Mercurial > repos > drosofff > lumpy
comparison lumpy.xml @ 1:aa514338711d draft
planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/lumpy commit bd0a0b0717fd7da2ff703668b21ff7db3677d61b
| author | drosofff |
|---|---|
| date | Tue, 06 Dec 2016 09:29:08 -0500 |
| parents | bbdc52775678 |
| children | 9f5761fe885d |
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| 0:bbdc52775678 | 1:aa514338711d |
|---|---|
| 69 </conditional> | 69 </conditional> |
| 70 | 70 |
| 71 </inputs> | 71 </inputs> |
| 72 | 72 |
| 73 <outputs> | 73 <outputs> |
| 74 <data format="tabular" name="histogram" type="data" label="${input_file.element_identifier} Fragment size distribution"> | 74 <data format="tabular" name="histogram" type="data" label="Lumpy on ${input_file.element_identifier}: Fragment size distribution"> |
| 75 <filter>seq_method['seq_method_list'] == "paired-end"</filter> | 75 <filter>seq_method['seq_method_list'] == "paired-end"</filter> |
| 76 </data> | 76 </data> |
| 77 <data format="bam" name="splits" type="data" label="${input_file.element_identifier} Split Reads (Bam format)"/> | 77 <data format="bam" name="splits" type="data" label="Lumpy on ${input_file.element_identifier}: Split Reads (Bam format)"/> |
| 78 <data format="bam" name="discordants" type="data" label="${input_file.element_identifier} Discordant Pairs (Bam format)"> | 78 <data format="bam" name="discordants" type="data" label="Lumpy on ${input_file.element_identifier}: Discordant Pairs (Bam format)"> |
| 79 <filter>seq_method['seq_method_list'] == "paired-end"</filter> | 79 <filter>seq_method['seq_method_list'] == "paired-end"</filter> |
| 80 </data> | 80 </data> |
| 81 <data format="vcf" name="vcf_call" type="data" label="${input_file.element_identifier} Variant Calling (vcf format)"/> | 81 <data format="vcf" name="vcf_call" type="data" label="Lumpy on ${input_file.element_identifier}: Variant Calling (vcf format)"/> |
| 82 </outputs> | 82 </outputs> |
| 83 | 83 |
| 84 <tests> | 84 <tests> |
| 85 <test> | 85 <test> |
| 86 <param name="input_file" value="sr.input.bam" ftype="bam"/> | 86 <param name="input_file" value="sr.input.bam" ftype="bam"/> |
| 91 <output name="vcf_call" file="output.vcf" ftype="vcf"/> | 91 <output name="vcf_call" file="output.vcf" ftype="vcf"/> |
| 92 </test> | 92 </test> |
| 93 </tests> | 93 </tests> |
| 94 | 94 |
| 95 <help> | 95 <help> |
| 96 Some help required | 96 |
| 97 **lumpy-sv manual** | |
| 98 | |
| 99 Read the lumpy-sv_ documentation for details on using lumpy. | |
| 100 | |
| 101 .. _lumpy-sv: https://github.com/arq5x/lumpy-sv | |
| 102 | |
| 103 **lumpy options** | |
| 104 | |
| 105 v 0.2.13 | |
| 106 Author: Ryan Layer (rl6sf@virginia.edu) | |
| 107 | |
| 108 Summary: Find structural variations in various signals. | |
| 109 | |
| 110 Options:: | |
| 111 | |
| 112 -g Genome file (defines chromosome order) | |
| 113 -e Show evidence for each call | |
| 114 -w File read windows size (default 1000000) | |
| 115 -mw minimum weight for a call | |
| 116 -msw minimum per-sample weight for a call | |
| 117 -tt trim threshold | |
| 118 -x exclude file bed file | |
| 119 -t temp file prefix, must be to a writeable directory | |
| 120 -P output probability curve for each variant | |
| 121 -b output BEDPE instead of VCF | |
| 122 -sr bam_file:<file name>, | |
| 123 id:<sample name>, | |
| 124 back_distance:<distance>, | |
| 125 min_mapping_threshold:<mapping quality>, | |
| 126 weight:<sample weight>, | |
| 127 min_clip:<minimum clip length>, | |
| 128 read_group:<string> | |
| 129 | |
| 130 -pe bam_file:<file name>, | |
| 131 id:<sample name>, | |
| 132 histo_file:<file name>, | |
| 133 mean:<value>, | |
| 134 stdev:<value>, | |
| 135 read_length:<length>, | |
| 136 min_non_overlap:<length>, | |
| 137 discordant_z:<z value>, | |
| 138 back_distance:<distance>, | |
| 139 min_mapping_threshold:<mapping quality>, | |
| 140 weight:<sample weight>, | |
| 141 read_group:<string> | |
| 142 | |
| 143 -bedpe bedpe_file:<bedpe file>, | |
| 144 id:<sample name>, | |
| 145 weight:<sample weight> | |
| 146 | |
| 97 </help> | 147 </help> |
| 98 | 148 |
| 99 <citations> | 149 <citations> |
| 100 <citation type="doi">10.1186/gb-2014-15-6-r84</citation> | 150 <citation type="doi">10.1186/gb-2014-15-6-r84</citation> |
| 101 </citations> | 151 </citations> |
