Closed kerimsecener closed 3 years ago
Hi Kerim, I made a new release replacing trim galore with a faster/better alternative. https://github.com/BIMSBbioinfo/pigx_rnaseq/releases/tag/v0.0.13
The guix package for this release should be available within a couple of days. Best, Bora
Hello,
I'm running pigx-rnaseq on three samples (paired-end): trim_galore log files seem fine to me, however in the snakejob log files I see this:
_mv: cannot stat ‘/fast/CF_Sequencing/work_dir/cfische/SP005/bulk_RNA_seq/pigx_work/pigx_output/trimmed_reads/GYWU-1219_EIA5_CTNNB1R1.good.fq.gz’: No such file or directory
"_GYWU-1219_EIA5_CTNNB1R1.good.fq.gz " is supposed to be the original fastq file name, I don't understand why the algorithm looks for it in the trimmed_reads folder ?
I'm attaching the yaml file, sample sheet, as well as error files. settings.yaml.txt trim_galore_GYWU_1219.log snakejob.trim_galore_pe.7.sh.e4460475.txt sample_sheet.csv
Thanks,
Kerim