Given a RadioSet of the sensitivity experiment type, and a list of drugs, the function will compute a signature for the effect gene expression on the molecular profile of a cell. The function returns the estimated coefficient, the t-stat, the p-value and the false discovery rate associated with that coefficient, in a 3 dimensional array, with genes in the first direction, drugs in the second, and the selected return values in the third.
radSensitivitySig(rSet, mDataType, radiation.types, features,
sensitivity.measure = "AUC_recomputed",
molecular.summary.stat = c("mean", "median", "first", "last", "or",
"and"), sensitivity.summary.stat = c("mean", "median", "first",
"last"), returnValues = c("estimate", "pvalue", "fdr"),
sensitivity.cutoff, standardize = c("SD", "rescale", "none"),
nthread = 1, verbose = TRUE, ...)[PharmacoSet] a PharmacoSet of the perturbation experiment type
[character] which one of the molecular data types to use in the analysis, out of dna, rna, rnaseq, snp, cnv
[character] a vector of radiation.types for which to compute the signatures. Should match the names used in the PharmacoSet.
[character] a vector of features for which to compute the signatures. Should match the names used in correspondant molecular data in PharmacoSet.
[character] which measure of the radiation sensitivity should the function use for its computations? Use the sensitivityMeasures function to find out what measures are available for each PSet.
What summary statistic should be used to summarize duplicates for cell line molecular profile measurements?
What summary statistic should be used to summarize duplicates for cell line sensitivity measurements?
[character] Which of estimate, t-stat, p-value and fdr should the function return for each gene?
Allows to provide upper and lower bounds to sensitivity measures in the cases where the values exceed physical values due to numerical or other errors.
[character] One of "SD", "rescale", or "none", for the form of standardization of the data to use. If "SD", the the data is scaled so that SD = 1. If rescale, then the data is scaled so that the 95 interquantile range lies in [0,1]. If none no rescaling is done.
[numeric] if multiple cores are available, how many cores should the computation be parallelized over?
[boolean] 'TRUE' if the warnings and other infomrative message shoud be displayed
additional arguments not currently fully supported by the function
[list] a 3D array with genes in the first dimension, radiation.types in the second, and return values in the third.
# NOT RUN {
data(Cleveland_small)
rad.sensitivity <- radSensitivitySig(Cleveland_small, mDataType="rna",
nthread=1, features = fNames(Cleveland_small, "rna")[1],
radiation.types=radiationTypes(Cleveland_small))
print(rad.sensitivity)
# }
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