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- 1OGS EVcouplings Configuration DI
- Build mutation Script
- Canavan Disease: Task 02 - Journal
- Canavan Disease: Task 03 - Journal
- Canavan Disease: Task 04 - Journal
- Canavan Disease: Task 07 - Journal
- Canavan Disease: Task 11 - Molecular Dynamics Simulation
- Canavan Disease 2011
- Canavans Disease
- ClustalW Above 60
- ClustalW Below 30
- ClustalW whole
- Cys152arg
- Disease list 2011
- Disorder general
- Disorder gerneral
- Fabry Disease 2011
- Fabry Disease Selected Mutations
- Foldx hexa
- GO Terms A4 HUMAN
- GO Terms BACR HALSA
- GO Terms HEXA HUMAN
- GO Terms INSL5 HUMAN
- GO Terms LAMP1 HUMAN
- GO Terms RET4 HUMAN
- GO annotation of the proteins
- GO terms general
- Gaucher Disease: Task 06 - Lab Journal
- Gaucher Disease 2011
- Go annotations here
- Hemo seq based pred
- Hemochromatosis 2011
- Hereditary hemochromatosis
- Hex A Reference sequence
- Homology-modelling HEXA/3bc9.pir
- Homology-modelling HEXA/3cui.pir
- Homology-modelling HEXA/3lut.pir,
- Homology-modelling HEXA/hh search output
- Homology-modelling HEXA/swissmodel 3CUI
- Homology-modelling HEXA/swissmodel 3LUT
- Homology-modelling HEXA/swissmodel ali
- Homology based structure prediction (Phenylketonuria)
- Imm ev hotspots
- MAFFT 30
- MAFFT 360
- MAFFT 60
- MAFFT whole
- MD Mutation436
- MD Mutation485
- MD WildType
- MD WildeType
- MSUD Q80E
- Main Page
- MapleSyrupDisease disease causing mutations
- Maple syrup urine disease 2011
- Mapping SNPs HEXA/DETAIL
- Metachromatic leukodistrophy
- Metachromatic leukodystrophy 2011
- Missense nonsense CFTR
- Modeller protocol BCKDHA
- Modeller protokoll BCKDHA
- Multiple Sequence Alignment: ClustalW - set 1
- Multiple Sequence Alignment: ClustalW - set 2
- Multiple Sequence Alignment: ClustalW - set 3
- Multiple Sequence Alignment: Espresso - set 1
- Multiple Sequence Alignment: Muscle - set 1
- Multiple Sequence Alignment: Muscle - set 2
- Multiple Sequence Alignment: Muscle - set 3
- Multiple Sequence Alignment: T-Coffee - set 1
- Multiple Sequence Alignment: T-Coffee - set 2
- Multiple Sequence Alignment: T-Coffee - set 3
- Normal mode analysis (Phenylketonuria)
- P01112 EVcouplings Configuration DI
- P01112 EVcouplings Configuration PLM
- PSIBlasttrainer.pl
- Pearson cc.r (Gaucher Disease)
- Phenylketonuria/Task2/Scripts
- Phenylketonuria/Task2 Scripts
- Phenylketonuria/Task6 Scripts
- Phenylketonuria 2011
- Prediction of Disordered Regions
- Prediction of transmembrane alpha-helices and signal peptides A4 HUMAN
- Prediction of transmembrane alpha-helices and signal peptides BACR HALSA
- Prediction of transmembrane alpha-helices and signal peptides HEXA HUMAN
- Prediction of transmembrane alpha-helices and signal peptides INSL5 HUMAN
- Prediction of transmembrane alpha-helices and signal peptides LAMP1 HUMAN
- Prediction of transmembrane alpha-helices and signal peptides RET4 HUMAN
- Protein Structure and Function Analysis (SS 2011)
- Protein Structure and Function Analysis (version: SS 2011)
- Protein Structure and Function Analysis (version: SS 2012)
- Protein structure prediction from evolutionary sequence variation (Phenylketonuria)
- Ras PLM Score Configuration
- Reference Sequence
- Reference sequence
- Researching SNPs (Phenylketonuria)
- Researching and mapping point mutations TSD Journal
- Rs1054374
- Rs1054374 SNAP
- Rs121907967
- Rs121907967 SNAP
- Rs121907968
- Rs121907968 SNAP
- Rs121907974
- Rs121907974 SNAP
- Rs121907979
- Rs121907979 SNAP
- Rs121907982
- Rs121907982 SNAP
- Rs1800430
- Rs1800430 SNAP
- Rs1800431
- Rs4777505
- Rs4777505 SNAP
- Rs61731240
- Rs61731240 SNAP
- Rs61747114
- Rs61747114 SNAP
- Run MD HEXA
- Runscript BCKDHA
- SNPs for Hema
- Secondary Structure Prediction
- Secstr general
- Seq.-based mut. analysis HEXA
- Sequence-based mutation analysis (Phenylketonuria)
- Sequence-based mutation analysis HEXA/Mutation Summary
- Sequence-based mutation analysis HEXA/rs4777505 SNAP
- Structural Alignments (Phenylketonuria)
- Structure-based mutation analysis (Phenylketonuria)
- Structure pdb
- Structures for P00439 in PDB
- TSD Modeller 3gh5 Edited Alignment
- Task3 protocoll
- Task 10 - Molecular Dynamics Simulations 2011
- Task 2 - Alignments with PAH Reference
- Task 3 - Normal Mode Analysis
- Task 3 - Sequence-based predictions 2011
- Task 5 - Mapping SNPs 2011
- Task 6 - EVfold
- Task 6 - Sequence-based mutation analysis 2011
- Task 7 - Structure-based mutation analysis 2011
- Task 8 - Molecular Dynamics Simulations 2011
- Task 9 - Normal Mode Analysis 2011
- Task alignments 2011
- Task homologyModelling 2011
- Task sequenceAnalysis
- Tastk 2
- Tastk 2: Alignments
- Tay-Sachs Disease 2011
- Tcoffee 30
- Tcoffee 60
- Tcoffee whole
- Transmembrane signal peptide general
- White brain matter