ANGSD: Analysis of next generation Sequencing Data

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  1. Direct Ancestry‏‎ (2 revisions)
  2. Pbs‏‎ (2 revisions)
  3. SuYeon‏‎ (2 revisions - redirect page)
  4. Glf files‏‎ (2 revisions)
  5. ErrorSykMethod‏‎ (2 revisions)
  6. Supersim‏‎ (2 revisions)
  7. LD‏‎ (2 revisions)
  8. Error estimation method‏‎ (2 revisions)
  9. Li2011‏‎ (2 revisions)
  10. Skotte‏‎ (2 revisions)
  11. Orlando2013‏‎ (2 revisions)
  12. Regionfile‏‎ (3 revisions)
  13. Kim2011‏‎ (3 revisions)
  14. SNP Calling‏‎ (3 revisions)
  15. SYKmaf‏‎ (3 revisions)
  16. Gatk‏‎ (3 revisions)
  17. ThetaStat‏‎ (3 revisions)
  18. Changes‏‎ (3 revisions)
  19. RealSFSmethod‏‎ (3 revisions)
  20. Vcf‏‎ (4 revisions)
  21. Korneliussen2013‏‎ (4 revisions)
  22. Misc example‏‎ (4 revisions)
  23. Nielsen2012‏‎ (4 revisions)
  24. Skotte2012‏‎ (4 revisions)
  25. Mismatch‏‎ (5 revisions)
  26. Genotype Distribution‏‎ (6 revisions)
  27. PCA‏‎ (7 revisions)
  28. Base quality‏‎ (7 revisions)
  29. Genotype likelihoods from alignments new‏‎ (8 revisions)
  30. Introduction‏‎ (8 revisions)
  31. Glcomparison‏‎ (8 revisions)
  32. SNP calling‏‎ (8 revisions)
  33. Haploid calling‏‎ (9 revisions)
  34. NGSadmix‏‎ (10 revisions)
  35. Angsd structure‏‎ (11 revisions)
  36. Depth‏‎ (13 revisions)
  37. Beagle input‏‎ (13 revisions)
  38. Authors‏‎ (14 revisions)
  39. Heterozygosity‏‎ (16 revisions)
  40. SnpFilters‏‎ (18 revisions)
  41. HWE test‏‎ (19 revisions)
  42. HWE and Inbreeding estimates‏‎ (20 revisions)
  43. Safv3‏‎ (20 revisions)
  44. Relatedness‏‎ (21 revisions)
  45. Fst‏‎ (23 revisions)
  46. Citing angsd‏‎ (23 revisions)
  47. Plink‏‎ (24 revisions)
  48. Genotype calling‏‎ (27 revisions)
  49. Contamination‏‎ (29 revisions)
  50. Abbababa‏‎ (31 revisions)

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