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: 6414956
total bases: 586719273
Q20 bases: 573948636(97.8234%)
Q30 bases: 556695819(94.8828%)

Read1 after filtering:
total reads: 4545028
total bases: 387825712
Q20 bases: 379043265(97.7355%)
Q30 bases: 367435380(94.7424%)

Filtering result:
reads passed filter: 4545028
reads failed due to low quality: 8043
reads failed due to too many N: 0
reads failed due to too short: 1861885
reads with adapter trimmed: 0
bases trimmed due to adapters: 0

Duplication rate (may be overestimated since this is SE data): 28.2574%

JSON report: SRX7656970.fastp.json
HTML report: SRX7656970.fastp.html

fastp --in1 SRX7656970.fastq.gz --out1 SRX7656970.fastp.fastq.gz --thread 6 --json SRX7656970.fastp.json --html SRX7656970.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: 14 seconds