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From: biohelp@hgmp.mrc.ac.uk (BIOSCI Administrator)
X-Newsgroups: bionet.software.acedb
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 1 Nov 1999 02:00:20 -0800
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(LAST REVISION: 14-AUG-99)

This BIOSCI "miniFAQ" is designed to answer the questions that come up
the *most frequently*.  The main BIOSCI FAQ (Frequently Asked
Questions) is accessible on the World Wide Web at URL
http://www.bio.net/.

If you can not find an answer to your question in this or other
documentation, the BIOSCI technical support staff answers e-mail
queries sent to

		       biosci-help@net.bio.net

We can only answer questions about the use of the newsgroups and
mailing lists.  We unfortunately do not have the staff to do Internet
information searches or answer scientific questions.  Please post
those to the appropriate BIOSCI/bionet newsgroups.


	Contents:
	--------
	0) BIOSCI NEEDS YOUR SUPPORT!!

	1) Using the WWW to access the BIOSCI/bionet newsgroups.

	2) What to do about "spams," i.e., junk mail, ads, etc.

	3) Examples of subscribing and unsubscribing to the mailing lists.

	4) The BIOSCI user address and research interest directory.


0) BIOSCI NEEDS YOUR SUPPORT!!
------------------------------
BIOSCI's government funding has been expended, and we are now
operating solely from advertising revenue that we have raised from our
Web site at http://www.bio.net/.  We need just a few minutes of your
time to help us serve you.

You can do two important things which will take very little time for
you individually and will immensely help us continue to help you.

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can post or reply to messages via your Web browser as
described in item #1 below.  Your usage helps attract sponsors. If you
contact any of our sponsors, please be sure to thank them for
supporting BIOSCI. It is critical for them to get this feedback if
they are to continue their sponsorship for the long term.

Second, if you work for a company or organization that provides
products or services of interest to the biology community, please pass
this message on to your marketing or marketing communications
department or other appropriate group.  Please ask them to help
support BIOSCI by sponsoring our Web site and explain the uses and
benefits of the system to the biology community. If they are
interested, they can then contact us for further information at our
tech support address, biosci-help@net.bio.net.


1) Using the WWW to access the BIOSCI/bionet newsgroups.
--------------------------------------------------------
All BIOSCI/bionet full newsgroups are accessible through the World
Wide Web (WWW) at URL http://www.bio.net.  One can read and reply
publicly or privately to both recent postings and archived messages
through one's Web browser if it is configured properly to send e-mail.
Each newsgroup is equipped with its own WAIS index.  The main BIOSCI
home page also has access to the BIO-JOURNALS Table of Contents
database WAIS index and the BIOSCI user address database described in
another item further below.


2) What to do about "spams," i.e., junk mail, ads, etc.
-------------------------------------------------------
BIOSCI is a set of parallel USENET newsgroups (the "bionet" groups),
mailing lists, and a hypermail archive at URL http://www.bio.net/.
The same postings are distributed on all media (except for a small
number of mailing-list-only groups at net.bio.net).  Unfortunately it
is becoming a despicable practice on the Internet (by a few people out
to make a fast buck) to do automated mass postings to thousands of
newsgroups and mailing lists.  These attempts to grab free advertising
are refered to as "spams" in the usual, somewhat boneheaded, net
terminology.  USENET is more susceptible to this practice, and many
spams originate on the USENET groups and then are passed on to the
mailing lists.  However, spammers also get lists of mailing addresses
and hit these too, so neither medium is immune.

What should you do personally if you get junk mail?
---------------------------------------------------
Just delete it and move on without reading it further.  Filing a
protest is becoming increasingly useless because spammers are often
disguising the addresses where the messages are sent from.  Unless you
really understand Internet mail systems, your attempt at protest by
sending replies to the message will often end up being sent to the
address of an innocent person that the spammer is victimizing.

What can BIOSCI/bionet do to protect its newsgroups?
----------------------------------------------------
The only solution currently available is to moderate the newsgroup.
If this newsgroup is already moderated, then you are in good shape.
Moderation protects the USENET distribution from about 95% of the
spams that are being sent to date and protects the mailing lists
completely.  Moderation means, however, that someone has to take the
time to review each message before it goes out.  We have set up
software here that simply allows the moderator to forward to an
address at net.bio.net messages that (s)he wishes to have distributed.
This takes no more time than that needed to read the message and pass
it on, say about 1 min. per message.

Most newsgroups currently have a discussion leader who is responsible
for their newsgroup.  The discussions leaders and their e-mail
addresses are listed in the BIOSCI Information Sheet which is
available on the Web at http://www.bio.net/.  If a newsgroup is being
hit with too many junk postings, please contact the discussion leader
for that group and see if there is interest in moderating the group.
Please do not assume that by simply posting a complaint to the
newsgroup itself, anyone on the BIOSCI staff will act on your
complaint.  With close to 100 newsgroups to run, the BIOSCI staff has
to rely on the discussion leaders of each newsgroup to report problems
directly to us at biosci-help@net.bio.net.

We will moderate any of our newsgroups if the discussion leader tells
us that the readership of the group wishes to do so and if a moderator
is willing to do the work.  For most BIOSCI/bionet groups, this
entails only a few minutes of work each day.

Moderating a newsgroup will resolve probably 95% of the junk postings
on the USENET distribution.  Unfortunately there are easy ways for
determined spammers to override the moderation mechanism on USENET,
but we can protect our e-mail subscribers from unwanted postings if
the newsgroup is moderated.  You can also access our newsgroups over
the WWW at URL http://www.bio.net.  While this Web interface will not
stop spammers from trying to post to the groups, this will give you
yet another way, besides using USENET news, to keep the junk out of
your personal mail files.  For those of you with local USENET news
systems, the Web interface will also give you faster access to new
newsgroups and recent postings.


3) Examples of subscribing and unsubscribing to the mailing lists.
------------------------------------------------------------------
PLEASE NOTE: The BIOSCI management does NOT act on
subscription/unsubscription requests that are posted improperly to the
newsgroups and mailing lists.  People who do this only bother everyone
on the lists to no avail.  Please be sure to follow the proper
procedures below.

Gory details are in the BIOSCI Information sheets on the Web at
http://www.bio.net.  Below we give an example utilizing the
METHODS-AND-REAGENTS list at both of our two BIOSCI sites:

Users in the Americas and Pacific Rim countries who use the BIOSCI
------------------------------------------------------------------
node at computer net.bio.net:
----------------------------

A) Determine the "listname" which is the <=8 character mail address
                                         ^^^^^^^^^^^^^
   for the group.  These can be found in the BIOSCI Info. Sheet.  For
   the METHODS-AND-REAGENTS group the mailing address is
   methods@net.bio.net.  The listname is the portion of the address to
   the left of the @ sign, i.e., "methods".  The listname is used with
   the "subscribe" and "unsubscribe" commands illustrated below.

B) Mail all commands in the body of a mail message addressed to
   biosci-server@net.bio.net.  Do NOT send commands to the newsgroup
   posting addresses!  Leave the Subject: line blank, any text on it
   will be ignored.

C) In the body of your message put one or more of the following
   commands with an "end" command on the last line, e.g.,

   subscribe methods
   unsubscribe methods
   end

   Do NOT put your e-mail address or other text on these lines.  The
   server only allows you to cancel your subscription if the address
   on your mail header matches the address on our mailing list.
   Please ask for help at biosci-help@net.bio.net if your address has
   changed, e.g., if you know you are on the list but the server tells
   you that you are not a member.


Users in Europe, Africa, and Central Asia who use the BIOSCI node at
--------------------------------------------------------------------
the UK-HGMP-Resource Centre (known as hgmp.mrc.ac.uk):
-----------------------------------------------------

A) Determine the "listname" which is the <=8 character mail address
                                         ^^^^^^^^^^^^^
   for the group.  These can be found in the BIOSCI Info. Sheet.  For
   the METHODS-AND-REAGENTS group the mailing address is
   methods@hgmp.mrc.ac.uk.  The listname is the portion of the address to
   the left of the @ sign, i.e., "methods".  The listname is used with
   the "subscribe" and "unsubscribe" commands illustrated below.

B) Mail all commands in the body of a mail message addressed to
   majordomo@hgmp.mrc.ac.uk.  Do NOT send commands to the newsgroup
   posting addresses!  Leave the Subject: line blank, any text on it
   will be ignored.

C) In the body of your message put one or more of the following
   commands with an "end" command on the last line, e.g.,

   subscribe methods
   unsubscribe methods
   end

   Please ask for help at biosci@hgmp.mrc.ac.uk if your address has
   changed, e.g., if you know you are on the list but the server tells
   you that you are not a member.


4) The BIOSCI user address and research interest directory.
-----------------------------------------------------------
Please take this opportunity to add your name, address, and research
interest information to the BIOSCI User Address Database if you have
not already done so.

You can fill out the address form directly through our Web page at URL
http://www.bio.net/adrform.html.

The address database is reindexed nightly for WWW access (the URL is
http://www.bio.net/).  If you are not directly on the Internet but can
reach it by e-mail, please use our waismail server to access the user
directory.  waismail use is described above.  You can also request a
user address form by e-mail from biosci-help@net.bio.net.

Please check your database entry from time-to-time to see if your
address information is still up-to-date.  Because of our limited
personnel resources, we ask that you resubmit a *complete* form to
revise your entry; we only replace complete entries and do not have
resources to edit old forms.







From owner-acedb@hgmp.mrc.ac.uk  Mon Nov  1 12:15:30 1999
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From: edgrif@sanger.ac.uk (Ed Griffiths)
X-Newsgroups: bionet.software.acedb
Subject: Re: Problem installing webace
Date: 1 Nov 1999 03:51:20 -0800
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Francois,

I think your problem is simple:


You have:

> 
> OK, I figured this out:
> 
> [root wmake]#export ACEDB_SRC=/home/Database/Soft/sources_acedb
> [root wmake]#export
> ACEDB_MACHINE=/home/Database/Soft/sources_acedb/wmake/LINUX_LIBC5_4
> 
> Just to check:
> 
> [root wmake]# echo $ACEDB_SRC
> /home/Database/Soft/sources_acedb
> [root wmake]# echo $ACEDB_MACHINE
> /home/Database/Soft/sources_acedb/wmake/LINUX_LIBC5_4
> 

but $ACEDB_MACHINE is not correct, you need to do this:


export ACEDB_MACHINE=LINUX_LIBC5_4



don't put the directory in front of the LINUX_LIBC5_4.


cheers Ed

 ------------------------------------------------------------------------------
| Ed Griffiths, Informatics Group,                                             |
|               The Sanger Centre, Wellcome Trust Genome Campus,               |
|               Hinxton, Cambridge CB10 1SA, UK                                |
|                                                                              |
| email: edgrif@sanger.ac.uk      URL: http://www.sanger.ac.uk/Users/edgrif    |
|   Tel: +44-1223-494780 (switch  +44 1223 834244) Fax: +44 1223 494919        |
 ------------------------------------------------------------------------------



From owner-acedb@hgmp.mrc.ac.uk  Mon Nov  1 13:13:59 1999
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From: vascoco@THEARMY.COM ("JS")
X-Newsgroups: bionet.software.acedb
Subject: AVAILBLE 6,000 SQ. FT. FACTORY FOR RENT IN UDYOG VIHAR,GURGAON
Date: 1 Nov 1999 05:15:26 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Distribution: world
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6,000 SQ. FT. INDUSTRIAL FACTORY AVAILBLE FOR RENT IN UDYOG VIHAR,
PHASE 5,GURGAON,HARYANA
WITH VERY REASONABLE RENT

CONTACT US IF YOU PLAN TO PUT UP A FACTORY THERE

JS

"ONE MAILING IN THIS LIST-YOU NEED NOT REPLY IN CASE NOT INTERESTED
-THERE IS NO REPEAT MAILING"





From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  2 03:10:42 1999
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From: pugu46@NS2.RBH.NTHAMES.NHS.UK (Photo Specialists)
X-Newsgroups: bionet.software.acedb
Subject: Photo Mouse Pads .....Great Christmas Gift!
Date: 1 Nov 1999 18:54:26 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 113
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                   GREAT CHRISTMAS GIFT IDEA!

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S


From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  2 06:45:32 1999
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From: sdgmh@thrwel@hotmail.com
X-Newsgroups: bionet.software.acedb
Subject: LOANS For Active NetWorkers!                                    [vihgb]
Date: 1 Nov 1999 22:44:03 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 63
Distribution: world
Message-ID: <199911020644.WAA28702@net.bio.net>
Reply-To: jo22c@bigfoot.com
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LOANS AVAILABLE TO ACTIVE NETWORKERS
YOU CAN BORROW MONEY AT 2% INTEREST
FOR FIFTEEN YEARS.

Use the money to pay off all your high interest loans and your
mortgage. Or use the money as investment capital.
Or save the money in a savings account. It's up to you how
you use the money!  There is no credit check. You can qualify
for these loans just by being an active networker.  This is a
brand new offer that was not available to anyone until very
recently. And it's made for networkers! I am not a financier;
I'm just someone who wants to see people who need it get
this information.  All of the loans are at only 2% interest, per
year. The interest is simple and not compound. You have
15 years to use all the money you can accumulate before you
ever have to do anything to settle the loans.

HOW do you get these loans?
There is a company that gives generous loans to networkers just
for helping them promote their opportunity. The loans are available
internationally. Any networker in the world can qualify for them.

WHAT must you do to qualify? You do a little advertising for the
company, just like I'm doing now. When you get about four
people interested, you have done the basic work you must do
to qualify for the loans. Active networkers should have no
trouble completing this work within a few weeks.

WHY should you do it? If you need a loan, you should get in
touch with me. Or if you have heavy debts to pay and need
some help, you should get in touch with me. Or if you're
cash-poor and need some operating capital, you should get
in touch with me.

This is an honest, easy borrowing opportunity. It is a unique,
unusual opportunity, the likes of which you have never seen
before. If you have no credit, or if your credit rating is poor,
that will not be a problem in getting these loans. You need
only do a little reasonable work in exchange for the loans.
There is no other qualification of any kind.

Why shouldn't you be one of the many people who will qualify
for these loans?

HOW MUCH can you borrow? WOW! I'm not telling you
right now, but believe me, the news is very good! You need
to reply to me so that I know you are interested.

WHEN can you have your first loan? It is possible to have
your loan within about a week after you qualify. And you can
qualify within a few weeks, if you are interested enough and
able to complete a fairly simple networking task for the company.

Thank you for listening to my message. Contact me by Reply
my E-mail with "Loans" on the subject line and you will get more
information. I will also send you advance information on our
new web page, and numbers you can call to get official literature
and application forms.

mailto:s2la@bigfoot.com?subject=Loans

Have A Blessed Day!



From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  2 12:55:24 1999
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From: "F. Coulier" <coulier@marseille.inserm.fr>
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Subject: Re: Problem installing webace
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In article
<Pine.OSF.4.10.9911011141420.6701-100000@griffin.sanger.ac.uk>,
  edgrif@sanger.ac.uk (Ed Griffiths) wrote:
> Francois,
>
> I think your problem is simple:
>
cut
>
> but $ACEDB_MACHINE is not correct, you need to do this:
>
> export ACEDB_MACHINE=LINUX_LIBC5_4
>
> don't put the directory in front of the LINUX_LIBC5_4.
>
> cheers Ed

Thanks a lot.

The problem was in fact double.
export ACEDB_MACHINE=LINUX_LIBC5_4 was not working any better than
export ACEDB_MACHINE=/home/Database/..../wmake/LINUX_LIBC5_4 because I
was in the wrong directory (sources_acedb/wmake/ instead of
sources_acedb/).
This was pointed out to me in another newsgroup.

Thanks to all who helped!

François

--
François Coulier,
"Laboratoire d'Oncologie Moléculaire" et "Atelier
de Bioinformatique et d'Imagerie",
INSERM Unité 119, 27 bd Leï Roure, 13009 Marseille


Sent via Deja.com http://www.deja.com/
Before you buy.


From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  2 18:27:59 1999
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From: Jamie Kincaid <jamie@thale.life.nottingham.ac.uk>
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Hi,
I've made some changes to my models.wrm and want to re-read the file , yet
when I do this using either tace or xace it core dumps while indexing.

I've tried re-reading the old models.wrm file and it still core dumps !

The xace client reports "reading in class comment" - which I don't have!
then reports "indexing" before core dumping.

Any ideas?

Jamie


-------------------------------------------------------------------------------
Jamie Kincaid
Nottingham Arabidopsis Stock Centre
School of Biological Sciences
University Park
The University of Nottingham
Nottingham
NG7 2RD

Office: 0115 951 3091

NASC website:	nasc.nott.ac.uk



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One idea,

Should I be re-reading models.wrm in an empty database?

jamie


-------------------------------------------------------------------------------
Jamie Kincaid
Nottingham Arabidopsis Stock Centre
School of Biological Sciences
University Park
The University of Nottingham
Nottingham
NG7 2RD

Office: 0115 951 3091

NASC website:	nasc.nott.ac.uk



From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  2 19:04:33 1999
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From: mieg@beta.crbm.cnrs-mop.fr (Danielle et jean Thierry-Mieg)
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you are definitelly supposed to be able to re-read modesl
in a full database
this is one of the mainassets of acedb

please let me know exactly what code version and machine you use

as a work around

do a
dump -s

and in a separate directory
install the new model file
mkdir database
and re-read all the files you dumped previously

=====

but this is definitely a terrible bug, which we have
note seen here or during testing

jean
---


From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  2 21:42:08 1999
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From: vdrake@WGN.NET (Vernon Drake)
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Subject: Super Inkjet Price
Date: 2 Nov 1999 13:41:06 -0800
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Hello!
 This regards the Epson cartages listed below which I saw on the Bio.net
page.
Super Inkjet Price. Could you tell me how I can order them.
Thank you
vdrake@wgn.net

EPSON

Epson - $8.00 - Black or 10 for $65.00 - All Models*
Epson - $12.00 - Color or 10 for $100.00 - All Models*



From owner-acedb@hgmp.mrc.ac.uk  Wed Nov  3 00:55:32 1999
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From: "W. Bill Ge" <ge.10@osu.edu>
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Hi, all,

Anyone knows how to change the list of columns in the graphic display of
sequence objects?

I am trying to delete some columns and add a few to the sequence graphs,
but do not know how. For ?Map objects, the display columns can be
changed by changing the view, but there is no ?View object associated
with sequence display that can be edited to change the columns listed
and their relative positions. The only thing that I can do now is select
or unselect the columns listed. 

Any hint is greatly appreciated!

Cheers,
Bill 
____________________________________________________________
http://pegasus.med.ohio-state.edu/~bill


From owner-acedb@hgmp.mrc.ac.uk  Wed Nov  3 06:45:33 1999
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From owner-acedb@hgmp.mrc.ac.uk  Wed Nov  3 09:45:30 1999
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From: edgrif@sanger.ac.uk (Ed Griffiths)
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Vernon,

This was unwanted spam, acedb is a scientific newsgroup not a spam newsgroup (as
it often must appear). You need to try to find out the originator of the spam to
get your inkjet prices. Please do _not_ append any further notes about inkjet
stuff to the acedb newsgroup, thank you.

Ed



On 2 Nov 1999, Vernon Drake wrote:

> Hello!
>  This regards the Epson cartages listed below which I saw on the Bio.net
> page.
> Super Inkjet Price. Could you tell me how I can order them.
> Thank you
> vdrake@wgn.net
> 
> EPSON
> 
> Epson - $8.00 - Black or 10 for $65.00 - All Models*
> Epson - $12.00 - Color or 10 for $100.00 - All Models*
> 
> 

 ------------------------------------------------------------------------------
| Ed Griffiths, Informatics Group,                                             |
|               The Sanger Centre, Wellcome Trust Genome Campus,               |
|               Hinxton, Cambridge CB10 1SA, UK                                |
|                                                                              |
| email: edgrif@sanger.ac.uk      URL: http://www.sanger.ac.uk/Users/edgrif    |
|   Tel: +44-1223-494780 (switch  +44 1223 834244) Fax: +44 1223 494919        |
 ------------------------------------------------------------------------------



From owner-acedb@hgmp.mrc.ac.uk  Wed Nov  3 09:59:50 1999
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From: rd@sanger.ac.uk (Richard Durbin)
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Subject: Re:  Graphical display of sequence
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Almost all columns in the sequence display have an associated Method
object.  There is a tag in this method object

	Right_priority <float>

The columns are sorted left to right on the value of this tag.  This
makes it easy to add another column.  If the values are within 0.01
then the columns are drawn on top of each other (can be useful if 
there is a really large number of columns).  There are also tags

	Max_mag UNIQUE Float	// don't show if more bases per line
	Min_mag UNIQUE Float	// don't show if fewer bases per line

in the Method class that, at least with recent versions of the code,
allow you to control at what range of zoom levels a column is shown.

We are working on storing specific configurations in View objects,
though not quite in the same way as with Maps.

Richard
---


From owner-acedb@hgmp.mrc.ac.uk  Thu Nov  4 18:25:24 1999
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From: davel@src.uchicago.edu (Dave Lorand)
X-Newsgroups: bionet.software.acedb
Subject: newbie trouble importing .ace files
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Hi,

I'm having trouble importing some .ace files which I created from
scratch.  The problem is probably my own lack of clues about ACEDB
syntax.  Here's what I've got (this is not genetic data, BTW):

---- added to wspec/models.wrm: ---------

?Action     Name UNIQUE Text

?Cycle      CycleAction Action

---- added to wspec/options.wrm: --------

_VAction        -V -CaseSensitive
_VCycle         -V -CaseSensitive

----------------- (end) -----------------

These models seem to import just fine, no syntax errors.  I should mention
that I'm not really using the "Name" tag of the Action class, because each
object has a name anyway (I'll get rid of that tag eventually, unless it
turns out that I need it).

The first .ace file I am importing is a list of "Action" objects.  The
beginning looks like this:

---- head -7 actions.ace ----------------
Action CLEAN

Action DNEG1

Action DNEG2

Action DSFEED
-----------------------------------------

It goes on like that with different names and no repetition (I piped the
names through a sort -u when I was generating the file).

The trouble comes when I try to import some Cycle objects.  I get syntax
errors right away.  Here's the first object:

---- head -6 cycles.ace -----------------
Cycle 9-41
CycleAction SPOON
CycleAction EXT
CycleAction OPEN
CycleAction FEED
CycleAction END
-----------------------------------------

ACEDB seems happy enough with the fist line, but the second line gives me
this error:

    ERROR: parse error near line 2 in 9-41: Unknown tag "SPOON"

This is ocnfusing, because what I thought I was doing is including an
Action object in the Cycle object.  "CycleAction" is meant to be a tag,
while "SPOON", "EXT", "OPEN", etc. are meant to be names of objects, not
tags.

Can anyone explain to me what I'm doing wrong?

Thanks in advance,

Dave

 ____________________________________________________________
| Dave Lorand, System Administrator | davel@src.uchicago.edu |
| Social Science Research Computing | 773-702-3792           |
| University of Chicago             | 773-702-2101 (fax)     |
+-----------------------------------+------------------------+


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From: matthews@GREENGENES.CIT.CORNELL.EDU (Dave Matthews)
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Subject: Re:  newbie trouble importing .ace files
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Hi Dave, The problem is in your model for ?Cycle:

?Cycle      CycleAction Action

should be

?Cycle      CycleAction ?Action


Have you already found the help on models and ace files in the ACEDB
Documentation Library?  Especially
http://ars-genome.cornell.edu/acedocs/models_guide.html
and
http://ars-genome.cornell.edu/acedocs/ace97/sam/exploring/

- Dave


From owner-acedb@hgmp.mrc.ac.uk  Fri Nov  5 05:11:15 1999
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From: signaturecenter@HOTMAIL.COM
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Subject: Convert your Signature to a Font for $9.95
Date: 4 Nov 1999 21:16:38 -0800
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Wouldn't it be nice to be able to:
	*Fax Signed Documents
	*Print Signed Letters
	*Easily insert your signature into any document

For just $9.95 you can do all this.

We will convert your signature to a font which can be accessed 
and
used in any program just like you now use Arial or Courier fonts.

We can convert signatures, initials, first names, last names
or whatever you choose to give us.

These fonts are useful, convenient and huge time savers.  Get
yours now and you'll see why Corporations and Universities have
been buying large numbers of these fonts from us for their 
employees.

Ordering is simple, just use the order form below and send it or 
fax it to 
us.
--------------------------
SignatureCenter Text Order Form

e-mail address(print large and clear): 
________________________________

Name for font (8 characters max-font will be called 
Signature-Name):

Payment Method:	__Check __Money order __Cash __Credit Card
(Visa, Mastercard, and American Express are accepted for credit 
card orders)
                        Credit Card 
Number:_____________________________
			Credit Card Exp. Date:________
			CardHolder Name:
			CardHolder Billing Address:

1. Cost for Signature Font is $9.95 (font will be returned by 
e-mail)
2. e-mail address is required; Signature font will be returned by 
e-mail.
3. If desired, signature font can be sent on a diskette by U.S. 
mail. Add $3
   shipping & handling for U.S. addresses or $6 for non-U.S. 
addresses.
4. For best results send your order in by mail.

Send Form To:	SignatureCenter
		#301, 1302 24th St. West
		Billings, Montana  59102
or FAX to: 	520-223-0861 (If faxing sign as large as 
possible)
Signature: (place below line - make sure no part of signature 
touches line)
           (make sure area around signature is free of all stray 
marks!!)
(For mailing, fold signature area in last so text above won't 
bleed onto it)
-----------------------------------------------------------------
-----------




 
 
 
 
 
 
 
 
 
 


From owner-acedb@hgmp.mrc.ac.uk  Sat Nov  6 01:16:14 1999
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From: matthews@GREENGENES.CIT.CORNELL.EDU (Dave Matthews)
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Subject: searching for #
Date: 5 Nov 1999 17:02:19 -0800
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In GrainGenes, "find trait_scores *#*" succeeds in tace and gifaceserver.

It fails in xace, webace and AceBrowser.  Presumably for different reasons.

"query find trait_study trait_scores=*#*" fails even in tace.

(All using ace4_7g)

- Dave


From owner-acedb@hgmp.mrc.ac.uk  Sun Nov  7 14:56:11 1999
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http://members.tripod.lycos.nl/svenb/index.html




From owner-acedb@hgmp.mrc.ac.uk  Mon Nov  8 00:35:45 1999
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SORRY IF THIS AD HAS OFFENDED YOU IN ANYWAY. IF YOU DO NOT LIKE THE AD PLEASE NO FLAMES, JUST DELETE, YOU TAKE MORE TIME TO COMPLAIN THEN TO JUST DELETE.
Now to explain how the whole process works. First of all, you tell us how many e-mail addresses you would like us to send your advertisement to--you may either e-mail, fax, or snail-mail a hard copy of your ad to us. 

We will then place your ad in our database so it will be ready to be sent out anytime thereafter. Say for instance you wanted 1-million e-mails sent--once we receive your payment it will take about  3-4 days to be completed, unless you desire a more lengthy time frame, or need it done faster.

Right about now you might be wondering why you should choose us above the competitors. Well, we can sum it up for you in one simple word: Assurance. We are able to e-mail you an uploaded log of your sending in order to provide you with verification. These maillogs will display the time and date of the mailings as well as the actual e-mail addresses that your ad was sent to along with a "recipient okay" tag. This tag will confirm the address.  We do not send you a whole log of the mailing, but just a portion of it, so you can see that we are doing the work. WE HAVE ALSO BEEN IN BUSINESS IN CA FOR OVER 2 YEARS.

In addition to this, we offer targeted lists just starting at $400.00 for 1 million. Finally, I must inform you that your ad, if being sent to AOL, may have all the HTML, colored and enlarged fonts as well as colored background. When you are ready to order, just contact us and we will e-mail you an work order for you to sign and send with your payment.   For the target lists it is best that you call or e-mail back to us letting us know what type of target and we will let you know if we have the target you are looking for.  

Some of our targets that we have are: business opportunity seekers, cigar smokers, people seeking health products, homeowners, all females, all males, adult site seekers, some of the major states in the US, online purchasers, singles, golf related interests, sports fanatics, please call for more info, most targets are on request basis, it really just depends on what you are searching for.  Our targets are gathered by search keywords or member directory data bases like from AOL, Bigfoot or Mindspring, etc.  Call for more info 209-669-3628.  Target types are subject to change.

It's all quite simple. 

The bottom line to effective bulk e-mailing is quality of the service and what it has to offer the customer. 

You can make your dreams come true with bulk e-mail--allow us to set you on your way. 

We offer the following prices: 

*General AOL Lists or other ISPs 
$200.00 for 1-million e-mails sent. 
$400.00 for 3-million e-mails sent. 
$600.00 for 5-million e-mails sent. 
$800.00 for 7-million e-mails sent. 
$1000.00 for 10-million e-mails sent. 

WE ALSO HAVE LARGER PACKAGES!


*Targeted Lists: 
$400.00 for 1-million e-mails sent. 
$700.00 for 2-million e-mails sent. 
$1,000.00 for 3-million e-mails sent.

Call for bigger packages!

Many people often ask us..Why are you so cheap compared to the others?  My only answer is that we do not have a big overhead, and we are a smaller company with the right tools where we don't work hard, our computers do the hard work for us.

The % of your response is hard to determine.  It will all depend on your product or service. 

FOR ALL OTHER AMOUNTS YOU MUST CALL FOR OUR PRICING. We also offer larger list packages. You will need to call for pricing. 

CALL NOW 209-669-3628, WE ARE ON THE WEST COAST SO PLEASE TAKE THIS INTO CONSIDERATION WHEN CALLING. YOU MAY CALL 7 DAYS A WEEK, ANYTIME!

Once you are ready to order, just e-mail or call and we will e-mail you a work order.

Bulk e-mailing sells itself, so when you are ready to make a positive change in your business just let us know.  Just as you responded to my e-mail ad you can have people respond to yours, so the answer to the question - "Does bulk e-mailing really work?" Yes it does.  You responded to a bulk e-mail ad didn't you? :)

CALL 209-669-3628

METHOD OF PAYMENT UNTIL THE HOLIDAYS ARE OVER IS, CASHIERS CHECK MONEY ORDER OR BANK WIRE.










---


From owner-acedb@hgmp.mrc.ac.uk  Mon Nov  8 00:45:38 1999
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From: OiC4cExwp@HKEM.COM
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Subject: INCREASE SALES 4 THE HOLIDAYS WITH BULK E-MAIL
Date: 7 Nov 1999 16:42:44 -0800
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Precedence: bulk

SORRY IF THIS AD HAS OFFENDED YOU IN ANYWAY. IF YOU DO NOT LIKE THE AD PLEASE NO FLAMES, JUST DELETE, YOU TAKE MORE TIME TO COMPLAIN THEN TO JUST DELETE.
Now to explain how the whole process works. First of all, you tell us how many e-mail addresses you would like us to send your advertisement to--you may either e-mail, fax, or snail-mail a hard copy of your ad to us. 

We will then place your ad in our database so it will be ready to be sent out anytime thereafter. Say for instance you wanted 1-million e-mails sent--once we receive your payment it will take about  3-4 days to be completed, unless you desire a more lengthy time frame, or need it done faster.

Right about now you might be wondering why you should choose us above the competitors. Well, we can sum it up for you in one simple word: Assurance. We are able to e-mail you an uploaded log of your sending in order to provide you with verification. These maillogs will display the time and date of the mailings as well as the actual e-mail addresses that your ad was sent to along with a "recipient okay" tag. This tag will confirm the address.  We do not send you a whole log of the mailing, but just a port
In addition to this, we offer targeted lists just starting at $400.00 for 1 million. Finally, I must inform you that your ad, if being sent to AOL, may have all the HTML, colored and enlarged fonts as well as colored background. When you are ready to order, just contact us and we will e-mail you an work order for you to sign and send with your payment.   For the target lists it is best that you call or e-mail back to us letting us know what type of target and we will let you know if we have the target yo
Some of our targets that we have are: business opportunity seekers, cigar smokers, people seeking health products, homeowners, all females, all males, adult site seekers, some of the major states in the US, online purchasers, singles, golf related interests, sports fanatics, please call for more info, most targets are on request basis, it really just depends on what you are searching for.  Our targets are gathered by search keywords or member directory data bases like from AOL, Bigfoot or Mindspring, etc
It's all quite simple. 

The bottom line to effective bulk e-mailing is quality of the service and what it has to offer the customer. 

You can make your dreams come true with bulk e-mail--allow us to set you on your way. 

We offer the following prices: 

*General AOL Lists or other ISPs 
$200.00 for 1-million e-mails sent. 
$400.00 for 3-million e-mails sent. 
$600.00 for 5-million e-mails sent. 
$800.00 for 7-million e-mails sent. 
$1000.00 for 10-million e-mails sent. 

WE ALSO HAVE LARGER PACKAGES!


*Targeted Lists: 
$400.00 for 1-million e-mails sent. 
$700.00 for 2-million e-mails sent. 
$1,000.00 for 3-million e-mails sent.

Call for bigger packages!

Many people often ask us..Why are you so cheap compared to the others?  My only answer is that we do not have a big overhead, and we are a smaller company with the right tools where we don't work hard, our computers do the hard work for us.

The % of your response is hard to determine.  It will all depend on your product or service. 

FOR ALL OTHER AMOUNTS YOU MUST CALL FOR OUR PRICING. We also offer larger list packages. You will need to call for pricing. 

CALL NOW 209-669-3628, WE ARE ON THE WEST COAST SO PLEASE TAKE THIS INTO CONSIDERATION WHEN CALLING. YOU MAY CALL 7 DAYS A WEEK, ANYTIME!

Once you are ready to order, just e-mail or call and we will e-mail you a work order.

Bulk e-mailing sells itself, so when you are ready to make a positive change in your business just let us know.  Just as you responded to my e-mail ad you can have people respond to yours, so the answer to the question - "Does bulk e-mailing really work?" Yes it does.  You responded to a bulk e-mail ad didn't you? :)

CALL 209-669-3628

METHOD OF PAYMENT UNTIL THE HOLIDAYS ARE OVER IS, CASHIERS CHECK MONEY ORDER OR BANK WIRE.












From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  9 13:16:46 1999
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From: "Emmett Power" <Emmett@MIB-Group.com>
X-Newsgroups: bionet.software.acedb
Subject: CEO WANTED FOR AI-BASED PHARMACEUTICAL START-UP
Date: Tue, 9 Nov 1999 12:47:28 -0000
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CEO WANTED FOR AI-BASED PHARMACEUTICAL START-UP

Our client is a start-up in the field of the application of artificial
intelligence-based knowledge management solutions for pharmaceutical and
biotechnology research and development. The company has an alliance with one
of the leading academic centres of excellence for computer-driven artificial
research in the world.

The company also has highly-experienced sales and technology directors in
place and an impressive list of non-executive directors. The company is now
negotiating with venture funders for funding and with a major pharmaceutical
company to develop and trial the product. We are now looking for a CEO to
complete the management team and to lead the company through the venture
funding, launch and flotation stages.

It is essential that the successful candidate carries credibility within
client organisations in the pharmaceutical and biotechnology sectors. As a
minimum requirement, he or she will have occupied a senior managerial
position, ideally within the pharmaceutical sector. By the nature of both
the industry and the product, the role will call for an individual of the
very highest intellectual calibre.


The CEO will receive an equity stake in the business and a
performance-related option package. The post will be based in the South East
of England. This is a chance to share in the wealth creation process and to
steer an exciting, intellectually-challenging business to flotation.

Please reply in the first instance by email or post with a resume to Emmett
Power, CEO, The MIB Group, 126 Aldersgate Street, London EC1A 4JQ, United
Kingdom, telephone: 0171 687 0352, fax: 0171 687 0358, email:
Emmett@MIB-Group.com.

All applications will be treated in the strictest confidence and will be
used for no other purpose than consideration for the post described above.

**Please excuse any inappropriate or cross-postings**






From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  9 15:45:54 1999
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From: wtom2@BOOTMAIL.COM ("Scott")
X-Newsgroups: bionet.software.acedb
Subject: Boost
Date: 8 Nov 1999 19:36:01 -0800
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From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  9 15:47:45 1999
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From: Keith Bradnam <keith@thale.life.nottingham.ac.uk>
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Subject: How to view overlapping sequences
Date: Tue, 9 Nov 1999 15:41:05 +0000
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This is all new to me, so my apologies in advance if there is something
obvious that I have missed.

I have previously used xace and also AceBrowser to access ACeDB.  With the
complete C. elegans genome sequence you can use the Sequence Map class to
look at all the overlapping cosmid sequences.  Bringing up a sequence
display for any one cosmid sequence then allows you to move up or down to
adjacent cosmid sequences and therefore you can proceed along a
chromosome without having to launch separate windows for each overlapping 
sequence.

In contrast, when working with our Arabidopsis database, it seems that you
cannot move between overlapping sequences.  There is no Sequence Map class
for the Arabidopsis database and I was therefore curious as to how this
overlapping information for C. elegans is curated.

Are the relationships between overlapping sequences specified in the
models.wrm file?  More specifically in the Overlap_left and Overlap_right
tags of the Sequence class?

I know that in the GenBank entries of C. elegans cosmid sequences, there
are remarks that specify what the adjacent cosmids are, so I suppose in
building ACeDB, the necessary information could be extracted from this.

I would like to know how it would be possible to construct a similar
Sequence Map class for Arabidopsis so that it would be possible to
'scroll' through overlapping sequences.  This will become more important
by next year as the Arabidopsis genome project nears completion.

Hope someone can help me, thanks.

Keith B.


~  Keith Bradnam - Developer, Arabidopsis Genome Resource (AGR)
~  University Park, University of Nottingham, NG7 2RD, UK
~  Tel: (0115) 951 3091 Web: http://synteny.nott.ac.uk/



From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  9 16:55:34 1999
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From: rd@sanger.ac.uk (Richard Durbin)
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Subject: Re:  How to view overlapping sequences
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Hello Keith,

Aha, you ended up with AGR.  Congratulations.

It is not a sequence map that you need.  What glues separate clone
sequences together in the worm database is the *LINK* objects in the
Sequence class.  They have the separate entries as subsequences, e.g.

  Sequence : "LINK_Y39B6B"
  Source	 "SUPERLINK_CB_V"
  Subsequence	 "B0399" 556032 599668
  Subsequence	 "B0399.1" 568119 608616
  Subsequence	 "B0399.2" 558575 550832
  Subsequence	 "C14B4" 358654 346803
  Subsequence	 "C14B4.2" 347961 335484
  Subsequence	 "C25F9" 441189 397306
  Subsequence	 "C43D7" 346906 311926
  Subsequence	 "F21D9" 282729 244387
  Subsequence	 "F55C9" 312029 282626
  Subsequence	 "Y39B6B" 1 207022
  Subsequence	 "T26H2" 244487 206919
  Subsequence	 "Y43F8A" 358551 397406
  Subsequence	 "M04C3" 454554 441086
  Subsequence	 "Y43F8B" 454454 556132
  Subsequence	 "Y43F8C" 599568 720059
  Subsequence	 "Y116F11A" 719951 733832
  Subsequence	 "M04C3.1" 446349 440693

We use the Overlap_right and Overlap_left tags in acedb to store the
overlap information, then use a script as in the next message to
rebuild the link objects, which are what acedb needs.

Richard
---


From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  9 16:59:41 1999
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Here is the perl script we use to make the LINK* objects.  A bit
C.elegans specific I am afraid.

It assumes that there is a chain of Overlap_right specifiying the
order of sequences, with a value to the right if and only if there is
an actual overlap, the value being the start position of the
right-overlapping sequence within the current sequence.

Richard

---------------------------------------------------------------------------

#!/usr/local/bin/perl

##########################################################
#
# Makelinks program which will link up cosmid sequences and 
# spanning subsequences based on Overlap_left/right info and
# the current LINK_*.  Makes one LINK_XXX for each set of
# entries with DNA and Overlap_right set non-zero and
# no Confidential_remark "not in Cambridge LINK".  XXX is 
# the leftmost entry name.  SUPERLINK_CB_* are also made 
# based on a hardwired table of left ends.
#
# Performs a number of checks to make sure of the integrity 
# of the new links
#
# 1) Will check that all sequences that previously were in a link
#    are put back into a link.
# 2) Will check that all subsequences from links are put back into 
#    links.
#
#    WARNING: Current implementation relies on the fact that 
#    all current primary links have names starting with "LINK".
#
# RD 990712 total rewrite of Steven Jones original using AcePerl
# now handle reversed sequences with Flipped tag set.
# -dump and -load options to separate reading database from making result.
# -flip_subseqs option a bit subtle - when attaching spanning subsequences
#    based on flipped sequences, reverse attachment info.  This is correct
#    only once, when sequences are newly flipped (but how to know that in
#    the future?).
#
##########################################################

use Getopt::Long ;

&GetOptions("dump!","load=s", "flip_subseqs!") ;

if ($opt_load) {
    open (FILE, "$opt_load") || die "failed to open dump file $opt_load\n" ;
    while (<FILE>) {
	chop ;
	($type, $seq, @a) = split /\t/ ;
	if ($type eq "SEQ") {
	    ($length{$seq}, $right{$seq}, $rightOffset{$seq}, $left{$seq},
	     $isFlipped{$seq}, $isExternal{$seq}, $isLinkCandidate{$seq}) = @a ;
	    $isGenomeSequence{$seq} = 1 ;
	} elsif ($type == "LINK") {
	    ($currSource{$seq}, $currStart{$seq}, $currEnd{$seq}) = @a ;
	} else {
	    die "bad line in load file: $type\t$seq\t$_\n" ;
	}
    }
} else {

	# get data from camace

    use Ace ;
    $campath = glob("~/acedb/ace4/cam") ;
    $camdb = Ace->connect(-path=>"$campath") || 
	die "failed to connect to database\n" ;

	# first get lots of info about Genome_sequence objects

    $it = $camdb->fetch_many(Genome_sequence => '*') ;
    while ($obj = $it->next) {
	$isGenomeSequence{$obj} = 1 ;
	$length{$obj} = $obj->DNA(2) ;
	if (!$length{$obj}) { warn "No length for $obj\n" ; }
	$right{$obj} = $obj->Overlap_right ;
	$rightOffset{$obj} = $obj->Overlap_right(2) ;
	$left{$obj} = $obj->Overlap_left ;
	if ($obj->at('Structure.Flipped')) { $isFlipped{$obj} = 1 ; }
	foreach ($obj->Confidential_remark) {
	    if (/^not in Cambridge LINK$/) { $isExternal{$obj} = 1 ; }
	}
	$isLinkCandidate{$obj} = (!$isExternal{$obj} && $length{$obj} > 0) ;
    }

	# then some info about current links

    $it = $camdb->fetch_many(Sequence => 'LINK*') ;
    while ($obj = $it->next) {
	foreach $a ($obj->at('Structure.Subsequence')) {
	    ($seq, $start, $end) = $a->row ;
	    $currSource{$seq} = $obj ;
	    $currStart{$seq} = $start ;
	    $currEnd{$seq} = $end ;
	}
    }
}

if ($opt_dump) {
    foreach $obj (keys %length) {
	print "SEQ\t$obj\t$length{$obj}\t$right{$obj}\t$rightOffset{$obj}\t$left{$obj}\t" ;
	print "$isFlipped{$obj}\t$isExternal{$obj}\t$isLinkCandidate{$obj}\n" ;
    }
    foreach $seq (keys %currSource) {
	print "LINK\t$seq\t$currSource{$seq}\t$currStart{$seq}\t$currEnd{$seq}\n" ;
    }

    exit 0 ;		# exit after dumping
}

###########################################
# make links
###########################################

foreach $seq (keys %isGenomeSequence) {
				# only keep seeds
    next if (!$isLinkCandidate{$seq} ||
	     ($left{$seq} && $isLinkCandidate{$left{$seq}} && $rightOffset{$left{$seq}}) ||
	     !$rightOffset{$seq} ||
	     !$isLinkCandidate{$right{$seq}}) ;

				# print LINK header
    $lk = "LINK_$seq" ;
    print "\nSequence $lk\n" ;
    print "From_laboratory CB\n" ;

				# loop over subsequences
    $startright=1 ;
    while ($isLinkCandidate{$seq}) {
	if ($isFlipped{$seq}) {
	    $start{$seq} = $startright + $length{$seq} - 1 ; 
	    $end{$seq} = $startright ; 
	} else {
	    $start{$seq} = $startright ; 
	    $end{$seq} = $startright + $length{$seq} - 1 ;
	}
	print "Subsequence $seq $start{$seq} $end{$seq}\n" ;
	$link{$seq} = $lk ;
	if (!$rightOffset{$seq}) { last ; } # POSS EXIT FROM LOOP
	$startright = $startright + $rightOffset{$seq} - 1 ;
	$seq = $right{$seq} ;
    }		
}

###########################################
#Re-map subsequences back onto the new links 
###########################################

foreach $seq (keys %currStart) {
    next if ($isGenomeSequence{$seq}) ;
    if ($seq =~ /(\S+)\.\d+/) { $parent = $1 ; }
    else { warn "no dot in subsequence name $seq\n" ; next ; }
    if (!$currStart{$parent}) { warn "no coord in link for parent $parent of $seq\n" ; next ; }
    if (!($currSource{$seq} eq $currSource{$parent})) { warn "parent $parent and child $seq in different links\n" ; next ; }
    if (!$link{$parent}) { warn "no new link for parent $parent of $seq\n" ; next ; }
    if ($isFlipped{$parent} && $opt_flip_subseqs)  {
	$start{$seq} = $start{$parent} + $currStart{$parent} - $currStart{$seq} ;
	$end{$seq} =  $start{$parent} + $currStart{$parent} - $currEnd{$seq} ;
    } else {
	$start{$seq} = $start{$parent} - $currStart{$parent} + $currStart{$seq} ;
	$end{$seq} = $start{$parent} - $currStart{$parent} + $currEnd{$seq} ;
    }
    print "\nSequence $link{$parent}\n";
    print "Subsequence $seq $start{$seq} $end{$seq}\n" ;
    $link{$seq} = $link{$parent} ;
}

###########################################
#Do a quick check to make sure that everything 
#that was in a link has been put back in one
###########################################

foreach $seq (keys %currSource) {
    if (!$link{$seq}) { warn "$seq not put back into a link\n" ; }
}

###########################################
# make superlinks
###########################################

%superinfo = ( "I" => "H06O01",		# left ends of superlinks
	       "IR" => "Y95D11A",
	       "II" => "T05A6",
	       "IIIL" => "F45H7",
	       "IIIR" => "K01F9",
	       "IV" => "F21D5",
	       "V" => "F07D3",
	       "X" => "B0272"
	       ) ;

foreach $chrom (keys %superinfo) {
    print "\nSequence SUPERLINK_CB_$chrom\n" ;
    print "From_laboratory CB\n" ;
    $pos = 1 ;
    $seq = $superinfo{$chrom} ;
    while ($seq) {
	if ($link{$seq}) {
	    $lk = $link{$seq} ;
	    while ($seq && $lk eq $link{$seq}) {
		$end = $end{$seq} ;
		$seq = $right{$seq} ;
	    }
	    $end += $pos - 1 ;
	    print "Subsequence $lk $pos $end\n" ;
	} elsif ($isLinkCandidate{$seq}) {
	    $end = $pos - 1 + $length{$seq} ;
	    if ($isFlipped{$seq}) {
		print "Subsequence $seq $end $pos\n" ;
	    } else {
		print "Subsequence $seq $pos $end\n" ;
	    }
	    $seq = $right{$seq} ;
	} elsif (!$isExternal{$seq}) {
	    $end = $pos - 1 + 1000 ;
	    print "Subsequence $seq $pos $end\n" ;
	    $seq = $right{$seq} ;
	} else {
	    last ;
	}
	$pos = $end + 101 ;
    }
}

############# end of file ################
---


From owner-acedb@hgmp.mrc.ac.uk  Tue Nov  9 18:23:17 1999
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On Tue, 9 Nov 1999, Richard Durbin wrote:

> Hello Keith,
> 
> Aha, you ended up with AGR.  Congratulations.

Thankyou, I started last Monday (which was the same day that I finally
submitted my thesis).  

Thanks for the help.  I won't pretend that I've got to grips with Acedb
yet (certainly not within a week).  I will hopefully be attending the
ACEDB course in January and that will help.

There is no urgent need for me to sort this out for the Arabidopsis
database as there is still a lot of sequence information to come before it
will be necessary to link things together.

One more question though.  The overlap information stored in the
Overlap_left and Overlap_right tags...does this come from the comment
field of the GenBank/EMBL entries?  Without a lof of BLAST searchs I don't
see how else you piece together which sequences overlap.  I'm therefore
uncertain of how applicable this is to A. thaliana as from what I have
seen so far, very few EMBL entries have information about how they
overlap...which begs the questions as to how our database knows that they
*do* overlap in the first place.

I shall try and refrain from asking you too many questions before I've
learnt a little more about ACEDB.

Thanks again for your help.

Keith

~  Keith Bradnam - Developer, Arabidopsis Genome Resource (AGR)
~  University Park, University of Nottingham, NG7 2RD, UK
~  Tel: (0115) 951 3091 Web: http://synteny.nott.ac.uk/

---


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-------------------------------------------------------

Dear Fellow Diver,

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The newsletter for active divers published by Scuba
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November 1, 1999

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TABLE OF CONTENTS

--Savvy Diver Tip: How to Always Surface Near the Boat
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________________________Savvy Diver Tip:
_____How to Always Surface Near the Boat

Keep it simple. Before leaving the anchor line, take a compass
reading and follow a simple path, such as swimming out on one
heading for a certain number of minutes and back on the
reciprocal for the same amount of time.  You'll have a better
chance of finding the line again, and in any event you'll surface
closer to the dive boat.

-------------------------------------------------------

____________________________GEAR REVIEW:
______________________Five Head Warmers

Thermal protection for your head is critical because that's
where you lose 40 percent or more of your body heat--the blood
vessels in your scalp do not constrict in cold water, leaving
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http://www.scubadiving.com/gear/hoods/   

-------------------------------------------------------

____________________________TRAINING:
________Energy to Burn on Your Next Dive

It's not uncommon to feel so wiped out by the third day of a
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stores high so you don't miss those dives you paid so much for?
Go to http://www.scubadiving.com/training/medicine/nofatigue/
for tips on maintaining your energy level during your dive trip.

-------------------------------------------------------

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-------------------------------------------------------

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-------------------------------------------------------

_________________________TRAVEL GUIDE:
_____________________________Curacao

Few destinations are as well-rounded as Curacao. Like its
Netherlands Antilles neighbor Bonaire to the east, the island
offers the freedom of shore diving, where the dive drill is as
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For your personal guide to diving one of the Caribbean's most
complete dive destinations, go to
http://www.scubadiving.com/travel/curacao2/

-------------------------------------------------------

_________________________THE TOP 10 LIST
______Signs You Need a Refresher Course:
(By the readers of www.scubadiving.com)

10) You ask someone which fin goes on the right foot and which
goes on the left.

9) You think a dive table is what your dive buddies sit around at
Denny's.

8) You ask where the second regulator hose has gone.

7) You see Mike Nelson wearing your gear on a Sea Hunt
re-run.

6) You are certain that the power inflator button on your BC
is to be pressed in order to quickly remove you from perceived
danger.

5) The local hyperbaric chamber technician has memorized your
DAN number.

4) You have signature fins, and the signature is "Lloyd Bridges."

3) You ask "Who is this DAN guy anyway?"

2) When asked for your dive planner, you hand over a bundle of
travel brochures.

1) You think "annual service" means polishing up your brass helmet.

Want more scuba humor? You'll find it in our Top 10 List archives
at: http://www.scubadiving.com/feature/topten/archives.shtml

-------------------------------------------------------

THIS FREE BOOK COULD SAVE YOU THOUSANDS!  Scuba gear costs
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is yours free with your paid subscription to Rodale's Scuba Diving.
Go to http://www.scubadiving.com/subs/saveyourgear.shtml

-------------------------------------------------------

_________________READER RATINGS:
_________________________Best Fish Life

In every issue of Scuba Diving magazine, we report our
readers' ratings of dive operators, accommodations and dive
destinations around the world. Below are the results of our survey
of fish life worldwide divided by region: Caribbean/Atlantic,
Indo-Pacific and North America. 

CARIBBEAN/ATLANTIC
Little Cayman: 93.2
Bonaire: 90.5
Cay Sal Banks, Bahamas: 88.2
St. Croix, USVIs: 88.0
Saba: 87.2

IND0-PACIFIC
Palau: 97.6
Egyptian Red Sea: 95.5
Galapagos Islands: 92.3
Fiji: 91.7
Yap, Micronesia: 90.9

NORTH AMERICA
British Columbia, Canada: 85.7
Islamorada, Fla. Keys: 85.3
Morehead City, N.C.: 81.1
Looe Key, Fla. Keys: 80.8
Tavernier, Fla. Keys: 77.3

Your opinion counts, too! Tell us about your last dive vacation,
and rate the destination, dive operator and resort.  Your input
will be included in our Readers' Choice Awards, to be published
in the Jan/Feb 2000 issue of Scuba Diving. Go to
http://www.scubadiving.com/readersrate

-------------------------------------------------------
________________________Savvy Diver Tip:
_____How to Avoid Cuts, Bites and Stings

A run-in with a sea urchin, stonefish, jellyfish or coelenterate
can sour even the best dive. The key to avoiding these potential
hazards is a healthy respect for the ocean environment. So:

-Get neutrally buoyant. 
-Keep your hands to yourself. 
-Beware of surge, current or swells that can sweep you into
these problematic denizens of the deep.

-------------------------------------------------------

If you like what you have read in Depth-Finder why not tell a
friend?  Go to http://www.scubadiving.com/tellafriend/

-------------------------------------------------------

This is a responsible e-mail sent by Scuba Diving magazine,
6600 Abercorn St., Suite 208, Savannah, GA 31405.
Tel: (912) 351-0855. E-mail: newsletter@depth-finder.com.

-------------------------------------------------------

Copyright 1999, Scuba Diving magazine






From owner-acedb@hgmp.mrc.ac.uk  Wed Nov 10 12:11:29 1999
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From owner-acedb@hgmp.mrc.ac.uk  Thu Nov 11 21:32:33 1999
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From: "Harold K. Moss" <nabiu@king.cts.com>
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Subject: Beef Insulin Crisis
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     Every day, beef insulin is becoming more and more scarce
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     If you or someone you know has been taking beef insulin
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From owner-acedb@hgmp.mrc.ac.uk  Fri Nov 12 00:05:45 1999
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From: okaichi@net.nagasaki-u.ac.jp
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I would like to disconect from bionet of acedb.
Please tell me how to disconect from it.

Kumio Okaichi.
---


From owner-acedb@hgmp.mrc.ac.uk  Fri Nov 12 09:39:18 1999
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Kumio

> I would like to disconect from bionet of acedb.
> Please tell me how to disconect from it.
> 
> Kumio Okaichi.
> ---



Try this from the from the BIOSCI faq:



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From owner-acedb@hgmp.mrc.ac.uk  Fri Nov 12 10:22:27 1999
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From owner-acedb@hgmp.mrc.ac.uk  Fri Nov 12 16:10:02 1999
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From: dsmith@UCSD.EDU (Doug Smith)
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Subject: Re:  How to view overlapping sequences
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I would be interested in the answer to the following question by Keith.
We currently use the blastcl3 client in Perl scripts to do this sort
of thing.

Also, a question re Overlap_right and Overlap_left:
There is asymmetry here.  The ace_4.7g models have an Int for Overlap-right
but not one for Overlap_left.  This Int, the overlap to the next 'leftward'
sequence, eg a cosmid, is apparently used in Richard's LINK script to generate
composite sequences.

But ... is there more to this?
Why would users also not be interested in the overlap to a 'rightward'
sequence?
Are Overlap_right and Overlap_left 'magic tags' in some sense?

Thanks
  -Doug



>On Tue, 9 Nov 1999, Richard Durbin wrote:
>
>> Hello Keith,
>>
>> Aha, you ended up with AGR.  Congratulations.
>
>Thankyou, I started last Monday (which was the same day that I finally
>submitted my thesis).
>
>Thanks for the help.  I won't pretend that I've got to grips with Acedb
>yet (certainly not within a week).  I will hopefully be attending the
>ACEDB course in January and that will help.
>
>There is no urgent need for me to sort this out for the Arabidopsis
>database as there is still a lot of sequence information to come before it
>will be necessary to link things together.
>
>One more question though.  The overlap information stored in the
>Overlap_left and Overlap_right tags...does this come from the comment
>field of the GenBank/EMBL entries?  Without a lof of BLAST searchs I don't
>see how else you piece together which sequences overlap.  I'm therefore
>uncertain of how applicable this is to A. thaliana as from what I have
>seen so far, very few EMBL entries have information about how they
>overlap...which begs the questions as to how our database knows that they
>*do* overlap in the first place.
>
>I shall try and refrain from asking you too many questions before I've
>learnt a little more about ACEDB.
>
>Thanks again for your help.
>
>Keith
>
>~  Keith Bradnam - Developer, Arabidopsis Genome Resource (AGR)
>~  University Park, University of Nottingham, NG7 2RD, UK
>~  Tel: (0115) 951 3091 Web: http://synteny.nott.ac.uk/
>
>---





From owner-acedb@hgmp.mrc.ac.uk  Fri Nov 12 16:55:48 1999
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From: gaune67@CLYDE.ROEHAMPTON.AC.UK (mwestew)
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From owner-acedb@hgmp.mrc.ac.uk  Fri Nov 12 19:08:06 1999
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From: "Marcel Dinger" <marcel@ihug.co.nz>
X-Newsgroups: bionet.software.acedb
Subject: Genamics SoftwareSeek
Date: Sat, 13 Nov 1999 08:03:50 +1300
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GENAMICS SOFTWARESEEK
The Largest Science Software Directory on Earth.
http://genamics.com/software/

Genamics SoftwareSeek now indexes well over 1000 freely-distributable and
commercial titles. Classifications include DNA sequence analysis, protein
structure analysis, RNA structure prediction, molecular modeling, image
analysis, and sequence alignment. All major platforms are supported, including,
Windows, Macintosh, Unix, and Linux. Over 150 online tools and resources that
run directly through your internet browser are also listed.

New software can be submitted on-line through our web-site.

Marcel Dinger,
Genamics.
http://genamics.com/software/





From owner-acedb@hgmp.mrc.ac.uk  Sat Nov 13 03:55:43 1999
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////////////////////////////////////////
 One time mailing, no need for removal.
////////////////////////////////////////

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From owner-acedb@hgmp.mrc.ac.uk  Sat Nov 13 11:42:23 1999
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DEAR FRIENDS,

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TO IMPORT ANY PRODUCT FROM THE WORLD.

PLEASE SEND E-MAIL MENTIONING THE PRODUCT YOU WANT TO EXPORT OR
IMPORT

MS RAJNI RAJ





From owner-acedb@hgmp.mrc.ac.uk  Sun Nov 14 08:11:07 1999
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From: s6s5@BOOM.COM
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From owner-acedb@hgmp.mrc.ac.uk  Mon Nov 15 03:13:59 1999
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From: "W. Bill Ge" <ge.10@osu.edu>
X-Newsgroups: bionet.software.acedb
Subject: subclass display
Date: Sun, 14 Nov 1999 12:36:19 -0500
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Hi, everyone,

I have got a problem displaying subclass in the main xace window. 

I define the a subclass as

Class MouseGene
Visible
Is_a_subclass_of Locus
Filter "IS Gene AND Species=Mouse"

And, I also added MouseGene to the layout.wrm and options.wrm files.
This new subclass does not show up in the main xace window. 

Whatelse should I do to show this subclass?

Thank you!

Bill 

-- 
____________________________________________________________
http://pegasus.med.ohio-state.edu/~bill


From owner-acedb@hgmp.mrc.ac.uk  Mon Nov 15 10:19:54 1999
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From: rd@sanger.ac.uk (Richard Durbin)
X-Newsgroups: bionet.software.acedb
Subject: Re:  How to view overlapping sequences
Date: 15 Nov 1999 10:19:49 -0000
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Overlap_left and Overlap_right are not "magic" tags, in the sense that the
acedb code itself does not know about them.  There is some code outside acedb,
in the form of the perl script that I mailed to the newsgroup and a C program
of Jean's (mieg@crbm.cnrs-mop.fr) called fixsuperlink that both use them.

In my models the Int is only attached to Overlap_right and not to Overlap_left
so as to avoid possible conflicts if the two values differed.  In AcePerl
notation, the value of the integer following the Overlap_left sequence name
would be x->Overlap_left->Overlap_right(2).

Richard
---


From owner-acedb@hgmp.mrc.ac.uk  Mon Nov 15 22:15:30 1999
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From: narayanfax@THEARMY.COM ("NARAYAN")
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SEND UPTO 2 PAGES OF FAXES ANYWHERE IN WORLD
--IN TEXT, MS WORD OR ANY SCANNED DOCUMENT FOR JUST RS.25/- FOR MORE
DETAILS SEND E-MAIL

NARAYAN





From owner-acedb@hgmp.mrc.ac.uk  Tue Nov 16 00:25:45 1999
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From: "Sergio Fernández" <sergioff@euskalnet.net>
X-Newsgroups: alt.comp.software,alt.english,alt.geo-software,alt.usage.english,bionet.software.acedb,bit.software,es.ciencia.electronica,es.comp.cracks,es.comp.lenguajes,es.misc.anuncios.trabajo.demandas,es.misc.anuncios.trabajo.ofertas,misc.education.langua
Subject: Soft de Ingles
Date: Tue, 16 Nov 1999 01:00:50 -0000
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Estoy interesado en perfeccionar mi ingles y al ver como clavan a los pobres
estudiantes en las academias, se me quitan las ganas de intentarlo.
Os escribo para ver si me podéis ayudar a encontrar un programa parecido o
similar que los que utilizan en las academias de ingles informatizadas para
practicar en mi casa.
Lo que busco es algo más económico que las 130.000 ptas. que me supondría
apuntarme a una academia, si tenéis alguna sugerencia o algo que me pueda
ayudar os lo agradecería muchísimo.
Si conocéis o usáis algún programa de los que ahora se comercializan me
gustaría que me dij