PLIERsparse | R Documentation |
sparse PLIER function (experimental)
PLIERsparse(
data,
priorMat,
svdres = NULL,
k = NULL,
L1 = NULL,
L2 = NULL,
L3 = NULL,
frac = 0.7,
max.iter = 350,
trace = F,
scale = T,
Chat = NULL,
maxPath = 10,
doCrossval = T,
penalty.factor = rep(1, ncol(priorMat)),
glm_alpha = 0.9,
minGenes = 10,
tol = 1e-06,
seed = 123456,
allGenes = F,
rseed = NULL,
pathwaySelection = c("complete", "fast"),
sparseL = 0.01,
sparseType = "SCAD"
)
data |
the data to be processed with genes in rows and samples in columns. Should be z-scored or set scale=T |
priorMat |
the binary prior information matrix with genes in rows and pathways/genesets in columns |
svdres |
Pre-computed result of the svd decomposition for data |
k |
The number of latent variables to return, leave as NULL to be set automatically using the num.pc "elbow" method |
L1 |
L1 constant, leave as NULL to automatically select a value |
L2 |
L2 constant, leave as NULL to automatically select a value |
L3 |
L3 constant, leave as NULL to automatically select a value. Sparsity in U should be instead controlled by setting frac |
frac |
The fraction of LVs that should have at least 1 prior inforamtion association, used to automatically set L3 |
max.iter |
Maximum number of iterations to perform |
trace |
Display progress information |
scale |
Z-score the data before processing |
Chat |
A ridge inverse of priorMat, used to select active pathways, expensive to compute so can be precomputed when running PLIER multiple times |
maxPath |
The maximum number of active pathways per latent variable |
doCrossval |
Whether or not to do real cross-validation with held-out pathway genes. Alternatively, all gene annotations are used and only pseudo-crossvalidation is done. The latter option may be preferable if some pathways of interest have few genes. |
penalty.factor |
A vector equal to the number of columns in priorMat. Sets relative penalties for different pathway/geneset subsets. Lower penalties will make a pathway more likely to be used. Only the relative values matter. Internally rescaled. |
glm_alpha |
Set the alpha for elastic-net |
minGenes |
The minimum number of genes a pathway must have to be considered |
tol |
Convergence threshold |
seed |
Set the seed for pathway cross-validation |
allGenes |
Use all genes. By default only genes in the priorMat matrix are used. |
rseed |
Set this option to use a random initialization, instead of SVD |
pathwaySelection |
Pathways to be optimized with elstic-net penalty are preselected based on ridge regression results. "Complete" uses all top pathways to fit individual LVs. "Fast" uses only the top pathways for the single LV in question. |
sparseL |
the lambda for sparsity on Z, default 0.02 |
sparseType |
sparsity inducing penalty to use (SCAD or L1) |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.