Overview
MalReBay is an R package for Bayesian molecular correction of malaria therapeutic efficacy studies (TES). Given paired genotyping data from a patient’s initial infection (Day 0) and a later recurrence, it estimates the posterior probability that the recurrence is a recrudescence (treatment failure, same parasite persisting) versus a reinfection (new parasite acquired after treatment).
Unlike rule-based allele-matching methods, MalReBay:
- models sequencing error, allelic dropout, and allele loss explicitly
- handles polyclonal infections (MOI > 1) at every locus
- incorporates local allele frequency information to weigh evidence
- uses a full Bayesian MCMC engine (Stan HMC-NUTS) for principled uncertainty quantification
- supports both length-polymorphic markers (microsatellites, MSP, GLURP) and amplicon sequencing (haplotype) data
Key Features
| Feature | Detail |
|---|---|
| Data types | Length-polymorphic markers and amplicon sequencing |
| MCMC engine | Stan HMC-NUTS via rstan — fast, well-mixing, gradient-based |
| Polyclonal infections | Analytically marginalises over within-host clone multiplicity |
| Error model | Estimates q_mismatch, q_loss, q_dropout from the data |
| Prior | Recrudescence probability fixed at 0.5 (no directional bias) |
| Convergence | Rank-normalised R̂, bulk/tail ESS, Geweke, Gelman-Rubin |
| Output | Per-patient posterior probability + match-counting comparison table |
Installation
# Install the development version from GitHub
remotes::install_github("SwissTPH/MalReBay")Note: MalReBay links against
rstanandStanHeaders. On first use the Stan model is compiled once and cached. This may take a few minutes but only happens once per R installation.