I am trying to wrap my head around this GSE entry:
This is a scRNA-seq study, using the technology m-CelSeq 2. As far as I understand, in this technology you sort cells into 384-well plates and then you sequence each cell in each well. Following this logic, each GSM entry should be the results of a single cell. However, there are only 319 GSMs, and the paper states that they sequenced 10,000 cells. What is, then, each sample in this dataset?