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This table compares the current GTR section titles to corresponding heading in various recommendations found in the following literature: | 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 | + | * '''ACMG''': American College Of Medical Genetics recommendations for standards for interpretation of sequence variations, see entry G17 at [http://www.acmgfoundation.org/AM/Template.cfm?Section=Content_Area_413&Template=/CM/ContentDisplay.cfm&ContentID=6328] |
| − | * '''CAP''': Clinical Laboratory Reports in Molecular Pathology, see at [http://www.archivesofpathology.org/doi/pdf/10.1043/1543-2165%282007%29131%5B852%3ACLRIMP%5D2.0.CO%3B2] | + | * '''CAP''': College of American Pathologists - Clinical Laboratory Reports in Molecular Pathology, see at [http://www.archivesofpathology.org/doi/pdf/10.1043/1543-2165%282007%29131%5B852%3ACLRIMP%5D2.0.CO%3B2] |
| − | * '''JMD''': Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report | + | * '''JMD''': Journal of Molecular Diagnostics - Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report, see at [http://moldiag.highwire.org/cgi/reprint/11/2/162] |
Note that GTR titles in parenthesis represnet parent sections. | Note that GTR titles in parenthesis represnet parent sections. | ||
| Line 18: | Line 18: | ||
| Test results and a brief interpretation | | Test results and a brief interpretation | ||
|- | |- | ||
| − | | Indications (Test Details) | + | | 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 | | Reason for testing | ||
| Indications for testing (Demographic information) | | Indications for testing (Demographic information) | ||
| Line 27: | Line 32: | ||
| Laboratory procedures performed (Billing information) | | Laboratory procedures performed (Billing information) | ||
| Test Ordered | | Test Ordered | ||
| + | |- | ||
| + | | Specimen (Test Details, Summary) | ||
| + | | Specimen type | ||
| + | | Specimen (within Laboratory/patient/sample identifiers) | ||
| + | | Specimen type | ||
|- | |- | ||
| Background (Test Information) | | Background (Test Information) | ||
| Line 36: | Line 46: | ||
| Methodology | | Methodology | ||
| Procedure | | Procedure | ||
| − | | | + | | (within supplemental information) |
|- | |- | ||
| References (Test Information) | | References (Test Information) | ||
| References | | References | ||
| − | | (Cite peer-reviewed medical literature or reliable Web sites, | + | | (Cite peer-reviewed medical literature or reliable Web sites, within Comments) |
| (within supplemental information) | | (within supplemental information) | ||
|- | |- | ||
| Line 48: | Line 58: | ||
| Guidance | | 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 | ||
| + | | (designated by type of procedure / methdology) | ||
| + | | (designated by type of procedure / methdology) | ||
| + | | (designated by type of procedure / methdology) | ||
| + | |- | ||
| + | | Cytogenetics | ||
| + | | (designated by type of procedure / methdology) | ||
| + | | (designated by type of procedure / methdology) | ||
| + | | (designated by type of procedure / methdology) | ||
| + | |- | ||
| + | | Gene Expression | ||
| + | | (designated by type of procedure / methdology) | ||
| + | | (designated by type of procedure / methdology) | ||
| + | | (designated by type of procedure / methdology) | ||
|} | |} | ||
Latest revision as of 09:15, 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 | (designated by type of procedure / methdology) | (designated by type of procedure / methdology) | (designated by type of procedure / methdology) |
| Cytogenetics | (designated by type of procedure / methdology) | (designated by type of procedure / methdology) | (designated by type of procedure / methdology) |
| Gene Expression | (designated by type of procedure / methdology) | (designated by type of procedure / methdology) | (designated by type of procedure / methdology) |
