Solving Medical Mysteries at the Stanford Center for Undiagnosed Diseases

Solving Medical Mysteries at the Stanford Center for Undiagnosed Diseases

Stanford Health Care via YouTube Direct link

Whole genome sequencing

13 of 35

13 of 35

Whole genome sequencing

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Solving Medical Mysteries at the Stanford Center for Undiagnosed Diseases

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  1. 1 Intro
  2. 2 The First Moment of Undiagnosed
  3. 3 Patient Story 1
  4. 4 Undiagnosed Diseases Network
  5. 5 New England Journal of Medicine
  6. 6 First 20 months
  7. 7 Types of omics
  8. 8 Genetic variation and phenotype
  9. 9 Rare diseases
  10. 10 Genetic testing
  11. 11 The nucleus of a cell
  12. 12 DNA DNA microarray
  13. 13 Whole genome sequencing
  14. 14 Previous genetic testing
  15. 15 Similarities
  16. 16 Veins
  17. 17 Vascular Longing
  18. 18 Looking Again
  19. 19 Metabolomics
  20. 20 Fly example
  21. 21 Data sharing networks
  22. 22 Genomics
  23. 23 Amelie
  24. 24 Clint
  25. 25 Diagnosis
  26. 26 Why
  27. 27 cytokine profiling
  28. 28 therapeutic approach
  29. 29 funders
  30. 30 Insurance Coverage
  31. 31 Diagnosis and Therapy
  32. 32 Genetics and Family
  33. 33 Genetics
  34. 34 Research
  35. 35 Evidence

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