Stream: genomics
Topics:
- GenomicStudy Resource (5 messages, latest: Apr 12 2022 at 16:01)
- R5 changes - MolecularSequence and 'Genomics Guidance' (30 messages, latest: Apr 12 2022 at 15:11)
- New publication: Best practices for interpretation of WGS (1 message, latest: Apr 11 2022 at 20:43)
- Question on block vote (3 messages, latest: Apr 07 2022 at 13:12)
- GenomeX Accelerator News (3 messages, latest: Apr 07 2022 at 04:00)
- Liquid Biopsies and Reporting in our IG (12 messages, latest: Mar 31 2022 at 17:32)
- FDA vs CPIC Pharmacogenomics Tables (2 messages, latest: Mar 30 2022 at 22:06)
- Study Level (37 messages, latest: Mar 28 2022 at 13:23)
- backporting "new resources" (10 messages, latest: Mar 21 2022 at 12:40)
- STU2 Publication process started (3 messages, latest: Mar 16 2022 at 15:01)
- R5 plan settled (2 messages, latest: Mar 14 2022 at 17:25)
- DR.presentedForm (12 messages, latest: Mar 04 2022 at 15:25)
- FISH result related data components (26 messages, latest: Mar 02 2022 at 23:19)
- MolecularSequence - rethink 'referenceSeq' (44 messages, latest: Mar 01 2022 at 17:27)
- Connectathon 30 - Genomic operations (3 messages, latest: Feb 28 2022 at 19:44)
- collab Genetic Operations May 2022 Connectathon (2 messages, latest: Feb 24 2022 at 20:53)
- How to represent Exon & MSI marker data (17 messages, latest: Feb 22 2022 at 16:05)
- DNA change type (22 messages, latest: Feb 17 2022 at 20:39)
- MolecularSequence for R5 (4 messages, latest: Feb 16 2022 at 17:13)
- how to express asco scale results in observation profiles (15 messages, latest: Feb 16 2022 at 16:24)
- Cytogenomic Result Interpretation in FHIR (9 messages, latest: Feb 15 2022 at 14:59)
- Technical change? FHIR-36011 (3 messages, latest: Feb 11 2022 at 21:13)
- GenomicsReport 0..0 JIRA ticket (55 messages, latest: Feb 11 2022 at 21:13)
- Name of our IG (10 messages, latest: Feb 10 2022 at 17:07)
- How to represent FISH lab test results (16 messages, latest: Feb 08 2022 at 00:45)
- genomics "coding systems" and HTA (32 messages, latest: Feb 07 2022 at 16:41)
- percentage tumor cells (5 messages, latest: Feb 01 2022 at 09:45)
- Flexible fields (5 messages, latest: Jan 27 2022 at 20:11)
- HGNC Gene ID (9 messages, latest: Jan 26 2022 at 09:43)
- biomarker slides (2 messages, latest: Jan 20 2022 at 10:50)
- Genomics & USCDIv3 (7 messages, latest: Jan 19 2022 at 16:46)
- RefSeq binding on component:genomic-ref-seq (1 message, latest: Jan 19 2022 at 11:09)
- Sanger confirmation/testing (61 messages, latest: Jan 18 2022 at 14:15)
- genomics standard extensions (2 messages, latest: Jan 17 2022 at 22:14)
- Understanding versions of the Genomics Reporting IG (3 messages, latest: Jan 11 2022 at 23:06)
- Jiras in WAITING FOR INPUT (21 messages, latest: Jan 11 2022 at 20:27)
- ✔ Genomics IG Version (2 messages, latest: Jan 11 2022 at 10:14)
- Representation of Repeat Expansions in FHIR (65 messages, latest: Dec 21 2021 at 00:16)
- More Genomics Operations (1 message, latest: Dec 20 2021 at 17:18)
- Tuesday call - Zoom issues (1 message, latest: Dec 14 2021 at 16:05)
- RNA fusions and additional annotations (11 messages, latest: Dec 07 2021 at 22:26)
- Grouper Profile Usefulness (181 messages, latest: Dec 02 2021 at 19:08)
- another question on Variant1 example (39 messages, latest: Nov 29 2021 at 19:45)
- Genomics and Biomarkers examples (11 messages, latest: Nov 23 2021 at 18:39)
- Simplifying Variant Guidance (12 messages, latest: Nov 23 2021 at 17:08)
- Proposal for new extension - Genomics File (128 messages, latest: Nov 23 2021 at 17:07)
- Epigenomics (4 messages, latest: Nov 15 2021 at 01:11)
- How to represent the test identifier (80 messages, latest: Nov 10 2021 at 22:41)
- Input on Article - can FHIR Scale to high volume production? (15 messages, latest: Nov 09 2021 at 22:03)
- No meeting Nov 2 (1 message, latest: Nov 02 2021 at 14:27)
- genotype and haplotype (19 messages, latest: Nov 01 2021 at 15:26)
- Variant valueCodeableConcept too constrained (3 messages, latest: Oct 18 2021 at 18:33)
- Biomarkers sync-up (15 messages, latest: Oct 15 2021 at 19:57)
- handling medication information such as drug class (33 messages, latest: Oct 14 2021 at 19:30)
- Clinvar Submission API (22 messages, latest: Oct 11 2021 at 18:41)
- MolecularVariant and Observation (25 messages, latest: Oct 11 2021 at 14:22)
- IG - Updated general page (40 messages, latest: Oct 08 2021 at 19:09)
- DiagnosticReport Discussion (12 messages, latest: Oct 06 2021 at 22:31)
- Examples wanted: MolecularSequence (3 messages, latest: Oct 04 2021 at 22:16)
- Wanted: SMEs (4 messages, latest: Oct 04 2021 at 22:13)
- JIRA for opening up 'media' on DiagnosticReport (1 message, latest: Oct 04 2021 at 16:49)
- Sep 2021 WGM (29 messages, latest: Sep 22 2021 at 14:22)
- Update to WGM agenda - times for Q3 and Q4 (1 message, latest: Sep 14 2021 at 18:30)
- Journal Article- Challenges/Benefits Labs using standards (3 messages, latest: Sep 01 2021 at 15:50)
- Improving Usability of IG (Topic from May 2021 WGM) (7 messages, latest: Jul 22 2021 at 12:58)
- 2021-05 WGM (13 messages, latest: May 27 2021 at 17:34)
- Ballot comments imported (5 messages, latest: May 21 2021 at 22:38)
- Connectathon 27 (23 messages, latest: May 21 2021 at 21:44)
- JIRA Stuck in "Create Account" Mode (4 messages, latest: May 20 2021 at 17:30)
- is there a break between Q4 and Q5 (3 messages, latest: May 19 2021 at 14:02)
- Fixing Genomics Link on "Main" FHIR page is getting critical (16 messages, latest: May 17 2021 at 17:06)
- Diagnostic Implication Definition in our IG (3 messages, latest: May 17 2021 at 16:48)
- somatic variant reporting (11 messages, latest: May 07 2021 at 01:10)
- Is there a FHIR subgroup meeting today 5/3 (5 messages, latest: May 03 2021 at 16:33)
- TMB AnswerList (8 messages, latest: Apr 22 2021 at 20:24)
- 1.1.0 ballot package not available in registry (2 messages, latest: Apr 22 2021 at 11:18)
- ISO and Genomics (3 messages, latest: Apr 20 2021 at 15:14)
- STU2 Theme: Uncallable subregions in a region studied (27 messages, latest: Apr 19 2021 at 14:32)
- PGx Example for IG - included in May Ballot (22 messages, latest: Apr 06 2021 at 16:58)
- Observation Searching + returning groupers (17 messages, latest: Apr 05 2021 at 19:52)
- Variation-code use (13 messages, latest: Apr 01 2021 at 13:42)
- Variation-code definition documentation (4 messages, latest: Apr 01 2021 at 13:19)
- Encoding new components in Variant profile (5 messages, latest: Apr 01 2021 at 12:50)
- Request for info on what is in the IG (2 messages, latest: Apr 01 2021 at 12:32)
- PGx clopidogrel study (1 message, latest: Mar 25 2021 at 01:27)
- semantic computing conference (1 message, latest: Mar 24 2021 at 03:22)
- Error in current build (9 messages, latest: Mar 23 2021 at 22:57)
- Multiple Category codes (13 messages, latest: Mar 15 2021 at 15:28)
- using observation.components (1 message, latest: Mar 05 2021 at 12:43)
- FHIR IG NIB for May 2021 (1 message, latest: Mar 03 2021 at 23:36)
- GenomicsBase profile on genomics-reporting IG (9 messages, latest: Mar 03 2021 at 15:57)
- FYI PharmGKB, CPIC curated info now displayed on ClinGen (1 message, latest: Feb 23 2021 at 21:55)
- Prep for May 2021 WGM - Tell us your time zone (again :)) (4 messages, latest: Feb 17 2021 at 15:50)
- Schedule OMOP Genomics Preso? (6 messages, latest: Feb 04 2021 at 00:11)
- Compound heterozygosity (16 messages, latest: Jan 31 2021 at 21:16)
- January 2021 Virtual WGM thread (45 messages, latest: Jan 28 2021 at 15:22)
- Structural Variants Spanning Multiple Genomic "Regions" (13 messages, latest: Jan 26 2021 at 14:30)
- Variantion Representation - a standard to create a compu... (1 message, latest: Jan 19 2021 at 21:12)
- Combining similar types of components (23 messages, latest: Jan 12 2021 at 16:21)
- Use of eMERGE images in our IG (2 messages, latest: Jan 11 2021 at 17:35)
- ConnectathonJanuary 2020 (7 messages, latest: Dec 22 2020 at 22:18)
- variant Inherited from (60 messages, latest: Dec 07 2020 at 08:45)
- HLA Haplotype from NGS data (11 messages, latest: Dec 01 2020 at 02:58)
- Stress Testing IG Implications with Examples (154 messages, latest: Nov 18 2020 at 15:08)
- Text examples / use cases (9 messages, latest: Nov 04 2020 at 23:39)
- Precision Of Boundaries (3 messages, latest: Nov 04 2020 at 18:03)
- LOINC Terms (2 messages, latest: Nov 02 2020 at 13:04)
- VCF2FHIR: Exomiser results (7 messages, latest: Oct 22 2020 at 13:59)
- V2 examples from LRI 2.5.1 (11 messages, latest: Oct 12 2020 at 15:05)
- Updated Genomics Guidance page (15 messages, latest: Oct 05 2020 at 21:43)
- FHIR R4b - Observation-genetics profiles (20 messages, latest: Sep 29 2020 at 05:18)
- Sep 2020 WGM Topics (39 messages, latest: Sep 25 2020 at 02:03)
- GA4GH Variation Representation Specification (5 messages, latest: Aug 17 2020 at 21:03)
- Functional Annotation / Variant Consequence / Functional Eff (35 messages, latest: Aug 11 2020 at 13:58)
- Block Vote: Tuesday, August 18th (7 messages, latest: Aug 10 2020 at 22:17)
- Finally — some REAL progress :) (1 message, latest: Aug 07 2020 at 02:14)
- CG Reporting IG STU2 to mCODE alignment (1 message, latest: Jul 28 2020 at 16:08)
- Pertinent negatives & no-call regions (10 messages, latest: Jul 27 2020 at 20:59)
- Sep 2020 WGM (5 messages, latest: Jul 27 2020 at 15:33)
- Connectathon 25 (5 messages, latest: Jul 27 2020 at 13:25)
- Standard terms from NCBI (42 messages, latest: Jul 27 2020 at 13:23)
- Usage of LOINC code 81247-9 for Genetic tests (7 messages, latest: Jul 27 2020 at 13:21)
- MolecularSequence (17 messages, latest: Jul 27 2020 at 13:09)
- Tracking WES data (4 messages, latest: Jul 27 2020 at 12:55)
- FHIR Connectathon shorthand track is on. (1 message, latest: Jul 21 2020 at 19:47)
- DiagnosticReport intent (2 messages, latest: Jul 15 2020 at 19:42)
- Representation of pipeline methodology (21 messages, latest: Jun 08 2020 at 13:45)
- FHIR R4.1 - Impact to Genomics Implementation Guidance (6 messages, latest: Jun 02 2020 at 22:30)
- O&O joint call is starting! (1 message, latest: May 21 2020 at 14:04)
- Connectathon 24 (251 messages, latest: May 18 2020 at 16:40)
- Genomics Guidance updates in FHIR Core (1 message, latest: May 18 2020 at 16:24)
- Updates to all key documents based on latest version of IG (30 messages, latest: May 15 2020 at 22:05)
- Update on TBD Code Systems for FHIR (33 messages, latest: May 14 2020 at 20:55)
- Observation-genetics vs Variant (3 messages, latest: May 12 2020 at 12:13)
- Hemizygotes as Complex Variants (7 messages, latest: May 10 2020 at 13:46)
- coding grouper resource (47 messages, latest: May 05 2020 at 14:04)
- COVID19 viral sequences? (35 messages, latest: May 05 2020 at 13:21)
- MSI & TMB profiles ready (7 messages, latest: May 05 2020 at 12:48)
- Representing Significance and Confidence in FHIR/HL7 specs (7 messages, latest: May 05 2020 at 12:15)
- Genomic allele start-end (20 messages, latest: Apr 28 2020 at 15:43)
- Associated Phenotype Nomenclature (60 messages, latest: Apr 27 2020 at 16:36)
- subType in Specimen DAM (2 messages, latest: Apr 21 2020 at 16:10)
- Lab Services spec in Order Catalog IG (3 messages, latest: Apr 17 2020 at 14:32)
- STU2 Theme: Implications (247 messages, latest: Apr 10 2020 at 16:39)
- driver/passenger mutation (63 messages, latest: Apr 08 2020 at 07:50)
- Zoom coordinates (3 messages, latest: Mar 31 2020 at 19:10)
- Representing tumor-normal sequencing tests? (117 messages, latest: Mar 31 2020 at 13:06)
- data-set samples and examples (9 messages, latest: Mar 31 2020 at 12:39)
- HGNC gene symbol (42 messages, latest: Mar 23 2020 at 14:40)
- how to use HGNC valueset? (4 messages, latest: Mar 22 2020 at 12:33)
- Need to include chromosome as a component to ObsVariant (31 messages, latest: Mar 16 2020 at 19:20)
- hgvs-shell (4 messages, latest: Mar 16 2020 at 14:58)
- Themes for STU2 (40 messages, latest: Mar 16 2020 at 14:49)
- Variant Origin - 'NOT' ? (17 messages, latest: Mar 15 2020 at 16:05)
- query variants in a specific region (84 messages, latest: Feb 18 2020 at 21:35)
- genetic test results (3 messages, latest: Jan 13 2020 at 16:03)
- mCODE Sept 2019 Ballot General CG Reporting-related comments (34 messages, latest: Dec 17 2019 at 21:52)
- IG FHIR Version (17 messages, latest: Dec 13 2019 at 17:30)
- Beacon API (14 messages, latest: Dec 11 2019 at 16:02)
- slides PGx CG IG use and proposal components versus profiles (25 messages, latest: Dec 10 2019 at 18:09)
- Validation issue for HGVS/HGNC code (12 messages, latest: Dec 09 2019 at 03:04)
- Validation issue for RelatedArtifact (14 messages, latest: Dec 06 2019 at 18:47)
- task recommendations (19 messages, latest: Nov 29 2019 at 16:16)
- GA4GH vs HL7 (9 messages, latest: Nov 29 2019 at 16:07)
- searching for Reports including all Observations (2 messages, latest: Nov 29 2019 at 15:50)
- FHIR lingo (6 messages, latest: Nov 25 2019 at 16:11)
- IG is officially published! (1 message, latest: Nov 21 2019 at 20:57)
- variation-code component (46 messages, latest: Nov 21 2019 at 15:29)
- identifier/coding systems and codes (8 messages, latest: Nov 21 2019 at 14:46)
- harmonize somatic and PGx profiles (36 messages, latest: Nov 21 2019 at 12:13)
- Level of Evidence versus Clinical Significance (101 messages, latest: Nov 21 2019 at 12:11)
- implementations (1 message, latest: Nov 21 2019 at 11:58)
- genotype display name profile (5 messages, latest: Nov 20 2019 at 16:16)
- Observation validation issue without effectiveDateTime (7 messages, latest: Nov 19 2019 at 20:06)
- task recommendation follow up (6 messages, latest: Nov 18 2019 at 17:40)
- Joint openEHR meeting, November (17 messages, latest: Nov 13 2019 at 06:55)
- Microbiology (2 messages, latest: Nov 12 2019 at 17:33)
- Representation of secondary findings (15 messages, latest: Nov 06 2019 at 18:28)
- mCODE: region-studied (4 messages, latest: Nov 01 2019 at 14:14)
- hgvs component(s) (26 messages, latest: Oct 30 2019 at 17:55)
- HPO codes (9 messages, latest: Oct 22 2019 at 15:23)
- Narrative auto-generation issue (4 messages, latest: Oct 16 2019 at 21:14)
- more examples (37 messages, latest: Oct 08 2019 at 18:15)
- Modelling of 'affected' status (18 messages, latest: Oct 07 2019 at 02:36)
- Multiple (LOINC) Codes (41 messages, latest: Oct 03 2019 at 16:34)
- Trailing slashes on CodeSystems (9 messages, latest: Oct 03 2019 at 12:01)
- Glossary (9 messages, latest: Sep 27 2019 at 02:32)
- Changes to genomic related CodeSystem URIs (11 messages, latest: Sep 26 2019 at 20:31)
- DiagnosticReport categories (9 messages, latest: Sep 26 2019 at 17:54)
- FYI - GENO value sets! (2 messages, latest: Sep 24 2019 at 20:55)
- obsVariant transcript/aa components (40 messages, latest: Sep 20 2019 at 19:02)
- DiagnosticReport codings? (5 messages, latest: Sep 19 2019 at 15:44)
- performing lab disclaimers (10 messages, latest: Sep 19 2019 at 14:26)
- genomeBuild on MolecularSequence (3 messages, latest: Sep 18 2019 at 19:23)
- chromosome-copy-number-change-type (8 messages, latest: Sep 17 2019 at 14:27)
- transcript and amino acid variants (3 messages, latest: Sep 17 2019 at 14:07)
- fusion genes (7 messages, latest: Sep 15 2019 at 17:29)
- Best practice guidelines for managing optional elements (8 messages, latest: Sep 14 2019 at 22:07)
- Atlanta Connectathon 2019 (15 messages, latest: Sep 14 2019 at 21:07)
- CoordinateSystem ValueSet (21 messages, latest: Sep 14 2019 at 20:22)
- Adding Report Comments to Genomics Report (6 messages, latest: Sep 14 2019 at 02:32)
- Adding extensions to Genomics Report (5 messages, latest: Sep 06 2019 at 20:13)
- Consanguinity (2 messages, latest: Sep 02 2019 at 14:21)
- Ironing out TBD LOINCs (7 messages, latest: Aug 20 2019 at 20:03)
- obs-structural-genetic-findin (14 messages, latest: Jul 29 2019 at 21:37)
- Cancer Interoperability Chat (42 messages, latest: Jul 22 2019 at 14:30)
- Describing TMB & Other Tests (22 messages, latest: Jul 19 2019 at 12:25)
- functional class (42 messages, latest: Jul 18 2019 at 15:47)
- multiple codings (1 message, latest: Jul 18 2019 at 08:02)
- affected genes/exons (4 messages, latest: Jul 17 2019 at 09:55)
- variant profile data-types (5 messages, latest: Jul 09 2019 at 19:31)
- IG profile naming conventions don't follow FHIR guidance (12 messages, latest: Jun 27 2019 at 23:10)
- CNV size (4 messages, latest: Jun 11 2019 at 11:20)
- devdays2019 (2 messages, latest: Jun 10 2019 at 18:33)
- structural variant change type (3 messages, latest: Jun 07 2019 at 20:54)
- variant start-end (5 messages, latest: Jun 06 2019 at 16:10)
- Issue with FamilyMemberHistory-Genomics profile (9 messages, latest: May 29 2019 at 22:37)
- multiple specimen (4 messages, latest: May 21 2019 at 16:13)
- Grahames view on must-support (1 message, latest: May 06 2019 at 19:00)
- CG Meetingroom (1 message, latest: May 06 2019 at 17:08)
- Public Validation (1 message, latest: May 05 2019 at 19:49)
- Montreal Connectathon 2019 (7 messages, latest: May 05 2019 at 18:46)
- allele frequency component (NFr) (5 messages, latest: May 03 2019 at 11:35)
- Montreal (2 messages, latest: Apr 16 2019 at 02:03)
- ISO TC (6 messages, latest: Mar 26 2019 at 07:41)
- CAP Cancer Protocols/electronic Cancer Checklists (eCC)/SDC (4 messages, latest: Mar 20 2019 at 14:50)
- panel orders (2 messages, latest: Mar 08 2019 at 13:57)
- Cytogenetic Nomenclature (14 messages, latest: Mar 08 2019 at 13:56)
- terminology to unified IG (17 messages, latest: Mar 06 2019 at 19:11)
- eMERGE pilot sub-stream (2 messages, latest: Mar 06 2019 at 15:55)
- page for IG and example PDFs added to confluence (1 message, latest: Mar 05 2019 at 17:31)
- Feb. 11 deadline for HL7 vocabulary harmonization (6 messages, latest: Feb 07 2019 at 21:27)
- todos before publishing (7 messages, latest: Jan 16 2019 at 18:16)
- "Must Support" versus "1..1" cardinality (1 message, latest: Jan 15 2019 at 18:51)
- Jan 2019 Connectathon (18 messages, latest: Jan 15 2019 at 18:35)
- Bad? Genetics example 3 in core Observation Resource (8 messages, latest: Jan 15 2019 at 15:48)
- Link DiagnosticReports hierarchically (4 messages, latest: Jan 14 2019 at 22:03)
- Jan 2019 WGM (2 messages, latest: Jan 14 2019 at 19:39)
- Region Studied Implementation (18 messages, latest: Jan 13 2019 at 21:08)
- validating against the IG (47 messages, latest: Jan 12 2019 at 15:50)
- Discussion on transcending V2? (1 message, latest: Jan 08 2019 at 16:55)
- consent scope for genomics testing (8 messages, latest: Jan 04 2019 at 15:06)
- Attaching VCF files (25 messages, latest: Dec 13 2018 at 03:05)
- Sequence / Observation comparison (68 messages, latest: Dec 04 2018 at 17:26)
- QA for MolecularSequence (15 messages, latest: Nov 28 2018 at 18:25)
- R4 MolecularSequence composite search params (16 messages, latest: Nov 27 2018 at 21:14)
- URI for HPO CodeSystem (10 messages, latest: Nov 16 2018 at 13:01)
- specimen.subject in IG (10 messages, latest: Nov 16 2018 at 07:59)
- Corrections of Terminology URIs in Core (24 messages, latest: Nov 07 2018 at 21:09)
- Genomic Observation Extensions in Core (2 messages, latest: Oct 29 2018 at 14:32)
- GF13626 has no resolution (1 message, latest: Oct 28 2018 at 14:39)
- GF13622 has no resolution (1 message, latest: Oct 28 2018 at 14:35)
- GF13623 has no resolution (10 messages, latest: Oct 28 2018 at 14:25)
- HGNC code (11 messages, latest: Oct 23 2018 at 10:53)
- Did you find this variant vs What variant did you find? (25 messages, latest: Oct 19 2018 at 20:56)
- CodeSystem URIs for genomics (60 messages, latest: Oct 16 2018 at 20:05)
- Phenopackets (8 messages, latest: Oct 15 2018 at 22:50)
- ValueSets (13 messages, latest: Oct 11 2018 at 18:12)
- Sequence.readDepth (7 messages, latest: Oct 11 2018 at 15:54)
- Winning Task (5 messages, latest: Oct 10 2018 at 19:35)
- Sequence.structureVariant (5 messages, latest: Oct 10 2018 at 15:00)
- Possible Typo (2 messages, latest: Oct 10 2018 at 00:25)
- WGM Agenda Update (1 message, latest: Oct 01 2018 at 22:22)
- Welcome to Baltimore! (4 messages, latest: Sep 30 2018 at 18:31)
- attaching genomic files (4 messages, latest: Sep 20 2018 at 19:35)
- Unable to locate Isolated DNA in the list of specimen types (2 messages, latest: Sep 10 2018 at 13:17)
- MPEG-G in FHIR? (1 message, latest: Sep 10 2018 at 08:23)
- Capturing Genomic Panel Definitions (124 messages, latest: Aug 31 2018 at 14:01)
- Specifying "Panels" during ordering (2 messages, latest: Aug 30 2018 at 13:24)
- ComplexMutations (9 messages, latest: Aug 30 2018 at 13:16)
- code for a Group that means family (9 messages, latest: Aug 15 2018 at 14:03)
- Secondary Findings - New Extension proposal (38 messages, latest: Aug 07 2018 at 18:43)
- IG build currently broke (19 messages, latest: Jul 25 2018 at 10:32)
- github collaboration rights (3 messages, latest: Jun 29 2018 at 16:49)
- Varnomen (9 messages, latest: Jun 12 2018 at 22:45)
- genomics DiagnosticReport/Observation with a little text (15 messages, latest: May 23 2018 at 03:35)
- ig Observation.component formatting (1 message, latest: May 14 2018 at 21:01)
- gene coding without the id (14 messages, latest: Apr 12 2018 at 23:25)
- Media (2 messages, latest: Apr 04 2018 at 14:36)
- Reporting IG (11 messages, latest: Apr 02 2018 at 15:42)
- FamilyHistory in the reporting IG (2 messages, latest: Mar 30 2018 at 01:42)
- LOINC and reference sequences (8 messages, latest: Mar 29 2018 at 14:31)
- IG Updated (3 messages, latest: Mar 26 2018 at 03:43)
- Medication Assessed (9 messages, latest: Mar 13 2018 at 16:36)
- FYI - Mother/Child record discussion (2 messages, latest: Mar 13 2018 at 15:29)
- Genetic Impact (28 messages, latest: Mar 06 2018 at 16:43)
- GA4GH (3 messages, latest: Feb 08 2018 at 00:20)
- Unified proposal (1 message, latest: Feb 02 2018 at 19:38)
- CG 2018 WGM New Orleans minutes (1 message, latest: Jan 28 2018 at 22:28)
- 201801 Connectathon (4 messages, latest: Jan 28 2018 at 20:54)
- IG discussion breakout (1 message, latest: Jan 27 2018 at 16:28)
- how to capture geneName (2 messages, latest: Mar 15 2017 at 20:47)
- Is there any extensions definition about Sequence ? (17 messages, latest: Dec 14 2016 at 18:52)
- Add exmaples and code systems for Sequence.quality (8 messages, latest: Aug 19 2016 at 16:53)
- Genomics IG problem (1 message, latest: Jul 29 2016 at 22:06)
- DiagnosticOrder disappeared (8 messages, latest: Jul 27 2016 at 14:27)
- phenotypes (1 message, latest: Jul 20 2016 at 19:35)
- HLA related changes (8 messages, latest: Jul 20 2016 at 13:21)
- Genomics Implementation Guidance (9 messages, latest: Jul 19 2016 at 20:46)
- Sequence.structureVariant cardinality (1 message, latest: Jul 19 2016 at 17:35)
- Sequence.coordinateSystem cardinality (7 messages, latest: Jul 11 2016 at 06:29)
- Implementation Guide (5 messages, latest: Jun 22 2016 at 19:42)
- observation-geneticsSequence cardinality (1 message, latest: Jun 14 2016 at 21:46)
- strategy for phasing sequence blocks (26 messages, latest: Jun 14 2016 at 14:40)
- Observation for Genetics > Allele Name (3 messages, latest: Jun 14 2016 at 14:38)
- Server for testing (5 messages, latest: Jun 06 2016 at 12:43)
- readCoverage (4 messages, latest: May 31 2016 at 22:29)
- readLength (3 messages, latest: May 31 2016 at 18:45)
- CG definitions (1 message, latest: May 31 2016 at 15:27)
- variant location (6 messages, latest: May 30 2016 at 13:27)
- China (3 messages, latest: May 30 2016 at 13:13)
- HLA profiles (6 messages, latest: May 26 2016 at 14:28)
- allelicFrequency (1 message, latest: May 18 2016 at 15:00)
- using gforge tracker (10 messages, latest: May 18 2016 at 14:40)
- Discussion at Montreal (3 messages, latest: May 09 2016 at 20:19)
- Transactions (8 messages, latest: May 09 2016 at 02:03)
- Survey for Connectathon 12- FHIR Genomics (1 message, latest: May 08 2016 at 13:56)
- Issues/suggestions (1 message, latest: May 07 2016 at 23:10)
- typo in sequence_example.xml (1 message, latest: May 07 2016 at 18:28)
- testing (1 message, latest: May 07 2016 at 14:16)
Last updated: Apr 12 2022 at 19:14 UTC
