Skip to main content

Table 1 The advantages and limitations of bioinformatics tools current available for analysis of polyclonal infections and estimation of MOI

From: Molecular approaches to determine the multiplicity of Plasmodium infections

Software/approach

Implementation

Data source

Advantage

Limitation

References

Fws

Fws statistics

SNPs

Provide a summary statistic of relative inbreeding and correlation with MOI

Does not provide a direct estimate of COI

Manske et al. [108]

estMOI

Perl scripts 

TDS

estimate MOI, SNP combinations and proportion in a specific genomic region

Partial genomic region, sufficient density of SNPs in an amplicon is required

Assefa et al. [107]

COIL

Perl scripts web interface

SNPs

Use genome-wide SNPs to infer the number of strains and their proportions

Does not infer haplotypes; sequence read counts are assumed to be unbiased and the SNPs are unlinked

Galinsky et al. [93]

SeekDeep

Perl scripts

TDS

No reference sequence required, direct estimation of amplicon haplotype cluster and frequency

Partial genomic region, threshold for haplotype cluster calls needs to be determined by empirical methods in each study

Hathaway et al. [104]

HaplotypR

R package

TDS

Direct estimation of haplotype cluster and frequency based quality filtering of sequencing reads

Partial genomic region, enough high polymorphism in the amplicon is required and unable to deal with indel of amplicon

Lerch et al. [102]

pfmix

R package

SNPs

Infer inbreeding coefficients using WGS to assess within-sample parasite infections

Does not infer haplotypes, sequence read counts are assumed to be unbiased and SNPs need to be unlinked

O’Brien et al. [110]

THE REAL McCOIL

Perl scripts web interface

SNPs

Infer the number of strains and their proportions

Does not infer haplotypes, sequence read counts are assumed to be unbiased and SNPs need to be unlinked

Chang et al. [94]

DEploid

R package

SNPs

Estimate the number of strains, their relative proportions, and the haplotypes

Reference panel required, more reference strains are better. Multiallelic variant not considered

Zhu et al. [111]

  1. SNPs single nucleotide polymorphism, TDS targeted deep sequencing, WGS whole genome sequencing, MOI multiplicity of infection