Mercurial > repos > galaxy-australia > dorado
comparison dorado.xml @ 7:34e128a6a6ed draft default tip
planemo upload for repository https://github.com/usegalaxy-au/tools-au/tree/master/tools/dorado commit 97793e41864a750b1c18c80b858c118e43ae8d97
author | galaxy-australia |
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date | Mon, 23 Jun 2025 03:09:42 +0000 |
parents | 5e67ea368004 |
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6:5e67ea368004 | 7:34e128a6a6ed |
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1 <tool id="dorado" name="Dorado" version="@VERSION@+galaxy0" python_template_version="3.5" profile="24.1"> | 1 <tool id="dorado" name="Dorado" version="@VERSION@+galaxy1" python_template_version="3.5" profile="24.1"> |
2 <description>basecaller for raw Oxford Nanopore data</description> | 2 <description>basecaller for raw Oxford Nanopore data</description> |
3 <macros> | 3 <macros> |
4 <import>macros.xml</import> | 4 <import>macros.xml</import> |
5 </macros> | 5 </macros> |
6 <expand macro="xrefs"/> | 6 <expand macro="xrefs"/> |
27 > summary.tsv | 27 > summary.tsv |
28 | 28 |
29 ]]></command> | 29 ]]></command> |
30 <inputs> | 30 <inputs> |
31 <param name="pod5_file" type="data" format="pod5" label="Raw pod5 file" help="Only pod5 is supported. You can convert fast5 to pod5 with the fast5 to pod5 tool."/> | 31 <param name="pod5_file" type="data" format="pod5" label="Raw pod5 file" help="Only pod5 is supported. You can convert fast5 to pod5 with the fast5 to pod5 tool."/> |
32 <param name="model" type="select" label="Basecalling model. See the Help section for info on model names."> | 32 <expand macro="model_param"/> |
33 <options from_data_table="dorado_models"> | |
34 <!-- only allow models that shipped in this container --> | |
35 <filter type="static_value" column="1" value="@CONTAINER_HASH@"/> | |
36 </options> | |
37 </param> | |
38 <param type="select" argument="--trim" label="DNA adapter and primer trimming" help="Detect and remove any adapter and/or primer sequences from the beginning and end of DNA reads. Note that if you intend to demultiplex the reads, trimming adapters and primers could interfere with correct demultiplexing."> | 33 <param type="select" argument="--trim" label="DNA adapter and primer trimming" help="Detect and remove any adapter and/or primer sequences from the beginning and end of DNA reads. Note that if you intend to demultiplex the reads, trimming adapters and primers could interfere with correct demultiplexing."> |
39 <option value="all" selected="true">Any. Trim any detected adapters or primers.</option> | 34 <option value="all" selected="true">Any. Trim any detected adapters or primers.</option> |
40 <option value="primers"> Primers. Trim any detected adapters or primers, but if barcoding is enabled the barcode sequences will not be trimmed.</option> | 35 <option value="primers"> Primers. Trim any detected adapters or primers, but if barcoding is enabled the barcode sequences will not be trimmed.</option> |
41 <option value="adapters"> Adapters. Trim any detected adapters, but primers will not be trimmed, and if barcoding is enabled then barcodes will not be trimmed either.</option> | 36 <option value="adapters"> Adapters. Trim any detected adapters, but primers will not be trimmed, and if barcoding is enabled then barcodes will not be trimmed either.</option> |
42 <option value="none"> None. Nothing will be trimmed.</option> | 37 <option value="none"> None. Nothing will be trimmed.</option> |
43 </param> | 38 </param> |
44 <!-- dev note: the barcode kits are hardcoded in https://github.com/nanoporetech/dorado/blob/release-v0.9/dorado/utils/barcode_kits.cpp --> | 39 <!-- dev note: the barcode kits are hardcoded in https://github.com/nanoporetech/dorado/blob/release-v0.9/dorado/utils/barcode_kits.cpp --> |
45 <param type="select" argument="--kit-name" optional="true" label="Enable barcoding with the selected kit name." help="Reads are classified into their barcode groups during basecalling. The classification will be reflected in the read group name as well as in the BC tag of the output record."> | 40 <param type="select" argument="--kit-name" optional="true" label="Enable barcoding with the selected kit name." help="Reads are classified into their barcode groups during basecalling. The classification will be reflected in the read group name as well as in the BC tag of the output record."> |
46 <expand macro="barcode_kits" /> | 41 <expand macro="barcode_kits"/> |
47 </param> | 42 </param> |
48 </inputs> | 43 </inputs> |
49 <outputs> | 44 <outputs> |
50 <data format="unsorted.bam" name="out_bam" label="Reads from ${on_string} basecalled by ${tool.name} with model ${model.fields.name}" from_work_dir="calls.bam"/> | 45 <data format="unsorted.bam" name="out_bam" label="Reads from ${on_string} basecalled by ${tool.name} with model ${model.fields.name}" from_work_dir="calls.bam"/> |
51 <data format="tsv" name="out_tsv" label="${tool.name} sequencing summary for ${on_string}" from_work_dir="summary.tsv"/> | 46 <data format="tsv" name="out_tsv" label="${tool.name} sequencing summary for ${on_string}" from_work_dir="summary.tsv"/> |