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annotate picard_SamToFastq.xml @ 19:5053a18d9bc8 draft

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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/picard commit 7036343b9ac0a0ffc2ce4f6db465b9298ef05e73
author iuc
date Mon, 16 Apr 2018 21:27:29 -0400
parents 465cbb0cf2eb
children 2a17c789e0a5
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1 <tool name="SamToFastq" id="picard_SamToFastq" version="@TOOL_VERSION@.@WRAPPER_VERSION@">
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2 <description>extract reads and qualities from SAM/BAM dataset and convert to fastq</description>
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3 <macros>
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4 <import>picard_macros.xml</import>
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5 <token name="@WRAPPER_VERSION@">0</token>
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6 </macros>
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7 <expand macro="requirements" />
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8 <command detect_errors="exit_code"><![CDATA[
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9
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10 echo "BAM" > $report && ## This is necessary for output dataset detection (see output tags below)
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12 @java_options@
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13 @symlink_element_identifier@
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15 picard
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16 SamToFastq
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18 INPUT='$escaped_element_identifier'
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19
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20 #if str( $output_per_rg ) == "true":
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21 OUTPUT_PER_RG=true
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22 OUTPUT_DIR=.
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23 #elif str( $output_per_rg ) == "false" and str( $interleave ) == "false":
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24 FASTQ=READ1.fastq
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25 SECOND_END_FASTQ=READ2.fastq
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26 UNPAIRED_FASTQ=UNPAIRED_READS.fastq
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27 #elif str( $output_per_rg ) == "false" and str( $interleave ) == "true":
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28 FASTQ=INTERLEAVED.fastq
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29 #end if
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30
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31 RE_REVERSE="${re_reverse}"
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32 INTERLEAVE="${interleave}"
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33 INCLUDE_NON_PF_READS="${include_non_pf_reads}"
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34 CLIPPING_ATTRIBUTE="${clipping_attribute}"
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35 CLIPPING_ACTION="${clipping_action}"
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36 READ1_TRIM="${read1_trim}"
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37
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38 #if int($read1_max_bases_to_write) > -1:
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39 READ1_MAX_BASES_TO_WRITE="${read1_max_bases_to_write}"
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40 #end if
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41
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42 READ2_TRIM="${read2_trim}"
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43
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44 #if int($read2_max_bases_to_write) > -1:
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45 READ2_MAX_BASES_TO_WRITE="${read2_max_bases_to_write}"
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46 #end if
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47
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48 INCLUDE_NON_PRIMARY_ALIGNMENTS="${include_non_primary_alignments}"
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50
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51 VALIDATION_STRINGENCY="${validation_stringency}"
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52 QUIET=true
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53 VERBOSITY=ERROR
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54
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55 ]]></command>
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56 <inputs>
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57
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58 <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"/>
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59 <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"/>
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60 <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"/>
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61 <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"/>
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62 <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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63 <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"/>
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64 <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"/>
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65 <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"/>
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66 <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)"/>
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67 <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"/>
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68 <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)"/>
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69 <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"/>
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70
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71 <expand macro="VS" />
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73 </inputs>
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74
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75 <outputs>
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76 <!-- here dataset discovery is based on fact that if OUTPUT_PER_RG=true this tool automatically adds .fastq extension to emitted files -->
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77 <data format="txt" name="report" label="SamToFastq run" hidden="true">
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78 <discover_datasets pattern="(?P&lt;designation&gt;.+)\.fastq" ext="fastqsanger" visible="true"/>
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79 </data>
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80 </outputs>
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81
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82 <tests>
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83 <test>
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84 <param name="inputFile" value="picard_SamToFastq.bam" ftype="bam"/>
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85 <param name="output_per_rg" value="false"/>
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86 <param name="re_reverse" value="true"/>
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87 <param name="interleave" value="true"/>
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88 <param name="include_non_pf_reads" value="false"/>
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89 <param name="clipping_attribute" value="null" />
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90 <param name="clipping_action" value="null" />
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91 <param name="read1_trim" value="0" />
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92 <param name="read1_max_bases_to_write" value="-1"/>
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93 <param name="read2_trim" value="0" />
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94 <param name="read2_max_bases_to_write" value="-1"/>
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95 <param name="include_non_primary_alignments" value="false"/>
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96 <output name="report">
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97 <assert_contents>
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98 <has_line line="BAM" />
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99 </assert_contents>
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100 <discovered_dataset designation="INTERLEAVED" file="picard_SamToFastq_test1.fq" ftype="fastqsanger"/>
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101 </output>
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102 </test>
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103 </tests>
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105
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106 <help>
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107
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108 **Purpose**
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109
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110 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.
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111
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112 -----
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113
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114 .. class:: warningmark
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115
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116 **DANGER: Multiple Outputs**
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117
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118 Generating per readgroup fastq (setting **OUTPUT_PER_RG** to True) may produce very large numbers of outputs. Know what you are doing!
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119
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120 @dataset_collections@
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121
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122 @description@
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123
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124 FASTQ=File
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125 F=File Output fastq file (single-end fastq or, if paired, first end of the pair fastq).
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126 Required. Cannot be used in conjuction with option(s) OUTPUT_PER_RG (OPRG)
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127
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128 SECOND_END_FASTQ=File
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129 F2=File Output fastq file (if paired, second end of the pair fastq). Default value: null.
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130 Cannot be used in conjuction with option(s) OUTPUT_PER_RG (OPRG)
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131
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132 UNPAIRED_FASTQ=File
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133 FU=File Output fastq file for unpaired reads; may only be provided in paired-fastq mode Default
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134 value: null. Cannot be used in conjuction with option(s) OUTPUT_PER_RG (OPRG)
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135
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136 OUTPUT_PER_RG=Boolean
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137 OPRG=Boolean Output a fastq file per read group (two fastq files per read group if the group is
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138 paired). Default value: false. Possible values: {true, false} Cannot be used in
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139 conjuction with option(s) SECOND_END_FASTQ (F2) UNPAIRED_FASTQ (FU) FASTQ (F)
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140
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141 OUTPUT_DIR=File
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142 ODIR=File Directory in which to output the fastq file(s). Used only when OUTPUT_PER_RG is true.
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143 Default value: null.
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144
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145 RE_REVERSE=Boolean
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146 RC=Boolean Re-reverse bases and qualities of reads with negative strand flag set before writing them
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147 to fastq Default value: true. Possible values: {true, false}
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148
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149 INTERLEAVE=Boolean
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150 INTER=Boolean Will generate an interleaved fastq if paired, each line will have /1 or /2 to describe
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151 which end it came from Default value: false. Possible values: {true, false}
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152
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153 INCLUDE_NON_PF_READS=Boolean
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154 NON_PF=Boolean Include non-PF reads from the SAM file into the output FASTQ files. PF means 'passes
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155 filtering'. Reads whose 'not passing quality controls' flag is set are non-PF reads.
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156 Default value: false. Possible values: {true, false}
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157
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158 CLIPPING_ATTRIBUTE=String
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159 CLIP_ATTR=String The attribute that stores the position at which the SAM record should be clipped Default
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160 value: null.
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161
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162 CLIPPING_ACTION=String
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163 CLIP_ACT=String The action that should be taken with clipped reads: 'X' means the reads and qualities
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164 should be trimmed at the clipped position; 'N' means the bases should be changed to Ns in
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165 the clipped region; and any integer means that the base qualities should be set to that
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166 value in the clipped region. Default value: null.
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167
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168 READ1_TRIM=Integer
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169 R1_TRIM=Integer The number of bases to trim from the beginning of read 1. Default value: 0.
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170
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171 READ1_MAX_BASES_TO_WRITE=Integer
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172 R1_MAX_BASES=Integer The maximum number of bases to write from read 1 after trimming. If there are fewer than
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173 this many bases left after trimming, all will be written. If this value is null then all
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174 bases left after trimming will be written. Default value: null.
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175
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176 READ2_TRIM=Integer
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177 R2_TRIM=Integer The number of bases to trim from the beginning of read 2. Default value: 0.
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178
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179 READ2_MAX_BASES_TO_WRITE=Integer
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180 R2_MAX_BASES=Integer The maximum number of bases to write from read 2 after trimming. If there are fewer than
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181 this many bases left after trimming, all will be written. If this value is null then all
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182 bases left after trimming will be written. Default value: null.
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183
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184 INCLUDE_NON_PRIMARY_ALIGNMENTS=Boolean
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185 If true, include non-primary alignments in the output. Support of non-primary alignments
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186 in SamToFastq is not comprehensive, so there may be exceptions if this is set to true and
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187 there are paired reads with non-primary alignments. Default value: false.
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188 Possible values: {true, false}
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189
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190 @more_info@
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191
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192 </help>
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193 <expand macro="citations" />
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194 </tool>