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- 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