Evidence map›Paper›PMID 35281805›Full record

SynthesisFrontiers in genetics2022

A Systematic Evaluation of Supervised Machine Learning Algorithms for Cell Phenotype Classification Using Single-Cell RNA Sequencing Data.

Xiaowen Cao, Li Xing, Elham Majd, Hua He, Junhua Gu, Xuekui Zhang

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

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

6 authors.

Xiaowen CaoSchool of Artificial Intelligence, Hebei University of Technology, Tianjin, China.
Li XingDepartment of Mathematics and Statistics, University of Saskatchewan, Saskatoon, SK, Canada.
Elham MajdDepartment of Mathematics and Statistics, University of Victoria, Victoria, BC, Canada.
Hua HeSchool of Science, Hebei University of Technology, Tianjin, China.
Junhua GuSchool of Artificial Intelligence, Hebei University of Technology, Tianjin, China.
Xuekui ZhangDepartment of Mathematics and Statistics, University of Victoria, Victoria, BC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The new technology of single-cell RNA sequencing (scRNA-seq) can yield valuable insights into gene expression and give critical information about the cellular compositions of complex tissues. In recent years, vast numbers of scRNA-seq datasets have been generated and made publicly available, and this has enabled researchers to train supervised machine learning models for predicting or classifying various cell-level phenotypes. This has led to the development of many new methods for analyzing scRNA-seq data. Despite the popularity of such applications, there has as yet been no systematic investigation of the performance of these supervised algorithms using predictors from various sizes of scRNA-seq datasets. In this study, 13 popular supervised machine learning algorithms for cell phenotype classification were evaluated using published real and simulated datasets with diverse cell sizes. This benchmark comprises two parts. In the first, real datasets were used to assess the computing speed and cell phenotype classification performance of popular supervised algorithms. The classification performances were evaluated using the area under the receiver operating characteristic curve, F1-score, Precision, Recall, and false-positive rate. In the second part, we evaluated gene-selection performance using published simulated datasets with a known list of real genes. The results showed that ElasticNet with interactions performed the best for small and medium-sized datasets. The NaiveBayes classifier was found to be another appropriate method for medium-sized datasets. With large datasets, the performance of the XGBoost algorithm was found to be excellent. Ensemble algorithms were not found to be significantly superior to individual machine learning methods. Including interactions in the ElasticNet algorithm caused a significant performance improvement for small datasets. The linear discriminant analysis algorithm was found to be the best choice when speed is critical; it is the fastest method, it can scale to handle large sample sizes, and its performance is not much worse than the top performers.

Indexed as

classificationensemble algorithmsgene selectionmachine learningsingle-cell RNA sequencingsupervised algorithms

Identifiers

PMID35281805
PMCPMC8905542

What OpenQuestion holds

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Registered trials

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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.