Deep learning enables accurate clustering with batch effect removal in single-cell RNA-seq analysis
Year: 2020
Type: article
Abstract: Single-cell RNA sequencing (scRNA-seq) can characterize cell types and states through unsupervised clustering, but the ever increasing number of cells and batch effect impose computational challenges. We present DESC, an unsupervised deep embedding algorithm that clusters scRNA-seq data by iteratively optimizing a clustering objective function. Through iterative self-learning, DESC gradually removes batch effects, as long as technical differences across batches are smaller than true biological variations. As a soft clustering algorithm, cluster assignment probabilities from DESC are biologically interpretable and can reveal both discrete and pseudotemporal structure of cells. Comprehensive evaluations show that DESC offers a proper balance of clustering accuracy and stability, has a small footprint on memory, does not explicitly require batch information for batch effect removal, and can utilize GPU when available. As the scale of single-cell studies continues to grow, we believe DESC will offer a valuable tool for biomedical researchers to disentangle complex cellular heterogeneity.
Source: Nature Communications
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $5,380
Awards: Computational and functional strategies to decipher lncRNAs in human atherosclerosis, Single-Cell Transcriptomic Analysis of Human Retina, G2456439923, Elucidation of Tissue-Specific Transcriptomic Profiles in Cardio-metabolic Disease, G476040624, G5195934471, G6216850549, Deconstructing and Modeling the Single Cell Architecture of the Age-Related Macular Degeneration Retina and RPE/Choroid, G792645035, Statistical Methods for Single-Cell Transcriptomics, Statistical Methods for Transcriptome Profiling Using RNA Sequencing, Adaptive and maladaptive repair after kidney injury
OpenAlex ID: W3021272327
