Chao-Chung Kuo
Chao-Chung Kuo
Below is the error message I got when I set `--report` in the command. I will also check it later. ``` Call DPs on whole genome. Computing read extension sizes...
Detailed discussion can be seen here: https://app.slack.com/client/TE6CZUZPH/activity In short, the problem is: When I run this command for Qiaseq protocol, ``` nextflow run nf-core/smrnaseq -profile docker,qiaseq -resume \ --mirtrace_species "hsa"...
### Description of the bug The empty `fastq` files appears in this command: ``` umi_tools \ extract \ -I Healthy_E72a.umi_dedup.sorted.fastq.gz \ -S Healthy_E72a.umi_extract.fastq.gz \ --extract-method=regex --bc-pattern='.+(?PAACTGTAGGCACCATCAAT){s