Evidence map›Paper›PMID 37756593›Full record

ArticleBriefings in bioinformatics2023

GOWDL: gene ontology-driven wide and deep learning model for cell typing of scRNA-seq data.

Antonino Fiannaca, Massimo La Rosa, Laura La Paglia, Salvatore Gaglio, Alfonso Urso

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Antonino FiannacaICAR-CNR, National Research Council of Italy, Via Ugo La Malfa 153, 90146, Palermo, Italy.ORCID 0000-0002-0114-4984
Massimo La RosaICAR-CNR, National Research Council of Italy, Via Ugo La Malfa 153, 90146, Palermo, Italy.ORCID 0000-0001-6718-7269
Laura La PagliaICAR-CNR, National Research Council of Italy, Via Ugo La Malfa 153, 90146, Palermo, Italy.ORCID 0000-0002-1077-5657
Salvatore GaglioICAR-CNR, National Research Council of Italy, Via Ugo La Malfa 153, 90146, Palermo, Italy.ORCID 0000-0002-5480-2100
Alfonso UrsoICAR-CNR, National Research Council of Italy, Via Ugo La Malfa 153, 90146, Palermo, Italy.ORCID 0000-0003-3018-1458

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell RNA-sequencing (scRNA-seq) allows for obtaining genomic and transcriptomic profiles of individual cells. That data make it possible to characterize tissues at the cell level. In this context, one of the main analyses exploiting scRNA-seq data is identifying the cell types within tissue to estimate the quantitative composition of cell populations. Due to the massive amount of available scRNA-seq data, automatic classification approaches for cell typing, based on the most recent deep learning technology, are needed. Here, we present the gene ontology-driven wide and deep learning (GOWDL) model for classifying cell types in several tissues. GOWDL implements a hybrid architecture that considers the functional annotations found in Gene Ontology and the marker genes typical of specific cell types. We performed cross-validation and independent external testing, comparing our algorithm with 12 other state-of-the-art predictors. Classification scores demonstrated that GOWDL reached the best results over five different tissues, except for recall, where we got about 92% versus 97% of the best tool. Finally, we presented a case study on classifying immune cell populations in breast cancer using a hierarchical approach based on GOWDL.

Indexed as

Deep LearningAlgorithmsGene OntologyGenomicsSingle-Cell Gene Expression AnalysisCell typingDeep learningGene ontologyMarker genesscRNA-seq

Identifiers

PMID37756593
PMCPMC10530315

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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.