I would like to know if I can pass a fastq file in trimmomatic, and then pass again its results. Also, how can I be sure that a fastq file that I downloaded from public sources has already been trimmed for quality?
I got some SRA fastq files that seems that they have already been trimmed, since their reads are not the same lengh. But when i look at them in the Fastqc, it redflags a significant number of reports (as for example GC contents and overrepresented sequences). When I pass it again in trimmomatic, some of the reports in Fastqc get a better. So my doubt is if it's ok to do this, pass them twice in the trimmomatic. In the comments are some examples of what I got.
Thanks
it can be done. But it would help us understand if you could tell us why two pass is necessary for your work.
The thing is that I got some SRA fastq files that seems that they have already been trimmed, since their reads are not the same lengh. But when i look at them in the Fastqc, it redflags a significant number of reports (as for example GC contents and overrepresented sequences). When I pass it again in trimmomatic, some of the reports in Fastqc get a better. So my doubt is if it's ok to do this, pass them twice in the trimmomatic. Here goes some images that explain what I got. (The Filename is after passing is with a 6 in the place of 5, It was a typo)
There are no restrictions on number of times in filtering reads.