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Deep Batch Integration and Denoise of Single-Cell RNA-Seq Data.

Lu QinGuangya ZhangShaoqiang ZhangYong Chen
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Numerous single-cell transcriptomic datasets from identical tissues or cell lines are generated from different laboratories or single-cell RNA sequencing (scRNA-seq) protocols. The denoising of these datasets to eliminate batch effects is crucial for data integration, ensuring accurate interpretation and comprehensive analysis of biological questions. Although many scRNA-seq data integration methods exist, most are inefficient and/or not conducive to downstream analysis. Here, DeepBID, a novel deep learning-based method for batch effect correction, non-linear dimensionality reduction, embedding, and cell clustering concurrently, is introduced. DeepBID utilizes a negative binomial-based autoencoder with dual Kullback-Leibler divergence loss functions, aligning cell points from different batches within a consistent low-dimensional latent space and progressively mitigating batch effects through iterative clustering. Extensive validation on multiple-batch scRNA-seq datasets demonstrates that DeepBID surpasses existing tools in removing batch effects and achieving superior clustering accuracy. When integrating multiple scRNA-seq datasets from patients with Alzheimer's disease, DeepBID significantly improves cell clustering, effectively annotating unidentified cells, and detecting cell-specific differentially expressed genes.
Keyphrases
  • single cell
  • rna seq
  • high throughput
  • deep learning
  • anaerobic digestion
  • magnetic resonance imaging
  • stem cells
  • high resolution
  • computed tomography
  • cell proliferation
  • bone marrow
  • pi k akt
  • genome wide identification