This wiki has undergone a migration to Confluence found Here

Difference between revisions of "CG"

From HL7Wiki
Jump to navigation Jump to search
Line 71: Line 71:
  
 
====Standards====
 
====Standards====
'''''ANSI/HL7 RPS, R1-2007'''''
 
 
:Pedigree Topic - Familiy History
 
:7/5/2007
 
 
 
'''''HL7 CGPED, R1-'''''
 
'''''HL7 CGPED, R1-'''''
 
 
:HL7 Version 3 Pedigree Topic - Familiy History
 
:HL7 Version 3 Pedigree Topic - Familiy History
:Last Ballot: Informative Ballot 1 - ???
+
:Last Ballot: Nomrative Ballot 1 - May, 2007
  
 
'''''HL7 CG_GV, R1'''''
 
'''''HL7 CG_GV, R1'''''
Line 87: Line 81:
 
'''''HL7 IG CG_GENO, R1'''''
 
'''''HL7 IG CG_GENO, R1'''''
 
:HL7 Version 3 Genotype, Release 1
 
:HL7 Version 3 Genotype, Release 1
:DSTU Ballot 1 - January 2009
+
:Last Ballot: DSTU Ballot 1 - January 2009
 +
 
 +
'''''HL7 IG LOINCGENVA, R1'''''
 +
:HL7 Version 2 Implementation Guide: Clinical Genomics; Fully LOINC-Qualified Genetic Variation Model, Release 1 (US Realm)
  
 
==Reference Links==
 
==Reference Links==

Revision as of 15:51, 5 March 2009

Main Page | Clinal Genomics (CG)

This page is for the CG TC

Mission and Charter

Mission

This group supports the HL7 mission to create and promote its standards by enabling the communication between interested parties of the clinical and personalized genomic data. The focus of clinical genomics work is the personalization (differences in individual's genome) of the genomic data and the linking to relevant clinical information.

File:CG.jpg

This Work Group will facilitate the development of common standards for clinical research information management across a variety of organizations -- including national and international government agencies and regulatory bodies, private research efforts, and sponsored research -- and thus the availability of safe and effective therapies by improving the processes and efficiencies associated with regulated clinical research.

Charter

Work Products and Contributions to HL7 Processes

The Work Group will collect, review, develop and document clinical genomics use cases in order to determine what data needs to be exchanged. The WG will review existing genomics standards formats such as BSML (Bioinformatics Sequence Markup Language), MAGE-ML (Microarray and GeneExpression Markup Language), LSID (Life Science Identifier) and other. This group will recommend enhancements to and/or extensions of HL7's normative standards for exchange of information about clinical genomic orders and observations.

In addition, Clinical Genomics will seek to assure that related or supportive standards produced by other HL7 groups are robust enough to accommodate their use in both research and clincal care use. The group will also monitor information interchange standards developed outside HL7, and attempt harmonization of information content and representation of such standards with the HL7 content and representation.

Formal Relationships with Other HL7 Groups

This Work Group will coordinate with a large number of other Work Groups in order to accomplish its mission. Strongest relationships will be with:

  • Orders and Observation
  • Clinical Statement
  • Clincal Decision Support
  • Regulated Clinical Research Information Management
  • Orders and Observations
  • Patient Care
  • Electronic Health Records
  • Modeling and Methodology
  • Structured Documents

Formal Relationships with Groups Outside of HL7

Decision Making

see Work Group Decision Making Documents[1]


Date of Last Revision Final March 2, 2009

CG Projects

Working Group Meetings

CG Working Group Meeting Agendas

Meeting Minutes

CG Working Group Meeting Minutes

Sub-Teams

CG Vocabulary

Domains

clinical Genomics

Clinical Genomics Facilitators

Modeling:

Amnon Shabo
shabo@il.ibm.com
IBM Rsearch Lab in Haifa

Publishing:

Grant Wood
Grant.Wood@imail.org
Intermountain Healthcare

Vocabulary:

Joyce Hernandez
joyce_hernandez@merck.com

Standards

HL7 CGPED, R1-

HL7 Version 3 Pedigree Topic - Familiy History
Last Ballot: Nomrative Ballot 1 - May, 2007

HL7 CG_GV, R1

HL7 Version 3 Standard: Genetic Variation, Release 1
Last Ballot: Normative Ballot 2 - January 2009

HL7 IG CG_GENO, R1

HL7 Version 3 Genotype, Release 1
Last Ballot: DSTU Ballot 1 - January 2009

HL7 IG LOINCGENVA, R1

HL7 Version 2 Implementation Guide: Clinical Genomics; Fully LOINC-Qualified Genetic Variation Model, Release 1 (US Realm)

Reference Links

BRIDG file release site http://gforge.nci.nih.gov/frs/?group_id=342

BRIDG Project site http://gforge.nci.nih.gov/projects/bridg-model/