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Showing below up to 100 results in range #101 to #200.

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  1. Sequence-based mutation analysis TSD‏‎ (109 revisions)
  2. Fabry Disease 2012‏‎ (108 revisions)
  3. Canavan Disease‏‎ (108 revisions)
  4. Normal mode analysis‏‎ (107 revisions)
  5. MD simulation analysis TSD‏‎ (107 revisions)
  6. Structure-based mutation analysis TSD‏‎ (106 revisions)
  7. Task 3 (MSUD)‏‎ (106 revisions)
  8. Phenylketonuria 2011‏‎ (105 revisions)
  9. Task 2: Sequence alignments (sequence searches and multiple alignments)‏‎ (104 revisions)
  10. Hemochromatosis Normal modes‏‎ (104 revisions)
  11. Gaucher Disease: Task 10 - Normal mode analysis‏‎ (102 revisions)
  12. Canavan Task 7 - Structure-based mutation analysis‏‎ (102 revisions)
  13. Structure-based mutation analysis GLA‏‎ (102 revisions)
  14. Fabry:Homology based structure predictions‏‎ (102 revisions)
  15. Sequence-based mutation analysis GLA‏‎ (102 revisions)
  16. MD Mutation485‏‎ (101 revisions)
  17. Task 9: Normal Mode Analysis‏‎ (100 revisions)
  18. Task 7: Research SNPs‏‎ (100 revisions)
  19. Sequence Alignments Gaucher Disease‏‎ (100 revisions)
  20. Mapping SNPs BCKDHA‏‎ (97 revisions)
  21. Predicting the Effect of SNPs (PKU)‏‎ (95 revisions)
  22. Task 9: Structure-based mutation analysis‏‎ (92 revisions)
  23. Maple syrup urine disease 2011‏‎ (92 revisions)
  24. Researching SNPs (Phenylketonuria)‏‎ (91 revisions)
  25. Normal Mode Analysis of Glucocerebrosidase‏‎ (91 revisions)
  26. Sequence Alignments HEXA‏‎ (89 revisions)
  27. Sequence Alignment GLA‏‎ (89 revisions)
  28. Structure-Based Mutation Analysis Hemochromatosis‏‎ (87 revisions)
  29. Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal‏‎ (86 revisions)
  30. Canavan Disease: Task 05 - Homology Modelling‏‎ (84 revisions)
  31. Maple Syrup Urine Disease 2012‏‎ (84 revisions)
  32. Resource software‏‎ (84 revisions)
  33. Task 6: Protein structure prediction from evolutionary sequence variation‏‎ (83 revisions)
  34. Normal Mode Analysis of ARSA‏‎ (82 revisions)
  35. Fabry:Normal mode analysis‏‎ (81 revisions)
  36. Fabry Disease 2011‏‎ (81 revisions)
  37. Researching And Mapping Point Mutations Hemochromatosis‏‎ (79 revisions)
  38. Researching SNPs (PKU)‏‎ (79 revisions)
  39. Gaucher Disease: Task 09 - Lab Journal‏‎ (79 revisions)
  40. Hemochromatosis 2012‏‎ (78 revisions)
  41. Rs61731240‏‎ (78 revisions)
  42. Metachromatic leukodystrophy reference aminoacids‏‎ (77 revisions)
  43. Fabry:Mapping point mutations‏‎ (77 revisions)
  44. Task 3 - Sequence-based predictions 2011‏‎ (77 revisions)
  45. Researching SNPs Gaucher Disease‏‎ (76 revisions)
  46. Normal Mode Analysis Hemochromatosis‏‎ (76 revisions)
  47. Task 4: Homology-based structure prediction‏‎ (75 revisions)
  48. Phenylketonuria‏‎ (73 revisions)
  49. Task 2 (MSUD)‏‎ (73 revisions)
  50. ARS A Sequence alignments‏‎ (72 revisions)
  51. Structure-based mutation analysis ARSA‏‎ (72 revisions)
  52. Protein Structure and Function Analysis (SS 2013)‏‎ (72 revisions)
  53. Maple Syrup Urine Disease‏‎ (71 revisions)
  54. Fabry:Sequence-based mutation analysis‏‎ (70 revisions)
  55. Fabry:Sequence alignments (sequence searches and multiple alignments)‏‎ (70 revisions)
  56. Sequence Alignments BCKDHA‏‎ (70 revisions)
  57. Normal Mode Analysis (PKU)‏‎ (69 revisions)
  58. Task 2: Multiple Sequence Alignment‏‎ (68 revisions)
  59. Structure-based mutation analysis HEXA‏‎ (68 revisions)
  60. Fabry:Sequence alignments (sequence searches and multiple alignments):Results‏‎ (68 revisions)
  61. Normal mode analysis Gaucher Disease‏‎ (67 revisions)
  62. Protein Structure and Function Analysis (version: SS 2011)‏‎ (66 revisions)
  63. Gaucher Disease - Task 06 - Lab Journal‏‎ (65 revisions)
  64. Canavan Disease: Task 04 - Structural Alignments‏‎ (64 revisions)
  65. Lab journal task 8‏‎ (64 revisions)
  66. Gaucher Disease: Task 04 - Lab Journal‏‎ (64 revisions)
  67. Structure-based mutation analysis Gaucher Disease‏‎ (64 revisions)
  68. Tay-Sachs Disease 2011‏‎ (62 revisions)
  69. Rs121907974‏‎ (61 revisions)
  70. Glucocerebrosidase mapping snps‏‎ (59 revisions)
  71. Task 7 (MSUD)‏‎ (58 revisions)
  72. ASPA Sequence Based Predictions‏‎ (58 revisions)
  73. AllBio Forum‏‎ (57 revisions)
  74. Task 6 (MSUD)‏‎ (56 revisions)
  75. Phenylketonuria 2012‏‎ (53 revisions)
  76. Rs4777505‏‎ (53 revisions)
  77. Fabry:Structure-based mutation analysis‏‎ (53 revisions)
  78. Mapping mutations of ARS A‏‎ (53 revisions)
  79. Sequence Alignments‏‎ (52 revisions)
  80. Task 9 - Normal Mode Analysis‏‎ (51 revisions)
  81. Gaucher Disease: Task 08 - LabJournal‏‎ (50 revisions)
  82. Molecular Dynamics Simulations‏‎ (50 revisions)
  83. Lab Journal - Task 8 (PAH)‏‎ (48 revisions)
  84. Rs1800430‏‎ (48 revisions)
  85. Rs61747114‏‎ (47 revisions)
  86. Lab journal task 4‏‎ (46 revisions)
  87. Task 6 - Protein structure prediction from evolutionary sequence variation‏‎ (46 revisions)
  88. Task 5: Researching SNPs‏‎ (46 revisions)
  89. Researching SNPs TSD Journal‏‎ (45 revisions)
  90. Homology modelling Gaucher Disease‏‎ (44 revisions)
  91. Molecular Dynamics Analysis GLA‏‎ (44 revisions)
  92. Reference Sequence BCKDHA‏‎ (44 revisions)
  93. Molecular Dynamics Simulations (PKU)‏‎ (44 revisions)
  94. Normal mode analysis GLA‏‎ (42 revisions)
  95. Canavan Disease: Task 06 - Protein Structure Prediction‏‎ (42 revisions)
  96. Gaucher Disease: Task 02 - Lab Journal‏‎ (42 revisions)
  97. Lab Journal - Task 6 (PAH)‏‎ (41 revisions)
  98. Fabry:Sequence-based analyses‏‎ (41 revisions)
  99. Fabry:Homology based structure predictions/Journal‏‎ (41 revisions)
  100. Rs121907982‏‎ (41 revisions)

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