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Showing below up to 100 results in range #21 to #120.

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  1. Sequence-based mutation analysis BCKDHA‏‎ (237 revisions)
  2. Gaucher Disease: Task 05 - Homology Modelling‏‎ (236 revisions)
  3. Task 4: Structural Alignments‏‎ (223 revisions)
  4. Task 3: Sequence-based predictions‏‎ (209 revisions)
  5. Homology based structure prediction (Phenylketonuria)‏‎ (205 revisions)
  6. Hemochromatosis: Sequence based predictions‏‎ (200 revisions)
  7. Gaucher Disease: Task 04 - Structural Alignment‏‎ (196 revisions)
  8. Structure-based mutation analysis‏‎ (196 revisions)
  9. Sequence-based mutation analysis (Phenylketonuria)‏‎ (195 revisions)
  10. Mapping SNPs HEXA‏‎ (192 revisions)
  11. Sequence-based predictions GLA‏‎ (190 revisions)
  12. Homology modelling TSD‏‎ (189 revisions)
  13. Sequence-based analyses of ARS A‏‎ (188 revisions)
  14. Task 4: Homology based structure predictions‏‎ (182 revisions)
  15. Sequence-based predictions TSD‏‎ (181 revisions)
  16. Molecular Dynamics Simulations HEXA‏‎ (177 revisions)
  17. Sequence-Based Mutation Analysis Hemochromatosis‏‎ (177 revisions)
  18. Sequence-based analyses Gaucher Disease‏‎ (176 revisions)
  19. Molecular Dynamics Simulations Analysis (PKU)‏‎ (174 revisions)
  20. Gaucher Disease‏‎ (174 revisions)
  21. Gaucher Disease: Task 07 - Research SNPs‏‎ (173 revisions)
  22. Homology Modeling of ARS A‏‎ (170 revisions)
  23. Sequence based mutation analysis of GBA‏‎ (169 revisions)
  24. Hemochromatosis 2011‏‎ (168 revisions)
  25. Sequence-based mutation analysis‏‎ (168 revisions)
  26. Hemochromatosis‏‎ (167 revisions)
  27. Task 6: Sequence-based mutation analysis‏‎ (166 revisions)
  28. Normal mode analysis HEXA‏‎ (165 revisions)
  29. Canavan Task 10 - Molecular Dynamics Simulations‏‎ (164 revisions)
  30. Sequence Alignments TSD‏‎ (164 revisions)
  31. Task 2: Alignments‏‎ (163 revisions)
  32. Homology Based Structure Predictions Hemochromatosis‏‎ (162 revisions)
  33. Canavan Task 9 - Normal Mode Analysis‏‎ (162 revisions)
  34. Sequence-based mutation analysis Gaucher Disease‏‎ (161 revisions)
  35. Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation‏‎ (160 revisions)
  36. Homology-based structure prediction (PKU)‏‎ (158 revisions)
  37. Gaucher Disease: Task 08 - Sequence-based mutation analysis‏‎ (156 revisions)
  38. Sequence-based mutation analysis of ARSA‏‎ (156 revisions)
  39. Structure-based mutation analysis (Phenylketonuria)‏‎ (155 revisions)
  40. Protein structure prediction from evolutionary sequence variation (Phenylketonuria)‏‎ (153 revisions)
  41. Structure-based mutation analysis (PKU)‏‎ (153 revisions)
  42. Sequence-based predictions (PKU)‏‎ (152 revisions)
  43. Gaucher Disease: Task 09 - Structure-based mutation analysis‏‎ (147 revisions)
  44. Sequence Alignments Hemochromatosis‏‎ (143 revisions)
  45. Canavan Disease: Task 07 - Researching SNPs‏‎ (142 revisions)
  46. Structure-based mutation analysis BCKDHA‏‎ (142 revisions)
  47. Sequence-based mutation analysis HEXA‏‎ (141 revisions)
  48. MD Mutation436‏‎ (140 revisions)
  49. Normal mode analysis (Phenylketonuria)‏‎ (140 revisions)
  50. Normal Mode Analysis BCKDHA‏‎ (139 revisions)
  51. Task 3: odba human Sequence-based predictions‏‎ (132 revisions)
  52. Glucocerebrosidase homology modelling‏‎ (132 revisions)
  53. Canavan Disease: Task 08 - Sequence-based Mutation Analysis‏‎ (130 revisions)
  54. Gaucher Disease 2012‏‎ (130 revisions)
  55. Task 7: MSUD - Structure-based mutation analysis‏‎ (129 revisions)
  56. Task 3 - Sequence-based predictions‏‎ (129 revisions)
  57. Mapping SNPs‏‎ (129 revisions)
  58. Task 10: Molecular Dynamics Analysis‏‎ (129 revisions)
  59. Structural Alignments (Phenylketonuria)‏‎ (127 revisions)
  60. Tay-Sachs Disease 2012‏‎ (127 revisions)
  61. Structure based mutation analysis of GBA‏‎ (126 revisions)
  62. Task 5 - Mapping SNPs Canavan‏‎ (126 revisions)
  63. Sequence Search and Multiple Sequence Alignment (PKU)‏‎ (126 revisions)
  64. Task 5: Homology Modeling‏‎ (125 revisions)
  65. Sequence and multiple alignments‏‎ (123 revisions)
  66. Homology Modelling GLA‏‎ (122 revisions)
  67. Molecular Dynamics Simulations Analysis Hemochromatosis‏‎ (122 revisions)
  68. Task 8: Sequence-based mutation analysis‏‎ (122 revisions)
  69. Task 6: MSUD - Sequence-based mutation analysis‏‎ (120 revisions)
  70. Canavan Disease: Task 09 - Structure-based Mutation Analysis‏‎ (120 revisions)
  71. Normal mode analysis TSD‏‎ (119 revisions)
  72. Task 7: Structure-based mutation analysis‏‎ (119 revisions)
  73. MD WildType‏‎ (117 revisions)
  74. Canavan Disease: Task 03 - Sequence-based Predictions‏‎ (116 revisions)
  75. Researching SNPs TSD‏‎ (116 revisions)
  76. Molecular Dynamics Simulations Analysis of Glucocerebrosidase‏‎ (116 revisions)
  77. Sequence-Based Predictions Hemochromatosis‏‎ (114 revisions)
  78. Gaucher Disease 2011‏‎ (114 revisions)
  79. Glucocerebrosidase sequence alignments‏‎ (112 revisions)
  80. Canavan Disease: Task 10 - Normal Mode Analysis‏‎ (112 revisions)
  81. Sequence-based mutation analysis TSD‏‎ (109 revisions)
  82. Fabry Disease 2012‏‎ (108 revisions)
  83. Canavan Disease‏‎ (108 revisions)
  84. MD simulation analysis TSD‏‎ (107 revisions)
  85. Normal mode analysis‏‎ (107 revisions)
  86. Task 3 (MSUD)‏‎ (106 revisions)
  87. Structure-based mutation analysis TSD‏‎ (106 revisions)
  88. Phenylketonuria 2011‏‎ (105 revisions)
  89. Hemochromatosis Normal modes‏‎ (104 revisions)
  90. Task 2: Sequence alignments (sequence searches and multiple alignments)‏‎ (104 revisions)
  91. Sequence-based mutation analysis GLA‏‎ (102 revisions)
  92. Canavan Task 7 - Structure-based mutation analysis‏‎ (102 revisions)
  93. Fabry:Homology based structure predictions‏‎ (102 revisions)
  94. Structure-based mutation analysis GLA‏‎ (102 revisions)
  95. Gaucher Disease: Task 10 - Normal mode analysis‏‎ (102 revisions)
  96. MD Mutation485‏‎ (101 revisions)
  97. Task 7: Research SNPs‏‎ (100 revisions)
  98. Sequence Alignments Gaucher Disease‏‎ (100 revisions)
  99. Task 9: Normal Mode Analysis‏‎ (100 revisions)
  100. Mapping SNPs BCKDHA‏‎ (97 revisions)

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