From owner-acedb@net.bio.net Tue Sep 07 23:00:00 1993
Path: biosci!rutgers!cis.ohio-state.edu!math.ohio-state.edu!uwm.edu!spool.mu.edu!agate!dog.ee.lbl.gov!slavsing.lbl.gov!user
From: jlmccarthy@lbl.gov (John L. McCarthy)
Newsgroups: bionet.software.acedb
Subject: Notes from ACEDB Workshop, part I
Message-ID: <jlmccarthy-080993095131@slavsing.lbl.gov>
Date: 8 Sep 93 16:42:17 GMT
Followup-To: bionet.software.acedb
Organization: Lawrence Berkeley Laboratory
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NNTP-Posting-Host: 128.3.252.43

By popular request, here are some very rough outline notes I took at the
ACEDB Workshop in Boston last month. I cannot vouch for their accuracy, but
hope I have not misquoted anyone too badly. Please post corrections and
clarifications to this newsgroup.

The full set of notes are about 20 pages long. I have broken them into two
parts to accomodate my news reader and mail software.

If you have questions about particular points, you probably should send
them directly to the people who made those points at the workshop.  A list
of workshop attendees with Email addresses was posted to this newsgroup a
few weeks ago.

A copy of this document is available via anonymous ftp
on weeds.mgh.harvard.edu  under pub/acedb-dev/doc

-John McCarthy, Lawrence Berkeley Laboratory


==================================================================
ACEDB Workshop  Wed 28-31 July 1993 Boston, MA 
Highlight notes from John McCarthy (LBL) jlmccarthy@lbl.gov 

more or less in chronological order, with TOPICS IN CAPS
see list of attendees for full names, addresses, etc.

Wed 28 July 
=================================
COMMUNICATIONS, GOPHER
Mike Cherry is providing ACEDB archive on his gopher server at
Stanford -- genome.stanford.edu.

Mike asks if people could please send notes to bionet.software.acedb
another thing that would be nice to have is FAQ - Brad will do this

weeds.mgh.harvard.edu has anonymous gopher+  login/server
Also experimenting with remote anonymous AATDB login aatdb
user name c-aatdb used for MacX
Mike used Richard's acedump to create gopher files.
WAIS paragraph format / from acedump    also textace

Brad notes that his gopher archive includes USDA sysad archive.

Brad Sherman did research for secure anonymous ftp

Mike: weeds is a separate machine, not cross mounted to anything, and
not used for anything else

stty script --  Otto points out that you can trap interupts with Bourne
shell
Brad points out that most vulnerable spot is within application.

anonymous FTP setup instructions,  
thor.ece.uc.edu
/pub/sun-faq/anon-ftp.script
guidelines:  . cert.org   /pub/tech.tips/anonymous.ftp

=========================================================
PRINTING FOR REMOTE USERS
richard: set ACEDB_LPR to null -- code checks for this.
maybe could do a script that turns print script into Email.
Michelle: also may want to print to a file  
(richard:  currently always goes into /PS directory).  
Stan: might be nice to have switch to disable all writing
could do changeroot to keep people restricted to specified area.

=================================
ACEDB NEW DEVELOPMENTS - Richard Durbin: 
ORGANIZATIONAL STATUS, what Richard and Jean are doing:
RD  -worm sequencing (2,5,10 Mb/yr)
      -sanger Centre  (RD joint head of informatics)
      -CGC map -> Cambridge  (worm cytogenetics center)
            Mary O'Callaghan doing this (moc@mrc-lmb.cam.ac.uk)
      -in house use: sequence (worm, yeast, human)
                             worm genetic map
   so RD will have less time for kernal development

Jean:  -Human mapping - Frensal (Genethon)
          -IGD
          -ports to various unix systems
          - management of kernal  (want to keep unified version)
             incorporate changes from others & redistribute
             also would like to make other's tools & modules available

RELEASES:
        1-10  now  (still backwards compatible with old databases)
        2-0 September? (model changes for maps, sequences)
                             running this in Cambridge now
                      but want to make other changes before release
              would like to get some feedback from this workshop first
     developers can get 2-0 code but should not use for databases
          that will be distributed, etc.
Will have AWK scripts for database restructuring from 1-10 to 2-0
Extra things in specifications directories, PS fonts, Xfonts.wrm,


NEW ARCHITECTURE FOR MAP DISPLAY-- RD
  columnar architecture/format will help
  would also be nice to have developers style guide

Stan: would be nice to have another level of indirection, so people
could map different names to std display code names -- intermediate
layer to make it easier to change models and yet maintain
compatibility with display modules.

RD: not convinced that another layer of indirection is good idea
may slow things down

RD: people should not expect that all the good ideas that get
suggested here will get implemented.  Commitment to maintain kernal.

------------------- break-----------------------
NEW DEVELOPMENTS (mostly in 1-10)
SUBCLASSES 
  -can appear on main window
  -can use in queries, .ace files
  -no code change required
specification
  -wspec/subclasses.wrm
  -read after models.wrm
  -ace file
      class genome_Sequence
      Subclass-of Sequence  //can be a subclass  (can have 2 parents?)
      Visible            //indicates whether displayed on main window
      Filter     "Genomic_canonical"  query
  How it works:
       Have 8 bits free per key in memory 
       -uses 1 bit per filter
       checks on object save
       when filter changes -- rescans entire class with query
       can't change entries in class class directly, reads from
subclasses.wrm
        
May be possible in future:
      to have different default display type for different subclasses
      
Used in 2.0
?Map   -  Chromosome
?Locus - gene, RFLP, etc.
?Interval - rearrangement, Chrom_Band, Hybrid cell line, ...
?Df_dup_defic     Inside
                           Outside
?Probe

2-0 has a models class 
so won't have ?class as part of keyset
you will get this type of info in other ways

2 possible ways to do sub-maps
  1 scale with some linear transformation
  2 interpolate between shared loci (now done in 1-10 physical map)

Otto: IGD has used clone grid as general model for 2-D maps

RD: map display now automatically transforms contig info in this way
 maybe could do some graphic to indicate where there are conflicts
  between different versions of maps

GRAPH PACKAGE additions
   filled arcs
   filled polygons (from Suzanna)

IMAGES (grey level: 256-->128)
      (a) in subwindow    graphPixels()
      (b) PIXEL_SCROLL graph type   (coordinates are pixels) 
            graph Pixel Background()

Possible Development
      -ASCII dump format for draw stack
      -stand alone drawing editor
 full color images will require more thought!
now easier to attach sub-menus to boxes

Otto: can pick up X colors and coordinates to use from XV
Suzanna: has done some things to display TIFF images

MAP PACKAGE
map.h     w7/mapcontrol.c
A. drawing coordinates  (zoom, centre, scroll, etc.)
B. columns of data (user toggleable)
C Cursor

MAP  *map
Look -> map -> mapCreate(column, ...         )
{float   min, max
Coordinate Functions
Locator (small green bar)

Stan: is this the way you would draw multiple (synteny) maps?
RD: not yet..., in the meantime can use TableMaker multi-map

Planned Enhancements
1. add a help line per column for display control
2. allow >32 columns
3. give names to sets of columns
4  ?   Multiple ?MAP's per window

Code:
     separate columns further
             ==>library of columns
     separate SEG's array per column    (convert (store),  destroy)
   put PICK control in MAP package
          -select   /  follow
          - neighbor       on/off  (key)  [e.g., to light up related
objects]

Sequence Fetch/Align
--------------------------
a. summon up SwissProt/PIR entry(s)
b. show multiple alignment based on BLAST segments  =BLIXEM
uses unix command
   fetch  -Bdbname (SP,PIR,EMBL,GB)
             -a accession number
             -P Pearson (FASTA) format
             -s  just  sequence ... no new line
   our version uses the EMBL CDROM index structu
From owner-acedb@net.bio.net Tue Sep 07 23:00:00 1993
Path: biosci!daresbury!doc.ic.ac.uk!warwick!uknet!pipex!uunet!europa.eng.gtefsd.com!howland.reston.ans.net!agate!dog.ee.lbl.gov!slavsing.lbl.gov!user
From: jlmccarthy@lbl.gov (John L. McCarthy)
Newsgroups: bionet.software.acedb
Subject: Notes from ACEDB Workshop, part 2 of 2
Message-ID: <jlmccarthy-080993095310@slavsing.lbl.gov>
Date: 8 Sep 93 16:44:30 GMT
Followup-To: bionet.software.acedb
Organization: Lawrence Berkeley Laboratory
Lines: 326
NNTP-Posting-Host: 128.3.252.43

This is the second part of some very rough outline notes I took at the
ACEDB Workshop in Boston last month. I cannot vouch for their accuracy, but
hope I have not misquoted anyone too badly. Please post corrections and
clarifications to this newsgroup.

The full set of notes are about 20 pages long. I have broken them into two
parts to accomodate my news reader and mail software.

If you have questions about particular points, you probably should send
them directly to the people who made those points at the workshop.  A list
of workshop attendees with Email addresses was posted to this newsgroup a
few weeks ago.

A copy of this document is available via anonymous ftp
on weeds.mgh.harvard.edu  under pub/acedb-dev/doc

-John McCarthy, Lawrence Berkeley Laboratory


====================FRIDAY=============================
AM demos & tutorial (very popular!)

GENETIC MAPS
an item gets put on genetic map if it has a name and coordinates
can set center and extent within ?Chromosome
interesting links to 2 and 3 point data, which displays distance difs
 nice quick visual summary of how well map fits expmtl data
menu items for show/highlight selected objects (from KeySet)

show = only display ones on keyset, highlight keeps others

[need better names of menu items "show Keyset items", "Highlight ]

middle button lets you recenter, also at bottom of page it scrolls 1/2
page at a time
middle button to left of left green bar (locator), also zooms
if you move it left and right with middle button, scales continuously

in ?Chromosome  Centre  x  y  y=initial spread when loci are displayd
                          Extent x y map coords of left & rt ends of
black bar
                  Error_factor  x=number that multiplies times 2nd number
    (treat with grain of salt because things get bumped right]
  Bigwood: might be nice to have this not be linear
Otto knows how this all works
          can be set different for dense maps

also can put anchor loci beside black bar by setting tag Marker gene
in ?Gene class
[really need Richard and Jean to define tags like these!!]

Private maps ... may go away (no longer in RD's 2.0)
physical chromo map: 
contigs can have gMap coords & get displayed on map
if you choose this item, it strings together contigs with gaps
shows boxes to left of scale representing clones, cDNA's etc via Keyset
in order to see distribution along the physical map
tied via pMap tags

Chrom-band class: can have dark, light, and color
also can set centromere, don't have telomere's

deficiencies and duplications
1,2, or thick bar  -- set as tag in rearrangement class
click to see name displayed above
GMap Data button shows things inside or outside rearrangements
displayed in dif colors - linked via ??? tags

linkage data has been tailored to C. elegans, but some use elsewhere
2ptdata, 3ptdata will be changed a lot in 2-0
2pt_data is for "selfed"
Wild Type A B AB
mendelian ratio 9 3 3 1
slots to show calculated distance and errors
they have 19 dif types of crosses represented in 2-0 data file
there is a description file that goes along with it (wdoc--should be
part of help/hints/metadata)

3pt_data: 
A-non-B recombinants
B-non-A recombinants
one or more unknown  markers
a5c12b
a 0 c 8 b   does not unambiguously determine order

with new system, can enter multi-point data, not just 3-point
could use to test RFLP's between known markers
on gMap, main markers shown by large squares, others by small
function lets you display relative likelihoods for selected locus
red line end points constrained by mult point data, def/dup, pMap

framework probably appropriate even if detailed calculations are not

Frank: what happens if you have contradictions (highlight in dark)
RD: can fix certain loci and recalculate others via keyset
[would also be nice to have screen dump with lines to explain each
component]

can throw out any particular data item and recalculate local set
Jean may be putting in additional info re LOD scores, etc for Genethon
for dif kinds of experimental data

======================lunch=============================
DATA LOADING Dave Matthews
asks RD to eliminate setenv ACEDB_SU
should give full main menu for everyone with write access

RD: C.elegans has moved towards on-line updates & master is db
DM: would like transaction report
         new objects created explicitly, implicitly
         objects changed, new fields added, fields replaced
         links made to existing objects
         deletes, renames of individual objects, data fields
SL: before a load, she dumps current db, then dumps new & does dif
  also knows what things should not happen.
Otto: could you query the lexique to see if new objs created?
    
RD: in past has thought would be good idea to have dry run input
Mike: does script to look up objects he expects to find in db
Brad: in prior project, did a transaction log and tools to operate on it 
     it took a lot of time to do, and was very little used
RD: thinks it would be easier to produce big file and tools to use it
maybe code in front of each input line to indicate what happens to it
Otto: what about dump option including session # for each object&tag
Mike: essentially an ACEDIFF where you do dump before you save
can do query to get all newly created & updated objects
RD: this gets back to yesterday's idea to be able to do keyset of
changed objects.
JM: can we do search for empty objects?
RD: other thing would be to do a more efficient acedif
make list of all things touched, acedump, quit
RD: it would be a good idea and not hard to do query for all items
that have been changed, and/or all empty items (italicized) also
thinks its reasonable to do acefile annotated with what happens tool
could pass over this to create summary report of what happened Problem
with dry run is that it would not reflect load A, then XREF A
Brad: no one has proposed automated solution to all this Wants data
providers to give him a text file that explains data file that can be
understood by undergraduate.  Thinks .ace files are going to be the
database for some time to come.  Needs to establish new strategies for
data collection in the lab.

=================IMAGES
Otto: Alex virtual file system can keep correspondence of virtual and
real machines
Frank: most neuroscience is 3-D image data, acquired via dif methods
hard to register dif types of info with one another (same scales, etc.)
proposes new standard class ?Image
?Image
           Text         //path to where image is stored
            Class      //type of image (postscript, gif, pict)
             size      //bits
            preferred display program
            might give many images
            Box      x  y   width height      parts of image
another thing you want to do is overlay, with approx registration

PACS - picture archiving and communications systems
most use Sybase, etc. 

Dave and Brad want to integrate geographic maps where stuff grows

RD: Hotspot  x y w h #Class
#Class Locus ?Locus
           Clone ?Clone
           etc. for all classes              (could be useful elsewhere)

Frank: general... how to indicate hotspots-draw box (or shade) 
as mouse passes over it, menu choice for display hotspots, 

Eric: medical community just beginning to do smart things with images,
so not likely to learn much from PACs, but GIS has already done a lot
and may have more to offer.

============break=============
METADATA: Cartinhour, McCarthy
Sam: already a fair amount of metadata in acedb
model itself, help files, hints
can extend in several directions...
e.g., to document tags and data fields
e.g., Chrom_band 
                gMap ?Chromosome int int

=====================================================
DOCUMENTATION
Mike: can take many forms ... 
Ian Dunham has chap in book on physical map databases
FAQ, tutorial, on-line help, clean up doc/ directory, doc list,
4 ace docs: intro, installation guide, config guide, syntax
Sam & John white papers on metadata
Sam: need new docs on table-maker, query language, tools
         perhaps a list of canned queries to cut & paste
       along with explanation of what it was intended to do
     (perhaps via //comment on query line)  RD has some too
programmers guide, how to do a new module, application
     RD: biblio.c is a nice eg for this
weeds has anonymous ftp incoming
Mary Callahan has written intro thing with RD
Sam & Mike contrib to book
RD not too enthusiastic about making help more of a database
Dave M: README would be even more helpful for installation
RD: this is currently in "Notes"
Mike: other newsgroups have had one person do FAQ and then put on
newsgroup & get redone periodically
Brad: volunteers to put together intial FAQ
other volunteers: Marc, Otto, Lisa, Sam, John, Richard, Jean, David,
Staffan, Brad, Edie (for review, etc. -- worked on commercial doc)
Eric: what about TeX info ala Gnu project?
Sam: will do intro manual re how to do create models
Doug: need virgin users to critique documents, interfaces, etc.

========================================================
ACEDB PLATFORMS & PERFORMANCE (Richard)
                                                     Performance
Sun Sparc
    I  (ipc)
    II (ipx, 470)
    10                                         
From owner-acedb@net.bio.net Sat Sep 11 23:00:00 1993
Path: biosci!uwm.edu!cs.utexas.edu!uunet!mcsun!julienas!jouy!moulon!decoux
From: decoux@moulon.inra.fr (ts)
Newsgroups: bionet.software.acedb
Subject: gateway WWW-ACEDB
Message-ID: <1993Sep12.144428.14066@inra.fr>
Date: 12 Sep 93 14:44:28 GMT
Sender: decoux@moulon (ts)
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Nntp-Posting-Host: moulon-gw




 
 Gateway WWW-ACEDB
 =================
 
 If you want to consult ACeDB and MycDB, try :
 
   * "http://moulon.inra.fr/acedb/acedb.html" to consult "A Caenorhabditis
elegans Data Base" (ACeDB).
 
   * "http://moulon.inra.fr/acedb/mycdb.html" to consult "Mycobacterium
DataBase". "Mycobacterium DataBase" is funded by the WHO and the Fondation
Raoul Follereau and is maintained by the Unite de Genetique Moleculaire
Bacterienne at the Institut Pasteur.
 
 
 To consult these databases, you can : 
 
    * If you know syntax of "tace" commands, enter your query in "SearchText".
    * otherwise you can make a complete Consultation of the database.  
 
 For more precisions, about "tace" syntax, just enter "help".
 
 
 If you want to create an ACEDB gateway, see (or contact me) :
 
          "http://moulon.inra.fr/acedb_conf_eng.html" 
                             ou
          "http://moulon.inra.fr/acedb_conf.html"  (version francaise)
 
 

-- 

Guy Decoux

From owner-acedb@net.bio.net Mon Sep 13 23:00:00 1993
Path: biosci!HERMES.CHPC.UTEXAS.EDU!mwitten
From: mwitten@HERMES.CHPC.UTEXAS.EDU
Newsgroups: bionet.software.acedb
Subject: CONGRESS: COMPUTATIONAL MEDICINE AND PUBLIC HEALTH (long)
Message-ID: <9309141757.AA08577@morpheus.chpc.utexas.edu>
Date: 14 Sep 93 17:57:00 GMT
Sender: daemon@net.bio.net
Distribution: biosci
Lines: 555


 ** NOTE CHANGES IN SUBMISSION AND REGISTRATION DEADLINES **

		FIRST WORLD CONGRESS
      ON COMPUTATIONAL MEDICINE, PUBLIC HEALTH AND
                     BIOTECHNOLOGY
                    24-28 April 1994
                   Hyatt Regency Hotel
                     Austin, Texas
----- (Feel Free To Cross Post This Announcement) ----

1.0 CONFERENCE OVERVIEW:  With increasing frequency, 
computational sciences are being exploited as a means 
with which to investigate biomedical processes at all 
levels of complexity; from molecular to systemic to 
demographic. Computational instruments are now used, 
not only as exploratory tools but also as diagnostic 
and prognostic tools. The appearance of high 
performance computing environments has, to a great 
extent, removed the problem of increasing the 
biological reality of the mathematical models. For the 
first time in the history of the field, practical 
biological reality is finally within the grasp of the 
biomedical modeler. Mathematical complexity is no 
longer as serious an issue as speeds of computation 
are now of the order necessary to allow extremely 
large and complex computational models to be analyzed. 
Large memory machines are now routinely available.  
Additionally, high speed, efficient, highly optimized 
numerical algorithms are under constant development. 
As these algorithms are understood and improved upon, 
many of them are transferred from software 
implementation to an implementation in the hardware 
itself; thereby further enhancing the available 
computational speed of current hardware. The purpose 
of this congress is to bring together a 
transdisciplinary group of researchers in medicine, 
public health, computer science, mathematics, nursing,
veterinary medicine, ecology, allied health, as well 
as numerous other disciplines, for the purposes of 
examining the grand challenge problems of the next 
decades. This will be a definitive meeting in that it 
will be the first World Congress of its type and will 
be held as a follow-up to the very well received 
Workshop On High Performance Computing In The Life 
Sciences and Medicine held by the University of Texas 
System Center For High Performance Computing in 1990.

Young scientists (graduate students, postdocs, etc.)
are encouraged to attend and to 
present their work in this increasingly interesting 
discipline. Funding is being solicited from NSF, NIH, 
DOE, Darpa, EPA, and private foundations, as well as 
other sources to assist in travel support and in the 
offsetting of expenses for those unable to attend 
otherwise. Papers, poster presentations, tutorials, 
focused topic workshops,  birds of a feather groups, 
demonstrations, and other suggestions are also 
solicited.

2.0 CONFERENCE SCOPE AND TOPIC AREAS: The Congress 
has a broad scope. If you are not sure
whether or not your subject fits the Congress 
scope, contact the conference organizers at one 
of the addresses below.

Subject areas include but are not limited to:
*Visualization/Sonification
 --- medical imaging
 --- molecular visualization as a clinical 
     research tool
 --- simulation visualization
 --- microscopy
 --- visualization as applied to problems 
     arising in computational molecular 
     biology and genetics or other non-traditional 
     disciplines
 --- telemedicine
*Computational Molecular Biology and Genetics
 --- computational ramifications of clinical 
     needs in the Human Genome, Plant Genome, 
     and Animal Genome Projects
 --- computational and grand challenge problems in
     molecular biology and genetics
 --- algorithms and methodologies
 --- issues of multiple datatype databases
*Computational Pharmacology, Pharmacodynamics, 
    Drug Design
*Computational Chemistry as Applied to Clinical Issues
*Computational Cell Biology, Physiology, 
    and Metabolism
 --- Single cell metabolic models (red blood cell)
 --- Cancer models
 --- Transport models
 --- Single cell interaction with external factors 
     models (laser, ultrasound, electrical stimulus)
*Computational Physiology and Metabolism
 --- Renal System
 --- Cardiovascular dynamics
 --- Liver function
 --- Pulmonary dynamics
 --- Auditory function, coclear dynamics, hearing
 --- Reproductive modeling: ovarian dynamics, 
     reproductive ecotoxicology, modeling the 
     hormonal cycle 
 --- Metabolic Databases and metabolic models
*Computational Demography, Epidemiology, and 
    Statistics/Biostatistics
 --- Classical demographic, epidemiologic, 
     and biostatistical modeling
 --- Modeling of the role of culture, poverty, 
     and other sociological issues as they 
     impact healthcare 
 --- Morphometrics
*Computational Disease Modeling
 --- AIDS
 --- TB
 --- Influenza
 --- Statistical Population Genetics Of Disease
     Processes
 --- Other
*Computational Biofluids
 --- Blood flow
 --- Sperm dynamics
 --- Modeling of arteriosclerosis and related
     processes
*Computational Dentistry, Orthodontics, and 
    Prosthetics
*Computational Veterinary Medicine 
 --- Computational issues in modeling non-human 
     dynamics such as equine, feline, canine dynamics 
     (physiological/biomechanical)
*Computational Allied Health Sciences
 --- Physical Therapy
 --- Neuromusic Therapy
 --- Respiratory Therapy
*Computational Radiology
 --- Dose modeling
 --- Treatment planning
*Computational Surgery
 --- Simulation of surgical procedures in VR worlds
 --- Surgical simulation as a precursor to surgical 
     intervention
 --- The Visible Human
*Computational Cardiology
*Computational Nursing
*Computational Models In Chiropractice
*Computational Neurobiology and Neurophysiology 
 --- Brain modeling
 --- Single neuron models
 --- Neural nets and clinical applications
 --- Neurophysiological dynamics 
 --- Neurotransmitter modeling
 --- Neurological disorder modeling (Alzheimer's 
     Disease, for example)
 --- The Human Brain Project
*Computational Models of Psychiatric and Psychological
    Processes
*Computational Biomechanics
 --- Bone Modeling
 --- Joint Modeling
*Computational Models of Non-traditional Medicine
 --- Acupuncture
 --- Other
*Computational Issues In Medical Instrumentation
 Design and Simulation
 --- Scanner Design 
 --- Optical Instrumentation
*Ethical issues arising in the use of computational
 technology in medical diagnosis and simulation
*The role of alternate reality methodologies
 and high performance environments in the medical and
 public health disciplines
*Issues in the use of high performance computing 
 environments in the teaching of health science 
 curricula
*The role of high performance environments
 for the handling of large medical datasets (high
 performance storage environments, high performance
 networking, high performance medical records 
 manipulation and management, metadata structures
 and definitions)
*Federal and private support for transdisciplinary 
 research in computational medicine and public health

3.0 CONFERENCE COMMITTEE

*CONFERENCE CHAIR: Matthew Witten, UT System Center 
For High Performance Computing, Austin, Texas
m.witten@chpc.utexas.edu

*CURRENT CONFERENCE DIRECTORATE: 
Regina Monaco, Mt. Sinai Medical Center
Dan Davison, University of Houston  
Chris Johnson, University of Utah 
Lisa Fauci, Tulane University 
Daniel Zelterman, University of Minnesota Minneapolis
James Hyman, Los Alamos National Laboratory
Richard Hart, Tulane University  
Dennis Duke, SCRI-Florida State University  
Sharon Meintz, University of Nevada Los Vegas  
Dean Sittig, Vanderbilt University  
Dick Tsur, UT System CHPC  
Dan Deerfield, Pittsburgh Supercomputing Center 
Istvan Gyori, University of Veszprem (Hungary)
Don Fussell, University of Texas at Austin  
Ken Goodman, University Of Miami School of Medicine  
Martin Hugh-Jones, Louisiana State University 
Stuart Zimmerman, MD Anderson Cancer Research Center  
John Wooley, DOE  
Sylvia Spengler, University of California Berkeley   
Robert Blystone, Trinity University 
Gregory Kramer, Santa Fe Institute
Franco Celada, NYU Medical Center
David Robinson, NIH, NHLBI
Jane Preson, MCC
Peter Petropoulos, Brooks Air Force Base
Marcus Pandy, University of Texas at Austin
George Bekey, University of Southern California
Stephen Koslow, NIH, NIMH
Fred Bookstein, University of Michigan Ann Arbor
Dan Levine, University of Texas at Arlington
Richard Gordon, University of Manitoba (Canada)
Stan Zeitz, Drexel University
Marcia McClure, University of Nevada Las Vegas
Renato Sabbatini, UNICAMP/Brazil (Brazil)
Hiroshi Tanaka, Tokyo Medical and Dental University (Japan)
Shusaku Tsumoto, Tokyo Medical and Dental University (Japan)

Additional conference directorate members are
being added and will be updated on the anonymous
ftp list as they agree.

4.0 CONTACTING THE CONFERENCE COMMITTEE: To contact
the congress organizers for any reason use any of the 
following pathways:

ELECTRONIC MAIL - compmed94@chpc.utexas.edu

FAX (USA)       - (512) 471-2445

PHONE (USA)     - (512) 471-2472

GOPHER: log into the University of Texas System-CHPC
select the Computational Medicine and Allied Health
menu choice

ANONYMOUS FTP: ftp.chpc.utexas.edu
               cd /pub/compmed94
POSTAL:
            Compmed 1994
      University of Texas System CHPC
	    Balcones Research Center
	    10100 Burnet Road, 1.154CMS
	    Austin, Texas 78758-4497 

5.0 SUBMISSION PROCEDURES: Authors must submit 5 

From owner-acedb@net.bio.net Tue Sep 14 23:00:00 1993
Path: biosci!FRODO.MGH.HARVARD.EDU!CHERRY
From: CHERRY@FRODO.MGH.HARVARD.EDU (Mike Cherry)
Newsgroups: bionet.software.acedb
Subject: ACEDB 1-21 available via Gopher
Message-ID: <930915130145.2020011c@Frodo.MGH.Harvard.EDU>
Date: 15 Sep 93 17:01:45 GMT
Sender: daemon@net.bio.net
Distribution: biosci
Lines: 73

The information from ACeDB release 1-21 is now available via Internet
Gopher from weeds.mgh.harvard.edu.

Once connected to the weeds.mgh.harvard.edu Gopher server select the
following menu item:

      5.  Arabidopsis Information (thale cress)/
 -->  6.  Caenorhabditis Inform/
      7.  Department of Molecular Biology, MGH/

Then the menus will change to:

 -->  1.  Help Searching the "<?>" databases.
      2.  ACEDB, A Caenorhabditis elegans Database (1-21) <?>
      3.  C. elegans Strains and Alleles (University of Texas)/
      4.  Caenorhabditis Genetics Center (CGC)/

See the Help document for more details on performing searches. The
ACEDB release 1-21 physcial map is also included in a text format. For
example: select menu item 2 and entering K09A10 . The search result
will be shown as:

 -->  1.  Clone_Pic : K09A10.
      2.  Contig : ctg1.

The Clone_Pic item looks like:

Clone_Pic : K09A10
Member of Contig: ctg1
Contig: ctg1 limits: -154 to 436
Limits of this partial view are: -117 to 53
----------------------Y48E9----------------------
---------------Y67G4---------------
-----------------------------------Y53C6-----------------------------------
  -------------Y48A8-------------
  -----Y27H10-----
  ------Y68B7------
           ---K05C4---
            --R10E1--
             ---C43D5---
                          ----F14B11----
                            ====K09A10====
                                 -------------------Y54F6!-------------------
                                 ---T10A7---
                                  -----C13G1-----
                                     ---SG25/36---
                                      ------K05G4------
                                      -SG23/3-
                                      ------C03C9------


This release of ACEDB include many abstracts from the Worm Breeder's
Gazette so you can search for general terms like kinase, neuro* or
homeo* to find several items of interest.

The Gopher .Link entry, for those that like this form, is:

Type=7
Name=ACEDB, A Caenorhabditis elegans Database (1-21)
Path=7/.index/Caenorhabditis_elegans_Genome
Host=weeds.mgh.harvard.edu
Port=70

The ACEDB software for Unix X-windows and the ACeDB database is
developed and maintained by Richard Durbin (MRC-LMB, U.K.) and Jean
Thierry-Mieg (CNRS, France).

Durbin R and Thierry-Mieg J (1991). A C elegans Database Documentation
code and data available from Anonymous FTP servers at lirmm.lirmm.fr,
cele.mrc-lmb.cam.ac.uk and ncbi.nlm.nih.gov.

Mike Cherry
cherry@frodo.mgh.harvard.edu

From owner-acedb@net.bio.net Thu Sep 16 23:00:00 1993
Path: biosci!FRODO.MGH.HARVARD.EDU!CHERRY
From: CHERRY@FRODO.MGH.HARVARD.EDU (Mike Cherry)
Newsgroups: bionet.software.acedb
Subject: AAtDB 1-5 now available
Message-ID: <930917010317.202008b5@Frodo.MGH.Harvard.EDU>
Date: 17 Sep 93 05:03:17 GMT
Sender: daemon@net.bio.net
Distribution: biosci
Lines: 242

AAtDB release 1-5

Release 1-5 of AAtDB, An Arabidopsis thaliana Database, is now
available for Unix workstations as well as through the Internet using
the Gopher and WAIS software clients.

This release of AAtDB includes several new and updated types of
information:

  o New and revised stock information provided by Mary Anderson of the
    Nottingham Arabidopsis Stock Centre.

  o Over one hundred new images of Arabidopsis ecotypes and mutations
    available from either the Ohio State or Nottingham stock centers.

  o Over one thousand new DNA sequences from GenBank including the
    sequence similarity of these sequences to entries in the protein
    sequence databases as defined by NCBI's BLASTX software.

  o Several new and updated Colleague entries.

  o New bibliographic information from Medline.


AAtDB Class Sizes in release 1-5:

  Class Name            Total Entries          New Entries in 1-4
 ===============      =================       ====================
   Allele                    293                       165
   Author                   4272                       243
   Chromosome                 25                         0
   Clone                   14606                         0
   Clone_Grid                  2                         0
   Colleague                1277                        15
   Contig                   1196                         0
   DNA                      2485                      1066
   Gene_Class                243                         2
   Gene_Product              187                        40
   Image                     235                       113
   Journal                   361                         8
   KeySet                     22                         4
   Keyword                  5369                       256
   Locus                    1398                       143
   Paper                    3535                       187
   Phenotype                1449                        54
   Population                 26                         6
   Probe                     426                         1
   Restriction               338                         0
   Sequence                 9006                      4097
   Source                     58                         1
   Strain                   5567                      1081
   2_point_data             3741                         0


AAtDB uses the ACEDB software developed by Richard Durbin (MRC-LMB,
U.K.) and Jean Thierry-Mieg (CNRS, France). The AAtDB project is
funded by the U.S. Department of Agriculture Plant Genome Research
Program through the National Agricultural Library. The AAtDB project
is staffed by members of the Department of Molecular Biology at
Massachusetts General Hospital and Harvard Medical School, Boston USA.
AAtDB is available without charge via Internet FTP transfer and remote
X-windows access (see below).

AAtDB features a wide variety of public information that is presented
using graphical, text, and tabular formats. The user interface, which
was designed to invite browsing, allows users to explore information
by pointing and clicking with the workstation mouse or by using a
versatile query facility. ACEDB allows all parts of the database to be
cross-referenced with each other. The large number of interconnections
provides a dense navigable network in which information can be located
from many different starting points (see sample screen in appendix).

All information contained within AAtDB was obtained directly from the
original authors or from publicly available collections and databases.
Updates to AAtDB are periodically distributed and the database is now
in its fifth data release. A partial list of the information AAtDB 1-5
contains includes:

-- The Hauge/Goodman cosmid physical map including greater than 14,000
cosmid clones. The contigs of the physical map are associated with the
genetic maps.

-- Genetic markers, including RFLP, RAPD, and "classical" markers.

-- Genetic maps, including the Integrated map from Hauge et al. (1993)
The Plant Journal, a visible marker map including many embryo
defective loci from David Meinke, and RAPD maps from Scolnik et al.
(1992) PNAS.

-- Primary F2 and RI population recombination data from the Goodman,
Meyerowitz, Scolnik, and Dean laboratories.

-- Primary 2-point data from M. Koorneef, D. Meinke, and others.

-- Strain list, now maintained and entered for AAtDB by Mary Anderson
at the Nottingham Arabidopsis Stock Centre. Includes many new entries
from the Nottingham and Ohio State stock centers.

-- List of Arabidopsis researchers, including postal mail address,
telephone and FAX numbers, electronic mail address, publications,
research interests, and research associates. Information on over 1200
colleagues is included.

-- All Arabidopsis DNA sequences from GenBank and EMBL DNA sequence
databases as well as the EST (expressed sequence tags, i.e., cDNA)
reports from the NCBI's dbEST database on the MSU and French
sequencing efforts, with over 2400 entries total.

-- NCBI BLASTX (six frame translations searched against the NCBI
non-redundant peptide database) defined peptide sequence homologies
for all DNA sequences included in AAtDB.

-- Phenotype descriptions from the Green Book by Meyerowitz and
Pruitt, updated with descriptions from the Nottingham and Ohio State
stock centers.

-- Scanned images of RFLP autoradiograms from the Goodman lab,
photographs of mutant plants from G. Redei and M. Anderson, and
ethidum bromide-stained restriction enzyme digests of RFLP probes
distributed by the ABRC.

-- Bibliographic citations, including references for all articles from
the Arabidopsis Information Service, currently numbering 3400.

AAtDB  1-5 utilitzes the new ACEDB  1.10 software providing fixes and
new features.  Note that the ACEDB  software is  now available for the
public Unix version called Linux  that runs on Intel 386 and 486 based
systems! For  more information about Linux retrieve  the  linux.readme
file via anonymous ftp or Gopher.

The ACEDB software is developed by Richard Durbin (MRC-LMB, Cambridge,
UK) and  Jean Thierry-Mieg (CNRS,  Montpellier,  France).  Precompiled
executables  of ACEDB are available for Sun SPARC (SunOS and Solaris),
DEC MIPS and Alpha, NeXT, IBM-6000, and Silicon Graphics  workstations
under  the X-windows environment  plus  Intel  386 and  486  computers
running Linux.  ACEDB can be compiled on Suns under Sunview or Sun386i
under OpenWindows, Alliant, and CONVEX computers.  A Macintosh version
is in development.

All  the  AAtDB  information  in  text  form  is  available   via  the
Arabidopsis Research  Companion, an  Internet  Gopher server available
from the host Weeds.MGH.Harvard.EDU. For convenience the bibliographic
references have been  converted to Macintosh  EndNote and the  general
bibliographic format called refer.   The new images  obtained from the
ABRC at Ohio State  University  are available as GIF files.  All these
files  are  available  via Gopher  and  anonymous ftp  from  the  host
Weeds.MGH.Harvard.EDU (IP 132.183.190.21).


Using Gopher to search AAtDB and retrieve information:

Internet  Gopher  was  developed by  the  University  of Minnesota. It
requires  a  computer that  is  connected  to  the worldwide  Internet
network. Software referred to as a Gopher client is available for most
types of  computer, most of these are available via anonymous ftp from
boombox.micro.umn.edu.

If your computer manager cannot provide you with one of the free
Gopher clients but you have access to telnet you can use a public
access account provided by the Department of Molecular Biology at
Massachusetts General Hospital.  Simply telnet to the host
Weeds.MGH.Harvard.EDU (IP 132.183.190.21), use the username gopher,
there is no password. A Gopher client will start that automatically
connects with the AAtDB Research Companion.  Text information can be
mailed from the public gopher account by using the "m" option.
However the images cannot be viewed using the public telnet account.
A Gopher client on your local computer is required to view images, or
you can transfer the images via an ftp or Gopher client to an
intermediate computer subsequently transferring the image to a
workstation or personal computer that can display GIF and JPEG images.


Remote Access to the Unix AAtDB database using X-windows

Remote access to the full Unix version of AAtDB is now available to
computers with a good Internet network connection and X-windows
software. This means that most Unix workstations using OpenWindows,
Motif, or any of a large number of other windowing environments based
on MIT's X-windows can access a remote server that will display the
graphic interface of AAtDB on the local computer's display. For
personal computers a variety of commercial X-windows emulation
software is available: Macintosh users can purchase eXodus (White Pine
Software) or MacX (Apple Computer), MS Windows users can use Vista
eXceed plus (Hummingbird Communications) or DESQview/X (Quarterdeck
Office Systems).

The basic procedure is to login on the host weeds.mgh.harvard.edu
using the username 'aatdb'; no password is required. If you are on a
Unix X-windows workstation you will need to issue the following
command before connecting with the server:

	% xhost weeds.mgh.harvard.edu

The above command is required to allow the AAtDB server to creat
From owner-acedb@net.bio.net Tue Sep 21 23:00:00 1993
Path: biosci!daresbury!doc.ic.ac.uk!warwick!pavo.csi.cam.ac.uk!nntp-serv!esr
From: esr@al.mrc-lmb.cam.ac.uk (Sonnhammer E./Durbin)
Newsgroups: bionet.software.acedb
Subject: Re: Notes from ACEDB Workshop, part I
Message-ID: <ESR.93Sep22164005@al.mrc-lmb.cam.ac.uk>
Date: 22 Sep 93 16:40:05 GMT
References: <jlmccarthy-080993095131@slavsing.lbl.gov>
Sender: news@infodev.cam.ac.uk (USENET news)
Followup-To: bionet.software.acedb
Organization: /hgmp0/esr/.organization
Lines: 35
In-Reply-To: jlmccarthy@lbl.gov's message of 8 Sep 1993 16:42:17 GMT
Nntp-Posting-Host: al.mrc-lmb.cam.ac.uk


Thanks John McCarthy for your excellent notes of the ACEDB workshop!

I feel obliged, however, to correct your notes on 'fetch' which
retrieves sequence data from external databases for either annotation
pop-up or multiple alignment of blast segments in 'Blixem'.

Your notes say:

>   Sequence Fetch/Align
>   --------------------------
>   a. summon up SwissProt/PIR entry(s)
>   b. show multiple alignment based on BLAST segments = BLIXEM
>   uses unix command
>      fetch  	-Bdbname (SP,PIR,EMBL,GB)
>		-a accession number
>		-P Pearson (FASTA) format
>		-s  just  sequence ... no new line
>      our version uses the EMBL CDROM index structure

The -P and -s options are incorrect.  They should be 

		-f Pearson (FASTA) format
		-q just sequence (on one line)


The fetch program used here in Cambridge is available by anonymous FTP
on cele.mrc-lmb.cam.ac.uk in /pub/acedb/fetch.tar.Z, which contains
further instructions. There are actually about 15 options at the
moment.  If you prefer to call your own 'fetch' from ACEDB, only the
-q option is necessary though.

Erik Sonnhammer
Sanger Centre
Cambridge, UK

From owner-acedb@net.bio.net Wed Sep 22 23:00:00 1993
Path: biosci!daresbury!doc.ic.ac.uk!agate!fly2.berkeley.edu!hcobb
From: hcobb@fly2.berkeley.edu (Henry J. Cobb)
Newsgroups: bionet.software.acedb
Subject: Re: Write locks in Acedb [Long and boresome, for code nerds only]
Message-ID: <HCOBB.93Sep23140612@fly2.berkeley.edu>
Date: 23 Sep 93 21:06:12 GMT
References: <1993Sep23.182732.1681@gserv1.dl.ac.uk>
Distribution: bionet
Organization: University of California, Berkeley
Lines: 49
NNTP-Posting-Host: fly2.berkeley.edu
In-reply-to: rd@uk.ac.cam.mrc-lmb's message of Thu, 23 Sep 1993 18:20:03 GMT


	I did not ask the question clearly enough, so let me take another
stab at it.

	My understanding of this program is somewhat incomplete (i.e.: I
haven't managed to read through the TAGS file...), but my presumption is
that the user grabs "write access" to the database and is then allowed an
extended browsing period where they build up a "delta" to be applied to the
database, which is then committed in a single call to sessionClose(true).

	The effect being that other readers of the database will see a
sudden, consistent change to the database, but that only one session will
be allowed into the "gather and modify" mode at a time.

	My suggestion was along the lines of only locking the database at
the "moment" of committing a change, with the option of alerting other
sessions (that were contemplating changes) that a change had been made to
the database, and giving them the option to abandon their (uncommitted)
changes or run a check for overlaps, or whatever.

	I would also like to hack the session ID "numbers" to include the
machine, user and (Unixy) process ID number.  This would be a step along
the way to providing a "virtual server" implemented in the file system
itself.

	The end result of my little plot would have "minor version numbers"
attached to the database where at certain points readers of the database
would notice that the version number had changed beneath them and flush
their little caches, while browsers would be left alone to complete their
"delta" and then when they choose to commit it be informed that a change
had taken place in the database and be allowed to step through the records
involved and combine the original, their changes and the other changes.

	This would, of course, update their "snapshot" of the database and
if further changes occurred while they were back into this browsing mode
they would face the same process over (from the new snapshot) when they
again try to commit.  (This also might prove helpful in merging together
versions of the database from different user sites).

	Now (fortunately) I wasn't born a biologist.  So it really isn't my
place to decide upon the policy of how the multiple writers, multiple
machine case should be handled.  But as a "Bjarne again" hacker I'd like to
implement the mechanism in the cleanest, simplest, most general manner,
exactly once.  I realize that the only program "guaranteed to work on all
machines" is Microsoft Word for Windows, but I do not want to pile up a
bunch of redundant backup systems.  Given the choice, I'd put my locking
code into a few functions and let the end-users replace those as needed.
--
	Henry J. Cobb	hcobb@fly2.berkeley.edu	SFB Tyrant

From owner-acedb@net.bio.net Wed Sep 22 23:00:00 1993
Path: biosci!daresbury!daresbury!news
From: rd@uk.ac.cam.mrc-lmb (Richard Durbin)
Newsgroups: bionet.software.acedb
Subject: Re: Write locks in Acedb
Message-ID: <1993Sep23.182732.1681@gserv1.dl.ac.uk>
Date: 23 Sep 93 18:20:03 GMT
Sender: list-admin@daresbury.ac.uk
Distribution: bionet
Lines: 23
Precedence: first-class
Original-To: acedb@uk.ac.daresbury, hcobb@fly2.berkeley.edu
Original-Cc: mieg@ppsw.cam.ac.uk


It is clear that semaphores are inappropriate for ACEDB, since they
are machine specific, and these days people almost always run in a NFS
network environment.  In fact I always disable them by setting SEM = 0!

There is in fact a lock file operating (database/lock.wrm), but that
has problems if a program dies ungracefully without removing the
lockfile.  For that reason ACEDB puts up a warning explanation if the
lock file is set, but allows you to override it.

I understood that there is an advisory record locking mechanism that
works across NFS, breaks the lock when the locking process dies, and
even handles remote disk server downs well.  This seems to me a good
candidate to replace semaphores.  Is the problem that it requires
lockd, which Henry says is not always available?  Even if so, we could
use this, with the overidable lock file as a backup.

The history of the code that manages all this (session.c) is that it
is old and has had a number of solutions layered on each other.  I
apologise for the mess.  Cleanups guaranteed to compile and work on
all machines would be appreciated.

Richard

From owner-acedb@net.bio.net Wed Sep 22 23:00:00 1993
Path: biosci!daresbury!doc.ic.ac.uk!warwick!uknet!pipex!howland.reston.ans.net!agate!fly2.berkeley.edu!hcobb
From: hcobb@fly2.berkeley.edu (Henry J. Cobb)
Newsgroups: bionet.software.acedb
Subject: Write locks in Acedb
Message-ID: <HCOBB.93Sep23105946@fly2.berkeley.edu>
Date: 23 Sep 93 17:59:46 GMT
References: <jlmccarthy-080993095310@slavsing.lbl.gov>
Followup-To: bionet.software.acedb
Organization: University of California, Berkeley
Lines: 14
NNTP-Posting-Host: fly2.berkeley.edu


	The semaphore system in Acedb seems to be slightly misused, and
anyway won't scale over NFS mounts.

	NFS guarantees only one atomic action (without the presence of
lockd, which is not universal):  File creation.

	So is there any objection to throwing out the Semaphores and other
junk and replacing this with a simple:

	open( lockfile, O_RDWR | O_CREATE | O_EXCL) or fail in
sessionClose()?
--
	Henry J. Cobb	hcobb@fly2.berkeley.edu	SFB Tyrant

From owner-acedb@net.bio.net Wed Sep 22 23:00:00 1993
Path: biosci!daresbury!daresbury!news
From: rd@uk.ac.cam.mrc-lmb (Richard Durbin)
Newsgroups: bionet.software.acedb
Subject: more on locks
Message-ID: <1993Sep23.214236.3664@gserv1.dl.ac.uk>
Date: 23 Sep 93 21:35:09 GMT
Sender: list-admin@daresbury.ac.uk
Distribution: bionet
Lines: 45
Precedence: first-class
Original-To: acedb@uk.ac.daresbury


Hmm. I think there are technical difficulties with Henry's
suggestions.

We lock the whole database so that only one user can every be
accumulating changes at one time.  When one user gets write access
that starts a new session and you lock against any others from getting
write access.  As changes are made they get written to disk (depends
on caches etc), but all objects touched in the new session are written
to new disk blocks.  Only when the user saves a session are the
indices and superblock rewritten, so up to that point any other user
starting up will get the old version.  (Also any crash will leave the
old version intact.)

Other users can not detect the update being made -- they have to quit
and start up again to pick it up.  Perhaps we could implement
something to check the superblock to check for this, but essentially
they would have to flush everything, in case it had changed.  The only
alternative would be a scan of all dynamically held data of all sorts,
which is a nightmare.

The problem with locking only during saving, which allows parallel
updating, is that if two users A and B take an object X, A edits it
and writes it back, and then B edits it tries to write it, the state B
is editing it from is not the last state of the database.  One
solution is to lock at the object level, not at the database level,
allowing several individuals to check out different objects.  However
that rapidly leads to deadlock situations, where two users are waiting
for each other to free something.  All very nasty.  Another is to do a
comparison when you save, to see if the object has changed under you.
But what to do if it has?  

Of course you are right that this is the same problem involved in
merging databases.  There we agreed that we need tools to highlight
clashes, but final fixing is up to the curator to manage.

As it is, the current sessions keep track of the user.  I don't see
the point in keeping the Unix pid.  Maybe the machine, though this
does not seem that relevant.  The date and time really should be there
-- currently they are not.  It is easy to add more information, since
the session is not just a "number", but also an ACEDB object.  We can
extend its model like any other (almost).  The "(almost)" is because
the sessions get treated slightly differently, being not under session
control themselves, and can only contain tags and data (Int, Float,
Text), not pointers to other objects.

From owner-acedb@net.bio.net Thu Sep 23 23:00:00 1993
Path: biosci!agate!overload.lbl.gov!dog.ee.lbl.gov!slavsing.lbl.gov!user
From: jlmccarthy@lbl.gov (John L. McCarthy)
Newsgroups: bionet.software.acedb
Subject: Re: gateway WWW-ACEDB
Message-ID: <jlmccarthy-240993085054@slavsing.lbl.gov>
Date: 24 Sep 93 15:49:02 GMT
References: <1993Sep12.144428.14066@inra.fr>
Followup-To: bionet.software.acedb
Organization: Lawrence Berkeley Laboratory
Lines: 60
NNTP-Posting-Host: 128.3.252.43

In article <1993Sep12.144428.14066@inra.fr>, decoux@moulon.inra.fr (ts)
wrote:

>  
>  Gateway WWW-ACEDB
>  =================
>  
>  If you want to consult ACeDB and MycDB, try :
>  
>    * "http://moulon.inra.fr/acedb/acedb.html" to consult "A Caenorhabditis
> elegans Data Base" (ACeDB).
>  
>    * "http://moulon.inra.fr/acedb/mycdb.html" to consult "Mycobacterium
> DataBase". "Mycobacterium DataBase" is funded by the WHO and the Fondation
> Raoul Follereau and is maintained by the Unite de Genetique Moleculaire
> Bacterienne at the Institut Pasteur.
>  
>  
>  To consult these databases, you can : 
>  
>     * If you know syntax of "tace" commands, enter your query in "SearchText".
>     * otherwise you can make a complete Consultation of the database.  
>  
>  For more precisions, about "tace" syntax, just enter "help".
>  
>  
>  If you want to create an ACEDB gateway, see (or contact me) :
>  
>           "http://moulon.inra.fr/acedb_conf_eng.html" 
>                              ou
>           "http://moulon.inra.fr/acedb_conf.html"  (version francaise)
> -- 
> 
> Guy Decoux

--
I finally had a chance to try these yesterday, and they are VERY
impressive.
It is the next best thing to running ACEDB itself.

For Mac users, the just-released NCSA Mosaic B1 (beta) is a very nice way
to access them on a color Macintosh. To get NCSA Mosaic for the Mac, you
can just

ftp ftp.ncsa.uiuc.edu
cd Mac/Mosaic
get NCSAMosaicMac.B1.sit.hqx

If you use Fetch (also from NCSA), it will automatically unbinhex the
result.
Then you can double click the result to decompress into working files.

 
+=====================================================================+
|  John L. McCarthy.               . | Internet:..JLMcCarthy@lbl.gov  |
|  Computer Science R&D  MS 50B-3238 | Bitnet: ...JLMCCARTHY@LBL      |
|  Lawrence Berkeley Laboratory     .| telephone: (510) 486-5307      |
|  1 Cyclotron Road                . |                                |
|  BERKELEY, CA 94720, U.S.A.      . | FAX:       (510) 486-4004      |
+=====================================================================+

From owner-acedb@net.bio.net Thu Sep 23 23:00:00 1993
Path: biosci!uwm.edu!cs.utexas.edu!usc!howland.reston.ans.net!agate!fly2.berkeley.edu!hcobb
From: hcobb@fly2.berkeley.edu (Henry J. Cobb)
Newsgroups: bionet.software.acedb
Subject: Re: more on locks
Message-ID: <HCOBB.93Sep24121839@fly2.berkeley.edu>
Date: 24 Sep 93 19:18:39 GMT
References: <1993Sep23.214236.3664@gserv1.dl.ac.uk>
Distribution: bionet
Organization: University of California, Berkeley
Lines: 22
NNTP-Posting-Host: fly2.berkeley.edu
In-reply-to: rd@uk.ac.cam.mrc-lmb's message of Thu, 23 Sep 1993 21:35:09 GMT


	Thanks, OK I won't mess with the policy of global database locking.

	But unless there is something else I've overlooked, I'll add a
section to filopen() (protected by a #ifndef NO_ATOMIC_CREATION (I hope
that nothing is really that broken)).

	I'll check for spec == "atomic" and do an open() with O_WRONLY |
O_CREAT | O_EXCL followed by an fdopen() for lockfile itself.

	Then I'll change the ...WriteLock functions to atomically create
the lockfile, or remove it, etc.

	Also I'd like to set a special protocol in the client/server setup
to request a break of the lock.

	All of the OS'es I am aware of have some procedure for atomic file
creation, and I know of no other IPC which is common to all of them.  If
this is a problem under say VMS or MVS or Novell or Appleshare, etc.,
please let me know.
--
	Henry J. Cobb	hcobb@fly2.berkeley.edu	SFB Tyrant

From owner-acedb@net.bio.net Fri Sep 24 23:00:00 1993
Path: biosci!uwm.edu!math.ohio-state.edu!howland.reston.ans.net!agate!overload.lbl.gov!bks
From: bks@s27w007.pswfs.gov (Bradley K. Sherman)
Newsgroups: bionet.software.acedb
Subject: Re: more on locks
Message-ID: <281t94$5ss@overload.lbl.gov>
Date: 25 Sep 93 16:57:08 GMT
References: <1993Sep23.214236.3664@gserv1.dl.ac.uk> <HCOBB.93Sep24121839@fly2.berkeley.edu>
Distribution: bionet
Organization: Dendrome, A Genome Database for Forest Trees
Lines: 24
NNTP-Posting-Host: s27w007.pswfs.gov

In article <HCOBB.93Sep24121839@fly2.berkeley.edu> hcobb@fly2.berkeley.edu (Henry J. Cobb) writes:
> ...
>	I'll check for spec == "atomic" and do an open() with O_WRONLY |
>O_CREAT | O_EXCL followed by an fdopen() for lockfile itself.
> ...
>	All of the OS'es I am aware of have some procedure for atomic file
>creation, and I know of no other IPC which is common to all of them.  If
>this is a problem under say VMS or MVS or Novell or Appleshare, etc.,
>please let me know.
> ...

There was a nasty problem with NFS and SunOS 3.x where calls such
as this (open (...O_CREAT...)) appeared to succeed but which did
not preempt similar calls from other workstations.  This was
caused by local file caching. I do not know if this feature of
Sun/NFS interaction has been fixed in subsequent releases, or
whether it plagues other NFS implementations.

    --bks
-- 
Bradley K. Sherman               P.O. Box 245                    
Computer Scientist               Berkeley, CA, 94701
Dendrome Project                 510-559-6437 FAX: 510-559-6440  
Institute of Forest Genetics     Internet: bks@s27w007.pswfs.gov

From owner-acedb@net.bio.net Sat Sep 25 23:00:00 1993
Path: biosci!agate!fly2.berkeley.edu!hcobb
From: hcobb@fly2.berkeley.edu (Henry J. Cobb)
Newsgroups: bionet.software.acedb
Subject: Re: more on locks
Message-ID: <HCOBB.93Sep26103706@fly2.berkeley.edu>
Date: 26 Sep 93 17:37:06 GMT
References: <1993Sep23.214236.3664@gserv1.dl.ac.uk> <HCOBB.93Sep24121839@fly2.berkeley.edu>
	<281t94$5ss@overload.lbl.gov>
Distribution: bionet
Organization: University of California, Berkeley
Lines: 23
NNTP-Posting-Host: fly2.berkeley.edu
In-reply-to: bks@s27w007.pswfs.gov's message of 25 Sep 1993 16:57:08 GMT


	OK gang, time for ultimate defensive driving here!

	First: the semaphores will not help NFS one little bit, so drop em.

	Now the plan:

1) Check to see if the file exists.

2) If it doesn't then open it for exclusive create with no buffering
(O_SYNC).

3) Write out the usual stuff.

4) (redundantly) flush it then close it.

5) Reopen the file for reading and check to see if it has what we
(hopefully) just wrote to it, and nothing more.

	Fail on any error, complain to the log files (with an option to
mail the Admin) and clean up whatever seems to be resonable.
--
	Henry J. Cobb	hcobb@fly2.berkeley.edu	SFB Tyrant

From owner-acedb@net.bio.net Sun Sep 26 23:00:00 1993
Path: biosci!bloom-beacon.mit.edu!gatech!howland.reston.ans.net!agate!overload.lbl.gov!bks
From: bks@s27w007.pswfs.gov (Bradley K. Sherman)
Newsgroups: bionet.software.acedb
Subject: bionet.software.acedb FAQ
Summary: Frequently Asked Questions about finding and getting
	started with the database system ACEDB.  ACEDB is used
	to collect information regarding the molecular biology
	of the genome.
Message-ID: <287bt8$fg4@overload.lbl.gov>
Date: 27 Sep 93 18:37:28 GMT
Reply-To: acedbfaq@s27w007.pswfs.gov
Followup-To: poster
Organization: Lawrence Berkeley Laboratory, Berkeley CA
Lines: 375
NNTP-Posting-Host: s27w007.pswfs.gov

Archive-name: acedb-faq
Last-modifed: 9/27/93
Version: 1.1

----------------------------------------------------------------------
Common Questions and Answers about ACEDB.

    This is the zeroth posting of this document.  Errors of
    commission or omission are unintentional.

    Please send comments and corrections to acedbfaq@s27w007.pswfs.gov.
    Curators of ACEDB databases should take note of Question 4 and
    keep me apprised of changes.

    I will submit the next version of this FAQ for Usenet
    archival storage.
        --Bradley K. Sherman

----------------------------------------------------------------------
List of questions in the ACEDB FAQ:

Q0:  What is ACEDB?
Q1:  What is the current version of ACEDB?
Q2:  What {hardware | software} do I need to run ACEDB?
Q3:  Where can I get ACEDB?
Q4:  What ACEDB databases exist?
Q5:  What written documentation exists for ACEDB?
Q6:  Where can I find further information about ACEDB?
Q7:  How should ACEDB be cited?
Q8:  Is ACEDB object-oriented?
Q411:Who contributed to this document?

----------------------------------------------------------------------
Q0:  What is ACEDB?

A0:  ACEDB is an acronym for A Caenorhabditis elegans Database.  It can
     refer to a database and data concerning the nematode C.  elegans,
     or to the database software alone.  This document is concerned
     primarily with the latter meaning.  ACEDB is being adapted by many
     groups to organize data about diverse species [see Q4].

     ACEDB allows for automatic cross-referencing of items when loaded
     and allows for hypertextual navigation of the links using a mouse.
     Certain special purpose graphical displays have been integrated
     into the software.  These reflect the efforts of molecular
     biologists in constructing genetic and physical maps of genomes.

     ACEDB was written and developed by Richard Durbin (MRC LMB
     Cambridge, England) and Jean Thierry-Mieg (CNRS, Montpellier,
     France), beginning circa 1990.  It is written in the C programming
     language and uses the X11 windowing system to provide a platform
     independent graphical user interface.  The source code is publicly
     available [See Q3].  Durbin & Thierry-Mieg continue to develop
     the system, with contributions from other groups including
     Lawrence Berkeley Laboratory and the European integrated Genome
     Project.

     A description by Durbin & Thierry-Mieg:
         ACEDB does not use an underlying relational database
	 schema, but a system we wrote ourselves in which data
	 are stored in objects that belong in classes.  This is
	 nevertheless a general database management system using
	 caches, session control, and a powerful query language.
	 Typical objects are clones, genes, alleles, papers,
	 sequences, etc.  Each object is stored as a tree,
	 following a hierarchical structure for the class (called
	 the "model").  Maps are derived from data stored in tree
	 objects, but precomputed and stored as tables for
	 efficiency.  The system of models allows flexibility
	 and efficiency of storage -missing data are not stored.
	 A major advantage is that the models can be extended
	 and refined without invalidating an existing database.
         Comments can be added to any node of an object.

         Current display modes are:
             TREE   for text type objects: papers, authors, genes
	            etc.
             GMAP   genetic map
             PMAP   physical map (Sulston contig style)
             SEQ    DNA sequence - symbolic, features, sequence
	            and translation
             GRID   hybridisation patterns for a probe to a clone
	            grid
             BIBLIO bibliography attached to any object display
	            modules under development:
             CMAP   whole chromosome physical map plot
             GEL    agarose gel simulation derived from sequence

----------------------------------------------------------------------
Q1:  What is the current version of ACEDB?

A1:  1-10.  It was released Summer 1993.  The next release will be
     2.0.

----------------------------------------------------------------------
Q2:  What {hardware | software} do I need to run ACEDB?

A2:  ACEDB currently runs on the following Unix sytems, under X11:
         Sun SPARCstation 1, 1+, 2, IPC, IPX:
         SPARCstation 10 running Solaris:
         DEC  DECstation3100, 5100 etc.
         DEC  Alpha/OSF-1
         Silicon Graphics Iris series
         PC 386/486 with Linux (public domain Unix)
    Other Unix:
        There exist, or have existed, ports onto Alliant, Hewlett-
	Packard, IBM R6000, NeXT, Convex.   You may have to contact
	the developer responsible for the port to make these real.
    Macintosh:
        A port to the Macintosh may become available by the end of 1993.


----------------------------------------------------------------------
Q3:  Where can I get ACEDB?

A3:  All the files are available in the following public access
     accounts (anonymous ftp sites) accessible via Internet:
          lirmm.lirmm.fr         (193.49.104.10)  genome/acedb
          cele.mrc-lmb.cam.ac.uk (131.11.84.1)    pub/acedb
          ncbi.nlm.nih.gov       (130.14.20.1)    repository/acedb

----------------------------------------------------------------------
Q4:  What ACEDB databases exist?

A4:  Database : ACeDB
     Species : Caenorhabditis elegans
     Availability :
     Current version: 1-10
     Curator : Jean Thierry-Mieg
     Curator : Richard Durbin
     Contact : rd@cele.mrc-lmb.cam.ac.uk
     Contact : mieg@kaa.cnrs-mop.fr
     Last_update : Sept. 1993

     Database : AAtDB
     Species : Arabadopsis thaliana
     Availability : 
     Curator : John Morris
     Current version: 1-5
     Contact : curator@frodo.mgh.harvard.edu
     Last_update : Sept. 1993

     Database : GrainGenes
     Species : Wheat, barley, oats, relatives
     Availability : Gopher greengenes.cit.cornell.edu port 70
     Availability : ACEDB version by ftp, on request from the curators
     Curator : David E. Matthews
     PI : Olin D. Anderson
     Contact : matthews@greengenes.cit.cornell.edu
     Contact : oandersn@wheat.usda.gov
     Last_update : Sept. 1993

     Database : SolGenes
     Coverage: Solanaceae - tomato, potato, pepper (eventually)
     Availability : Beta ACEDB via login or tar file
     Curator : Edie Paul
     Contact : epaul@nightshade.cit.cornell.edu
     Last_update : Sept. 1993

     Database : RiceGenes
     Species : Rice (O. sative)
     Availability : under development, login at own risk
     Curator : Edie Paul
     Contact : epaul@nightshade.cit.cornell.edu
     Last_update : Sept. 1993

     Database : SoyBase
     Species : Soybeans
     Curator :  Lisa Lorenzen
     PI : Randy Shoemaker
     Contact : lorenzen@mendel.agron.iastate.edu
     Last_update : Sept. 1993

     Database : TreeGenes
     Species : Forest trees, Pinus taeda
     Availability : contact curator
     Curator : Bradley K. Sherman
     PI : David B. Neale
     Contact : Dendrome@s27w007.pswfs.gov
     Contact : bks@s27w007.pswfs.gov
     Contact : dbn@s27w007.pswfs.gov
     Last_update : Sept. 1993

     Database : 21Bdb
     Species : Homo sapiens
     Availability : by request, via ftp, gopher
     Curator : Donn F. Davy
     Contact : DFDavy@lbl.gov
     Contact : aggarwal@genome.lbl.gov
     Focus : STS content mapping & sequencing of Human Chromosome 21
     PI : Jasper Rine
     PI : Michael Palazzolo
     PI : Chris Martin
     PI : Jan-Fang Cheng
     Last_update : Sept. 1993

     Database : Flydb
     Species : Drosophila melanogaster
     Availability : by request only, via ftp
     Curator : Suzanna E. Lewis
     Contact : SELewis@lbl.gov
     Focus : STS content mapping project summary
     PI : Gerald Rubin
     PI : Mike Palazzolo
     PI : Dan Hartl
     PI : Alan Spradling
     Last_update : Sept. 1993

     Database : ChlamyDB
     Species : Chlamydomonas
     PI : Elizabeth Harris
     Last_update : Sept. 1993

     Database : AAnDB
     Species : Aspergillus nidulans
     PI : LeLand Ellis
     Last_update : Sept. 1993

     Species : Bovine
     PI : LeLand Ellis
     Last_update : Sept. 1993

     Species : Sorghum
     PI : LeLand Ellis
     Last_update : Sept. 1993

     Darabase : MycDB
     Species : Mycobacterium
     PI : Staffan Bergh
     PI : Thierry Garnier
     Last_update : Sept. 1993

     Database : EcoDB
     Species : E. coli
     PI : Staffan Bergh
     Last_update : Sept. 1993

     PI : Scott Chasalow
     Species : Potato
     Contact : Scottish Crop Institute, Dundee
     Last_update : Sept. 1993

     PI : George Murphy
     PI : David Flanders
     Species : Arabidopsis t.
     Contact : J. Innes Center, Norwich, England
     Last_update : Sept. 1993

     PI : David Bentley
     Species : Homo sap.
     Contact : Sanger Centre, Cambridge, England
     Last_update : Sept. 1993

     Database : MaizeDB
     Species : Maize
     Curator : Mary Polacco
     Contact : University of Missouri, Columbia, MO
     Last_update : Sept. 1993

     [Curators:  Please submit an entire paragraph in
      this format for inclusion or update. --bks]


----------------------------------------------------------------------
Q5:  What written documentation exists for ACEDB?

A5:  The primary documents are included in the Software
     distribution in the wdoc subdirectory:
         acedb -- A C. elegans Database: I. Users' Guide.
         acedb -- A C. elegans Database: II. Installation Guide.
         acedb -- A C. elegans Database: III. Configurat
From owner-acedb@net.bio.net Sun Sep 26 23:00:00 1993
Path: biosci!bloom-beacon.mit.edu!gatech!europa.eng.gtefsd.com!library.ucla.edu!agate!overload.lbl.gov!bks
From: bks@s27w007.pswfs.gov (Bradley K. Sherman)
Newsgroups: bionet.software.acedb
Subject: Re: bionet.software.acedb FAQ
Message-ID: <287ef9$g17@overload.lbl.gov>
Date: 27 Sep 93 19:21:13 GMT
References: <287bt8$fg4@overload.lbl.gov>
Organization: Dendrome, A Genome Database for Forest Trees
Lines: 20
NNTP-Posting-Host: s27w007.pswfs.gov


The first error in the FAQ is that my Organization was
listed as Lawrence Berkeley Laboratory.  This is an
artifact of the posting software and route and will
be corrected in future postings.

The Institute of Forest Genetics is part of the United
States Forest Service of the USDA.  Funding for the
Dendrome project comes in large part from the USDA
ARS / National Agricultural Library Plant Genome Database
project.

Sorry for any misunderstanding.

    --bks
-- 
Bradley K. Sherman               P.O. Box 245                    
Computer Scientist               Berkeley, CA, 94701
Dendrome Project                 510-559-6437 FAX: 510-559-6440  
Institute of Forest Genetics     Internet: bks@s27w007.pswfs.gov

From owner-acedb@net.bio.net Wed Sep 29 23:00:00 1993
Path: biosci!daresbury!doc.ic.ac.uk!warwick!uknet!pipex!uunet!haven.umd.edu!cville-srv.wam.umd.edu!usenet
From: asmarina@next03epsl.wam.umd.edu (Ghermay Araya)
Newsgroups: bionet.software.acedb
Subject: RESAMPLING SOLUTIONS TO PROBLEMS
Message-ID: <28fj81$1a8@cville-srv.wam.umd.edu>
Date: 30 Sep 93 21:31:45 GMT
Reply-To: THE ACM BUT HEADS
Organization: University of Maryland College Park
Lines: 178
NNTP-Posting-Host: next02wor.wam.umd.edu

SOLUTIONS AND PROBLEMS TO PREVIOUS POSTING:


 Resampling, (bootstrapping, etc.), is revolutionizing the practice of  
statistic, and the way it is taught.  For articles, and information on  
software + books, results of classroom trails, and descriptions of pending  
projects in which teachers can become involved, contact the University of  
Maryland's Resampling Project. We are especially interested in class  
testers.  Contact:
	 Resampling Project,
	 attn. P.G. Bruce
	 College of Business
	 University of Maryland,
	 College Park, MD  20742. 
          Phone: 703-522-2713
	 FAX 703-522-5846
	 email pcbruce@wam.umd.edu 
	 
	 (mark attn. P. C. Bruce). 
         please provide  both  postal and email address.



SOLUTIONS:

Solution, Puzzle 1:
        
1.  Three urns - "0,0"; "0,1"; "1,1".
        
2.  Choose an urn at random. [Can do this on the computer 
        
with random selection of urn numbers, and then "If"]
        
3.  Choose the first element in the chosen urn's vector.  If 
        
"1", stop trial and make no further record.  If "0", continue.
        
4.  Record the second element in the chosen urn's vector on 
        
the scoreboard.  
        
5.  Repeat (2 - 5), and calculate the proportion "0s" on 
        
scoreboard. (Answer should be 2/3.)
        
                
        
NUMBERS (1 2 3) a         '"1" denotes a selection of urn 1 (u1),
                          '"2" urn 2, "3" urn 3
NUMBERS (6 6) u1          '"u1" has two pennies (6's)
NUMBERS (7 7) u2          '"u2" has two nickels (7's)
NUMBERS (6 7) u3          '"u3" has one penny & one nickel
REPEAT 1000
  SAMPLE 1 a b            'Select an urn at random
  IF b =1                 'If urn selector says urn 1
    SHUFFLE u1 u1         'shuffle urn 1
    TAKE u1 1 c11         'take one coin from urn 1, call it c11
    IF c11=6              'if the coin is a penny
      TAKE u1 2 c12       'take the second coin
      IF c12=6            'if the second coin is a penny
        SCORE 6 z         'keep track of the second coin result
      END                 'end IF conditions
    END
  END
  
  IF b =2                 'if urn selector says urn 2
    SHUFFLE u2 u2         'etc. as above
    TAKE u2 1 c21
      IF c21=6
        TAKE u2 2 c22
        IF c22=6
          SCORE 6 z
        END
      END
    END
        
    IF b =3
      SHUFFLE u3 u3
      TAKE u3 1 c31
      IF c31=6
        TAKE u3 2 c32
        IF c32=6
          SCORE 6 z
        END
      END
    END
 
END                        'End the experiment, go back and
                           'repeat until 1000 repetitions
                           'are complete
COUNT z = 6 k
DIVIDE k 1000 kk
PRINT kk
        

Answer:        KK       =       0.34



Solution:  Puzzle 2
 
1.  Put a white ball (later have the computer call it "7" to 
        
avoid confusion) or black (call it "8") in the urn with 
        
probability .5.
        
2.  Put in a white and shuffle the two balls.
        
3.  Take out a ball.  If black, stop and make no record.  
        
4.  (If result of (3) is white):  Take out the remaining 
        
ball, examine, and record its color.
        
5.  Repeat steps 1-4 (say) until 1000 trials (with 1000 
        
recordings) have been completed.  (Alternatively, one can divide 
        
the number of repetitions by the number of records in the 
        
scoreboard).  
        
6.  Count the number and compute the proportion of whites 
        
(7s) among the trials where the result of step (3) is white.  
        
Carroll gives the answer as 2/3 (p. 32).
        
COPY (7 8) A        '7=WHITE COUNTER, 8=BLACK COUNTER.
        
REPEAT 1000
  SHUFFLE A B       'SHUFFLE THE TWO COUNTERS
  TAKE B 1 C        'TAKE A COUNTER FOR THE BAG
  CONCAT C 7 D      'JOIN A WHITE COUNTER TO THE BAG
  SHUFFLE D E       'SHUFFLE THE BAG
  TAKE E 1 F        'TAKE OUT A COUNTER
  IF F =7           'IF THE COUNTER YOU TAKE OUT IS WHITE
    TAKE E 2 G      'TAKE THE OTHER ONE
    SCORE G Z       'RECORD THIS SECOND ONE'S COLOR
  END
END                 'END THE REPEAT LOOP, GO BACK AND REPEAT
COUNT Z =7 K        'COUNT HOW MANY TIMES SECOND ONE WAS WHITE
DIVIDE K ZZ KK      'EXPRESS AS A PROPORTION OF THE NUMBER OF
                    'TRIALS ON WHICH THE FIRST ONE WAS WHITE.
PRINT KK
        
Answer:         KK       =    0.66356





FROM PREVIOUS MESSAGE:
PROBLEMS:

Two Puzzles:  Does your reasoning lead you astray on the following  
puzzles?  Most people's does.  Here are resampling (simulation) solutions  
that illustrate how such an approach, though less sophisticated than a  
formulaic one, yields correct answers and offers fewer opportunities to go  
wrong. 

        
        
1)  "Three identical boxes each contain two coins. In one 
box both are pennies, in the second both are nickels, 
and in the third there is one penny and one nickel. 
        
A man chooses a box at random and takes out a coin.  If 
the coin is a penny, what is the probability that the 
other coin in the box is also a penny?"   [from Goldberg, 
1960, p. 99]
       
        
2)  A bag contains one counter, known to be either white or black. A white  
counter is put in, the bag shaken, and a counter drawn out, which proves  
to be white.  What is now the chance of drawing a white counter?  From  
Lewis Carroll's PILLOW PROBLEMS (1895/1958) (p. 2, via Martin Gardner)

From owner-acedb@net.bio.net Thu Sep 30 23:00:00 1993
Path: biosci!NET.BIO.NET!kristoff
From: kristoff@NET.BIO.NET (David Kristofferson)
Newsgroups: bionet.software.acedb
Subject: IMPORTANT BIOSCI INFORMATION
Message-ID: <9310010900.AA04979@net.bio.net>
Date: 1 Oct 93 09:00:03 GMT
Sender: kristoff@net.bio.net
Distribution: biosci
Lines: 243


Three important items follow: BIOSCI archive searching by e-mail, the
BIOSCI FAQ, and the BIOSCI User Address Directory form.  If you have
not yet listed yourself in our e-mail address directory, please take a
few minutes to complete and return the form below.  If your address
information has changed since you listed yourself, please send us an
updated form.

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				kristoff@net.bio.net



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This notice will be mailed bimonthly to each newsgroup.  You should
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                  ---------------------------------

If you don't want to use a text editor, you can also use Dan
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> To add yourself to the database just point your
> gopher client at merlot.welch.jhu.edu and select the following:
> 
> -->  15. Searching For Biologists/
> 
>  -->  9.  E-mail Addresses of Biosci-Bionet Users/
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>   -->  1.  Add (or Correct) Your Address to the BIOSCI User Address
> Data..
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> 
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or Rob Harper's gopher site in Europe as follows:

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> 
> The path to the questionare is as follows.
> 
>    ---> 10. Finnish EMBnet BioBox/
> 
>         ---> 8.  FAQ Files/
> 
>                               FAQ Files
> 
>       1.  EMBnet: Information.
>       2.  EMBnet: Internet resources guide.
>       3.  A Biologist's Guide to Internet Resources/
>       4.  All FAQs (Frequently Asked Questions) Searches and Archives/
>   --->5.  Bionauts Address Database (questionaire) <TEL>


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DO NOT DELETE THEM FROM THE FORM OR ALTER THEM.  One suggested use is
to list the names of the newsgroups in which you participate.  Please
use the MAILING LIST name (see below - the latest version of the list
can be requested from biosci@net.bio.net) instead of the USENET name
even if you don't participate by e-mail.  WAIS might get confused by
the periods in the USENET names.  This allows one to retrieve via WAIS
or waismail the list of participants in a particular group.

For example:

comment: ARABIDOPSIS PLANT-BIOLOGY BIONEWS

On the comment: lines
use these names below ---- NOT the USENET names below

MAILING LIST NAME          USENET Newsgroup Name
-----------------          ---------------------
ACEDB-SOFT                 bionet.software.acedb
AGEING                     bionet.molbio.ageing
AGROFORESTRY               bionet.agroforestry
ARABIDOPSIS                bionet.genome.arabidopsis
BIOFORUM                   bionet.general
BIO-INFORMATION-THEORY     bionet.info-theory
BIONAUTS                   bionet.users.addresses
BIONEWS                    bionet.announce
BIO-JOURNALS               bionet.journals.contents
BIO-MATRIX                 bionet.molbio.bio-matrix
BIO-SOFTWARE               bionet.software
CHROMOSOMES                bionet.genome.chromosomes
COMPUTATIONAL-BIOLOGY      bionet.biology.computational
DROSOPHILA                 bionet.drosophila
EMBL-DATABANK              bionet.molbio.embldatabank
EMPLOYMENT                 bionet.jobs
GDB                        bionet.molbio.gdb
GENBANK-BB                 bionet.molbio.genbank
GENETIC-LINKAGE            bionet.molbio.gene-linkage
HIV-MOLECULAR-BIOLOGY      bionet.molbio.hiv
HUMAN-GENOME-PROGRAM       bionet.molbio.genome-program
IMMUNOLOGY                 bionet.immunology
INFO-GCG                   bionet.software.gcg
JOURNAL-NOTES              bionet.journals.note
METHODS-AND-REAGENTS       bionet.molbio.methds-reagnts
MOLECULAR-EVOLUTION        bionet.molbio.evolution
NEUROSCIENCE               bionet.neuroscience
N2-FIXATION                bionet.biology.n2-fixation
PHOTOSYNTHESIS             bionet.photosynthesis
PLANT-BIOLOGY              bionet.plants
POPULATION-BIOLOGY         bionet.population-bio
PROTEIN-ANALYSIS           bionet.molbio.proteins
PROTEIN-CRYSTALLOGRAPHY    bionet.xtallography
RAPD                       bionet.molbio.rapd
SCIENCE-RESOURCES          bionet.sci-resources
TROPICAL-BIOLOGY           bionet.biology.tropical
VIROLOGY                   bionet.virology
WOMEN-IN-BIOLOGY           bionet.women-in-bio
YEAST                      bionet.molbio.yeast

Listing newsgroups on the comment: line is optional, of course.

Thanks again for your cooperation!



--------------- please cut here and return portion below ---------------

New information or Update to old record (enter N or U): 
date (DD-MM-YY): 
first name: 
middle initial: 
family name: 
job title: 
e-mail address: 
e-mail network: 
phone number: 
FAX number: 
institution: 
address1: 
address2: 
address3: 
city: 
state/province: 
country: 
postal code: 
research interest: 
research interest: 
comment: 
comment: 
comment: 
comment: 
comment: 

