EIRIRSampliconsequencingcoregenometranslocationselectionRDTalignmentIPTpACTPfPRVgscTajima'sDMDAHe(heterozygosity)SMCCOIintrogressioninversiontSNEK13(kelch13)SNPWGSlocusmicrosatellitephasingclonalsuperinfectionIPTiactivecasedetectionCNVsWGAincidenceITNscoalescenceIlluminaNanoporebarcodelowcomplexityalleleGWASPacBioIBDMOIpassivecasedetectionindelDBSPCAsequencingcoveragestructuralvariantmonogenomicNGSIBSnucleotidediversity(pi/π)recombinationFwslinkageprevalencereferencegenomehaplotypeLLINdiscordantreadssubtelomericdeepsequencingreactivecasedetectiondiversityFree!persistencemicrohaplotypemolecularinversionprobesSTRpolygenomicEIRIRSampliconsequencingcoregenometranslocationselectionRDTalignmentIPTpACTPfPRVgscTajima'sDMDAHe(heterozygosity)SMCCOIintrogressioninversiontSNEK13(kelch13)SNPWGSlocusmicrosatellitephasingclonalsuperinfectionIPTiactivecasedetectionCNVsWGAincidenceITNscoalescenceIlluminaNanoporebarcodelowcomplexityalleleGWASPacBioIBDMOIpassivecasedetectionindelDBSPCAsequencingcoveragestructuralvariantmonogenomicNGSIBSnucleotidediversity(pi/π)recombinationFwslinkageprevalencereferencegenomehaplotypeLLINdiscordantreadssubtelomericdeepsequencingreactivecasedetectiondiversityFree!persistencemicrohaplotypemolecularinversionprobesSTRpolygenomic

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.


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