Mercurial > repos > bgruening > trim_galore
view test-data/sanger_full_range_report_results1gz.txt @ 16:cc01cbc4e7f7 draft default tip
"planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/trim_galore commit 276a0ec327f5369c16563696047f0d31577c353f"
author | bgruening |
---|---|
date | Fri, 08 Oct 2021 09:57:12 +0000 |
parents | 313e04fe07cd |
children |
line wrap: on
line source
SUMMARISING RUN PARAMETERS ========================== Input filename: input_1.fastq.gz Trimming mode: single-end Trim Galore version: 0.6.7 Cutadapt version: 3.4 Python version: could not detect Number of cores used for trimming: 4 Quality Phred score cutoff: 20 Quality encoding type selected: ASCII+33 Unable to auto-detect most prominent adapter from the first specified file (count Illumina: 0, count Nextera: 0, count smallRNA: 0) Defaulting to Illumina universal adapter ( AGATCGGAAGAGC ). Specify -a SEQUENCE to avoid this behavior). Adapter sequence: 'AGATCGGAAGAGC' (Illumina TruSeq, Sanger iPCR; default (inconclusive auto-detection)) Maximum trimming error rate: 0.1 (default) Minimum required adapter overlap (stringency): 1 bp Minimum required sequence length before a sequence gets removed: 20 bp Output file will be GZIP compressed This is cutadapt 3.4 with Python 3.9.6 Command line parameters: -j 4 -e 0.1 -q 20 -O 1 -a AGATCGGAAGAGC input_1.fastq.gz Processing reads on 4 cores in single-end mode ... Finished in 0.01 s (5217 µs/read; 0.01 M reads/minute). === Summary === Total reads processed: 2 Reads with adapters: 1 (50.0%) Reads written (passing filters): 2 (100.0%) Total basepairs processed: 188 bp Quality-trimmed: 20 bp (10.6%) Total written (filtered): 167 bp (88.8%) === Adapter 1 === Sequence: AGATCGGAAGAGC; Type: regular 3'; Length: 13; Trimmed: 1 times No. of allowed errors: 1-9 bp: 0; 10-13 bp: 1 Bases preceding removed adapters: A: 0.0% C: 100.0% G: 0.0% T: 0.0% none/other: 0.0% Overview of removed sequences length count expect max.err error counts 1 1 0.5 0 1 RUN STATISTICS FOR INPUT FILE: input_1.fastq.gz ============================================= 2 sequences processed in total Sequences removed because they became shorter than the length cutoff of 20 bp: 0 (0.0%)