RDML.AsTable {RDML} | R Documentation |
Represents fields of RDML
object as data.frame
Description
Formats particular fields of RDML
object as data.frame
s,
filters or passes them to RDML.GetFData
and RDML.SetFData
functions.
Arguments
.default |
|
name.pattern |
expression to form |
add.columns |
|
treat.null.as.na |
if value is |
... |
additional columns |
Details
By default input this function forms data.frame
with following columns:
- exp.id
experiment$id
- run.id
run$id
- react.id
react$id
- position
react$position
- sample
react$sample
- target
data$tar$id
- target.dyeId
target[[data$id]]$dyeId
- sample.type
sample[[react$sample]]$type
You can overload default
columns list by parameter .default
but note that columns
exp.id, run.id, react.id, target
are necessary for usage
AsTable
output as
input for GetFData
and SetFData
.
Additional columns can be
introduced by specifying them at input parameter ...
(see Examples).
All default and additional columns accession expressions must be named.
Experiment, run, react and data to which belongs each fluorescence data vector
can be accessed by experiment, run, react, data
(see Examples).
Result table does not contain data from experiments with ids starting with '.'!
Author(s)
Konstantin A. Blagodatskikh <k.blag@yandex.ru>, Stefan Roediger <stefan.roediger@b-tu.de>, Michal Burdukiewicz <michalburdukiewicz@gmail.com>
Examples
## Not run:
## internal dataset stepone_std.rdml (in 'data' directory)
## generated by Applied Biosystems Step-One. Contains qPCR data.
library(chipPCR)
PATH <- path.package("RDML")
filename <- paste(PATH, "/extdata/", "stepone_std.rdml", sep ="")
stepone <- RDML$new(filename)
## Mark fluorescense data which Cq > 30 and add quantities to
## AsTable output.
## Names for fluorescense data will contain sample name and react
## positions
tab <- stepone$AsTable(
name.pattern = paste(react$sample$id, react$position),
add.columns = list(cq30 = if(data$cq >= 30) ">=30" else "<30",
quantity = sample[[react$sample$id]]$quantity$value)
)
## Show cq30 and quantities
tab[, c("cq30", "quantity")]
## Get fluorescence values for 'std' type samples
## in format ready for ggplot function
library(dplyr)
fdata <- stepone$GetFData(
filter(tab, sample.type == "std"),
long.table = TRUE)
## Plot fdata with colour by cq30 and shape by quantity
library(ggplot2)
ggplot(fdata, aes(x = cyc, y = fluor,
group = fdata.name,
colour = cq30,
shape = as.factor(quantity))) +
geom_line() + geom_point()
## End(Not run)