I have the scRNAseq data sequenced by BGI, which can be processed by cellranger. but the result always show "Low Fraction Reads in Cells" as the fig showed.
does anyone know the reason, I also tested my pipeline with 10X test data, result is ok.
is there with any mistake I made or some bug between BGI and cellranger
This indicates a problem with the sample/libraries. Did you start with significantly more cells than recommended by 10x protocol?