bioRxivBioinformaticsPreprint
QuImputer: an LD-informed QUBO/Ising formulation of genotype imputation with quantum-hardware execution
Abstract
Genotype imputation offers a biological application for optimization methods that may eventually run on larger quantum computers. We developed QuImputer to encode allele-frequency priors and signed linkage disequilibrium (LD) in a reduced Ising/QUBO objective, with only missing genotypes represented as optimization variables. The same objective can be passed to exhaustive classical search, quantum approximate optimization algorithm simulation, or quantum hardware. We evaluated the formulation on 100 rice accessions across 12 chromosomes, estimating LD and allele frequency from the same post-masking observed matrix supplied to Beagle 5.4. Evaluation was restricted to known truth at sites with exact dosage coding and an alternate allele that was not the major allele, with MAF below 0.50, yielding 1.88 billion scored genotypes. Beagle achieved higher rare-ALT sensitivity (2.52% versus 0.54%), F1 (0.047 versus 0.011), Matthews correlation coefficient (0.088 versus 0.044), and pooled hard-call dosage R-squared (0.231 versus 0.014). QuImputer produced fewer false ALT calls, with Type I error of 0.038% versus 0.223%. Analyses of a chromosome-1 subset showed limited local LD support for many masked rare-ALT carriers. In five small IBM Fez validation problems, the selected minimum-energy outputs matched unique all-reference exact optima; the pooled frequency of those optima was 1.21-2.63%. Further IBM Fez executions covered eleven sparse instances with 12-97 variables and a separate 120-variable instance, retaining all measurements. Selected outputs recovered the exact optima in eight instances through 49 variables. Larger instances remained below the all-reference baseline; noiseless comparisons distinguished finite-shot sampling from deviations in hardware output. QuImputer provides an LD-informed formulation and a route to quantum-hardware execution, together with an empirical assessment of the limitations of the evaluated configuration. These results establish a basis for studying richer information models and alternative classical or quantum solvers.
- organism: plant (other)
- assay: whole-genome sequencing
- research focus: imputation
- approach: statistical model
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- AlphaImpute2: Fast and accurate pedigree and population based imputation for hundreds of thousands of individuals in livestock populations
Andrew Whalen, John M. Hickey·bioRxiv·Sep 16, 2020
- Selphi: Empowering GWAS Discovery through Enhanced Genotype Imputation
Adriano De Marino, Abdallah Amr Mahmoud, … Puya G. Yazdi·medRxiv·Dec 18, 2023
- Why are rare variants hard to impute? Coalescent models reveal theoretical limits in existing algorithms.
Yichen Si, Brett R. Vanderwerff, Sebastian K. Zöllner·GeneticsPeer-reviewed·Feb 5, 2021
- Rapid and accurate genotype imputation from low coverage short read, long read, and cell free DNA sequence
Zilong Li, Anders Albrechtsen, Robert William Davies·bioRxiv·Jul 18, 2024
- Genotype imputation and error estimation in connected multiparental populations
Chaozhi Zheng, Eligio Bossolini, … Fred A. van Eeuwijk·GeneticsPeer-reviewed·Aug 17, 2026
- A one penny imputed genome from next generation reference panels
Brian L. Browning, Ying Zhou, Sharon R. Browning·The American Journal of Human GeneticsPeer-reviewed·Aug 9, 2018