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SCOT: Single-Cell Multi-Omics Alignment with Optimal Transport.


ABSTRACT: Recent advances in sequencing technologies have allowed us to capture various aspects of the genome at single-cell resolution. However, with the exception of a few of co-assaying technologies, it is not possible to simultaneously apply different sequencing assays on the same single cell. In this scenario, computational integration of multi-omic measurements is crucial to enable joint analyses. This integration task is particularly challenging due to the lack of sample-wise or feature-wise correspondences. We present single-cell alignment with optimal transport (SCOT), an unsupervised algorithm that uses the Gromov-Wasserstein optimal transport to align single-cell multi-omics data sets. SCOT performs on par with the current state-of-the-art unsupervised alignment methods, is faster, and requires tuning of fewer hyperparameters. More importantly, SCOT uses a self-tuning heuristic to guide hyperparameter selection based on the Gromov-Wasserstein distance. Thus, in the fully unsupervised setting, SCOT aligns single-cell data sets better than the existing methods without requiring any orthogonal correspondence information.

SUBMITTER: Demetci P 

PROVIDER: S-EPMC8812493 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

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SCOT: Single-Cell Multi-Omics Alignment with Optimal Transport.

Demetci Pinar P   Santorella Rebecca R   Sandstede Björn B   Noble William Stafford WS   Singh Ritambhara R  

Journal of computational biology : a journal of computational molecular cell biology 20220101 1


Recent advances in sequencing technologies have allowed us to capture various aspects of the genome at single-cell resolution. However, with the exception of a few of co-assaying technologies, it is not possible to simultaneously apply different sequencing assays on the same single cell. In this scenario, computational integration of multi-omic measurements is crucial to enable joint analyses. This integration task is particularly challenging due to the lack of sample-wise or feature-wise corres  ...[more]

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