Closed NicMAlexandre closed 3 years ago
It looks like I may have used the wrong input file for the next step. Disregard.
excellent, I was just going through the CHANGELOG to see whether there was anything that might affect your processing (it might still be a good idea to upgrade to 0.6.6 if you have time...).
Hi Felix,
Will do! My apologies.
On Tue, May 25, 2021 at 9:03 AM Felix Krueger @.***> wrote:
excellent, I was just going through the CHANGELOG to see whether there was anything that might affect your processing (it might still be a good idea to upgrade to 0.6.6 if you have time...).
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I ran the following on paired-end RNASeq data:
TrimGalore-0.6.0/./trim_galore --paired --retain_unpaired --phred33 --output_dir trimmed_reads --length 36 -q 5 --stringency 1 -e 0.1 $1 $2
When looking at the fastqc report, I am still seeing adapter content. Are the above parameters correct?