Closed titand98 closed 3 years ago
You command line uses -a -dont_gzip
. Specifying -a
overrides the adapter auto-detection, and instead tries to use -dont_gzip
as the adapter sequence (which isn't allowed). I would also try to use weird symbols in the directory file, e.g. ()!/#
etc, as they will most likely cause trouble. The following command should work just fine:
trim_galore --fastqc -o ../trimmed_files/ SRR1777087.1.fastq.gz
thanks sir.issue resolved
base) erpl@erpl-HP-Z840-Workstation:~/sayak/pilot study/downloaded_Raw_files$ trim_galore --fastqc -a -dont_gzip o ../trimmed_files(trial)/ SRR1777087.1 _Multicore support not enabled. Proceeding with single-core trimming. Path to Cutadapt set as: 'cutadapt' (default) Cutadapt seems to be working fine (tested command 'cutadapt --version') Cutadapt version: 3.1 single-core operation. No quality encoding type selected. Assuming that the data provided uses Sanger encoded Phred scores (default)
Adapter sequence must contain DNA characters only (A,C,T,G or N)!
I have tried commenting out line 2 two lines in perl file still getting that error else{ # default
unless ($adapter =~ /^[ACTGNXactgnx]+$/){
plz help!!!!!!!!!!!!!!!!!!