方法对比
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| 多组学单细胞RNA测序分析× | 通路富集分析× | |
|---|---|---|
| 领域 | 生物信息学 | 生物信息学 |
| 方法族 | Process / pipeline | Process / pipeline |
| 起源年份≠ | 2015–2021 (rapid maturation with CITE-seq 2017; Seurat v4 2021) | 2003–2005 |
| 提出者≠ | Pioneered by Rahul Satija (Seurat), Oliver Stegle and John Marioni (MOFA+), and the broader single-cell genomics community | Mootha et al. (2003); systematised by Subramanian et al. (2005) |
| 类型≠ | Integrative computational pipeline | Statistical functional annotation method |
| 开创性文献≠ | Hao, Y., Hao, S., Andersen-Nissen, E., Mauck, W. M., Zheng, S., Butler, A., Lee, M. J., Wilk, A. J., Darby, C., Zager, M., Hoffman, P., Stoeckius, M., Papalexi, E., Mimitou, E. P., Jain, J., Srivastava, A., Stuart, T., Fleming, L. M., Yeung, B., Rogers, A. J., McElrath, J. M., Blish, C. A., Gottardo, R., Smibert, P., & Satija, R. (2021). Integrated analysis of multimodal single-cell data. Cell, 184(13), 3573–3587.e29. link ↗ | Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., & Mesirov, J. P. (2005). Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles. Proceedings of the National Academy of Sciences, 102(43), 15545–15550. DOI ↗ |
| 别名 | scMulti-omics, single-cell multi-omics, multimodal single-cell analysis, paired single-cell omics | PEA, overrepresentation analysis, ORA, functional enrichment analysis |
| 相关 | 6 | 6 |
| 摘要≠ | Multi-omics single-cell RNA-seq analysis integrates two or more molecular layers — such as gene expression (scRNA-seq), chromatin accessibility (scATAC-seq), or surface protein abundance (CITE-seq) — measured simultaneously or co-profiled in the same individual cells. By aligning these modalities in a shared low-dimensional space, researchers gain a mechanistically richer picture of cell identity, regulatory state, and phenotype than any single assay can provide. | Pathway enrichment analysis (PEA) is a statistical approach that takes a list of genes or proteins of interest — typically derived from a differential expression or proteomics experiment — and identifies which pre-defined biological pathways or functional gene sets are represented more often than expected by chance. By mapping individual molecular changes onto curated pathway knowledge bases such as KEGG, Gene Ontology, or Reactome, PEA translates long gene lists into interpretable biological processes, making it a central tool in the post-analysis of high-throughput omics experiments. |
| ScholarGate数据集 ↗ |
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