From owner-rapd@net.bio.net Sat Sep 03 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!daresbury!trane.uninett.no!eunet.no!nuug!EU.net!uunet!munnari.oz.au!news.Hawaii.Edu!uhunix.uhcc.Hawaii.Edu!stiles
From: stiles@uhunix.uhcc.Hawaii.Edu (John Stiles)
Subject: Re: Next PLANT GENOME meetings
Message-ID: <Cv45Gq.5Hv@news.Hawaii.Edu>
Sender: news@news.Hawaii.Edu
Organization: University of Hawaii
References: <wfl1-250894002541@132.236.3.90>
Date: Thu, 25 Aug 1994 23:05:14 GMT
Lines: 27

In article <wfl1-250894002541@132.236.3.90> wfl1@cornell.edu (Warren Frank Lamboy) writes:
>Does anyone know when the next Plant Genome meetings will be held,
>and whom I might contact for more information?  Thank you.
>
>-- 
>Warren F. Lamboy
>Dept. of Horticultural Sciences and
>   USDA-ARS Plant Genetic Resources Unit
>Cornell University
>Geneva, NY 14456-0462
>warren_lamboy@cornell.edu

Plant Gemone III
January 15-19
Town & Country Hotel
San Diego, CA

For information contact:

     Scherago International, Inc.
       Tel. (212) 643-1750
       Fax. (212) 643-1758
       Email Scherago@Biotechnet.com


John
stiles@uhunix.uhcc.hawaii.edu

From owner-rapd@net.bio.net Mon Sep 05 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!agate!library.ucla.edu!europa.eng.gtefsd.com!newsxfer.itd.umich.edu!gatech!swrinde!howland.reston.ans.net!vixen.cso.uiuc.edu!news.uoregon.edu!netnews.nwnet.net!ns1.nodak.edu!badlands!dahleen
From: dahleen@badlands.NoDak.edu (Lynn S Dahleen)
Subject: Re: codominance take 2 (or more!)
Sender: usenet@ns1.nodak.edu (Usenet login)
Message-ID: <Cvpv81.xn7@ns1.nodak.edu>
Date: Tue, 6 Sep 1994 16:31:13 GMT
References: <CunrKC.KJ6@ucdavis.edu> <Kath.Nesbitt-300894155114@mg1_98.plant.utas.edu.au>
Nntp-Posting-Host: badlands.nodak.edu
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: In my lab we are having trouble with the cutting oout and re-amplification
: bit, do you have any suggestions?  
Kath,  
Try cutting the band out and placing the agarose/acrylamide fragment in 
50 to 100 microliters of water. Let that sit overnight.  The next day, 
set up a 100 ul PCR reaction using the original primers and 2 ul of the 
eluate from the gel frag.  This should give you a pretty substantial 
amount of the band you are interested in.


People are also trying to clone the band
: for sequencing.

As for cloning, add 1 ul (about 5 units) of Klenow to the above reaction, 
and incubate 30 minutes at 37 degrees C.  This should effectivly blunt 
end the amplification product. (Yes, klenow seems to work fine in both 
Taq, Tfl, and Vent buffer).  Run the resulting DNA out on a gel, cut out 
the band (there should be lots of it if all worked well).  Take a 0.5 ml 
eppi and punch a small hole in the bottom of it.  Plug the hole with 
glass wool, and place your gel fragment in the modified tube.  Then place 
the whole set-up in a 1.5 ml eppi and spin for 15 min at max speed.  
Extract the resulting liquid 2X with phenol and 2X with CHCl3 and then 
EtOH precipitate.  Mix with the blunt ended vector of choice and ligate 
(use an excess of ligase) overnight at room temp.  Transform using any 
standard method.

Hope this helps.  
Dave Horvath
USDA/ARS/NCSL
Fargo, ND  

PS. I am also curious as to how one gets a heteroduplex with PCR.

: Kath Nesbitt

: P.s. It seems that I have to make more text than I'm replying to for this
: news-server to post my questions.  Sometimes I just don't understand
: computers!!! I wonder if that's enough text for it.

From owner-rapd@net.bio.net Tue Sep 06 23:00:00 1994
Path: biosci!JOPLIN.BIOSCI.ARIZONA.EDU!mount
From: mount@JOPLIN.BIOSCI.ARIZONA.EDU ("Dr. David Mount")
Newsgroups: bionet.molbio.rapd
Subject: (none)
Date: 7 Sep 1994 12:22:09 -0700
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unsubscribe

From owner-rapd@net.bio.net Wed Sep 07 23:00:00 1994
Path: biosci!ACAD.URSINUS.EDU!kgoddard
From: kgoddard@ACAD.URSINUS.EDU
Newsgroups: bionet.molbio.rapd
Subject: seeking human primers
Date: 8 Sep 1994 12:45:03 -0700
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We would be most grateful if anyone could recommend some primers which reveal
differences within human populations.  

From owner-rapd@net.bio.net Thu Sep 08 23:00:00 1994
Path: biosci!zoology.uni-frankfurt.d400.de!Streit
From: Streit@zoology.uni-frankfurt.d400.de (PCN-Benutzer)
Newsgroups: bionet.molbio.rapd
Subject: request
Date: 9 Sep 1994 08:05:07 -0700
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Sorry, if we do not keep up to your normal standarts of communication.
We are a group of molecular ecologists and we are interested in information
about joining your network.
We do not even know, if this is the right adress, but if there's anybody out
there please respond. (Our e-mail system is now installed for about 1 hour
and therefore we are very proud that we can handle it.)

thank you in advance

AK ™K™LOGIE Uni-Frankfurt/Deutschland

From owner-rapd@net.bio.net Sun Sep 11 23:00:00 1994
Path: biosci!agate!howland.reston.ans.net!EU.net!sunic!trane.uninett.no!daresbury!not-for-mail
From: J R Beeching <J.R.Beeching@bath.ac.uk>
Newsgroups: bionet.molbio.rapd
Subject: RFLP / RAPD band profile database
Date: 12 Sep 1994 13:44:41 +0100
Lines: 22
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Original-To: BIO-SOFTWARE <bio-soft@dl.ac.uk>

Dear All,

I am looking for some software, preferably public domain, which can be
used to store and compare RFLP and/or RAPD band profile data.  Ideally it
should be able to accept cumulative date from different probes or primers.
It should also have the capability to be interrogated in order to determine
whether or not a pattern from a new organism is already in the database.

If there is much interest and many replies I will post a compilation.

Thank you for your help.

John

-------------------------------------------------------------------
| John Beeching                 E-mail: J.R.Beeching@bath.ac.uk   |
| Biology & Biochemistry                                          |
| University of Bath                                              |
| Bath BA2 7AY                  Phone:  +44 (0)225 826826 ext 5193|
| U.K.                          Fax:    +44 (0)225 826779         |
-------------------------------------------------------------------


From owner-rapd@net.bio.net Tue Sep 13 23:00:00 1994
Path: biosci!YVAX.BYU.EDU!FARMERJ
From: FARMERJ@YVAX.BYU.EDU
Newsgroups: bionet.molbio.rapd
Subject: Re: There is no rapd FAQ, but... (addresses)
Date: 14 Sep 1994 08:32:10 -0700
Organization: Brigham Young University
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Sender: daemon@net.bio.net
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In my last posting, I did not have the address for users in the European-Africa area. 
You can request assistance from either of the addresses below.

biosci-help@net.bio.net 

biosci@daresbury.ac.uk 

Best wishes.

James Farmer
FARMERJ@YVAX.BYU.EDU

From owner-rapd@net.bio.net Tue Sep 13 23:00:00 1994
Path: biosci!YVAX.BYU.EDU!FARMERJ
From: FARMERJ@YVAX.BYU.EDU
Newsgroups: bionet.molbio.rapd
Subject: There is no FAQ, but...
Date: 14 Sep 1994 08:12:29 -0700
Organization: Brigham Young University
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NNTP-Posting-Host: net.bio.net

In a recent message, Hilton referred to rapd FAQ.  I would like to remind
everyone, especially newcomers, that there is no FAQ.  However, it is possible
to search the archives.  If you do not know how, request information from
BIOSCI-HELP@NET.BIO.NET or the equivalent address at DANSBURY for the European
and African users.

Jim Farmer
FARMERJ@YVAX.BYU.EDU

From owner-rapd@net.bio.net Tue Sep 13 23:00:00 1994
Path: biosci!agate!howland.reston.ans.net!pipex!uknet!fulcrum!bham!bcs88.bham.ac.uk!user
From: A.C.Hilton@bham.ac.uk (Wiggy)
Newsgroups: bionet.molbio.rapd
Subject: Re: RFLP / RAPD band profile database
Date: 14 Sep 1994 08:43:59 GMT
Organization: University of Birmingham
Lines: 39
Distribution: bionet
Message-ID: <A.C.Hilton-1409940947160001@bcs88.bham.ac.uk>
References: <351ifp$7be@mserv1.dl.ac.uk>
NNTP-Posting-Host: bcs88.bham.ac.uk

In article <351ifp$7be@mserv1.dl.ac.uk>, J R Beeching
<J.R.Beeching@bath.ac.uk> wrote:

> Dear All,
> 
> I am looking for some software, preferably public domain, which can be
> used to store and compare RFLP and/or RAPD band profile data.  Ideally it
> should be able to accept cumulative date from different probes or primers.
> It should also have the capability to be interrogated in order to determine
> whether or not a pattern from a new organism is already in the database.
> 
> If there is much interest and many replies I will post a compilation.
> 
> Thank you for your help.
> 
> John
> 
> -------------------------------------------------------------------
> | John Beeching                 E-mail: J.R.Beeching@bath.ac.uk   |
> | Biology & Biochemistry                                          |
> | University of Bath                                              |
> | Bath BA2 7AY                  Phone:  +44 (0)225 826826 ext 5193|
> | U.K.                          Fax:    +44 (0)225 826779         |
> -------------------------------------------------------------------

There was some discussion on this topic a few months ago and a compilation
of possible analysis software posted to this group. You may want to check
the FAQ.

Wig.

-- 
      **********************************************************
      ** It's because I come from Wigan that my name is Wiggy,**
      ** and nothing to do with my head................Honest!**
      **                                                      **
      **                 A.C.Hilton@bham.ac.uk                **
      **********************************************************
                         

From owner-rapd@net.bio.net Tue Sep 13 23:00:00 1994
Path: biosci!jab000.uesp.ansp.br!gkuhar
From: gkuhar@jab000.uesp.ansp.br (GORAN KUHAR JEZOVSEK)
Newsgroups: bionet.molbio.rapd
Subject: info primers
Date: 13 Sep 1994 23:46:56 -0700
Organization: UNESP
Lines: 11
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <2e746181@jab000.uesp.ansp.br>
Reply-To: GORAN KUHAR JEZOVSEK <GKUHAR@jab000.uesp.ansp.br>
NNTP-Posting-Host: net.bio.net

I would like to know if anybody has the information about random or specific primers for maize fingerprinting, or any microsattelite sequences?
Thanks a lot.

Goran Kuhar.
-- 

       GORAN KUHAR JEZOVSEK                   E-mail: gkuhar@jab000.uesp.ansp.br
FACULDADE CIENCIAS AGRARIAS E VETERINARIAS    Fone  :  (0163) 23-2500
       JABOTICABAL/ UNESP                     Endereco: Rod. Carlos Tonanni,Km 5
                                              14870-000  Jaboticabal   SP


From owner-rapd@net.bio.net Wed Sep 14 23:00:00 1994
Path: biosci!EMUNIX.EMICH.EDU!bio_hannan%emuvax.dnet.emich.edu
From: bio_hannan%emuvax.dnet.emich.edu@EMUNIX.EMICH.EDU
Newsgroups: bionet.molbio.rapd
Subject: RE: RAPD for plant ID
Date: 15 Sep 1994 10:27:14 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 10
Sender: daemon@net.bio.net
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Message-ID: <9409151726.AA01823@emunix.emich.edu>
NNTP-Posting-Host: net.bio.net

Stewart,
	I have been working on developing clone-specific profiles in Iris
lacustris and have been able to find consistent banding patterns for
all shoots within single clones that also differ between clones.  We had
to sample multiple shoots from single clones to find those fragments that
consistently appeared in all shoots.  We always find a number of bands that
sho w up only inconsistently within clones.

Gary Hannan
bio_hannan@emunix.emich.edu

From owner-rapd@net.bio.net Wed Sep 14 23:00:00 1994
Path: biosci!FAPQ.FAPESP.BR!Carteiro
From: Carteiro@FAPQ.FAPESP.BR
Newsgroups: bionet.molbio.rapd
Subject: Mail not delivered yet. Please do not reply.
Date: 15 Sep 1994 11:00:07 -0700
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Lines: 33
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NNTP-Posting-Host: net.bio.net

-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+- begin-
-------------------------------------------------------------------------------
This mail was not delivered yet. Some "daemon" in the system may
be hung. The system will retry later.
  Virtually,
  Fapesp's PostPerson.
-------------------------------------------------------------------------------
`From gkuhar Mon, 12 Sep 94 10:11:13 C remote from jab000
`Received:  by jab000.uesp.ansp.br (UUPC/extended 0.0);
`           Mon, 12 Sep 94 10:11:13 C
`Message-id: <2e746181@jab000.uesp.ansp.br>
`Date:      Mon, 12 Sep 94 10:11:13 C
`From:      GORAN KUHAR JEZOVSEK <gkuhar@jab000.uesp.ansp.br>
`Organization: UNESP
`Reply-To:  GORAN KUHAR JEZOVSEK <GKUHAR@JAB000.UESP.ANSP.BR>
`To:        rapd@net.bio.net
`Subject:   info primers
`
`I would like to know if anybody has the information about random or specific p
`rimers for maize fingerprinting, or any microsattelite sequences?
`Thanks a lot.
`
`Goran Kuhar.
`-- 
`
`       GORAN KUHAR JEZOVSEK                   E-mail: gkuhar@jab000.uesp.ansp.
`br
`FACULDADE CIENCIAS AGRARIAS E VETERINARIAS    Fone  :  (0163) 23-2500
`       JABOTICABAL/ UNESP                     Endereco: Rod. Carlos Tonanni,Km
` 5
`                                              14870-000  Jaboticabal   SP
`
-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+- end-

From owner-rapd@net.bio.net Wed Sep 14 23:00:00 1994
Path: biosci!agate!howland.reston.ans.net!cs.utexas.edu!uunet!panix!ddsw1!godot.cc.duq.edu!newsfeed.pitt.edu!dsinc!netnews.upenn.edu!msuinfo!harbinger.cc.monash.edu.au!news.uwa.edu.au!newsman.csu.murdoch.edu.au!Stewart.Washer
From: Washer@csuvax1.murdoch.edu.au (Stewart Washer)
Newsgroups: bionet.molbio.rapd
Subject: RAPD for plant ID
Date: 15 Sep 1994 06:53:30 GMT
Lines: 11
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Xdisclaimer: No attempt was made to authenticate the sender's name.

I wish to use RAPD to compare a group of plants to see if any are from
the same original clone. Are RAPDs stable enough to do this beyond
"reasonable" doubt ? Also, what sort of sensitivity do they have in
regards to picking up differences between closely related individuals ?

Any help or advice would be greatly appreciated !

                             Stewart Washer
                             Murdoch University
                             Western Australia
                             email (Washer@csuvax1.murdoch.edu.au)

From owner-rapd@net.bio.net Sun Sep 18 23:00:00 1994
Newsgroups: bionet.celegans,bionet.molbio.rapd
Path: biosci!bcm!cs.utexas.edu!news.uta.edu!wbar.uta.edu!patrick
From: patrick@wbar.uta.edu (Patrick Phillips)
Subject: RAPD on C. elegans
Message-ID: <1994Sep19.180655.9508@news.uta.edu>
Sender: news@news.uta.edu (USENET News System)
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Organization: /usr/local/lib/news/organization
Date: Mon, 19 Sep 1994 18:06:55 GMT
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Xref: biosci bionet.celegans:111 bionet.molbio.rapd:775

We are just starting a project using RAPDs with everyone's favorite
nematode, C. elegans.  Is anyone out there working with this method
in C. elegans?  I would like to know which primers should for sure work
with N2 before I do a lot of playing around.

For those experienced RAPDers in b.m.rapd, what seems to be the probability
that a particular primer will amplify at all?  I've only tried four
primers so far, and none have amplified (I know the DNA and PCR reagents
are good).  I have no way of knowing whether something is going wrong with
the PCR (like the annealing temp), or if the primers just aren't hitting
anything.  Before I try 100 more primers, I'd like to know what others have
experienced.

Patrick Phillips
Biology Department
University of Texas at Arlington
patrick@wbar.uta.edu
(817) 273-2409


From owner-rapd@net.bio.net Mon Sep 19 23:00:00 1994
Path: biosci!cbr.for.csiro.au!charlie.bell
From: charlie.bell@cbr.for.csiro.au (Charlie Bell)
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPD on C. elegans
Date: 20 Sep 1994 16:06:40 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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Sender: daemon@net.bio.net
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NNTP-Posting-Host: net.bio.net


>For those experienced RAPDers in b.m.rapd, what seems to be the probability
>that a particular primer will amplify at all?  I've only tried four
>primers so far, and none have amplified (I know the DNA and PCR reagents
>are good).  I have no way of knowing whether something is going wrong with
>the PCR (like the annealing temp), or if the primers just aren't hitting
>anything.  Before I try 100 more primers, I'd like to know what others have
>experienced.
>
>Patrick Phillips
>Biology Department
>University of Texas at Arlington
>patrick@wbar.uta.edu
>(817) 273-2409
>
>
We have screened the first 520 Operon primers on DNA from Pinus Radiata and 
Eucalyptus nitens and found that only about 10% do not amplify under the 
conditions that we have standardised on. We can usually get these 10% to 
work by just changing the MgCl2 concentration.


From owner-rapd@net.bio.net Mon Sep 19 23:00:00 1994
Path: biosci!EMUNIX.EMICH.EDU!bio_hannan%emuvax.dnet.emich.edu
From: bio_hannan%emuvax.dnet.emich.edu@EMUNIX.EMICH.EDU
Newsgroups: bionet.molbio.rapd
Subject: E. elegans RAPDs
Date: 20 Sep 1994 07:31:52 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 6
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Message-ID: <9409201433.AA20749@emunix.emich.edu>
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Over what time period  have you tried the four primers?  It is possible that
amplifications just stop for a while for no apparent reason.  But if other
systems in the same lab were working, the lack of amplification is not
as likely to be a random shutdown of amplification reactions.

gary Hannan

From owner-rapd@net.bio.net Tue Sep 20 23:00:00 1994
Path: biosci!GNU.AI.MIT.EDU!bw
From: bw@GNU.AI.MIT.EDU (Bruce Waldman)
Newsgroups: bionet.molbio.rapd
Subject: Research Position/ Molecular Ecology of New Zealand Frogs
Date: 21 Sep 1994 05:18:16 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 38
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Distribution: world
Message-ID: <9409211213.AA03638@apple-gunkies.gnu.ai.mit.edu>
NNTP-Posting-Host: net.bio.net

Research Scientist/Postdoctoral Fellow

BEHAVIOUR, ECOLOGY AND POPULATION GENETICS OF NEW ZEALAND FROGS

A research position to study behavioural ecology and population genetics of
native New Zealand frogs (genus Leiopelma) is available starting 1 November
1994 (or other date to be negotiated).  The successful candidate will be
involved in various research projects concerned with the behaviour
(e.g. parental care of brood) and ecology (e.g. dispersal) of these unique
frogs.  A major portion of the work will involve analyses of genetic
variation within and among populations using PCR-based methodologies (e.g.
microsatellites, RAPDs) and other fingerprinting techniques (minisatellites,
mtDNA).  The application of these methodologies to conservation biology, both
with respect to these endangered frogs and other threatened New Zealand fauna,
will be stressed.

Applicants should have experience in methods of DNA purification and analyses.
Knowledge of techniques for constructing and screening genomic libraries would
be an advantage.  Research will also involve fieldwork, surveying behaviour of
frogs in natural conditions.  Funding is initially for one year, with
possibilities of extension for a further two years.  Appointment may be made
as a Research Scientist, Postdoctoral Fellow, or Research Assistant,
depending on applicant's qualifications and final budget allocation.

Please contact me if you are interested, or would like further details.
Letters of application should include details of previous experience with
molecular methods, c.v., and names and contact information (phone/fax/email)
of referees who know your work.


Bruce Waldman
Department of Zoology
University of Canterbury
Christchurch, New Zealand

Telephone: +64 3 364 2066
FAX:       +64 3 364 2024
Email:     waldman_b@ix.wcc.govt.nz

From owner-rapd@net.bio.net Wed Sep 21 23:00:00 1994
Path: biosci!bcm!cs.utexas.edu!uunet!news.delphi.com!usenet
From: Tony <san17@delphi.com>
Newsgroups: bionet.molbio.rapd
Subject: Anyone here can help me with RFLP Linkage Analysis
Date: Wed, 21 Sep 94 22:21:35 -0500
Organization: Delphi (info@delphi.com email, 800-695-4005 voice)
Lines: 3
Message-ID: <RO4V40P.san17@delphi.com>
NNTP-Posting-Host: bos1b.delphi.com

Could anyone assist me in info about this procedure, that is--
RFLP Linkage Analysis.
Thanks

From owner-rapd@net.bio.net Wed Sep 21 23:00:00 1994
Path: biosci!jab000.uesp.ansp.br!gkuhar
From: gkuhar@jab000.uesp.ansp.br (GORAN KUHAR JEZOVSEK)
Newsgroups: bionet.molbio.rapd
Subject: (none)
Date: 22 Sep 1994 04:19:18 -0700
Organization: UNESP
Lines: 13
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <2e807123@jab000.uesp.ansp.br>
Reply-To: GORAN KUHAR JEZOVSEK <GKUHAR@jab000.uesp.ansp.br>
NNTP-Posting-Host: net.bio.net

Do someone have information about the use of PCR-RFLPs in plants ?
If so, in which references?

Thanks

Goran Kuhar
-- 

       GORAN KUHAR JEZOVSEK                   E-mail: gkuhar@jab000.uesp.ansp.br
FACULDADE CIENCIAS AGRARIAS E VETERINARIAS    Fone  :  (0163) 23-2500
       JABOTICABAL/ UNESP                     Endereco: Rod. Carlos Tonanni,Km 5
                                              14870-000  Jaboticabal   SP


From owner-rapd@net.bio.net Wed Sep 21 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!agate!howland.reston.ans.net!swrinde!sgiblab!munnari.oz.au!newsroom.utas.edu.au!ml.csiro.au!mac-1303.ml.csiro.au!chris.bolch
From: Christopher J. S. Bolch <chris.bolch@ml.csiro.au>
Subject: Sequencing PCR product
Message-ID: <1994Sep22.063608.16290@ml.csiro.au>
X-Xxmessage-Id: <AAA76384FD016251@mac-1303.ml.csiro.au>
X-Xxdate: Thu, 22 Sep 94 16: 38:28 GMT
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Organization: CSIRO Division of Fisheries, Hobart, Tasmania
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Date: Thu, 22 Sep 1994 06:36:08 GMT
Lines: 7

I have heard recently that it is possible to sequence PCR products
directly either by usual means or by cycle sequencing.  Is it as simple
as that or does one need to clone the fragments first?  Does sequencing
of the product directly have any pitfalls or problems?  I imagine that
excess primer could be a problem.

Chris

From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Path: biosci!vt.edu!fishgen
From: fishgen@vt.edu (Bruce  J. Turner)
Newsgroups: bionet.molbio.rapd
Subject: expanding the subject base of the rapd network
Date: 23 Sep 1994 11:38:53 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 17
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199409231834.LAA23867@net.bio.net>
NNTP-Posting-Host: net.bio.net

In postings today, Kevin O'Donnell and David MacHugh both suggested that
the subject base of the rapd network be expanded to other sorts of
molecular markers.  I agree, especially since microsatellites are very
likely going to have an enormous impact on the field.  I think we should
become something like a "molecular techniques in population genetics" net,
with  members employing, and discussing the relative merits of,  different
techniques as they become available. Rapds are still of interest to many
people, but I think it fair to say that they are now one of several
different techniquess one might use, rather than a focal technique that
nearly all people will use.  It is likely that very nearly all the future
molecular markers will be based on pcr amplification (some are already
referring to them as "amplicons") and this technique, and the ever-present
problems inherent in isolating good DNA from many different organisms, can
serve as a common thread for discussions even if different people are using
different markers.



From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Path: biosci!MERCURY.UARK.EDU!drhoads
From: drhoads@MERCURY.UARK.EDU (doug rhoads)
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPD Newsgroup
Date: 23 Sep 1994 11:16:16 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 49
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <1CE1B2807C6@uamercury.uark.edu>
NNTP-Posting-Host: net.bio.net

At 05:12 PM 9/23/94 GMT, David MacHugh wrote:
>In article <CwL8sJ.5M1@jura.sasa.gov.uk>, odonnell@sasa.gov.uk (Kevin
>O'Donnell) wrote:
>
>>
>> I find this newsgroup the most useful of all of the BIONET newsgroups,
>> (along with the Diagnostics list), and have a suggestion as to how it
>> could be made even more useful, to me at least.
>>
>> As all of the participants seem to be using RAPDs for much the same
>> sort of purpose, would it make sense to expand the subject matter of
>> the group to take in AFLPs, SSRs, RFLPs etc.?  This would mean a
>> molecular markers group rather than a RAPDs group but this would make
>> sense to me.
>>
>> This may be one of those questions which gets flogged to death
>> every so often, so apologies if I am going over old ground.  However,
>> I would be interested in what others think of this idea.
>>
>> Kevin O'Donnell
>> Scottish Agricultural Science Agency
>> Edinburgh
>> Scotland
>
>I reckon this is a worthwile idea. Without meaning to demean RAPDs, VNTRs
>(in the broad sense) are much more widely used. SSRs are the workhorses of
>gene mapping and are undoubtedly about to revolutionise population and
>evolutionary genetics too. Basically it would be great to have a forum for
>all types of molecular markers, not just RAPDs.

>    *********************************************************************
>    *         (__)  David MacHugh,        E-mail: dmachugh@mail.tcd.ie  *

Well, I guess I need to throw away all my RAPD primers.  We're working in 
the dark ages.  I believe all of the techniques are similar enough in the 
general approach perhaps a molecular mapping forum is what is desired.  
After all we can only deal with the `I don't have bands in my RAPDs any 
more' or `there are bands in my negative control' questions.  Do we really 
need a name change??  I would speculate that would only be with recruitment 
of new newsies.  Perhaps our network leaders could comment on what happens 
with a name change.  I have seen similar discussions in other groups and I 
would hate for us to fragment to far and wide.
 

Doug Rhoads                  || Dept. of Biological Sciences
drhoads@mercury.uark.edu     || 601 Science Engineering
drhoads@uafsysb.uark.edu     || University of Arkansas
501-575-3251                 || Fayetteville, AR 72701


From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!agate!howland.reston.ans.net!news.sprintlink.net!pipex!jura.sasa.gov.uk!news
From: odonnell@sasa.gov.uk (Kevin O'Donnell)
Subject: RAPD Newsgroup
Organization: Scottish Agricultural Science Agency
Date: Fri, 23 Sep 1994 15:09:55 GMT
Message-ID: <CwL8sJ.5M1@jura.sasa.gov.uk>
X-Newsreader: WinVN 0.91.3
Sender: news@jura.sasa.gov.uk (Usenet)
Lines: 19


I find this newsgroup the most useful of all of the BIONET newsgroups,
(along with the Diagnostics list), and have a suggestion as to how it
could be made even more useful, to me at least. 

As all of the participants seem to be using RAPDs for much the same
sort of purpose, would it make sense to expand the subject matter of
the group to take in AFLPs, SSRs, RFLPs etc.?  This would mean a 
molecular markers group rather than a RAPDs group but this would make
sense to me.

This may be one of those questions which gets flogged to death
every so often, so apologies if I am going over old ground.  However,
I would be interested in what others think of this idea.
 
Kevin O'Donnell
Scottish Agricultural Science Agency    
Edinburgh
Scotland                                           

From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!agate!howland.reston.ans.net!pipex!jura.sasa.gov.uk!news
From: odonnell@sasa.gov.uk (Kevin O'Donnell)
Subject: Automatic Data Collection
Organization: Scottish Agricultural Science Agency
Date: Fri, 23 Sep 1994 15:01:34 GMT
Message-ID: <CwL8En.5FK@jura.sasa.gov.uk>
X-Newsreader: WinVN 0.91.3
Sender: news@jura.sasa.gov.uk (Usenet)
Lines: 19

We are interested in constructing a RAPD band library for potato 
varieties and would like to use a system for automatically
registering and characterising the bands generated on RAPD gels,
and entering this information into a database which can then be 
interogatted to identify unknown varieties in blind tests. in other words,
once the data is entered, it will be able to identify any of the
varieties from their banding patterns.

Has anyone tried using a gel scanner to construct a library
of RAPD band patterns for use in variety testing?  If so, would you like
to share your experiences? I am particularly interested in how many
varieties your software was able to descriminate between and how reliably.
Is there a particular type of hardware or software that you would
 recommend,and so on.
  
Kevin O'Donnell
Scottish Agricultural Science Agency    
Edinburgh
Scotland                                           

From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!rutgers!gatech!howland.reston.ans.net!EU.net!ieunet!tcdcs!news.tcd.ie!gen033.gen.tcd.ie!user
From: dmachugh@mail.tcd.ie (David MacHugh)
Subject: Re: RAPD Newsgroup
Message-ID: <dmachugh-230994171217@gen033.gen.tcd.ie>
Followup-To: bionet.molbio.rapd
Sender: usenet@news.tcd.ie (TCD News System )
Organization: Genetics Department, Trinity College, Dublin 2. IRELAND
References: <CwL8sJ.5M1@jura.sasa.gov.uk>
Date: Fri, 23 Sep 1994 17:12:17 GMT
Lines: 41

In article <CwL8sJ.5M1@jura.sasa.gov.uk>, odonnell@sasa.gov.uk (Kevin
O'Donnell) wrote:

> 
> I find this newsgroup the most useful of all of the BIONET newsgroups,
> (along with the Diagnostics list), and have a suggestion as to how it
> could be made even more useful, to me at least. 
> 
> As all of the participants seem to be using RAPDs for much the same
> sort of purpose, would it make sense to expand the subject matter of
> the group to take in AFLPs, SSRs, RFLPs etc.?  This would mean a 
> molecular markers group rather than a RAPDs group but this would make
> sense to me.
> 
> This may be one of those questions which gets flogged to death
> every so often, so apologies if I am going over old ground.  However,
> I would be interested in what others think of this idea.
>  
> Kevin O'Donnell
> Scottish Agricultural Science Agency    
> Edinburgh
> Scotland

I reckon this is a worthwile idea. Without meaning to demean RAPDs, VNTRs
(in the broad sense) are much more widely used. SSRs are the workhorses of
gene mapping and are undoubtedly about to revolutionise population and
evolutionary genetics too. Basically it would be great to have a forum for
all types of molecular markers, not just RAPDs.                            
       

-- 
    *********************************************************************
    *         (__)  David MacHugh,        E-mail: dmachugh@mail.tcd.ie  *  
            
    *         (@*)  Bovine Genetics,      Phone:  (353)-1-7021088       *
    *  /-------\u'  Genetics Department,  Fax:    (353)-1-6798558       *
    * / |     ||    Trinity College,                                    *
    *   ||----||    Dublin 2.                                           *
    *   ^^    ^^    Ireland.                                            *
    *********************************************************************
 

From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Path: biosci!CHUMA.CAS.USF.EDU!karl
From: karl@CHUMA.CAS.USF.EDU ("Stephen A. Karl")
Newsgroups: bionet.molbio.rapd
Subject: Re: Sequencing PCR product
Date: 23 Sep 1994 09:27:33 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 53
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.3.87.9409231232.B21996-0100000@chuma>
References: <1994Sep22.063608.16290@ml.csiro.au>
NNTP-Posting-Host: net.bio.net

On Thu, 22 Sep 1994, Christopher J. S. Bolch wrote:

> I have heard recently that it is possible to sequence PCR products
> directly either by usual means or by cycle sequencing.  Is it as simple
> as that or does one need to clone the fragments first?  Does sequencing
> of the product directly have any pitfalls or problems?  I imagine that
> excess primer could be a problem.
> 
> Chris
> 
> 
  We are currently using US Biochemicals PCR Sequenase Sequencing Kit 
(Actually, we have ordered the missing enzymes separately and have 
"converted" our existing Sequenase V2.0 kits).  It uses Exonuclease I to 
digest single stranded DNA (i.e. primers) in ~5 microL of PCR amplified 
DNA (directly).  The free nucleotides (from the exo reaction and the dNTP 
added for the PCR) are dephosphorylated with Shrimp alk-Phosphatase and 
the resulting DNA is used directly in a standard Sequenase reaction.  In 
addition, we have been using AT Biochem (1-800-282-4626) Long Ranger Gel 
solution under standard conditions (i.e. NOT glycerol tolerant - the new 
Sequenase protocol has the Sequenase and Pyrophos. enzymes mixed in a 
glycerol buffer and suggests that a glycerol tolerant gel be used).  We 
have tried both the standard Sequenase labeling and a modified 3 nt 
labeling approach when the sequence just after the primer is known 
(details are available in the kit directions or from USB).  The 3 nt 
techniques seems to give better results but both work well.  With the 3 
nt technique we easily get to within 2 nt of the labeled primer.
  Although we have only made 3 sequencing attempts (30 independent
reactions) the gels are working very, very well (i.e. easily 300 bp of good
sequence, few if any "hard stops" that are normally observed in PCR
template sequencing, short exposure times with 35S - 2 days on average 
and nice even band intensities).
  Like everyone, I have tried everything (cycle sequencing, Lambda exo,
standard Sequenase, single stranded amps, spin col. etc) and this is by
far the easiest and BEST (that is results wise) technique that I have
used.  Just in case you are now wondering - I do not work for USB (and in
fact have a general dislike and contempt for these companies that are
making so much money from so little work!).  

FYI,
Steve


Stephen Karl
Department of Biology
University of South Florida
4202 East Fowler Ave, LIF 169
Tampa, Florida 33620-5150
Voice (813) 974-1592
Fax   (813) 974-3263
EMail Karl@.chuma.cas.usf.edu



From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Path: biosci!rutgers!gatech!swrinde!howland.reston.ans.net!news.cac.psu.edu!news.tc.cornell.edu!travelers.mail.cornell.edu!newsstand.cit.cornell.edu!NewsWatcher!user
From: wfl1@cornell.edu (Warren Frank Lamboy)
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPD Newsgroup
Followup-To: bionet.molbio.rapd
Date: Fri, 23 Sep 1994 02:18:31 -1200
Organization: Cornell University
Lines: 17
Sender: wfl1@cornell.edu (Verified)
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NNTP-Posting-Host: 132.236.3.42

In article <CwL8sJ.5M1@jura.sasa.gov.uk>, odonnell@sasa.gov.uk (Kevin
O'Donnell) wrote:

> 
> I find this newsgroup . . . (text deleted)           

I don't see any need for a name change for the group, but I, too would
welcome extending the subject matter discussed to other types of molecular
markers.

-- 
Warren F. Lamboy                            "It's easy if you know how to
Dept. of Horticultural Sciences and          do it, but it's impossible if
   USDA-ARS Plant Genetic Resources Unit     you don't know how to do it."
Cornell University
Geneva, NY 14456-0462
warren_lamboy@cornell.edu

From owner-rapd@net.bio.net Thu Sep 22 23:00:00 1994
Path: biosci!CSCGPO.ANU.EDU.AU!lce652
From: lce652@CSCGPO.ANU.EDU.AU (Livinus Emebiri)
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPD Newsgroup
Date: 23 Sep 1994 16:44:19 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 14
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <9409232346.AA16334@cscgpo.anu.edu.au>
NNTP-Posting-Host: net.bio.net

>I find this newsgroup the most useful of all of the BIONET newsgroups,
>(along with the Diagnostics list), and have a suggestion as to how it
>could be made even more useful, to me at least.

I agree with you that this news group has been most useful and informative
(to me at least), and welcome the suggestion to expand its subject matter
coverage. No doubt it will be even more informative, but will this not
amount to an encroachment into  the Diagnostics List field of interest ?



Livinus Emebiri



From owner-rapd@net.bio.net Sun Sep 25 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!agate!howland.reston.ans.net!pipex!jura.sasa.gov.uk!news
From: odonnell@sasa.gov.uk (Kevin O'Donnell)
Subject: Re: RAPD Newsgroup
Organization: Scottish Agricultural Science Agency
Date: Mon, 26 Sep 1994 07:53:37 GMT
Message-ID: <Cwq8LD.JA4@jura.sasa.gov.uk>
X-Newsreader: WinVN 0.91.3
References: <9409232346.AA16334@cscgpo.anu.edu.au>
Sender: news@jura.sasa.gov.uk (Usenet)
Lines: 32

In article <9409232346.AA16334@cscgpo.anu.edu.au>, lce652@CSCGPO.ANU.EDU.AU (Livinus Emebiri) says:
>
>I agree with you that this news group has been most useful and informative
>(to me at least), and welcome the suggestion to expand its subject matter
>coverage. No doubt it will be even more informative, but will this not
>amount to an encroachment into  the Diagnostics List field of interest ?
>

No, I don't think so. However, as a few people have mailed me to ask about
the Diagnostics list, perhaps I should say what it is.  Diagnost is a 
prototype bionet group i.e. currently available as an email list only. It
provides a forum for discussion about using and developing techniques
for the detection and identification of pests and pathogens.  The group
covers all techniques from antibodies (ELISA) to DNA (PCR, LCR etc.).
Subscribers come from a variety of backgrounds -plant, vet, medical, 
where people are using the same techniques for the same purpose.  

If you are interested, you can subscribe to diagnost by sending the
message:  subscribe diagnost  to this address: biosci-server@net.bio.net
leaving the subject line blank.

I should declare an interest by saying that I am one of the discussion
leaders for diagnost.  As for overlap, well diagnostics uses some of 
the techniques used for molecular markers but in a different context, IMO.

I am interested in both groups because I have an interest in variety
testing of plants, as well as their diseases.  

Kevin O'Donnell
Scottish Agricultural Science Agency    
Edinburgh
Scotland                                           

From owner-rapd@net.bio.net Sun Sep 25 23:00:00 1994
Path: biosci!YVAX.BYU.EDU!FARMERJ
From: FARMERJ@YVAX.BYU.EDU
Newsgroups: bionet.molbio.rapd
Subject: Comment on expanding this newsgroup
Date: 26 Sep 1994 09:00:24 -0700
Organization: Brigham Young University
Lines: 92
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <01HHKBFEKDJM91WEHY@yvax.byu.edu>
NNTP-Posting-Host: net.bio.net

In light of the current discussion about expanding this newsgroup, I posted the following
message to BIOSCI-HELP@NET.BIO.NET and received the following response.  What
do you think?  

James Farmer
farmerj@yvax.byu.edu

>> There is some discussion in the rapd newsgroup about
>> expanding the scope to include other techniques of
>> molecular mapping.  I do not know where it will lead. 
>> If the decision were made to expand, it would be a good
>> idea to change the name of the group.  Is that
>> feasible?  If so, what would be required to obtain
>> permission?  I would like to know the answers to these
>> questions, and your general advice, before the
>> discussion goes much further.
>> 
>> Thanks
>> 
>> James Farmer
>> farmerj@yvax.byu.edu
>> 
>
>I include the charter for the CHROMOSOMES group.  Please look it over
>and see if you think whether or not you would be duplicating the
>purpose of that group.  If so, then those discussions should be held in
>the CHROMOSOMES group.
>
>                   Sincerely,
>
>                   Dave Kristofferson
>                   BIOSCI/bionet Manager
>
>                   biosci-help@net.bio.net
>
>
>Information for CHROMOSOMES/bionet.genome.chromosomes
>
>USENET newsgroup name: bionet.genome.chromosomes
>
>Mailing list name: CHROMOSOMES
>
>E-mail addresses: bio-chrom@net.bio.net
>                  bio-chrom@daresbury.ac.uk
>
>Discussion leaders:
>
>Greg Lennon
>Human Genome Center, L-452
>Lawrence Livermore National Laboratory
>Livermore, CA 94550
>greg@mendel.llnl.gov
>
>Bruce A. Roe
>Department of Chemistry and Biochemistry
>University of Oklahoma
>620 Parrington Oval
>Norman, Oklahoma 73019
>broe@aardvark.ucs.uoknor.edu
>
>
>CHROMOSOMES/bionet.genome.chromosomes charter:
>
>Name:  bio-chrom   MAPPING AND SEQUENCING OF EUCARYOTE
CHROMOSOMES
>
>    Greg Lennon and Bruce Roe propose to be discussion leaders
>for a new news group that would replace the .chromosome22 news group
>and the autoseqs@net.bio.net e-mail list.   
>
>The topics open for discussion in this new, combined, news group include:
>
>  1. Physical mapping of human, mouse, and other eucaryote chromosomes
>
>  2. Large-scale sequencing of cDNAs and chromosomes
>
>  3. Mapping of human, mouse, and other eucaryote cDNAs to chromosomes
>
>  4. Selection of chromosome-specific cDNAs
>
>  5. Generation of chromosome-specific clones and sequences
>     (STSs, microsatellites, etc.)  
>
>  6. Announcements and requests for probes.
>
>with an emphasis on theory, techniques and discoveries.  The overall
>purpose of this new, combined news group is to bring research groups
>with an interest in genomic-level research and automated methods for
>studying eucaryote genomes together to exchange ideas and protocols, 
>probes and mapping information, and to discuss other issues relevant
>to large scale mapping and sequencing.
>

From owner-rapd@net.bio.net Mon Sep 26 23:00:00 1994
Path: biosci!CABI.org!D.BRAYFORD
From: D.BRAYFORD@CABI.org ("David Brayford ", IMI)
Newsgroups: bionet.molbio.rapd
Subject: RAPD amplification
Date: 27 Sep 1994 00:27:18 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 17
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <2E87C9BB@smtp-gateway.cgnet.com>
NNTP-Posting-Host: net.bio.net


There does seem to be potential overlap between an expanded RAPD group and 
the Eukaryotic Chromosomes newsgroup.  One possibility would be to merge the 
whole lot into one.  However, I feel that this would then be too broad. 
 Also, we use PCR methodologies to analyse variation in fungi and plant 
pathogenic bacteria.  Where would the prokaryotic interests of users such as 
us then fit in??

I venture to suggest that the RAPD newsgroup should be expanded to cover all 
PCR-based methodologies as applied to eukaryotic and prokaryotic organisms, 
and that it should be kept separate from the Eukaryotic Chromosomes 
newsgroup.  The name could then be changed from RAPD to PCR.  I think this 
would keep the group focussed, whilst reflecting the expanding horizons of 
how these techniques are being used.

Dave Brayford
International Mycological Institute

From owner-rapd@net.bio.net Mon Sep 26 23:00:00 1994
Path: biosci!PIRA.CENA.USP.BR!DAVHMOON
From: DAVHMOON@PIRA.CENA.USP.BR
Newsgroups: bionet.molbio.rapd
Subject: Re. Robocycler
Date: 27 Sep 1994 12:00:45 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 8
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <MAILQUEUE-101.940927155923.626@pira.cena.usp.br>
NNTP-Posting-Host: net.bio.net

Hi netters,
Is any one out there using a Stratagene Robocycler??
They are just launching this model in Brasil with claims of reduced 
cycling times of up to 30%, extended block life etc. etc. etc.
I would be grateful to receive any feed back about this machine.
Thanks in advance,
David H. Moon


From owner-rapd@net.bio.net Tue Sep 27 23:00:00 1994
Path: biosci!FAPQ.FAPESP.BR!Carteiro
From: Carteiro@FAPQ.FAPESP.BR
Newsgroups: bionet.molbio.rapd
Subject: Mail not delivered yet. Please do not reply.
Date: 28 Sep 1994 15:05:17 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 36
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <86C19B5EA004763B@fapq.fapesp.br>
Reply-To: Carteiro@fapq.fapesp.br
NNTP-Posting-Host: net.bio.net

-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+-+- begin-
-------------------------------------------------------------------------------
This mail was not delivered yet. Some "daemon" in the system may
be hung. The system will retry later.
  Virtually,
  Fapesp's PostPerson.
-------------------------------------------------------------------------------
`From gkuhar Mon, 26 Sep 94 11:44:15 C remote from jab000
`Received:  by jab000.uesp.ansp.br (UUPC/extended 0.0);
`           Mon, 26 Sep 94 11:44:15 C
`Message-id: <2e86ec4f@jab000.uesp.ansp.br>
`Date:      Mon, 26 Sep 94 11:44:15 C
`From:      GORAN KUHAR JEZOVSEK <gkuhar@jab000.uesp.ansp.br>
`Organization: UNESP
`Reply-To:  GORAN KUHAR JEZOVSEK <GKUHAR@JAB000.UESP.ANSP.BR>
`To:        rapd@net.bio.net
`Subject:   looking for position
`
`I am looking for a laboratory to extend my knowledge on the use of RAPD and PC
`R related molecular markers. I would be interested in a two or three year peri
`od of working. No restrictions. A PhD course would also be desirable.
`Thanks a lot.
`
`Goran Kuhar
`
`email: gkuhar@jab000.uesp.ansp.br
`-- 
`
`       GORAN KUHAR JEZOVSEK                   E-mail: gkuhar@jab000.uesp.ansp.
`br
`FACULDADE CIENCIAS AGRARIAS E VETERINARIAS    Fone  :  (0163) 23-2500
`       JABOTICABAL/ UNESP                     Endereco: Rod. Carlos Tonanni,Km
` 5
`                                              14870-000  Jaboticabal   SP
`
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From owner-rapd@net.bio.net Tue Sep 27 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!agate!library.ucla.edu!europa.eng.gtefsd.com!howland.reston.ans.net!EU.net!ieunet!tcdcs!news.tcd.ie!gen033.gen.tcd.ie!user
From: dmachugh@mail.tcd.ie (David MacHugh)
Subject: Re: RAPD amplification
Message-ID: <dmachugh-280994114207@gen033.gen.tcd.ie>
Followup-To: bionet.molbio.rapd
Sender: usenet@news.tcd.ie (TCD News System )
Organization: Genetics Department, Trinity College, Dublin 2. IRELAND
References: <2E87C9BB@smtp-gateway.cgnet.com>
Date: Wed, 28 Sep 1994 11:42:07 GMT
Lines: 39

In article <2E87C9BB@smtp-gateway.cgnet.com>, D.BRAYFORD@CABI.org ("David
Brayford ", IMI) wrote:

> 
> There does seem to be potential overlap between an expanded RAPD group and 
> the Eukaryotic Chromosomes newsgroup.  One possibility would be to merge the 
> whole lot into one.  However, I feel that this would then be too broad. 
>  Also, we use PCR methodologies to analyse variation in fungi and plant 
> pathogenic bacteria.  Where would the prokaryotic interests of users such as 
> us then fit in??
> 
> I venture to suggest that the RAPD newsgroup should be expanded to cover all 
> PCR-based methodologies as applied to eukaryotic and prokaryotic organisms, 
> and that it should be kept separate from the Eukaryotic Chromosomes 
> newsgroup.  The name could then be changed from RAPD to PCR.  I think this 
> would keep the group focussed, whilst reflecting the expanding horizons of 
> how these techniques are being used.


A broad-based newsgroup pertaining to PCR would perhaps overlap with the
methds-reagnts group to a great extent. More appropriate titles might be
"bionet.molbio.mol-polymorphs" or "bionet.molbio.mol-markers", even
"bionet.molbio.PCR-polymorphs" etc. I think a name change along these lines
would expand the scope of the newsgroup without attracting too many
irrelevant postings.

David.


-- 
    *********************************************************************
    *         (__)  David MacHugh,        E-mail: dmachugh@mail.tcd.ie  *
    *         (@*)  Bovine Genetics,      Phone:  (353)-1-7021088       *
    *  /-------\u'  Genetics Department,  Fax:    (353)-1-6798558       *
    * / |     ||    Trinity College,                                    *
    *   ||----||    Dublin 2.                                           *
    *   ^^    ^^    Ireland.                                            *
    *********************************************************************
 

From owner-rapd@net.bio.net Tue Sep 27 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!daresbury!trane.uninett.no!sunic!pipex!jura.sasa.gov.uk!news
From: odonnell@sasa.gov.uk (Kevin O'Donnell)
Subject: Re: Comment on expanding this newsgroup
Organization: Scottish Agricultural Science Agency
Date: Wed, 28 Sep 1994 14:00:14 GMT
Message-ID: <CwuEwE.BBE@jura.sasa.gov.uk>
X-Newsreader: WinVN 0.91.3
References: <01HHKBFEKDJM91WEHY@yvax.byu.edu>
Sender: news@jura.sasa.gov.uk (Usenet)
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In article <01HHKBFEKDJM91WEHY@yvax.byu.edu>, FARMERJ@YVAX.BYU.EDU says:
>
>In light of the current discussion about expanding this newsgroup, I posted the following
>message to BIOSCI-HELP@NET.BIO.NET and received the following response.  What
>do you think?  

(From D. Kristofferson:)
>>I include the charter for the CHROMOSOMES group.  Please look it over
>>and see if you think whether or not you would be duplicating the
>>purpose of that group.  If so, then those discussions should be held in
>>the CHROMOSOMES group.
>>
(from chromosomes charter:)
>>>with an emphasis on theory, techniques and discoveries.  The overall
>>purpose of this new, combined news group is to bring research groups
>>with an interest in genomic-level research and automated methods for
>>studying eucaryote genomes together to exchange ideas and protocols, 
>>probes and mapping information, and to discuss other issues relevant
>>to large scale mapping and sequencing.
>>


Oh dear.  I started the ball rolling on this and it has had the totally 
unintended effect of calling the existence of the group into question.

In answer to the above query, the bits I've copied
state clearly that bionet.chromosomes is about sequencing and mapping
genomes. I see this as completely different to the subject matter of
RAPD as that is concerned with variation within and between populations
(broadly speaking).  So, whereas I'm still keen to see other methods 
included I don't think that a merger with chromosomes is a good idea.

  
Kevin O'Donnell
Scottish Agricultural Science Agency    
Edinburgh
Scotland                                           

From owner-rapd@net.bio.net Wed Sep 28 23:00:00 1994
Newsgroups: bionet.molbio.rapd
Path: biosci!bcm!cs.utexas.edu!swrinde!elroy.jpl.nasa.gov!netline-fddi.jpl.nasa.gov!nntp-server.caltech.edu!news.claremont.edu!paris.ics.uci.edu!csulb.edu!library.ucla.edu!news.mic.ucla.edu!unixg.ubc.ca!quartz.ucs.ualberta.ca!tribune.usask.ca!sue!news
From: DURKIN@Meena.CC.URegina.CA (192403285)
Subject: Query: Looking for good orthopteran CytB & 16s rDNA primers
Sender: news@sue.cc.uregina.ca
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Date: Thu, 29 Sep 1994 05:02:18 GMT
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Organization: University of Regina, Regina, Sask., Canada
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Greetings:

I am working on a project to determine the phylogeny of Acrididae 
grasshoppers via RFLPs.  I have looked in the Simple Fool's Guide
for appropriate primers to amplify the 16s rDNA and CytB regions of 
the mitochondrial DNA.  The closest match they give is for Drosophila;
I was wondering if anyone has had personal experience with the Drosophila
primers for orthopterans and if so, how they have worked out.  If anyone
has information regarding appropriate orthopteran primers or knows of 
a suitable recent reference, please contact me via E-mail.

Thanks in advance,

Jonathan Durkin
durkin@meena.cc.uregina.ca

From owner-rapd@net.bio.net Wed Sep 28 23:00:00 1994
Path: biosci!UCONNVM.UCONN.EDU!CSIMON
From: CSIMON@UCONNVM.UCONN.EDU (Chris)
Newsgroups: bionet.molbio.rapd
Subject: Good orthopteran Cytb & 16S primers
Date: 29 Sep 1994 08:44:51 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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Distribution: world
Message-ID: <199409291544.IAA24910@net.bio.net>
NNTP-Posting-Host: net.bio.net

Hi Jonathan-  My colleagues and I have just finished a paper that contains
an appendix of over 70 "universal" PCR primers.  These primers are
presented in comparative format to show how conserved they are.  We compare
the primers to human (or cow), xenopus, urchin, nematode, fly, bee, locust,
and sometimes additional taxa.  The body of the paper reviews weighting DNA
data for phylogenetic analysis, mitochondrial gene evolution, and the
phylogenetic usefulness of various mitochondrial genes (with an emphasis
on insects).  The reference is:  Simon, C., F. Frati, A. Beckenbach,
B. Crespi, H. Liu, and P. Flook.  1994.  Evolution, Weighting, and phylogene-
tic usefulness of mitochondrial genes with a compilation of conserved PCR
primers.  Annals of the Entomological Society of America  in press
[November 1994, pp. 1-51].  You might also wish to join Bug-net, the
insect molecular systematics network by sending a message to Crespi@SFU.CA
Good Luck, Chris

CHRIS SIMON                      PHONE: 203-486-4640
ECOL. EVOL. BIOLOGY U-43           FAX: 203-486-6364
UNIVERSITY OF CONNECTICUT       BITNET: CSIMON@UCONNVM
STORRS, CT  06269             INTERNET: CSIMON@UCONNVM.UCONN.EDU

From owner-rapd@net.bio.net Wed Sep 28 23:00:00 1994
Path: biosci!jab000.uesp.ansp.br!gkuhar
From: gkuhar@jab000.uesp.ansp.br (GORAN KUHAR JEZOVSEK)
Newsgroups: bionet.molbio.rapd
Subject: looking for position
Date: 28 Sep 1994 18:07:12 -0700
Organization: UNESP
Lines: 13
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <2e86ec4f@jab000.uesp.ansp.br>
Reply-To: GORAN KUHAR JEZOVSEK <GKUHAR@jab000.uesp.ansp.br>
NNTP-Posting-Host: net.bio.net

I am looking for a laboratory to extend my knowledge on the use of RAPD and PCR related molecular markers. I would be interested in a two or three year period of working. No restrictions. A PhD course would also be desirable.
Thanks a lot.

Goran Kuhar

email: gkuhar@jab000.uesp.ansp.br
-- 

       GORAN KUHAR JEZOVSEK                   E-mail: gkuhar@jab000.uesp.ansp.br
FACULDADE CIENCIAS AGRARIAS E VETERINARIAS    Fone  :  (0163) 23-2500
       JABOTICABAL/ UNESP                     Endereco: Rod. Carlos Tonanni,Km 5
                                              14870-000  Jaboticabal   SP


