Mercurial > repos > devteam > picard
annotate picard_SamToFastq.xml @ 12:05087b27692a draft
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 7491208ca0c917a053798a48c3e54c3e30e95d92
| author | devteam |
|---|---|
| date | Sun, 27 Nov 2016 15:11:50 -0500 |
| parents | 5eaa8a968300 |
| children | 7e6fd3d0f16e |
| rev | line source |
|---|---|
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3a3234d7a2e8
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 00a7926c285bc4a339bd7deebf40b28f39c7d947-dirty
devteam
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1 <tool name="SamToFastq" id="picard_SamToFastq" version="@TOOL_VERSION@.0"> |
| 5 | 2 <description>extract reads and qualities from SAM/BAM dataset and convert to fastq</description> |
| 3 <macros> | |
| 4 <import>picard_macros.xml</import> | |
| 5 </macros> | |
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3a3234d7a2e8
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 00a7926c285bc4a339bd7deebf40b28f39c7d947-dirty
devteam
parents:
5
diff
changeset
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6 <expand macro="requirements" /> |
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05087b27692a
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 7491208ca0c917a053798a48c3e54c3e30e95d92
devteam
parents:
9
diff
changeset
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7 <command detect_errors="exit_code"><![CDATA[ |
| 5 | 8 |
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12
05087b27692a
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 7491208ca0c917a053798a48c3e54c3e30e95d92
devteam
parents:
9
diff
changeset
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9 echo "BAM" > $report && ## This is necessary for output dataset detection (see output tags below) |
| 5 | 10 |
| 11 @java_options@ | |
| 12 | |
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12
05087b27692a
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 7491208ca0c917a053798a48c3e54c3e30e95d92
devteam
parents:
9
diff
changeset
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13 picard |
| 5 | 14 SamToFastq |
| 15 | |
| 16 INPUT="${inputFile}" | |
| 17 | |
| 18 #if str( $output_per_rg ) == "true": | |
| 19 OUTPUT_PER_RG=true | |
| 20 OUTPUT_DIR=. | |
| 21 #elif str( $output_per_rg ) == "false" and str( $interleave ) == "false": | |
| 22 FASTQ=READ1.fastq | |
| 23 SECOND_END_FASTQ=READ2.fastq | |
| 24 UNPAIRED_FASTQ=UNPAIRED_READS.fastq | |
| 25 #elif str( $output_per_rg ) == "false" and str( $interleave ) == "true": | |
| 26 FASTQ=INTERLEAVED.fastq | |
| 27 #end if | |
| 28 | |
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9227b8c3093b
Updated command line format per dev team standards.
devteam <devteam@galaxyproject.org>
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29 RE_REVERSE="${re_reverse}" |
| 5 | 30 INTERLEAVE="${interleave}" |
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9227b8c3093b
Updated command line format per dev team standards.
devteam <devteam@galaxyproject.org>
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31 INCLUDE_NON_PF_READS="${include_non_pf_reads}" |
| 5 | 32 CLIPPING_ATTRIBUTE="${clipping_attribute}" |
| 33 CLIPPING_ACTION="${clipping_action}" | |
| 34 READ1_TRIM="${read1_trim}" | |
| 35 | |
| 36 #if int($read1_max_bases_to_write) > -1: | |
| 37 READ1_MAX_BASES_TO_WRITE="${read1_max_bases_to_write}" | |
| 0 | 38 #end if |
| 5 | 39 |
| 40 READ2_TRIM="${read2_trim}" | |
| 41 | |
| 42 #if int($read2_max_bases_to_write) > -1: | |
| 43 READ2_MAX_BASES_TO_WRITE="${read2_max_bases_to_write}" | |
| 0 | 44 #end if |
| 5 | 45 |
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9227b8c3093b
Updated command line format per dev team standards.
devteam <devteam@galaxyproject.org>
parents:
0
diff
changeset
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46 INCLUDE_NON_PRIMARY_ALIGNMENTS="${include_non_primary_alignments}" |
| 0 | 47 |
| 5 | 48 |
| 49 VALIDATION_STRINGENCY="${validation_stringency}" | |
| 50 QUIET=true | |
| 51 VERBOSITY=ERROR | |
| 52 | |
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12
05087b27692a
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 7491208ca0c917a053798a48c3e54c3e30e95d92
devteam
parents:
9
diff
changeset
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53 ]]></command> |
| 0 | 54 <inputs> |
| 55 | |
| 5 | 56 <param format="sam,bam" name="inputFile" type="data" label="Select SAM/BAM dataset or dataset collection" help="If empty, upload or import a SAM/BAM dataset"/> |
| 57 <param name="output_per_rg" type="boolean" checked="False" label="Do you want to output a fastq file per read group (two fastq files per read group if the group is paired)" help="OUTPUT_PER_RG; default=False"/> | |
| 58 <param name="re_reverse" type="boolean" checked="True" label="Re-reverse bases and qualities of reads with negative strand flag set before writing them to fastq" help="RE_REVERSE; default=True"/> | |
| 59 <param name="interleave" type="boolean" label="Will generate an interleaved fastq if paired, each line will have /1 or /2 to describe which end it came from" help="INTERLEAVE; default=False"/> | |
| 60 <param name="include_non_pf_reads" type="boolean" label="Include non-PF reads from the SAM/BAM dataset into the output FASTQ" help="INCLUDE_NON_PF_READS; PF means 'passes filtering'. Reads whose 'not passing quality controls' flag is set are non-PF reads; default=False"/> | |
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9
5eaa8a968300
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 1869970193a1878acbc0f8a79b81dd02b37f1dc1
devteam
parents:
8
diff
changeset
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61 <param name="clipping_attribute" type="text" value="null" label="The attribute that stores the position at which the SAM/BAM record should be clipped" help="CLIPPING_ATTRIBUTE; default=null"/> |
|
5eaa8a968300
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 1869970193a1878acbc0f8a79b81dd02b37f1dc1
devteam
parents:
8
diff
changeset
|
62 <param name="clipping_action" type="text" value="null" label="The action that should be taken with clipped reads: 'X' means the reads and qualities should be trimmed at the clipped position; 'N' means the bases should be changed to Ns in the clipped region; and any integer means that the base qualities should be set to that value in the clipped region" help="CLIPPING_ACTION; default=null"/> |
| 5 | 63 <param name="read1_trim" type="integer" value="0" min="0" label="The number of bases to trim from the beginning of read 1" help="READ1_TRIM; default=0"/> |
| 64 <param name="read1_max_bases_to_write" type="integer" value="-1" label="The maximum number of bases to write from read 1 after trimming" help="READ1_MAX_BASES_TO_WRITE; If there are fewer than this many bases left after trimming, all will be written. If this value is null then all bases left after trimming will be written; default=null (-1)"/> | |
| 65 <param name="read2_trim" type="integer" value="0" min="0" label="The number of bases to trim from the beginning of read 2" help="READ2_TRIM; default=0"/> | |
| 66 <param name="read2_max_bases_to_write" type="integer" value="-1" label="The maximum number of bases to write from read 2 after trimming" help="READ2_MAX_BASES_TO_WRITE; If there are fewer than this many bases left after trimming, all will be written. If this value is null then all bases left after trimming will be written; default=null (-1)"/> | |
| 67 <param name="include_non_primary_alignments" type="boolean" label="If true, include non-primary alignments in the output" help="INCLUDE_NON_PRIMARY_ALIGNMENTS; Support of non-primary alignments in SamToFastq is not comprehensive, so there may be exceptions if this is set to true and there are paired reads with non-primary alignments; default=False"/> | |
| 68 | |
| 69 <expand macro="VS" /> | |
| 70 | |
| 71 </inputs> | |
| 72 | |
| 0 | 73 <outputs> |
| 5 | 74 <!-- here dataset discovery is based on fact that if OUTPUT_PER_RG=true this tool automatically adds .fastq extension to emitted files --> |
| 75 <data format="txt" name="report" label="SamToFastq run" hidden="true"> | |
| 76 <discover_datasets pattern="(?P<designation>.+)\.fastq" ext="fastqsanger" visible="true"/> | |
| 0 | 77 </data> |
| 78 </outputs> | |
| 5 | 79 |
| 0 | 80 <tests> |
| 5 | 81 <test> |
| 82 <param name="inputFile" value="picard_SamToFastq.bam" ftype="bam"/> | |
| 83 <param name="output_per_rg" value="false"/> | |
| 84 <param name="re_reverse" value="true"/> | |
| 85 <param name="interleave" value="true"/> | |
| 86 <param name="include_non_pf_reads" value="false"/> | |
| 87 <param name="clipping_attribute" value="null" /> | |
| 88 <param name="clipping_action" value="null" /> | |
| 89 <param name="read1_trim" value="0" /> | |
| 90 <param name="read1_max_bases_to_write" value="-1"/> | |
| 91 <param name="read2_trim" value="0" /> | |
| 92 <param name="read2_max_bases_to_write" value="-1"/> | |
| 93 <param name="include_non_primary_alignments" value="false"/> | |
| 94 <output name="report"> | |
| 95 <assert_contents> | |
| 96 <has_line line="BAM" /> | |
| 97 </assert_contents> | |
| 98 <discovered_dataset designation="INTERLEAVED" file="picard_SamToFastq_test1.fq" ftype="fastqsanger"/> | |
| 99 </output> | |
| 100 </test> | |
| 0 | 101 </tests> |
| 5 | 102 |
| 103 | |
| 0 | 104 <help> |
| 105 | |
| 5 | 106 **Purpose** |
| 0 | 107 |
| 5 | 108 Extracts read sequences and qualities from the input SAM/BAM dataset and outputs them in Sanger fastq format. In the RE_REVERSE=True mode (default behavior), if the read is aligned and the alignment is to the reverse strand on the genome, the read's sequence from input SAM.BAM dataset will be reverse-complemented prior to writing it to fastq in order restore correctly the original read sequence as it was generated by the sequencer. |
| 0 | 109 |
| 5 | 110 ----- |
| 0 | 111 |
| 5 | 112 .. class:: warningmark |
| 0 | 113 |
| 5 | 114 **DANGER: Multiple Outputs** |
| 0 | 115 |
| 5 | 116 Generating per readgroup fastq (setting **OUTPUT_PER_RG** to True) may produce very large numbers of outputs. Know what you are doing! |
| 0 | 117 |
| 5 | 118 @dataset_collections@ |
| 0 | 119 |
| 5 | 120 @description@ |
| 0 | 121 |
| 5 | 122 FASTQ=File |
| 123 F=File Output fastq file (single-end fastq or, if paired, first end of the pair fastq). | |
| 124 Required. Cannot be used in conjuction with option(s) OUTPUT_PER_RG (OPRG) | |
| 125 | |
| 126 SECOND_END_FASTQ=File | |
| 127 F2=File Output fastq file (if paired, second end of the pair fastq). Default value: null. | |
| 128 Cannot be used in conjuction with option(s) OUTPUT_PER_RG (OPRG) | |
| 129 | |
| 130 UNPAIRED_FASTQ=File | |
| 131 FU=File Output fastq file for unpaired reads; may only be provided in paired-fastq mode Default | |
| 132 value: null. Cannot be used in conjuction with option(s) OUTPUT_PER_RG (OPRG) | |
| 133 | |
| 134 OUTPUT_PER_RG=Boolean | |
| 135 OPRG=Boolean Output a fastq file per read group (two fastq files per read group if the group is | |
| 136 paired). Default value: false. Possible values: {true, false} Cannot be used in | |
| 137 conjuction with option(s) SECOND_END_FASTQ (F2) UNPAIRED_FASTQ (FU) FASTQ (F) | |
| 138 | |
| 139 OUTPUT_DIR=File | |
| 140 ODIR=File Directory in which to output the fastq file(s). Used only when OUTPUT_PER_RG is true. | |
| 141 Default value: null. | |
| 142 | |
| 143 RE_REVERSE=Boolean | |
| 144 RC=Boolean Re-reverse bases and qualities of reads with negative strand flag set before writing them | |
| 145 to fastq Default value: true. Possible values: {true, false} | |
| 146 | |
| 147 INTERLEAVE=Boolean | |
| 148 INTER=Boolean Will generate an interleaved fastq if paired, each line will have /1 or /2 to describe | |
| 149 which end it came from Default value: false. Possible values: {true, false} | |
| 150 | |
| 151 INCLUDE_NON_PF_READS=Boolean | |
| 152 NON_PF=Boolean Include non-PF reads from the SAM file into the output FASTQ files. PF means 'passes | |
| 153 filtering'. Reads whose 'not passing quality controls' flag is set are non-PF reads. | |
| 154 Default value: false. Possible values: {true, false} | |
| 0 | 155 |
| 5 | 156 CLIPPING_ATTRIBUTE=String |
| 157 CLIP_ATTR=String The attribute that stores the position at which the SAM record should be clipped Default | |
| 158 value: null. | |
| 159 | |
| 160 CLIPPING_ACTION=String | |
| 161 CLIP_ACT=String The action that should be taken with clipped reads: 'X' means the reads and qualities | |
| 162 should be trimmed at the clipped position; 'N' means the bases should be changed to Ns in | |
| 163 the clipped region; and any integer means that the base qualities should be set to that | |
| 164 value in the clipped region. Default value: null. | |
| 165 | |
| 166 READ1_TRIM=Integer | |
| 167 R1_TRIM=Integer The number of bases to trim from the beginning of read 1. Default value: 0. | |
| 168 | |
| 169 READ1_MAX_BASES_TO_WRITE=Integer | |
| 170 R1_MAX_BASES=Integer The maximum number of bases to write from read 1 after trimming. If there are fewer than | |
| 171 this many bases left after trimming, all will be written. If this value is null then all | |
| 172 bases left after trimming will be written. Default value: null. | |
| 173 | |
| 174 READ2_TRIM=Integer | |
| 175 R2_TRIM=Integer The number of bases to trim from the beginning of read 2. Default value: 0. | |
| 176 | |
| 177 READ2_MAX_BASES_TO_WRITE=Integer | |
| 178 R2_MAX_BASES=Integer The maximum number of bases to write from read 2 after trimming. If there are fewer than | |
| 179 this many bases left after trimming, all will be written. If this value is null then all | |
| 180 bases left after trimming will be written. Default value: null. | |
| 181 | |
| 182 INCLUDE_NON_PRIMARY_ALIGNMENTS=Boolean | |
| 183 If true, include non-primary alignments in the output. Support of non-primary alignments | |
| 184 in SamToFastq is not comprehensive, so there may be exceptions if this is set to true and | |
| 185 there are paired reads with non-primary alignments. Default value: false. | |
| 186 Possible values: {true, false} | |
| 187 | |
| 188 @more_info@ | |
| 0 | 189 |
| 190 </help> | |
| 191 </tool> | |
| 5 | 192 |
| 193 |