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CCB: ISMB2005 Alternative Splicing Special Interest Group meeting, June 23-24, 2005, Detroid, Michigan, USA
- General Conference Site: http://biolinfo.org/as-sig/2005/
- Presenters Here is the list of accepted speakers for AS-SIG 2005 (in alphabetic order):
- Volker Brendel, Iowa State University, USA
- Tom Cooper, Baylor College of Medicine, USA
- Xiang-Dong Fu, UCSD, USA
- Michael Hiller, University of Jena, Germany
- Viive Howell, University of Michigan, USA
- Katherina Kechris, UCSF, USA
- Roscoe Klinck, University of Sherbrooke, Canada
- Chris Lee, UCLA, USA
- Ji-Ann Lee, UCLA, USA
- Dick Madden, University of Sherbrooke, Canada
- Wojciech Makalowski, Pennsylvania State University, USA
- Stephen Mount, University of Maryland, USA
- Sandy Pan, University of Toronto, Canada
- Shoba Ranganathan, Macquarie University, Australia
- Ronen Shemesh, Compugen, Israel
- Stefan Stamm, University Erlangen-Nurenberg, Germany
- Alphonse Thanaraj, EBI, UK
- Yi Xing, UCLA, USA
- Gene Yeo, Salk Institute, USA
- Xiang Zhang, Columbia University, USA
- Mihaela Zavolan, University of Basel, Switzerland
The organizers of AS-SIG would
like to invite you to participate in the first ISMB Special Interest Group
meeting on Alternative Splicing, on June 23-24, 2005 at Detroit, Michigan,
USA. This workshop is scheduled immediately before ISMB2005,
June 25-29, 2005 and is jointly sponsored by the RNA
Society and ISCB.
AS-SIG follows on from the highly
successful Alternative Splicing SIG
meeting held at the Pacific Symposium of Biocomputing, 2004.
Alternative splicing generates
multiple products from a single gene and is a major mechanism responsible
for diversity in the transcriptome of higher organisms.
This is an exciting time in the field of alternative splicing, combining new
discoveries from genomics, bioinformatics and molecular biology. Long
considered to be an interesting but less common form of regulation, alternative
splicing has emerged as a ubiquitous mechanism of regulation, thanks to genome
analysis of human and other higher organisms. Whereas the Human Genome
Project has produced a net result of 25,000 – 30,000 genes, alternative
splicing evidently produces over 100,000 distinct transcript forms. Identifying,
quantifying and analyzing the regulation, function and evolution of these forms
constitutes a “Human Transcriptome Project”, and will require as
remarkable and as concerted an effort as the Human Genome Project. Above
all, it will require close collaboration between bioinformaticists and experimentalists,
to build a community of shared tools, databases, nomenclature and standards
that permit everyone to contribute what they do best, while benefiting from
what everyone else has done. The AS-SIG aims to establish a permanent
forum for bioinformaticists and experimentalists to come together in this field.
AS-SIG will address the latest results and questions in this exciting field,
and to bring together bioinformaticists and experimentalists, focusing on questions
that demand their collaborative inputs.
Besides oral and poster presentation
sessions, the workshop will address the issue of data standards to pave
the way for the international efforts directed towards the human transcriptome
analysis.
The purpose of this SIG is to cover
the latest results and questions in this exciting field, and to bring together
bioinformaticists and experimentalists, focusing on questions that demand
their collaboration.The
SIG will include studies of alternative splicing both in human and other
organisms, and will consist of two days of talks (approximately 20 minutes
each), and a poster session.
- The meeting sessions will follows; four major thematic areas:
- Technologies: new experimental
approaches for high-throughput discovery, quantification, and functional
analysis of alternative splice forms in both mRNA and protein. These
include splice-variant measurement technologies such as microarrays; laboratory
protocols/assays; validation techniques; and novel instrumentation platforms.
- Biology: Biological mechanisms
of splicing and regulation; biological functions such as the impact of
splice variants on protein structure and biological pathways; phenomena
such as nonsense-mediated decay and disease associations.
- Bioinformatics: algorithms
and analysis of alternative splicing, including topics such as analysis
of alternative splicing evidence, products, and functional impact; comparative
genomics; alternative splicing regulation; and data-mining.
- Databases, Standards, and Community
Building for the “Human Transcriptome Project”: our
research community is in effect building a catalog of the 100,000+ transcript
forms found in human (and other transcriptomes), including their precise
structures, products, regulation, functional and experimental annotation. This
massive project, comparable in scale to the Human Genome Project, requires
the efforts of the entire community, as well as agreed standards for
sharing data, i.e. a common database, data standards, and shared tools. What
data and tool standards do we need? What nomenclature must we agree
on? How can we unify our efforts via a common database? How
can we integrate data from genomics, bioinformatics and traditional experiments? How
can we enable community annotation, curation and validation?
- Venue, Registration and Accommodation
The meeting will be held at the Detroit Marriott
at the Renaissance Center, Detroit, Michigan, USA.
AS-SIG registration
will be along with ISMB2005 registration.
ISMB2005 conference
rates have been extended to cover pre-conference days required to attend
AS-SIG. For more information on hotels offering special rates, please
see ISMB2005 Housing.
Hotel reservation will have to be made along with the SIG registration.
- Organizers:
- Professor Chistopher Lee, Chair, University of California Los Angeles, USA
- Prof. Shoba Ranganathan, Co-Chair, Macquarie University, Sydney, Australia
- Professor Stefan Stamm, Co-Chair, University of Erlangen-Nuremberg, Germany
- Dr. Hui Wang, Co-Chair, Affymetrix Inc., USA
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