Background: Most existing algorithms for modeling and analyzing molecular networks assume a static or time-invariant network topology. Such view, however, does not render the temporal evolution of the underlying biological process as molecular networks are typically "re-wired" over time in response to cellular development and environmental changes. In our previous work, we formulated the inference of time-varying or dynamic networks as a tracking problem, where the target state is the ensemble of edges in the network. We used the Kalman filter to track the network topology over time. Unfortunately, the output of the Kalman filter does not reflect known properties of molecular networks, such as sparsity.
Results: To address the problem of inferring sparse time-varying networks from a set of under-sampled measurements, we propose the Approximate Kernel RecONstruction (AKRON) Kalman filter. AKRON supersedes the Lasso regularization by starting from the Lasso-Kalman inferred network and judiciously searching the space for a sparser solution. We derive theoretical bounds for the optimality of AKRON. We evaluate our approach against the Lasso-Kalman filter on synthetic data. The results show that not only does AKRON-Kalman provide better reconstruction errors, but it is also better at identifying if edges exist within a network. Furthermore, we perform a real-world benchmark on the lifecycle (embryonic, larval, pupal, and adult stages) of the
Conclusions: We show that the networks inferred by the AKRON-Kalman filter are sparse and can detect more known gene-to-gene interactions for the
Ditzler, G., Bouaynaya, N., Shterenberg, R. et al. (2019). Approximate kernel reconstruction for time-varying networks. BioData Mining 12, 5 (2019). https://doi.org/10.1186/s13040-019-0192-1
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