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: 4209903
Q20 bases: 4113317(97.7057%)
Q30 bases: 3982610(94.601%)

Read1 after filtering:
total reads: 23547
total bases: 1972438
Q20 bases: 1923174(97.5024%)
Q30 bases: 1860329(94.3162%)

Filtering result:
reads passed filter: 23547
reads failed due to low quality: 50
reads failed due to too many N: 0
reads failed due to too short: 26403
reads with adapter trimmed: 0
bases trimmed due to adapters: 0

Duplication rate (may be overestimated since this is SE data): 24.432%

JSON report: SRX7656985.fastp.json
HTML report: SRX7656985.fastp.html

fastp --in1 SRX7656985.fastq.gz --out1 SRX7656985.fastp.fastq.gz --thread 6 --json SRX7656985.fastp.json --html SRX7656985.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/3ILL-30_5ILL/polyA.fa 
fastp v0.23.4, time used: 2 seconds