Ian I agree, and indeed, the word I meant was genetic, which lead to a type on generic. However, the care provision model is quite generic, but that was off discussion.
A lot of the content might be useful in different formats, but the best is to have that consistent over standards and implementations. Vriendelijke groet, William Goossen directeur Results 4 Care -----Original Message----- From: David Moner <[email protected]> To: For openEHR clinical discussions <openehr-clinical at openehr.org> Sent: Thu, Nov 11, 2010 12:31 pm Subject: Re: Research Topic Hello, We are involved in a small project for modelling genetic diagnosis reports and genetic variations with EN13606 archetypes. It has just started, but I hope we can have some results during the next months. David 2010/11/11 Ian McNicoll <Ian.McNicoll at oceaninformatics.com> An interesting project might be to see how the concepts identified in that work, can be best modelled in openEHR, making use of existing CKM archetypes wherever possible. Ian Dr Ian McNicoll office / fax +44(0)1536 414994 mobile +44 (0)775 209 7859 skype ianmcnicoll ian.mcnicoll at oceaninformatics.com Clinical analyst, Ocean Informatics openEHR Clinical Knowledge Editor www.openehr.org/knowledge Honorary Senior Research Associate, CHIME, UCL BCS Primary Health Care SG Group www.phcsg.org On 11 November 2010 09:30, William Goossen <williamtfgoossen at cs.com> wrote: > The HL7 community has created a message for genetic information exchange. It > does include a significant effort in modeling of the knowledge behind, a > good starting point for the ontology. > > Vriendelijke groet, > > William Goossen > directeur Results 4 Care > > -----Original Message----- > From: Hasti Ziaimatin <h.ziaimatin at uq.edu.au> > To: openehr-clinical at openehr.org <openehr-clinical at openehr.org> > Sent: Thu, Nov 11, 2010 12:40 am > Subject: Research Topic > > Hi All, > > I?m a PhD student at the University of Queensland in Brisbane, Australia. > I?m currently performing research, in collaboration with other members of > the team, on creating an ontology for depicting a health information system > model for a heterogeneous group of genetic disorders affecting skeletal > development. > > I have recently come across openEHR archetypes. I have an interest in this > area and would like to kindly ask for your help in finding a research topic > which I may be able to relate to creating a knowledgebase to assist > clinicians in capturing gene and protein information as well as help with > the diagnosis of rare and unknown cases of these genetic Skeletal disorders. > Semantic Web technologies will be used for creating this knowledge base. > > Thanks in advance. > Hasti Ziaimatin > > = > > _______________________________________________ > > > openEHR-clinical mailing list > > > openEHR-clinical at openehr.org > > > http://lists.chime.ucl.ac.uk/mailman/listinfo/openehr-clinical > > > > _______________________________________________ > openEHR-clinical mailing list > openEHR-clinical at openehr.org > http://lists.chime.ucl.ac.uk/mailman/listinfo/openehr-clinical > _______________________________________________ openEHR-clinical mailing list openEHR-clinical at openehr.org http://lists.chime.ucl.ac.uk/mailman/listinfo/openehr-clinical -- David Moner Cano Grupo de Inform?tica Biom?dica - IBIME Instituto ITACA http://www.ibime.upv.es Universidad Polit?cnica de Valencia (UPV) Camino de Vera, s/n, Edificio G-8, Acceso B, 3? planta Valencia ? 46022 (Espa?a) _______________________________________________ openEHR-clinical mailing list openEHR-clinical at openehr.org http://lists.chime.ucl.ac.uk/mailman/listinfo/openehr-clinical -------------- next part -------------- An HTML attachment was scrubbed... URL: <http://lists.openehr.org/mailman/private/openehr-clinical_lists.openehr.org/attachments/20101111/7094638f/attachment.html>
