Training activity information
Details
Review referrals; analyse, interpret, and report results for Next Generation Sequencing (NGS) panels for patients referred for investigation of rare disease using HGVS nomenclature to describe genomic sequence changes.
Type
Entrustable training activity (ETA)
Evidence requirements
Evidence the activity has been undertaken by the trainee repeatedly, consistently, and effectively over time, in a range of situations. This may include occasions where the trainee has not successfully achieved the outcome of the activity themselves. For example, because it was not appropriate to undertake the task in the circumstances or the trainees recognised their own limitations and sought help or advice to ensure the activity reached an appropriate conclusion.
Reflection at multiple timepoints on the trainee learning journey for this activity.
Relevant learning outcomes
| # | Outcome |
|---|---|
| # 1 |
Outcome
Triage referrals for rare disease genomic investigations. |
| # 2 |
Outcome
Perform targeted and chromosomal analysis for patients referred for investigation of rare disease. |
| # 3 |
Outcome
Interpret genomic variants to investigate the clinical significance using appropriate nomenclature. |
| # 4 |
Outcome
Interpret and report genomic testing for Next Generation Sequencing (NGS) panels. |