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Nathan Leroy

dblp:370/4727 · DBLP profile ↗
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2ranked-venue papers
0as first author
2since 2021 · last 2024
0000-0002-7354-7213ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 60% Computational science and engineering · 40%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › functional genomics › functional enrichment analysis
gene set enrichment analysis
0.812024
DeepGSEA: explainable deep gene set enrichment analysis for single-cell transcriptomic data · Bioinform. 2024
Computational science and engineering › model interpretability
interpretable deep learning
0.812024
DeepGSEA: explainable deep gene set enrichment analysis for single-cell transcriptomic data · Bioinform. 2024
Bioinformatics and computational biology › single-cell analysis
single-cell transcriptomics
0.812024
DeepGSEA: explainable deep gene set enrichment analysis for single-cell transcriptomic data · Bioinform. 2024
Bioinformatics and computational biology › bioinformatics infrastructure
biological data management
0.712023
GEOfetch: a command-line tool for downloading data and standardized metadata from GEO and SRA · Bioinform. 2023
Computational science and engineering › data infrastructure
metadata standardization
0.712023
GEOfetch: a command-line tool for downloading data and standardized metadata from GEO and SRA · Bioinform. 2023

Methods — techniques the papers use, named apart from their topics

prototype-based neural network · 0.8deep learning · 0.8command-line tool · 0.7
YearPublicationVenuePosition
2024 DeepGSEA: explainable deep gene set enrichment analysis for single-cell transcriptomic data
abstract
MOTIVATION: Gene set enrichment (GSE) analysis allows for an interpretation of gene expression through pre-defined gene set databases and is a critical step in understanding different phenotypes. With the rapid development of single-cell RNA sequencing (scRNA-seq) technology, GSE analysis can be performed on fine-grained gene expression data to gain a nuanced understanding of phenotypes of interest. However, with the cellular heterogeneity in single-cell gene profiles, current statistical GSE analysis methods sometimes fail to identify enriched gene sets. Meanwhile, deep learning has gained traction in applications like clustering and trajectory inference in single-cell studies due to its prowess in capturing complex data patterns. However, its use in GSE analysis remains limited, due to interpretability challenges. RESULTS: In this paper, we present DeepGSEA, an explainable deep gene set enrichment analysis approach which leverages the expressiveness of interpretable, prototype-based neural networks to provide an in-depth analysis of GSE. DeepGSEA learns the ability to capture GSE information through our designed classification tasks, and significance tests can be performed on each gene set, enabling the identification of enriched sets. The underlying distribution of a gene set learned by DeepGSEA can be explicitly visualized using the encoded cell and cellular prototype embeddings. We demonstrate the performance of DeepGSEA over commonly used GSE analysis methods by examining their sensitivity and specificity with four simulation studies. In addition, we test our model on three real scRNA-seq datasets and illustrate the interpretability of DeepGSEA by showing how its results can be explained. AVAILABILITY AND IMPLEMENTATION: https://github.com/Teddy-XiongGZ/DeepGSEA.
Guangzhi Xiong, Nathan Leroy, Stefan Bekiranov, Nathan C. Sheffield, Aidong Zhang 0001
Bioinform.2
2023 GEOfetch: a command-line tool for downloading data and standardized metadata from GEO and SRA
abstract
MOTIVATION: The Gene Expression Omnibus has become an important source of biological data for secondary analysis. However, there is no simple, programmatic way to download data and metadata from Gene Expression Omnibus (GEO) in a standardized annotation format. RESULTS: To address this, we present GEOfetch-a command-line tool that downloads and organizes data and metadata from GEO and SRA. GEOfetch formats the downloaded metadata as a Portable Encapsulated Project, providing universal format for the reanalysis of public data. AVAILABILITY AND IMPLEMENTATION: GEOfetch is available on Bioconda and the Python Package Index (PyPI).
Oleksandr Khoroshevskyi, Nathan Leroy, Vincent P. Reuter, Nathan C. Sheffield
Bioinform.2