Thank you. I appreciate your help. I have not tried your answer yet because I found an R package, Sierra that seems to have a function for splitting a bam file into multiple bam files for every cell, "https://rdrr.io/github/VCCRI/Sierra/man/SplitBam.html". Have you ever tried this?
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Assuming your data was processed by
cellrangerthere should be a BAM fie withCBtags in it. Using those to split the file would be the way to go.Some background info: https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/output/bam#bam-bc-tags
There are some approaches outlined in the blog linked by @igor in this thread: scRNAseq: Split FASTQ into cell specific FASTQ Files