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From: schnee@iti.CS.Uni-Magdeburg.De (Roland Schnee)
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Subject: GCB2001
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Dear Ladies and Gentlemen!

The German Conference on Bioinformatics 2001 will take place from
October 7-10, 2001 in Braunschweig, Germany.

For further information, please see the following URL:
http://www.bioinfo.de/gcb01/


Roland Schnee

---


From owner-bio-srs@hgmp.mrc.ac.uk  Tue Aug  7 16:32:54 2001
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To: bionet-software-srs@moderators.isc.org
From: "Igor Evsikov" <ievsikov@flowpath.com>
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Subject: Scientific and engineering expresson calculator+grapher * unit converter/(MATRIX^COMPLEX)
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New version:

http://www.simtel.net/pub/pd/17596.shtml

WiSCy99 v4.26 for (Windows'9x/NT/2000) is the complete and-to-use scientific
calculator.  The results of calculation can be visualization, printing as
graphic, as text or saving to disk. Unit Converter is pre-configured to
convert over 500 units in 30 categories and editor for custom units
conversion.Periodic table of the elements utility provides basic and
extended properties of the elements.
Complex and MATRIX operations is available.

      - Arithmetic and logical operators and functions
      - Common functions such as exp, ln, sqrt, sqr, bnml etc.
      - Common, trigonometric, hyperbolic complex functions
      - Trigonometric, Hyperbolic  functions
      - Numerical Integration
      - Equations can be solved
      - Special functions (Gamma, Bessel's, Si, Ci, erf, erfc, Fresnel's)
      - Statistic functions (Average, Standard deviation, Sum, Random,
        Gauss random, statistical variance, etc )
      - FOR-type loop
      - if (...) then (...) else (...) function
      - Tape of results
      - Assistant and debug: error position fixed
      - Plot f(X), Contour Plot f(X,Y), Color Shading  f(X,Y),
        real 3D-Plot f(X,Y), Derivative, Fit.
      - Print results, graphics and print preview
      - Save graphics to BMP, WMF, EMF formats
      - Matrix Operations(A+B=C, A-B=C, A*B=C, inverse(A)=C,
        Power(A,n)=C, det |A|=C[1.1], Solve A(X)=C)
      - Decimal, Hexadecimal and Binary bases
      - Fixed point, Scientific, Engineering and Sexagesimal notations
      - Radian and Degree modes for trigonometric functions
      - Precision: 10-12 significant digits.
      - Range: _(3.4E-4392 to 1.1E+4392)
      - 10 pre defined variables, user define variables
      - User define functions
      - 30 user defined constants (up to 16000), search and edit file
        with constants.
      - Stack for expressions (up to 16000)
      - Stack for results (up to 16000)
      - Unit Converter
      - Custom unit converter
      - Evaluate expressions from file
      - Simple tape calculator
      - Periodic table of the elements

Special requirements: None.

Changes: Added Periodic table of the elements
         More than 400 units in 20 categories


Igor Evsikov
ievsikov@flowpath.com













From owner-bio-srs@hgmp.mrc.ac.uk  Mon Aug 13 10:32:44 2001
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From: willy_valdivia@ndsu.nodak.edu (Willy Valdivia)
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Subject: virtual conference
Organization: BIOSCI/MRC Human Genome Mapping Project Resource Centre
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         First Virtual Conference in Genomics and Bioinformatics

October 15 & 16, 2001

At World-Wide Access Grid Locations

Sequencing projects and genomics research has led to an explosive rate of 
data accumulation and to a shift in the way biological research is 
conducted. Bioinformatic tools of the post-genome era are providing new 
insights about gene expression patterns, intron/exon structure, 
post-translational changes and protein interactions as well as phylogenetic 
relationships.  Parallel analysis of thousands of genes using microarray 
technology has become a multi-disciplinary endeavor in which unsupervised 
and supervised learning is applied for gene expression clustering and/or 
classification.  Although genomic technologies offer an enormous scientific 
potential to understand organisms at the molecular level, new challenges on 
the horizon are envisioned.  There is a need for improvement of microarray 
technology, data standardization, and tools for integration of multiple 
databases and data mining.  Other necessary needs include the improvement 
of bioinformatic tools and statistical approaches for sequence analysis, 
gene annotation, categorization of protein families, protein-protein 
interactions, and phylogenetic studies.

The goal for the First Virtual Conference in Genomics and Bioinformatics is 
to increase the exchange of ideas and establish new ways of interaction and 
collaboration among scientists around the world.

For the 2001 Virtual Conference, topics include:

Functional Genomics

Structural Genomics

Computational Approaches for Gene Expression Analysis

Metabolic Profiling

Genomic Data Standardization and Management

Implications of Genomic Research

Proteomics

Invited speakers and Participation:

For the First Conference, invited speakers and reviewers represent 
institutions including:

Argonne National Laboratory

Brookhaven National Laboratory

Cold Spring Harbor Laboratory

First Genetic Trust, Inc.

Massachusetts Institute of Technology

National Center for Genome Resources

National Institute of Standars and Technology

North Dakota State University

Ohio State University

Stanford University

UC Berkeley

Although registration is required, there are no required registration fees 
to participate in the conference.  To participate at the Fargo Access Grid 
Node or one of several other Nodes around the world, please register 
through our web page

http://www.ndsu.nodak.edu/virtual-genomics/registration.htm

 Abstract and Papers:

In addition to the invited presentations, we invite participants to 
consider additional participation through abstracts and papers.  This is a 
fully refereed meeting and each submitted abstract will be peer-reviewed. 
Abstracts should describe unpublished research that is not under review. 
Abstracts describing novel applications and theoretical contributions are 
also requested.  An abstract of no more than 250 words should be submitted 
by August 31, 2001. Please submit your abstract through our web page 
http://www.ndsu.nodak.edu/virtual-genomics/abstract.htm

Accepted abstracts will be invited for a complete paper to be submitted by 
September 21, 2001.  Papers should not be more than 20 pages long using 11 
point font times new roman, 1.5 line spacing, and 3 cm margins on all four 
sides on letter size paper.  An electronic document session will be 
scheduled following the conference to allow the maximum participation 
between the attendees and the authors. Accepted documents as well documents 
submitted by invited speakers will be available in electronic version in 
the "Proceedings of the Virtual Conferences of Genomics and 
Bioinformatics."

Deadline: August 31, 2001 for abstracts

Deadline: September 21, 2001 complete documents

Useful links:

Access Grid locations in the US and around the world:

http://www-fp.mcs.anl.gov/fl/accessgrid/ag-nodes.htm


Registration to attend the meeting in Fargo, North Dakota

http://www.ndsu.nodak.edu/virtual-genomics/registration.htm

Link to submit your abstract

http://www.ndsu.nodak.edu/virtual-genomics/abstract.htm

Susbcribe to our e-mail list

http://listserv.nodak.edu/scripts/wa.exe?SUBED1=virtual-genomics&A=1

E-mail your questions to

Edward_Deckard@ndsu.nodak.edu

Willy_Valdivia@ndsu.nodak.edu

 

---


From owner-bio-srs@hgmp.mrc.ac.uk  Mon Aug 20 10:19:34 2001
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To: bionet-software-srs@moderators.isc.org
From: Guy Bottu <gbottu@bigben.vub.ac.be>
Newsgroups: bionet.software.srs
Subject: about hyperlinling to an SRS server
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	Dear colleages,

I do not know how many of you use hypertext pages that contain
hyperlinks pointing to an SRS server. I mean links like 
<A HREF="http://ben.vub.ac.be/srs6bin/wgetz?-e+[swissprot:papa_carpa]">PAPA_CARPA</A>
>From SRS version 6.1.1 on this retrieves a page with the entry a simple
text instead of parsed text with hyperlinks inserted. Did you also
notice this ? I have send a message to the SRS support.

	Sincerely,
	Guy Bottu


From owner-bio-srs@hgmp.mrc.ac.uk  Tue Aug 28 13:22:49 2001
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To: bionet-software-srs@moderators.isc.org
From: John Broxholme <johnb@well.ox.ac.uk>
Newsgroups: bionet.software.srs
Subject: getz problem
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Any ideas why the following should not work:

johnb@zeon /// getz "libs=[embl-Description: abc2*] & [libs-org:human]"
error: unknown set or databank, "libs"

when the following does:

johnb@zeon /// getz "[embl-Description: abc2*] & [embl-org:human]"
EMBL:AF216833
EMBL:HS18235

(I'm using SRS6.1.0.1, if that makes any difference)

Thanks in advance,

John

-- 
John Broxholme
Wellcome Trust Centre for Human Genetics
Roosevelt Drive, Oxford, OX3 7BN, UK 
Tel: (+44 1865) 287611 FAX: 287664
e-fax: (+44 0870) 1370921


From owner-bio-srs@hgmp.mrc.ac.uk  Wed Aug 29 09:13:08 2001
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To: bionet-software-srs@uunet.uu.net
From: Tim Cutts <timc@chiark.greenend.org.uk>
Newsgroups: bionet.software.srs
Subject: Re: getz problem
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In article <3B864A35.908A3F5F@well.ox.ac.uk>,
John Broxholme  <johnb@well.ox.ac.uk> wrote:
>
>Any ideas why the following should not work:
>
>johnb@zeon /// getz "libs=[embl-Description: abc2*] & [libs-org:human]"
>error: unknown set or databank, "libs"
>
>when the following does:
>
>johnb@zeon /// getz "[embl-Description: abc2*] & [embl-org:human]"
>EMBL:AF216833
>EMBL:HS18235

libs is for combining complete databases, whereas you're trying to treat
it as a result set.

In this case you don't need it.  The second version of your query is
the correct form, but you could use the following more verbose form,
which is probably what you were aiming at:

getz "[libs={embl}-des: abc2*] & [libs-org:human]"

although I just tried a similar query here, using SRS 5.1, and it was
very slow indeed, so there seems to be a potentially really bad
implementation inefficiency in SRS 5.1 for this sort of query.
Hopefully it's better in SRS 6.x

I use both result sets and libs={} assignments to always retrieve the
latest version of a sequence from genbank and genbanknew:

For example:

getz -e "(q22714=[libs={genbank genbanknew}-id:X12345]) ! q22714<genbanknew"

This query works as follows:

1)  Query both Genbank and GenbankNew for id X12345, and store the
results in set q22714
2)  Find those entries in q22714 which have a link to genbanknew (in
other words, have an updated version in genbanknew)
3)  Remove these entries from the result set.

Hopefully this neatly demonstrates the difference between querying
multiple libraries and assigning to a result set.

Tim.

-- 
"It is the job of Sales and Marketing to insulate those who know what
they're talking about from each other"
  -- I know who said this, but I'm not telling.


From owner-bio-srs@hgmp.mrc.ac.uk  Wed Aug 29 09:13:34 2001
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From: gilbertd@bio.indiana.edu (Don Gilbert)
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Subject: IUBio bio-data warehouse
Organization: BIOSCI/MRC Human Genome Mapping Project Resource Centre
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We are testing the waters of interest for additional bio-data
formats distributed from IUBio archive
(http://iubio.bio.indiana.edu) and Bio-Mirror
(http://bio-mirror.net/). We could make available GCG formats of
a standard bio-data set including genbank-embl, swissprot-trembl
and others.   We are also testing the idea of redistributing
EMBOSS indices and SRS indices, and would appreciate hearing of
any of this would be of interest to you.

IUBio hopes to be part of developing bio-grid efforts,
with help from partners with more advanced information grid
work. Indiana U. has a set of researchers actively involved in
information grid efforts: in computer science, including the
Globus grid project, in physics where grid efforts are essential
for their huge data set, and information technology.
IUBio also has good network connectivity with the world. 

-- Don Gilbert
IUBio archivist.
-- d.gilbert--bioinformatics--indiana-u--bloomington-in-47405
-- gilbertd@bio.indiana.edu

---


