Mercurial > repos > bgruening > trim_galore
comparison test-data/paired_example_results2.txt @ 18:b94789823aad draft default tip
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/trim_galore commit f8ccc97b827b98db1bcf42073d3c5eb4e3f134c4
author | bgruening |
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date | Sat, 10 May 2025 08:09:10 +0000 |
parents | cd7e644cae1d |
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17:eefb644655a5 | 18:b94789823aad |
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1 | 1 |
2 SUMMARISING RUN PARAMETERS | 2 SUMMARISING RUN PARAMETERS |
3 ========================== | 3 ========================== |
4 Input filename: input_1.fastq | 4 Input filename: input_1.fastq |
5 Trimming mode: paired-end | 5 Trimming mode: paired-end |
6 Trim Galore version: 0.6.7 | 6 Trim Galore version: 0.6.10 |
7 Cutadapt version: 3.4 | 7 Cutadapt version: 5.0 |
8 Python version: could not detect | 8 Python version: 3.12.10 |
9 Number of cores used for trimming: 4 | 9 Number of cores used for trimming: 4 |
10 Quality Phred score cutoff: 20 | 10 Quality Phred score cutoff: 20 |
11 Quality encoding type selected: ASCII+33 | 11 Quality encoding type selected: ASCII+33 |
12 Using Nextera adapter for trimming (count: 29). Second best hit was smallRNA (count: 0) | 12 Using Nextera adapter for trimming (count: 29). Second best hit was smallRNA (count: 0) |
13 Adapter sequence: 'CTGTCTCTTATA' (Nextera Transposase sequence; auto-detected) | 13 Adapter sequence: 'CTGTCTCTTATA' (Nextera Transposase sequence; auto-detected) |
14 Maximum trimming error rate: 0.1 (default) | 14 Maximum trimming error rate: 0.1 (default) |
15 Minimum required adapter overlap (stringency): 1 bp | 15 Minimum required adapter overlap (stringency): 1 bp |
16 Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp | 16 Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp |
17 | 17 |
18 | 18 |
19 This is cutadapt 3.4 with Python 3.9.6 | 19 This is cutadapt 5.0 with Python 3.12.10 |
20 Command line parameters: -j 4 -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_1.fastq | 20 Command line parameters: -j 4 -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_1.fastq |
21 Processing reads on 4 cores in single-end mode ... | 21 Processing single-end reads on 4 cores ... |
22 Finished in 0.01 s (117 µs/read; 0.51 M reads/minute). | |
23 | 22 |
24 === Summary === | 23 === Summary === |
25 | 24 |
26 Total reads processed: 99 | 25 Total reads processed: 99 |
27 Reads with adapters: 52 (52.5%) | 26 Reads with adapters: 52 (52.5%) |
33 | 32 |
34 === Adapter 1 === | 33 === Adapter 1 === |
35 | 34 |
36 Sequence: CTGTCTCTTATA; Type: regular 3'; Length: 12; Trimmed: 52 times | 35 Sequence: CTGTCTCTTATA; Type: regular 3'; Length: 12; Trimmed: 52 times |
37 | 36 |
37 Minimum overlap: 1 | |
38 No. of allowed errors: | 38 No. of allowed errors: |
39 1-9 bp: 0; 10-12 bp: 1 | 39 1-9 bp: 0; 10-12 bp: 1 |
40 | 40 |
41 Bases preceding removed adapters: | 41 Bases preceding removed adapters: |
42 A: 9.6% | 42 A: 9.6% |
83 | 83 |
84 SUMMARISING RUN PARAMETERS | 84 SUMMARISING RUN PARAMETERS |
85 ========================== | 85 ========================== |
86 Input filename: input_2.fastq | 86 Input filename: input_2.fastq |
87 Trimming mode: paired-end | 87 Trimming mode: paired-end |
88 Trim Galore version: 0.6.7 | 88 Trim Galore version: 0.6.10 |
89 Cutadapt version: 3.4 | 89 Cutadapt version: 5.0 |
90 Python version: could not detect | 90 Python version: 3.12.10 |
91 Number of cores used for trimming: 4 | 91 Number of cores used for trimming: 4 |
92 Quality Phred score cutoff: 20 | 92 Quality Phred score cutoff: 20 |
93 Quality encoding type selected: ASCII+33 | 93 Quality encoding type selected: ASCII+33 |
94 Using Nextera adapter for trimming (count: 29). Second best hit was smallRNA (count: 0) | 94 Using Nextera adapter for trimming (count: 29). Second best hit was smallRNA (count: 0) |
95 Adapter sequence: 'CTGTCTCTTATA' (Nextera Transposase sequence; auto-detected) | 95 Adapter sequence: 'CTGTCTCTTATA' (Nextera Transposase sequence; auto-detected) |
96 Maximum trimming error rate: 0.1 (default) | 96 Maximum trimming error rate: 0.1 (default) |
97 Minimum required adapter overlap (stringency): 1 bp | 97 Minimum required adapter overlap (stringency): 1 bp |
98 Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp | 98 Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp |
99 | 99 |
100 | 100 |
101 This is cutadapt 3.4 with Python 3.9.6 | 101 This is cutadapt 5.0 with Python 3.12.10 |
102 Command line parameters: -j 4 -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_2.fastq | 102 Command line parameters: -j 4 -e 0.1 -q 20 -O 1 -a CTGTCTCTTATA input_2.fastq |
103 Processing reads on 4 cores in single-end mode ... | 103 Processing single-end reads on 4 cores ... |
104 Finished in 0.03 s (256 µs/read; 0.23 M reads/minute). | |
105 | 104 |
106 === Summary === | 105 === Summary === |
107 | 106 |
108 Total reads processed: 99 | 107 Total reads processed: 99 |
109 Reads with adapters: 58 (58.6%) | 108 Reads with adapters: 58 (58.6%) |
115 | 114 |
116 === Adapter 1 === | 115 === Adapter 1 === |
117 | 116 |
118 Sequence: CTGTCTCTTATA; Type: regular 3'; Length: 12; Trimmed: 58 times | 117 Sequence: CTGTCTCTTATA; Type: regular 3'; Length: 12; Trimmed: 58 times |
119 | 118 |
119 Minimum overlap: 1 | |
120 No. of allowed errors: | 120 No. of allowed errors: |
121 1-9 bp: 0; 10-12 bp: 1 | 121 1-9 bp: 0; 10-12 bp: 1 |
122 | 122 |
123 Bases preceding removed adapters: | 123 Bases preceding removed adapters: |
124 A: 12.1% | 124 A: 12.1% |