View source: R/read_files_functions.R
merge_sampleID | R Documentation |
A generic function that merges the protein data with the sample identifiers or sample names. If the file does not have sample identifiers the function generates it automatically.
merge_sampleID(iden, data_files, genepix_vars, method)
iden |
A character indicating the name of the object to be used under data_files. |
data_files |
A list of data objects with names utilised by iden. |
genepix_vars |
A list of specific definitions of the experiment design.
See |
method |
A description of the background correction to be used.
See |
a data frame merged with corresponding sample ID's. The sample ID are specified in the sample ID files
## Not run: ### Define the genepix_vars genepix_vars <- array_vars( channel = "635", chip_path = system.file("extdata", "array_data/machine1/", package="protGear"), totsamples = 21, blockspersample = 2, mig_prefix = "_first", machine = 1, ## optional date_process = "0520" ) ## the path where the micro-array data is located data_path <- paste0(genepix_vars$chip_path) filenames <- list.files(genepix_vars$chip_path, pattern = "*.txt$|*.gpr$", full.names = FALSE ) ## create a list of all the files data_files <- purrr::map( .x = filenames, .f = read_array_files, data_path = data_path, genepix_vars = genepix_vars ) data_files <- purrr::set_names(data_files, purrr::map(filenames, name_of_files)) ## merge the lab data with samples and perform bg correction merge_sampleID(iden = "KK2-06", data_files = data_files, genepix_vars =genepix_vars,method = "subtract_global" ) ## End(Not run)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.