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  1. Introduction to the GATK‏‎ (360 revisions)
  2. Base quality score recalibration‏‎ (279 revisions)
  3. Variant quality score recalibration‏‎ (241 revisions)
  4. Genome Sequencing and Analysis Group‏‎ (226 revisions)
  5. GenomicAnnotator‏‎ (213 revisions)
  6. Genomic Annotator Data Tables‏‎ (168 revisions)
  7. HLA caller algorithm‏‎ (147 revisions)
  8. Unified genotyper‏‎ (138 revisions)
  9. Best Practice Variant Detection with the GATK v2‏‎ (118 revisions)
  10. Creating Amplicon Sequences‏‎ (111 revisions)
  11. Xiaoming (Sherman) Jia‏‎ (108 revisions)
  12. Local realignment around indels‏‎ (101 revisions)
  13. Best Practice Variant Detection with the GATK v3‏‎ (89 revisions)
  14. VariantFiltrationWalker‏‎ (74 revisions)
  15. Managing user input‏‎ (64 revisions)
  16. SelectVariants‏‎ (64 revisions)
  17. FullCallingPipeline.q‏‎ (59 revisions)
  18. Genomic Annotator - Detailed Example‏‎ (59 revisions)
  19. Somatic Indel Detector‏‎ (58 revisions)
  20. BCF2‏‎ (55 revisions)
  21. VariantEval‏‎ (53 revisions)
  22. Variant Optimizer‏‎ (53 revisions - redirect page)
  23. Whole genome, low-pass v1‏‎ (51 revisions)
  24. Merging batched call sets‏‎ (51 revisions)
  25. VariantAnnotator‏‎ (50 revisions)
  26. Frequently Asked Questions‏‎ (48 revisions)
  27. Parallelism and the GATK‏‎ (45 revisions)
  28. GATK resource bundle‏‎ (45 revisions)
  29. Understanding the Unified Genotyper's VCF files‏‎ (44 revisions)
  30. GATK-Queue‏‎ (44 revisions)
  31. CombineVariants‏‎ (43 revisions)
  32. Input files for the GATK‏‎ (41 revisions)
  33. Data Processing Pipeline‏‎ (37 revisions)
  34. Whole genome, deep coverage v1‏‎ (37 revisions)
  35. Interface with BEAGLE imputation software‏‎ (35 revisions)
  36. Sting BWA/C bindings‏‎ (35 revisions)
  37. Home Page‏‎ (35 revisions)
  38. GATK development process‏‎ (35 revisions)
  39. SequenomValidationConverter‏‎ (35 revisions)
  40. Adding Genomic Annotations Using SnpEff and VariantAnnotator‏‎ (34 revisions)
  41. Depth of Coverage v3.0‏‎ (33 revisions)
  42. Built-in command-line arguments‏‎ (30 revisions)
  43. Running the GATK for the first time‏‎ (30 revisions)
  44. Redistributing walkers‏‎ (29 revisions)
  45. Downloading the GATK‏‎ (28 revisions)
  46. Read-backed phasing algorithm‏‎ (27 revisions)
  47. Queue QScripts‏‎ (27 revisions)
  48. Genomic Annotator - refGene Table - How It Was Created‏‎ (25 revisions)
  49. Genotype and Validate‏‎ (25 revisions)
  50. PacBio Data Processing Guidelines‏‎ (25 revisions)

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