Supplementary processed data for Chandler et al. Single-cell transcriptomics identifies aberrant glomerular angiogenic signalling in the early stages of a murine model of WT1 kidney disease

<strong><em>Summary datafiles for Chandler et al.</em></strong> Processed single-cell RNA sequencing data, derived from murine glomeruli (isolated using the dynabead technique) from <em>n = 2</em> wild-type <em>Wt1^+/+</em> (Ctrl) and <em>n = 2</em> mutant <em>Wt1^R394W/+</em> (Mut) littermates of WT1 glomerulopathy, followed by 10x Genomics Chromium v3 platform. Please refer to associated scripts for analysis of the data: https://github.com/daniyal-jafree1995/collaborations/blob/main/Chandleretal_2022_WT1glomerulopathyscRNAseq.R File descriptions as below: barcodes.tsv.gz - barcodes file required for input to Read10X function in Seurat features.tsv.gz - features file required for input to Read10X function in Seurat matrix.mtx.gz - matrix file required for input to Read10X function in Seurat WT1_scRNAseq.rds - RDS file containing processed and annotated Seurat object for downstream analysis*Chandler等人研究相关汇总数据集文件* 本数据集包含经处理的单细胞RNA测序（single-cell RNA sequencing）数据，样本来源于采用磁珠分选技术（dynabead）分离得到的小鼠肾小球，取自2只野生型*Wt1^+/+*（对照组，Ctrl）与2只突变型*Wt1^R394W/+*（突变组，Mut）的WT1肾小球病同窝仔鼠，后续采用10x Genomics Chromium v3平台完成测序。数据分析所用配套脚本可参见：https://github.com/daniyal-jafree1995/collaborations/blob/main/Chandleretal_2022_WT1glomerulopathyscRNAseq.R 文件说明如下： 1. `barcodes.tsv.gz`：Seurat工具`Read10X`函数输入所需的条形码文件 2. `features.tsv.gz`：Seurat工具`Read10X`函数输入所需的特征文件 3. `matrix.mtx.gz`：Seurat工具`Read10X`函数输入所需的矩阵文件 4. `WT1_scRNAseq.rds`：包含已完成处理与注释的Seurat对象的RDS文件，可用于下游分析