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Showing below up to 50 results in range #51 to #100.

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  1. Task 2: Alignments‏‎ (163 revisions)
  2. Homology Based Structure Predictions Hemochromatosis‏‎ (162 revisions)
  3. Canavan Task 9 - Normal Mode Analysis‏‎ (162 revisions)
  4. Sequence-based mutation analysis Gaucher Disease‏‎ (161 revisions)
  5. Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation‏‎ (160 revisions)
  6. Homology-based structure prediction (PKU)‏‎ (158 revisions)
  7. Sequence-based mutation analysis of ARSA‏‎ (156 revisions)
  8. Gaucher Disease: Task 08 - Sequence-based mutation analysis‏‎ (156 revisions)
  9. Structure-based mutation analysis (Phenylketonuria)‏‎ (155 revisions)
  10. Structure-based mutation analysis (PKU)‏‎ (153 revisions)
  11. Protein structure prediction from evolutionary sequence variation (Phenylketonuria)‏‎ (153 revisions)
  12. Sequence-based predictions (PKU)‏‎ (152 revisions)
  13. Gaucher Disease: Task 09 - Structure-based mutation analysis‏‎ (147 revisions)
  14. Sequence Alignments Hemochromatosis‏‎ (143 revisions)
  15. Structure-based mutation analysis BCKDHA‏‎ (142 revisions)
  16. Canavan Disease: Task 07 - Researching SNPs‏‎ (142 revisions)
  17. Sequence-based mutation analysis HEXA‏‎ (141 revisions)
  18. Normal mode analysis (Phenylketonuria)‏‎ (140 revisions)
  19. MD Mutation436‏‎ (140 revisions)
  20. Normal Mode Analysis BCKDHA‏‎ (139 revisions)
  21. Glucocerebrosidase homology modelling‏‎ (132 revisions)
  22. Task 3: odba human Sequence-based predictions‏‎ (132 revisions)
  23. Gaucher Disease 2012‏‎ (130 revisions)
  24. Canavan Disease: Task 08 - Sequence-based Mutation Analysis‏‎ (130 revisions)
  25. Task 10: Molecular Dynamics Analysis‏‎ (129 revisions)
  26. Mapping SNPs‏‎ (129 revisions)
  27. Task 7: MSUD - Structure-based mutation analysis‏‎ (129 revisions)
  28. Task 3 - Sequence-based predictions‏‎ (129 revisions)
  29. Tay-Sachs Disease 2012‏‎ (127 revisions)
  30. Structural Alignments (Phenylketonuria)‏‎ (127 revisions)
  31. Sequence Search and Multiple Sequence Alignment (PKU)‏‎ (126 revisions)
  32. Structure based mutation analysis of GBA‏‎ (126 revisions)
  33. Task 5 - Mapping SNPs Canavan‏‎ (126 revisions)
  34. Task 5: Homology Modeling‏‎ (125 revisions)
  35. Sequence and multiple alignments‏‎ (123 revisions)
  36. Molecular Dynamics Simulations Analysis Hemochromatosis‏‎ (122 revisions)
  37. Task 8: Sequence-based mutation analysis‏‎ (122 revisions)
  38. Homology Modelling GLA‏‎ (122 revisions)
  39. Canavan Disease: Task 09 - Structure-based Mutation Analysis‏‎ (120 revisions)
  40. Task 6: MSUD - Sequence-based mutation analysis‏‎ (120 revisions)
  41. Normal mode analysis TSD‏‎ (119 revisions)
  42. Task 7: Structure-based mutation analysis‏‎ (119 revisions)
  43. MD WildType‏‎ (117 revisions)
  44. Molecular Dynamics Simulations Analysis of Glucocerebrosidase‏‎ (116 revisions)
  45. Canavan Disease: Task 03 - Sequence-based Predictions‏‎ (116 revisions)
  46. Researching SNPs TSD‏‎ (116 revisions)
  47. Gaucher Disease 2011‏‎ (114 revisions)
  48. Sequence-Based Predictions Hemochromatosis‏‎ (114 revisions)
  49. Canavan Disease: Task 10 - Normal Mode Analysis‏‎ (112 revisions)
  50. Glucocerebrosidase sequence alignments‏‎ (112 revisions)

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