Events
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ECCB 2010 Workshop:
Annotation, interpretation and management of Mutations (AIMM2010) - Call for Papers
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http://www.unbsj.ca/sase/csas/data/aimm2010/
This year's will workshop showcase the state of the art in extraction and
reuse of genotype-phenotype information. Annotation of mutations with their
impact on phenotypic expression is crucial to understanding genetic
mechanisms involved in phenotypic processes and ultimately in complex
diseases. Managing this knowledge is key to generating novel hypotheses.
Despite the existence of literature and databases describing impacts
of mutations, association studies fail to deliver linkage to
phenotypes which is the most important contemporary research interest.
Extraction of such information from scientific literature is a
promising research field and existing solutions are ready to be
deployed as services and as semantic web services.
***Early bird registration has been extended until 21 July!***
The third GATE training course will take place at Concordia University
in Montréal, Canada, from August 30th to September 3rd 2010. This event
will follow the format of the earlier May 2010 course, but with the
addition of a new training track covering linked data and ontologies.
Further details on the material to be covered:
https://gate.ac.uk/family/training.html
Registration, travel and accommodation:
https://gate.ac.uk/conferences/montreal-2010/index.html
=========================================================================================
ECCB 2010 Workshop:
Annotation, interpretation and management of Mutations (AIMM2010) - Call for Papers
=========================================================================================
http://www.unbsj.ca/sase/csas/data/aimm2010/
Full paper submission deadline extended by 1 week to August 2
This year's will workshop showcase the state of the art in extraction and
reuse of genotype-phenotype information. Annotation of mutations with their
impact on phenotypic expression is crucial to understanding genetic
mechanisms involved in phenotypic processes and ultimately in complex
diseases. Managing this knowledge is key to generating novel hypotheses.
Despite the existence of literature and databases describing impacts
of mutations, association studies fail to deliver linkage to
phenotypes which is the most important contemporary research interest.
Extraction of such information from scientific literature is a
promising research field and existing solutions are ready to be
deployed as services and as semantic web services.
