Evidence map›Paper›PMID 39468737›Full record

ArticleBioinformatics (Oxford, England)2024

GEEES: inferring cell-specific gene-enhancer interactions from multi-modal single-cell data.

Shuyang Chen, Sündüz Keleş

Abstract read
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Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Shuyang ChenDepartment of Statistics, University of Wisconsin-Madison, Madison, WI 53706, United States.
Sündüz KeleşDepartment of Statistics, University of Wisconsin-Madison, Madison, WI 53706, United States.ORCID 0000-0001-9048-0922

Funding

Statistical Methods for the Analysis of ChlP-chip DataR01HG003747 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI KELES, SUNDUZ · 2007 to 2024
$4.8M
Statistical methods for co-expression network analysis of population-scale scRNA-seq dataR21HG012881 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI KELES, SUNDUZ · 2023 to 2023
$408k
Chan Zuckerberg InitiativeNHGRI NIH HHS R01 HG003747NHGRI NIH HHS R21 HG012881NIH HHS HG003747
6 · The paper itself

Abstract

motivationGene-enhancer interactions are central to transcriptional regulation. Current multi-modal single-cell datasets that profile transcriptome and chromatin accessibility simultaneously in a single cell are yielding opportunities to infer gene-enhancer associations in a cell type specific manner. Computational efforts for such multi-modal single-cell datasets thus far focused on methods for identification and refinement of cell types and trajectory construction. While initial attempts for inferring gene-enhancer interactions have emerged, these have not been evaluated against benchmark datasets that materialized from bulk genomic experiments. Furthermore, existing approaches are limited to inferring gene-enhancer associations at the level of grouped cells as opposed to individual cells, thereby ignoring regulatory heterogeneity among the cells.

resultsWe present a new approach, GEEES for "Gene EnhancEr IntEractions from Multi-modal Single Cell Data," for inferring gene-enhancer associations at the single-cell level using multi-modal single-cell transcriptome and chromatin accessibility data. We evaluated GEEES alongside several multivariate regression-based alternatives we devised and state-of-the-art methods using a large number of benchmark datasets, providing a comprehensive assessment of current approaches. This analysis revealed significant discrepancies between gold-standard interactions and gene-enhancer associations derived from multi-modal single-cell data. Notably, incorporating gene-enhancer distance into the analysis markedly improved performance across all methods, positioning GEEES as a leading approach in this domain. While the overall improvement in performance metrics by GEEES is modest, it provides enhanced cell representation learning which can be leveraged for more effective downstream analysis. Furthermore, our review of existing experimentally driven benchmark datasets uncovers their limited concordance, underscoring the necessity for new high-throughput experiments to validate gene-enhancer interactions inferred from single-cell data. AVAILABILITY AND IMPLEMENTATION: https://github.com/keleslab/GEEES.

Indexed as

ChromatinEnhancer Elements, GeneticSingle-Cell AnalysisAlgorithmsComputational BiologyHumansTranscriptomeChromatin

Identifiers

PMID39468737
PMCPMC11549018

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.