Dong Sherry, Deng Kaiwen, Huang Xiuzhen
Skyline High School, Ann Arbor, MI 48103, United States.
National AI Campus and Department of Computational Biomedicine, Cedars-Sinai Medical Center, West Hollywood, CA 90069, United States.
Bioinform Adv. 2024 Apr 8;4(1):vbae054. doi: 10.1093/bioadv/vbae054. eCollection 2024.
Annotating cell types is a challenging yet essential task in analyzing single-cell RNA sequencing data. However, due to the lack of a gold standard, it is difficult to evaluate the algorithms fairly and an overfitting algorithm may be favored in benchmarks. To address this challenge, we developed a deep learning-based single-cell type prediction tool that assigns the cell type to 265 different cell types for humans, based on data from approximately five million cells.
We achieved a median area under the ROC curve (AUC) of 0.93 when evaluated across datasets. We found that inconsistent labeling in the existing database generated by different labs contributed to the mistakes of the model. Therefore, we used cell ontology to correct the annotations and retrained the model, which resulted in 0.971 median AUC. Our study reveals a limiting factor of the accuracy one may achieve with the current database annotation and points to the solutions towards an algorithm-based correction of the gold standard for future automated cell annotation approaches.
The code is available at: https://github.com/SherrySDong/Hierarchical-Correction-Improves-Automated-Single-cell-Type-Annotation. Data used in this study are listed in Supplementary Table S1 and are retrievable at the CZI database.
在分析单细胞RNA测序数据时,注释细胞类型是一项具有挑战性但又至关重要的任务。然而,由于缺乏金标准,很难公平地评估算法,并且在基准测试中可能会青睐过拟合算法。为应对这一挑战,我们开发了一种基于深度学习的单细胞类型预测工具,该工具基于约五百万个细胞的数据,将细胞类型分配给人类的265种不同细胞类型。
在跨数据集评估时,我们实现了ROC曲线下面积(AUC)中位数为0.93。我们发现不同实验室生成的现有数据库中的标签不一致导致了模型的错误。因此,我们使用细胞本体来校正注释并重新训练模型,这使得AUC中位数达到0.971。我们的研究揭示了当前数据库注释可能达到的准确性的一个限制因素,并指出了未来自动细胞注释方法基于算法校正金标准的解决方案。