Call for Papers and Posters
Discovery of Molecularly Targeted
Therapies
Pacific Symposium on Biocomputing
January 5-8, 2016
Fairmont Orchid Resort
The Big Island of Hawaii, USA
Motivation
The delivery of personalized
healthcare is predicated on the application of the best available scientific
knowledge to the practice of medicine in order to promote health, improve
outcomes and enhance patient safety. Unfortunately, current approaches to basic
science research and clinical care are poorly integrated, yielding clinical
decision-making processes that do not take advantage of up-to-date scientific
knowledge. Basic scientists investigating the biological basis for a given
disease may regularly encounter synergistic effects spanning two or more
bio-molecular entities or processes that can contribute to our understanding of
the mechanisms underlying phenomena such as the etiologic basis of the targeted
disease state or potential response to therapeutic agents. However, systematic
approaches to the use of that knowledge in order to directly inform the
selection of targeted molecular therapies for Òreal worldÓ patients are
extremely limited.
There are an increasing number of
multi-modelling and in-silico
knowledge synthesis techniques that can provide investigators with the tools to
quickly generate hypotheses concerning the relationships between entities found
in heterogeneous collections of scientific data — for example, exploring
potential linkages among genes, phenotypes and molecularly targeted therapeutic
agents, thus enabling the Òforward engineeringÓ of treatment strategies based
on knowledge generated via basic science studies. Ultimately, the goal of such
methodologies is to accelerate the identification of actionable research
questions that can make direct contributions to clinical practice. Given increasing concerns over the
barriers to the timely translation of discoveries from the laboratory to the
clinic or broader population settings, such high-throughput hypothesis
generation and testing is highly desirable. These needs are particularly
critical in numerous disease areas where the availability of new therapeutic
agents is constrained, thus calling for the re-use and repositioning of
existing treatments.
Session Topics
In response to the challenges
and opportunities enumerated above, this session will specifically focus on the
use of multi-modeling approaches for improving molecularly targeted therapies
and precision medicine. We invite submissions which integrate multiple data
types, including but not limited to: clinical trial, electronic health record, drug
toxicity, genomic, pharmacogenomic, proteomic, metabolomic, microbiome, exposome
and structural data. Examples of submission topics emphasizing novel
methodologies and applications include:
Methodology:
Novel methods for multi-scale
data integration
Probabilistic models and
predictive methods
Machine learning applications
Systems biology and network
analysis
Visualization techniques for
integrating disparate data types
Novel data resources and
databases for molecularly targeted therapies
Application areas:
Drug-target interactions
Drug repurposing or
repositioning
Synergistic drug combinations
Patient response and outcome
Off-target effects and adverse
events
Drug-drug interactions
Pharmacokinetics
Pharmacodynamics
Session
Organizers
Philip R.O. Payne, PhD, The Ohio State University, Philip.Payne@osumc.edu
Kun Huang, PhD, The Ohio State University, Kun.Huang@osumc.edu
Nigam Shah, MBBS, PhD, Stanford University, nigam@standford.edu
Primary contact for all inquiries: Philip.Payne@osumc.edu
Submission
Information
Please
note that the submitted papers are reviewed and accepted on a competitive
basis. At least three reviewers will be assigned to each submitted manuscript.
Important Dates
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Paper
submissions due: July 27, 2015 August 3, 2015
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Notification
of paper acceptance: September 14, 2015
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Camera-ready
final paper due: October 5, 2015
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Deadline
for poster abstracts: November 17, 2015
Paper Format
Please see the PSB paper format template and instructions at http://psb.stanford.edu/psb-online/psb-submit.
The file formats we accept are: postscript (*.ps) and Adobe Acrobat
(*.pdf)). Attached files should be named with the last name of the first author
(e.g. altman.ps or altman.pdf). 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:
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The
email address of the corresponding author.
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The
specific PSB session that should review the paper or abstract.
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The
submitted paper contains original, unpublished results, and is not currently
under consideration elsewhere.
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All
co-authors concur with the contents of the paper.
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 cannot 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.