Authors
Oskar Henriksson, Carlos Améndola, Jose Israel Rodriguez, Polly Y Yu
Published in
Journal of mathematical biology. Volume 91. Issue 4. Pages 34. Sep 10, 2025. Epub Sep 10, 2025.
Abstract
A fundamental question in the field of molecular computation is what computational tasks a biochemical system can carry out. In this work, we focus on the problem of finding the maximum likelihood estimate (MLE) for log-affine models. We revisit a construction due to Gopalkrishnan of a mass-action system with the MLE as its unique positive steady state, which is based on choosing a basis for the kernel of the design matrix of the model. We extend this construction to allow for any finite spanning set of the kernel, and explore how the choice of spanning set influences the dynamics of the resulting network, including the existence of boundary steady states, the deficiency of the network, and the rate of convergence. In particular, we prove that using a Markov basis as the spanning set guarantees global stability of the MLE steady state.
PMID:
40928650
Bibliographic data and abstract were imported from PubMed on 10 Sep 2025.
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