Ultra-high throughput single-cell analysis of proteins and RNAs by split-pool synthesis
The authors demonstrate split-pool barcoding for protein and targeted RNA measurements in cell lines, human blood-cell material and mouse cells. Large theoretical barcode capacity is distinct from measured event recovery. Uneven RNA detection, cell losses, exclusions, doublets and source discrepancies limit interpretation; no clinical or UAP validation follows.
Complete supplied main and correction text; partial supplemental visuals