Mercurial > repos > fwuennemann > kb_python
comparison genap2_kb_python/kb_count.xml @ 0:e8d93f1429c2 draft
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author | fwuennemann |
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date | Fri, 16 Apr 2021 18:18:21 +0000 |
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children | dbcb26e2a1db |
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-1:000000000000 | 0:e8d93f1429c2 |
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1 <tool id="kb_python" name="kb_python" version="@VERSION@+galaxy0"> | |
2 <description>performs gene and feature quantification on single-cell sequencing data.</description> | |
3 <macros> | |
4 <import>macros.xml</import> | |
5 </macros> | |
6 <requirements> | |
7 <requirement type="package" version="0.25.1">kb-python</requirement> | |
8 </requirements> | |
9 <stdio> | |
10 <exit_code range="1:" /> | |
11 <exit_code range=":-1" /> | |
12 <regex match="Error:" /> | |
13 <regex match="Exception:" /> | |
14 <regex match="Exception :" /> | |
15 </stdio> | |
16 <command detect_errors="exit_code"><![CDATA[ | |
17 mkdir ./index | |
18 && mkdir ./kb_outs | |
19 #if $refTranscriptSource.TranscriptSource == "history": | |
20 && ln -s '${refTranscriptSource.h_index.index_file}' './index/kb_ref.idx' | |
21 && ln -s '${refTranscriptSource.h_index.t2g_file}' './index/t2g.txt' | |
22 #if $workflow == "lamanno" or $workflow == "nucleus": | |
23 && ln -s '${refTranscriptSource.h_index.history_lamanno.cdna_t2c}' './index/cdna_t2c.txt' | |
24 && ln -s '${refTranscriptSource.h_index.history_lamanno.intron_t2c}' './index/intron_t2c.txt' | |
25 #end if | |
26 #set $index_path = './index' | |
27 #else if $refTranscriptSource.TranscriptSource == "built": | |
28 && kb ref -i ./index/kb_ref.idx | |
29 -g ./index/t2g.txt | |
30 -f1 ./index/cdna.fa | |
31 --workflow $workflow | |
32 #if $workflow == "lamanno" or $workflow == "nucleus": | |
33 -f2 ./index/intron.fa | |
34 -c1 ./index/cdna_t2c.txt | |
35 -c2 ./index/intron_t2c.txt | |
36 --workflow $workflow | |
37 #end if | |
38 #if $workflow != "kite": | |
39 '${refTranscriptSource.s_index.genomic_fasta}' | |
40 '${refTranscriptSource.s_index.genomic_gtf}' | |
41 #else: | |
42 '${refTranscriptSource.s_index.kite_table}' | |
43 #end if | |
44 #set $index_path = './index' | |
45 #end if | |
46 && kb count | |
47 -t \${GALAXY_SLOTS:-1} | |
48 -i $index_path/kb_ref.idx | |
49 -g $index_path/t2g.txt | |
50 #if $workflow == "lamanno" or $workflow == "nucleus": | |
51 -c1 $index_path/cdna_t2c.txt | |
52 -c2 $index_path/intron_t2c.txt | |
53 #end if | |
54 -x $technology | |
55 #if $whitelist: | |
56 --whitelist '${optional.whitelist}' | |
57 #end if | |
58 #if $optional.multimap: | |
59 --mm | |
60 #end if | |
61 --workflow $workflow | |
62 #if $extra_dtype != "none": | |
63 $extra_dtype | |
64 #end if | |
65 -o ./kb_outs | |
66 --cellranger | |
67 $FASTQ1 | |
68 $FASTQ2 | |
69 ]]> | |
70 </command> | |
71 <inputs> | |
72 <param name="workflow" label="Select the workflow you want to use:" type="select" multiple="false" format="text" help="Type of workflow. Use `lamanno` for RNA velocity based on La Manno et al. 2018 logic. | |
73 Use `nucleus` for RNA velocity on single-nucleus RNA-seq reads. Use `kite` for feature barcoding. Use `kite:10xFB` for 10x Genomics Feature Barcoding technology."> | |
74 <option value="standard">standard</option> | |
75 <option value="lamanno">lamanno</option> | |
76 <option value="nucleus">nucleus</option> | |
77 <option value="kite">kite</option> | |
78 </param> | |
79 <expand macro="index"/> | |
80 <param name="technology" label="Select the scRNA-seq technology:" type="select" multiple="false" format="text" help="Choose the scRNA-seq technology used to generate the fastq data."> | |
81 <option value="10XV1">10XV1</option> | |
82 <option value="10XV2">10XV2</option> | |
83 <option value="10XV3">10XV3</option> | |
84 <option value="CELSEQ">CELSEQ</option> | |
85 <option value="CELSEQ2">CELSEQ2</option> | |
86 <option value="DROPSEQ">DROPSEQ</option> | |
87 <option value="INDROPSV1">INDROPSV1</option> | |
88 <option value="INDROPSV2">INDROPSV2</option> | |
89 <option value="INDROPSV3">INDROPSV3</option> | |
90 <option value="SCRUBSEQ">SCRUBSEQ</option> | |
91 <option value="SURECELL">SURECELL</option> | |
92 </param> | |
93 <param name="FASTQ1" label="Select the R1 fastq file:" type="data" format="fastqsanger.gz" multiple="false"/> | |
94 <param name="FASTQ2" label="Select the R2 fastq file:" type="data" format="fastqsanger.gz" multiple="false"/> | |
95 <param name="extra_dtype" type="select" label="Do you want any additional output data type beside CellRanger?"> | |
96 <option value="none" selected = "true">No</option> | |
97 <option value="--loom">Loom</option> | |
98 <option value="--h5ad">H5ad</option> | |
99 </param> | |
100 <section name="optional" title="Optional commands" expanded="false"> | |
101 <param name="whitelist" type="data" format="tsv,tabular" optional="true" label="Whitelist file" help="Whitelisted barcodes to correct to. If not provided and bustools supports the technology, a pre-packaged whitelist is used. If not, the bustools | |
102 whitelist command is used."/> | |
103 <param name="multimap" type="boolean" optional="true" label="Include multi pseudoaligned reads?" help="Do you want to include reads that pseudoalign to multiple genes?"/> | |
104 </section> | |
105 </inputs> | |
106 <outputs> | |
107 <data name="barcodes" label="cellranger barcodes" format="txt" from_work_dir="kb_outs/counts_unfiltered/cellranger/barcodes.tsv"/> | |
108 <data name="genes" label="cellranger genes" format="txt" from_work_dir="kb_outs/counts_unfiltered/cellranger/genes.tsv"/> | |
109 <data name="matrix" label="cellranger matrix" format="mtx" from_work_dir="kb_outs/counts_unfiltered/cellranger/matrix.mtx" /> | |
110 <data name="inspect" label="inspect_report" format="json" from_work_dir="kb_outs/inspect.json"/> | |
111 <data name="runinfo" label="run info" format="json" from_work_dir="kb_outs/run_info.json"/> | |
112 <data name="kbinfo" label="kb info" format="json" from_work_dir="kb_outs/kb_info.json"/> | |
113 <data name="kb_ref" label="kb_ref.idx" format="kallisto.idx" from_work_dir="index/kb_ref.idx"/> | |
114 <data name="t2g" label="t2g.txt" format="txt" from_work_dir="index/t2g.txt"/> | |
115 <data name="cdna_t2c" label="-c1 cdna_t2c.txt" format="txt" from_work_dir="index/cdna_t2c.txt"> | |
116 <filter>workflow == "lamanno"</filter> | |
117 </data> | |
118 <data name="intron_t2c" label="-c2 intron_t2c.txt" format="txt" from_work_dir="index/intron_t2c.txt"> | |
119 <filter>workflow == "lamanno"</filter> | |
120 </data> | |
121 <data name="adata" label="adata.h5ad" format="h5ad" from_work_dir="kb_outs/counts_unfiltered/adata.h5ad"> | |
122 <filter >extra_dtype == "--h5ad"</filter> | |
123 </data> | |
124 <data name="adata" label="adata.loom" format="loom" from_work_dir="kb_outs/counts_unfiltered/adata.loom"> | |
125 <filter>extra_dtype == "--loom"</filter> | |
126 </data> | |
127 </outputs> | |
128 <tests> | |
129 <expand macro="tests"/> | |
130 </tests> | |
131 <help><![CDATA[ | |
132 This is a galaxy wrapper for kallisto-bustools (kb) for quantification of different types of single-cell sequencing data. The main kallisto-bustools homepage can be found under: | |
133 'kallisto-bustools<https://www.kallistobus.tools/>'. | |
134 | |
135 The kb count command runs the kallisto and bustools programs. It can be used for pre-processing of data from a variety of single-cell RNA-seq technologies, | |
136 and for a number of different workflows (e.g. production of gene count matrices, RNA velocity analyses, etc.). | |
137 | |
138 The kb package is developed and maintained by the Pachterlab under the MIT License. | |
139 ]]></help> | |
140 <citations> | |
141 <citation type="doi">https://doi.org/10.1101/673285</citation> | |
142 </citations> | |
143 </tool> |