<?xml version="1.0" encoding="ISO-8859-1" ?>
<!DOCTYPE bix SYSTEM "rez/bix.dtd"> 
<!-- PUBLIC "http://iubio.bio.indiana.edu/grid/runner/docs//bix.dtd" -->

<bix>

<package>
<id>biapps</id>

<xpackage>
<id>emboss</id>

<env>EMBOSSDIR=/bio/mb/emboss/</env>
<env>EMBOSS_ACDROOT=/bio/mb/emboss/share/EMBOSS/acd</env>
<env>PLPLOT_LIB=/bio/mb/emboss/share/EMBOSS</env>
<env>empath=/bio/mb/emboss/bin/</env>
<env>PATH=/bio/mb/emboss/bin/:/usr/bin:/bin:/usr/sbin:/sbin:/usr/local/bin:/usr/local/sbin</env>
<!-- 

env settings for emboss
!urk needs /bio/mb/emboss/bin in PATH for wossname to work == why? 
 because ... nucleus/embgroup.c is looking at system path ! and must
 find embossy name to proceed
 
these also are in emboss .c: EMBOSS_DATA EMBOSS_ROOT 
    if(ajNamGetValueC("DATA", &fname))
    if(ajNamRootInstall(&fname)) /* just emboss/data under installation */
    if(ajNamRoot(&fname))       /* just emboss/data under source */

solaris needs this for shared lib path:
LD_LIBRARY_PATH=...
macosx needs this
DYLD_LIBRARY_PATH=/bio/mb/emboss-shared/lib

-->

 <command>
  <id>emboss-packinfo</id>
  <menu>About/EMBOSS</menu>
  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">EMBOSS</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About</label>
    <value type="title">European Molecular Biology Open Source Suite (EMBOSS)</value>
   </par>
   <par>
    <id>HELP</id>
    <label>Help</label>
    <value type="url">http://www.uk.embnet.org/Software/EMBOSS/</value>
   </par>
<par><label>version</label><value type="title">2.2.0</value></par>
<par><label>date</label><value type="title">Fri Feb  1 04:36:47 EST 2002</value></par>
<par><label>hostname</label><value type="title">dghome-osx</value></par>

	<par><label>reference source</label>
		<value type="url">ftp://ftp.uk.embnet.org/pub/EMBOSS/EMBOSS-latest.tar.gz</value>
	</par>
	<par><label>working source</label>
		<value type="url">ftp://iubio.bio.indiana.edu/molbio/emboss/EMBOSS-2.2.0.tar.gz</value>
	</par>

  </parlist>
</command>

</xpackage>

<xpackage>
<id>GCG</id>

 <command>
  <id>gcg-packinfo</id>
  <menu>About/GCG</menu>
  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">GCG</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About</label>
    <value type="title">Genetics Computer Group software suite (GCG)</value>
   </par>
   <par>
    <id>HELP</id>
    <label>Help</label>
    <value type="url">http://www.gcg.com/</value>
   </par>
  </parlist>
</command>

</xpackage>

<xpackage>
<id>ncbitools</id>
<env>NCBI=/bio/mb/ncbi/ncbirc</env>
<env>ncbipath=/bio/mb/ncbi/bin/</env>

 <command>
<id>ncbitools-packinfo</id>
  <menu>About/NCBI Tools</menu>
  <parlist>
   <par>
    <id>TITLE</id> <value type="title">NCBI Tools</value>
   </par>
   <par>
    <id>INFO</id> <label>About</label>
    <value type="title">
    National Center for Biotechnology Information(NCBI) Tool Kit.
    Includes BLAST and related software.
    </value>
   </par>
   <par>
    <id>HELP</id> <label>Help</label>
    <value type="url">http://www.ncbi.nih.gov/IEB/ToolBox/</value>
   </par>
	<par><label>version</label><value type="title">Dec 2001</value></par>
	<par><label>date</label><value type="title">Thu Dec 20 11:43:53 EST 2001</value></par>

	<par><label>reference source</label>
		<value type="url">ftp://ncbi.nlm.nih.gov/toolbox/ncbi_tools/ncbi.tar.gz</value>
	</par>
	<par><label>working source</label>
		<value type="url">ftp://iubio.bio.indiana.edu/molbio/ncbi/ncbi_tools/ncbi-01dec.tar.gz</value>
	</par>

  </parlist>
</command>
</xpackage>

<xpackage>
<id>fasta</id>

<env>FASTLIBS=/bio/mb/data/fastalib</env>
<env>fastapath=/bio/mb/fasta/bin/</env>

 <command>
	<id>fasta-packinfo</id>
  <menu>About/FastA</menu>
  <parlist>
   <par>
    <id>TITLE</id> <value type="title">The FASTA program package</value>
   </par>
   <par>
    <id>INFO</id> <label>About</label>
    <value type="title">
    The FASTA program package, version 3,
contains many programs for searching DNA and
protein databases and one program (prss3) for evaluating
statistical significance from randomly shuffled sequences.
    Copyright 1988, 1991, 1992, 1994, 1995, 1996, 1999 by William R.
Pearson and the University of Virginia.
    </value>
   </par>
   <par>
		<label>Citations</label>
    <value type="title">
   	see W. R. Pearson and D. J. Lipman (1988),
"Improved Tools for Biological Sequence Analysis", PNAS
85:2444-2448 (Pearson and Lipman, 1988); W. R.  Pearson (1996)
"Effective protein sequence comparison" Meth. Enzymol.
266:227-258 (Pearson, 1996); Pearson et. al. (1997) Genomics
46:24-36 (Zhang et al., 1997);  Pearson, (1999) Meth. in
Molecular Biology 132:185-219 (Pearson, 1999).
    </value>
   </par>

   <par>
    <id>HELP</id> <label>Help</label>
    <value type="url"> </value>
   </par>
	<par><label>version</label><value type="title">34t10d3</value></par>
	<par><label>date</label><value type="title">4 Jan 2001</value></par>

	<par><label>reference source</label>
		<value type="url">ftp://ftp.virginia.edu/pub/fasta/fasta3.shar.Z</value>
	</par>
	<par><label>working source</label>
   <value type="url">ftp://iubio.bio.indiana.edu/molbio/search/fasta/fasta34t10d3.shar.Z</value>
	</par>

   <par>
		<label>Comparison of FASTA3 programs</label>
    <value type="text/plain">
<![CDATA[
              Table I. Comparison programs in the FASTA3 package
-------------------------------------------------------------------------------
fasta3             Compare a protein sequence to a protein sequence database or
                   a  DNA  sequence  to a DNA sequence database using the FASTA
                   algorithm (Pearson and Lipman, 1988, Pearson, 1996).  Search
                   speed and selectivity are controlled with the ktup(wordsize)
                   parameter.  For protein comparisons, ktup =  2  by  default;
                   ktup  =1 is more sensitive but slower.  For DNA comparisons,
                   ktup=6 by default; ktup=3 or ktup=4 provides  higher  sensi-
                   tivity;  ktup=1  should  be  used  for oligonucleotides (DNA
                   query lengths < 20).

ssearch3           Compare a protein sequence to a protein sequence database or
                   a  DNA  sequence to a DNA sequence database using the Smith-
                   Waterman algorithm (Smith and Waterman, 1981).  ssearch3  is
                   about 10-times slower than FASTA3, but is more sensitive for
                   full-length protein sequence comparison.

fastx3/ fasty3     Compare a DNA sequence to a protein  sequence  database,  by
                   comparing  the  translated  DNA sequence in three frames and
                   allowing gaps  and  frameshifts.   fastx3  uses  a  simpler,
                   faster algorithm for alignments that allows frameshifts only
                   between codons; fasty3 is slower but produces better  align-
                   ments  with  poor  quality sequences because frameshifts are
                   allowed within codons.

tfastx3/ tfasty3   Compare a protein sequence to a DNA sequence database,  cal-
                   culating  similarities  with  frameshifts to the forward and
                   reverse orientations.

tfasta3            Compare a protein sequence to a DNA sequence database,  cal-
                   culating similarities (without frameshifts) to the 3 forward
                   and three reverse reading frames.  tfastx3 and  tfasty3  are
                   preferred    because    they   calculate   similarity   over
                   frameshifts.

fastf3/tfastf3     Compares an ordered peptide mixture, as would be obtained by
                   Edman degredation of a CNBr cleavage of a protein, against a
                   protein (fastf) or DNA (tfastf) database.

fasts3/tfasts3     Compares set of short peptide fragments,  as  would  be  ob-
                   tained from mass-spec. analysis of a protein, against a pro-
                   tein (fasts) or DNA (tfasts) database.
]]>    
    </value>
   </par>

  </parlist>
</command>
</xpackage>

<xpackage>
<id>samplebix</id>

 <command>
<!-- package info -->
  <id>sample-packinfo</id>
  <menu>About/Bio App Samples</menu>
  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">Bioinformatics Application samples</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About</label>
    <value type="title">
<![CDATA[
This is a set of commonly used sample bioinformatics programs which have 
a command line interface, amenable to automated use from various other
programs.  The means to automate their use lies in a computable description
of program inputs, outputs and command options.  
]]>    
    </value>
   </par>
   <par>
    <id>HELP</id>
    <label>Help</label>
    <value type="url">http://iubio.bio.indiana.edu/grid/runner/</value>
   </par>
  </parlist>
</command>

 <command>
  <id>clustalw</id>
  <menu>About/Clustal multiple alignment</menu>
  <menu>Sequence Alignment/Clustal multiple alignment</menu>
  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">Clustal W Alignment</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About Clustal W</label>
    <value type="title">Clustal W - for multiple sequence alignment 
by Des Higgins and colleagues. Clustal W is a general purpose multiple 
alignment program for DNA or proteins.</value>
   </par>

   <par>
	 <id>HELP</id>
	 <label>Help with Clustal W</label>
	 <value type="url">file:/bio/mb/docs/clustalw.txt</value>
	 <!-- http://www-igbmc.u-strasbg.fr/BioInfo/ClustalW/ -->
	 <!-- there should be another clustal doc source ?? -->
	 </par>
  </parlist>
 </command>

 <command>
  <id>cap</id>
  <menu>About/CAP contig assembly</menu>
  <menu>Sequence Alignment/CAP contig assembly</menu>

  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">CAP Contig Assembly</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About CAP</label>
    <value type="title"> A Contig Assembly Program by Xiaoqiu Huang</value>
   </par>
	<par>
	 <id>HELP</id>
	 <label>Help with CAP</label>
	 <value type="url">file:/bio/mb/docs/cap.txt</value>
	</par>
  </parlist>
 </command>

 <command>
  <id>fastdnaml</id>
  <menu>About/FastDNAml</menu>
  <menu>Phylogeny/FastDNAml</menu>
  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">FastDNAml</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About FastDNAml</label>
    <value type="title">A faster DNA maximum likelihood phylogeny estimator.
 fastDNAml is a program derived from Joseph Felsenstein  version 3.3 DNAML
 (part of his PHYLIP package).  Users should consult the documentation for
 DNAML before using this program.
 Produced by Gary Olsen, Hideo Matsuda, Ray Hagstrom, and Ross Overbeek.</value>
   </par>

	<par>
	 <id>HELP</id>
	 <label>Help with FastDNAml</label>
	 <value type="url">http://geta.life.uiuc.edu/~gary/programs/fastDNAml.html</value>
	</par>
 </parlist>
 </command>

 <command>
  <id>tacg</id>
  <menu>About/tacg</menu>
  <menu>Restriction Map/tacg</menu>

  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">tacg restriction map</value>
   </par>
   <par>
    <id>HELP</id>
    <label>Help with tacg</label>
<!-- value.url = file:/bio/mb/docs/tacg2.main.html -->
<!-- this is v3: -->
    <value type="url">http://tacg.sourceforge.net/</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About tacg</label>
    <value type="title">tacg analyzes a DNA sequence for restriction enzyme sites, 
nucleic acid patterns version 2, by Harry Mangalam</value>
	</par>
 </parlist>
 </command>

     
 <command>
  <id>bixinfo</id>
  <menu>About/Bix command language</menu>
  <parlist>
   <par>
    <id>TITLE</id>
    <value type="title">BIX - BioInformatics application/command Xml</value>
   </par>
   <par>
    <id>INFO</id>
    <label>About</label>
    <value type="title">
<![CDATA[
 sample.bix.xml
 d.gilbert, jan02
 XML doctype/magic string for this format is <bix>
 bix.DTD  - BioInformatics application/command Xml

 rewrite of clustal.command (BOP structure format)
 d.gilbert, dec97
 rewrite of clustal.html (seqpup) and clustalw.config (seqlab)
 as general parseable structure for specifying app parameters
 for use w/ a corba client=server interface  
 
 magic string for this format is "Content=type: biocompute/command"
 format 
  key = value
  key = { structured.value }
  newlines or ';' separate key=value pairs in a structure
  values that include white space need to be quoted with "" or ''

 see bopper.idl and ReadCommand.java for current key words  (these may change)
 key words match fields in the bopper.idl, and are case=insensitive 

 commandKeys = { "id", "transport", "action", "filepath", "parlist", "command" };
 parameterKeys = { "id", "label", "value", "ifelseRules", "runSwitch" };
 containerKeys = { "required", "parlist" };
 choiceKeys = { "multiple", "minToShow", "parlist" };
 dataKeys = { "datatype", "dataflow", "filename", "flavor", "data" };

 ID values are case=sensitive, unique strings.
 reference IDs and other variables as $ID 
 $serverurl, $tempdir, and $tempname are variables that are set 
   by server (remote or local) at runtime

 TITLE, INFO and HELP are special par ids 

]]>
    </value>
   </par>
   <par>
    <id>HELP</id>
    <label>Help</label>
    <value type="url">http://iubio.bio.indiana.edu/grid/runner/docs/bix.dtd</value>
   </par>
  </parlist>
</command>
</xpackage>

</package>

</bix>
