Entering edit mode
20 months ago
myoui3122010
▴
30
I used singleR to annotate the data, where the ref was common cells between original dataset and the matrix generated by me using Kallisto-bustools.
meta$annotation_cell_class <- orig_metadata$annotation_cell_class[match(meta$cell_barcode, orig_metadata$cell_barcode)]
But singleR assigned most NA cells to one type of cell. Based on expression pattern majority of Non-neuron express less than 2000 gene, should i filter them out as I don't require them. And should I just annotate them based on clusters from original annotation.
Thanks for your time
Left: SingleR, Right: Copied from Original data