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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. Homology-modelling HEXA‏‎ (241 revisions)
  20. Canavan Task 2 - Sequence alignments‏‎ (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. Sequence Alignments TSD‏‎ (164 revisions)
  50. Canavan Task 10 - Molecular Dynamics Simulations‏‎ (164 revisions)
  51. Task 2: Alignments‏‎ (163 revisions)
  52. Homology Based Structure Predictions Hemochromatosis‏‎ (162 revisions)
  53. Canavan Task 9 - Normal Mode Analysis‏‎ (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. Gaucher Disease: Task 08 - Sequence-based mutation analysis‏‎ (156 revisions)
  58. Sequence-based mutation analysis of ARSA‏‎ (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. Canavan Disease: Task 07 - Researching SNPs‏‎ (142 revisions)
  66. Structure-based mutation analysis BCKDHA‏‎ (142 revisions)
  67. Sequence-based mutation analysis HEXA‏‎ (141 revisions)
  68. MD Mutation436‏‎ (140 revisions)
  69. Normal mode analysis (Phenylketonuria)‏‎ (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. Canavan Disease: Task 08 - Sequence-based Mutation Analysis‏‎ (130 revisions)
  74. Gaucher Disease 2012‏‎ (130 revisions)
  75. Task 7: MSUD - Structure-based mutation analysis‏‎ (129 revisions)
  76. Task 3 - Sequence-based predictions‏‎ (129 revisions)
  77. Task 10: Molecular Dynamics Analysis‏‎ (129 revisions)
  78. Mapping SNPs‏‎ (129 revisions)
  79. Structural Alignments (Phenylketonuria)‏‎ (127 revisions)
  80. Tay-Sachs Disease 2012‏‎ (127 revisions)
  81. Task 5 - Mapping SNPs Canavan‏‎ (126 revisions)
  82. Sequence Search and Multiple Sequence Alignment (PKU)‏‎ (126 revisions)
  83. Structure based mutation analysis of GBA‏‎ (126 revisions)
  84. Task 5: Homology Modeling‏‎ (125 revisions)
  85. Sequence and multiple alignments‏‎ (123 revisions)
  86. Homology Modelling GLA‏‎ (122 revisions)
  87. Molecular Dynamics Simulations Analysis Hemochromatosis‏‎ (122 revisions)
  88. Task 8: Sequence-based mutation analysis‏‎ (122 revisions)
  89. Canavan Disease: Task 09 - Structure-based Mutation Analysis‏‎ (120 revisions)
  90. Task 6: MSUD - Sequence-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. Molecular Dynamics Simulations Analysis of Glucocerebrosidase‏‎ (116 revisions)
  95. Canavan Disease: Task 03 - Sequence-based Predictions‏‎ (116 revisions)
  96. Researching SNPs TSD‏‎ (116 revisions)
  97. Gaucher Disease 2011‏‎ (114 revisions)
  98. Sequence-Based Predictions Hemochromatosis‏‎ (114 revisions)
  99. Canavan Disease: Task 10 - Normal Mode Analysis‏‎ (112 revisions)
  100. Glucocerebrosidase sequence alignments‏‎ (112 revisions)
  101. Sequence-based mutation analysis TSD‏‎ (109 revisions)
  102. Canavan Disease‏‎ (108 revisions)
  103. Fabry Disease 2012‏‎ (108 revisions)
  104. Normal mode analysis‏‎ (107 revisions)
  105. MD simulation analysis TSD‏‎ (107 revisions)
  106. Task 3 (MSUD)‏‎ (106 revisions)
  107. Structure-based mutation analysis TSD‏‎ (106 revisions)
  108. Phenylketonuria 2011‏‎ (105 revisions)
  109. Task 2: Sequence alignments (sequence searches and multiple alignments)‏‎ (104 revisions)
  110. Hemochromatosis Normal modes‏‎ (104 revisions)
  111. Fabry:Homology based structure predictions‏‎ (102 revisions)
  112. Sequence-based mutation analysis GLA‏‎ (102 revisions)
  113. Gaucher Disease: Task 10 - Normal mode analysis‏‎ (102 revisions)
  114. Structure-based mutation analysis GLA‏‎ (102 revisions)
  115. Canavan Task 7 - Structure-based mutation analysis‏‎ (102 revisions)
  116. MD Mutation485‏‎ (101 revisions)
  117. Task 7: Research SNPs‏‎ (100 revisions)
  118. Sequence Alignments Gaucher Disease‏‎ (100 revisions)
  119. Task 9: Normal Mode Analysis‏‎ (100 revisions)
  120. Mapping SNPs BCKDHA‏‎ (97 revisions)
  121. Predicting the Effect of SNPs (PKU)‏‎ (95 revisions)
  122. Task 9: Structure-based mutation analysis‏‎ (92 revisions)
  123. Maple syrup urine disease 2011‏‎ (92 revisions)
  124. Normal Mode Analysis of Glucocerebrosidase‏‎ (91 revisions)
  125. Researching SNPs (Phenylketonuria)‏‎ (91 revisions)
  126. Sequence Alignment GLA‏‎ (89 revisions)
  127. Sequence Alignments HEXA‏‎ (89 revisions)
  128. Structure-Based Mutation Analysis Hemochromatosis‏‎ (87 revisions)
  129. Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal‏‎ (86 revisions)
  130. Resource software‏‎ (84 revisions)
  131. Maple Syrup Urine Disease 2012‏‎ (84 revisions)
  132. Canavan Disease: Task 05 - Homology Modelling‏‎ (84 revisions)
  133. Task 6: Protein structure prediction from evolutionary sequence variation‏‎ (83 revisions)
  134. Normal Mode Analysis of ARSA‏‎ (82 revisions)
  135. Fabry:Normal mode analysis‏‎ (81 revisions)
  136. Fabry Disease 2011‏‎ (81 revisions)
  137. Gaucher Disease: Task 09 - Lab Journal‏‎ (79 revisions)
  138. Researching And Mapping Point Mutations Hemochromatosis‏‎ (79 revisions)
  139. Researching SNPs (PKU)‏‎ (79 revisions)
  140. Rs61731240‏‎ (78 revisions)
  141. Hemochromatosis 2012‏‎ (78 revisions)
  142. Fabry:Mapping point mutations‏‎ (77 revisions)
  143. Task 3 - Sequence-based predictions 2011‏‎ (77 revisions)
  144. Metachromatic leukodystrophy reference aminoacids‏‎ (77 revisions)
  145. Normal Mode Analysis Hemochromatosis‏‎ (76 revisions)
  146. Researching SNPs Gaucher Disease‏‎ (76 revisions)
  147. Task 4: Homology-based structure prediction‏‎ (75 revisions)
  148. Phenylketonuria‏‎ (73 revisions)
  149. Task 2 (MSUD)‏‎ (73 revisions)
  150. Structure-based mutation analysis ARSA‏‎ (72 revisions)
  151. Protein Structure and Function Analysis (SS 2013)‏‎ (72 revisions)
  152. ARS A Sequence alignments‏‎ (72 revisions)
  153. Maple Syrup Urine Disease‏‎ (71 revisions)
  154. Fabry:Sequence-based mutation analysis‏‎ (70 revisions)
  155. Fabry:Sequence alignments (sequence searches and multiple alignments)‏‎ (70 revisions)
  156. Sequence Alignments BCKDHA‏‎ (70 revisions)
  157. Normal Mode Analysis (PKU)‏‎ (69 revisions)
  158. Task 2: Multiple Sequence Alignment‏‎ (68 revisions)
  159. Fabry:Sequence alignments (sequence searches and multiple alignments):Results‏‎ (68 revisions)
  160. Structure-based mutation analysis HEXA‏‎ (68 revisions)
  161. Normal mode analysis Gaucher Disease‏‎ (67 revisions)
  162. Protein Structure and Function Analysis (version: SS 2011)‏‎ (66 revisions)
  163. Gaucher Disease - Task 06 - Lab Journal‏‎ (65 revisions)
  164. Lab journal task 8‏‎ (64 revisions)
  165. Gaucher Disease: Task 04 - Lab Journal‏‎ (64 revisions)
  166. Structure-based mutation analysis Gaucher Disease‏‎ (64 revisions)
  167. Canavan Disease: Task 04 - Structural Alignments‏‎ (64 revisions)
  168. Tay-Sachs Disease 2011‏‎ (62 revisions)
  169. Rs121907974‏‎ (61 revisions)
  170. Glucocerebrosidase mapping snps‏‎ (59 revisions)
  171. Task 7 (MSUD)‏‎ (58 revisions)
  172. ASPA Sequence Based Predictions‏‎ (58 revisions)
  173. AllBio Forum‏‎ (57 revisions)
  174. Task 6 (MSUD)‏‎ (56 revisions)
  175. Rs4777505‏‎ (53 revisions)
  176. Mapping mutations of ARS A‏‎ (53 revisions)
  177. Fabry:Structure-based mutation analysis‏‎ (53 revisions)
  178. Phenylketonuria 2012‏‎ (53 revisions)
  179. Sequence Alignments‏‎ (52 revisions)
  180. Task 9 - Normal Mode Analysis‏‎ (51 revisions)
  181. Gaucher Disease: Task 08 - LabJournal‏‎ (50 revisions)
  182. Molecular Dynamics Simulations‏‎ (50 revisions)
  183. Rs1800430‏‎ (48 revisions)
  184. Lab Journal - Task 8 (PAH)‏‎ (48 revisions)
  185. Rs61747114‏‎ (47 revisions)
  186. Lab journal task 4‏‎ (46 revisions)
  187. Task 6 - Protein structure prediction from evolutionary sequence variation‏‎ (46 revisions)
  188. Task 5: Researching SNPs‏‎ (46 revisions)
  189. Researching SNPs TSD Journal‏‎ (45 revisions)
  190. Molecular Dynamics Analysis GLA‏‎ (44 revisions)
  191. Reference Sequence BCKDHA‏‎ (44 revisions)
  192. Molecular Dynamics Simulations (PKU)‏‎ (44 revisions)
  193. Homology modelling Gaucher Disease‏‎ (44 revisions)
  194. Normal mode analysis GLA‏‎ (42 revisions)
  195. Gaucher Disease: Task 02 - Lab Journal‏‎ (42 revisions)
  196. Canavan Disease: Task 06 - Protein Structure Prediction‏‎ (42 revisions)
  197. Fabry:Homology based structure predictions/Journal‏‎ (41 revisions)
  198. Lab Journal - Task 6 (PAH)‏‎ (41 revisions)
  199. Fabry:Sequence-based analyses‏‎ (41 revisions)
  200. Rs121907982‏‎ (41 revisions)
  201. Task 5 - Researching SNPs‏‎ (40 revisions)
  202. Task 5 - Mapping SNPs 2011‏‎ (39 revisions)
  203. Rs1054374‏‎ (39 revisions)
  204. Task 9: MSUD - Normal Mode Analysis‏‎ (39 revisions)
  205. Task 4 (MSUD)‏‎ (39 revisions)
  206. Task 9 (MSUD)‏‎ (39 revisions)
  207. Fabry:Sequence-based mutation analysis/Journal‏‎ (38 revisions)
  208. Canavan Task 8 - Molecular Dynamics Simulations‏‎ (36 revisions)
  209. Molecular Dynamics Simulations Analysis Gaucher Disease‏‎ (36 revisions)
  210. Task 5: Mapping point mutations‏‎ (36 revisions)
  211. Lab Journal of Task 3 (MSUD)‏‎ (36 revisions)
  212. Task 5 (MSUD)‏‎ (36 revisions)
  213. Metachromatic leukodystrophy‏‎ (35 revisions)
  214. Gaucher Disease: Task 03 - Lab Journal‏‎ (34 revisions)
  215. Task 10 - Journal (PKU)‏‎ (34 revisions)
  216. Molecular Dynamics Simulations TSD‏‎ (33 revisions)
  217. Metachromatic leukodystrophy 2011‏‎ (33 revisions)
  218. Rs121907979‏‎ (33 revisions)
  219. Task 3 - Normal Mode Analysis‏‎ (32 revisions)
  220. Task alignments‏‎ (32 revisions)
  221. Lab Journal - Task 5 (PAH)‏‎ (32 revisions)
  222. Sequence Alignments Protocol TSD‏‎ (32 revisions)
  223. Rs121907968‏‎ (32 revisions)
  224. Gaucher Disease: Task 05 - Lab Journal‏‎ (32 revisions)
  225. Rs121907967‏‎ (31 revisions)
  226. ARSA search protocol‏‎ (31 revisions)
  227. Protein Structure and Function Analysis (version: SS 2012)‏‎ (31 revisions)
  228. Lab Journal - Task 4 (PAH)‏‎ (30 revisions)
  229. Task 10 (MSUD)‏‎ (30 revisions)
  230. Lab journal Task 7‏‎ (28 revisions)
  231. Workflow homology modelling glucocerebrosidase‏‎ (28 revisions)
  232. Sequence-based predictions Protocol TSD‏‎ (27 revisions)
  233. Gaucher Task07 Protocol‏‎ (27 revisions)
  234. CD task2 protocol‏‎ (27 revisions)
  235. M82L‏‎ (26 revisions)
  236. Task 8 (MSUD)‏‎ (25 revisions)
  237. Task 8 - Molecular Dynamics Simulations 2011‏‎ (25 revisions)
  238. Task alignments 2012‏‎ (25 revisions)
  239. Task2 Hemochromatosis Protocol‏‎ (25 revisions)
  240. Phenylketonuria/Task3/Scripts‏‎ (25 revisions)
  241. Sequence and structure based mutation analysis of GBA‏‎ (25 revisions)
  242. Molecular Dynamics Simulations Hemochromatosis‏‎ (25 revisions)
  243. Lab journal‏‎ (24 revisions)
  244. BCKDHA‏‎ (24 revisions)
  245. Canavan Disease: Task 02 - Journal‏‎ (24 revisions)
  246. Task 2 lab journal (MSUD)‏‎ (24 revisions)
  247. Lab Journal - Task 9 (PAH)‏‎ (24 revisions)
  248. Modeller protocol BCKDHA‏‎ (24 revisions)
  249. Mapping SNPs GLA‏‎ (23 revisions)
  250. Fabry:Mapping point mutations/Journal‏‎ (23 revisions)

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