Mercurial > repos > bgruening > trim_galore
comparison test-data/paired_collection_example_results3.txt @ 4:2c1f0fe810f7 draft
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author | bgruening |
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date | Wed, 15 Apr 2015 11:32:11 -0400 |
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children | 11962ce40855 |
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3:eb546ac2aab2 | 4:2c1f0fe810f7 |
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1 | |
2 SUMMARISING RUN PARAMETERS | |
3 ========================== | |
4 Input filename: ./input_mate1 | |
5 Trimming mode: paired-end | |
6 Trim Galore version: 0.3.7 | |
7 Quality Phred score cutoff: 20 | |
8 Quality encoding type selected: ASCII+33 | |
9 Adapter sequence: 'AGATCGGAAGAGC' | |
10 Maximum trimming error rate: 0.1 (default) | |
11 Minimum required adapter overlap (stringency): 1 bp | |
12 Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp | |
13 | |
14 | |
15 cutadapt version 1.1 | |
16 Command line parameters: -f fastq -e 0.1 -q 20 -O 1 -a AGATCGGAAGAGC ./input_mate1 | |
17 Maximum error rate: 10.00% | |
18 Processed reads: 100 | |
19 Trimmed reads: 20 ( 20.0%) | |
20 Total basepairs: 24894 (0.0 Mbp) | |
21 Trimmed basepairs: 26 (0.0 Mbp) (0.10% of total) | |
22 Too short reads: 0 ( 0.0% of processed reads) | |
23 Too long reads: 0 ( 0.0% of processed reads) | |
24 Total time: 0.00 s | |
25 Time per read: 0.03 ms | |
26 | |
27 === Adapter 1 === | |
28 | |
29 Adapter 'AGATCGGAAGAGC', length 13, was trimmed 20 times. | |
30 | |
31 Lengths of removed sequences | |
32 length count expected | |
33 1 16 25.0 | |
34 2 2 6.2 | |
35 3 2 1.6 | |
36 | |
37 | |
38 RUN STATISTICS FOR INPUT FILE: ./input_mate1 | |
39 ============================================= | |
40 100 sequences processed in total | |
41 | |
42 | |
43 SUMMARISING RUN PARAMETERS | |
44 ========================== | |
45 Input filename: ./input_mate2 | |
46 Trimming mode: paired-end | |
47 Trim Galore version: 0.3.7 | |
48 Quality Phred score cutoff: 20 | |
49 Quality encoding type selected: ASCII+33 | |
50 Adapter sequence: 'AGATCGGAAGAGC' | |
51 Maximum trimming error rate: 0.1 (default) | |
52 Minimum required adapter overlap (stringency): 1 bp | |
53 Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp | |
54 | |
55 | |
56 cutadapt version 1.1 | |
57 Command line parameters: -f fastq -e 0.1 -q 20 -O 1 -a AGATCGGAAGAGC ./input_mate2 | |
58 Maximum error rate: 10.00% | |
59 Processed reads: 100 | |
60 Trimmed reads: 24 ( 24.0%) | |
61 Total basepairs: 24354 (0.0 Mbp) | |
62 Trimmed basepairs: 36 (0.0 Mbp) (0.15% of total) | |
63 Too short reads: 0 ( 0.0% of processed reads) | |
64 Too long reads: 0 ( 0.0% of processed reads) | |
65 Total time: 0.01 s | |
66 Time per read: 0.10 ms | |
67 | |
68 === Adapter 1 === | |
69 | |
70 Adapter 'AGATCGGAAGAGC', length 13, was trimmed 24 times. | |
71 | |
72 Lengths of removed sequences | |
73 length count expected | |
74 1 15 25.0 | |
75 2 7 6.2 | |
76 3 1 1.6 | |
77 4 1 0.4 | |
78 | |
79 | |
80 RUN STATISTICS FOR INPUT FILE: ./input_mate2 | |
81 ============================================= | |
82 100 sequences processed in total | |
83 | |
84 Total number of sequences analysed for the sequence pair length validation: 100 | |
85 | |
86 Number of sequence pairs removed because at least one read was shorter than the length cutoff (20 bp): 1 (1.00%) |