raw data for quantification of D12 and D18/19 immunocytochemistry

Underlying data for quantification graphs shown in Figure 3<br>cppipe files: CellProfiler v.3.1.9 was used to generate the pipelines for each image set (one differentiation protocol, 3 channels, 2 timepoints).<br>quantification.xlsx: The raw data generated after running the pipelines were copied to a spreadsheet. 'Cells / Nuclei (%)' column shows the percentage of cells positive for SOX2 at D12 and TBR2 at D18/19. 'Intracellular APOE / Cells (%)' column shows the percentage of intracellular APOE-positive cells amongst SOX2- and TBR2-positive cells. These 2 columns are presented as bar graphs on Figure 3 of the manuscript.<br>

图3所示定量图表的基础数据集<br>cppipe文件：使用CellProfiler v3.1.9为每组图像集生成分析管道（涵盖1种分化方案、3个通道、2个时间点）。<br>quantification.xlsx：运行上述分析管道后得到的原始数据被导入电子表格。其中，"细胞/细胞核占比（%）"列展示了D12时点SOX2阳性细胞、D18/19时点TBR2阳性细胞的占比；"胞内APOE/细胞占比（%）"列则展示了SOX2与TBR2阳性细胞中，胞内APOE阳性细胞的占比。上述两列数据以柱状图形式呈现于本文稿的图3中。