MOIFree!PfPRpassivecasedetectionNanoporelocusLLINcoalescenceIPTiindelCOIHe(heterozygosity)ampliconsequencingGWASCNVK13(kelch13)VgscIRSRDTIlluminaIBDtSNEtranslocationrecombinationallelereferencegenomeprevalenceactivecasedetectionbarcodereactivecasedetectionWGShaplotypeACTsuperinfectionmonogenomicIPTpalignmentdiscordantreadslinkagepersistencediversitycoregenomesequencingcoveragesWGAITNslowcomplexityPCAmolecularinversionprobesMDAphasingSMCEIRinversionTajima'sDSTRdeepsequencingmicrosatellitemicrohaplotypeNGSFwsintrogressionincidenceDBSnucleotidediversity(pi/π)clonalselectionsubtelomericpolygenomicstructuralvariantSNPPacBioIBSMOIFree!PfPRpassivecasedetectionNanoporelocusLLINcoalescenceIPTiindelCOIHe(heterozygosity)ampliconsequencingGWASCNVK13(kelch13)VgscIRSRDTIlluminaIBDtSNEtranslocationrecombinationallelereferencegenomeprevalenceactivecasedetectionbarcodereactivecasedetectionWGShaplotypeACTsuperinfectionmonogenomicIPTpalignmentdiscordantreadslinkagepersistencediversitycoregenomesequencingcoveragesWGAITNslowcomplexityPCAmolecularinversionprobesMDAphasingSMCEIRinversionTajima'sDSTRdeepsequencingmicrosatellitemicrohaplotypeNGSFwsintrogressionincidenceDBSnucleotidediversity(pi/π)clonalselectionsubtelomericpolygenomicstructuralvariantSNPPacBioIBS

GEM 2021 Bingo - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. MOI
  2. Free!
  3. PfPR
  4. passive case detection
  5. Nanopore
  6. locus
  7. LLIN
  8. coalescence
  9. IPTi
  10. indel
  11. COI
  12. He (heterozygosity)
  13. amplicon sequencing
  14. GWAS
  15. CNV
  16. K13 (kelch13)
  17. Vgsc
  18. IRS
  19. RDT
  20. Illumina
  21. IBD
  22. tSNE
  23. translocation
  24. recombination
  25. allele
  26. reference genome
  27. prevalence
  28. active case detection
  29. barcode
  30. reactive case detection
  31. WGS
  32. haplotype
  33. ACT
  34. superinfection
  35. monogenomic
  36. IPTp
  37. alignment
  38. discordant reads
  39. linkage
  40. persistence
  41. diversity
  42. core genome
  43. sequencing coverage
  44. sWGA
  45. ITNs
  46. low complexity
  47. PCA
  48. molecular inversion probes
  49. MDA
  50. phasing
  51. SMC
  52. EIR
  53. inversion
  54. Tajima's D
  55. STR
  56. deep sequencing
  57. microsatellite
  58. microhaplotype
  59. NGS
  60. Fws
  61. introgression
  62. incidence
  63. DBS
  64. nucleotide diversity (pi/π)
  65. clonal
  66. selection
  67. subtelomeric
  68. polygenomic
  69. structural variant
  70. SNP
  71. PacBio
  72. IBS