Mercurial > repos > iuc > umi_tools_group
comparison macros.xml @ 17:428735be9764 draft default tip
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/umi_tools commit bc1b362f6783d3fc0ed0f42c14687001d7ff5f7a
author | iuc |
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date | Sat, 05 Oct 2024 13:08:51 +0000 |
parents | 257be15474a7 |
children |
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16:257be15474a7 | 17:428735be9764 |
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2 <macros> | 2 <macros> |
3 | 3 |
4 <!-- macros applying to all umi_tools --> | 4 <!-- macros applying to all umi_tools --> |
5 | 5 |
6 <token name="@TOOL_VERSION@">1.1.5</token> | 6 <token name="@TOOL_VERSION@">1.1.5</token> |
7 <token name="@VERSION_SUFFIX@">0</token> | 7 <token name="@VERSION_SUFFIX@">1</token> |
8 <token name="@PROFILE@">21.01</token> | 8 <token name="@PROFILE@">23.1</token> |
9 <xml name="requirements"> | 9 <xml name="requirements"> |
10 <requirements> | 10 <requirements> |
11 <requirement type="package" version="@TOOL_VERSION@">umi_tools</requirement> | 11 <requirement type="package" version="@TOOL_VERSION@">umi_tools</requirement> |
12 <yield /> | 12 <yield /> |
13 </requirements> | 13 </requirements> |
102 <when value="single"> | 102 <when value="single"> |
103 <param name="input_read1" type="data" format="@FASTQ_FORMATS@" label="Reads in FASTQ format" /> | 103 <param name="input_read1" type="data" format="@FASTQ_FORMATS@" label="Reads in FASTQ format" /> |
104 <expand macro="barcode1_macro"/> | 104 <expand macro="barcode1_macro"/> |
105 </when> | 105 </when> |
106 <when value="paired"> | 106 <when value="paired"> |
107 <param name="input_read1" type="data" format="@FASTQ_FORMATS@" label="Reads in FASTQ format" /> | 107 <param name="input_read1" type="data" format="@FASTQ_FORMATS@" label="Forward reads in FASTQ format" /> |
108 <param name="input_read2" type="data" format="@FASTQ_FORMATS@" label="Reads in FASTQ format" /> | 108 <param name="input_read2" type="data" format="@FASTQ_FORMATS@" label="Reverse reads in FASTQ format" /> |
109 <expand macro="barcode1_macro"/> | 109 <expand macro="barcode1_macro"/> |
110 <expand macro="barcode2_macro"/> | 110 <expand macro="barcode2_macro"/> |
111 <yield/> | 111 <yield/> |
112 </when> | 112 </when> |
113 <when value="paired_collection"> | 113 <when value="paired_collection"> |
150 | 150 |
151 <!-- macros for count, dedup, and group --> | 151 <!-- macros for count, dedup, and group --> |
152 | 152 |
153 <token name="@LINK_SAM_BAM_INPUT@"><![CDATA[ | 153 <token name="@LINK_SAM_BAM_INPUT@"><![CDATA[ |
154 #if $input.is_of_type("sam"): | 154 #if $input.is_of_type("sam"): |
155 ## TODO dedup has problems with SAM input in some cases | 155 ## sam input is not supported for paired data |
156 ## https://github.com/CGATOxford/UMI-tools/issues/483 | 156 ## https://github.com/CGATOxford/UMI-tools/issues/483 |
157 ## so convert it to sorted BAM for now | 157 ## so convert it to sorted BAM |
158 ## #set $input_file = $input | 158 ## #set $input_file = $input |
159 samtools sort --no-PG '$input' > 'input.bam' && | 159 samtools sort --no-PG '$input' -O BAM > 'input.bam' && |
160 samtools index -b 'input.bam' && | 160 samtools index -b 'input.bam' && |
161 #set $input_file = 'input.bam' | 161 #set $input_file = 'input.bam' |
162 #else: | 162 #else: |
163 ln -sf '${input}' 'input.bam' && | 163 ln -sf '${input}' 'input.bam' && |
164 ln -sf '$input.metadata.bam_index' 'input.bam.bai' && | 164 ln -sf '$input.metadata.bam_index' 'input.bam.bai' && |
165 #set $input_file = 'input.bam' | 165 #set $input_file = 'input.bam' |
166 #end if | 166 #end if |
167 ]]></token> | 167 ]]></token> |
168 <token name="@SET_INPUT_TYPE@"><![CDATA[ | 168 <token name="@SET_INPUT_TYPE@"><![CDATA[ |
169 ## TODO see comment in LINK_SAM_BAM_INPUT | 169 ## see comment in LINK_SAM_BAM_INPUT |
170 ## #if $input.is_of_type("sam"): | 170 ## #if $input.is_of_type("sam"): |
171 ## --in-sam | 171 ## --in-sam |
172 ## #end if | 172 ## #end if |
173 ]]></token> | 173 ]]></token> |
174 | 174 |
509 <expand macro="sanitize_tag" /> | 509 <expand macro="sanitize_tag" /> |
510 </param> | 510 </param> |
511 <param argument="--assigned-status-tag" type="text" optional="true" label="Bam tag describing whether read is assigned to a gene" help="By default, this is set as the same tag as --gene-tag"> | 511 <param argument="--assigned-status-tag" type="text" optional="true" label="Bam tag describing whether read is assigned to a gene" help="By default, this is set as the same tag as --gene-tag"> |
512 <expand macro="sanitize_tag" /> | 512 <expand macro="sanitize_tag" /> |
513 </param> | 513 </param> |
514 <param argument="--skip-tags-regex" name="skip_tags_regex" type="text" label="Skip any reads where the gene matches this tag" value="" > | 514 <param argument="--skip-tags-regex" type="text" label="Skip any reads where the gene matches this tag" value="" > |
515 <expand macro="barcode_sanitizer" /> | 515 <expand macro="barcode_sanitizer" /> |
516 </param> | 516 </param> |
517 <param argument="--per-contig" type="boolean" truevalue="--per-contig" falsevalue="" label="Deduplicate per contig" help="Field 3 in BAM; RNAME. All reads with the same contig will be considered to have the same alignment position. This is useful if your library prep generates PCR duplicates with non identical alignment positions such as CEL-Seq. In this case, you would align to a reference transcriptome with one transcript per gene" /> | 517 <param argument="--per-contig" type="boolean" truevalue="--per-contig" falsevalue="" label="Deduplicate per contig" help="Field 3 in BAM; RNAME. All reads with the same contig will be considered to have the same alignment position. This is useful if your library prep generates PCR duplicates with non identical alignment positions such as CEL-Seq. In this case, you would align to a reference transcriptome with one transcript per gene" /> |
518 <param argument="--gene-transcript-map" type="data" format="tabular" optional="true" label="Tabular file mapping genes to transripts" /> | 518 <param argument="--gene-transcript-map" type="data" format="tabular" optional="true" label="Tabular file mapping genes to transripts" /> |
519 <param argument="--per-cell" name="per_cell" type="boolean" truevalue="--per-cell" falsevalue="" label="Group reads only if they have the same cell barcode" /> | 519 <param argument="--per-cell" type="boolean" truevalue="--per-cell" falsevalue="" label="Group reads only if they have the same cell barcode" /> |
520 </section> | 520 </section> |
521 </xml> | 521 </xml> |
522 <token name="@SC_OPTIONS@"><![CDATA[ | 522 <token name="@SC_OPTIONS@"><![CDATA[ |
523 #if str($sc.gene_tag) != "": | 523 #if str($sc.gene_tag) != "": |
524 --gene-tag '$sc.gene_tag' | 524 --gene-tag '$sc.gene_tag' |