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Integrating single-cell datasets with ambiguous batch information by incorporating molecular network features
Briefings in Bioinformatics ( IF 9.5 ) Pub Date : 2021-08-19 , DOI: 10.1093/bib/bbab366
Ji Dong 1 , Peijie Zhou 2 , Yichong Wu 3 , Yidong Chen 4 , Haoling Xie 5 , Yuan Gao 5 , Jiansen Lu 5 , Jingwei Yang 5 , Xiannian Zhang 6 , Lu Wen 5 , Tiejun Li 3 , Fuchou Tang 5
Affiliation  

With the rapid development of single-cell sequencing techniques, several large-scale cell atlas projects have been launched across the world. However, it is still challenging to integrate single-cell RNA-seq (scRNA-seq) datasets with diverse tissue sources, developmental stages and/or few overlaps, due to the ambiguity in determining the batch information, which is particularly important for current batch-effect correction methods. Here, we present SCORE, a simple network-based integration methodology, which incorporates curated molecular network features to infer cellular states and generate a unified workflow for integrating scRNA-seq datasets. Validating on real single-cell datasets, we showed that regardless of batch information, SCORE outperforms existing methods in accuracy, robustness, scalability and data integration.

中文翻译:

通过结合分子网络特征将单细胞数据集与模糊的批次信息相结合

随着单细胞测序技术的飞速发展,全球多个大型细胞图谱项目相继启动。然而,由于确定批次信息的模糊性,整合具有不同组织来源、发育阶段和/或重叠很少的单细胞 RNA-seq (scRNA-seq) 数据集仍然具有挑战性,这对于当前批次尤为重要-效果校正方法。在这里,我们介绍了 SCORE,这是一种简单的基于网络的集成方法,它结合了策划的分子网络特征来推断细胞状态并生成用于集成 scRNA-seq 数据集的统一工作流程。通过对真实的单细胞数据集进行验证,我们表明,无论批次信息如何,SCORE 在准确性、稳健性、可扩展性和数据集成方面都优于现有方法。
更新日期:2021-08-19
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