MOI alignment EIR translocation MDA structural variant microhaplotype locus GWAS diversity active case detection reference genome molecular inversion probes clonal incidence Fws monogenomic SMC Tajima's D IBD ACT passive case detection barcode reactive case detection amplicon sequencing IRS nucleotide diversity (pi/π) Free! ITNs tSNE Vgsc persistence discordant reads DBS K13 (kelch13) inversion PCA introgression IPTi polygenomic IBS allele RDT selection linkage subtelomeric microsatellite sequencing coverage recombination Illumina COI WGS deep sequencing CNV coalescence haplotype PacBio superinfection indel Nanopore prevalence STR SNP sWGA low complexity LLIN PfPR NGS core genome IPTp He (heterozygosity) phasing MOI alignment EIR translocation MDA structural variant microhaplotype locus GWAS diversity active case detection reference genome molecular inversion probes clonal incidence Fws monogenomic SMC Tajima's D IBD ACT passive case detection barcode reactive case detection amplicon sequencing IRS nucleotide diversity (pi/π) Free! ITNs tSNE Vgsc persistence discordant reads DBS K13 (kelch13) inversion PCA introgression IPTi polygenomic IBS allele RDT selection linkage subtelomeric microsatellite sequencing coverage recombination Illumina COI WGS deep sequencing CNV coalescence haplotype PacBio superinfection indel Nanopore prevalence STR SNP sWGA low complexity LLIN PfPR NGS core genome IPTp He (heterozygosity) phasing
(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.
MOI
alignment
EIR
translocation
MDA
structural variant
microhaplotype
locus
GWAS
diversity
active case detection
reference genome
molecular inversion probes
clonal
incidence
Fws
monogenomic
SMC
Tajima's D
IBD
ACT
passive case detection
barcode
reactive case detection
amplicon sequencing
IRS
nucleotide diversity (pi/π)
Free!
ITNs
tSNE
Vgsc
persistence
discordant reads
DBS
K13 (kelch13)
inversion
PCA
introgression
IPTi
polygenomic
IBS
allele
RDT
selection
linkage
subtelomeric
microsatellite
sequencing coverage
recombination
Illumina
COI
WGS
deep sequencing
CNV
coalescence
haplotype
PacBio
superinfection
indel
Nanopore
prevalence
STR
SNP
sWGA
low complexity
LLIN
PfPR
NGS
core genome
IPTp
He (heterozygosity)
phasing