diff test-data/sanger_full_range_report_results1.txt @ 15:084bbd8ba7b8 draft

planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/trim_galore commit 10a9de2adae04249830c880cf0c55edaa196f3f7

--- a/test-data/sanger_full_range_report_results1.txt	Thu Jun 01 12:15:10 2017 -0400
+++ b/test-data/sanger_full_range_report_results1.txt	Tue Jul 30 06:26:49 2019 -0400
@@ -3,8 +3,9 @@
 ==========================
 Input filename: input_1.fastq
 Trimming mode: single-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: 'AGATCGGAAGAGC' (Illumina TruSeq, Sanger iPCR; default (inconclusive auto-detection))
@@ -13,10 +14,10 @@
 Minimum required sequence length before a sequence 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 AGATCGGAAGAGC input_1.fastq
-Trimming 1 adapter with at most 10.0% errors in single-end mode ...
-Finished in 0.01 s (5000 us/read; 0.01 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 AGATCGGAAGAGC input_1.fastq
+Processing reads on 1 core in single-end mode ...
+Finished in 0.00 s (1608 us/read; 0.04 M reads/minute).
 
 === Summary ===
 
@@ -46,7 +47,6 @@
 length	count	expect	max.err	error counts
 1	1	0.5	0	1
 
-
 RUN STATISTICS FOR INPUT FILE: input_1.fastq
 =============================================
 2 sequences processed in total