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siVAE: interpretable deep generative models for single-cell transcriptomes

delete2023-02-20
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OA
AI
Y
Yongin Choi
李若馨 (Ruoxin Li)
G
Gerald Quon *
DOI:10.1186/s13059-023-02850-ydelete
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Abstract

Abstract

En 中文
Neural networks such as variational autoencoders (VAE) perform dimensionality reduction for the visualization and analysis of genomic data, but are limited in their interpretability: it is unknown which data features are represented by each embedding dimension. We present siVAE, a VAE that is interpretable by design, thereby enhancing downstream analysis tasks. Through interpretation, siVAE also identifies gene modules and hubs without explicit gene network inference. We use siVAE to identify gene modules whose connectivity is associated with diverse phenotypes such as iPSC neuronal differentiation efficiency and dementia, showcasing the wide applicability of interpretable generative models for genomic data analysis.
Keywords:
GENE REGULATORY NETWORKS
RNA-SEQ
ANALYSIS REVEALS
DIFFERENTIATION
COEXPRESSION
IDENTIFICATION
INFERENCE
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Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.

Journal

G
Genome Biology
IF:
9.4
Papers:
6.3K
Citations:
7.3W

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U
university of california davis
Scholars:
3.4W
Papers: 2.6W
Citations: 45
University of California System cover
University of California System
Scholars:
37.5W
Papers: 33.7W
Citations: 6.6K