normalise | R Documentation |
This function creates a list in which your settings, the raw counts and normalised counts are stored,
using the result from a call to load_rcc()
.
normalise(
nacho_object,
housekeeping_genes = nacho_object[["housekeeping_genes"]],
housekeeping_predict = nacho_object[["housekeeping_predict"]],
housekeeping_norm = nacho_object[["housekeeping_norm"]],
normalisation_method = nacho_object[["normalisation_method"]],
n_comp = nacho_object[["n_comp"]],
remove_outliers = nacho_object[["remove_outliers"]],
outliers_thresholds = nacho_object[["outliers_thresholds"]]
)
nacho_object |
[list] A list object of class |
housekeeping_genes |
[character] A vector of names of the miRNAs/mRNAs
that should be used as housekeeping genes. Default is |
housekeeping_predict |
[logical] Boolean to indicate whether the housekeeping genes
should be predicted ( |
housekeeping_norm |
[logical] Boolean to indicate whether the housekeeping normalisation
should be performed. Default is |
normalisation_method |
[character] Either |
n_comp |
[numeric] Number indicating the number of principal components to compute.
Cannot be more than n-1 samples. Default is |
remove_outliers |
[logical] A boolean to indicate if outliers should be excluded. |
outliers_thresholds |
[list] List of thresholds to exclude outliers. |
Outliers definition (remove_outliers = TRUE
):
Binding Density (BD
) < 0.1
Binding Density (BD
) > 2.25
Field of View (FoV
) < 75
Positive Control Linearity (PCL
) < 0.95
Limit of Detection (LoD
) < 2
Positive normalisation factor (Positive_factor
) < 0.25
Positive normalisation factor (Positive_factor
) > 4
Housekeeping normalisation factor (house_factor
) < 1/11
Housekeeping normalisation factor (house_factor
) > 11
[list] A list containing parameters and data.
access
[character] Value passed to load_rcc()
in id_colname
.
housekeeping_genes
[character] Value passed to load_rcc()
or normalise()
.
housekeeping_predict
[logical] Value passed to load_rcc()
.
housekeeping_norm
[logical] Value passed to load_rcc()
or normalise()
.
normalisation_method
[character] Value passed to load_rcc()
or normalise()
.
remove_outliers
[logical] Value passed to normalise()
.
n_comp
[numeric] Value passed to load_rcc()
.
data_directory
[character] Value passed to load_rcc()
.
pc_sum
[data.frame] A data.frame
with n_comp
rows and four columns:
"Standard deviation", "Proportion of Variance", "Cumulative Proportion" and "PC".
nacho
[data.frame] A data.frame
with all columns from the sample sheet ssheet_csv
and all computed columns, i.e., quality-control metrics and counts, with one sample per row.
outliers_thresholds
[list] A list
of the quality-control thresholds used.
raw_counts
[data.frame] Raw counts with probes as rows and samples as columns.
With "CodeClass"
(first column), the type of the probes and
"Name"
(second column), the Name of the probes.
normalised_counts
[data.frame] Normalised counts with probes as rows and samples as columns.
With "CodeClass"
(first column)), the type of the probes and
"Name"
(second column), the name of the probes.
data(GSE74821)
GSE74821_norm <- normalise(
nacho_object = GSE74821,
housekeeping_norm = TRUE,
normalisation_method = "GEO",
remove_outliers = TRUE
)
if (interactive()) {
library(GEOquery)
library(NACHO)
# Import data from GEO
gse <- GEOquery::getGEO(GEO = "GSE74821")
targets <- Biobase::pData(Biobase::phenoData(gse[[1]]))
GEOquery::getGEOSuppFiles(GEO = "GSE74821", baseDir = tempdir())
utils::untar(
tarfile = file.path(tempdir(), "GSE74821", "GSE74821_RAW.tar"),
exdir = file.path(tempdir(), "GSE74821")
)
targets$IDFILE <- list.files(
path = file.path(tempdir(), "GSE74821"),
pattern = ".RCC.gz$"
)
targets[] <- lapply(X = targets, FUN = iconv, from = "latin1", to = "ASCII")
utils::write.csv(
x = targets,
file = file.path(tempdir(), "GSE74821", "Samplesheet.csv")
)
# Read RCC files and format
nacho <- load_rcc(
data_directory = file.path(tempdir(), "GSE74821"),
ssheet_csv = file.path(tempdir(), "GSE74821", "Samplesheet.csv"),
id_colname = "IDFILE"
)
# (re)Normalise data by removing outliers
nacho_norm <- normalise(
nacho_object = nacho,
remove_outliers = TRUE
)
# (re)Normalise data with "GLM" method and removing outliers
nacho_norm <- normalise(
nacho_object = nacho,
normalisation_method = "GLM",
remove_outliers = TRUE
)
}
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