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. 2018 May 2;17:185. doi: 10.1186/s12936-018-2337-y

Table 2.

Comparison of three methods for determination of multiplicity of infection (MOI) of P. vivax: long fragment (422 bp) of pvmsp1 amplicon deep sequencing, short fragment (117 bp) of pvmsp1 amplicon deep sequencing, and microsatellite marker genotyping

Amplicon deep sequencing
Long fragment (422 bp)
Amplicon deep sequencing
Short fragment (117 bp)
Microsatellite markersa
Number of subject 135 135 58
Median MOI 2 1 1
Mean MOIa 2.16a 1.64b 1.07c
Max MOI 6 4 3
No. polyclonal 84 62 3
% polyclonal 62.2 45.9 5.2
No. alleles 88 29 24
Heterozygosity (He) 0.92 0.84 0.77

Significant differences were detected in mean MOI among the three methods as indicated by the superscripts (Tukey–Kramer HSD test, P < 0.05)

He: Expected heterozygosity corrected for sample size

aRefer to Lo et al. (2015) [39]