WARNING: you specified the options for cutting by quality, but forogt to enable any of cut_front/cut_tail/cut_right. This will have no effect.
Detecting adapter sequence for read1...
No adapter detected for read1

Read1 before filtering:
total reads: 3920762
total bases: 349980816
Q20 bases: 342286451(97.8015%)
Q30 bases: 331993063(94.8604%)

Read1 after filtering:
total reads: 2482075
total bases: 211469055
Q20 bases: 206674169(97.7326%)
Q30 bases: 200450570(94.7896%)

Filtering result:
reads passed filter: 2482075
reads failed due to low quality: 4953
reads failed due to too many N: 0
reads failed due to too short: 1433734
reads with adapter trimmed: 0
bases trimmed due to adapters: 0

Duplication rate (may be overestimated since this is SE data): 28.5008%

JSON report: SRX7656990.fastp.json
HTML report: SRX7656990.fastp.html

fastp --in1 SRX7656990.fastq.gz --out1 SRX7656990.fastp.fastq.gz --thread 6 --json SRX7656990.fastp.json --html SRX7656990.fastp.html --cut_mean_quality 30 --trim_front1 10 --trim_front2 10 --adapter_fasta /mmfs1/gscratch/scrubbed/strigg/analyses/20250415_RNAseq/polyA.fa 
fastp v0.23.4, time used: 9 seconds