Mercurial > repos > iuc > seq2hla
comparison seq2hla.xml @ 0:52bba1cd3823 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/seq2hla commit 96f219ed86ce674def72c73393d3c29c87cb56e5"
author | iuc |
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date | Thu, 20 Feb 2020 18:27:07 -0500 |
parents | |
children | 5a7cd6c39085 |
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1 <tool id="seq2hla" name="seq2HLA" version="2.2.0"> | |
2 <description>HLA genotype and expression from RNA-seq</description> | |
3 <requirements> | |
4 <!-- needed because of some non POSIX compliant wc usage --> | |
5 <requirement type="package" version="8.31">coreutils</requirement> | |
6 <requirement type="package" version="2.2">seq2hla</requirement> | |
7 </requirements> | |
8 <command detect_errors="exit_code"><![CDATA[ | |
9 seq2HLA --runName='$run_name' -1 '$fastq_input1' -2 '$fastq_input2' | |
10 #if str($trim) != '': | |
11 --trim3=$trim | |
12 #end if | |
13 -p \${GALAXY_SLOTS:-1} >> '$seq2hla_log' | |
14 && cp -p '${run_name}-ClassI.HLAgenotype2digits' '${c1_genotype2digits}' | |
15 && cp -p '${run_name}-ClassI.HLAgenotype4digits' '${c1_genotype4digits}' | |
16 && echo '#Locus_RPKM' | cat - '${run_name}-ClassI.expression' | sed 's/^\(.*\): \([0-9.]*\).*$/\1_\2/' | tr '_' '\t' > '${c1_expression}' | |
17 && cp -p '${run_name}-ClassII.HLAgenotype4digits' '${c2_genotype4digits}' | |
18 && echo '#Locus_RPKM' | cat - '${run_name}-ClassII.expression' | sed 's/^\(.*\): \([0-9.]*\).*$/\1_\2/' | tr '_' '\t' > '${c2_expression}' | |
19 && cp -p '${run_name}.ambiguity' '${ambiguity}' | |
20 ]]></command> | |
21 <inputs> | |
22 <param name="run_name" type="text" value="sample1" label="Name prefix for this analysis"> | |
23 <validator type="regex" message="Use letters,digits,_.-">^[A-Za-z0-9_\-+.]+$</validator> | |
24 </param> | |
25 <param name="fastq_input1" type="data" format="fastqsanger" label="Select first set of reads" help="Specify dataset with forward reads"/> | |
26 <param name="fastq_input2" type="data" format="fastqsanger" label="Select second set of reads" help="Specify dataset with reverse reads"/> | |
27 <param name="trim" type="integer" value="" min="0" optional="true" label="Trim bases from 3 prime" | |
28 help="trim this many bases from the low-quality end of each read" /> | |
29 </inputs> | |
30 <outputs> | |
31 <data format="txt" name="seq2hla_log" label="${tool.name} on ${on_string}: ${run_name} logfile"/> | |
32 <data format="tabular" name="c1_genotype2digits" label="${tool.name} on ${on_string}: ${run_name}-ClassI.HLAgenotype2digits"/> | |
33 <data format="tabular" name="c1_genotype4digits" label="${tool.name} on ${on_string}: ${run_name}-ClassI.HLAgenotype4digits"/> | |
34 <data format="tabular" name="c2_genotype4digits" label="${tool.name} on ${on_string}: ${run_name}-ClassII.HLAgenotype4digits"/> | |
35 <data format="tabular" name="c1_expression" label="${tool.name} on ${on_string}: ${run_name}-ClassI.expression"/> | |
36 <data format="tabular" name="c2_expression" label="${tool.name} on ${on_string}: ${run_name}-ClassII.expression"/> | |
37 <data format="tabular" name="c2_expression" label="${tool.name} on ${on_string}: ${run_name}-ClassII.expression"/> | |
38 <data format="txt" name="ambiguity" label="${tool.name} on ${on_string}: ${run_name}.ambiguity"/> | |
39 </outputs> | |
40 <tests> | |
41 <test> | |
42 <param name="run_name" value="test"/> | |
43 <param name="fastq_input1" ftype="fastqsanger" value="reads1.fastq"/> | |
44 <param name="fastq_input2" ftype="fastqsanger" value="reads2.fastq"/> | |
45 <output name="c1_genotype4digits"> | |
46 <assert_contents> | |
47 <has_text text="A*24:02" /> | |
48 </assert_contents> | |
49 </output> | |
50 </test> | |
51 </tests> | |
52 <help><![CDATA[ | |
53 | |
54 **seq2HLA** *HLA typing from RNA-Seq sequence reads* | |
55 | |
56 Release: 2.2 | |
57 | |
58 seq2HLA_ is an in-silico method, written in python and R, which takes standard RNA-Seq sequence reads in fastq format | |
59 as input, uses a bowtie index comprising all HLA alleles and outputs the most likely HLA class I and class II genotypes (in 4 digit resolution), | |
60 a p-value for each call, and the expression of each class | |
61 | |
62 **Inputs** | |
63 | |
64 Paired read fastq files with illumina style IDs. | |
65 | |
66 | |
67 **Outputs** | |
68 | |
69 1. <prefix>-ClassI.HLAgenotype2digits => 2 digit result of Class I | |
70 2. <prefix>-ClassII.HLAgenotype2digits => 2 digit result of Class II | |
71 3. <prefix>-ClassI.HLAgenotype4digits => 4 digit result of Class I | |
72 4. <prefix>-ClassII.HLAgenotype4digits => 4 digit result of Class II | |
73 5. <prefix>.ambiguity => reports typing ambuigities (more than one solution for an allele possible) | |
74 6. <prefix>-ClassI.expression => expression of Class I alleles | |
75 7. <prefix>-ClassII.expression => expression of Class II alleles | |
76 | |
77 | |
78 ClassI.HLAgenotype4digits | |
79 | |
80 ======= ======== =========== ======== ============ | |
81 #Locus Allele 1 Confidence Allele 2 Confidence | |
82 ======= ======== =========== ======== ============ | |
83 A A*03:01 0.000510333 A*02:01' 0.0005975604 | |
84 B B*50:01 0.001271273 B*58:02 3.52561e-05 | |
85 C C*04:01 0.06362723 C*06:02 0.04725865 | |
86 ======= ======== =========== ======== ============ | |
87 | |
88 | |
89 ClassI.expression | |
90 | |
91 ======= ====== | |
92 #Locus RPKM | |
93 ======= ====== | |
94 A 89.59 | |
95 B 139.66 | |
96 C 184.42 | |
97 ======= ====== | |
98 | |
99 | |
100 .. _seq2HLA: https://bitbucket.org/sebastian_boegel/seq2hla | |
101 | |
102 ]]></help> | |
103 <citations> | |
104 <citation type="doi">10.1186/gm403</citation> | |
105 </citations> | |
106 </tool> |