multiDGD: A versatile deep generative model for multi-omics data

Recent technological advancements in single-cell genomics have enabled joint profiling of gene expression and alternative modalities at unprecedented scale. Consequently, the complexity of multi-omics data sets is increasing massively. Existing models for multi-modal data are typically limited in functionality or scalability, making data integration and downstream analysis cumbersome. We present multiDGD, a scalable deep generative model providing a probabilistic framework to learn shared representations of transcriptome and chromatin accessibility. It shows outstanding performance on data reconstruction without feature selection. We demonstrate on several data sets from human and mouse that multiDGD learns well-clustered joint representations. We further find that probabilistic modeling of sample covariates enables post-hoc data integration without the need for fine-tuning. Additionally, we show that multiDGD can detect statistical associations between genes and regulatory regions conditioned on the learned representations. multiDGD is available as an scverse-compatible package on GitHub.

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Publication Details

Journal
Nature Communications
Published
2024-11-20
DOI
https://doi.org/10.1038/s41467-024-53340-z
Citations
23
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
5.38

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article

multiDGD: A versatile deep generative model for multi-omics data

Viktoria Schuster, Sarah Amalia Teichmann, Anders Krogh, Emma Dann
23 citations
Nature Communications
Bioinformatics and Genomic Networks
5.38
article

multiDGD: A versatile deep generative model for multi-omics data

Viktoria Schuster, Sarah Amalia Teichmann, Anders Krogh, Emma Dann
article en
23 citations

Abstract

Recent technological advancements in single-cell genomics have enabled joint profiling of gene expression and alternative modalities at unprecedented scale. Consequently, the complexity of multi-omics data sets is increasing massively. Existing models for multi-modal data are typically limited in functionality or scalability, making data integration and downstream analysis cumbersome. We present multiDGD, a scalable deep generative model providing a probabilistic framework to learn shared representations of transcriptome and chromatin accessibility. It shows outstanding performance on data reconstruction without feature selection. We demonstrate on several data sets from human and mouse that multiDGD learns well-clustered joint representations. We further find that probabilistic modeling of sample covariates enables post-hoc data integration without the need for fine-tuning. Additionally, we show that multiDGD can detect statistical associations between genes and regulatory regions conditioned on the learned representations. multiDGD is available as an scverse-compatible package on GitHub.

Nature CommunicationsVol. 15(1)
University of Copenhagen (DK), Wellcome/MRC Cambridge Stem Cell Institute (GB), University of Cambridge (GB), Wellcome Sanger Institute (GB)
Wellcome, Novo Nordisk, Novo Nordisk Fonden
Openalex Percentile: Top 3%
Bioinformatics and Genomic Networks
5.38
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