Pages with the most revisions
From Bioinformatikpedia
Showing below up to 100 results in range #21 to #120.
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- Sequence-based mutation analysis BCKDHA (237 revisions)
- Gaucher Disease: Task 05 - Homology Modelling (236 revisions)
- Task 4: Structural Alignments (223 revisions)
- Task 3: Sequence-based predictions (209 revisions)
- Homology based structure prediction (Phenylketonuria) (205 revisions)
- Hemochromatosis: Sequence based predictions (200 revisions)
- Gaucher Disease: Task 04 - Structural Alignment (196 revisions)
- Structure-based mutation analysis (196 revisions)
- Sequence-based mutation analysis (Phenylketonuria) (195 revisions)
- Mapping SNPs HEXA (192 revisions)
- Sequence-based predictions GLA (190 revisions)
- Homology modelling TSD (189 revisions)
- Sequence-based analyses of ARS A (188 revisions)
- Task 4: Homology based structure predictions (182 revisions)
- Sequence-based predictions TSD (181 revisions)
- Molecular Dynamics Simulations HEXA (177 revisions)
- Sequence-Based Mutation Analysis Hemochromatosis (177 revisions)
- Sequence-based analyses Gaucher Disease (176 revisions)
- Molecular Dynamics Simulations Analysis (PKU) (174 revisions)
- Gaucher Disease (174 revisions)
- Gaucher Disease: Task 07 - Research SNPs (173 revisions)
- Homology Modeling of ARS A (170 revisions)
- Sequence based mutation analysis of GBA (169 revisions)
- Hemochromatosis 2011 (168 revisions)
- Sequence-based mutation analysis (168 revisions)
- Hemochromatosis (167 revisions)
- Task 6: Sequence-based mutation analysis (166 revisions)
- Normal mode analysis HEXA (165 revisions)
- Canavan Task 10 - Molecular Dynamics Simulations (164 revisions)
- Sequence Alignments TSD (164 revisions)
- Task 2: Alignments (163 revisions)
- Homology Based Structure Predictions Hemochromatosis (162 revisions)
- Canavan Task 9 - Normal Mode Analysis (162 revisions)
- Sequence-based mutation analysis Gaucher Disease (161 revisions)
- Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation (160 revisions)
- Homology-based structure prediction (PKU) (158 revisions)
- Gaucher Disease: Task 08 - Sequence-based mutation analysis (156 revisions)
- Sequence-based mutation analysis of ARSA (156 revisions)
- Structure-based mutation analysis (Phenylketonuria) (155 revisions)
- Protein structure prediction from evolutionary sequence variation (Phenylketonuria) (153 revisions)
- Structure-based mutation analysis (PKU) (153 revisions)
- Sequence-based predictions (PKU) (152 revisions)
- Gaucher Disease: Task 09 - Structure-based mutation analysis (147 revisions)
- Sequence Alignments Hemochromatosis (143 revisions)
- Canavan Disease: Task 07 - Researching SNPs (142 revisions)
- Structure-based mutation analysis BCKDHA (142 revisions)
- Sequence-based mutation analysis HEXA (141 revisions)
- MD Mutation436 (140 revisions)
- Normal mode analysis (Phenylketonuria) (140 revisions)
- Normal Mode Analysis BCKDHA (139 revisions)
- Task 3: odba human Sequence-based predictions (132 revisions)
- Glucocerebrosidase homology modelling (132 revisions)
- Canavan Disease: Task 08 - Sequence-based Mutation Analysis (130 revisions)
- Gaucher Disease 2012 (130 revisions)
- Task 7: MSUD - Structure-based mutation analysis (129 revisions)
- Task 3 - Sequence-based predictions (129 revisions)
- Mapping SNPs (129 revisions)
- Task 10: Molecular Dynamics Analysis (129 revisions)
- Structural Alignments (Phenylketonuria) (127 revisions)
- Tay-Sachs Disease 2012 (127 revisions)
- Structure based mutation analysis of GBA (126 revisions)
- Task 5 - Mapping SNPs Canavan (126 revisions)
- Sequence Search and Multiple Sequence Alignment (PKU) (126 revisions)
- Task 5: Homology Modeling (125 revisions)
- Sequence and multiple alignments (123 revisions)
- Homology Modelling GLA (122 revisions)
- Molecular Dynamics Simulations Analysis Hemochromatosis (122 revisions)
- Task 8: Sequence-based mutation analysis (122 revisions)
- Task 6: MSUD - Sequence-based mutation analysis (120 revisions)
- Canavan Disease: Task 09 - Structure-based Mutation Analysis (120 revisions)
- Normal mode analysis TSD (119 revisions)
- Task 7: Structure-based mutation analysis (119 revisions)
- MD WildType (117 revisions)
- Canavan Disease: Task 03 - Sequence-based Predictions (116 revisions)
- Researching SNPs TSD (116 revisions)
- Molecular Dynamics Simulations Analysis of Glucocerebrosidase (116 revisions)
- Sequence-Based Predictions Hemochromatosis (114 revisions)
- Gaucher Disease 2011 (114 revisions)
- Glucocerebrosidase sequence alignments (112 revisions)
- Canavan Disease: Task 10 - Normal Mode Analysis (112 revisions)
- Sequence-based mutation analysis TSD (109 revisions)
- Fabry Disease 2012 (108 revisions)
- Canavan Disease (108 revisions)
- MD simulation analysis TSD (107 revisions)
- Normal mode analysis (107 revisions)
- Task 3 (MSUD) (106 revisions)
- Structure-based mutation analysis TSD (106 revisions)
- Phenylketonuria 2011 (105 revisions)
- Hemochromatosis Normal modes (104 revisions)
- Task 2: Sequence alignments (sequence searches and multiple alignments) (104 revisions)
- Sequence-based mutation analysis GLA (102 revisions)
- Canavan Task 7 - Structure-based mutation analysis (102 revisions)
- Fabry:Homology based structure predictions (102 revisions)
- Structure-based mutation analysis GLA (102 revisions)
- Gaucher Disease: Task 10 - Normal mode analysis (102 revisions)
- MD Mutation485 (101 revisions)
- Task 7: Research SNPs (100 revisions)
- Sequence Alignments Gaucher Disease (100 revisions)
- Task 9: Normal Mode Analysis (100 revisions)
- Mapping SNPs BCKDHA (97 revisions)