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Rojalin Mishra

Publications and source records attributed to Rojalin Mishra.

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Design Verification of the Quantum Control Stack

This paper describes the verification of the classical software and hardware stack that is used to control cold atom- and superconducting-based quantum computing hardware. The paper serves both as an introduction to quantum computing and to how classical device verification techniques can be employed there. Two main challenges in building a quantum control stack are generating precise deterministic-timing operations at the edge and scaled-out processing in the middle layer. Both challenges are to do with a certain kind of functional performance correctness. And, as usual, the design lives under tight power, memory and latency constraints. The quantum control stack is a complex interaction of algorithms, software runtimes and digital hardware. We take inspiration from modern software approaches to engineering, such as continuous integration and hardware automation, to quickly ship experimental features to customers in the field.

quant-ph

A Quantitative Understanding of Human Sex Chromosomal Genes

In the last few decades, the human allosomes are engrossed in an intensive attention among researchers. The allosomes are now already been sequenced and found there are about 2000 and 78 genes in human X and Y chromosomes respectively. The hemizygosity of the human X chromosome in males exposes recessive disease alleles, and this phenomenon has prompted decades of intensive study of X-linked disorders. By contrast, the small size of the human Y chromosome, and its prominent long-arm heterochromatic region suggested absence of function beyond sex determination. But the present problem is to accomplish whether a given sequence of nucleotides i.e. a DNA is a Human X or Y chromosomal genes or not, without any biological experimental support. In our perspective, a proper quantitative understanding of these genes is required to justify or nullify whether a given sequence is a Human X or Y chromosomal gene. In this paper, some of the X and Y chromosomal genes have been quantified in genomic and proteomic level through Fractal Geometric and Mathematical Morphometric analysis. Using the proposed quantitative model, one can easily make probable justification or deterministic nullification whether a given sequence of nucleotides is a probable Human X or Y chromosomal gene or not, without seeking any biological experiment. Of course, a further biological experiment is essential to validate it as the probable Human X or Y chromosomal gene homologue. This study would enable Biologists to understand these genes in more quantitative manner instead of their qualitative features.

q-bio.GN