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(Created page with "This table compares the current GTR outline to various recommendations found in the literature:") |
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− | This table compares the current GTR | + | 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 [http://www.acmgfoundation.org/AM/Template.cfm?Section=Content_Area_413&Template=/CM/ContentDisplay.cfm&ContentID=6328] | ||
+ | * '''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''': 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. | ||
+ | |||
+ | {| class="wikitable" | ||
+ | |- | ||
+ | ! 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) | ||
+ | |} |
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) |