Evidence map›Paper›PMID 37402002›Full record

ArticleInterdisciplinary sciences, computational life sciences2023

scFED: Clustering Identifying Cell Types of scRNA-Seq Data Based on Feature Engineering Denoising.

Yang Liu, Feng Li, Junliang Shang, Jinxing Liu, Juan Wang, Daohui Ge

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Article in Interdisciplinary sciences, computational life sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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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.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yang LiuSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.ORCID http://orcid.org/0000-0001-6708-0808
Feng LiSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China. lifeng_10_28@163.com.
Junliang ShangSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Jinxing LiuSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Juan WangSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Daohui GeSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.

Funding

National Natural Science Foundation of China 61902216National Natural Science Foundation of China 61972226National Natural Science Foundation of China 62172253National Natural Science Foundation of China 62172254
6 · The paper itself

Abstract

Recently developed single-cell RNA-seq (scRNA-seq) technology has given researchers the chance to investigate single-cell level of disease development. Clustering is one of the most essential strategies for analyzing scRNA-seq data. Choosing high-quality feature sets can significantly enhance the outcomes of single-cell clustering and classification. But computationally burdensome and highly expressed genes cannot afford a stabilized and predictive feature set for technical reasons. In this study, we introduce scFED, a feature-engineered gene selection framework. scFED identifies prospective feature sets to eliminate the noise fluctuation. And fuse them with existing knowledge from the tissue-specific cellular taxonomy reference database (CellMatch) to avoid the influence of subjective factors. Then present a reconstruction approach for noise reduction and crucial information amplification. We apply scFED on four genuine single-cell datasets and compare it with other techniques. According to the results, scFED improves clustering, decreases dimension of the scRNA-seq data, improves cell type identification when combined with clustering algorithms, and has higher performance than other methods. Therefore, scFED offers certain benefits in scRNA-seq data gene selection.

Indexed as

RNA-SeqSequence Analysis, RNASingle-Cell AnalysisAlgorithmsCluster AnalysisComputational BiologyHumansSingle-Cell Gene Expression AnalysisClassificationClusteringFeature engineeringReconstructionscRNA-seq

Identifiers

PMID37402002

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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.