This wiki has undergone a migration to Confluence found Here
Difference between revisions of "Outline comparison table"
Jump to navigation
Jump to search
| Line 72: | Line 72: | ||
| 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 |