Polarization screening and induced carrier density at the interface of LaAlO3_3 overlayer on SrTiO3_3 (001)

We investigate the role of lattice polarization in determination of induced carrier density at the $n$-type interface of LaAlO$_3$ overlayer on SrTiO$_3$ (001) by carrying out density-functional-theory calculations. When no oxygen vacancy or defect is present, the magnitude of polarization screening in the LaAlO$_3$ layers is found to be correlated with the carrier charge induced at the interface. For the interfaces with a few LaAlO$_3$ layers, the induced charge carrier is compensated by the electrostatic screening and consequently its density remains far less than 0.5 electrons per unit cell.Comment: 4 pages, 4 figure

Special Session on Industry 4.0

No abstract available

Applications of degree estimate for subalgebras

Let $K$ be a field of positive characteristic and $K$ be the free algebra of rank two over $K$. Based on the degree estimate done by Y.-C. Li and J.-T. Yu, we extend the results of S.J. Gong and J.T. Yu's results: (1) An element $p(x,y)\in K$ is a test element if and only if $p(x,y)$ does not belong to any proper retract of $K$; (2) Every endomorphism preserving the automorphic orbit of a nonconstant element of $K$ is an automorphism; (3) If there exists some injective endomorphism $\phi$ of $K$ such that $\phi(p(x,y))=x$ where $p(x,y)\in K$, then $p(x,y)$ is a coordinate. And we reprove that all the automorphisms of $K$ are tame. Moreover, we also give counterexamples for two conjectures established by Leonid Makar-Limanov, V. Drensky and J.-T. Yu in the positive characteristic case.Comment: 12 page

Worldwide genetic variation of the IGHV and TRBV immune receptor gene families in humans.

The immunoglobulin heavy variable (IGHV) and T cell beta variable (TRBV) loci are among the most complex and variable regions in the human genome. Generated through a process of gene duplication/deletion and diversification, these loci can vary extensively between individuals in copy number and contain genes that are highly similar, making their analysis technically challenging. Here, we present a comprehensive study of the functional gene segments in the IGHV and TRBV loci, quantifying their copy number and single-nucleotide variation in a globally diverse sample of 109 (IGHV) and 286 (TRBV) humans from over a 100 populations. We find that the IGHV and TRBV gene families exhibit starkly different patterns of variation. In addition to providing insight into the different evolutionary paths of the IGHV and TRBV loci, our results are also important to the adaptive immune repertoire sequencing community, where the lack of frequencies of common alleles and copy number variants is hampering existing analytical pipelines