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annotate repenrich.xml @ 4:d359ec9f0fe1 draft

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planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/repenrich commit 0ec9810f3c05456fa8f19329a56eb1db32e218e5
author drosofff
date Tue, 30 May 2017 19:52:36 -0400
parents 1805b262c12d
children ea5bba2c569f
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d359ec9f0fe1 planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/repenrich commit 0ec9810f3c05456fa8f19329a56eb1db32e218e5
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1 <tool id="repenrich" name="RepEnrich" version="1.2.0">
0
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2 <description>Repeat Element Profiling</description>
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3 <requirements>
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4 <requirement type="package" version="1.2.0">bowtie</requirement>
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5 <requirement type="package" version="0.1.19">samtools</requirement>
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6 <requirement type="package" version="2.20.1">bedtools</requirement>
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7 <requirement type="package" version="1.69">biopython</requirement>
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8 </requirements>
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9 <stdio>
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10 <exit_code range="1:" level="fatal" description="Tool exception" />
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11 </stdio>
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12 <command detect_errors="exit_code"><![CDATA[
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13 #import re
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14 #set input_base = 'Sample'
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15 #set baseReference = 'Genome'
0
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16 ln -f -s '$genome' '${baseReference}.fa' &&
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17 ln -f -s '$input_fastq' '${input_base}.fastq' &&
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18 #if $seq_method.seq_method_list == "paired-end":
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19 ln -f -s '$input2_fastq' '${input_base}_2.fastq' &&
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20 #end if
0
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21 bowtie-build '$genome' ${baseReference} &&
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22 python $__tool_directory__/RepEnrich_setup.py $repeatmasker ${baseReference}.fa setup_folder_${baseReference} &&
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23 #if $seq_method.seq_method_list == "single-read":
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24 bowtie $baseReference -p \${GALAXY_SLOTS:-4} -t -m 1 -S --max ${input_base}_multimap.fastq ${input_base}.fastq ${input_base}_unique.sam 2>bowtie_alignments.txt &&
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25 TOTAL=\$(grep 'reads processed:' bowtie_alignments.txt | cut -d ' ' -f 4) &&
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26 NONALIGNED=\$(grep 'reads that failed to align:' bowtie_alignments.txt | cut -d ' ' -f 7) &&
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27 echo \$((\$TOTAL-\$NONALIGNED)) > bowtie_aligned.numb &&
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28 #else:
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29 bowtie $baseReference -p \${GALAXY_SLOTS:-4} -t -m 1 -S --max ${input_base}_multimap.fastq -1 ${input_base}.fastq -2 ${input_base}_2.fastq ${input_base}_unique.sam 2>bowtie_alignments.txt &&
d359ec9f0fe1 planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/repenrich commit 0ec9810f3c05456fa8f19329a56eb1db32e218e5
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30 TOTAL=\$(grep 'reads processed:' bowtie_alignments.txt | cut -d ' ' -f 4) &&
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31 NONALIGNED=\$(grep 'reads that failed to align:' bowtie_alignments.txt | cut -d ' ' -f 7) &&
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32 echo \$((\$TOTAL-\$NONALIGNED)) > bowtie_aligned.numb &&
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33 #end if
0
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34 samtools view -bS ${input_base}_unique.sam > ${input_base}_unique.bam &&
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35 samtools sort ${input_base}_unique.bam ${input_base}_unique_sorted &&
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36 mv ${input_base}_unique_sorted.bam ${input_base}_unique.bam &&
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37 samtools index ${input_base}_unique.bam &&
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38 rm ${input_base}_unique.sam &&
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39 #if $seq_method.seq_method_list == "single-read":
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40 python $__tool_directory__/RepEnrich.py $repeatmasker ${input_base} ${input_base} setup_folder_${baseReference} ${input_base}_multimap.fastq ${input_base}_unique.bam --cpus "\${GALAXY_SLOTS:-4}" &&
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41 #else:
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42 python $__tool_directory__/RepEnrich.py $repeatmasker ${input_base} ${input_base} setup_folder_${baseReference} ${input_base}_multimap_1.fastq --fastqfile2 ${input_base}_multimap_2.fastq ${input_base}_unique.bam --cpus "\${GALAXY_SLOTS:-4}" --pairedend TRUE &&
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43 #end if
0
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44 cp $input_base/${input_base}_class_fraction_counts.txt class_fraction_counts.tabular &&
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45 cp $input_base/${input_base}_family_fraction_counts.txt family_fraction_counts.tabular &&
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46 cp $input_base/${input_base}_fraction_counts.txt fraction_counts.tabular
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47 ]]></command>
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48 <!-- basic error handling -->
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49 <inputs>
4
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50 <conditional name="seq_method">
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51 <param help="Paired-end or single-read sequencing" label="Sequencing method" name="seq_method_list" type="select">
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52 <option selected="True" value="single-read">Single-read sequencing</option>
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53 <option value="paired-end">Paired-end sequencing</option>
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54 </param>
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55 <when value="single-read">
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56 <param format="fastq,fastqsanger" label="Single-reads" name="input_fastq" type="data" help="accepted formats: fastq, fastqsanger" />
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57 </when>
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58 <when value="paired-end">
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59 <param format="fastq,fastqsanger" label="1st paired-end sequencing dataset" name="input_fastq" type="data" help="accepted formats: fastq, fastqsanger" />
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60 <param format="fastq,fastqsanger" label="2nd paired-end sequencing dataset" name="input2_fastq" type="data" help="accepted formats: fastq, fastqsanger" />
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61 </when>
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62 </conditional>
0
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63 <param format="fasta" label="Reference genome in fasta format" name="genome" type="data" />
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64 <param format="txt" label="RepeatMasker description file" name="repeatmasker" type="data" help="see help section"/>
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65 </inputs>
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66
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67 <outputs>
1
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68 <data format="tabular" name="bowtie_alignments" label="RepEnrich on ${on_string}: reads aligned" from_work_dir="bowtie_aligned.numb">
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69 </data>
0
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70 <data format="tabular" name="class_fraction_counts" label="RepEnrich on ${on_string}: class fraction counts" from_work_dir="class_fraction_counts.tabular">
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71 </data>
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72 <data format="tabular" name="family_fraction_counts" label="RepEnrich on ${on_string}: family fraction counts" from_work_dir="family_fraction_counts.tabular">
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73 </data>
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74 <data format="tabular" name="fraction_counts" label="RepEnrich on ${on_string}: fraction counts" from_work_dir="fraction_counts.tabular">
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75 </data>
4
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76 <data format="tabular" name="bowtieoutput" label="bowtie aligments" from_work_dir="bowtie_alignments.txt">
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77 </data>
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78 </outputs>
0
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79
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80 <tests>
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81 <test>
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82 <param name="seq_method_list" value="single-read"/>
0
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83 <param name="input_fastq" value="Samp.fastq" ftype="fastq"/>
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84 <param name="genome" value="chrM.fa" ftype="fasta"/>
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85 <param name="repeatmasker" value="chrM_repeatmasker.txt" ftype="txt"/>
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86 <output name="bowtie_alignments" file="aligned_reads.tab" ftype="tabular"/>
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87 <output name="class_fraction_counts" file="Samp_class_fraction_counts.tabular" ftype="tabular"/>
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88 <output name="family_fraction_counts" file="Samp_family_fraction_counts.tabular" ftype="tabular"/>
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89 <output name="fraction_counts" file="Samp_fraction_counts.tabular" ftype="tabular"/>
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90 </test>
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91 </tests>
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92
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93 <help>
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94
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95 **What it does**
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96
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97 Reads are mapped to the genome using the Bowtie1 aligner. Reads mapping uniquely to the genome are assigned to subfamilies of repetitive elements based on their degree of overlap to RepeatMasker annotated genomic instances of each repetitive element subfamily. Reads mapping to multiple locations are separately mapped to repetitive element assemblies – referred to as repetitive element psuedogenomes – built from RepeatMasker annotated genomic instances of repetitive element subfamilies. RepEnrich then return tables of counts merged from both strategies, that can be further processed in statistical analysis for differential expression. For detailed information see the `original publication`_.
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98
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99 .. _original publication: https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-15-583
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100
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101 **Inputs**
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102
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103 *Reference genome* : reference genome in fasta format
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104
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105 *Sequencing dataset*: Single-reads sequencing dataset. Paired-end sequencing dataset in not implemented yet
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106
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107 *RepeatMasker description file*: a txt repeatmasker file which can be downloaded from http://www.repeatmasker.org/genomicDatasets/RMGenomicDatasets.html
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108
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109 This file looks like:
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110
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111 <![CDATA[
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112
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113 SW perc perc perc query position in query matching repeat position in repeat
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114
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115 score div. del. ins. sequence begin end (left) repeat class/family begin end (left) ID
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116
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117 16 20.2 5.9 0.0 chrM 1211 1261 (18263) + (TTTTA)n Simple_repeat 1 54 (0) 84486
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118
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119 13 23.9 2.2 2.2 chrM 2014 2059 (17465) + (TTA)n Simple_repeat 1 46 (0) 84487
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120
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121 24 18.8 5.3 2.6 chrM 3924 3999 (15525) + (TAT)n Simple_repeat 1 78 (0) 84488
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122
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123 18 4.5 0.0 0.0 chrM 5961 5983 (13541) + (AT)n Simple_repeat 1 23 (0) 84489
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124
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125 13 25.9 4.0 4.0 chrM 6247 6320 (13204) + (ATTTAT)n Simple_repeat 1 74 (0) 84490
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126
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127 11 14.6 7.5 2.4 chrM 8783 8822 (10702) + (CTAATT)n Simple_repeat 1 42 (0) 84491
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128
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129 17 19.0 0.0 8.6 chrM 9064 9126 (10398) + A-rich Low_complexity 1 58 (0) 84492
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130
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131 13 21.0 5.9 1.9 chrM 11723 11773 (7751) + (ATA)n Simple_repeat 1 53 (0) 84493
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132
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133 66 20.4 12.3 12.3 chrM 12823 13001 (6523) C LSU-rRNA_Cel rRNA (1) 2431 2253 84494
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134
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135 16 16.6 0.0 2.9 chrM 14361 14396 (5128) + (ATT)n Simple_repeat 1 35 (0) 84495
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136
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137 44 2.4 0.0 0.0 chrM 15966 16007 (3517) + (TA)n Simple_repeat 1 42 (0) 84496
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138
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139 35 5.3 0.0 0.0 chrM 16559 16597 (2927) + (AT)n Simple_repeat 1 39 (0) 84497
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141 36 2.9 0.0 0.0 chrM 16922 16956 (2568) + (AT)n Simple_repeat 1 35 (0) 84498
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142
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143 37 0.0 0.0 0.0 chrM 17040 17071 (2453) + (TA)n Simple_repeat 1 32 (0) 84499
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145 20 4.3 0.0 0.0 chrM 17417 17440 (2084) + (T)n Simple_repeat 1 24 (0) 84500
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146
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147 31 6.9 6.3 1.5 chrM 17451 17513 (2011) + (TA)n Simple_repeat 1 66 (0) 84501
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148
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149 26 17.0 0.0 0.0 chrM 19469 19514 (10) + A-rich Low_complexity 1 46 (0) 84502
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150
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151 ]]>
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152
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153 Users may filter this file so that it contains only desired items (for instance only satellites, repeats and transposons)
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154
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155 **Outputs**
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156
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157 (1) Fraction counts, (2) Family fraction counts and (3) Class fraction counts are returned in tabular format, for further statistical tests differential expression analysis or graphics
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158
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159 **RepEnrich**
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160
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161 This Galaxy tool is a wrapper of the RepEnrich tool by steven_criscione@brown.edu et al. whose code and manual are available in `GitHub`_.
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162
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163 .. _GitHub: https://github.com/nskvir/RepEnrich
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164
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165 Python scripts RepEnrich.py and RepEnrich_setup.py have been adapted to python 3. Note that sorting of Fraction counts, Family fraction counts and Class fraction counts is different with this Galaxy wrapper or with RepEnrich as found in the `RepEnrich code repository`_. However, this different sorting does not affect subsequent statistical analyses
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166
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167 .. _RepEnrich code repository: https://github.com/nskvir/RepEnrich
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168
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169 **Execution time**
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170
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171 .. class:: warningmark
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172
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173 This tool includes steps to index the reference genome, index repeat sequences and align reads to these indexes. Therefore the run time may be **long to very long**.
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174
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175 .. class:: infomark
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176
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177 For more information on the tools, please visit our `code repository`_.
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178
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179 If you would like to give us feedback or you run into any trouble, please send an email to artbio.ibps@gmail.com
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180
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181 This tool wrapper is developed by the `ARTbio team`_ at the `Institut de Biologie Paris Seine (IBPS)`_.
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182
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183 .. _code repository: https://github.com/ARTbio/tools-artbio/tree/master/tools/
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184 .. _ARTbio team: http://artbio.fr
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185 .. _Institut de Biologie Paris Seine (IBPS): http://www.ibps.upmc.fr/en/core-facilities/bioinformatics
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186
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187 </help>
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188
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189 <citations>
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190 <citation type="doi">10.1186/1471-2164-15-583</citation>
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191 </citations>
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192 </tool>