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  1. 1OGS EVcouplings Configuration DI
  2. Build mutation Script
  3. Canavan Disease: Task 02 - Journal
  4. Canavan Disease: Task 03 - Journal
  5. Canavan Disease: Task 04 - Journal
  6. Canavan Disease: Task 07 - Journal
  7. Canavan Disease: Task 11 - Molecular Dynamics Simulation
  8. Canavan Disease 2011
  9. Canavans Disease
  10. ClustalW Above 60
  11. ClustalW Below 30
  12. ClustalW whole
  13. Cys152arg
  14. Disease list 2011
  15. Disorder general
  16. Disorder gerneral
  17. Fabry Disease 2011
  18. Fabry Disease Selected Mutations
  19. Foldx hexa
  20. GO Terms A4 HUMAN
  21. GO Terms BACR HALSA
  22. GO Terms HEXA HUMAN
  23. GO Terms INSL5 HUMAN
  24. GO Terms LAMP1 HUMAN
  25. GO Terms RET4 HUMAN
  26. GO annotation of the proteins
  27. GO terms general
  28. Gaucher Disease: Task 06 - Lab Journal
  29. Gaucher Disease 2011
  30. Go annotations here
  31. Hemo seq based pred
  32. Hemochromatosis 2011
  33. Hereditary hemochromatosis
  34. Hex A Reference sequence
  35. Homology-modelling HEXA/3bc9.pir
  36. Homology-modelling HEXA/3cui.pir
  37. Homology-modelling HEXA/3lut.pir,
  38. Homology-modelling HEXA/hh search output
  39. Homology-modelling HEXA/swissmodel 3CUI
  40. Homology-modelling HEXA/swissmodel 3LUT
  41. Homology-modelling HEXA/swissmodel ali
  42. Homology based structure prediction (Phenylketonuria)
  43. Imm ev hotspots
  44. MAFFT 30
  45. MAFFT 360
  46. MAFFT 60
  47. MAFFT whole
  48. MD Mutation436
  49. MD Mutation485
  50. MD WildType
  51. MD WildeType
  52. MSUD Q80E
  53. Main Page
  54. MapleSyrupDisease disease causing mutations
  55. Maple syrup urine disease 2011
  56. Mapping SNPs HEXA/DETAIL
  57. Metachromatic leukodistrophy
  58. Metachromatic leukodystrophy 2011
  59. Missense nonsense CFTR
  60. Modeller protocol BCKDHA
  61. Modeller protokoll BCKDHA
  62. Multiple Sequence Alignment: ClustalW - set 1
  63. Multiple Sequence Alignment: ClustalW - set 2
  64. Multiple Sequence Alignment: ClustalW - set 3
  65. Multiple Sequence Alignment: Espresso - set 1
  66. Multiple Sequence Alignment: Muscle - set 1
  67. Multiple Sequence Alignment: Muscle - set 2
  68. Multiple Sequence Alignment: Muscle - set 3
  69. Multiple Sequence Alignment: T-Coffee - set 1
  70. Multiple Sequence Alignment: T-Coffee - set 2
  71. Multiple Sequence Alignment: T-Coffee - set 3
  72. Normal mode analysis (Phenylketonuria)
  73. P01112 EVcouplings Configuration DI
  74. P01112 EVcouplings Configuration PLM
  75. PSIBlasttrainer.pl
  76. Pearson cc.r (Gaucher Disease)
  77. Phenylketonuria/Task2/Scripts
  78. Phenylketonuria/Task2 Scripts
  79. Phenylketonuria/Task6 Scripts
  80. Phenylketonuria 2011
  81. Prediction of Disordered Regions
  82. Prediction of transmembrane alpha-helices and signal peptides A4 HUMAN
  83. Prediction of transmembrane alpha-helices and signal peptides BACR HALSA
  84. Prediction of transmembrane alpha-helices and signal peptides HEXA HUMAN
  85. Prediction of transmembrane alpha-helices and signal peptides INSL5 HUMAN
  86. Prediction of transmembrane alpha-helices and signal peptides LAMP1 HUMAN
  87. Prediction of transmembrane alpha-helices and signal peptides RET4 HUMAN
  88. Protein Structure and Function Analysis (SS 2011)
  89. Protein Structure and Function Analysis (version: SS 2011)
  90. Protein Structure and Function Analysis (version: SS 2012)
  91. Protein structure prediction from evolutionary sequence variation (Phenylketonuria)
  92. Ras PLM Score Configuration
  93. Reference Sequence
  94. Reference sequence
  95. Researching SNPs (Phenylketonuria)
  96. Researching and mapping point mutations TSD Journal
  97. Rs1054374
  98. Rs1054374 SNAP
  99. Rs121907967
  100. Rs121907967 SNAP

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