mliiv

If I understand the output correctly, there should be 2 files per sample, usually it's *_L001_R1_001.fastq.gz which is read 1 having cell barcodes, and *_L001_R2_001.fastq.gz which is read 2 with...

Hi @gbloeb if I remember correctly, then I dropped the idea of filtering the loom file with loomR since no luck with really fixing the error. Instead, I prepared the...