While high-throughput sequencing (HTS) has enabled the rapid and inexpensive acquisition of large quantities of genetic sequencing data, HTS data may not fully reflect characteristics of the environment being sequenced. A common step in generating HTS data is multiplexing, which reduces the cost of studying many samples by enabling sample processing in a single sequencing batch. Unfortunately multiplexing can incur sample-to-sample misclassification of observations, with misclassification rates varying by sequencing chemistry and batch. In this paper, we propose a statistical model to link the source sample to observed count data. Because many latent misclassification matrices could connect the source and observed data, directly computing likelihoods is infeasible, and so we propose an importance sampling method to estimate the likelihood of a candidate source matrices. We demonstrate the performance of our proposed method using a simulation study and an application to a vaginal microbiome dataset.
No takes yet. Share an insight, caveat, or question.
Shi et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: