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Ziyi Chai

dblp:369/6661 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2024
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 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
1 paper
Bioinformatics and computational biology · 92% Computational science and engineering · 8%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis
cell type annotation
0.812024
CTISL: a dynamic stacking multi-class classification approach for identifying cell types from single-cell RNA-seq data · Bioinform. 2024
Bioinformatics and computational biology
single-cell analysis
0.812024
CTISL: a dynamic stacking multi-class classification approach for identifying cell types from single-cell RNA-seq data · Bioinform. 2024
Bioinformatics and computational biology › single-cell analysis › single-cell RNA sequencing
single-cell RNA-seq analysis
0.812024
CTISL: a dynamic stacking multi-class classification approach for identifying cell types from single-cell RNA-seq data · Bioinform. 2024
Computational science and engineering
ensemble learning
0.212024
CTISL: a dynamic stacking multi-class classification approach for identifying cell types from single-cell RNA-seq data · Bioinform. 2024
Bioinformatics and computational biology › genomics
machine learning for genomics
0.212024
CTISL: a dynamic stacking multi-class classification approach for identifying cell types from single-cell RNA-seq data · Bioinform. 2024

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

support vector machine · 0.8stacking ensemble · 0.8logistic regression · 0.8
YearPublicationVenuePosition
2024 CTISL: a dynamic stacking multi-class classification approach for identifying cell types from single-cell RNA-seq data
abstract
MOTIVATION: Effective identification of cell types is of critical importance in single-cell RNA-sequencing (scRNA-seq) data analysis. To date, many supervised machine learning-based predictors have been implemented to identify cell types from scRNA-seq datasets. Despite the technical advances of these state-of-the-art tools, most existing predictors were single classifiers, of which the performances can still be significantly improved. It is therefore highly desirable to employ the ensemble learning strategy to develop more accurate computational models for robust and comprehensive identification of cell types on scRNA-seq datasets. RESULTS: We propose a two-layer stacking model, termed CTISL (Cell Type Identification by Stacking ensemble Learning), which integrates multiple classifiers to identify cell types. In the first layer, given a reference scRNA-seq dataset with known cell types, CTISL dynamically combines multiple cell-type-specific classifiers (i.e. support-vector machine and logistic regression) as the base learners to deliver the outcomes for the input of a meta-classifier in the second layer. We conducted a total of 24 benchmarking experiments on 17 human and mouse scRNA-seq datasets to evaluate and compare the prediction performance of CTISL and other state-of-the-art predictors. The experiment results demonstrate that CTISL achieves superior or competitive performance compared to these state-of-the-art approaches. We anticipate that CTISL can serve as a useful and reliable tool for cost-effective identification of cell types from scRNA-seq datasets. AVAILABILITY AND IMPLEMENTATION: The webserver and source code are freely available at http://bigdata.biocie.cn/CTISLweb/home and https://zenodo.org/records/10568906, respectively.
Ziyi Chai, Yan Liu 0038, Chen Li 0021, Yu Jiang 0014, Quanzhong Liu
Bioinform.2