Description Usage Arguments Details Value See Also Examples
View source: R/superPC_pathway_tValues.R
If we sample from the null, distribution, first parametrically
resample the response vector before model analysis (f we calculate Student
t statistics from the true distribution instead, the response matrix is
untouched). Then extract principal components (PCs) from the gene pathway,
and return the test statistics associated with the first numPCs
principal components at a set of threshold values based on the values of
the parametrically resampled response (for the null distribution) or the
response itself (for the true distribution).
1 2 3 4 5 6 7 8 9 10 | PathwaytValues(
pathway_vec,
geneArray_df,
response_mat,
responseType = c("survival", "regression", "categorical"),
control = FALSE,
n.threshold = 20,
numPCs = 1,
min.features = 3
)
|
pathway_vec |
A character vector of the measured -Omes in the chosen gene pathway. These should match a subset of the rownames of the gene array. |
geneArray_df |
A "tall" pathway data frame (p \times N). Each subject or tissue sample is a column, and the rows are the -Ome measurements for that sample. |
response_mat |
A response matrix corresponding to |
responseType |
A character string. Options are |
control |
Should the responses be parametrically resampled to generate
a control distribution? Defaults to |
n.threshold |
The number of bins into which to split the feature scores
in the |
numPCs |
The number of PCs to extract from the pathway. |
min.features |
What is the smallest number of genes allowed in each pathway? This argument must be kept constant across all calls to this function which use the same pathway list. Defaults to 3. |
This is a wrapper function to call superpc.train
and superpc.st
. This wrapper is designed to facilitate
apply calls (in parallel or serially) of these two functions over a list
of gene pathways. When numPCs
is equal to 1, we recommend using a
simplify-style apply variant, such as sapply
(shown in
lapply
) or parSapply
(shown in
clusterApply
), then transposing the resulting
matrix.
If control = TRUE
, the RandomControlSample
suite of
functions first parametrically bootstrapps the response. This control
response will be used to contrstruct a null distribution against which to
compare the results calculated with the original response values.
If control = TRUE
, a matrix with numPCs
rows and
n.threshold
columns. The matrix values are model
t-statisics for each PC included (rows) at each threshold level
(columns).
If control = TRUE
, the same matrix as above is contained as the
tscor
element of a list (the first element). The other list
elements are PCs_mat
(the matrix of PCs) and loadings
(the
matrix of -Ome loadings corresponding to the PCs).
pathway_tScores
; pathway_tControl
;
RandomControlSample
; superpc.train
;
superpc.st
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 | # DO NOT CALL THIS FUNCTION DIRECTLY.
# Use SuperPCA_pVals() instead
## Not run:
data("colon_pathwayCollection")
data("colonSurv_df")
colon_OmicsSurv <- CreateOmics(
assayData_df = colonSurv_df[, -(2:3)],
pathwayCollection_ls = colon_pathwayCollection,
response = colonSurv_df[, 1:3],
respType = "surv"
)
asthmaGenes_char <-
getTrimPathwayCollection(colon_OmicsSurv)[["KEGG_ASTHMA"]]$IDs
resp_mat <- matrix(
c(getEventTime(colon_OmicsSurv), getEvent(colon_OmicsSurv)),
ncol = 2
)
PathwaytValues(
pathway_vec = asthmaGenes_char,
geneArray_df = t(getAssay(colon_OmicsSurv)),
response_mat = resp_mat,
responseType = "survival"
)
PathwaytValues(
pathway_vec = asthmaGenes_char,
geneArray_df = t(getAssay(colon_OmicsSurv)),
response_mat = resp_mat,
responseType = "survival",
control = TRUE
)
## End(Not run)
|
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