Mercurial > repos > petr-novak > various_galaxy_tools
comparison gff2bed.xml @ 0:696e702ebf74 draft
"planemo upload commit 0f6eca49bafc3c946189d793161a7f81d595e1a1-dirty"
author | petr-novak |
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date | Mon, 09 May 2022 08:26:30 +0000 |
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children | 639c0edb7e64 |
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1 <tool id="gff2bed1" name="GFF-to-BED" version="1.0.1"> | |
2 <description>converter</description> | |
3 <edam_operations> | |
4 <edam_operation>operation_3434</edam_operation> | |
5 </edam_operations> | |
6 <command interpreter="python">gff_to_bed_converter.py $input $out_file1</command> | |
7 <inputs> | |
8 <param format="gff" name="input" type="data" label="Convert this dataset"/> | |
9 </inputs> | |
10 <outputs> | |
11 <data format="bed" name="out_file1" /> | |
12 </outputs> | |
13 <tests> | |
14 <test> | |
15 <param name="input" value="5.gff" ftype="gff"/> | |
16 <output name="out_file1" file="gff2bed_out.bed"/> | |
17 </test> | |
18 <test> | |
19 <param name="input" value="gff2bed_in2.gff" ftype="gff"/> | |
20 <output name="out_file1" file="gff2bed_out2.bed"/> | |
21 </test> | |
22 <test> | |
23 <!-- Test conversion of gff3 file. --> | |
24 <param name="input" value="5.gff3" ftype="gff"/> | |
25 <output name="out_file1" file="gff2bed_out3.bed"/> | |
26 </test> | |
27 </tests> | |
28 <help> | |
29 | |
30 **What it does** | |
31 | |
32 This tool converts data from GFF format to BED format (scroll down for format description). | |
33 | |
34 -------- | |
35 | |
36 **Example** | |
37 | |
38 The following data in GFF format:: | |
39 | |
40 chr22 GeneA enhancer 10000000 10001000 500 + . TGA | |
41 chr22 GeneA promoter 10010000 10010100 900 + . TGA | |
42 | |
43 Will be converted to BED (**note** that 1 is subtracted from the start coordinate):: | |
44 | |
45 chr22 9999999 10001000 enhancer 0 + | |
46 chr22 10009999 10010100 promoter 0 + | |
47 | |
48 ------ | |
49 | |
50 .. class:: infomark | |
51 | |
52 **About formats** | |
53 | |
54 **BED format** Browser Extensible Data format was designed at UCSC for displaying data tracks in the Genome Browser. It has three required fields and several additional optional ones: | |
55 | |
56 The first three BED fields (required) are:: | |
57 | |
58 1. chrom - The name of the chromosome (e.g. chr1, chrY_random). | |
59 2. chromStart - The starting position in the chromosome. (The first base in a chromosome is numbered 0.) | |
60 3. chromEnd - The ending position in the chromosome, plus 1 (i.e., a half-open interval). | |
61 | |
62 The additional BED fields (optional) are:: | |
63 | |
64 4. name - The name of the BED line. | |
65 5. score - A score between 0 and 1000. | |
66 6. strand - Defines the strand - either '+' or '-'. | |
67 7. thickStart - The starting position where the feature is drawn thickly at the Genome Browser. | |
68 8. thickEnd - The ending position where the feature is drawn thickly at the Genome Browser. | |
69 9. reserved - This should always be set to zero. | |
70 10. blockCount - The number of blocks (exons) in the BED line. | |
71 11. blockSizes - A comma-separated list of the block sizes. The number of items in this list should correspond to blockCount. | |
72 12. blockStarts - A comma-separated list of block starts. All of the blockStart positions should be calculated relative to chromStart. The number of items in this list should correspond to blockCount. | |
73 13. expCount - The number of experiments. | |
74 14. expIds - A comma-separated list of experiment ids. The number of items in this list should correspond to expCount. | |
75 15. expScores - A comma-separated list of experiment scores. All of the expScores should be relative to expIds. The number of items in this list should correspond to expCount. | |
76 | |
77 **GFF format** General Feature Format is a format for describing genes and other features associated with DNA, RNA and Protein sequences. GFF lines have nine tab-separated fields:: | |
78 | |
79 1. seqname - Must be a chromosome or scaffold. | |
80 2. source - The program that generated this feature. | |
81 3. feature - The name of this type of feature. Some examples of standard feature types are "CDS", "start_codon", "stop_codon", and "exon". | |
82 4. start - The starting position of the feature in the sequence. The first base is numbered 1. | |
83 5. end - The ending position of the feature (inclusive). | |
84 6. score - A score between 0 and 1000. If there is no score value, enter ".". | |
85 7. strand - Valid entries include '+', '-', or '.' (for don't know/care). | |
86 8. frame - If the feature is a coding exon, frame should be a number between 0-2 that represents the reading frame of the first base. If the feature is not a coding exon, the value should be '.'. | |
87 9. group - All lines with the same group are linked together into a single item. | |
88 | |
89 </help> | |
90 </tool> |