A Systematic Framework for the Interpretation of Copy Number Variants - Webinar - Ambry Genetics

A Systematic Framework for the Interpretation of Copy Number Variants - Webinar - Ambry Genetics

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Evidence Categories

14 of 38

14 of 38

Evidence Categories

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A Systematic Framework for the Interpretation of Copy Number Variants - Webinar - Ambry Genetics

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  1. 1 Intro
  2. 2 Disclaimer
  3. 3 Variant Interpretation
  4. 4 Guidelines
  5. 5 Deletions
  6. 6 Duplications
  7. 7 The Current Scene
  8. 8 Proposed Changes
  9. 9 Classification System
  10. 10 Uncouple Classification from Clinical Significance
  11. 11 Clinical Significance
  12. 12 Why is this important
  13. 13 Quantitative Points Based Evaluation Framework
  14. 14 Evidence Categories
  15. 15 Special Considerations
  16. 16 Consistency
  17. 17 Other Supporting Information
  18. 18 Gene Number
  19. 19 Data
  20. 20 Case Based Evidence
  21. 21 Segregation
  22. 22 NonSegregation
  23. 23 Case Control Studies
  24. 24 Family History
  25. 25 Calculator Tool
  26. 26 Scoring Mattress
  27. 27 Calculating Appropriate Classification
  28. 28 Improving Interlaboratory Concordance
  29. 29 Metric Based Classifications
  30. 30 Duplicates
  31. 31 Full Set
  32. 32 Summary
  33. 33 Questions
  34. 34 How is the metric updated
  35. 35 Do you see the value to the clinician
  36. 36 concordance rates
  37. 37 publication date
  38. 38 closing remarks

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