| gen-wg -- AMIA Genomics Working Group | ||||||||||||||||||||||||
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| About gen-wg | ||||||||||||||||||||||||
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Mission/Purpose: The attempts to sequence the entire genome of humans and associated pathogens is already generating large volumes of information with clinical relevance for prevention, diagnosis, treatment, and prognosis. The impact of this information on clinical information systems is not yet fully understood, nor are the potential contributions that clinical information systems can make in helping unravel the relationship between the genetic background of a patient and their experience of disease. The goal of this working group is to focus on opportunities within medical informatics that arise in the context of the storage, retrieval, analysis and dissemination of genomic information. The interests therefore include, for example, linking clinical databases to genomic databases, modifying the electronic medical record to accommodate the molecular medicine of the 21st century, methods for decision support in the post-genomic era, the design of clinical trials in the context of the genome projects, and any other pursuits in which genomic information interacts with medical information systems.
To see the collection of prior postings to the list, visit the gen-wg Archives. (The current archive is only available to the list members.) |
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| Using gen-wg | ||||||||||||||||||||||||
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To post a message to all the list members, send email to
gen-wg@mailman.amia.org.
You can subscribe to the list, or change your existing subscription, in the sections below. |
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| Subscribing to gen-wg | ||||||||||||||||||||||||
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Subscribe to gen-wg by filling out the following form. This is a closed list, which means your subscription will be held for approval. You will be notified of the list moderator's decision by email. This is also a hidden list, which means that the list of members is available only to the list administrator.
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version 2.1.9 |