View source: R/timecourseTable.R
timecourseTable | R Documentation |
This function constructs a time course table of which rows are genomic features and columns time points. values can be normalized expression levels or log2-fold changes compared to a control time point. The time course table is used for clustering analysis.
timecourseTable(
object,
value = "expression",
control.group = NULL,
lib.norm = TRUE,
norm.method = "rpkm",
subset = NULL,
filter = FALSE,
pvalue = "fdr",
pvalue.threshold = 0.05,
abs.fold = 2,
direction = "both",
...
)
object |
a |
value |
a character string, either " |
control.group |
a character string giving the time point to
be compared with, i.e., the denominator in the fold changes. It
should match one of the time points in the |
lib.norm |
logical indicating whether or not use effective
library size (see "Details" in |
norm.method |
a character string specifying the normalization
method if |
subset |
an optinal character vector giving a subset of genomic features, if not NULL, time course table is generated for only this subset of genomic features. |
filter |
logical, whether to drop the genomic features
shows no significant changes (defined by |
pvalue |
character string specify the type of p-values:
" |
pvalue.threshold |
a numeric value giving threshold of selected p-value, significant changes have lower (adjusted) p-values than the threshold. |
abs.fold |
a numeric value, the least minimum log2-fold
changes. The returned genomic regions have changes
with absolute log2-fold changes exceeding |
direction |
character string specify the direction of fold
changes. " |
... |
additional arguments passing to |
A TCA
object
If "expression
" in value
is chosen, the average
normalized expression values of replicates for each group will
be calculated and returned.
Mengjun Wu
data(tca_ATAC)
tca_ATAC <- DBanalysis(tca_ATAC)
tca_ATAC <- timecourseTable(tca_ATAC, value = 'expression',
lib.norm = TRUE, norm.method = 'rpkm')
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