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