Newsletter No. 8

September 2004

(Previous HGVS & HUGO-MDI newsletters may be found on our website at: www.genomic.unimelb.edu.au/hgvs/newsletters.html, these may be helpful for new members to familiarize themselves with our projects).

HGVS NEWS

Forthcoming Scientific & Annual General Meeting of HGVS - time to register

HGVS Scientific & Annual General Meeting Toronto, Canada, 26th October; Abstracts & registrations now being accepted, closing date for abstracts Sept. 19 deadline -see details below. If you know you are attending, please register now. If you wish to present an oral presentation please register and send your abstract in ASAP, last year we had an oversupply of abstracts! However, you do not need to present an abstract to attend the meeting.

Elections

Four new Board members need to be elected for a three year term. A call for nominations will be made this week by the Secretary Dr. Bill Oetting. Any member wishing to stand for nomination should put in their proposal to the nominating committee via Rania when the call is made or now but in any event by September 30.

HGVS Booth

The Society will host an exhibitor's booth once again at the American Society of Human Genetics Annual Meeting. The booth allocated is number 1028 located in Publishers Row. If you are at ASHG please drop by the booth and meet us. We are calling on members to volunteer to man the booth for short periods, those interested please contact Rania.

CORRESPONDENCE

Anyone wishing to make an announcement of interest to members in these newsletters please send a short paragraph to Rania at (horaitis@medstv.unimelb.edu.au) to be included in the next issue.

New Locus Specific Database

Database of sequence variation in two associated genes, ENG and ALK1. http://www.hht.org/web/

Dr. Paul Westwood, Molecular Genetics Service, Molecular Medicine Centre, Western General Hospital, Edinburgh, UK

CALENDAR OF EVENTS

CALL FOR ABSTRACTS

HGVS Scientific and Annual General Meeting

Toronto, Canada

Registration
Abstracts
Sponsorship Opportunities
Contact Us

Date:

 

Tuesday 26th October 2004

The biggest HGVS event of the year! TIME TO REGISTER NOW!

Venue:

Quebec Room, ASHG Conference Hotel: Fairmont, Royal York, Toronto.

Time:

 

 

Speakers to arrive: 7:45AM
Registration: 8:00AM
Conference Start: 8:45AM
Conference finish 7:00PM
Mixer: 7:00PM- 8:00PM

Registration:

 

 

 

 

Fee includes administrative costs, conference materials, coffee breaks, a buffet luncheon and mixer.

HGVS members: CAN $109
Non-HGVS member: CAN $145
All students: CAN $100
All costs in Canadian dollars (CAN). 1 CAN $ = ~ 0.715 US $ at 18th May 2004

(HGVS members receive a 25% reduction in meeting registrations. To join HGVS click here).

Abstracts:

 

Closing date is 19th September 2004 however the earlier you submit the more chance you will have of presenting. All those who send abstracts MUST register to have their abstract considered. Later abstracts MAY be considered. Registrations without presentations are also accepted.

Associated with:

A satellite meeting of the American Society of Human Genetics Annual Meeting


Mutation Detection 2005

VIII International Symposium of Mutations in the Genome

Santorini, Greece

May 31- June 4, 2005

This meeting aims to bring together all those interested in Mutation Detection methods and their application in Biology, Medicine and Agriculture. It is a forum where developers of methodology can exchange ideas, and those responsible for diagnostics can compare results with specific methods. Those in agriculture, microbiology and non-medical fields are encouraged to attend. A meeting report and selected papers from the last meeting in Palm Cove, Australia was published in Vol. 23, No. 5 in Human Mutation.

The Mutation Detection Symposium this year will be held on the island of Santorini, Greece. These symposia have a tradition of a wonderful cultural program that compliments the scientific program allowing all participants to freely interact and exchange ideas in magnificent surroundings with plenty of time for communication between the invited inventors and major users and committed audience who have experience in mutation detection. There is a strictly limited number of 170 registrants on a 1st come 1st served basis to allow maximum interaction between delegates. For more information see the Website: http://www.genomic.unimelb.edu.au/santorini.htm

If you are interested in attending or sponsoring you should indicate your interest to Rania as this meeting has a strictly limited number of 170.

Invited Speakers:

A. Athanassiadou, Greece Analysis of Parkinsons Disease
J. Barton, USA Electronic Detection
S. Beck, UK Human Epigenome Project
A. Brookes, UK Phenotype in Databases
C. Cantor, USA Mass Spectrometry Analysis
N. Carter, UK Arrays
S. Chanock, USA Cancer Genetics
H. Clausen-Schaumann, Germany Force Sensors
R. Cotton, Australia Collecting Mutations
R. Davis, USA*(not yet confirmed) Molecular Inverted Probes
J.T. den Dunnen, Netherlands The Diagnostic Lab
P-Y. Kwok Genotyping and Methods
K. Lohman, USA Parallel Sequencing
M. Nilsson, Sweden Ligation Amplification
G. Patrinos, Netherlands Locus Specific Databases
S. Quake, USA Micro Fluidics
R. Sandaltzopoulos, Greece Single Molecule Detection
J. Schouten, Netherlands MLPA
S. Sunyaef, USA Prediction of Effect
A-C Syvanen, Sweden Genotyping
M. Trau, Australia Nanoparticles
G. Traverso, UK Protein Truncation Test
J. Van Ness, USA Isothermal Amplification
R. Wooster, UK Cancer Genome Project

 

© Copyright HGVS 2004 Created by Rania Horaitis Posted 7 Sept. 2004
Coordinator Rania Horaitis horaitis@mail.medstv.unimelb.edu.au