Description Usage Arguments Details Value Author(s) References See Also
Various plotting routines, used for diagnostic purposes
1 2 3 4 5 6 7 8 9 10 11 12 | checkCCV(data, useRank = FALSE, f = 1/2)
checkModel(data, fit, model = c("gamma", "lognormal", "lnnmv"),
number = 9, nb = 10, cluster = 1, groupid = NULL)
checkVarsQQ(data, groupid, ...)
checkVarsMar(data, groupid, xlab, ylab, ...)
plotMarginal(fit, data, kernel = "rect", n = 100,
bw = "nrd0", adjust = 1, xlab, ylab,...)
plotCluster(fit, data, cond = NULL, ncolors = 123, sep=TRUE,
transform=NULL)
## S3 method for class 'ebarraysEMfit'
plot(x, data, plottype="cluster", ...)
|
data |
data, as a “matrix” or “ExpressionSet” |
useRank |
logical. If |
f |
passed on to |
fit, x |
object of class “ebarraysEMfit”, typically produced by a
call to |
model |
which theoretical model use for Q-Q plot. Partial string matching is allowed |
number |
number of bins for checking model assumption. |
nb |
number of data rows included in each bin for checking model assumption |
cluster |
check model assumption for data in that cluster |
groupid |
an integer vector indicating which group each sample belongs to. groupid for samples not included in the analysis should be 0. |
kernel, n, bw, adjust |
passed on to |
cond |
a vector specifying the condition for each replicate |
ncolors |
different number of colors in the plot |
xlab, ylab |
labels for x-axis and y-axis |
sep |
whether or not to draw horizontal lines between clusters |
transform |
a function to transform the original data in plotting |
plottype |
a character string specifying the type of the plot. Available options are "cluster" and "marginal". The default plottype "cluster" employs function 'plotCluster' whereas the "marginal" plottype uses function 'plotMarginal'. |
... |
extra arguments are passed to the |
checkCCV
checks the constant coefficient of variation assumption
made in the GG and LNN models.
checkModel
generates QQ plots for subsets of (log) intensities
in a small window. They are used to check the Log-Normal assumption on
observation component of the LNN and LNNMV models and the Gamma
assumption on observation component of the GG model.
checkVarsQQ
generates QQ plot for gene specific sample
variances. It is used to check the assumption of a scaled inverse
chi-square prior on gene specific variances, made in the LNNMV model.
checkVarsMar
is another diagnostic tool to check this
assumption. The density histogram of gene specific sample variances
and the density of the scaled inverse chi-square distribution with
parameters estimated from data will be plotted.
checkMarginal
generates predictive marginal distribution from
fitted model and compares with estimated marginal (kernel) density of
data. Available for the GG and LNN models only.
plotCluster
generate heatmap for gene expression data with clusters
checkModel
, checkVarsQQ
and checkVarsMar
return an object of class
“trellis”, using function in the Lattice package. Note that in
certain situations, these may need to be explicitly ‘print’-ed to have
any effect.
Ming Yuan, Ping Wang, Deepayan Sarkar, Michael Newton, and Christina Kendziorski
Newton, M.A., Kendziorski, C.M., Richmond, C.S., Blattner, F.R. (2001). On differential variability of expression ratios: Improving statistical inference about gene expression changes from microarray data. Journal of Computational Biology 8:37-52.
Kendziorski, C.M., Newton, M.A., Lan, H., Gould, M.N. (2003). On parametric empirical Bayes methods for comparing multiple groups using replicated gene expression profiles. Statistics in Medicine 22:3899-3914.
Newton, M.A. and Kendziorski, C.M. Parametric Empirical Bayes Methods for Microarrays in The analysis of gene expression data: methods and software. Eds. G. Parmigiani, E.S. Garrett, R. Irizarry and S.L. Zeger, New York: Springer Verlag, 2003.
Newton, M.A., Noueiry, A., Sarkar, D., and Ahlquist, P. (2004). Detecting differential gene expression with a semiparametric hierarchical mixture model. Biostatistics 5: 155-176.
Yuan, M. and Kendziorski, C. (2006). A unified approach for simultaneous gene clustering and differential expression identification. Biometrics 62(4): 1089-1098.
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