TL;DR
MixTwice is an empirical Bayesian method designed for large-scale peptide array hypothesis testing, improving detection power and reproducibility by estimating effect and variance distributions.
Contribution
It introduces a novel two-mixing-distribution model for effect and variance estimation, enhancing false discovery rate control in high-dimensional peptide data.
Findings
Accurately estimates generative parameters in simulations.
Effectively identifies non-null peptides in rheumatoid arthritis data.
Demonstrates strong reproducibility in real data applications.
Abstract
Peptide microarrays have emerged as a powerful technology in immunoproteomics as they provide a tool to measure the abundance of different antibodies in patient serum samples. The high dimensionality and small sample size of many experiments challenge conventional statistical approaches, including those aiming to control the false discovery rate (FDR). Motivated by limitations in reproducibility and power of current methods, we advance an empirical Bayesian tool that computes local false discovery rate statistics and local false sign rate statistics when provided with data on estimated effects and estimated standard errors from all the measured peptides. As the name suggests, the \verb+MixTwice+ tool involves the estimation of two mixing distributions, one on underlying effects and one on underlying variance parameters. Constrained optimization techniques provide for model fitting of…
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