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: 3069935
total bases: 275283112
Q20 bases: 269057604(97.7385%)
Q30 bases: 260791358(94.7357%)

Read1 after filtering:
total reads: 2023416
total bases: 171920953
Q20 bases: 167949141(97.6897%)
Q30 bases: 162781900(94.6842%)

Filtering result:
reads passed filter: 2023416
reads failed due to low quality: 3536
reads failed due to too many N: 0
reads failed due to too short: 1042983
reads with adapter trimmed: 0
bases trimmed due to adapters: 0

Duplication rate (may be overestimated since this is SE data): 23.6049%

JSON report: SRX7656966.fastp.json
HTML report: SRX7656966.fastp.html

fastp --in1 SRX7656966.fastq.gz --out1 SRX7656966.fastp.fastq.gz --thread 6 --json SRX7656966.fastp.json --html SRX7656966.fastp.html --cut_mean_quality 30 --trim_front1 10 --trim_front2 10 --adapter_fasta /mmfs1/gscratch/scrubbed/strigg/analyses/20250415_RNAseq_2/polyA.fa 
fastp v0.23.4, time used: 13 seconds