readQpcrBatch {qpcrNorm} | R Documentation |
This function reads in data from multiple qPCR experiments from the one batch.
Each text file in the batch must meet the structure required by readQpcr
.
Note: In order to qualify as a batch, it is assumed that the same set of primers
are being analyzed in each experiment.
readQpcrBatch(..., filenames = character(), qc = FALSE)
... |
Filenames separated by a comma. |
filenames |
Character vector specifying file names. |
qc |
Logical value, TRUE if a QC filter ctQc should be applied to the data. If qc = F, the replicate Ct values will be averaged. See ctQc . |
If the function is called with no arguments readQpcrBatch()
all the files in the working directory are
read and put into a qpcrBatch
object.
All files must conform to the following structure:
1st column = names denoting genes or primer pairs
2nd column = plate index of each gene or primer pair
remaining columns = (replicate) Ct values
other annotation fields may be added after the Ct value columns. /cr /cr
Currently fields appearing after the Ct value columns are not associated with the output of this function.
Note: the majority of arguments to readQpcr are identical to those supplied to read.table. These have been included to
give the user greater control over data input, should the data deviate from a standard tab-delimited file structure.
For a set of standard tab-delimited text files, specifying the filenames
should be sufficient.
A qpcrBatch
object.
Jess Mar jess@jimmy.harvard.edu
## myBatch <- readQpcrBatch()