Mercurial > repos > artbio > manta
comparison manta.xml @ 5:f55d45b0c6d1 draft
"planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/manta commit 86427647db100383faa432008b58e768b56ac416"
author | artbio |
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date | Tue, 09 Jun 2020 06:23:39 -0400 |
parents | d09254e37c68 |
children | cb5691381acb |
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4:d09254e37c68 | 5:f55d45b0c6d1 |
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22 ln -s '$bam_input.normal_bam_file.metadata.bam_index' normal.bai && | 22 ln -s '$bam_input.normal_bam_file.metadata.bam_index' normal.bai && |
23 ln -s '$bam_input.tumor_bam_file' tumor.bam && | 23 ln -s '$bam_input.tumor_bam_file' tumor.bam && |
24 ln -s '$bam_input.tumor_bam_file.metadata.bam_index' tumor.bai && | 24 ln -s '$bam_input.tumor_bam_file.metadata.bam_index' tumor.bai && |
25 #end if | 25 #end if |
26 | 26 |
27 #if str( $set_configuration.set_configuration_switch ) == "Customized": | |
28 sed -i 's/minCandidateVariantSize = 8/minCandidateVariantSize = $set_configuration.minCandidateVariantSize/' ./configManta.py.ini && | |
29 sed -i 's/rnaMinCandidateVariantSize = 1000/rnaMinCandidateVariantSize = $set_configuration.rnaMinCandidateVariantSize/' ./configManta.py.ini && | |
30 sed -i 's/minEdgeObservations = 3/minEdgeObservations = $set_configuration.minEdgeObservations/' ./configManta.py.ini && | |
31 sed -i 's/graphNodeMaxEdgeCount = 10/graphNodeMaxEdgeCount = $set_configuration.graphNodeMaxEdgeCount/' ./configManta.py.ini && | |
32 sed -i 's/minCandidateSpanningCount = 3/minCandidateSpanningCount = $set_configuration.minCandidateSpanningCount/' ./configManta.py.ini && | |
33 sed -i 's/minScoredVariantSize = 50/minScoredVariantSize = $set_configuration.minScoredVariantSize/' ./configManta.py.ini && | |
34 sed -i 's/minDiploidVariantScore = 10/minDiploidVariantScore = $set_configuration.minDiploidVariantScore/' ./configManta.py.ini && | |
35 sed -i 's/minPassDiploidVariantScore = 20/minPassDiploidVariantScore = $set_configuration.minPassDiploidVariantScore/' ./configManta.py.ini && | |
36 sed -i 's/minPassDiploidGTScore = 15/minPassDiploidGTScore = $set_configuration.minPassDiploidGTScore/' ./configManta.py.ini && | |
37 sed -i 's/minSomaticScore = 10/minSomaticScore = $set_configuration.minSomaticScore/' ./configManta.py.ini && | |
38 sed -i 's/minPassSomaticScore = 30/minPassSomaticScore = $set_configuration.minPassSomaticScore/' ./configManta.py.ini && | |
39 sed -i 's/enableRemoteReadRetrievalForInsertionsInGermlineCallingModes = 1/enableRemoteReadRetrievalForInsertionsInGermlineCallingModes = $set_configuration.enableRemoteReadRetrievalForInsertionsInGermlineCallingModes/' ./configManta.py.ini && | |
40 sed -i 's/enableRemoteReadRetrievalForInsertionsInCancerCallingModes = 0/enableRemoteReadRetrievalForInsertionsInCancerCallingModes = $set_configuration.enableRemoteReadRetrievalForInsertionsInCancerCallingModes/' ./configManta.py.ini && | |
41 sed -i 's/useOverlapPairEvidence = 0/useOverlapPairEvidence = $set_configuration.useOverlapPairEvidence/' ./configManta.py.ini && | |
42 #end if | |
43 | |
44 #if str( $set_configuration.set_configuration_switch ) == "Custom_config_file": | 27 #if str( $set_configuration.set_configuration_switch ) == "Custom_config_file": |
45 cp '$set_configuration.CustomConfigFile' ./configManta.py.ini && | 28 cp '$set_configuration.CustomConfigFile' ./configManta.py.ini && |
29 #end if | |
30 #if str( $set_configuration.set_configuration_switch ) == "Customized": | |
31 rm ./configManta.py.ini && | |
32 python $__tool_directory__/customConfigManta.py | |
33 --minCandidateVariantSize '$set_configuration.minCandidateVariantSize' | |
34 --rnaMinCandidateVariantSize '$set_configuration.rnaMinCandidateVariantSize' | |
35 --minEdgeObservations '$set_configuration.minEdgeObservations' | |
36 --graphNodeMaxEdgeCount '$set_configuration.graphNodeMaxEdgeCount' | |
37 --minCandidateSpanningCount '$set_configuration.minCandidateSpanningCount' | |
38 --minScoredVariantSize '$set_configuration.minScoredVariantSize' | |
39 --minDiploidVariantScore '$set_configuration.minDiploidVariantScore' | |
40 --minPassDiploidVariantScore '$set_configuration.minPassDiploidVariantScore' | |
41 --minPassDiploidGTScore '$set_configuration.minPassDiploidGTScore' | |
42 --minSomaticScore '$set_configuration.minSomaticScore' | |
43 --minPassSomaticScore '$set_configuration.minPassSomaticScore' | |
44 --enableRemoteReadRetrievalForInsertionsInGermlineCallingModes '$set_configuration.enableRemoteReadRetrievalForInsertionsInGermlineCallingModes' | |
45 --enableRemoteReadRetrievalForInsertionsInCancerCallingModes '$set_configuration.enableRemoteReadRetrievalForInsertionsInCancerCallingModes' | |
46 --useOverlapPairEvidence '$set_configuration.useOverlapPairEvidence' && | |
46 #end if | 47 #end if |
47 | 48 |
48 configManta.py --referenceFasta='${reference_fasta_filename}' | 49 configManta.py --referenceFasta='${reference_fasta_filename}' |
49 --config='./configManta.py.ini' | 50 --config='./configManta.py.ini' |
50 #if str( $bam_input.bam_input_selector ) == "not_tumor_bam": | 51 #if str( $bam_input.bam_input_selector ) == "not_tumor_bam": |
51 --bam='normal.bam' | 52 --bam='normal.bam' |
52 #else if str( $bam_input.bam_input_selector ) == "tumor_bam": | 53 #else if str( $bam_input.bam_input_selector ) == "tumor_bam": |
53 --bam='normal.bam' | 54 --bam='normal.bam' |
54 --tumorBam='tumor.bam' | 55 --tumorBam='tumor.bam' |
55 #end if | 56 #end if |
56 --runDir='${run_dir}' | 57 --runDir='${run_dir}' |
57 --scanSizeMb=${advanced.scanSizeMb} | 58 --scanSizeMb=${advanced.scanSizeMb} |
58 --callMemMb=${advanced.callMemMb} && | 59 --callMemMb=${advanced.callMemMb} && |
59 | 60 |
60 ln -s -f '${run_dir}/runWorkflow.py' '${run_manta_workflow}' && | |
61 ln -s -f './configManta.py.ini' '${set_conf_file}' && | |
62 python2 '${run_dir}/runWorkflow.py' -m local -j \${GALAXY_SLOTS:-4} | 61 python2 '${run_dir}/runWorkflow.py' -m local -j \${GALAXY_SLOTS:-4} |
63 | 62 |
64 ]]></command> | 63 ]]></command> |
65 | 64 |
66 <inputs> | 65 <inputs> |
67 <expand macro="reference_source_conditional" /> | 66 <expand macro="reference_source_conditional" /> |
68 | |
69 <conditional name="bam_input"> | 67 <conditional name="bam_input"> |
70 <param name="bam_input_selector" type="select" label="Just 'normal' BAM file or 'normal' + 'tumor' BAM files" help="Select between a single normal BAM file or a pair of normal / tumor BAM files"> | 68 <param name="bam_input_selector" type="select" label="Single 'normal' or 'normal vs tumor' analysis" help="Select between a single normal BAM file or a pair of normal/tumor BAM files"> |
71 <option value="not_tumor_bam">Normal</option> | 69 <option value="not_tumor_bam">Normal</option> |
72 <option value="tumor_bam">Normal + Tumor</option> | 70 <option value="tumor_bam">Normal + Tumor</option> |
73 </param> | 71 </param> |
74 | |
75 <when value="not_tumor_bam"> | 72 <when value="not_tumor_bam"> |
76 <param name="normal_bam_file" type="data" format="bam" label="select normal BAM" help="Select the files you wish to send to Manta (normal sample, it must be in BAM format)." /> | 73 <param name="normal_bam_file" type="data" format="bam" label="select normal BAM" help="Select the files you wish to send to Manta (normal sample, it must be in BAM format)." /> |
77 </when> | 74 </when> |
78 | |
79 <when value='tumor_bam'> | 75 <when value='tumor_bam'> |
80 <param name="normal_bam_file" type="data" format="bam" label="select normal BAM" help="Select the files you wish to send to Manta (normal sample, it must be in BAM format)." /> | 76 <param name="normal_bam_file" type="data" format="bam" label="select normal BAM" help="Select the files you wish to send to Manta (normal sample, it must be in BAM format)." /> |
81 <param name="tumor_bam_file" type="data" format="bam" label="select tumor BAM" help="Select the files you wish to send to Manta (tumor sample, it must be in BAM format)." /> | 77 <param name="tumor_bam_file" type="data" format="bam" label="select tumor BAM" help="Select the files you wish to send to Manta (tumor sample, it must be in BAM format)." /> |
82 </when> | 78 </when> |
83 </conditional> | 79 </conditional> |
84 | |
85 <param name="additional_param" type="select" multiple="true" display="checkboxes" label="Additional parameters" > | 80 <param name="additional_param" type="select" multiple="true" display="checkboxes" label="Additional parameters" > |
86 <option value="exome">Set options for WES input: turn off depth filters</option> | 81 <option value="exome">Set options for WES input: turn off depth filters</option> |
87 <option value="rna">Set options for RNA-Seq input. Must specify exactly one bam input file</option> | 82 <option value="rna">Set options for RNA-Seq input. Must specify exactly one bam input file</option> |
88 <option value="unstrandedRNA">Set if RNA-Seq input is unstranded: Allows splice-junctions on either strand</option> | 83 <option value="unstrandedRNA">Set if RNA-Seq input is unstranded: Allows splice-junctions on either strand</option> |
89 </param> | 84 </param> |
90 | |
91 <section name="advanced" title="Advanced options" expanded="false"> | 85 <section name="advanced" title="Advanced options" expanded="false"> |
92 | |
93 <param name="callMemMb" type="integer" value="8000" label="Set default task memory requirements" help="The maximum memory size to assign to tasks" /> | 86 <param name="callMemMb" type="integer" value="8000" label="Set default task memory requirements" help="The maximum memory size to assign to tasks" /> |
94 <param name="scanSizeMb" type="integer" value="12" label="Set maximum sequence region size" help="The maximum sequence region size (in megabases) scanned by each task during SV Locus graph generation. (default: 12)" /> | 87 <param name="scanSizeMb" type="integer" value="12" label="Set maximum sequence region size" help="The maximum sequence region size (in megabases) scanned by each task during SV Locus graph generation. (default: 12)" /> |
95 <!-- <param name="generateEvidenceBam" type="boolean" checked="False" truevalue="-s" falsevalue="" label="Generate a bam of supporting reads for all SVs" help="Click yes for generating a BAM of supporting reads for all SVs."/> --> | 88 <!-- <param name="generateEvidenceBam" type="boolean" checked="False" truevalue="-s" falsevalue="" label="Generate a bam of supporting reads for all SVs" help="Click yes for generating a BAM of supporting reads for all SVs."/> --> |
96 | |
97 </section> | 89 </section> |
98 | |
99 <!-- <expand macro="manta_configuration"/> --> | |
100 | |
101 <conditional name="set_configuration"> | 90 <conditional name="set_configuration"> |
102 <param name="set_configuration_switch" type="select" label="Do you want to change default configuration settings?"> | 91 <param name="set_configuration_switch" type="select" label="Do you want to change default configuration settings?"> |
103 <option value="Default_config_file">Default Manta Configuration File</option> | 92 <option value="Default_config_file">Default Manta Configuration File</option> |
104 <option value="Custom_config_file">Upload your Own Configuration File</option> | 93 <option value="Custom_config_file">Upload your Own Configuration File</option> |
105 <option value="Customized">Customize a Configuration File using this Galaxy Form</option> | 94 <option value="Customized">Customize a Configuration File using this Galaxy Form</option> |
124 <param name="enableRemoteReadRetrievalForInsertionsInGermlineCallingModes" type="integer" value="1" label="enableRemoteReadRetrievalForInsertionsInGermlineCallingModes" help="Remote read retrieval is used ot improve the assembly of putative insertions by retrieving any mate reads in remote locations with poor mapping quality. This feature can be enabled/disabled separately for germline and cancer calling below."/> | 113 <param name="enableRemoteReadRetrievalForInsertionsInGermlineCallingModes" type="integer" value="1" label="enableRemoteReadRetrievalForInsertionsInGermlineCallingModes" help="Remote read retrieval is used ot improve the assembly of putative insertions by retrieving any mate reads in remote locations with poor mapping quality. This feature can be enabled/disabled separately for germline and cancer calling below."/> |
125 <param name="enableRemoteReadRetrievalForInsertionsInCancerCallingModes" type="integer" value="0" label="enableRemoteReadRetrievalForInsertionsInCancerCallingModes" help="Here 'CancerCallingModes' includes tumor-normal subtraction and tumor-only calling. 'GermlineCallingModes' includes all other calling modes."/> | 114 <param name="enableRemoteReadRetrievalForInsertionsInCancerCallingModes" type="integer" value="0" label="enableRemoteReadRetrievalForInsertionsInCancerCallingModes" help="Here 'CancerCallingModes' includes tumor-normal subtraction and tumor-only calling. 'GermlineCallingModes' includes all other calling modes."/> |
126 <param name="useOverlapPairEvidence" type="integer" value="0" label="useOverlapPairEvidence" help="Set if an overlapping read pair will be considered as evidence. Set this value <= 0 to skip overlapping read pairs."/> | 115 <param name="useOverlapPairEvidence" type="integer" value="0" label="useOverlapPairEvidence" help="Set if an overlapping read pair will be considered as evidence. Set this value <= 0 to skip overlapping read pairs."/> |
127 </when> | 116 </when> |
128 </conditional> | 117 </conditional> |
129 | |
130 <param name="runworkflow_file_check" type="boolean" label="output manta run_workflow file" checked="False" help="Show run_workflow file on history"/> | |
131 <param name="config_file_check" type="boolean" label="output conf file" checked="False" help="Show configuration file on history"/> | 118 <param name="config_file_check" type="boolean" label="output conf file" checked="False" help="Show configuration file on history"/> |
132 <param name="candidateSV_check" type="boolean" label="Unscored candidate SV and indels" checked="False" | 119 <param name="candidateSV_check" type="boolean" label="Unfiltered structural variants" checked="False" |
133 help="Show unfiltered structural variants"/> | 120 help="All unscored structural variant candidates"/> |
134 <param name="candidateSmallIndels_check" type="boolean" label="all snvs" checked="False" | 121 <param name="candidateSmallIndels_check" type="boolean" label="Unfiltered small indel candidates" checked="False" |
135 help="Subset of the Unscored candidate SV and indels, containing only simple insertion and deletion variants"/> | 122 help="Subset of the unscored candidates, containing only small indel variants"/> |
136 <param name="diploidSV_check" type="boolean" label="filtered variants in diploid model" checked="False" | 123 <param name="diploidSV_check" type="boolean" label="Score-filtered variants in diploid model" checked="False" |
137 help="Show filtered variants in a diploid (only normal) model. In the case of a tumor/normal subtraction, the scores in this file *do not* | 124 help="Show filtered variants in a diploid (only normal) model. In the case of a tumor/normal subtraction, the scores in this file *do not* |
138 reflect any information from the tumor sample" /> | 125 reflect any information from the tumor sample" /> |
139 <param name="somaticSV_check" type="boolean" label="SVs and indels scored under a somatic variant model" checked="False" | |
140 help="This file will only be produced if a tumor sample alignment file is supplied during configuration"/> | |
141 </inputs> | 126 </inputs> |
142 | |
143 <outputs> | 127 <outputs> |
144 <data format="txt" name="run_manta_workflow" label="Parameters for running Manta"> | 128 <data format="tabular" name="conf_file" label="conf_file.ini" from_work_dir="./configManta.py.ini"> |
145 <filter>runworkflow_file_check == True</filter> | |
146 </data> | |
147 | |
148 <data format="tabular" name="set_conf_file" label="conf_file.ini"> | |
149 <filter>config_file_check == True</filter> | 129 <filter>config_file_check == True</filter> |
150 </data> | 130 </data> |
151 <data format="vcf_bgzip" name="candidateSV" label="Manta unfiltered SVs" from_work_dir="MantaWorkflow/results/variants/candidateSV.vcf.gz"> | 131 <data format="vcf_bgzip" name="candidateSV" label="Manta unfiltered variants" from_work_dir="MantaWorkflow/results/variants/candidateSV.vcf.gz"> |
152 <filter>candidateSV_check == True</filter> | 132 <filter>candidateSV_check == True</filter> |
153 </data> | 133 </data> |
154 <data format="vcf_bgzip" name="candidateSmallIndels" label="Manta unfiltered Small Indels" from_work_dir="MantaWorkflow/results/variants/candidateSmallIndels.vcf.gz"> | 134 <data format="vcf_bgzip" name="candidateSmallIndels" label="Manta unfiltered indels" from_work_dir="MantaWorkflow/results/variants/candidateSmallIndels.vcf.gz"> |
155 <filter>candidateSmallIndels_check == True</filter> | 135 <filter>candidateSmallIndels_check == True</filter> |
156 </data> | 136 </data> |
157 <data format="vcf_bgzip" name="diploidSV" label="Manta SVs (diploid model)" from_work_dir="MantaWorkflow/results/variants/diploidSV.vcf.gz"> | 137 <data format="vcf_bgzip" name="diploidSV" label="Score-filtered Variants (diploid model)" from_work_dir="MantaWorkflow/results/variants/diploidSV.vcf.gz"> |
158 <filter>diploidSV_check == True</filter> | 138 <filter>diploidSV_check == True</filter> |
159 </data> | 139 </data> |
160 <data format="vcf_bgzip" name="somaticSV" label="Manta SVs (somatic model)" from_work_dir="MantaWorkflow/results/variants/somaticSV.vcf.gz"> | 140 <data format="vcf_bgzip" name="somaticSV" label="Score-filtered Variants (somatic model)" from_work_dir="MantaWorkflow/results/variants/somaticSV.vcf.gz"> |
161 <filter>somaticSV_check == True</filter> | 141 <filter>bam_input['bam_input_selector'] == 'tumor_bam'</filter> |
162 </data> | 142 </data> |
163 </outputs> | 143 </outputs> |
164 | |
165 <tests> | 144 <tests> |
166 <test> | 145 <test> |
167 <param name="reference_source_selector" value="cached"/> | 146 <param name="reference_source_selector" value="cached"/> |
168 <param name="index" value="hg19"/> | 147 <param name="index" value="hg19"/> |
169 <param name="bam_input_selector" value="tumor_bam" dbkey="hg19"/> | 148 <param name="bam_input_selector" value="tumor_bam" dbkey="hg19"/> |
170 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> | 149 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> |
171 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> | 150 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> |
172 <param name="set_configuration_switch" value="Default_config_file"/> | 151 <param name="set_configuration_switch" value="Default_config_file"/> |
173 <param name="callMemMb" value="1000"/> | 152 <param name="callMemMb" value="1000"/> |
174 <param name="candidateSmallIndels_check" value="True"/> | 153 <param name="candidateSmallIndels_check" value="True"/> |
175 <param name="somaticSV_check" value="True"/> | 154 <output name="candidateSmallIndels" file="candidateSmallIndels.vcf.gz" decompress="true" lines_diff="6"/> |
176 <output name="candidateSmallIndels" file="candidateSmallIndels.vcf.gz" decompress="true" lines_diff="4"/> | 155 <output name="somaticSV" file="somaticSV.vcf.gz" decompress="true" lines_diff="6"/> |
177 <output name="somaticSV" file="somaticSV.vcf.gz" decompress="true" lines_diff="4"/> | 156 </test> |
178 </test> | 157 <test> |
179 <test> | |
180 <param name="reference_source_selector" value="cached"/> | 158 <param name="reference_source_selector" value="cached"/> |
181 <param name="index" value="hg19"/> | 159 <param name="index" value="hg19"/> |
182 <param name="bam_input_selector" value="tumor_bam" dbkey="hg19"/> | 160 <param name="bam_input_selector" value="tumor_bam" dbkey="hg19"/> |
183 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> | 161 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> |
184 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> | 162 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> |
163 <param name="set_configuration_switch" value="Customized"/> | |
164 <param name="callMemMb" value="1000"/> | |
165 <param name="candidateSmallIndels_check" value="True"/> | |
166 <output name="candidateSmallIndels" file="candidateSmallIndels.vcf.gz" decompress="true" lines_diff="6"/> | |
167 <output name="somaticSV" file="somaticSV.vcf.gz" decompress="true" lines_diff="6"/> | |
168 </test> | |
169 <test> | |
170 <param name="reference_source_selector" value="cached"/> | |
171 <param name="index" value="hg19"/> | |
172 <param name="bam_input_selector" value="tumor_bam" dbkey="hg19"/> | |
173 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> | |
174 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> | |
185 <param name="set_configuration_switch" value="Default_config_file"/> | 175 <param name="set_configuration_switch" value="Default_config_file"/> |
186 <param name="callMemMb" value="1000"/> | 176 <param name="callMemMb" value="1000"/> |
187 <param name="candidateSmallIndels_check" value="True"/> | 177 <param name="candidateSmallIndels_check" value="True"/> |
188 <output name="candidateSmallIndels" file="candidateSmallIndels.vcf.gz" decompress="true" lines_diff="4"/> | 178 <output name="candidateSmallIndels" file="candidateSmallIndels.vcf.gz" decompress="true" lines_diff="6"/> |
179 <output name="somaticSV" file="somaticSV.vcf.gz" decompress="true" lines_diff="6"/> | |
189 </test> | 180 </test> |
190 <test> | 181 <test> |
191 <param name="reference_source_selector" value="history"/> | 182 <param name="reference_source_selector" value="history"/> |
192 <param name="ref_file" ftype="fasta" value="hg19_region.fa"/> | 183 <param name="ref_file" ftype="fasta" value="hg19_region.fa"/> |
193 <param name="bam_input_selector" value="tumor_bam"/> | 184 <param name="bam_input_selector" value="tumor_bam"/> |
194 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> | 185 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> |
195 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> | 186 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> |
196 <param name="set_configuration_switch" value="Default_config_file"/> | 187 <param name="set_configuration_switch" value="Default_config_file"/> |
197 <param name="callMemMb" value="1000"/> | 188 <param name="callMemMb" value="1000"/> |
198 <param name="candidateSV_check" value="True"/> | 189 <param name="candidateSV_check" value="True"/> |
199 <output name="candidateSV" file="candidateSV.vcf.gz" decompress="true" lines_diff="4"/> | 190 <output name="candidateSV" file="candidateSV.vcf.gz" decompress="true" lines_diff="6"/> |
191 <output name="somaticSV" file="somaticSV.vcf.gz" decompress="true" lines_diff="6"/> | |
200 </test> | 192 </test> |
201 <test> | 193 <test> |
202 <param name="reference_source_selector" value="history"/> | 194 <param name="reference_source_selector" value="history"/> |
203 <param name="ref_file" ftype="fasta" value="hg19_region.fa"/> | 195 <param name="ref_file" ftype="fasta" value="hg19_region.fa"/> |
204 <param name="bam_input_selector" value="tumor_bam"/> | 196 <param name="bam_input_selector" value="tumor_bam"/> |
205 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> | 197 <param name="normal_bam_file" ftype="bam" value="HCC1954_normal.bam"/> |
206 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> | 198 <param name="tumor_bam_file" ftype="bam" value="HCC1954_tumor.bam"/> |
207 <param name="set_configuration_switch" value="Default_config_file"/> | 199 <param name="set_configuration_switch" value="Default_config_file"/> |
208 <param name="callMemMb" value="1000"/> | 200 <param name="callMemMb" value="1000"/> |
209 <param name="candidateSmallIndels_check" value="True"/> | 201 <param name="candidateSmallIndels_check" value="True"/> |
210 <output name="candidateSmallIndels" file="candidateSmallIndels.vcf.gz" decompress="true" lines_diff="4"/> | 202 <output name="candidateSmallIndels" file="candidateSmallIndels.vcf.gz" decompress="true" lines_diff="6"/> |
211 </test> | 203 <output name="somaticSV" file="somaticSV.vcf.gz" decompress="true" lines_diff="6"/> |
212 </tests> | 204 </test> |
213 | 205 </tests> |
214 <help><![CDATA[ | 206 <help><![CDATA[ |
215 **Outputs** | 207 **Outputs** |
216 The primary Manta outputs are a set of VCF 4.1 files. Currently there are 3 VCF files | 208 The primary Manta outputs are a set of VCF 4.1 files. Currently there are 3 VCF files |
217 created for a germline analysis, and an additional somatic VCF is produced for a | 209 created for a germline analysis, and an additional somatic VCF is produced for a |
218 tumor/normal subtraction. These files are: | 210 tumor/normal subtraction. These files are: |
331 most compute intensive scatter-phase tasks of graph | 323 most compute intensive scatter-phase tasks of graph |
332 creation and candidate generation. | 324 creation and candidate generation. |
333 | 325 |
334 For further info see: https://github.com/Illumina/manta | 326 For further info see: https://github.com/Illumina/manta |
335 | 327 |
336 ]]></help> | 328 ]]></help> |
337 | |
338 <citations> | 329 <citations> |
339 <citation type="doi">10.1093/bioinformatics/btv710</citation> | 330 <citation type="doi">10.1093/bioinformatics/btv710</citation> |
340 </citations> | 331 </citations> |
341 | |
342 </tool> | 332 </tool> |