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CG WG Call Notes leading to 2014 January WGM
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Contents
- 1 November 12, 2013 -- Weekly call
- 2 Proposed Agenda
- 3 Attendees
- 4 Draft Minutes
- 5 November 5, 2013 -- Weekly call
- 6 Proposed Agenda
- 7 Attendees
- 8 Draft Minutes
- 9 October 29, 2013 -- Weekly call
- 10 Proposed Agenda
- 11 Attendees
- 12 Draft Minutes
- 13 October 22, 2013 -- Weekly call
- 14 Proposed Agenda
- 15 Attendees
- 16 Draft Minutes
- 17 October 15, 2013 -- Weekly call
- 18 Proposed Agenda
- 19 Attendees
- 20 Draft Minutes
- 21 October 8, 2013 -- Weekly call
- 22 Proposed Agenda
- 23 Attendees
- 24 Draft Minutes
November 12, 2013 -- Weekly call
Proposed Agenda
- Present and discuss in detail the FHIR resources
Attendees
- Amnon Shabo,Ruby Russell, Grant Wood, Gil Alterovitz, Larry Babb, Tom (CBMI), Siew Lam, Scott Botle
Draft Minutes
- Amnon's comments:
- How do the FHIR resources represent genotype-phenotype associations?
- How do you distinguish between interpretive phenotype and observed phenotype?
- How do we characterize a genotype-phenotype association while keeping each side of the association modular, e.g., representing observed phenotype using other standards for clinical data?
- Interperation should be separated from the class represneting the genomic observation, so thast it can have its own time stamp, mehod, performer, etc.
- Should distinguish between types (levels) of analyses mentioned in the various FHIR resources, e.g., Sequencing Analysis is different than the Genetic Analysis - the former is lower level analysis at the genomic side, while the the latter is more of a clinical genomics analysis
- Having FHIR Resources named after common representations like VCF and GVF as not flexible and should be abstracted a bit, e.g., through a wrapper of VCF-like formats that could include various existing formats and new ones in the future
- Larry:
- the FHIR Resource Genetic Analysis roughly follows an older version of the v2 message for genetic testing results, and that version has been recongnized to be limited and not being able to accomodate all use cases
- e.g., genotypes and phenotypes could have many to many relationships, and not necessarily as defined by some testing order
- Amnon:
- this discussion is held in the context of the effort to develop an agreed-upon Clinical Genomics Domain Information Model(s)
- therefore, all lessons learnt from existing specifications and pilots should inform the design of the CG DIM in a way that will result in an encompassing model that can be derived to produce different standards but still aligned semantically
- so, it's a top-down approached, informed by bottom-up reality...
November 5, 2013 -- Weekly call
Proposed Agenda
- Discuss and vote on whether to endorse the familial relation codes harmonization proposal
- Sorting out our projects in Project Insight
Attendees
- Amnon Shabo,Ruby Russell, Grant Wood, Gil Alterovitz, Mollie, Larry Babb, Yan Heras, Lloyd McKenzie
Draft Minutes
- Motion to endorse the familial relation codes harmonization proposal passed unanimously
- Discussion of projects listed under CG in HL7 Project Insight:
- HL7 CG-omics Domain Analysis Model
- send email to group announcing the intention to to retire this project
- if content is informative for other work - please advise group and lead discussion on a weekly call
- Gene Expression (project 867)
- send email to group to retire this project,
- if content is informative for other work please advise group and lead discussion on a weekly call
- Clinical Sequencing
- rename and expand scope, after January ballot
- Genetic Variation CMET (project 693)
- deprecate
- Pedigree Topic - ISO Ballot (project 479)
- put on hold/inactive -
- Cytogenetics Lab Result (project 663)
- status should equal published and complete but doesn't - need to clarify
- Canonical Pedigree - Family History (project 729)
- should list Published and completed because that's where we published the US Implemenetaion Guide for the Pedigree spec - need to clarify
- Pedigree release 2
- on hold
- Aligning the CG DAM, DIM, and FHIR Resources is easier as these are all under development
- goal to make first step in Jan ballot
- HL7 CG-omics Domain Analysis Model
October 29, 2013 -- Weekly call
Proposed Agenda
- Discuss the familial relation codes harmonization proposal
Attendees
- Amnon Shabo, Siew Lam, Ruby Russell, Grant Wood, Scott Bolte, Lloyd McKenzie, Phil Pochon, Chris Pack, Mollie, Larry Babb, Yan Heras
Draft Minutes
- Discuss the familial relation codes harmonization proposal
- Mollie: needs to run due diligence and understand its implications on current standard specifications and implementations
- Amnon:
- it's independent of the FHIR discussion and of any type of standard structure like v3, v2, CDA or FHIR
- it's an improved vocabulary that all standards can utilize
- standards can bind to it dynamically or extract subsets of it and bind to statically
- Motion to send out the harmonization proposal to the entire CG listserv and ask for comments, as well as reach out to Kevin Hughes team to check their feedback and possible implications on their implementation of the Pedigree spec that utilizes the current version of the vocabulary
- Lloyd seconded it
- Lam will send out an article with recommendations from genetic counselors
- Mollie will look into HGVS recommendations
- No objections or abstains and motion passed
October 22, 2013 -- Weekly call
Proposed Agenda
- Update on the Global Alliance by Gil
Attendees
- Amnon Shabo, Siew Lam, Gil Alterovitz, Ruby Russell, Grant Wood, Scott Bolte
Draft Minutes
- Discussed the correspondence of Scott, Lloyd and Kevin on Family History and FHIR
October 15, 2013 -- Weekly call
Proposed Agenda
- Discuss the CG DIM project
Attendees
- Amnon Shabo, Siew Lam, Grant Wood, Gil Alterovitz, Mollie, Phil Pochon, Yan Heras
Draft Minutes
- Amnon went through a slide deck, each containing a model underlying one of the specs developed by the HL7 Clinical Genomics group, and then presented a sketch of thought on where we could go with the DIM
October 8, 2013 -- Weekly call
Proposed Agenda
- Discuss the revised Project Scope Statement of CG Domain Information Model(s)
- See discussion on modeling issues at the project wiki page: http://wiki.hl7.org/index.php?title=Clinical_Genomics_Domain_Information_Model(s)_Project#Modeling_Discussion
- Need to submit the Cambridge WGM Meeting Minutes by the end of this week
- Change of WGM schedule
- From Wednesday & Thursday to Tuesday & Wednesday
- Do we need all session in both days?
- Accommodates joints with AP and OO with solo meetings before the joints
- So far we had a day and a half
- We could run from Tuesday Q2 to Wednesday Q3
Attendees
- Amnon Shabo, Siew Lam, Grant Wood, Larry Babb, Gil Alterovitz, Jenny, Ruby Russell, Mollie
Draft Minutes
- Grant will start the Cambridge WGM minutes by inserting the attendees in each session; Amnon will add to it minutes as he can recall and send out to the mailing list so that people can add to it
- Discussed the revisions to the CG DIM PSS and hearing no objections decided to resubmit to DESD
- Discussed initial modeling considerations of the DIM
- Amnon brought up the GTR, v2, v3 and FHIR models and made comments on the current differences
- Is research use case part of the DIM?
- Mollie said it should be clinically oriented with transnational capabilities at the most
- Amnon said it's Universal in the sense that we start from common denominator and then allow each environment to constrain it as need; e.g., for clinical it should be highly constrained