OPEN CALL FOR PAPERS - BMC Bioinformatics Special Issue
=================================================

Following the Event:
================

ECCB Workshop: http://www.eccb2010.org/index.php/workshops/workshop2
AIMM2010 Annotation, Interpretation and Management of Mutations
http://www.unbsj.ca/sase/csas/data/aimm2010/

A call for papers is now open to all workshop participants and newcomers
who could not attend the AIMM 2010 event. See the link below for details
of the Special Issue on the AIMM Theme.

AIMM Themes
===========

OPEN CALL FOR PAPERS - BMC Bioinformatics Special Issue
=================================================

Following the Event:
================

ECCB Workshop: http://www.eccb2010.org/index.php/workshops/workshop2
AIMM2010 Annotation, Interpretation and Management of Mutations
http://www.unbsj.ca/sase/csas/data/aimm2010/

A call for papers is now open to all workshop participants and newcomers
who could not attend the AIMM 2010 event. See the link below for details
of the Special Issue on the AIMM Theme.

AIMM Themes
===========

=========================================================================================
ECCB 2010 Workshop:
Annotation, interpretation and management of Mutations (AIMM2010) - Call for Papers
=========================================================================================

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

=========================================================================================
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.