摘要
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. Graphical abstract: [Figure not available: see fulltext.]
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 590-601 |
| 页数 | 12 |
| 期刊 | Interdisciplinary Sciences – Computational Life Sciences |
| 卷 | 15 |
| 期 | 4 |
| DOI | |
| 出版状态 | 已出版 - 12月 2023 |
| 已对外发布 | 是 |
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