# HG changeset patch # User abims-sbr # Date 1519739231 18000 # Node ID 9c0044eff621322a60bbbab587da57fd2893aa16 # Parent e0bea88bb09fc4680175cdb21a82a8d421925531 planemo upload for repository https://github.com/abims-sbr/adaptsearch commit 273a9af69b672b2580cd5dec4c0e67a4a96fb0fe diff -r e0bea88bb09f -r 9c0044eff621 BlastAlign.xml --- a/BlastAlign.xml Thu Jan 18 09:02:24 2018 -0500 +++ b/BlastAlign.xml Tue Feb 27 08:47:11 2018 -0500 @@ -1,4 +1,4 @@ - + Align the nucleic acid sequences using BLASTN @@ -35,7 +35,7 @@ && ln -s '$input.element_identifier'".fasta.phy" out.phy && ln -s '$input.element_identifier'".fasta.nxs" out.nxs - #if $fasta_out.value == True + #if $output_format.value == "fasta" && python $__tool_directory__/scripts/S01_phylip2fasta.py out.phy out.fasta #end if @@ -50,15 +50,23 @@ - - + + + + + + - @@ -72,9 +80,7 @@ - - - + @@ -86,10 +92,8 @@ - - - - + + @@ -100,8 +104,7 @@ - - + @@ -113,10 +116,20 @@ - - - - + + + + + +
+ + + + + +
+ +
@@ -171,17 +184,21 @@ Default : 0 Default is finding the reference sequence by blasting all sequences against all sequences, only randomly subsampling when it thinks the blast output file might be too large. +** Output format :** + The user have the choice between three format (only one is returned per run) : fasta, phylip, and nexus. -------- **Outputs** + +The output format is - - 'Alignment_{input.name}_phylip' : + - 'Blastalign_on_{input.name}_phylip' : the aligned sequences in Phylip format. - - 'Alignment_{input.name}_nexus' : + - 'Blastalign_on_{input.name}_nexus' : the aligned sequences in Nexus format. - - 'Alignment_{input_file}_fasta' : + - 'Blastalign_on_{input_file}_fasta' : the aligned sequences in Fasta format if the option "fasta format" is checked. --------- @@ -191,6 +208,7 @@ **Version 2.1 - 17/01/2018** + - New parameter "output format" - Applied some bugfixes and minor improvments **Version 2.0 - 21/04/2017**