A deep learning adversarial autoencoder with dynamic batching displays high performance in denoising and ordering scRNA-seq data.

iScience

Laboratory of Muscle Stem Cells & Gene Regulation, NIAMS, NIH, Bethesda, MD, USA.

Published: March 2024

AI Article Synopsis

  • Single-cell RNA sequencing (scRNA-seq) helps researchers understand variations in gene expression among individual cells, offering insights into cell type diversity and disease processes.
  • Despite its advantages, scRNA-seq can face issues like low capture rates and data dropout, leading to noisy results.
  • The study introduces a new deep learning model called the dynamic batching adversarial autoencoder (DB-AAE), which effectively denoises scRNA-seq data, improves the accuracy of biological signals, and enhances the performance of other algorithms used in analysis.

Article Abstract

By providing high-resolution of cell-to-cell variation in gene expression, single-cell RNA sequencing (scRNA-seq) offers insights into cell heterogeneity, differentiating dynamics, and disease mechanisms. However, challenges such as low capture rates and dropout events can introduce noise in data analysis. Here, we propose a deep neural generative framework, the dynamic batching adversarial autoencoder (DB-AAE), which excels at denoising scRNA-seq datasets. DB-AAE directly captures optimal features from input data and enhances feature preservation, including cell type-specific gene expression patterns. Comprehensive evaluation on simulated and real datasets demonstrates that DB-AAE outperforms other methods in denoising accuracy and biological signal preservation. It also improves the accuracy of other algorithms in establishing pseudo-time inference. This study highlights DB-AAE's effectiveness and potential as a valuable tool for enhancing the quality and reliability of downstream analyses in scRNA-seq research.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10867661PMC
http://dx.doi.org/10.1016/j.isci.2024.109027DOI Listing

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