Mercurial > repos > bgruening > trim_galore
diff test-data/paired_example_results2.txt @ 15:084bbd8ba7b8 draft
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/trim_galore commit 10a9de2adae04249830c880cf0c55edaa196f3f7
author | bgruening |
---|---|
date | Tue, 30 Jul 2019 06:26:49 -0400 |
parents | 80cd83b11214 |
children | cd7e644cae1d |
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--- a/test-data/paired_example_results2.txt Thu Jun 01 12:15:10 2017 -0400 +++ b/test-data/paired_example_results2.txt Tue Jul 30 06:26:49 2019 -0400 @@ -3,8 +3,9 @@ ========================== Input filename: input_1.fastq Trimming mode: paired-end -Trim Galore version: 0.4.3 -Cutadapt version: 1.13 +Trim Galore version: 0.6.3 +Cutadapt version: 2.4 +Number of cores used for trimming: 1 Quality Phred score cutoff: 20 Quality encoding type selected: ASCII+33 Adapter sequence: 'CTGTCTCTTATA' (Nextera Transposase sequence; auto-detected) @@ -13,10 +14,10 @@ Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp -This is cutadapt 1.13 with Python 3.5.3 -Command line parameters: -f fastq -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_1.fastq -Trimming 1 adapter with at most 10.0% errors in single-end mode ... -Finished in 0.01 s (101 us/read; 0.59 M reads/minute). +This is cutadapt 2.4 with Python 3.7.3 +Command line parameters: -j 1 -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_1.fastq +Processing reads on 1 core in single-end mode ... +Finished in 0.01 s (75 us/read; 0.80 M reads/minute). === Summary === @@ -73,7 +74,6 @@ 80 1 0.0 1 1 86 1 0.0 1 1 - RUN STATISTICS FOR INPUT FILE: input_1.fastq ============================================= 99 sequences processed in total @@ -83,8 +83,9 @@ ========================== Input filename: input_2.fastq Trimming mode: paired-end -Trim Galore version: 0.4.3 -Cutadapt version: 1.13 +Trim Galore version: 0.6.3 +Cutadapt version: 2.4 +Number of cores used for trimming: 1 Quality Phred score cutoff: 20 Quality encoding type selected: ASCII+33 Adapter sequence: 'CTGTCTCTTATA' (Nextera Transposase sequence; auto-detected) @@ -93,43 +94,43 @@ Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp -This is cutadapt 1.13 with Python 3.5.3 -Command line parameters: -f fastq -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_2.fastq -Trimming 1 adapter with at most 10.0% errors in single-end mode ... -Finished in 0.01 s (100 us/read; 0.60 M reads/minute). +This is cutadapt 2.4 with Python 3.7.3 +Command line parameters: -j 1 -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_2.fastq +Processing reads on 1 core in single-end mode ... +Finished in 0.00 s (50 us/read; 1.19 M reads/minute). === Summary === -Total reads processed: 100 -Reads with adapters: 59 (59.0%) -Reads written (passing filters): 100 (100.0%) +Total reads processed: 99 +Reads with adapters: 58 (58.6%) +Reads written (passing filters): 99 (100.0%) -Total basepairs processed: 25,100 bp -Quality-trimmed: 746 bp (3.0%) -Total written (filtered): 23,276 bp (92.7%) +Total basepairs processed: 24,849 bp +Quality-trimmed: 745 bp (3.0%) +Total written (filtered): 23,035 bp (92.7%) === Adapter 1 === -Sequence: CTGTCTCTTATA; Type: regular 3'; Length: 12; Trimmed: 59 times. +Sequence: CTGTCTCTTATA; Type: regular 3'; Length: 12; Trimmed: 58 times. No. of allowed errors: 0-9 bp: 0; 10-12 bp: 1 Bases preceding removed adapters: - A: 11.9% - C: 39.0% - G: 8.5% - T: 40.7% + A: 12.1% + C: 37.9% + G: 8.6% + T: 41.4% none/other: 0.0% Overview of removed sequences length count expect max.err error counts -1 16 25.0 0 16 +1 16 24.8 0 16 2 7 6.2 0 7 -3 1 1.6 0 1 +3 1 1.5 0 1 4 2 0.4 0 2 6 2 0.0 0 2 -9 2 0.0 0 2 +9 1 0.0 0 1 10 1 0.0 1 1 13 1 0.0 1 1 14 2 0.0 1 2 @@ -156,10 +157,9 @@ 67 1 0.0 1 1 80 1 0.0 1 1 - RUN STATISTICS FOR INPUT FILE: input_2.fastq ============================================= -100 sequences processed in total +99 sequences processed in total Total number of sequences analysed for the sequence pair length validation: 99