Description Usage Arguments Details Value Examples
Tidy, augment, and glance methods for MArrayLM objects, which contain the results of gene-wise linear models to microarray datasets. This class is the output of the lmFit and eBayes functions.
Tidying method for a MA list
Tidy an EList expression object
1 2 3 4 5 6 7 8 9 10 11 12 13 14 |
x |
|
intercept |
whether the |
... |
extra arguments, not used |
data |
original expression matrix; if missing, |
addTargets |
Add sample level information. Default is FALSE. |
Tidying this fit computes one row per coefficient per gene, while
augmenting returns one row per gene, with per-gene statistics included.
(This is thus a rare case where the augment
output has more rows
than the tidy
output. This is a side effect of the fact that the
input to limma is not tidy but rather a one-row-per-gene matrix).
The output of tidying functions is always a data frame without rownames.
tidy
returns one row per gene per coefficient. It always
contains the columns
gene |
The name of the gene (extracted from the rownames of the input matrix) |
term |
The coefficient being estimated |
estimate |
The estimate of each per-gene coefficient |
Depending on whether the object comes from eBayes
, it may also
contain
statistic |
Empirical Bayes t-statistic |
p.value |
p-value computed from t-statistic |
lod |
log-of-odds score |
augment
returns one row per gene, containing the original
gene expression matrix if provided. It then adds columns containing
the per-gene statistics included in the MArrayLM object, each prepended
with a .:
.gene |
gene ID, obtained from the rownames of the input |
.sigma |
per-gene residual standard deviation |
.df.residual |
per-gene residual degrees of freedom |
The following columns may also be included, depending on which have been
added by lmFit
and eBayes
:
.AMean |
average intensity across probes |
.statistic |
moderated F-statistic |
.p.value |
p-value generated from moderated F-statistic |
.df.total |
total degrees of freedom per gene |
.df.residual |
residual degrees of freedom per gene |
.s2.post |
posterior estimate of residual variance |
glance
returns one row, containing
rank |
rank of design matrix |
df.prior |
empirical Bayesian prior degrees of freedom |
s2.prior |
empirical Bayesian prior residual standard deviation |
tidy
returns a data frame with one row per gene-sample
combination, with columns
gene |
gene name |
sample |
sample name (from column names) |
value |
expressions on log2 scale |
tidy
returns a data frame with one row per gene-sample
combination, with columns
gene |
gene name |
sample |
sample name (from column names) |
value |
expressions on log2 scale |
weight |
present if |
other columns |
if present and if |
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 | if (require("limma")) {
# create random data and design
set.seed(2014)
dat <- matrix(rnorm(1000), ncol=4)
dat[, 1:2] <- dat[, 1:2] + .5 # add an effect
rownames(dat) <- paste0("g", 1:nrow(dat))
des <- data.frame(treatment = c("a", "a", "b", "b"),
confounding = rnorm(4))
lfit <- lmFit(dat, model.matrix(~ treatment + confounding, des))
eb <- eBayes(lfit)
head(tidy(lfit))
head(tidy(eb))
if (require("ggplot2")) {
# the tidied form puts it in an ideal form for plotting
ggplot(tidy(lfit), aes(estimate)) + geom_histogram(binwidth=1) +
facet_wrap(~ term)
ggplot(tidy(eb), aes(p.value)) + geom_histogram(binwidth=.2) +
facet_wrap(~ term)
}
}
|
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