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Showing below up to 50 results starting with #401.

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  1. Report (host object)‏‎ (3 revisions)
  2. Explain my genes (workflow)‏‎ (3 revisions)
  3. Match genes and metabolites (analysis)‏‎ (3 revisions)
  4. Plot scatter chart (analysis)‏‎ (3 revisions)
  5. Super annotate table (analysis)‏‎ (3 revisions)
  6. Virtual biology‏‎ (3 revisions)
  7. Download model (analysis)‏‎ (3 revisions)
  8. Merge peak callers (analysis)‏‎ (3 revisions)
  9. Blast alignment coverage (analysis)‏‎ (3 revisions)
  10. ArticleComparator (analysis)‏‎ (3 revisions)
  11. QUAST‏‎ (3 revisions)
  12. Jupyter‏‎ (3 revisions)
  13. SNP (reference type)‏‎ (3 revisions)
  14. Sequence minimal unique length (analysis)‏‎ (3 revisions)
  15. Perfectosape (analysis)‏‎ (3 revisions)
  16. Structures - PDB‏‎ (3 revisions)
  17. Probes - Affymetrix ST‏‎ (3 revisions)
  18. Convert diagram to Transpath (analysis)‏‎ (3 revisions)
  19. Transcript structure analysis‏‎ (3 revisions)
  20. Infer network (analysis)‏‎ (3 revisions)
  21. Report generator for quality control analysis‏‎ (3 revisions)
  22. Find gene fusions from RNA-seq (workflow)‏‎ (3 revisions)
  23. 1-dimensional arterial tree model‏‎ (3 revisions)
  24. Genes (reference type)‏‎ (3 revisions)
  25. Proteins - PDB‏‎ (3 revisions)
  26. Isoform TE (analysis)‏‎ (3 revisions)
  27. Drugs - DrugBank‏‎ (3 revisions)
  28. Merge peaks (analysis)‏‎ (3 revisions)
  29. Find miRNA feed forward loops with CMA (analysis)‏‎ (3 revisions)
  30. ArticleTrackCreator (analysis)‏‎ (3 revisions)
  31. Group table rows (analysis)‏‎ (3 revisions)
  32. Create miRNA promoters (analysis)‏‎ (3 revisions)
  33. Illumina metylation probes to track (analysis)‏‎ (3 revisions)
  34. Reference type‏‎ (3 revisions)
  35. Analyze any DNA sequence, EMBL (workflow)‏‎ (3 revisions)
  36. Convert diagram to pairs (analysis)‏‎ (3 revisions)
  37. Transcriptome mappability (analysis)‏‎ (3 revisions)
  38. Copy data element (analysis)‏‎ (3 revisions)
  39. Matrices (reference type)‏‎ (3 revisions)
  40. Find genome variants and indels from RNA-seq (workflow)‏‎ (3 revisions)
  41. Categories - ExPASy‏‎ (3 revisions)
  42. Optimization document‏‎ (3 revisions)
  43. Cis-module sets near given genes (analysis)‏‎ (3 revisions)
  44. 3D viewer‏‎ (3 revisions)
  45. Genes - BKL‏‎ (3 revisions)
  46. Treatment Simulation (analysis)‏‎ (3 revisions)
  47. Identification of cis-regulatory modules with given pattern of TF-classes (analysis)‏‎ (3 revisions)
  48. Make GTF for riboseq alignment (analysis)‏‎ (3 revisions)
  49. Merge simulation results (analysis)‏‎ (3 revisions)
  50. Select keynodes with top targets (analysis)‏‎ (3 revisions)

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