J1 mouse embryonic stem cells (cultured in medium) were facs sorted and processed in two batches. Single cell RNA-Seq was performed using Single Cell RNA Barcoding and Sequencing (SCRB-Seq) with unique molecular identifiers (UMI) and libraries were generated using Nextera XT (Illumina) kit. Furthermore, spike-ins (ERCC) were added. The read count matrix was downsampled to 10000 genes.
scrbseq_gene_cnts
An object of class data.frame with 10000 rows and 58 columns.
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE75790.