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SSCC: A Novel Computational Framework for Rapid and Accurate Clustering Large-scale Single Cell RNA-seq Data

机译:SSCC:一种新型的计算框架用于快速准确地聚类大规模单细胞RNA-seq数据

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摘要

>Clustering is a prevalent analytical means to analyze >single cell RNA sequencing (scRNA-seq) data but the rapidly expanding data volume can make this process computationally challenging. New methods for both accurate and efficient clustering are of pressing need. Here we proposed Spearman >subsampling-clustering->classification (SSCC), a new clustering framework based on random projection and feature construction, for large-scale scRNA-seq data. SSCC greatly improves clustering accuracy, robustness, and computational efficacy for various state-of-the-art algorithms benchmarked on multiple real datasets. On a dataset with 68,578 human blood cells, SSCC achieved 20% improvement for clustering accuracy and 50-fold acceleration, but only consumed 66% memory usage, compared to the widelyused software package SC3. Compared to k-means, the accuracy improvement of SSCC can reach 3-fold. An R implementation of SSCC is available at .
机译:>聚类是一种用于分析>单细胞 RNA测序(scRNA-seq)数据的流行分析方法,但是快速扩展的数据量可能会使此过程在计算上具有挑战性。迫切需要用于精确和有效聚类的新方法。在这里,我们针对大型scRNA-seq数据提出了Spearman >子采样-聚类->分类(SSCC),它是一种基于随机投影和特征构造的新聚类框架。对于在多个真实数据集上进行基准测试的各种最新算法,SSCC极大地提高了聚类准确性,鲁棒性和计算效率。与拥有广泛使用的软件包SC3相比,在具有68,578个人类血细胞的数据集上,SSCC的聚类准确性和50倍加速提高了20%,但仅消耗了66%的内存使用量。与k-means相比,SSCC的精度提高了3倍。可在上获得SSCC的R实现。

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