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  1. .snapfunrc
  2. 1OGS EVcouplings Configuration DI
  3. ARSA search protocol
  4. ASPA
  5. ASPA Homology Modelling
  6. ASPA Mapping SNPs
  7. ASPA Molecular Dynamics Simulation Analysis
  8. ASPA Normal Mode Analysis
  9. ASPA Sequence Alignments
  10. ASPA Sequence Based Mutation Analysis
  11. ASPA Structure Based Mutation Analysis
  12. Ala305glu
  13. All-blast.sh
  14. All-hhblits.sh
  15. All-psiblast.sh
  16. AllBio Forum
  17. Alpha galactosidase reference amino acid
  18. Alpha galactosidase reference nucleotide
  19. Animated Gifs
  20. Automated Evaluation of Homoloy Models
  21. BLAST
  22. BLOSUM62 matrix
  23. Beta-hexosaminidase subunit alpha
  24. Blast results Mamalian search
  25. Build mutation Script
  26. CD task10 protocol
  27. CD task2 protocol
  28. CD task5 protocol
  29. CD task6 protocol
  30. CD task7 protocol
  31. CD task8 protocol
  32. CD task9 protocol
  33. Canavans Disease
  34. ClustalW Above 60
  35. ClustalW Below 30
  36. ClustalW whole
  37. CompareCath.py
  38. Compiled list of SNPS
  39. Cys152arg
  40. DbSNP Silent Mutations Parser
  41. Devide psiblast out.pl
  42. Disopred
  43. Disorder general
  44. Disorder gerneral
  45. Dssp
  46. Example sequence
  47. FASTA
  48. Fabian Grandke
  49. Fabry:Annotated SNPs
  50. Fabry:Mapping point mutations/HGMD
  51. Fabry:Mapping point mutations/OMIM data
  52. Fabry:Mapping point mutations/SNPdbe data
  53. Fabry:Mapping point mutations/SNPedia data
  54. Fabry:Sequence alignments (sequence searches and multiple alignments):Results
  55. Fabry:Structure-based mutation analysis/FoldXtables
  56. Fabry Disease Mutation Analysis Sequence PSSM
  57. Fabry Disease mutation analysis sequence msa sequences
  58. Fabry Disease sequence-based prediction of tm-helices and signal peptides A4 HUMAN
  59. Fabry Disease sequence-based prediction of tm-helices and signal peptides BARC HALSA
  60. Fabry Disease sequence-based prediction of tm-helices and signal peptides GLA
  61. Fabry Disease sequence-based prediction of tm-helices and signal peptides INSL5 HUMAN
  62. Fabry Disease sequence-based prediction of tm-helices and signal peptides LAMP1 HUMAN
  63. Fabry Disease sequence-based prediction of tm-helices and signal peptides RET4 HUMAN
  64. Fabry Disease sequence prediction GO terms venn
  65. Fabry Disease swiss 1KTB graphics
  66. Fabry Disease swiss 3CC1 graphics
  67. Fabry Disease swiss 3HG3 graphics
  68. FoldX Difference Mutant/Wildtype
  69. Foldx hexa
  70. Format to wiki table.r
  71. GO Terms A4 HUMAN
  72. GO Terms BACR HALSA
  73. GO Terms HEXA HUMAN
  74. GO Terms INSL5 HUMAN
  75. GO Terms LAMP1 HUMAN
  76. GO Terms RET4 HUMAN
  77. GO annotation of the proteins
  78. GO terms general
  79. Gaucher Disease: Task 04 - Lab Journal
  80. Gaucher Disease: Task 06 - Lab Journal
  81. Gaucher Disease: Task 07 - Research SNPs
  82. Gaucher Disease: Task 08 - LabJournal
  83. Gaucher Disease: Task 09 - Lab Journal: run minimise.sh
  84. Gaucher Disease: Task 10 - Lab Journal
  85. Gaucher Task05 Protocol
  86. Gaucher Task07 Protocol
  87. Gaucher Task09 Protocol
  88. Gaucher Task10 Protocol
  89. Gaucher dbSNP Deletions
  90. Gaucher dbSNP Missense
  91. Gaucher dbSNP Synonymous
  92. Gaucher hgmd mutations
  93. Glu285ala
  94. Glucocerebrosidase disease causing mutations
  95. Glucocerebrosidase mapping snps
  96. Glucocerebrosidase neutral mutations
  97. Go annotations here
  98. HEXA Reference sequence
  99. HFE HUMAN NM
  100. HHSearch
  101. Hemo Task7 Minimise Table
  102. Hemo Task7 SCWRL FoldX Table
  103. Hemo seq based pred
  104. Hemochromatosis ALL SNP TABLE
  105. Hemochromatosis DBSNP SNP TABLE
  106. Hemochromatosis HGMD SNP TABLE
  107. Hemochromatosis PSSM Matrix
  108. Hemochromatosis SNP Mapping MSA
  109. Hemochromatosis SNPdbe SNP TABLE
  110. Hemochromatosis SS Alignments
  111. Hemochromatosis gromacs energy table pictures
  112. Hemochromatosis gromacs mdp
  113. Hereditary hemochromatosis
  114. Hex A Reference sequence
  115. Hhr2tsv
  116. Homology-modelling HEXA
  117. Homology-modelling HEXA/3bc9.pir
  118. Homology-modelling HEXA/3cui.pir
  119. Homology-modelling HEXA/3lut.pir,
  120. Homology-modelling HEXA/hh search output
  121. Homology-modelling HEXA/swissmodel 3CUI
  122. Homology-modelling HEXA/swissmodel 3LUT
  123. Homology-modelling HEXA/swissmodel ali
  124. Homology Based Structure Predictions Hemochromatosis Alignments
  125. How to search dbSNP
  126. Imm ev hotspots
  127. Isoform CRA a
  128. Isoform CRA b
  129. Iupred
  130. Journal structure based mutation analysis (PKU)
  131. Jpred
  132. Lab Journal -Task 4 (PAH)
  133. Lab Journal - Task 10 (PAH)
  134. Lab Journal - Task 2 (PAH)
  135. Lab Journal - Task 4 (PAH)
  136. Lab Journal - Task 5 (PAH)
  137. Lab Journal - Task 6 (PAH)
  138. Lab Journal - Task 7 (PAH)
  139. Lab Journal - Task 8 (PAH)
  140. Lab Journal - Task 9 (PAH)
  141. Lab Journal Hemochromatosis Task9
  142. Lab Journal Task 3 Hemo
  143. Lab Journal of Task 4 (MSUD)
  144. Lab journal Task 7
  145. Lab journal task 4
  146. Lab journal task 5
  147. Lab journal task 8
  148. Labjournal NMA-Hemochromatosis
  149. List of known Hex A mutations
  150. M82L
  151. MAFFT 30
  152. MAFFT 360
  153. MAFFT 60
  154. MAFFT whole
  155. MDP condiguration (PKU)
  156. MD Mutation436
  157. MD Mutation485
  158. MD WildType
  159. MD WildeType
  160. MSUD Task 9 Protocoll
  161. MapleSyrupDisease disease causing mutations
  162. Mapping SNPs HEXA
  163. Mapping SNPs HEXA/DETAIL
  164. Metachromatic leukodistrophy
  165. Metachromatic leukodystrophy reference aminoacids
  166. Metachromatic leukodystrophy reference nucleotide
  167. Missense nonsense CFTR
  168. Missense nonsense HFE
  169. Modeller.py
  170. Modeller protokoll BCKDHA
  171. Molecular Dynamics Simulation of ARSA
  172. Molecular Dynamics Simulations Gaucher Disease Scripts
  173. Molecular Dynamics Simulations HEXA
  174. Msa-conservation.py
  175. Multiple Alignment Mammalian PheOH
  176. Multiple Sequence Alignment: ClustalW - set 1
  177. Multiple Sequence Alignment: ClustalW - set 2
  178. Multiple Sequence Alignment: ClustalW - set 3
  179. Multiple Sequence Alignment: Espresso - set 1
  180. Multiple Sequence Alignment: Muscle - set 1
  181. Multiple Sequence Alignment: Muscle - set 2
  182. Multiple Sequence Alignment: Muscle - set 3
  183. Multiple Sequence Alignment: T-Coffee - set 1
  184. Multiple Sequence Alignment: T-Coffee - set 2
  185. Multiple Sequence Alignment: T-Coffee - set 3
  186. MutEn.pl
  187. Normal Mode Analysis of ARSA
  188. Normal mode analysis GLA supplementary
  189. Normal mode analysis HEXA
  190. Overlap between all databases (HGMD free)
  191. P01112 EVcouplings Configuration DI
  192. P01112 EVcouplings Configuration PLM
  193. P01112 EVfold Configuration DI
  194. P01112 EVfold Configuration PLM
  195. PSI-BLAST
  196. PSIBlasttrainer.pl
  197. PSSM
  198. PSSM of close homologous sequences
  199. Phenylalanine hydroxylase reference mRNA
  200. Phenylketonuria
  201. Phenylketonuria/Task2/Scripts
  202. Phenylketonuria/Task2 Scripts
  203. Phenylketonuria/Task3/Scripts
  204. Phenylketonuria/Task6 Scripts
  205. Polyphobius.pl
  206. Poodle
  207. Prediction of Disordered Regions
  208. Prediction of transmembrane alpha-helices and signal peptides A4 HUMAN
  209. Prediction of transmembrane alpha-helices and signal peptides BACR HALSA
  210. Prediction of transmembrane alpha-helices and signal peptides HEXA HUMAN
  211. Prediction of transmembrane alpha-helices and signal peptides INSL5 HUMAN
  212. Prediction of transmembrane alpha-helices and signal peptides LAMP1 HUMAN
  213. Prediction of transmembrane alpha-helices and signal peptides RET4 HUMAN
  214. ProtFun2.2 output
  215. Protein Structure and Function Analysis (SS 2011)
  216. Protocol
  217. Protocol-msud-task5 protocol
  218. Protocol search
  219. PsiPred of Mutated PAH
  220. Psipred
  221. Ras DI Score Configuration
  222. Ras PLM Score Configuration
  223. Reference Alignment BCKDHA
  224. Reference Sequence
  225. Reference Sequence (pdb)
  226. Reference Sequence Aspartoacyclase
  227. Reference mRNA of Glucocerebrosidase
  228. Reference sequence
  229. Researching and mapping point mutations TSD Journal
  230. Resource data
  231. Resource language
  232. Resource literature
  233. Rs1054374
  234. Rs1054374 SNAP
  235. Rs121907967
  236. Rs121907967 SNAP
  237. Rs121907968
  238. Rs121907968 SNAP
  239. Rs121907974
  240. Rs121907974 SNAP
  241. Rs121907979
  242. Rs121907979 SNAP
  243. Rs121907982
  244. Rs121907982 SNAP
  245. Rs1800430
  246. Rs1800430 SNAP
  247. Rs1800431
  248. Rs4777505
  249. Rs4777505 SNAP
  250. Rs61731240

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