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| Analiza ekspresji różnicowej RNA-seq wspomagana uczeniem maszynowym× | Analiza wzbogacenia szlaków× | |
|---|---|---|
| Dziedzina | Bioinformatyka | Bioinformatyka |
| Rodzina | Process / pipeline | Process / pipeline |
| Rok powstania≠ | 2015–2019 (rapid development period) | 2003–2005 |
| Twórca≠ | Multiple groups; scVI (Lopez et al., 2018) and DCA (Eraslan et al., 2019) are landmark tools | Mootha et al. (2003); systematised by Subramanian et al. (2005) |
| Typ≠ | Computational bioinformatics pipeline | Statistical functional annotation method |
| Źródło pierwotne≠ | Lopez, R., Regier, J., Cole, M. B., Jordan, M. I., & Yosef, N. (2018). Deep generative modeling for single-cell transcriptomics. Nature Methods, 15(12), 1053–1058. 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 ↗ |
| Inne nazwy | ML-based DE analysis, deep learning RNA-seq DE, neural network differential expression, ML-augmented transcriptomics | PEA, overrepresentation analysis, ORA, functional enrichment analysis |
| Pokrewne≠ | 5 | 6 |
| Podsumowanie≠ | Machine learning-assisted RNA-seq differential expression analysis augments classical statistical DE testing (DESeq2, edgeR, limma-voom) with ML models — including neural networks, random forests, and variational autoencoders — to better handle the high dimensionality, zero-inflation, and batch effects inherent in RNA-seq count data. The approach improves feature selection, noise reduction, and detection power, especially in large or complex experimental designs. | 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. |
| ScholarGateZbiór danych ↗ |
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