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: 4033781
total bases: 362706301
Q20 bases: 354716937(97.7973%)
Q30 bases: 344003838(94.8436%)

Read1 after filtering:
total reads: 2641321
total bases: 224143903
Q20 bases: 219059038(97.7314%)
Q30 bases: 212455265(94.7852%)

Filtering result:
reads passed filter: 2641321
reads failed due to low quality: 5252
reads failed due to too many N: 0
reads failed due to too short: 1387208
reads with adapter trimmed: 0
bases trimmed due to adapters: 0

Duplication rate (may be overestimated since this is SE data): 25.7435%

JSON report: SRX7656987.fastp.json
HTML report: SRX7656987.fastp.html

fastp --in1 SRX7656987.fastq.gz --out1 SRX7656987.fastp.fastq.gz --thread 6 --json SRX7656987.fastp.json --html SRX7656987.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: 11 seconds