Related Experiment Video
Updated: May 26, 2026

Analyzing Multifactorial RNA-Seq Experiments with DiCoExpress
Published on: July 29, 2022
Atlas-level single-cell integration and clustering-free differential expression analysis with GEDI 2.0
Arsham Mikaeili Namini1,2, Ali Saberi2,3, Hamed S Najafabadi1,2,4
1Department of Human Genetics, McGill University, Montreal, QC H3A 1Y2, Canada.
Motivation:
GEDI is a generative framework for multi-sample, multi-condition single-cell analysis that performs batch correction, latent representation learning, and clustering-free differential expression within a unified model. However, the original implementation suffered from prohibitive memory use and runtime, preventing its application to modern atlas-scale datasets.
Results:
We present GEDI 2.0, a complete high-performance reimplementation featuring a standalone C++ computational core with pre-allocated workspaces, strict sparse-matrix preservation, optimized BLAS routines, and multi-threaded block-coordinate descent. Across extensive benchmarks spanning up to 500 000 cells and 10 000 features, GEDI 2.0 achieves 40%-63.6% mean reduction in peak memory, 2.98× mean single-threaded speedups, and up to 11.5× acceleration with parallel execution, while maintaining full numerical equivalence to the original method. These improvements enable GEDI 2.0 to analyze million-cell datasets, a scale not achievable with the legacy implementation. GEDI 2.0 provides R and Python interfaces and seamless interoperability with common single-cell workflows.
Availability And Implementation:
Source code, documentation, reproducible codebase, and tutorials are available at https://github.com/csglab/gedi2.

