft.random":
"random" option has been renamed to
"random.hard", butinit.z="random" will work as before due to partial
matching.z.list is used with
algo != "EM" are also fixed.MEDseq_fit now checks for and terminates in the
presence of both types of missingnessTraMineR function seqhasmiss,
i.e. now also accounts for void values.plot.MEDcriterion added as a wrapper to
plot.MEDseq with related type, for
convenience:plot(x$BIC) is now equivalent to
plot(x, type="bic").MEDseq_control arg. dist.mat
no longer governs ASW calculations: it still defaults"CU", "CUN",
"UU", & "UUN" models for clusters with
only one observation.G=1.print.MEDseq now works again for all models with
G=1.vapply in place of tapply.TraMineR (>= 2.2-10) in
DESCRIPTION Imports: field due to
col.entr & seqhasmiss.plot.MEDseq:
sortv options "from.start" and
"from.end" borrowed from TraMineR whenseriated is "observations" or
"both" for the "clusters", "i",
& "I" type plots.type="gating" when:
x.axis is supplied via the ...
construct.TraMineR type
plots when using extra args. via ....seriated="none" is supplied.MoE_entropy and MoE_AvePP both gain the
arg. group for computing the average entropiesFALSE, i.e. old behaviour.TraMineR::seqdef.matrixStats (>= 1.0.0) + related minor speed-ups.CITATION commands & updated
License: GPL (>= 3).seqdef added as an exact copy of
TraMineR::seqdef, to enable experiencedMEDseq & TraMineR to use the
former without needing to explicitly load the latter.MEDseq_clustnames gains the arg.
weighted=FALSE for use when size=TRUE:weighted arg. to
plot.MEDseq where relevant.dist_freqwH added for calculating pairwise
dissimilarity matrix associated withwKModes(..., freq.weighted=TRUE) for subsequent use
(e.g. silhouettes).plot.MEDseq function’s type arg. gains
the option "dH",2.2-4 or later of the
TraMineR package is installed.plot.MEDseq also gains the "similarity"
option for its type argument.MEDseq_AvePP added.wKModes now also returns x$tot.withindiff
(i.e. sum(x$withindiff)).wKModes when
freq.weighted=TRUE.type="dbsvals" &
type="aswvals" in plot.MEDseq.plot.MEDseq related to its
seriated arg. in G=1 settings.MEDseq_fit & wKModes.G>1.G>1.MEDseq_meantime gains the map.size arg.
and a related print method.summary (and related print) methods
for MEDCriterion objects.MEDseq_entropy added.TraMineR
release w.r.t. "mt" & "ms" plots.WKModes (& thus related
MEDseq_control init.z"kmodes"/"kmodes2"), by further
altering klaR::kmodes:
wKModes
arg. random (defaults to TRUE).modes is supplied as a number with
aggregated data, e.g. "kmodes2".MEDseq_fit & other functions now work for sequence
alphabets of any size;dbs function when supplying
clusters with a noise component.sapply replaced with vapply, with other
negligible speed-ups.init.z options "kmodes" &
"kmodes2" in MEDseq_control, with new function
wKModesklaR::kmodes functionklaR package has been removed from the
DESCRIPTION Suggests: field).plot.MEDseq gains the arg. subset, for use
with the TraMineR type plots:MEDseq_fit to crash when
weights are supplied and unique=FALSE.unique=TRUE, the default).type="ms" plots for models with a
noise component when SPS=TRUE.noise.gate in
MEDseq_compare for G=2 models w/ noise &
gating covariates.G in MEDseq_fit.plot.MEDseq gains a number of new arguments:
soft allows soft cluster membership probabilities to be
used for the "d", "f", "Ht",
"ms","mt" type plots (default:
soft=TRUE) + the "i" & "I"
plots (default: soft=FALSE), in aWeightedCluster::fuzzyseqplot(): previously,
all but the "ms" plot used thesoft=FALSE, implicitly).sortv allows overriding the smeth arg. to
instead order observations in certain plotsseriated is one of "observations" or
"both") by the "dbs" or "asw"
values;WeightedCluster::fuzzyseqplot(),sortv="membership" is provided for soft=TRUE
type="I" plots.weighted (TRUE, by default) allows control
over whether the weights (if any) are used;"d", "f", "Ht",
"i", "I", "ms", &
"mt" type plots.MEDseq_clustnames &
MEDseq_nameclusts functions and added SPS arg.
to plot.MEDseq,MEDseq_meantime, MEDseq_stderr, &
various/more print/summary methods: now
certain plots &seriated options "observations" &
"both" can now be used for "i" type
plots,"i" & "I"
type plots for weighted data with seriated observations.predict, fitted, &
residuals methods for "MEDgating" objects,
i.e. x$gating.MEDseq_meantime gains the arg. wt.size
(defaults to FALSE).modtype="CU".itmax arg. to MEDseq_control: the
2nd element of this arg. governs the maximum number of100 to 1000, which is liable to slownnet::multinom, but generally
reduces the required number of EM iterations.Suggests: package viridisLite now only invoked
if available.x$gating object, especially for
equalPro modelsweights arg. is explicitly
supplied to MEDseq_fit"stslist" object passed via
seqs has the "weights" attribute.MEDseq_fit when the number of
states exceeds 9,gating formulas when there are duplicates.get_MEDseq_results and how its optional
args. are internally handled by plot.MEDseq.gating formula which
are not found in covars.type="mean" option renamed to
type="central" in plot.MEDseq.type="ms" plots now work properly when
seriated="clusters" or seriated="both"."mt"
TraMineR type plots.MEDseq_meantime when
MAP=FALSE.print.MEDseq for models where DBS
&/or ASW statistics weren’t computed."d", "f", "Ht",
"i", & "I" plot types now properly account
for sampling weights.TraMineR further, plot.MEDseq
also gains the type options "ms" &
"mt".opti="medoid"
setting.criterion="bic" is now the default for
MEDseq_control, MEDseq_compare, andget_MEDseq_results (previously "dbs"), with
modifications to print & summary
functions.print.MEDseqtheta) & plotted
(plot.MEDseq(..., type="mean")) always:preczero argument has thus been removed from both
functions.MEDseq_meantime gains two new arguments (see
documentation for more details):
weighted (default: TRUE, old:
FALSE) allows the sampling weights to be used,prop (default: FALSE) divides the output
when norm=TRUE by the sequence length.MEDseq_control gains the arg. random=TRUE,
governing tie-breaking of estimated central sequencerandom=FALSE.plot.MEDseq arg. quant.scale=FALSE
replaces old arg. log.scale: quantiles now usedtype="precision".init.z="kmedoids" initialisation via
pam for unweighted sequences, by using thepamonce option,
based on the cluster package’s version number.init.z gains the options "kmodes" &
"kmodes2", though only for unweighted
sequences:klaR (>= 0.6-13) package.plot.MEDseq gains the arg. smeth,
governing the seriation method to be used ("TSP", by
default).init.z="kmedoids" is now itself
initialised by Ward’s hierarchical clustering.opti settings (esp. "mode").SPS arg. (default=FALSE) to
print.MEDtheta & summary.MEDseq.dbs gains the optional/experimental arg.
clusters - no change to default.seriated arg. to
plot.MEDseq:
seriate to avoid conflict with
function seriation::seriate.seriated options
"clusters"/"both" for models with no noise
component.seriated="observations" (the default) now also works
for type="I" plots.seriated="clusters" now also works for
type="dbsvals" & type="aswvals"
plots.MEDseq_fit now always internally normalises the
weights to sum to the sample size.noise.gate=FALSE.noise.gate=FALSE when G=2.MEDseq_stderr now respects the algo,
opti, & noise.gate settings of the
original model.MEDseq_compare now returns & prints
opti info where relevant.print & summary methods for
MEDgating objects if equalPro=TRUE.MEDseq_fit now coerces "character"
covariates to "factor".print method for MEDlambda
objects also.plot.MEDseq(..., type="gating").print.MEDseqCompare gains the args. maxi
& rerank=FALSE.G=1 models.viridisLite (>= 0.2.0) to
Suggests: (for
plot.MEDseq(..., type="precision")).matrixStats (>= 0.53.1) and
TraMineR (>= 1.6) in Imports:.summary.MEDseq gains the printing-related
argumentsclassification=TRUE, parameters=FALSE, and
gating=FALSE.x$params$lambda now inherits the MEDlambda
class,print method as per
x$params$theta.x$params$tau now has informative
dimnames.x.axis to
plot.MEDseq(..., type="gating").rmarkdown to Suggests:.MEDseq_stderr is provided for computing the standard
errors of theget_MEDseq_results when what="MAP"
and non-noise models are chosen.summary on x$gating.plot.MEDseq when
type="clusters" for small sample sizes.donttest
examples.These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.