Previous changeset 0:2ac846969812 (2014-06-27) Next changeset 2:b007d9642911 (2015-07-16) |
Commit message:
planemo upload for repository https://github.com/lparsons/galaxy_tools/tree/master/tools/fastq_join commit 394834f8f34909961cfbf6252fefbdc63342d78d |
modified:
README.txt fastq-join.xml |
removed:
test-data/test.sam test-data/testout.txt |
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diff -r 2ac846969812 -r 593a729e5706 README.txt --- a/README.txt Fri Jun 27 15:39:38 2014 -0400 +++ b/README.txt Mon Jul 13 11:45:19 2015 -0400 |
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@@ -1,19 +1,18 @@ -== fastq-join Galaxy Wrapper == +== fastq-join Galaxy Wrapper == -This is a Galaxy wrapper for the fastq-join tool from ea-utils suite. +This is a Galaxy wrapper for the fastq-join tool from ea-utils suite. -** Installation ** +** Installation ** -Installation from a tool shed provides the necessary tool dependencies. +Installation from a tool shed provides the necessary tool dependencies. -Otherwise, make sure fastq-join is in the path. -Move the test data files to your galaxy root test-data. -Move the xml files to a subdirectory of your tools directory and add lines in tool_conf.xml to point to them. -Restart the Galaxy server. +Otherwise, make sure fastq-join is in the path. +Move the test data files to your galaxy root test-data. +Move the xml files to a subdirectory of your tools directory and add lines in tool_conf.xml to point to them. +Restart the Galaxy server. -** Attribution ** +** Attribution ** -The ea-utils package and associated documentation can be found at: http://code.google.com/p/ea-utils/ +The ea-utils package and associated documentation can be found at: http://code.google.com/p/ea-utils/ -The galaxy wrapper code was written by Lance Parsons (lparsons@princeton.edu), Lewis-Sigler Institute for Integrative Genomics, Princeton University. -The code is housed on BitBucket at: https://bitbucket.org/lance_parsons/ea_utils_galaxy_wrapper +The galaxy wrapper code was written by Lance Parsons (lparsons@princeton.edu), Lewis-Sigler Institute for Integrative Genomics, Princeton University. |
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diff -r 2ac846969812 -r 593a729e5706 fastq-join.xml --- a/fastq-join.xml Fri Jun 27 15:39:38 2014 -0400 +++ b/fastq-join.xml Mon Jul 13 11:45:19 2015 -0400 |
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@@ -1,10 +1,16 @@ -<tool id="fastq_join" name="fastq-join" version="1.1.2-484"> - <description> - Joins paired-end reads on the overlapping ends</description> +<tool id="fastq_join" name="fastq-join" version="0.1.1"> + <description> - Joins two paired-end reads on the overlapping ends</description> + <requirements> <requirement type="package" version="1.1.2-484">ea-utils</requirement> </requirements> - <command> - fastq-join + + <stdio> + <exit_code range="1:" level="fatal" description="Unknown error occurred" /> + </stdio> + + <command><![CDATA[ + fastq-join -v '$splitChar' -p $pctMaxDiff -m $minOverlap @@ -13,8 +19,10 @@ #end if $read1 $read2 - -o $outputUnmatched1 -o $outputUnmatched2 -o $outputJoined + -o $outputUnmatched1 -o $outputUnmatched2 -o $outputJoined + ]]> </command> + <inputs> <param format="fastq, fastqillumina, fastqsanger, fastqsolexa" name="read1" type="data" label="Read 1 Fastq" /> <param format="fastq, fastqillumina, fastqsanger, fastqsolexa" name="read2" type="data" label="Read 2 Fastq" /> @@ -25,18 +33,14 @@ </inputs> <outputs> - <data format="input" format_source="read1" name="outputJoined" label="${tool.name} on ${on_string} (joined)"/> - <data format="input" format_source="read1" name="outputUnmatched1" label="${tool.name} on ${on_string} (unmatched1)"/> - <data format="input" format_source="read2" name="outputUnmatched2" label="${tool.name} on ${on_string} (unmatched2)"/> + <data format_source="read1" name="outputJoined" label="${tool.name} on ${on_string} (joined)"/> + <data format_source="read1" name="outputUnmatched1" label="${tool.name} on ${on_string} (unmatched1)"/> + <data format_source="read2" name="outputUnmatched2" label="${tool.name} on ${on_string} (unmatched2)"/> <data format="tabular" name="outputStitchLengthReport" label="${tool.name} on ${on_string} (stitch length report)"> <filter>stitchLengthReport</filter> </data> </outputs> - <stdio> - <exit_code range="1:" level="fatal" description="Unknown error occurred" /> - </stdio> - <tests> <test> <param name="read1" value="test_read1.fastq" /> @@ -47,7 +51,7 @@ </test> </tests> - <help> + <help><![CDATA[ Overview -------- fastq-join joins two paired-end reads on the overlapping ends. @@ -61,5 +65,27 @@ Verbose stitch length report is a report for each joined paired of reads showing how large the overlapping section was. This tool uses sqr(distance)/len for anchored alignment quality algorithm. It's a good measure of anchored alignment quality, akin to squared-deviation for means. This tool uses the fastq-join program that is part of the ea-utils suite. See http://code.google.com/p/ea-utils/wiki/FastqJoin for details. +]]> </help> + + <citations> + <citation type="bibtex"> + @article{aronesty_comparison_2013, + title = {Comparison of {Sequencing} {Utility} {Programs}}, + volume = {7}, + issn = {18750362}, + url = {http://benthamopen.com/ABSTRACT/TOBIOIJ-7-1}, + doi = {10.2174/1875036201307010001}, + language = {en}, + number = {1}, + urldate = {2015-07-10}, + journal = {The Open Bioinformatics Journal}, + author = {Aronesty, Erik}, + month = jan, + year = {2013}, + pages = {1--8} + } + </citation> + </citations> + </tool> |
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diff -r 2ac846969812 -r 593a729e5706 test-data/test.sam --- a/test-data/test.sam Fri Jun 27 15:39:38 2014 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 |
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b'@@ -1,100 +0,0 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diff -r 2ac846969812 -r 593a729e5706 test-data/testout.txt --- a/test-data/testout.txt Fri Jun 27 15:39:38 2014 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 |
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@@ -1,29 +0,0 @@ -reads 100 -version 1.32 -mapped reads 11 -mapped bases 377 -phred 33 -forward 0 -reverse 11 -len max 48 -len mean 34.2727 -len stdev 9.4137 -mapq mean 255.0000 -mapq stdev 0.0000 -mapq Q1 255.00 -mapq median 255.00 -mapq Q3 255.00 -snp rate 0.000000 -pct mismatch 0.0000 -base qual mean 31.5650 -base qual stdev 3.2627 -%A 27.5862 -%C 34.4828 -%G 16.7109 -%T 21.2202 -%PCRPRIMER1 8.753316 -%PCRPRIMER1+1 45.358090 -%PCRPRIMER1+2 9.814324 -%PCRPRIMER2+1 36.074271 -num ref seqs 4 -num ref aligned 4 |