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