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Tejasvi Channagiri

Publications and source records attributed to Tejasvi Channagiri.

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Control Occupation Kernel Regression for Nonlinear Control-Affine Systems

This manuscript presents an algorithm for obtaining an approximation of a nonlinear high order control affine dynamical system. Controlled trajectories of the system are leveraged as the central unit of information via embedding them in vector-valued reproducing kernel Hilbert space (vvRKHS). The trajectories are embedded as the so-called higher order control occupation kernels which represent an operator on the vvRKHS corresponding to iterated integration after multiplication by a given controller. The solution to the system identification problem is then the unique solution of an infinite dimensional regularized regression problem. The representer theorem is then used to express the solution as finite linear combination of these occupation kernels, which converts an infinite dimensional optimization problem to a finite dimensional optimization problem. The vector valued structure of the Hilbert space allows for simultaneous approximation of the drift and control effectiveness components of the control affine system. Several experiments are performed to demonstrate the effectiveness of the developed approach.

math.OC

DSBplot: Indels in DNA Double-strand Break Repair Experiments

Double-strand breaks (DSBs) in DNA are naturally occurring destructive events in all organisms that may lead to genome instability. Cells employ various repair methods known as non-homologous end joining (NHEJ), microhomology mediated end joining (MMEJ), and homology-directed recombination (HDR). These repair processes may lead to DNA sequence variations (e.g., nucleotide insertions, deletions, and substitutions) at the location of the break. Studying DNA DSB repair processes often involves the use of high throughput sequencing assays to precisely quantify the sequence variations near the break with software tools. Often methods of assessing and visualizing these data have not taken into account the full complexity of the sequencing data, such as the frequency, type, and position of the sequence variations in a single comprehensive representation. Here we present a method that allows visualization of the overall variation pattern as well as comparison of these patterns among experimental setups.

q-bio.GN