Least Squares Separate (LSS) Analysis for fMRI Data.
The fmrilss package provides an efficient and flexible implementation of the Least Squares Separate (LSS) method for fMRI analysis, as proposed by Mumford et al. (2012). This approach models each trial with a separate GLM, making it a powerful technique for multivariate pattern analysis (MVPA) and connectivity studies where trial-specific estimates are needed.
The package offers multiple backends, from a simple reference implementation to a highly optimized, parallel C++ engine, all accessible through a clean, unified interface.
- Five Implementations: Includes a highly optimized C++ version, an optimized R version, standard vectorized R and C++ versions, and a simple R loop for testing and validation.
- Parallel Processing: The optimized C++ version uses OpenMP for multi-threaded execution to maximize performance on modern hardware.
- Flexible & Modern Interface: A clean
lss(Y, X, Z, Nuisance)signature that is powerful and intuitive. - Nuisance Regression: Built-in support for projecting out nuisance regressors (e.g., motion parameters, physiological noise) before the LSS analysis.
- CRAN-Compliant: Built with portable configurations suitable for CRAN submission.
You can install the development version of fmrilss from GitHub with:
# install.packages("devtools")
devtools::install_github("bbuchsbaum/fmrilss")The primary function is lss(), which takes your data Y, trial design X, experimental regressors Z, and optional nuisance regressors.
library(fmrilss)
# 1. Generate synthetic data
set.seed(123)
n_timepoints <- 120
n_trials <- 15
n_voxels <- 50
# Trial design matrix (X): one column per trial
X <- matrix(0, n_timepoints, n_trials)
onsets <- seq(from = 5, to = n_timepoints - 10, length.out = n_trials)
for(i in 1:n_trials) {
X[onsets[i]:(onsets[i] + 4), i] <- 1
}
colnames(X) <- paste0("Trial_", 1:n_trials)
# Experimental regressors (Z): intercept and condition-specific effects
# These are experimental regressors we want to model and get beta estimates for,
# but not trial-wise (e.g., condition differences, block effects)
Z <- cbind(Intercept = 1, LinearTrend = scale(1:n_timepoints, center = TRUE, scale = FALSE))
# Nuisance regressors: e.g., 6 motion parameters
Nuisance <- matrix(rnorm(n_timepoints * 6), n_timepoints, 6)
# Data (Y): timepoints x voxels
# (Simulate some effects for demonstration)
true_betas <- matrix(rnorm(n_trials * n_voxels, 0, 1.5), n_trials, n_voxels)
Y <- Z %*% matrix(c(10, -0.2), 2, n_voxels) +
X %*% true_betas +
Nuisance %*% matrix(rnorm(6 * n_voxels, 0, 2), 6, n_voxels) +
matrix(rnorm(n_timepoints * n_voxels, 0, 0.8), n_timepoints, n_voxels)
colnames(Y) <- paste0("Voxel_", 1:n_voxels)
# 2. Run LSS analysis
# Example 1: Basic LSS with default intercept
# If Z is NULL, an intercept is automatically added.
beta_estimates <- lss(Y, X)
# Example 2: LSS with experimental regressors (intercept + condition effects)
beta_fixed <- lss(Y, X, Z = Z)
# Example 3: LSS with experimental regressors and nuisance regression
beta_clean <- lss(Y, X, Z = Z, Nuisance = Nuisance)
# Example 4: Use the super-fast, parallelized C++ implementation
beta_fast <- lss(Y, X, Z = Z, Nuisance = Nuisance, method = "cpp_optimized")
# The result is a (trials x voxels) matrix of beta estimates
print(dim(beta_fast))
#> [1] 15 50
print(beta_fast[1:5, 1:4])Mumford, J. A., Turner, B. O., Ashby, F. G., & Poldrack, R. A. (2012). Deconvolving BOLD activation in event-related designs for multivoxel pattern classification analyses. NeuroImage, 59(3), 2636-2643.
GPL-3