Mercurial > repos > mvdbeek > generate_sliding_windows
changeset 4:cb2d94bb6772 draft
Uploaded
author | mvdbeek |
---|---|
date | Wed, 15 Apr 2015 09:08:37 -0400 |
parents | 3dcce035dd6c |
children | 79e43a3b0883 |
files | generate_sliding_windows.xml tool-data/all_fasta.loc.sample tool_data_table_conf.xml.sample |
diffstat | 3 files changed, 41 insertions(+), 2 deletions(-) [+] |
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--- a/generate_sliding_windows.xml Wed Apr 15 07:57:55 2015 -0400 +++ b/generate_sliding_windows.xml Wed Apr 15 09:08:37 2015 -0400 @@ -1,4 +1,4 @@ -<tool id="generate_sliding_windows" name="generate_sliding_windows" version="0.1.2"> +<tool id="generate_sliding_windows" name="generate_sliding_windows" version="0.1.3"> <description>Split fasta sequence in nucleotide windows</description> <requirements> <requirement type="package" version="1.65">biopython</requirement> @@ -11,7 +11,21 @@ generate_sliding_windows.py --input "$input" --output "$output" --window $window --step $step ]]></command> <inputs> - <param type="data" name="input" label="input fasta file" help="select fasta file for which you wish to generate a multi-fasta file in a sliding window fashion" format="fasta" /> + <conditional name="refFastaSource"> + <param help="" label="Will you select a fasta sequence from your history or use a pre-installed sequence?" name="fastaSource" type="select"> + <option value="history">Use one from the history</option> + <option value="pre-installed">Use a pre-installed fasta sequence</option> + </param> + <when value="pre-installed"> + <param help="if you wish to have your fasta sequence listed contact instance administrator" label="Select a fasta sequence" name="input" type="select"> + <options from_data_table="all_fasta"> + </options> + </param> + </when> + <when value="history"> + <param format="fasta" label="Select a fasta file for which you wish to generate a multi-fasta file in a sliding window fashion" name="input" type="data" /> + </when> + </conditional> <param type="integer" name="window" value="21" min="1" label="window size" help="Specifiy the size of the windows that should be generated"/> <param type="integer" name="step" value="21" min="1" label="step size" help="Specify the distance with which windows should be spaced apart."/> </inputs>
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool-data/all_fasta.loc.sample Wed Apr 15 09:08:37 2015 -0400 @@ -0,0 +1,18 @@ +#This file lists the locations and dbkeys of all the fasta files +#under the "genome" directory (a directory that contains a directory +#for each build). The script extract_fasta.py will generate the file +#all_fasta.loc. This file has the format (white space characters are +#TAB characters): +# +#<unique_build_id> <dbkey> <display_name> <file_path> +# +#So, all_fasta.loc could look something like this: +# +#apiMel3 apiMel3 Honeybee (Apis mellifera): apiMel3 /path/to/genome/apiMel3/apiMel3.fa +#hg19canon hg19 Human (Homo sapiens): hg19 Canonical /path/to/genome/hg19/hg19canon.fa +#hg19full hg19 Human (Homo sapiens): hg19 Full /path/to/genome/hg19/hg19full.fa +# +#Your all_fasta.loc file should contain an entry for each individual +#fasta file. So there will be multiple fasta files for each build, +#such as with hg19 above. +#
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool_data_table_conf.xml.sample Wed Apr 15 09:08:37 2015 -0400 @@ -0,0 +1,7 @@ +<tables> + <!-- Locations of all fasta files under genome directory --> + <table name="all_fasta" comment_char="#"> + <columns>value, dbkey, name, path</columns> + <file path="tool-data/all_fasta.loc" /> + </table> +</tables>