Pages with the most revisions
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Showing below up to 250 results in range #101 to #350.
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- Sequence-based mutation analysis TSD (109 revisions)
- Fabry Disease 2012 (108 revisions)
- Canavan Disease (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)
- Hemochromatosis Normal modes (104 revisions)
- Task 2: Sequence alignments (sequence searches and multiple alignments) (104 revisions)
- Canavan Task 7 - Structure-based mutation analysis (102 revisions)
- Fabry:Homology based structure predictions (102 revisions)
- Sequence-based mutation analysis GLA (102 revisions)
- Gaucher Disease: Task 10 - Normal mode analysis (102 revisions)
- Structure-based mutation analysis GLA (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)
- Canavan Disease: Task 05 - Homology Modelling (84 revisions)
- Maple Syrup Urine Disease 2012 (84 revisions)
- Resource software (84 revisions)
- Task 6: Protein structure prediction from evolutionary sequence variation (83 revisions)
- Normal Mode Analysis of ARSA (82 revisions)
- Fabry Disease 2011 (81 revisions)
- Fabry:Normal mode analysis (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)
- ARS A Sequence alignments (72 revisions)
- Structure-based mutation analysis ARSA (72 revisions)
- Protein Structure and Function Analysis (SS 2013) (72 revisions)
- Maple Syrup Urine Disease (71 revisions)
- Fabry:Sequence-based mutation analysis (70 revisions)
- Fabry:Sequence alignments (sequence searches and multiple alignments) (70 revisions)
- Sequence Alignments BCKDHA (70 revisions)
- Normal Mode Analysis (PKU) (69 revisions)
- Task 2: Multiple Sequence Alignment (68 revisions)
- Fabry:Sequence alignments (sequence searches and multiple alignments):Results (68 revisions)
- Structure-based mutation analysis HEXA (68 revisions)
- Normal mode analysis Gaucher Disease (67 revisions)
- Protein Structure and Function Analysis (version: SS 2011) (66 revisions)
- Gaucher Disease - Task 06 - Lab Journal (65 revisions)
- Lab journal task 8 (64 revisions)
- Gaucher Disease: Task 04 - Lab Journal (64 revisions)
- Structure-based mutation analysis Gaucher Disease (64 revisions)
- Canavan Disease: Task 04 - Structural Alignments (64 revisions)
- Tay-Sachs Disease 2011 (62 revisions)
- Rs121907974 (61 revisions)
- Glucocerebrosidase mapping snps (59 revisions)
- Task 7 (MSUD) (58 revisions)
- ASPA Sequence Based Predictions (58 revisions)
- AllBio Forum (57 revisions)
- Task 6 (MSUD) (56 revisions)
- Phenylketonuria 2012 (53 revisions)
- Rs4777505 (53 revisions)
- Mapping mutations of ARS A (53 revisions)
- Fabry:Structure-based mutation analysis (53 revisions)
- Sequence Alignments (52 revisions)
- Task 9 - Normal Mode Analysis (51 revisions)
- Gaucher Disease: Task 08 - LabJournal (50 revisions)
- Molecular Dynamics Simulations (50 revisions)
- Rs1800430 (48 revisions)
- Lab Journal - Task 8 (PAH) (48 revisions)
- Rs61747114 (47 revisions)
- Task 5: Researching SNPs (46 revisions)
- Lab journal task 4 (46 revisions)
- Task 6 - Protein structure prediction from evolutionary sequence variation (46 revisions)
- Researching SNPs TSD Journal (45 revisions)
- Molecular Dynamics Analysis GLA (44 revisions)
- Reference Sequence BCKDHA (44 revisions)
- Molecular Dynamics Simulations (PKU) (44 revisions)
- Homology modelling Gaucher Disease (44 revisions)
- Canavan Disease: Task 06 - Protein Structure Prediction (42 revisions)
- Normal mode analysis GLA (42 revisions)
- Gaucher Disease: Task 02 - Lab Journal (42 revisions)
- Fabry:Sequence-based analyses (41 revisions)
- Rs121907982 (41 revisions)
- Fabry:Homology based structure predictions/Journal (41 revisions)
- Lab Journal - Task 6 (PAH) (41 revisions)
- Task 5 - Researching SNPs (40 revisions)
- Task 9 (MSUD) (39 revisions)
- Task 5 - Mapping SNPs 2011 (39 revisions)
- Rs1054374 (39 revisions)
- Task 4 (MSUD) (39 revisions)
- Task 9: MSUD - Normal Mode Analysis (39 revisions)
- Fabry:Sequence-based mutation analysis/Journal (38 revisions)
- Task 5: Mapping point mutations (36 revisions)
- Lab Journal of Task 3 (MSUD) (36 revisions)
- Task 5 (MSUD) (36 revisions)
- Canavan Task 8 - Molecular Dynamics Simulations (36 revisions)
- Molecular Dynamics Simulations Analysis Gaucher Disease (36 revisions)
- Metachromatic leukodystrophy (35 revisions)
- Task 10 - Journal (PKU) (34 revisions)
- Gaucher Disease: Task 03 - Lab Journal (34 revisions)
- Molecular Dynamics Simulations TSD (33 revisions)
- Metachromatic leukodystrophy 2011 (33 revisions)
- Rs121907979 (33 revisions)
- Task 3 - Normal Mode Analysis (32 revisions)
- Task alignments (32 revisions)
- Lab Journal - Task 5 (PAH) (32 revisions)
- Sequence Alignments Protocol TSD (32 revisions)
- Rs121907968 (32 revisions)
- Gaucher Disease: Task 05 - Lab Journal (32 revisions)
- Protein Structure and Function Analysis (version: SS 2012) (31 revisions)
- Rs121907967 (31 revisions)
- ARSA search protocol (31 revisions)
- Lab Journal - Task 4 (PAH) (30 revisions)
- Task 10 (MSUD) (30 revisions)
- Lab journal Task 7 (28 revisions)
- Workflow homology modelling glucocerebrosidase (28 revisions)
- CD task2 protocol (27 revisions)
- Sequence-based predictions Protocol TSD (27 revisions)
- Gaucher Task07 Protocol (27 revisions)
- M82L (26 revisions)
- Sequence and structure based mutation analysis of GBA (25 revisions)
- Molecular Dynamics Simulations Hemochromatosis (25 revisions)
- Task 8 (MSUD) (25 revisions)
- Task2 Hemochromatosis Protocol (25 revisions)
- Task 8 - Molecular Dynamics Simulations 2011 (25 revisions)
- Task alignments 2012 (25 revisions)
- Phenylketonuria/Task3/Scripts (25 revisions)
- Modeller protocol BCKDHA (24 revisions)
- Lab journal (24 revisions)
- BCKDHA (24 revisions)
- Canavan Disease: Task 02 - Journal (24 revisions)
- Task 2 lab journal (MSUD) (24 revisions)
- Lab Journal - Task 9 (PAH) (24 revisions)
- Lab Journal Hemochromatosis Task9 (23 revisions)
- Mapping SNPs GLA (23 revisions)
- Fabry:Mapping point mutations/Journal (23 revisions)
- Table Templates (21 revisions)
- Task 1: Collect information on the individual disease (21 revisions)
- Lab Journal - Task 3 (PAH) (21 revisions)
- TSD Homology modelling protocol (21 revisions)
- Gaucher Task06 Protocol (21 revisions)
- Task 7 - Structure-based mutation analysis (20 revisions)
- Example/Template (20 revisions)
- Sequence-based mutation analysis TSD Journal (20 revisions)
- PAH Structure (20 revisions)
- Structure-based mutation analysis TSD Journal (19 revisions)
- CD task4 protocol (19 revisions)
- Canavan Disease: Task 07 - Supplement (19 revisions)
- ASPA Normal Mode Analysis (19 revisions)
- CD task10 protocol (18 revisions)
- Fabry:Sequence-based analyses/Journal (18 revisions)
- Task 8: Molecular Dynamics Simulations (17 revisions)
- CD task7 protocol (17 revisions)
- Protocol BCKDHA MD (17 revisions)
- Fabry:Sequence alignments (sequence searches and multiple alignments)/Scripts (17 revisions)
- Canavan Disease 2011 (17 revisions)
- Fabry:Molecular Dynamics Simulations (17 revisions)
- Phenylketonuria/Task2 Scripts (17 revisions)
- Run MD HEXA (17 revisions)
- Fabry:Structure-based mutation analysis/Journal (17 revisions)
- Task 10 - Normal Mode Analysis (16 revisions)
- Lab Journal of Task 5 (MSUD) (16 revisions)
- Q125E (16 revisions)
- Molecular Dynamics Simulations BCKDHA (16 revisions)
- Task homologyModelling (16 revisions)
- Task homologyModelling 2011 (16 revisions)
- Reference amino acid sequence of Glucocerebrosidase (15 revisions)
- Task 9 Structure-based mutation analysis (15 revisions)
- Parse output.pl (15 revisions)
- Psipred (15 revisions)
- Collection of scripts (15 revisions)
- Task 6 - Sequence-based mutation analysis (14 revisions)
- Go annotations here (14 revisions)
- ASPA Homology Modelling (14 revisions)
- Protocol-msud-task5 protocol (14 revisions)
- Disease list 2011 (14 revisions)
- Task 9 Lab Journal (MSUD) (14 revisions)
- Phenylalanine hydroxylase reference (14 revisions)
- Task Structural Alignments (14 revisions)
- Task3 Hemochromatosis Protocol (14 revisions)
- MSUP-task7-journal (14 revisions)
- Run.pl (14 revisions)
- Main Page (14 revisions)
- Fabian Grandke (14 revisions)
- DLD (13 revisions)
- Y438N (13 revisions)
- CD task6 protocol (13 revisions)
- Journal structure based mutation analysis (PKU) (13 revisions)
- Task alignments 2011 (13 revisions)
- Seq.-based mut. analysis HEXA (13 revisions)
- Phenylketonuria/Task2/Scripts (13 revisions)
- Task diseaseInfo (13 revisions)
- Task3 protocoll (13 revisions)
- Task 2 - Alignments with PAH Reference (13 revisions)
- Task4 Hemochromatosis Protocol (13 revisions)
- Task5 Hemochromatosis Protocol (13 revisions)
- ASPA Mapping SNPs (12 revisions)
- Mapping SNPs HEXA/DETAIL (12 revisions)
- Resource wiki (12 revisions)
- Multiple Sequence Alignment: ClustalW - set 1 (12 revisions)
- Normal mode analysis GLA supplementary (12 revisions)
- Lab Journal - Task 7 (PAH) (12 revisions)
- DBT (12 revisions)
- Fabry:Normal mode analysis/Journal (11 revisions)
- Phenylketonuria/Task6 Scripts (11 revisions)
- Reference Sequence (11 revisions)
- Task 6 Lab Journal (MSUD) (11 revisions)
- Disease list (11 revisions)
- Hemochromatosis SS Alignments (11 revisions)
- Homology Based Structure Predictions Hemochromatosis Alignments (11 revisions)
- Supplementary data normal mode glucocerebrosidase (11 revisions)
- Canavan Disease: Task 09 - Supplement (11 revisions)
- Task 8 Lab Journal (MSUD) (11 revisions)
- Using Modeller for TASK 4 (11 revisions)
- Task6 Hemochromatosis Protocol (10 revisions)
- Canavan Disease: Task 07 - Journal (10 revisions)
- Protocol (10 revisions)
- Sequence-based mutation analysis BCKDHA protocol (10 revisions)
- Animated Gifs (10 revisions)
- MD WildeType (10 revisions)
- ASPA Sequence Based Mutation Analysis (10 revisions)
- MD simulation analysis TSD Journal (10 revisions)
- ASPA Structure Based Mutation Analysis (10 revisions)
- Task 7 - Structure-based mutation analysis 2011 (10 revisions)
- F409C (10 revisions)
- Task 4 Protocol (10 revisions)
- Task 8: MSUD - Molecular Dynamics Simulations (10 revisions)
- C264W (10 revisions)
- Y166N (9 revisions)
- G249S (9 revisions)
- CD task5 protocol (9 revisions)
- Task 11 - Molecular Dynamics Simulation (9 revisions)
- Disopred (9 revisions)
- CD task8 protocol (9 revisions)
- Prediction of Disordered Regions (9 revisions)