incidenceintrogressionmonogenomicallelepassivecasedetectionmolecularinversionprobesEIRIBDFwsclonalampliconsequencingdiversityIBSCNVIPTpmicrosatellitebarcodedeepsequencingITNshaplotypeNanoporealignmentsequencingcoveragereactivecasedetectionIlluminaMDAmicrohaplotypeSNPNGSPfPRHe(heterozygosity)STRVgscACTLLINreferencegenomeWGSCOIcoregenomeindelphasinglocusPCAselectionRDTMOIGWASTajima'sDrecombinationpersistencesubtelomericinversionactivecasedetectionpolygenomicsuperinfectionSMCtranslocationDBSIPTilowcomplexityIRSnucleotidediversity(pi/π)PacBiotSNEFree!sWGAK13(kelch13)linkagecoalescencediscordantreadsprevalencestructuralvariantincidenceintrogressionmonogenomicallelepassivecasedetectionmolecularinversionprobesEIRIBDFwsclonalampliconsequencingdiversityIBSCNVIPTpmicrosatellitebarcodedeepsequencingITNshaplotypeNanoporealignmentsequencingcoveragereactivecasedetectionIlluminaMDAmicrohaplotypeSNPNGSPfPRHe(heterozygosity)STRVgscACTLLINreferencegenomeWGSCOIcoregenomeindelphasinglocusPCAselectionRDTMOIGWASTajima'sDrecombinationpersistencesubtelomericinversionactivecasedetectionpolygenomicsuperinfectionSMCtranslocationDBSIPTilowcomplexityIRSnucleotidediversity(pi/π)PacBiotSNEFree!sWGAK13(kelch13)linkagecoalescencediscordantreadsprevalencestructuralvariant

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