Open danledinh opened 2 years ago
sorry it is not suported now. one way to speed up could be split the fastq for cell barcode matching and merge them after alignment to genome.
@LuyiTian , would you recommend this splitting solution for bam files too? I already have barcode called and mapped reads in bam files. Should I split the bam by chromosome and run each separately to speed up the computation?
Thanks.
Is there a way to define number of cores, RAM usage, etc. for the pipelines?