Authors
Schäffer, D. E., Kang, H., Aksu, E. D., Edelman, D., Berger, B.
Abstract
Data from single-cell RNA sequencing (scRNA-seq) and the Assay for Transposase-Accessible Chromatin (scATAC-seq) are high-dimensional, sparse, and undesirably capture technical variability between experiments or batches. Many analysis methods thus seek to produce a low-dimensional cell-by-feature embedding space that groups together biologically similar cells across batches while distancing dissimilar cells. Here, we introduce ensemble refinement for scRNA-seq and scATAC-seq embeddings, inspired by ensemble methods from statistical machine learning, and implement BatchRefiner, a fast post-processing tool to enhance batch integration. We extensively benchmark widely-used scRNA-seq embedding methods on both batch integration and biological conservation over a wide range of datasets, before and after the addition of BatchRefiner. We extend these benchmarking approaches to provide the first comprehensive benchmark of batch integration for scATAC-seq embedding methods, including BatchRefiner. Importantly, we formalize a significance statistic, which we use to demonstrate BatchRefiner's significant improvement in batch integration across a wide range of embedding methods, atlas-scale datasets, and established metrics.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 27 Aug 2026.
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