I’m trying to assemble reads using spades on galaxy.org. spades but I get a mistake. from the fastqc of the reads I noticed that they have residues of the universal illuminates adapters used for sequencing. I tried to clean the sequences by inserting on trimmomatic also the adapters provided by the company, but I still have spades error. Do any of you know how I could solve the problem and assemble the reads?
Trimmomatic hasn't been updated in 5 years, probably you can try fastp? fastp is much faster, simpler, more accurate with more functions. fastp is still being actively developed.
Please post
galaxyrelated help questions on their help forum for prompt response: https://help.galaxyproject.org/They can see your data on
galaxyand should be able to provide direct help.