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authorCalvin Morrison <mutantturkey@gmail.com>2014-09-09 17:53:01 -0400
committerCalvin Morrison <mutantturkey@gmail.com>2014-09-09 17:53:01 -0400
commita9b3d721ac6057a84377cdeedafa986f7cf35b95 (patch)
tree9b3b3fced96978edafa1c2ebbc0a912539009495 /src/galaxy
parent3f3633d36cb033da5a7d616463a32397bd77c478 (diff)
parent62067f0ca6db19fcdedc84476e68ba3864062f54 (diff)
Merge branch 'master' of github.com:EESI/quikrHEADmaster
Diffstat (limited to 'src/galaxy')
-rw-r--r--src/galaxy/multifasta2otu.xml6
-rw-r--r--src/galaxy/quikr.xml20
-rw-r--r--src/galaxy/quikr_train.xml18
3 files changed, 5 insertions, 39 deletions
diff --git a/src/galaxy/multifasta2otu.xml b/src/galaxy/multifasta2otu.xml
index b80f8b2..eebe246 100644
--- a/src/galaxy/multifasta2otu.xml
+++ b/src/galaxy/multifasta2otu.xml
@@ -1,10 +1,10 @@
<tool id="multifasta" name="Multifasta">
<description>Get Abundances on Multiple Files</description>
- <command interpreter="bash">multifasta_to_otu -k $kmer -s $db -f &lt;( echo
+ <command>bash -c "multifasta_to_otu -k $kmer -s $db -f &lt;( echo
#for $input in $inputs:
-"${input}"
+${input}
#end for
- | xargs -n 1 ) -o $output</command>
+ | xargs -n 1 ) -o $output"</command>
<inputs>
<param name="inputs" multiple="true" type="data" format="fasta" label="input fasta"/>
<param name="db" type="data" format="data" label="trained database"/>
diff --git a/src/galaxy/quikr.xml b/src/galaxy/quikr.xml
index 89729be..65d604b 100644
--- a/src/galaxy/quikr.xml
+++ b/src/galaxy/quikr.xml
@@ -11,23 +11,7 @@
<data name="output" format="tabular"/>
</outputs>
<help>
-**What it does**
-
-This tool counts the length of each fasta sequence in the file. The output file has two columns per line (separated by tab): fasta titles and lengths of the sequences. The option *How many characters to keep?* allows to select a specified number of letters from the beginning of each FASTA entry.
-
------
-
-**Example**
-
-Suppose you have the following FASTA formatted sequences from a Roche (454) FLX sequencing run::
-
- &gt;EYKX4VC02EQLO5 length=108 xy=1826_0455 region=2 run=R_2007_11_07_16_15_57_ TCCGCGCCGAGCATGCCCATCTTGGATTCCGGCGCGATGACCATCGCCCGCTCCACCACG TTCGGCCGGCCCTTCTCGTCGAGGAATGACACCAGCGCTTCGCCCACG &gt;EYKX4VC02D4GS2 length=60 xy=1573_3972 region=2 run=R_2007_11_07_16_15_57_ AATAAAACTAAATCAGCAAAGACTGGCAAATACTCACAGGCTTATACAATACAAATGTAAfa
-
-Running this tool while setting **How many characters to keep?** to **14** will produce this::
-
- EYKX4VC02EQLO5 108
- EYKX4VC02D4GS2 60
-
-
</help>
</tool>
+
+
diff --git a/src/galaxy/quikr_train.xml b/src/galaxy/quikr_train.xml
index b5f5291..a33d866 100644
--- a/src/galaxy/quikr_train.xml
+++ b/src/galaxy/quikr_train.xml
@@ -9,23 +9,5 @@
<data name="output" format="data"/>
</outputs>
<help>
-**What it does**
-
-This tool counts the length of each fasta sequence in the file. The output file has two columns per line (separated by tab): fasta titles and lengths of the sequences. The option *How many characters to keep?* allows to select a specified number of letters from the beginning of each FASTA entry.
-
------
-
-**Example**
-
-Suppose you have the following FASTA formatted sequences from a Roche (454) FLX sequencing run::
-
- &gt;EYKX4VC02EQLO5 length=108 xy=1826_0455 region=2 run=R_2007_11_07_16_15_57_ TCCGCGCCGAGCATGCCCATCTTGGATTCCGGCGCGATGACCATCGCCCGCTCCACCACG TTCGGCCGGCCCTTCTCGTCGAGGAATGACACCAGCGCTTCGCCCACG &gt;EYKX4VC02D4GS2 length=60 xy=1573_3972 region=2 run=R_2007_11_07_16_15_57_ AATAAAACTAAATCAGCAAAGACTGGCAAATACTCACAGGCTTATACAATACAAATGTAAfa
-
-Running this tool while setting **How many characters to keep?** to **14** will produce this::
-
- EYKX4VC02EQLO5 108
- EYKX4VC02D4GS2 60
-
-
</help>
</tool>