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: 50000
total bases: 4152179
Q20 bases: 4059846(97.7763%)
Q30 bases: 3935225(94.7749%)

Read1 after filtering:
total reads: 23235
total bases: 1941355
Q20 bases: 1892431(97.4799%)
Q30 bases: 1830363(94.2828%)

Filtering result:
reads passed filter: 23235
reads failed due to low quality: 65
reads failed due to too many N: 0
reads failed due to too short: 26700
reads with adapter trimmed: 0
bases trimmed due to adapters: 0

Duplication rate (may be overestimated since this is SE data): 25.156%

JSON report: SRX7656969.fastp.json
HTML report: SRX7656969.fastp.html

fastp --in1 SRX7656969.fastq.gz --out1 SRX7656969.fastp.fastq.gz --thread 6 --json SRX7656969.fastp.json --html SRX7656969.fastp.html --cut_mean_quality 30 --trim_front1 10 --trim_front2 10 --reads_to_process 50000 --adapter_fasta /mmfs1/gscratch/scrubbed/strigg/analyses/20250407_RNAseq/adapter_fasta/polyA.fa 
fastp v0.23.4, time used: 2 seconds