Mercurial > repos > edward-kirton > phrap
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Migrated tool version 1.0.0 from old tool shed archive to new tool shed repository
author | edward-kirton |
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date | Tue, 07 Jun 2011 17:41:56 -0400 |
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<tool id="phrap" name="Phrap" version="1.0.0"> <description>Assemble long reads/short contigs</description> <command interpreter='bash'>phrap_wrapper.sh $label $fasta_infile $qual_infile $fasta_outfile $qual_outfile $singlets_outfile $fasta_outfile.extra_files_path</command> <inputs> <param name="label" type="text" value="seqs" label="Label for naming contig sequences (e.g. library or sample name)" help="Contigs will be named LABEL.Contig1, ..." /> <param name="fasta_infile" type="data" format="fasta" label="Long reads or contig sequences" /> <param name="qual_infile" type="data" format="qual" optional='True' label="Optional sequence quality scores (Phred-scaled)" /> </inputs> <outputs> <data name="fasta_outfile" format="fasta" /> <data name="qual_outfile" format="qual" label="Contig quality scores" /> <data name="singlets_outfile" format="fasta" label="Singlets Fasta" /> </outputs> <help> **What it does** phrap ("phragment assembly program", or "phil's revised assembly program"; a homonym of "frappe" = French for "swat") -- a program for assembling shotgun DNA sequence data. Key features: allows use of entire read (not just trimmed high quality part); uses a combination of user-supplied and internally computed data quality information to improve accuracy of assembly in the presence of repeats; constructs contig sequence as a mosaic of the highest quality parts of reads (rather than a consensus); provides extensive information about assembly (including quality values for contig sequence) to assist trouble-shooting; able to handle very large datasets. **Notes** phrap is great for assembling Sanger shotgun reads but should not be used for next-generation data (e.g. Illumina, Solid, 454, etc.). However phrap is useful for combining short-read assemblies from Velvet or Abyss (i.e. results from using multiple k-mer parameters). When used for this purpose, you should filter out short sequences first (e.g. less than 200-1000bp, depending on number of contigs). **Reference** http://www.phrap.org/phredphrap/phrap.html </help> </tool>