SIMS:用于单细胞 RNA 测序分析的深度学习标签转移工具。

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2024-06-12 Epub Date: 2024-05-31 DOI:10.1016/j.xgen.2024.100581
Jesus Gonzalez-Ferrer, Julian Lehrer, Ash O'Farrell, Benedict Paten, Mircea Teodorescu, David Haussler, Vanessa D Jonsson, Mohammed A Mostajo-Radji
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引用次数: 0

摘要

细胞图谱是对新样本进行自动细胞标记的重要参考,但现有的分类算法在准确性方面却举步维艰。在此,我们介绍 SIMS(用于单细胞的可扩展、可解释的机器学习),这是一种用于单细胞 RNA 分类的低代码数据高效管道。我们针对不同组织和物种的数据集对 SIMS 进行了基准测试。我们证明了 SIMS 在大脑细胞分类中的功效,即使使用较小的训练集也能达到很高的准确率(见图 1)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SIMS: A deep-learning label transfer tool for single-cell RNA sequencing analysis.

Cell atlases serve as vital references for automating cell labeling in new samples, yet existing classification algorithms struggle with accuracy. Here we introduce SIMS (scalable, interpretable machine learning for single cell), a low-code data-efficient pipeline for single-cell RNA classification. We benchmark SIMS against datasets from different tissues and species. We demonstrate SIMS's efficacy in classifying cells in the brain, achieving high accuracy even with small training sets (<3,500 cells) and across different samples. SIMS accurately predicts neuronal subtypes in the developing brain, shedding light on genetic changes during neuronal differentiation and postmitotic fate refinement. Finally, we apply SIMS to single-cell RNA datasets of cortical organoids to predict cell identities and uncover genetic variations between cell lines. SIMS identifies cell-line differences and misannotated cell lineages in human cortical organoids derived from different pluripotent stem cell lines. Altogether, we show that SIMS is a versatile and robust tool for cell-type classification from single-cell datasets.

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