The relationship between Lp affine surface area and curvature measures is investigated. As a result, a new representation of the existing notion of Lp affine surface area depending only on curvature measures is derived. Direct proofs of the equivalence between this new representation and those previously known are provided. The proofs show that the new representation is, in a sense, “polar” to that of Lutwak’s and “dual” to that of Schutt & Werner’s.

We propose a derived version of non-archimedean analytic geometry. Intuitively, a derived non-archimedean analytic space consists of an ordinary non-archimedean analytic space equipped with a sheaf of derived rings. Such a naive definition turns out to be insufficient. In this paper, we resort to the theory of pregeometries and structured topoi introduced by Jacob Lurie. We prove the following three fundamental properties of derived non-archimedean analytic spaces: (1) The category of ordinary non-archimedean analytic spaces embeds fully faithfully into the ∞-category of derived non-archimedean analytic spaces. (2) The ∞-category of derived non-archimedean analytic spaces admits fiber products. (3) The ∞-category of higher non-archimedean analytic Deligne-Mumford stacks embeds fully faithfully into the ∞-category of derived non-archimedean analytic spaces. The essential image of this embedding is spanned by n-localic discrete derived non-archimedean analytic spaces. We will further develop the theory of derived non-archimedean analytic geometry in our subsequent works. Our motivations mainly come from intersection theory, enumerative geometry and mirror symmetry.

Next-generation sequencing technology enables the routine detection of bacterial pathogens for clinical diagnostics and genetic research. Whole-genome sequencing has been of importance in the epidemiologic analysis of bacterial pathogens. However, few whole-genome sequencing-based genotyping pipelines are available for practical applications. Here, we present the whole-genome sequencing-based single nucleotide polymorphism(SNP) genotyping method and apply to the evolutionary analysis of methicillin-resistant Staphylococcus aureus. The SNP genotyping method calls genome variants using next-generation sequencing reads of whole genomes and calculates the pair-wise Jaccard distances of the genome variants. The method may reveal the high-resolution whole-genome SNP profiles and the structural variants of different isolates of methicillin-resistant S. aureus(MRSA) and methicillin-susceptible S. aureus(MSSA) strains. The phylogenetic analysis of whole genomes and particular regions may monitor and track the evolution and the transmission dynamic of bacterial pathogens. The computer pro- grams of the whole genome sequencing-based SNP genotyping methods are available to the public at https://github. com/ cyinbox/NGS.

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Some filtrations of the tensor product of a highest weight module and a lowest weight module over quantum group Uq(g)are constructed in[1]and one can use them to define a two-sided ideal of the modified quantized enveloping algebra. It is shown that the quotient algebra inherits a canonical basis from the modified quantized enveloping algebra and is dual to the quantum coordinate algebra defined by Kashiwara for a symmetrizable Kac–Moody algebra g.