Mercurial > repos > hackdna > fastqc
diff fastqc_checker.xml @ 0:d8d131d08779 draft default tip
Initial upload.
author | hackdna |
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date | Tue, 21 May 2013 11:48:53 -0400 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/fastqc_checker.xml Tue May 21 11:48:53 2013 -0400 @@ -0,0 +1,57 @@ +<tool id="fastqc_checker_1" name="FastQC checker" version="1.0.0"> + <description>for quality control of high throughput sequence data</description> + + <command interpreter="python"> + fastqc_checker.py -e ${GALAXY_DATA_INDEX_DIR}/shared/jars/FastQC/fastqc -o $output $input + </command> + + <inputs> + <param format="fastq" name="input" type="data" label="Source files" multiple="true"/> + </inputs> + <outputs> + <data format="txt" name="output"/> + </outputs> + + <help> + +.. class:: infomark + +**Purpose** + +FastQC aims to provide a simple way to do some quality control checks on raw +sequence data coming from high throughput sequencing pipelines. +It provides a modular set of analyses which you can use to give a quick +impression of whether your data has any problems of +which you should be aware before doing any further analysis. + +**FastQC documentation** + +This is a Galaxy interface to the external package FastQC_. +Specific documentation on FastQC can be found on that site. + + .. _FastQC: http://www.bioinformatics.bbsrc.ac.uk/projects/fastqc/ + +----- + +.. class:: infomark + +**Inputs and outputs** + +This wrapper will accept one or more fastq files. + +The tool produces a single output file that contains summary of all the results, including the following: + +- Basic Statistics +- Per base sequence quality +- Per sequence quality scores +- Per base sequence content +- Per base GC content +- Per sequence GC content +- Per base N content +- Sequence Length Distribution +- Sequence Duplication Levels +- Overrepresented sequences +- Kmer Content + + </help> +</tool>