From owner-rapd@net.bio.net Sun Dec 01 22:00:00 1996
Path: biosci!MAILSERV.CUHK.EDU.HK!b086712
From: b086712@MAILSERV.CUHK.EDU.HK (PC Shaw)
Newsgroups: bionet.molbio.rapd
Subject: Rapd data analysis
Date: 2 Dec 1996 02:54:19 -0800
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I am a RAPD user. I encounter a problem in analysis the RAPD data for 
phylogenetic studies. The similarity indexes ( the ratio between the 
common bands shared in two samples and the total number of bands of 
the two samples) from different primers show different results. Some 
primers show that they are very similar while other show they are not. So 
What should I do ? How many primers should be tried in order to give a 
confident result ?

Could anyone solve my problem, please send to s941800@mailserv.cuhk.hk

Thank you very much!

K.Ngan



From owner-rapd@net.bio.net Sun Dec 01 22:00:00 1996
Path: biosci!EMUVAX.EMICH.EDU!bio_hannan
From: bio_hannan@EMUVAX.EMICH.EDU (Gary Hannan)
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis
Date: 2 Dec 1996 06:42:38 -0800
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>I am a RAPD user. I encounter a problem in analysis the RAPD data for
>phylogenetic studies. The similarity indexes ( the ratio between the
>common bands shared in two samples and the total number of bands of
>the two samples) from different primers show different results. Some
>primers show that they are very similar while other show they are not. So
>What should I do ? How many primers should be tried in order to give a
>confident result ?
>
>Could anyone solve my problem, please send to s941800@mailserv.cuhk.hk
>
>Thank you very much!
>
>K.Ngan

I believe that RAPD band data are inappropriate for phylogenetic analysis,
regardless of the method used to analyze the data.  The fatal problem with
RAPD data is the serious issue concerning homology.  There is no way to
establish the homology of bands without (at least) performing southerns of
all bands used, and in all taxa studied.  An even this is only a rough
guide to homology- small insertions/deletions/point mutations could go
undetected.  We have already seen in the literature examples of apparently
identical bands being non-homologous using southerns.

Gary Hannan



From owner-rapd@net.bio.net Sun Dec 01 22:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Louis van de Zande <L.P.W.G.M.van.de.Zande@biol.RUG.NL>
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis
Date: 2 Dec 1996 15:06:39 -0000
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Original-To: rapd@dl.ac.UK

> I am a RAPD user. I encounter a problem in analysis the RAPD data for 
> phylogenetic studies. The similarity indexes ( the ratio between the 
> common bands shared in two samples and the total number of bands of 
> the two samples) from different primers show different results. Some 
> primers show that they are very similar while other show they are not. So 
> What should I do ? How many primers should be tried in order to give a 
> confident result ?
> 
> Could anyone solve my problem, please send to s941800@mailserv.cuhk.hk
> 
> Thank you very much!
> 
> K.Ngan
> 

Stop using RAPD for phylogenetic analysis (unless you have very 
closely related species). They will not give you sound quantitative 
data. See: Journal of Evolutionary Biology 8, 645-656, 1995.

Louis van de Zande




From owner-rapd@net.bio.net Sun Dec 01 22:00:00 1996
Path: biosci!esvax.dnet.dupont.com!rafalski
From: rafalski@esvax.dnet.dupont.com (Antoni Rafalski)
Newsgroups: bionet.molbio.rapd
Subject: RAPDs fo phylogenetic analysis
Date: 2 Dec 1996 08:39:24 -0800
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Regarding message by Gary Hannan:

There are several examples in the literature of successful use of RAPDs
for phylogenetic analysis (for example Tibayrenc, M., Neubauer, K.,
Barnabe, C., Guerrini, F., Skarecky, D., Ayala, F.J. Genetic
characterization of six parazitic protozoa: Parity between random-primer
DNA typing and multilocus enzyme electrophoresis PNAS 1993   90:
1335-1339). Of course, the method is more appropriate for relatively
closely realted individuals. Non-homologous similar-sized bands could
pose a problem, however, they are usually in minority and contribute to
some noise in the data, the more polymorphic bands you analyse the
better off you are. Methods exist to confirm homology of the bands, if
deemed necessary (for example Williams et al. Methods in Enzymology
218(1993) 704-740).
	Classical methods of phylogenetic analysis, of course, suffer from
similar problems: something that looks similar is not always homologous
(for example a phenotypic characteristic that may have evolved
independently)
To answer the originally asked question, the more polymoprhic bands you
analyze the better it is. Try to analyze the data after collecting 50,
100, 150 polymorphic bands and see if your results are consistent.

Antoni Rafalski

From owner-rapd@net.bio.net Sun Dec 01 22:00:00 1996
Path: biosci!EM.AGR.CA!vincentd
From: vincentd@EM.AGR.CA (Daniel Vincent)
Newsgroups: bionet.molbio.rapd
Subject: Inhibitor of Taq polymerase
Date: 2 Dec 1996 11:16:40 -0800
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Last year, someone wrote that vitamin E
used as a stabilizing agent in some
mineral and paraffin oil inhibits Taq
polymerase. If that person recognizes
him/herself, please write me back. I
would like to have more information.

Thanks.

From owner-rapd@net.bio.net Mon Dec 02 22:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Roland Koelliker <koelliker@ipw.agrl.ethz.ch>
Newsgroups: bionet.molbio.rapd
Subject: Genetic variability in 4n grasses
Date: 3 Dec 1996 12:08:46 -0000
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Dear netters
I'm working on genetic variability of meadow fescue (2n) using RAPD
markers. For comparison I'd like to investigate some Lolium perenne
cultivars. Since most of these cultivars are 4n I wonder if I ran in
difficulties comparing data from meadow fescue with the one of 4n Lolium
perenne. What do you think about that? Is there any literature to this
subject?
Thank you for your help.



Roland Koelliker	                  
Swiss Fed Inst Technol               
Plant Sciences                              
ETH-Zentrum, LFW-C47         
CH-8092 Zurich                          
Tel ++41-1-632 3888
Fax ++41-1-632 1153
e-mail: koelliker@ipw.agrl.ethz.ch

From owner-rapd@net.bio.net Mon Dec 02 22:00:00 1996
Path: biosci!ihnp4.ucsd.edu!swrinde!howland.erols.net!feed1.news.erols.com!news.bbnplanet.com!cpk-news-hub1.bbnplanet.com!cpk-news-feed1.bbnplanet.com!ox.mc.edu!usenet
From: Robert Hamilton <rhamilton@mc.edu>
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis
Date: 3 Dec 1996 23:09:07 GMT
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  Homology is a
>sticky issue, and even the same-sized fragment does not necessarily mean
>the fragments are homologous.
>

>Gary Hannan
>
>
>
This is true. SIMILARITY is NEVER a good measure of homolgy. Just because 
two fragments DON'T hybridize in a Southern does not mean that they are 
NOT homologous, particularly in closely realted species. An assessment of 
homology requires more knowledge than sequence similarity provides, be it 
via RAPDs or actual sequence data. 


From owner-rapd@net.bio.net Mon Dec 02 22:00:00 1996
Path: biosci!EMUVAX.EMICH.EDU!bio_hannan
From: bio_hannan@EMUVAX.EMICH.EDU (Gary Hannan)
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis
Date: 2 Dec 1996 16:35:32 -0800
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>Dear Gary,
>I'm interested by your reply, I wonder if I could trouble you to dig out
>some of the references you refer to.  I've only seen one so far and
>wasn't quite happy with the methodoloy used.  However I did have a long
>chat with someone at a conference recently who left me pretty convinced that
>her rapd bands were not homologous.  Still, I'm baffled - why should,
>non-homologous bands in a fingerprint be, quite coincidentally,
>the same size?.  It keeps me awake at night, not least because I've just
>spent several months generating rapd fingerprints with a view to making
>phylogenetic inferences.
>
>Yours sleeplessly,
>Alastair
>
>: ***************************************************************************
>: Alastair Hamilton	    | **.           .***.   .***.           .***.   .
>: Institute of Aquaculture  | | | *       * | | | * | | | *       * | | | * |
>: University of Stirling    | | | | *   * | | | *   * | | | *   * | | | *   *
>: Stirling                  | * | | | * | | | *       * | | | * | | | *
>: FK9 4LA                   |   '***'   '***'           '***'   '***'
>:
>: Tel: 01786 467878 X7919                      Fax: 01786 472133
>
>  ***************************************************************************
>
>

Quiros, et al. 1995.  Analysis of a set of RAPD markers by hybridization
sequencing in Brassica: a note of caution.  Plant Cell Rep. 14:630-634.

Ayliffe, et al.  1994.  Heteroduplex molecules formed between allelic
sequences cause nonparental RAPD bands.  Nucleic Acids Res. 22:1632-1636.

Clark & Lanigan.  1993.  Prospects for estimating nucleotide divergence
with RAPDs.  Mol. Biol. Evol. 10:1096-1111.

My question in response to your homology question would be: why should same
(or undetectably different size) bands in a fingerprint be, quite
conicidentally, homologous?  or, why should two bands that are similar
enough in size to run at nearly the same rate (at least close enough to not
be judged as different sizes) be assuemd to _be_ homologous?  Homology is a
sticky issue, and even the same-sized fragment does not necessarily mean
the fragments are homologous.

I just think RAPDs have a place as a tool, but phylogeny reconstruction is
a very risky application for it.

Gary Hannan




From owner-rapd@net.bio.net Tue Dec 03 22:00:00 1996
Path: biosci!ihnp4.ucsd.edu!swrinde!howland.erols.net!news.bbnplanet.com!cam-news-hub1.bbnplanet.com!uunet!in3.uu.net!192.89.123.24!nntp.inet.fi!news.funet.fi!news.helsinki.fi!news
From: Kari.Kammiovirta@Helsinki.Fi (Kari Kammiovirta)
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis
Date: 4 Dec 1996 14:29:44 GMT
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In article <199612021054.SAA20496@hpg50a.csc.cuhk.edu.hk>, 
b086712@MAILSERV.CUHK.EDU.HK says...
>
>I am a RAPD user. I encounter a problem in analysis the RAPD data for 
>phylogenetic studies. The similarity indexes ( the ratio between the 
>common bands shared in two samples and the total number of bands of 
>the two samples) from different primers show different results. Some 
>primers show that they are very similar while other show they are not. 
So 
>What should I do ? How many primers should be tried in order to give a 
>confident result ?
>
>Could anyone solve my problem, please send to s941800@mailserv.cuhk.hk
>
>Thank you very much!
>
>K.Ngan
>
Hi,

You don't tell are you trying to investigate among one species or 
between. Among species I have heard someone said something about 10-20 
primers is enough. After that dendrograms don't change anymore. 
Between species you should try something else, like microsatellites, 
because the checking of the bands is too enormous task.
Good luck,

Kari


From owner-rapd@net.bio.net Tue Dec 03 22:00:00 1996
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From: Martin Sanders <service@lazarlab.com>
Newsgroups: bionet.molbio.rapd
Subject: FREE pH Measurement booklet
Date: 4 Dec 1996 17:58:45 GMT
Organization: NetVision LTD.
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A free pH booklet is available which contains valuable information on 
basic pH measurement theory, pH measurement techniques, selecting the 
proper pH electrode for a particular application, and a pH  
troubleshooting guide.  The booklet is available from Lazar Research 
Labs. Inc. by emailing service@lazarlab.com or faxing 1-213-931-1434.  
The booklet can also be obtained from the Lazar web site at 
http://www.lazarlab.com


From owner-rapd@net.bio.net Wed Dec 04 22:00:00 1996
Path: biosci!MVET.UNIZAR.ES!pcatalan
From: pcatalan@MVET.UNIZAR.ES (PILAR CATALAN RODRIGUEZ)
Newsgroups: bionet.molbio.rapd
Subject: micro-sat Dioscoriaceae
Date: 5 Dec 1996 02:09:28 -0800
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Dear Sir/Madam,

I am interested in getting information on microsatellite of species of the plant 
family Dioscoriaceae. Any help on primers' design, efficiency, and obtained 
results would be very appreciate.

Yours faithfully,

Pilar Catalan


Dr. Pilar Catalan
Department of Agriculture
University of Zaragoza (Spain)

From owner-rapd@net.bio.net Thu Dec 05 22:00:00 1996
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From: landryp@ERE.UMontreal.CA (Landry Pierre-Alexandre)
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis
Date: 6 Dec 96 15:07:57 GMT
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b086712@MAILSERV.CUHK.EDU.HK (PC Shaw) writes:

>I am a RAPD user. I encounter a problem in analysis the RAPD data for 
>phylogenetic studies. The similarity indexes ( the ratio between the 
>common bands shared in two samples and the total number of bands of 
>the two samples) from different primers show different results. Some 
>primers show that they are very similar while other show they are not. So 
>What should I do ? How many primers should be tried in order to give a 
>confident result ?

>Could anyone solve my problem, please send to s941800@mailserv.cuhk.hk

>Thank you very much!

>K.Ngan


The use of RAPD bands in phylogenetic studies raises many questions. The 
choice of the similarity index is critical. I have worked with RAPD 
distance to reconstruct phylogenies for the last 8 months. Basically, I 
found that relationships among closely-related taxa are usually correctly 
recovered (i.e. below the level of the family), but that over this 
taxonomical limit the results become unreliable. For the number of 
primers to use, I think that it depends of the specimens you are 
comparing. I would suggest to make a little bootstrap among the primers 
you have used, and to verify the stability of the calculated distances 
for an increasing number of primers. When your estimates become stable 
(you can assess that rapidly by looking at it graphically), you can 
consider that the addition of new information will not change the 
results. For my part, I saw that 12 primers were sufficient.
Anyways, I have submitted a paper comparing 4 different similarity 
indexes (JAccard, Dice, Russel & Rao and simple matching) with increasing 
number of primers, in an experimental design including specimens of 
increasing phylogenetic distances. It was sent to Zoologica scripta about 
7 weeks ago.

Ax

From owner-rapd@net.bio.net Thu Dec 12 22:00:00 1996
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From: lemieuxs@IRO.UMontreal.CA (Sebastien Lemieux)
Newsgroups: bionet.molbio.rapd
Subject: RAPDs for phylogenetic analysis...
Date: 12 Dec 1996 21:35:54 GMT
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Hi all,

  I've been listening to the recent discussion about the analysis of
RADP band pattern for phylogeny reconstruction and I've been wondering
if any one has ever summarized the major arguments against the use of
RAPD for phylogeny reconstruction?

------------------ Sebastien Lemieux, Microbio/CS -------------------
	     Breaking the Second Half of the Genetic Code

  ctggaagggt taatttactc ccataaaaga gcagaaatcc tggatctttg ggtgtataac

From owner-rapd@net.bio.net Thu Dec 12 22:00:00 1996
Path: biosci!BRADLEY.BRADLEY.EDU!rrs
From: rrs@BRADLEY.BRADLEY.EDU (Robert Stephens)
Newsgroups: bionet.molbio.rapd
Subject: Re: RAPDs for phylogenetic analysis...
Date: 13 Dec 1996 07:33:06 -0800
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I believe there was a paper in Cladistics within the last several issues.

rrs@bradley.bradley.edu
Robert Rhea Stephens
Biology Department
Bradley University
Peoria, IL 61625

On 12 Dec 1996, Sebastien Lemieux wrote:

> Hi all,
> 
>   I've been listening to the recent discussion about the analysis of
> RADP band pattern for phylogeny reconstruction and I've been wondering
> if any one has ever summarized the major arguments against the use of
> RAPD for phylogeny reconstruction?
> 
> ------------------ Sebastien Lemieux, Microbio/CS -------------------
> 	     Breaking the Second Half of the Genetic Code
> 
>   ctggaagggt taatttactc ccataaaaga gcagaaatcc tggatctttg ggtgtataac
> 
> 


From owner-rapd@net.bio.net Thu Dec 12 22:00:00 1996
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From: krutovsk@fsl.orst.edu (Konstantin Krutovskii)
Newsgroups: bionet.molbio.rapd
Subject: Faculty Research Assistant/Plant Molecular Geneticist
Date: Wed, 11 Dec 1996 23:05:50
Organization: Forestry Sciences Lab
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Position Number: 002-825

     Faculty Research Assistant/Research Associate, Plant Molecular 
     Genetics

     Location: Department of Forest Science, Oregon State University, 
     Corvallis, OR

     Date Available: March 1, 1997

     Closing Date: January 13, 1997 

     Position Responsibilities:     

     We seek a molecular geneticist to work as part of the Tree Genetic 
     Engineering Research Cooperative (TGERC) at Oregon State University. 
      The TGERC is a consortium supported by 13 Members, mostly forest 
     industries, that are seeking improved means for genetic manipulation 
     of poplar trees.  The applicant's primary responsibility in the Coop 
     will be production of novel plasmid constructs to be used in 
     Agrobacterium transformation, and analysis of the transgenic trees 
     produced.  They will work closely with other TGERC staff doing tissue 
     culture, transformation, and gene isolation.  The constructs will be 
     composed primarily of floral homeotic genes intended for induction of 
     sexual sterility; however, they will also work with other genes 
     relevant to ongoing Cooperative projects on insect, disease, and 
     herbicide resistance.  

     Specifically, responsibilities will include: 

     1.   Development of strategies for producing binary constructs with 
     various genes for Agrobacterium transformation of poplar.  

     2.   Configuration of genes and plasmid vectors, verifying 
     structure/sequence, and transformation into Agrobacterium strains.  

     3.   Analysis of transgenic plants for gene incorporation, 
     expression, and delivery of desired traits.  

     5.   Supervision of students, technicians, and other workers to 
     help carry out laboratory studies.

     6.   Participation in writing Coop reports and publications for 
     scientific journals.  

     7.   Effective oral communication of results at annual Coop meeting 
     and other scientific forums.  

     8.   Collaboration with Coop staff to write grants to obtain 
     supplemental funding for research.  

     Education and experience:    

     A B.S. degree in molecular genetics or a related field, and at 
     least two years of experience with recombinant DNA manipulation, 
     are essential.  Knowledge of plant molecular biology and experience 
     in plant transformation techniques are desirable.  Experience and 
     demonstrated competence in the following areas are particularly 
     important:

     1.   Advanced recombinant DNA manipulation of plasmid vectors. 

     2.   Molecular analyses, including DNA sequencing, PCR, and 
     Southern, northern, and western blots. 

     3.   Written and oral communication. 

     4.   Collaboration with colleagues, subordinates, and superiors. 

     5.   Long- and short-term organization and planning of work. 

     Employment conditions:

     The job will be filled at the rank of either Research Assistant 
     (B.S., M.S., or Ph.D.) or Research Associate (Ph.D.), depending 
     upon career track of candidate, in the Department of Forest Science 
     at Oregon State University.  We are also open to the applicant 
     taking a more scientific role in the work, as would Ph.D.s in a 
     Research Associate position (e.g., writing papers for publication), 
     or a more technical role, as would most with only a B.S. (limited 
     writing, mostly directed lab work).  The appointment is a 
     full-time, 12-month, fixed-term position; reappointment is at the 
     discretion of the Dean.  The employee will report directly to 
     Cooperative Director.  The salary will be in the range of $24,000 
     to $32,004/year, depending on qualifications.  Medical, dental, and 
     life insurance plans are available.  

     To apply:

     Send a letter of application describing your qualifications and 
     interests in the position, a resume, transcripts, and the names, 
     email addresses, and fax numbers of four references by January 13, 
     1997 to Sandra Lewis, Office Manager, Dept. of Forest Science, 020 
     Forestry Sciences Laboratory, Oregon State University, Corvallis, 
     OR 97331-7501.  For more information contact Prof. Steve Strauss, 
     phone 541/737-6578, email strauss@FSL.orst.edu, fax 541/737-1393.  


     OREGON STATE UNIVERSITY IS AN AFFIRMATIVE ACTION/EQUAL OPPORTUNITY 
     EMPLOYER AND HAS A POLICY OF BEING RESPONSIVE TO THE NEEDS OF 
     DUAL-CAREER COUPLES.  


From owner-rapd@net.bio.net Mon Dec 16 22:00:00 1996
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.molbio.rapd
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 17 Dec 1996 02:00:48 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 239
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199612171000.CAA23520@net.bio.net>
NNTP-Posting-Host: net.bio.net

(LAST REVISION: 30-JUL-95)

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.
--------------------------------------------------------
As of 10 December 1995, 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
--------------------------------------------------------------------
computer daresbury.ac.uk (also known as dl.ac.uk):
-------------------------------------------------

To subscribe and unsubscribe to/from the BIOSCI lists, you need to
specify the full USENET newsgroup name with "bionet-news." prepended.
The USENET newsgroup names are listed in the BIOSCI Information sheet
on the Web at http://www.bio.net/.  For the METHODS-AND-REAGENTS list
the USENET newsgroup name is bionet.molbio.methds-reagnts, thus the
appropriate commands are

    sub bionet-news.bionet.molbio.methds-reagnts

    unsub bionet-news.bionet.molbio.methds-reagnts

These commands are included in a message addressed to mxt@dl.ac.uk,
NOT to the newsgroup mailing addresses.  As usual, include the text in
the body of the message as text on the Subject: line is ignored.

To unsubscribe from all the lists at the UK node, use

    unsub bionet-news

Please note that if the address in the list is different than the one
in your mail message header, you will not be able to unsubscribe by
this method. If you have problems, please mail biosci@daresbury.ac.uk.


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.

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net

From owner-rapd@net.bio.net Tue Dec 17 22:00:00 1996
Path: biosci!rutgers!gatech!csulb.edu!hammer.uoregon.edu!arclight.uoregon.edu!news.uoregon.edu!newsfeed.orst.edu!news.orst.edu!gus.FSL.ORST.EDU!krutovsk
From: krutovsk@fsl.orst.edu (Konstantin Krutovskii)
Newsgroups: bionet.molbio.rapd
Subject: GRADUATE ASSISTANTSHIPS - PLANT/TREE MOLECULAR GENETICS
Date: Tue, 17 Dec 1996 21:16:12
Organization: Forestry Sciences Lab
Lines: 44
Message-ID: <krutovsk.156.001545BC@fsl.orst.edu>
NNTP-Posting-Host: gus.fsl.orst.edu
X-Newsreader: Trumpet for Windows [Version 1.0 Rev A]

GRADUATE ASSISTANTSHIPS - PLANT/TREE MOLECULAR GENETICS

Two Graduate Research Assistantships are available in the Department of Forest 
Science at Oregon State University beginning July 1997.  Students must apply and
be accepted into either the Department of Forest Science, the Molecular and 
Cellular Biology Program, or the Genetics Program at OSU.  Doctoral students are
preferred, but outstanding students who lack a Masters are also encouraged to 
apply.  Students should have excellent grades and GRE scores; strong course 
and/or research experience in molecular genetics; and demonstrated ability to 
write and speak English well.  Three to five years of half-time support, and 
tuition remission, are available subject to adequate performance in research and
coursework.  

Students may work on a variety of topics related to gene identification, genetic
engineering, and genome mapping.  Most work in the laboratory deals with poplars
and Douglas-fir.   Students may develop other areas for research, however, 
current topics of interest include:

- Isolation and manipulation of floral homeotic genes for engineering of 
reproductive development

-Effects of matrix attachment regions on gene silencing in transgenic poplars

-Population genetic studies of gene diversity and gene flow using microsatellite
markers

-Genetic engineering of systems for inducible sterility/fertility 

-Molecular engineering of genotype independent transformation systems

-Ecophysiological consequences of genetic engineering for lignin modification

-Development of microsatellite marker-maps and use for QTL analysis 


For information or an application form (specify department), contact Steve 
Strauss, Dept. of Forest Science, Oregon State University, Corvallis, OR 
97331-7501, fax 541 737 1393, phone -6578, strauss@FSL.orst.edu







From owner-rapd@net.bio.net Sun Dec 22 22:00:00 1996
Path: biosci!rutgers!news.sgi.com!su-news-hub1.bbnplanet.com!news.bbnplanet.com!cpk-news-hub1.bbnplanet.com!newsfeed.internetmci.com!masternews.telia.net!newssrv.ita.tip.net!news.keyworld.net!news
From: Kenneth Briffa <kennbrif@keyworld.net>
Newsgroups: bionet.molbio.yeast,bionet.molbio.rapd
Subject: Method of DNA extraction from yeast
Date: Mon, 23 Dec 1996 23:17:28 -0800
Organization: ESI, Malta.
Lines: 9
Message-ID: <32BF8388.19C3@keyworld.net>
Reply-To: kennbrif@keyworld.net
NNTP-Posting-Host: ppp40.keyworld.net
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 3.0 (Win16; I)
Xref: biosci bionet.molbio.yeast:6285 bionet.molbio.rapd:1760

Hello, I'm an undergraduate preparing my dissertation project. The
project involves RAPD from brewer's yeast. I've been trying to extract
the DNA from the yeasts using benzyl chloride but the yield is not good
enough. Does anyone know any method to extract the DNA from yeasts
without using any enzymes?

Cheers,
Kenneth Briffa
University of Malta

From owner-rapd@net.bio.net Thu Dec 26 22:00:00 1996
Path: biosci!rutgers!cnn.Princeton.EDU!udel-eecis!gatech!csulb.edu!hammer.uoregon.edu!arclight.uoregon.edu!news.uoregon.edu!newsfeed.orst.edu!news.orst.edu!gus.FSL.ORST.EDU!krutovsk
From: krutovsk@fsl.orst.edu (Konstantin Krutovskii)
Newsgroups: bionet.molbio.rapd
Subject: GRADUATE ASSISTANTSHIPS - PLANT/TREE MOLECULAR GENETICS
Date: Tue, 17 Dec 1996 21:16:12
Organization: Forestry Sciences Lab
Lines: 44
Message-ID: <krutovsk.156.001545BC@fsl.orst.edu>
NNTP-Posting-Host: gus.fsl.orst.edu
X-Newsreader: Trumpet for Windows [Version 1.0 Rev A]

GRADUATE ASSISTANTSHIPS - PLANT/TREE MOLECULAR GENETICS

Two Graduate Research Assistantships are available in the Department of Forest 
Science at Oregon State University beginning July 1997.  Students must apply and
be accepted into either the Department of Forest Science, the Molecular and 
Cellular Biology Program, or the Genetics Program at OSU.  Doctoral students are
preferred, but outstanding students who lack a Masters are also encouraged to 
apply.  Students should have excellent grades and GRE scores; strong course 
and/or research experience in molecular genetics; and demonstrated ability to 
write and speak English well.  Three to five years of half-time support, and 
tuition remission, are available subject to adequate performance in research and
coursework.  

Students may work on a variety of topics related to gene identification, genetic
engineering, and genome mapping.  Most work in the laboratory deals with poplars
and Douglas-fir.   Students may develop other areas for research, however, 
current topics of interest include:

- Isolation and manipulation of floral homeotic genes for engineering of 
reproductive development

-Effects of matrix attachment regions on gene silencing in transgenic poplars

-Population genetic studies of gene diversity and gene flow using microsatellite
markers

-Genetic engineering of systems for inducible sterility/fertility 

-Molecular engineering of genotype independent transformation systems

-Ecophysiological consequences of genetic engineering for lignin modification

-Development of microsatellite marker-maps and use for QTL analysis 


For information or an application form (specify department), contact Steve 
Strauss, Dept. of Forest Science, Oregon State University, Corvallis, OR 
97331-7501, fax 541 737 1393, phone -6578, strauss@FSL.orst.edu







From owner-rapd@net.bio.net Thu Dec 26 22:00:00 1996
Path: biosci!rutgers!news.cis.ohio-state.edu!nntp.sei.cmu.edu!bb3.andrew.cmu.edu!newsfeed.pitt.edu!portc02.blue.aol.com!howland.erols.net!newsfeed.internetmci.com!masternews.telia.net!newssrv.ita.tip.net!news.keyworld.net!news
From: Kenneth Briffa <kennbrif@keyworld.net>
Newsgroups: bionet.molbio.yeast,bionet.molbio.rapd
Subject: Method of DNA extraction from yeast
Date: Mon, 23 Dec 1996 23:17:28 -0800
Organization: ESI, Malta.
Lines: 9
Message-ID: <32BF8388.19C3@keyworld.net>
Reply-To: kennbrif@keyworld.net
NNTP-Posting-Host: ppp40.keyworld.net
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 3.0 (Win16; I)
Xref: biosci bionet.molbio.yeast:6334 bionet.molbio.rapd:1762

Hello, I'm an undergraduate preparing my dissertation project. The
project involves RAPD from brewer's yeast. I've been trying to extract
the DNA from the yeasts using benzyl chloride but the yield is not good
enough. Does anyone know any method to extract the DNA from yeasts
without using any enzymes?

Cheers,
Kenneth Briffa
University of Malta

From owner-rapd@net.bio.net Mon Dec 30 22:00:00 1996
Path: biosci!MBCRR.HARVARD.EDU!bsturner
From: bsturner@MBCRR.HARVARD.EDU (Bradley Turner)
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis->Similarity vs homology
Date: 31 Dec 1996 08:52:51 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 48
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199612311652.LAA22215@mbcrr.harvard.edu>
NNTP-Posting-Host: net.bio.net


Hi Robert Hamilton,

I'm very interested in your comment differentiating Homology and Similarity,
I was wondering if you (or other RAPD netters) would be able to share some
references that would discuss these differences at greater length or depth?

Thank You,
Brad Turner

**************************************************************
		    Bradley Turner
	        Beth Israel Deaconess
                    Medical Center

Harvard Medical School		617-667-1215 phone
Division of Gastroenterology	617-667-2767 fax
Room Dana 536			bsturner@mbcrr.harvard.edu
330 Brookline Avenue		bturner@bidmc.harvard.edu
Boston, MA 02215, USA		turner@sprcore.bidmc.harvard.edu
**************************************************************



BEGIN INCLUDED MESSAGE-------------------------------------------------------

From rhamilton@mc.edu Wed Dec  4 02:59:24 1996
To: rapd@net.bio.net
From: Robert Hamilton <rhamilton@mc.edu>
Subject: Re: Rapd data analysis
Date: 3 Dec 1996 23:09:07 GMT

  Homology is a
>sticky issue, and even the same-sized fragment does not necessarily mean
>the fragments are homologous.
>

>Gary Hannan
>
>
>
This is true. SIMILARITY is NEVER a good measure of homolgy. Just because 
two fragments DON'T hybridize in a Southern does not mean that they are 
NOT homologous, particularly in closely realted species. An assessment of 
homology requires more knowledge than sequence similarity provides, be it 
via RAPDs or actual sequence data. 

END OF INCLUDED MESSAGE------------------------------------------------------

From owner-rapd@net.bio.net Mon Dec 30 22:00:00 1996
Path: biosci!agate!howland.erols.net!cam-news-hub1.bbnplanet.com!news.bbnplanet.com!cpk-news-hub1.bbnplanet.com!cpk-news-feed1.bbnplanet.com!ox.mc.edu!usenet
From: Robert Hamilton <rhamilton@mc.edu>
Newsgroups: bionet.molbio.rapd
Subject: Re: Rapd data analysis->Similarity vs homology
Date: 31 Dec 1996 19:50:52 GMT
Organization: Mississippi College
Lines: 3
Message-ID: <5abqqs$si9@ox.mc.edu>
References: <199612311652.LAA22215@mbcrr.harvard.edu>
NNTP-Posting-Host: mobo.mc.edu
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 1.22 (Windows; I; 16bit)

This issue has not been fully discussed with reference to the type of 
data associated with RAPDs.


