This work introduces ensemble refinement for scRNA-seq and scATAC-seq embeddings, inspired by ensemble methods from statistical machine learning, and implements BatchRefiner, a fast post-processing tool to enhance batch integration.
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.
Batch integration is a central preprocessing step in single-cell genomics, where datasets collected across experiments, donors, and protocols must be combined despite pervasive technical batch effects. The leading integration methods produce a shared low-dimensional embedding, which discards the corrected gene-expressi...
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Results indicate that discrete, anchor-constrained latent modeling provides a powerful and biologically coherent solution for unpaired single-cell multi-omics integration, and scCoA-VQA can accurately capture the meaningful regulatory structure.
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Advances in single-cell RNA sequencing (scRNA-seq) enable the exploration of cellular heterogeneity at single-cell resolution. Accurate cell clustering is a prerequisite for delineating these identities; however, the inherent sparsity and prevalent dropout noise of scRNA-seq data pose major algorithmic challenges. Exis...
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Correcting batch effects and integrating single-cell sequencing datasets has been a crucial step in large-scale biological studies. Many methods have been published for this task, with complementary strengths in various scenarios. Our previous work, LIGER, leveraging integrative non-negative matrix factorization (iNMF)...
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