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