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Difference between revisions of "Outline comparison table"
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| N/A | | N/A | ||
| Testing of other family members, Genetic counseling, Resources for additional information | | Testing of other family members, Genetic counseling, Resources for additional information | ||
+ | |- | ||
+ | | Genetic Variations | ||
+ | | N/A | ||
+ | | N/A | ||
+ | | N/A | ||
+ | |- | ||
+ | | Cytogenetics | ||
+ | | N/A | ||
+ | | N/A | ||
+ | | N/A | ||
+ | |- | ||
+ | | Gene Expression | ||
+ | | N/A | ||
+ | | N/A | ||
+ | | N/A | ||
+ | |- | ||
+ | | Other Testings | ||
+ | | N/A | ||
+ | | N/A | ||
+ | | N/A | ||
|} | |} |
Revision as of 07:16, 7 November 2011
This table compares the current GTR section titles to corresponding heading in various recommendations found in the following literature:
- ACMG: American College Of Medical Genetics recommendations for standards for interpretation of sequence variations, see entry G17 at [1]
- CAP: College of American Pathologists - Clinical Laboratory Reports in Molecular Pathology, see at [2]
- JMD: Journal of Molecular Diagnostics - Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report, see at [3]
Note that GTR titles in parenthesis represnet parent sections.
GTR | ACMG | CAP | JMD |
---|---|---|---|
Findings (Test Details) | Genotype and/or haplotype | Results | Test results and a brief interpretation |
Interpretation (Test Details) and Overall Interpretation (Summary) | Interpretation including clinical implications | Interpretations (optionally distinguish between clinical and analytic) | Test results and a brief interpretation (grouped within the report) |
Indications (Test Details, Summary) | Reason for testing | Indications for testing (Demographic information) | Indication for testing/specimen sent |
Test Performed (Test Details) | Test Performed | Laboratory procedures performed (Billing information) | Test Ordered |
Specimen (Test Details, Summary) | Specimen type | Specimen (within Laboratory/patient/sample identifiers) | Specimen type |
Background (Test Information) | Limitations of the assay | (free description under Comments) | Ancillary information/information for specialists / supplemental information |
Methodology (Test Information) | Methodology | Procedure | (within supplemental information) |
References (Test Information) | References | (Cite peer-reviewed medical literature or reliable Web sites, within Comments) | (within supplemental information) |
Recommendations (Summary) | Recommendations | Comment | Guidance |
FollowUp Genetic Tests (Recommendations / Summary) | Follow-up test recommendations | N/A | Follow-up testing / Additional testing that may be useful for clarifying the test result |
Follow Up Visits To Specialists (Recommendations / Summary) | N/A | N/A | N/A |
Recommended Actions(Recommendations / Summary) | N/A | N/A | Testing of other family members, Genetic counseling, Resources for additional information |
Genetic Variations | N/A | N/A | N/A |
Cytogenetics | N/A | N/A | N/A |
Gene Expression | N/A | N/A | N/A |
Other Testings | N/A | N/A | N/A |