Entering edit mode
11.1 years ago
roll
▴
350
I am running fastq_screen to pick up the contaminants from my fastq file.
The program runs successfully but finds no match. I have used the same data with FastQC and it finds some of the comtaminants in the same data.
Can anyone advise why fastq_screen can not find a match?
what kind of contaminants are you looking for? Which databases do you have specified in your .conf file for the application?
I am looking for the adapters/trimmers. I have the contaminant file from FastQC which I converted into fasta format and indexed it using bowtie. That is my in my .conf file.
You'll need to share the command line you typed, and your config file, before we can help you.