Pages with the most revisions
From Bioinformatikpedia
Showing below up to 50 results in range #101 to #150.
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- Sequence-based mutation analysis TSD (109 revisions)
- Canavan Disease (108 revisions)
- Fabry Disease 2012 (108 revisions)
- Normal mode analysis (107 revisions)
- MD simulation analysis TSD (107 revisions)
- Structure-based mutation analysis TSD (106 revisions)
- Task 3 (MSUD) (106 revisions)
- Phenylketonuria 2011 (105 revisions)
- Task 2: Sequence alignments (sequence searches and multiple alignments) (104 revisions)
- Hemochromatosis Normal modes (104 revisions)
- Sequence-based mutation analysis GLA (102 revisions)
- Gaucher Disease: Task 10 - Normal mode analysis (102 revisions)
- Structure-based mutation analysis GLA (102 revisions)
- Canavan Task 7 - Structure-based mutation analysis (102 revisions)
- Fabry:Homology based structure predictions (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)
- Predicting the Effect of SNPs (PKU) (95 revisions)
- Task 9: Structure-based mutation analysis (92 revisions)
- Maple syrup urine disease 2011 (92 revisions)
- Normal Mode Analysis of Glucocerebrosidase (91 revisions)
- Researching SNPs (Phenylketonuria) (91 revisions)
- Sequence Alignment GLA (89 revisions)
- Sequence Alignments HEXA (89 revisions)
- Structure-Based Mutation Analysis Hemochromatosis (87 revisions)
- Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal (86 revisions)
- Resource software (84 revisions)
- Canavan Disease: Task 05 - Homology Modelling (84 revisions)
- Maple Syrup Urine Disease 2012 (84 revisions)
- Task 6: Protein structure prediction from evolutionary sequence variation (83 revisions)
- Normal Mode Analysis of ARSA (82 revisions)
- Fabry:Normal mode analysis (81 revisions)
- Fabry Disease 2011 (81 revisions)
- Gaucher Disease: Task 09 - Lab Journal (79 revisions)
- Researching And Mapping Point Mutations Hemochromatosis (79 revisions)
- Researching SNPs (PKU) (79 revisions)
- Rs61731240 (78 revisions)
- Hemochromatosis 2012 (78 revisions)
- Fabry:Mapping point mutations (77 revisions)
- Task 3 - Sequence-based predictions 2011 (77 revisions)
- Metachromatic leukodystrophy reference aminoacids (77 revisions)
- Normal Mode Analysis Hemochromatosis (76 revisions)
- Researching SNPs Gaucher Disease (76 revisions)
- Task 4: Homology-based structure prediction (75 revisions)
- Phenylketonuria (73 revisions)
- Task 2 (MSUD) (73 revisions)
- Structure-based mutation analysis ARSA (72 revisions)
