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Supervised dimensionality reduction for exploration of single-cell data by Hybrid Subset Selection - Linear Discriminant Analysis

View ORCID ProfileMeelad Amouzgar, David R. Glass, Reema Baskar, Inna Averbukh, Samuel C. Kimmey, Albert G. Tsai, Felix J. Hartmann, Sean C. Bendall
doi: https://doi.org/10.1101/2022.01.06.475279
Meelad Amouzgar
1Department of Pathology, Stanford University, Stanford, CA, USA
2Immunology Graduate Program, Stanford University, Stanford, CA, USA
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  • ORCID record for Meelad Amouzgar
David R. Glass
1Department of Pathology, Stanford University, Stanford, CA, USA
2Immunology Graduate Program, Stanford University, Stanford, CA, USA
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  • For correspondence: drglass@stanford.edu bendall@stanford.edu
Reema Baskar
1Department of Pathology, Stanford University, Stanford, CA, USA
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Inna Averbukh
1Department of Pathology, Stanford University, Stanford, CA, USA
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Samuel C. Kimmey
1Department of Pathology, Stanford University, Stanford, CA, USA
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Albert G. Tsai
1Department of Pathology, Stanford University, Stanford, CA, USA
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Felix J. Hartmann
1Department of Pathology, Stanford University, Stanford, CA, USA
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Sean C. Bendall
1Department of Pathology, Stanford University, Stanford, CA, USA
2Immunology Graduate Program, Stanford University, Stanford, CA, USA
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  • For correspondence: drglass@stanford.edu bendall@stanford.edu
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Abstract

Single-cell technologies generate large, high-dimensional datasets encompassing a diversity of omics. Dimensionality reduction enables visualization of data by representing cells in two-dimensional plots that capture the structure and heterogeneity of the original dataset. Visualizations contribute to human understanding of data and are useful for guiding both quantitative and qualitative analysis of cellular relationships. Existing algorithms are typically unsupervised, utilizing only measured features to generate manifolds, disregarding known biological labels such as cell type or experimental timepoint. Here, we repurpose the classification algorithm, linear discriminant analysis (LDA), for supervised dimensionality reduction of single-cell data. LDA identifies linear combinations of predictors that optimally separate a priori classes, enabling users to tailor visualizations to separate specific aspects of cellular heterogeneity. We implement feature selection by hybrid subset selection (HSS) and demonstrate that this flexible, computationally-efficient approach generates non-stochastic, interpretable axes amenable to diverse biological processes, such as differentiation over time and cell cycle. We benchmark HSS-LDA against several popular dimensionality reduction algorithms and illustrate its utility and versatility for exploration of single-cell mass cytometry, transcriptomics and chromatin accessibility data.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted January 06, 2022.
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Supervised dimensionality reduction for exploration of single-cell data by Hybrid Subset Selection - Linear Discriminant Analysis
Meelad Amouzgar, David R. Glass, Reema Baskar, Inna Averbukh, Samuel C. Kimmey, Albert G. Tsai, Felix J. Hartmann, Sean C. Bendall
bioRxiv 2022.01.06.475279; doi: https://doi.org/10.1101/2022.01.06.475279
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Supervised dimensionality reduction for exploration of single-cell data by Hybrid Subset Selection - Linear Discriminant Analysis
Meelad Amouzgar, David R. Glass, Reema Baskar, Inna Averbukh, Samuel C. Kimmey, Albert G. Tsai, Felix J. Hartmann, Sean C. Bendall
bioRxiv 2022.01.06.475279; doi: https://doi.org/10.1101/2022.01.06.475279

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