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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
  101. Rs121907968
  102. Rs121907968 SNAP
  103. Rs121907974
  104. Rs121907974 SNAP
  105. Rs121907979
  106. Rs121907979 SNAP
  107. Rs121907982
  108. Rs121907982 SNAP
  109. Rs1800430
  110. Rs1800430 SNAP
  111. Rs1800431
  112. Rs4777505
  113. Rs4777505 SNAP
  114. Rs61731240
  115. Rs61731240 SNAP
  116. Rs61747114
  117. Rs61747114 SNAP
  118. Run MD HEXA
  119. Runscript BCKDHA
  120. SNPs for Hema
  121. Secondary Structure Prediction
  122. Secstr general
  123. Seq.-based mut. analysis HEXA
  124. Sequence-based mutation analysis (Phenylketonuria)
  125. Sequence-based mutation analysis HEXA/Mutation Summary
  126. Sequence-based mutation analysis HEXA/rs4777505 SNAP
  127. Structural Alignments (Phenylketonuria)
  128. Structure-based mutation analysis (Phenylketonuria)
  129. Structure pdb
  130. Structures for P00439 in PDB
  131. TSD Modeller 3gh5 Edited Alignment
  132. Task3 protocoll
  133. Task 10 - Molecular Dynamics Simulations 2011
  134. Task 2 - Alignments with PAH Reference
  135. Task 3 - Normal Mode Analysis
  136. Task 3 - Sequence-based predictions 2011
  137. Task 5 - Mapping SNPs 2011
  138. Task 6 - EVfold
  139. Task 6 - Sequence-based mutation analysis 2011
  140. Task 7 - Structure-based mutation analysis 2011
  141. Task 8 - Molecular Dynamics Simulations 2011
  142. Task 9 - Normal Mode Analysis 2011
  143. Task alignments 2011
  144. Task homologyModelling 2011
  145. Task sequenceAnalysis
  146. Tastk 2
  147. Tastk 2: Alignments
  148. Tay-Sachs Disease 2011
  149. Tcoffee 30
  150. Tcoffee 60
  151. Tcoffee whole
  152. Transmembrane signal peptide general
  153. White brain matter

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