Call For Papers & Participation |
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A large international
effort to define the fine patterns of sequence variation along the human
genome has been carried out using samples of four human populations. The
aim was to generate a genome-wide validated SNP resource and survey of
the patterns of allelic association and common haplotypes useful for designing
association studies. The outcome of this “HapMap” project
is the genotypes of over three million SNPs in DNA samples of individuals
from Africa, China, Utah, and Japan. This project is providing an unprecedented
amount of empirical data on the patterns of linkage disequilibrium across
the human genome that is fueling a large number of population genetic
analyses. A goal of the HapMap project is the selection of a subset of
the common SNPs to serve as a representative set of the entire common
variation. Methods for the selection of subsets of SNPs have proliferated,
and their effectiveness in different disease architectures and populations
still needs to be evaluated. However, the use of the HapMap data in other
aspects of study design and for the analysis of association studies has
received comparatively less attention. For example, methods which estimate
power and sample size for genetic studies using the empirically observed
patterns of LD are yet to be fully developed. Also, what is the power
of whole-genome direct association studies with putative causal variants
(i.e. non-synonymous cSNPs)? Questions about power are critically important,
as it is evident that the failures of replication that have plagued the
literature of disease association studies are likely to be the result
of underpowered studies. There are many other questions, for example:
What are the criteria to reject a gene or region for causality on a disease?
What are the necessary tools to better present the data from the HapMap
with other relevant annotations in a seamless way to allow the selection
of SNPs for particular candidate gene/region studies? What additional
information about selection, population history, recombination and related
phenomena can be gleaned from the HapMap data and future studies? |
Full Paper Submissions |
PSB will publish accepted full papers in an archival proceedings indexed in MEDLINE. All contributed papers will be rigorously peer-reviewed by at least three referees. A limited number of papers will be selected for a oral presentation to the full assembled conference. Accepted poster abstracts will be distributed at the conference separately from the archival Proceedings. To be eligible for Proceedings publication, each full paper must be accompanied by a cover letter stating that it contains original unpublished results not currently under consideration elsewhere. All papers must be submitted to russ.altman@smi.stanford.edu in electronic format. The file formats we accept are: postscript (*.ps), adobe acrobat (*.pdf) and Microsoft Word documents (*.doc). Attached files should be named with the last name of the first author (e.g. altman.ps, altman.pdf, or altman.doc). Hardcopy submissions or unprocessed TEX or LATEX files will be rejected without review. Each paper must be accompanied by a cover letter. The cover letter must state the following:
Submitted papers are limited to twelve (12) pages in our publication format. Please format your paper according to instructions found at: http://psb.stanford.edu/psb-online/psb-submit/ If figures can not be easily resized and placed precisely in the text, then it should be clear that with appropriate modifications, the total manuscript length would be within the page limit. Color pictures can be printed at the expense of the authors. The fee is $500 per page of color pictures, payable at the time of camera ready submission. |
Posters and Computer Demonstrations |
The poster session at PSB is another possibility to present results or to share ideas in the Conference. Posters are exhibited several days during the conference and include topics from all PSB sessions. Computer stations for live software or Web site demonstrations are also available during the conference and are encouraged as a complement to a poster or presentation. In order to be included in the Abstracts booklet to be distributed at the conference, one-page posters abstracts should be submitted by November 1 to russ.altman@smi.stanford.edu. Posters are not peer-reviewed nor indexed in MEDLINE. |
FAQ |
Q1. How can my paper be included in PSB's hardbound proceedings?
Q2. How does a PSB publication compare to a journal publication?
Q3. If I do not want to submit a full paper to PSB, but wish to participate?
Q4. How can I obtain travel support to come to PSB?
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Conference Information |
The Pacific Symposium on Biocomputing (PSB 2006) is an international, multidisciplinary conference for the presentation and discussion of current research in the theory and application of computational methods in problems of biological significance. The symposium is a forum for the presentation of work in databases, algorithms, interfaces, visualization, modeling and other computational methods, as applied to the data-rich areas of molecular biology. PSB 2006 will be held January 3-7, 2006, on The Grand Wailea Resort, Wailea, Maui, Hawaii. For more information see the official PSB 2006 Web page: http://psb.stanford.edu |
Session Chairs | ||
Andrew G. Clark |
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Andrew Collins |
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Francisco M. De La Vega Applied Biosystems Foster City, CA, USA E-mail:delavefm @ appliedbiosystems.com (Main Contact) |
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Kenneth K. Kidd |