getRobustWeightsSingleBinary: Single-omics SmCCA with Binary Phenotype

In SmCCNet: Sparse Multiple Canonical Correlation Network Analysis Tool

Single-omics SmCCA with Binary Phenotype

Description

Compute aggregated (SmCCA) canonical weights for single omics data with quantitative phenotype (subampling enabled).

Usage

getRobustWeightsSingleBinary(
  X1,
  Trait,
  Lambda1,
  s1 = 0.7,
  SubsamplingNum = 1000,
  K = 3
)

Arguments

X1	An n\times p_1 data matrix (e.g. mRNA) with p_1 features and n subjects.
Trait	An n\times 1 trait (phenotype) data matrix for the same n subjects.
Lambda1	LASSO penalty parameter for X1. Lambda1 needs to be between 0 and 1.
s1	Proportion of mRNA features to be included, default at s1 = 0.7. s1 needs to be between 0 and 1, default is set to 0.7.
SubsamplingNum	Number of feature subsamples. Default is 1000. Larger number leads to more accurate results, but at a higher computational cost.
K	Number of hidden components for PLSDA, default is set to 3.

Value

A partial least squared weight matrix with p_1 rows. Each column is the canonical correlation weights based on subsampled X1 features. The number of columns is SubsamplingNum.

Examples

X <- matrix(rnorm(600,0,1), nrow = 60)
Y <- rbinom(60,1,0.5)
Ws <- getRobustWeightsSingleBinary(X1 = X, Trait = as.matrix(Y), Lambda1 = 0.8, 
0.7, SubsamplingNum = 10)

SmCCNet documentation built on May 29, 2024, 10:49 a.m.