To facilitate single-cell multi-omics analysis and improve reproducibility, we present single-cell pipeline for end-to-end data integration (SPEEDI), a fully automated end-to-end framework for batch inference, data integration, and cell-type labeling. SPEEDI introduces data-driven batch inference and transforms the often heterogeneous data matrices obtained from different samples into a uniformly annotated and integrated dataset. Without requiring user input, it automatically selects parameters and executes pre-processing, sample integration, and cell-type mapping. It can also perform downstream analyses of differential signals between treatment conditions and gene functional modules. SPEEDI's data-driven batch-inference method works with widely used integration and cell-typing tools. By developing data-driven batch inference, providing full end-to-end automation, and eliminating parameter selection, SPEEDI improves reproducibility and lowers the barrier to obtaining biological insight from these valuable single-cell datasets. The SPEEDI interactive web application can be accessed at https://speedi.princeton.edu/. A record of this paper's transparent peer review process is included in the supplemental information.
Automated single-cell omics end-to-end framework with data-driven batch inference.
具有数据驱动批量推理的自动化单细胞组学端到端框架
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作者:Wang Yuan, Thistlethwaite William, Tadych Alicja, Ruf-Zamojski Frederique, Bernard Daniel J, Cappuccio Antonio, Zaslavsky Elena, Chen Xi, Sealfon Stuart C, Troyanskaya Olga G
| 期刊: | Cell Systems | 影响因子: | 7.700 |
| 时间: | 2024 | 起止号: | 2024 Oct 16; 15(10):982-990 |
| doi: | 10.1016/j.cels.2024.09.003 | 研究方向: | 细胞生物学 |
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