Mercurial > repos > iuc > beacon2_cnv
comparison cnv.xml @ 1:997f15134095 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/beacon2-import commit 23f6d9e5e91c43d5ab68e604205e06785635f42f
author | iuc |
---|---|
date | Mon, 19 Aug 2024 10:50:07 +0000 |
parents | 25424cc216f9 |
children | 398000f8de7d |
comparison
equal
deleted
inserted
replaced
0:25424cc216f9 | 1:997f15134095 |
---|---|
29 --end $advanced_settings.end | 29 --end $advanced_settings.end |
30 #end if | 30 #end if |
31 #if str($advanced_settings.chromosome) | 31 #if str($advanced_settings.chromosome) |
32 --chromosome '$advanced_settings.chromosome' | 32 --chromosome '$advanced_settings.chromosome' |
33 #end if | 33 #end if |
34 #if str($advanced_settings.variantStateId) | 34 #if str($advanced_settings.variantStateId) and $advanced_settings.variantStateId != "" |
35 --variantStateId '$advanced_settings.variantStateId' | 35 --variantStateId '$advanced_settings.variantStateId' |
36 #end if | |
37 #if str($advanced_settings.variantState) | |
38 --variantState '$advanced_settings.variantState' | |
39 #end if | 36 #end if |
40 #if str($advanced_settings.sequenceId) | 37 #if str($advanced_settings.sequenceId) |
41 --sequenceId '$advanced_settings.sequenceId' | 38 --sequenceId '$advanced_settings.sequenceId' |
39 #end if | |
40 #if str($advanced_settings.variantType) | |
41 --variantType '$advanced_settings.variantType' | |
42 #end if | |
43 #if str($advanced_settings.primarySite) | |
44 --primarySite '$advanced_settings.primarySite' | |
45 #end if | |
46 #if str($advanced_settings.diseaseType) | |
47 --diseaseType '$advanced_settings.diseaseType' | |
48 #end if | |
49 #if str($advanced_settings.gene) | |
50 --gene '$advanced_settings.gene' | |
42 #end if | 51 #end if |
43 > cnv_query_findings.json | 52 > cnv_query_findings.json |
44 ]]></command> | 53 ]]></command> |
45 <expand macro="configfile"/> | 54 <expand macro="configfile"/> |
46 <inputs> | 55 <inputs> |
51 <param argument="--analysisId" optional="true" type="text" label="ANALYSIS ID" value="" help="" /> | 60 <param argument="--analysisId" optional="true" type="text" label="ANALYSIS ID" value="" help="" /> |
52 <param argument="--individualId" optional="true" type="text" label="INDIVIDUAL ID" value="" help="" /> | 61 <param argument="--individualId" optional="true" type="text" label="INDIVIDUAL ID" value="" help="" /> |
53 <param argument="--start" optional="true" type="integer" label="START" value="" help="Start position" /> | 62 <param argument="--start" optional="true" type="integer" label="START" value="" help="Start position" /> |
54 <param argument="--end" optional="true" type="integer" label="END" value="" help="End position" /> | 63 <param argument="--end" optional="true" type="integer" label="END" value="" help="End position" /> |
55 <param argument="--chromosome" optional="true" type="text" label="CHROMOSOME" value="" help="Chromosome numbers (without chr)" /> | 64 <param argument="--chromosome" optional="true" type="text" label="CHROMOSOME" value="" help="Chromosome numbers (without chr)" /> |
56 <param argument="--variantStateId" optional="true" type="text" label="VARIANT STATE ID" value="" help="E.g EFO:0030067" /> | 65 <param argument="variantStateId" optional="true" type="select" label="GENDERS" help=""> |
57 <param argument="--variantState" optional="true" type="text" label="VARIANT STATE" value="" help="E.g. copy number loss" /> | 66 <option value="EFO:0030070">EFO:0030070: copy number gain</option> |
67 <option value="EFO:0030071">EFO:0030071: low-level copy number gain</option> | |
68 <option value="EFO:0030072">EFO:0030072: high-level copy number gain</option> | |
69 <option value="EFO:0030073">EFO:0030073: focal genome amplification</option> | |
70 <option value="EFO:0030067">EFO:0030067: copy number loss</option> | |
71 <option value="EFO:0030068">EFO:0030068: low-level copy number loss</option> | |
72 <option value="EFO:0020073">EFO:0020073: high-level copy number loss</option> | |
73 <option value="EFO:0030069">EFO:0030069: complete genomic deletion</option> | |
74 <option value="" selected="True">non specific</option> | |
75 </param> | |
58 <param argument="--sequenceId" optional="true" type="text" label="SEQUENCE ID" value="" help="E.g. refseq:NC_000011.10" /> | 76 <param argument="--sequenceId" optional="true" type="text" label="SEQUENCE ID" value="" help="E.g. refseq:NC_000011.10" /> |
77 <param argument="--gene" optional="true" type="text" label="GENE NAME" value="" help="Gene name e.g. 'AL645728.1'" /> | |
78 <param argument="--variantType" optional="true" type="text" label="VARIANT TYPE" value="" help="Variant Type 'DEL' or 'DUP'" /> | |
79 <param argument="--primarySite" optional="true" type="text" label="PRIMARY SITE" value="" help="Primary Site, e.g. 'brain'" /> | |
80 <param argument="--diseaseType" optional="true" type="text" label="DISEASE TYPE" value="" help="Disease Type, e.g. 'adnexal and skin appendage neoplasms'" /> | |
59 </section> | 81 </section> |
60 </inputs> | 82 </inputs> |
61 <outputs> | 83 <outputs> |
62 <data name="out_cnv_query" format="json" label="${tool.name} on ${on_string}: CNV Query" from_work_dir="cnv_query_findings.json" /> | 84 <data name="out_cnv_query" format="json" label="${tool.name} on ${on_string}: CNV Query" from_work_dir="cnv_query_findings.json" /> |
63 </outputs> | 85 </outputs> |
64 <tests> | 86 <tests> |
65 <test expect_num_outputs="1"> | 87 <test expect_num_outputs="1"> |
66 <param name="database" value="beacon" /> | 88 <param name="database" value="beacon" /> |
67 <param name="collection" value="cnv" /> | 89 <param name="collection" value="test" /> |
68 <param name="db_host" value="20.108.51.167" /> | 90 <param name="db_host" value="20.108.51.167" /> |
69 <param name="chromosome" value="1" /> | 91 <param name="chromosome" value="17" /> |
70 <param name="start" value="243618689" /> | 92 <param name="start" value="43044295" /> |
71 <param name="end" value="243620819" /> | 93 <param name="end" value="43170245" /> |
94 <param name="primarySite" value="breast" /> | |
95 <param name="diseaseType" value="adnexal and skin appendage neoplasms" /> | |
96 <param name="gene" value="BRCA1" /> | |
72 <param name="variantStateId" value="EFO:0030068" /> | 97 <param name="variantStateId" value="EFO:0030068" /> |
73 <output name="out_cnv_query"> | 98 <output name="out_cnv_query"> |
74 <assert_contents><has_text_matching expression="_id"/></assert_contents> | 99 <assert_contents><has_text_matching expression="_id"/></assert_contents> |
75 </output> | 100 </output> |
76 </test> | 101 </test> |