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- Canavan Disease: Task 07 - Supplement
- Canavan Disease: Task 08 - Sequence-based Mutation Analysis
- Canavan Disease: Task 08 - Supplement
- Canavan Disease: Task 09 - Structure-based Mutation Analysis
- Canavan Disease: Task 09 - Supplement
- Canavan Disease: Task 10 - Normal Mode Analysis
- Canavan Disease: Task 11 - Molecular Dynamics Simulation
- Canavan Disease 2011
- Canavan Disease 2012
- Canavan Task 10 - Molecular Dynamics Simulations
- Canavan Task 2 - Sequence alignments
- Canavan Task 3 - Sequence-based predictions
- Canavan Task 4 - Homology based structure predictions
- Canavan Task 6 - Sequence-based mutation analysis
- Canavan Task 7 - Structure-based mutation analysis
- Canavan Task 8 - Molecular Dynamics Simulations
- Canavan Task 9 - Normal Mode Analysis
- Canavans Disease
- ClustalW Above 60
- ClustalW Below 30
- ClustalW whole
- CompareCath.py
- Compiled list of SNPS
- Cys152arg
- DBT
- DLD
- DbSNP Silent Mutations Parser
- Devide psiblast out.pl
- Disease list
- Disease list 2011
- Disopred
- Disorder general
- Disorder gerneral
- Dssp
- Example/Template
- Example sequence
- F409C
- FASTA
- Fabian Grandke
- Fabry:Alpha-galactosidase sequence
- Fabry:Annotated SNPs
- Fabry:Mapping point mutations/HGMD
- Fabry:Mapping point mutations/OMIM data
- Fabry:Mapping point mutations/SNPdbe data
- Fabry:Mapping point mutations/SNPedia data
- Fabry:Normal mode analysis/Deformation Energies
- Fabry:Sequence alignments (sequence searches and multiple alignments):Results
- Fabry:Structure-based mutation analysis/FoldXtables
- Fabry:Structure-based mutation analysis/MinimiseTables
- Fabry Disease Mutation Analysis Sequence PSSM
- Fabry Disease mutation analysis sequence msa sequences
- Fabry Disease sequence-based prediction of tm-helices and signal peptides A4 HUMAN
- Fabry Disease sequence-based prediction of tm-helices and signal peptides BARC HALSA
- Fabry Disease sequence-based prediction of tm-helices and signal peptides GLA
- Fabry Disease sequence-based prediction of tm-helices and signal peptides INSL5 HUMAN
- Fabry Disease sequence-based prediction of tm-helices and signal peptides LAMP1 HUMAN
- Fabry Disease sequence-based prediction of tm-helices and signal peptides RET4 HUMAN
- Fabry Disease swiss 1KTB graphics
- Fabry Disease swiss 3CC1 graphics
- Fabry Disease swiss 3HG3 graphics
- FoldX Difference Mutant/Wildtype
- Foldx hexa
- Format to wiki table.r
- G249S
- 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
- Gaucher Disease: Task 02 - Alignments
- Gaucher Disease: Task 02 - Lab Journal
- Gaucher Disease: Task 03 - Lab Journal
- Gaucher Disease: Task 03 - Sequence-based predictions
- Gaucher Disease: Task 04 - Lab Journal
- Gaucher Disease: Task 04 - Structural Alignment
- Gaucher Disease: Task 05 - Homology Modelling
- Gaucher Disease: Task 05 - Lab Journal
- Gaucher Disease: Task 06 - Lab Journal
- Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation
- Gaucher Disease: Task 07 - Research SNPs
- Gaucher Disease: Task 08 - LabJournal
- Gaucher Disease: Task 08 - Sequence-based mutation analysis
- Gaucher Disease: Task 09 - Lab Journal
- Gaucher Disease: Task 09 - Lab Journal: run minimise.sh
- Gaucher Disease: Task 09 - Structure-based mutation analysis
- Gaucher Disease: Task 10 - Lab Journal
- Gaucher Disease: Task 10 - Normal mode analysis
- Gaucher Disease - Task 06 - Lab Journal
- Gaucher Disease 2012
- Gaucher Task05 Protocol
- Gaucher Task06 Protocol
- Gaucher Task07 Protocol
- Gaucher Task09 Protocol
- Gaucher Task10 Protocol
- Gaucher dbSNP Deletions
- Gaucher dbSNP Missense
- Gaucher dbSNP Synonymous
- Gaucher hgmd mutations
- Glu285ala
- Glucocerebrosidase disease causing mutations
- Glucocerebrosidase neutral mutations
- Go annotations here
- HEXA Reference sequence
- HFE HUMAN NM
- HHSearch
- Hemo Task7 Minimise Table
- Hemo Task7 SCWRL FoldX Table
- Hemo seq based pred
- Hemochromatosis
- Hemochromatosis: Sequence based predictions
- Hemochromatosis 2012
- Hemochromatosis ALL SNP TABLE
- Hemochromatosis DBSNP SNP TABLE
- Hemochromatosis HGMD SNP TABLE
- Hemochromatosis Normal modes
- Hemochromatosis PSSM Matrix
- Hemochromatosis SNP Mapping MSA
- Hemochromatosis SNPdbe SNP TABLE
- Hemochromatosis SS Alignments
- Hemochromatosis gromacs energy table pictures
- Hemochromatosis gromacs mdp
- Hereditary hemochromatosis
- Hex A Reference sequence
- Hhr2tsv
- Homology-modelling HEXA
- 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 Predictions Hemochromatosis
- Homology Based Structure Predictions Hemochromatosis Alignments
- Homology based Structure prediction protocol BCKDHA
- Homology based structure predictions BCKDHA
- Homology modelling Gaucher Disease
- Homology modelling TSD
- How to search dbSNP
- I326T
- Imm ev hotspots
- Isoform CRA a
- Isoform CRA b
- Iupred
- Jpred
- Lab Journal -Task 4 (PAH)
- Lab Journal - Task 10 (PAH)
- Lab Journal - Task 7 (PAH)
- Lab Journal Hemochromatosis Task9
- Lab Journal Task 3 Hemo
- Lab Journal of Task 3 (MSUD)
- Lab Journal of Task 4 (MSUD)
- Lab Journal of Task 5 (MSUD)
- Lab journal
- Lab journal Task 7
- Lab journal task 2
- Lab journal task 4
- Lab journal task 5
- Lab journal task 8
- Labjournal NMA-Hemochromatosis
- List of known Hex A mutations
- M82L
- MAFFT 30
- MAFFT 360
- MAFFT 60
- MAFFT whole
- MDP condiguration (PKU)
- MD Mutation436
- MD Mutation485
- MD WildType
- MD WildeType
- MD simulation analysis TSD
- MD simulation analysis TSD Journal
- MSUD Q80E
- MSUD Task 9 Protocoll
- MSUP-task7-journal
- Main Page
- MapleSyrupDisease disease causing mutations
- Maple Syrup Urine Disease
- Maple Syrup Urine Disease 2012
- Maple syrup urine disease 2011
- Mapping SNPs BCKDHA
- Mapping SNPs HEXA
- Mapping SNPs HEXA/DETAIL
- Metachromatic leukodistrophy
- Missense nonsense CFTR
- Missense nonsense HFE
- Modeller.py
- Modeller protocol BCKDHA
- Modeller protokoll BCKDHA
- Molecular Dynamics Analysis BCKDHA
- Molecular Dynamics Simulations Analysis Gaucher Disease
- Molecular Dynamics Simulations Analysis Hemochromatosis
- Molecular Dynamics Simulations BCKDHA
- Molecular Dynamics Simulations Gaucher Disease
- Molecular Dynamics Simulations Gaucher Disease Scripts
- Molecular Dynamics Simulations HEXA
- Molecular Dynamics Simulations Hemochromatosis
- Molecular Dynamics Simulations TSD
- Molecular Dynamics Simulations TSD Journal
- Msa-conservation.py
- 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
- MutEn.pl
- Mutation Minimization Plots (PKU)
- Normal Mode Analysis BCKDHA
- Normal Mode Analysis Hemochromatosis
- Normal mode analysis GLA supplementary
- Normal mode analysis Gaucher Disease
- Normal mode analysis HEXA
- Normal mode analysis TSD
- Normal mode analysis TSD Journal
- Overlap between all databases (HGMD free)
- P01112 EVcouplings Configuration DI
- P01112 EVcouplings Configuration PLM
- P01112 EVfold Configuration DI
- P01112 EVfold Configuration PLM
- PAH G312D
- PAH I65T
- PAH P275S
- PAH P281L
- PAH R158Q
- PAH R261Q
- PAH R408W
- PAH R71H
- PAH Structure
- PAH T266A
- PAH T278N
- PSI-BLAST
- PSIBlasttrainer.pl
- PSSM
- PSSM of close homologous sequences
- Parse output.pl
- Pearson cc.r (Gaucher Disease)
- Phenylalanine hydroxylase reference
- Phenylalanine hydroxylase reference mRNA
- Phenylketonuria/Task2/Scripts
- Phenylketonuria/Task2 Scripts
- Phenylketonuria/Task3/Scripts
- Phenylketonuria/Task6 Scripts
- Phenylketonuria 2011
- Polyphobius.pl
- Poodle
- 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
- ProtFun2.2 output
- Protein Structure and Function Analysis (SS 2011)
- Protein Structure and Function Analysis (SS 2013)
- Protein Structure and Function Analysis (version: SS 2011)
- Protein Structure and Function Analysis (version: SS 2012)
- Protocol
- Protocol-msud-task5 protocol
- Protocol BCKDHA MD
- Protocol search
- Psipred
- Q125E
- QMEAN score information BCKDHA
- R265W
- Ras DI Score Configuration
- Ras PLM Score Configuration
- Reference Alignment BCKDHA
- Reference Sequence
- Reference Sequence (pdb)
- Reference Sequence Aspartoacyclase
- Reference Sequence BCKDHA
- Reference amino acid sequence of Glucocerebrosidase
- Reference mRNA of Glucocerebrosidase
- Reference nucleotide sequence of Glucocerebrosidase
- Reference sequence
- Reference sequence (uniprot)
- Researching And Mapping Point Mutations Hemochromatosis
- Researching SNPs Gaucher Disease
- Researching SNPs TSD
- Researching SNPs TSD Journal
- Researching and mapping point mutations TSD Journal
- Resource data
- Resource discussion
- Resource language
- Resource literature
- Resource software
- Resource wiki
- 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-blast.pl
- Run.pl
- Run MD HEXA
- Runscript BCKDHA
- Runscript for foldx
- SNPdbe conservation score (PKU)
- SNPs for Hema
- Scrip pdb distance check.py
- Script calc hotspot.py
- Script distance check.py
- Script rank contacts.py
- Secondary Structure Prediction
- Secondary Structure Prediction BCKDHA
- Secstr general
- Seq.-based mut. analysis HEXA
- Sequence-Based Mutation Analysis Hemochromatosis
- Sequence-Based Predictions Hemochromatosis
- Sequence-based analyses Gaucher Disease
- Sequence-based mutation analysis BCKDHA
- Sequence-based mutation analysis BCKDHA protocol
- Sequence-based mutation analysis Gaucher Disease
- Sequence-based mutation analysis HEXA
- Sequence-based mutation analysis HEXA/Mutation Summary
- Sequence-based mutation analysis HEXA/rs4777505 SNAP
- Sequence-based mutation analysis TSD
- Sequence-based mutation analysis TSD Journal
- Sequence-based predictions HEXA
- Sequence-based predictions Protocol TSD
- Sequence-based predictions TSD
- Sequence Alignments
- Sequence Alignments BCKDHA
- Sequence Alignments Gaucher Disease
- Sequence Alignments HEXA
- Sequence Alignments Hemochromatosis
- Sequence Alignments Protocol TSD
- Sequence Alignments TSD
- Sift probability HFE
- SignalP scores TSD
- Solution HFE SNPs
- Structure-Based Mutation Analysis Hemochromatosis
- Structure-based mutation analysis BCKDHA
- Structure-based mutation analysis Gaucher Disease
- Structure-based mutation analysis HEXA
- Structure-based mutation analysis TSD
- Structure-based mutation analysis TSD Journal
- Structure pdb
- Structures for P00439 in PDB
- Supplementary data normal mode glucocerebrosidase
- Swismsmodel 2gk1 alignment
- Swissmodel 1o7a alignment
- Swissmodel 2gjx alignment
- TSD Homology modelling protocol
- TSD Modeller 1o7a 2D
- TSD Modeller 1o7a Simple
- TSD Modeller 2gk1 2D
- TSD Modeller 2gk1 Simple
- TSD Modeller 3gh5 2D
- TSD Modeller 3gh5 Edited Alignment
- TSD Modeller 3gh5 Simple
- TSD NM 000520.3 NM 000520.4 NW
- TSD PolyPhen2 Full Ouput
- TSD SIFT Scaled Probailities
- TSD createMap.pl
- TSD synonymous SNPs from dbSNP
- Table Templates
- Task04 protocol
- Task10 Hemochromatosis Protocol
- Task2 Hemochromatosis Protocol
- Task3 Hemochromatosis Protocol
- Task3 protocol
- Task3 protocoll
- Task4 Hemochromatosis Protocol
- Task5 Hemochromatosis Protocol
- Task6-MSUP-journal
- Task6 Hemochromatosis Protocol
- Task7 Hemochromatosis Protocol
- Task8 Hemochromatosis Protocol
- Task9 Hemochromatosis Protocol
- Task 10: Molecular Dynamics Analysis
- Task 10 (MSUD)
- Task 10 - Molecular Dynamics Simulations
- Task 10 - Molecular Dynamics Simulations 2011
- Task 10 - Normal Mode Analysis
- Task 10 Lab Journal (MSUD)
- Task 11 - Molecular Dynamics Simulation
- Task 1: Collect information on the individual disease
- Task 2: Alignments
- Task 2: Multiple Sequence Alignment
- Task 2: Sequence alignments (sequence searches and multiple alignments)
- Task 2 (MSUD)
- Task 2 (MUSD) Additional Results
- Task 2 - Alignments with PAH Reference
- Task 2 lab journal (MSUD)
- Task 3: Sequence-based predictions
- Task 3: odba human Sequence-based predictions
- Task 3 (MSUD)
- Task 3 - Normal Mode Analysis
- Task 3 - Sequence-based predictions 2011
- Task 3 - Sequence-based predictions 2012
- Task 4: Homology-based structure prediction
- Task 4: Homology based structure predictions
- Task 4: Structural Alignments
- Task 4 (MSUD)
- Task 4 Protocol
- Task 5: Homology Modeling
- Task 5: Mapping point mutations
- Task 5: Researching SNPs
- Task 5 (MSUD)
- Task 5 - Mapping SNPs
- Task 5 - Mapping SNPs 2011
- Task 5 - Mapping SNPs Canavan
- Task 5 - Researching SNPs
- Task 6: MSUD - Sequence-based mutation analysis
- Task 6: Protein structure prediction from evolutionary sequence variation
- Task 6: Sequence-based mutation analysis
- Task 6 (MSUD)
- Task 6 - EVfold
- Task 6 - Protein structure prediction from evolutionary sequence variation
- Task 6 - Sequence-based mutation analysis
- Task 6 - Sequence-based mutation analysis 2011
- Task 6 Lab Journal (MSUD)
- Task 7: MSUD - Structure-based mutation analysis
- Task 7: Research SNPs
- Task 7: Structure-based mutation analysis
- Task 7 (MSUD)
- Task 7 - Structure-based mutation analysis
- Task 7 - Structure-based mutation analysis 2011
- Task 7 Research SNPs
- Task 8: MSUD - Molecular Dynamics Simulations
- Task 8: Molecular Dynamics Simulations
- Task 8: Sequence-based mutation analysis
- Task 8 (MSUD)
- Task 8 - Molecular Dynamics Simulations
- Task 8 - Molecular Dynamics Simulations 2011
- Task 8 Lab Journal (MSUD)
- Task 8 Sequence-based mutation analysis
- Task 9: MSUD - Normal Mode Analysis
- Task 9: Normal Mode Analysis
- Task 9: Structure-based mutation analysis
- Task 9 (MSUD)
- Task 9 - Normal Mode Analysis
- Task 9 - Normal Mode Analysis 2011
- Task 9 Lab Journal (MSUD)
- Task 9 Structure-based mutation analysis
- Task Homology Modelling
- Task Structural Alignments
- Task alignments
- Task alignments 2011
- Task alignments 2012
- Task diseaseInfo
- Task homologyModelling
- Task homologyModelling 2011
- Task sequenceAnalysis
- Tastk 2
- Tastk 2: Alignments
- Tay-Sachs Disease 2011
- Tay-Sachs Disease 2012
- Tcoffee 30
- Tcoffee 60
- Tcoffee whole
- Tpr precision.pl
- Transmembrane signal peptide general
- Tyr231X
- Using Modeller for TASK 4
- Werner Syndrome
- White brain matter
- Y166N
- Y438N