Hi there,
Thank you for developing fastp.
I try to run it on a 3'seq experiment (without any option for polyA trimming), and fastp i) does not detect any adapters, ii) does not trim any reads.
And in practice, I know that I do have many reads spanning the polyA tail and then the adapter sequence, as this one
CCCAACGAAACTAGACGAGCTAACTAAGAATAGCTAAAAGAGCACACCCGTCTATGTAGCAAAAAAAAAAAAAAAAAAGATCGGAAGAGCAACCGTCTGAA
So, is there any parameter to add, so that it can detect such case ?
Thanks
Here is the command line I used :
fastp --qualified_quality_phred 0 --disable_trim_poly_g --length_required 10 -i input.fastq.gz -o input_trimmed.fastq.gz -j input.fastp.json -h input.fastp.html --thread 2
Nicolas
Hi there, Thank you for developing fastp. I try to run it on a 3'seq experiment (without any option for polyA trimming), and fastp i) does not detect any adapters, ii) does not trim any reads. And in practice, I know that I do have many reads spanning the polyA tail and then the adapter sequence, as this one
CCCAACGAAACTAGACGAGCTAACTAAGAATAGCTAAAAGAGCACACCCGTCTATGTAGCAAAAAAAAAAAAAAAAAAGATCGGAAGAGCAACCGTCTGAA
So, is there any parameter to add, so that it can detect such case ? Thanks Here is the command line I used :fastp --qualified_quality_phred 0 --disable_trim_poly_g --length_required 10 -i input.fastq.gz -o input_trimmed.fastq.gz -j input.fastp.json -h input.fastp.html --thread 2
Nicolas