ArticleBioinformatics (Oxford, England)2025
FastSCODE: an accelerated SCODE algorithm for inferring gene regulatory networks on manycore processors.
Article in Bioinformatics (Oxford, England), 2025. 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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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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Who cites it
1 citing paper in PubMed.
- CellCraft: an extensible visual programming application for gene regulatory network inference.Bioinformatics (Oxford, England) · 2026Article
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5 authors.
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Abstract
summarySCODE reconstructs gene regulatory networks from single-cell RNA sequencing (scRNA-seq) data using an ordinary differential equation (ODE) model, and has been successfully applied to a wide range of scRNA-seq datasets, including mouse, human, and plant cells. However, its computational performance is limited when processing large datasets due to its sequential execution flow and repeated optimization loops. To overcome this limitation, we have developed FastSCODE, a batch computing version of the SCODE algorithm optimized for acceleration on manycore processors such as GPUs. FastSCODE performs batch computation on multiple gene expression profiles and optimizes the parameters of a linear ODE model using manycore computing. Compared to the original implementation, FastSCODE achieves up to 6000× improvement in performance (from about one month to 10 min) on the CeNGEN scRNA-seq dataset when using multiple GPUs. AVAILABILITY AND IMPLEMENTATION: FastSCODE is publicly available on GitHub at https://github.com/cxinsys/fastscode.
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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.