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.
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