Pages with the most revisions

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Showing below up to 100 results in range #1 to #100.

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  1. Molecular Dynamics Analysis BCKDHA‏‎ (584 revisions)
  2. Sequence-based predictions (Phenylketonuria)‏‎ (500 revisions)
  3. Gaucher Disease: Task 03 - Sequence-based predictions‏‎ (471 revisions)
  4. Homology based structure predictions BCKDHA‏‎ (413 revisions)
  5. Secondary Structure Prediction BCKDHA‏‎ (408 revisions)
  6. Canavan Task 6 - Sequence-based mutation analysis‏‎ (377 revisions)
  7. Werner Syndrome‏‎ (363 revisions)
  8. Sequence-based predictions‏‎ (353 revisions)
  9. Canavan Task 4 - Homology based structure predictions‏‎ (350 revisions)
  10. Sequence-based predictions HEXA‏‎ (343 revisions)
  11. Canavan Task 3 - Sequence-based predictions‏‎ (336 revisions)
  12. Sequence searches and multiple sequence alignments (Phenylketonuria)‏‎ (304 revisions)
  13. Gaucher Disease: Task 02 - Alignments‏‎ (275 revisions)
  14. Canavan Disease: Task 02 - Alignments‏‎ (268 revisions)
  15. Canavan Disease 2012‏‎ (268 revisions)
  16. Molecular Dynamcis analysis‏‎ (262 revisions)
  17. Homology based structure predictions‏‎ (255 revisions)
  18. Glucocerebrosidase sequence based prediction‏‎ (251 revisions)
  19. Canavan Task 2 - Sequence alignments‏‎ (241 revisions)
  20. Homology-modelling HEXA‏‎ (241 revisions)
  21. Sequence-based mutation analysis BCKDHA‏‎ (237 revisions)
  22. Gaucher Disease: Task 05 - Homology Modelling‏‎ (236 revisions)
  23. Task 4: Structural Alignments‏‎ (223 revisions)
  24. Task 3: Sequence-based predictions‏‎ (209 revisions)
  25. Homology based structure prediction (Phenylketonuria)‏‎ (205 revisions)
  26. Hemochromatosis: Sequence based predictions‏‎ (200 revisions)
  27. Structure-based mutation analysis‏‎ (196 revisions)
  28. Gaucher Disease: Task 04 - Structural Alignment‏‎ (196 revisions)
  29. Sequence-based mutation analysis (Phenylketonuria)‏‎ (195 revisions)
  30. Mapping SNPs HEXA‏‎ (192 revisions)
  31. Sequence-based predictions GLA‏‎ (190 revisions)
  32. Homology modelling TSD‏‎ (189 revisions)
  33. Sequence-based analyses of ARS A‏‎ (188 revisions)
  34. Task 4: Homology based structure predictions‏‎ (182 revisions)
  35. Sequence-based predictions TSD‏‎ (181 revisions)
  36. Sequence-Based Mutation Analysis Hemochromatosis‏‎ (177 revisions)
  37. Molecular Dynamics Simulations HEXA‏‎ (177 revisions)
  38. Sequence-based analyses Gaucher Disease‏‎ (176 revisions)
  39. Molecular Dynamics Simulations Analysis (PKU)‏‎ (174 revisions)
  40. Gaucher Disease‏‎ (174 revisions)
  41. Gaucher Disease: Task 07 - Research SNPs‏‎ (173 revisions)
  42. Homology Modeling of ARS A‏‎ (170 revisions)
  43. Sequence based mutation analysis of GBA‏‎ (169 revisions)
  44. Hemochromatosis 2011‏‎ (168 revisions)
  45. Sequence-based mutation analysis‏‎ (168 revisions)
  46. Hemochromatosis‏‎ (167 revisions)
  47. Task 6: Sequence-based mutation analysis‏‎ (166 revisions)
  48. Normal mode analysis HEXA‏‎ (165 revisions)
  49. Canavan Task 10 - Molecular Dynamics Simulations‏‎ (164 revisions)
  50. Sequence Alignments TSD‏‎ (164 revisions)
  51. Task 2: Alignments‏‎ (163 revisions)
  52. Canavan Task 9 - Normal Mode Analysis‏‎ (162 revisions)
  53. Homology Based Structure Predictions Hemochromatosis‏‎ (162 revisions)
  54. Sequence-based mutation analysis Gaucher Disease‏‎ (161 revisions)
  55. Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation‏‎ (160 revisions)
  56. Homology-based structure prediction (PKU)‏‎ (158 revisions)
  57. Sequence-based mutation analysis of ARSA‏‎ (156 revisions)
  58. Gaucher Disease: Task 08 - Sequence-based mutation analysis‏‎ (156 revisions)
  59. Structure-based mutation analysis (Phenylketonuria)‏‎ (155 revisions)
  60. Structure-based mutation analysis (PKU)‏‎ (153 revisions)
  61. Protein structure prediction from evolutionary sequence variation (Phenylketonuria)‏‎ (153 revisions)
  62. Sequence-based predictions (PKU)‏‎ (152 revisions)
  63. Gaucher Disease: Task 09 - Structure-based mutation analysis‏‎ (147 revisions)
  64. Sequence Alignments Hemochromatosis‏‎ (143 revisions)
  65. Structure-based mutation analysis BCKDHA‏‎ (142 revisions)
  66. Canavan Disease: Task 07 - Researching SNPs‏‎ (142 revisions)
  67. Sequence-based mutation analysis HEXA‏‎ (141 revisions)
  68. Normal mode analysis (Phenylketonuria)‏‎ (140 revisions)
  69. MD Mutation436‏‎ (140 revisions)
  70. Normal Mode Analysis BCKDHA‏‎ (139 revisions)
  71. Glucocerebrosidase homology modelling‏‎ (132 revisions)
  72. Task 3: odba human Sequence-based predictions‏‎ (132 revisions)
  73. Gaucher Disease 2012‏‎ (130 revisions)
  74. Canavan Disease: Task 08 - Sequence-based Mutation Analysis‏‎ (130 revisions)
  75. Task 10: Molecular Dynamics Analysis‏‎ (129 revisions)
  76. Mapping SNPs‏‎ (129 revisions)
  77. Task 3 - Sequence-based predictions‏‎ (129 revisions)
  78. Task 7: MSUD - Structure-based mutation analysis‏‎ (129 revisions)
  79. Tay-Sachs Disease 2012‏‎ (127 revisions)
  80. Structural Alignments (Phenylketonuria)‏‎ (127 revisions)
  81. Sequence Search and Multiple Sequence Alignment (PKU)‏‎ (126 revisions)
  82. Structure based mutation analysis of GBA‏‎ (126 revisions)
  83. Task 5 - Mapping SNPs Canavan‏‎ (126 revisions)
  84. Task 5: Homology Modeling‏‎ (125 revisions)
  85. Sequence and multiple alignments‏‎ (123 revisions)
  86. Molecular Dynamics Simulations Analysis Hemochromatosis‏‎ (122 revisions)
  87. Task 8: Sequence-based mutation analysis‏‎ (122 revisions)
  88. Homology Modelling GLA‏‎ (122 revisions)
  89. Task 6: MSUD - Sequence-based mutation analysis‏‎ (120 revisions)
  90. Canavan Disease: Task 09 - Structure-based Mutation Analysis‏‎ (120 revisions)
  91. Task 7: Structure-based mutation analysis‏‎ (119 revisions)
  92. Normal mode analysis TSD‏‎ (119 revisions)
  93. MD WildType‏‎ (117 revisions)
  94. Canavan Disease: Task 03 - Sequence-based Predictions‏‎ (116 revisions)
  95. Molecular Dynamics Simulations Analysis of Glucocerebrosidase‏‎ (116 revisions)
  96. Researching SNPs TSD‏‎ (116 revisions)
  97. Gaucher Disease 2011‏‎ (114 revisions)
  98. Sequence-Based Predictions Hemochromatosis‏‎ (114 revisions)
  99. Glucocerebrosidase sequence alignments‏‎ (112 revisions)
  100. Canavan Disease: Task 10 - Normal Mode Analysis‏‎ (112 revisions)

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