Pages with the most revisions

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Showing below up to 50 results in range #571 to #620.

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  1. Sequence alignments (sequence searches and multiple alignments)‏‎ (1 revision - redirect page)
  2. Task 5‏‎ (1 revision - redirect page)
  3. Glucocerebrosidase reference nucleotide‏‎ (1 revision - redirect page)
  4. Rs121907974 SNAP‏‎ (1 revision)
  5. PAH T266A‏‎ (1 revision)
  6. MapleSyrupDisease disease causing mutations‏‎ (1 revision)
  7. TSD Modeller 3gh5 2D‏‎ (1 revision)
  8. Phenylketonuria/Task3‏‎ (1 revision - redirect page)
  9. Fabry Disease sequence-based prediction of tm-helices and signal peptides GLA‏‎ (1 revision)
  10. Task 10 (MUSD)‏‎ (1 revision - redirect page)
  11. Imm ev hotspots‏‎ (1 revision)
  12. Task 3‏‎ (1 revision - redirect page)
  13. Runscript BCKDHA‏‎ (1 revision)
  14. Task 8: MSUP - Molecular Dynamics Simulations‏‎ (1 revision - redirect page)
  15. Fabry Disease sequence-based prediction of tm-helices and signal peptides INSL5 HUMAN‏‎ (1 revision)
  16. Isoform CRA a‏‎ (1 revision)
  17. ClustalW Above 60‏‎ (1 revision)
  18. Drexler‏‎ (1 revision - redirect page)
  19. Researching and mapping point mutations TSD Journal‏‎ (1 revision)
  20. Overlap between all databases (HGMD free)‏‎ (1 revision)
  21. MAFFT 360‏‎ (1 revision)
  22. Fabry:Mapping point mutations/OMIM data‏‎ (1 revision)
  23. Rs121907979 SNAP‏‎ (1 revision)
  24. TSD Modeller 3gh5 Simple‏‎ (1 revision)
  25. Homology-modelling HEXA/swissmodel 3LUT‏‎ (1 revision)
  26. Fabry Disease sequence-based prediction of tm-helices and signal peptides LAMP1 HUMAN‏‎ (1 revision)
  27. Isoform CRA b‏‎ (1 revision)
  28. Sequence-based predictions GLA diagrams‏‎ (1 revision)
  29. ClustalW Below 30‏‎ (1 revision)
  30. Tcoffee 30‏‎ (1 revision)
  31. Task 3: obda human Sequence-based predictions‏‎ (1 revision - redirect page)
  32. MAFFT 60‏‎ (1 revision)
  33. TSD NM 000520.3 NM 000520.4 NW‏‎ (1 revision)
  34. Fabry:Sequence alignments (sequence searches and multiple alignments):Journal‏‎ (1 revision - redirect page)
  35. Fabry Disease sequence-based prediction of tm-helices and signal peptides RET4 HUMAN‏‎ (1 revision)
  36. Iupred‏‎ (1 revision)
  37. ClustalW whole‏‎ (1 revision)
  38. Tcoffee 60‏‎ (1 revision)
  39. Gaucher dbSNP Deletions‏‎ (1 revision)
  40. P01112 EVcouplings Configuration PLM‏‎ (1 revision)
  41. MAFFT whole‏‎ (1 revision)
  42. Rs121907982 SNAP‏‎ (1 revision)
  43. TSD PolyPhen2 Full Ouput‏‎ (1 revision)
  44. Hemochromatosis SNP Mapping MSA‏‎ (1 revision)
  45. Tcoffee whole‏‎ (1 revision)
  46. Gaucher dbSNP Missense‏‎ (1 revision)
  47. P01112 EVfold Configuration DI‏‎ (1 revision)
  48. Benjamin Drexler‏‎ (1 revision)
  49. PSSM‏‎ (1 revision)
  50. Task 6 Lab Journal (MUSD)‏‎ (1 revision - redirect page)

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