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Stefano Mangiola

dblp:279/4690 · DBLP profile ↗
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2ranked-venue papers
1as first author
2since 2021 · last 2023
0000-0001-7474-836XORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 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 · 70% Computational science and engineering · 30%
Artificial intelligence
1 paper
Probabilistic and Bayesian machine learning · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis
single-cell RNA sequencing
0.512021
Interfacing Seurat with the R tidy universe · Bioinform. 2021
Computational science and engineering
software interoperability
0.512021
Interfacing Seurat with the R tidy universe · Bioinform. 2021
Machine learning › Probabilistic and Bayesian machine learning › hierarchical modeling
hierarchical bayesian model
0.212023
cellsig plug-in enhances CIBERSORTx signature selection for multidataset transcriptomes with sparse multilevel modelling · Bioinform. 2023

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

sparse modelling · 1.3bayesian sparse multilevel model · 1.3tidyverse · 0.5
YearPublicationVenuePosition
2023 cellsig plug-in enhances CIBERSORTx signature selection for multidataset transcriptomes with sparse multilevel modelling
abstract
MOTIVATION: The precise characterization of cell-type transcriptomes is pivotal to understanding cellular lineages, deconvolution of bulk transcriptomes, and clinical applications. Single-cell RNA sequencing resources like the Human Cell Atlas have revolutionised cell-type profiling. However, challenges persist due to data heterogeneity and discrepancies across different studies. One limitation of prevailing tools such as CIBERSORTx is their inability to address hierarchical data structures and handle nonoverlapping gene sets across samples, relying on filtering or imputation. RESULTS: Here, we present cellsig, a Bayesian sparse multilevel model designed to improve signature estimation by adjusting data for multilevel effects and modelling for gene-set sparsity. Our model is tailored to large-scale, heterogeneous pseudobulk and bulk RNA sequencing data collections with nonoverlapping gene sets. We tested the performances of cellsig on a novel curated Human Bulk Cell-type Catalogue, which harmonizes 1435 samples across 58 datasets. We show that cellsig significantly enhances cell-type marker gene ranking performance. This approach is valuable for cell-type signature selection, with implications for marker gene validation, single-cell annotation, and deconvolution benchmarks. AVAILABILITY AND IMPLEMENTATION: Codes and the interactive app are available at https://github.com/stemangiola/cellsig; and the database is available at https://doi.org/10.5281/zenodo.7582421.
Md. Abdullah-Al-Kamran Khan, Yuhan Sun 0001, Alexander D. Barrow, Anthony T. Papenfuss, Stefano Mangiola
Bioinform.6
2021 Interfacing Seurat with the R tidy universe
abstract
MOTIVATION: Seurat is one of the most popular software suites for the analysis of single-cell RNA sequencing data. Considering the popularity of the tidyverse ecosystem, which offers a large set of data display, query, manipulation, integration and visualization utilities, a great opportunity exists to interface the Seurat object with the tidyverse. This interface gives the large data science community of tidyverse users the possibility to operate with familiar grammar. RESULTS: To provide Seurat with a tidyverse-oriented interface without compromising efficiency, we developed tidyseurat, a lightweight adapter to the tidyverse. Tidyseurat displays cell information as a tibble abstraction, allowing intuitively interfacing Seurat with dplyr, tidyr, ggplot2 and plotly packages powering efficient data manipulation, integration and visualization. Iterative analyses on data subsets are enabled by interfacing with the popular nest-map framework. AVAILABILITY AND IMPLEMENTATION: The software is freely available at cran.r-project.org/web/packages/tidyseurat and github.com/stemangiola/tidyseurat. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Stefano Mangiola, Maria A. Doyle, Anthony T. Papenfuss
Bioinform.1