Mercurial > repos > iuc > fargene
view test-data/paired/retrievedFragments/trimmedReads/reads__1_retrieved.fastq_trimming_report.txt @ 0:6f743c615c41 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/fargene commit 867e4a6fad4c2622ad69517e2d4d9ba185109b72"
author | iuc |
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date | Thu, 28 Nov 2019 14:39:41 -0500 |
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SUMMARISING RUN PARAMETERS ========================== Input filename: /home/ubuntu/data/fargene/tutorial/tutorialdata/tutorial_output_1/retrievedFragments/reads__1_retrieved.fastq Trimming mode: paired-end Trim Galore version: 0.6.3 Cutadapt version: 1.18 Number of cores used for trimming: 1 Quality Phred score cutoff: 30 Quality encoding type selected: ASCII+33 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 for both reads before a sequence pair gets removed: 20 bp This is cutadapt 1.18 with Python 2.7.15 Command line parameters: -j 1 -e 0.1 -q 30 -O 1 -a AGATCGGAAGAGC /home/ubuntu/data/fargene/tutorial/tutorialdata/tutorial_output_1/retrievedFragments/reads__1_retrieved.fastq Processing reads on 1 core in single-end mode ... Finished in 0.01 s (27 us/read; 2.19 M reads/minute). === Summary === Total reads processed: 393 Reads with adapters: 102 (26.0%) Reads written (passing filters): 393 (100.0%) Total basepairs processed: 39,300 bp Quality-trimmed: 156 bp (0.4%) Total written (filtered): 39,001 bp (99.2%) === Adapter 1 === Sequence: AGATCGGAAGAGC; Type: regular 3'; Length: 13; Trimmed: 102 times. No. of allowed errors: 0-9 bp: 0; 10-13 bp: 1 Bases preceding removed adapters: A: 24.5% C: 35.3% G: 31.4% T: 8.8% none/other: 0.0% Overview of removed sequences length count expect max.err error counts 1 72 98.2 0 72 2 24 24.6 0 24 3 3 6.1 0 3 4 2 1.5 0 2 6 1 0.1 0 1 RUN STATISTICS FOR INPUT FILE: /home/ubuntu/data/fargene/tutorial/tutorialdata/tutorial_output_1/retrievedFragments/reads__1_retrieved.fastq ============================================= 393 sequences processed in total