EBarrays (version 2.36.0)

ebplots: Various plotting routines in the EBarrays package

Description

Various plotting routines, used for diagnostic purposes

Usage

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)
"plot"(x, data, plottype="cluster", ...)

Arguments

data
data, as a ``matrix'' or ``ExpressionSet''
useRank
logical. If TRUE, ranks of means and c.v.-s are used in the scatterplot
f
passed on to lowess
fit, x
object of class ``ebarraysEMfit'', typically produced by a call to emfit
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 density
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 qqmath, histogram and xyplot call used to produce the final result

Value

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.

Details

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

References

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.

See Also

emfit, lowess