115 research outputs found
Effects of quenched impurities on surface diffusion, spreading, and ordering of O/W(110)
We study how quenched impurities affect the surfacediffusion and ordering of strongly interactingadsorbate atoms on surfaces. To this end, we carry out Monte Carlo simulations for a lattice-gas model of O/W(110), including small concentrations of immobile impurities which block their adsorption sites. We examine the behavior of the diffusion coefficients and order parameters as a function of coverage corresponding to various ordered phases at low temperatures. The effects of impurities are examined under both equilibrium and nonequilibrium conditions, and the results are compared to recent studies on a completely clean surface. We find that even minute impurity concentrations affect the diffusion behavior considerably in equilibrium. The effects are strongest in ordered phases and close to phase boundaries, where quenched impurities lead to a reduction of order, which in turn leads to significant changes in the collective diffusion and phase behavior. As the impurity concentration is increased to a level of a few percent of the total surface area, the reduction in order becomes particularly prominent at high coverages. Further studies under nonequilibrium conditions reveal that nonequilibrium effects are strong in the absence of impurities, while for surfaces covered by impurities the nonequilibrium effects are relatively weaker.Peer reviewe
One-pot synthesis, crystallization and deracemization of isoindolinones from achiral reactants
The synthesis, crystallization, and complete solid-state deracemization of isoindolinones was realized in one pot simply by grinding achiral reaction components in a suitable solvent with an achiral catalyst. Previously, this concept was applied to a reversible reaction, but herein we showed that it could also be used in combination with reactions in which product formation is irreversible. A controlled final configuration of the product was obtained by using small amounts of chiral additives or seed crystals of the product
A Note on Computations of D-brane Superpotential
We develop some computational methods for the integrals over the 3-chains on
the compact Calabi-Yau 3-folds that plays a prominent role in the analysis of
the topological B-model in the context of the open mirror symmetry. We discuss
such 3-chain integrals in two approaches. In the first approach, we provide a
systematic algorithm to obtain the inhomogeneous Picard-Fuchs equations. In the
second approach, we discuss the analytic continuation of the period integral to
compute the 3-chain integral directly. The latter direct integration method is
applicable for both on-shell and off-shell formalisms.Comment: 61 pages, 5 figures; v2: typos corrected, minor changes, references
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Diamond deposition on modified silicon substrates: Making diamond atomic force microscopy tips for nanofriction experiments
Fine-crystalline diamond particles are grown on standard Si atomic force microscopy tips, using hot filament-assisted chemical vapor deposition. To optimize the conditions for diamond deposition, first a series of experiments is carried out using silicon substrates covered by point-topped pyramids as obtained by wet chemical etching. The apexes and the edges of the silicon pyramids provide favorable sites for diamond nucleation and growth. The investigation of the deposited polycrystallites is done by means of optical microscopy, scanning electron microscopy and micro-Raman spectroscopy. The resulting diamond-terminated tips are tested in ultra high vacuum using contact-mode atomic force microscope on a stepped surface of sapphire showing high stability, sharpness, and hardnes
Voorwaarts met de milieuprestaties van de Nederlandse open-teelt sectoren: een verkenning naar 2020 ten behoeve van 'Telen met toekomst'
Dit rapport beschrijft het overheidsbeleid voor landbouw en milieu op het gebied van nutriënten en gewasbeschermingsmiddelen, en de daaruit afgeleide doelen welke voor de bedrijven binnen 'Telen met toekomst' gesteld zullen worden. Verder worden beschreven de huidige milieuprestaties van de vier sectoren en de tekortkomingen ten aanzien van milieudoelstellingen en oplossingsrichtingen om de gestelde doelen te kunnen gaan voldoe
Holonomic functions of several complex variables and singularities of anisotropic Ising n-fold integrals
Lattice statistical mechanics, often provides a natural (holonomic) framework
to perform singularity analysis with several complex variables that would, in a
general mathematical framework, be too complex, or could not be defined.
Considering several Picard-Fuchs systems of two-variables "above" Calabi-Yau
ODEs, associated with double hypergeometric series, we show that holonomic
functions are actually a good framework for actually finding the singular
manifolds. We, then, analyse the singular algebraic varieties of the n-fold
integrals , corresponding to the decomposition of the magnetic
susceptibility of the anisotropic square Ising model. We revisit a set of
Nickelian singularities that turns out to be a two-parameter family of elliptic
curves. We then find a first set of non-Nickelian singularities for and , that also turns out to be rational or ellipic
curves. We underline the fact that these singular curves depend on the
anisotropy of the Ising model. We address, from a birational viewpoint, the
emergence of families of elliptic curves, and of Calabi-Yau manifolds on such
problems. We discuss the accumulation of these singular curves for the
non-holonomic anisotropic full susceptibility.Comment: 36 page
The Genome of the Netherlands:design, and project goals
Within the Netherlands a national network of biobanks has been established (Biobanking and Biomolecular Research Infrastructure-Netherlands (BBMRI-NL)) as a national node of the European BBMRI. One of the aims of BBMRI-NL is to enrich biobanks with different types of molecular and phenotype data. Here, we describe the Genome of the Netherlands (GoNL), one of the projects within BBMRI-NL. GoNL is a whole-genome-sequencing project in a representative sample consisting of 250 trio-families from all provinces in the Netherlands, which aims to characterize DNA sequence variation in the Dutch population. The parent-offspring trios include adult individuals ranging in age from 19 to 87 years (mean = 53 years; SD = 16 years) from birth cohorts 1910-1994. Sequencing was done on blood-derived DNA from uncultured cells and accomplished coverage was 14-15x. The family-based design represents a unique resource to assess the frequency of regional variants, accurately reconstruct haplotypes by family-based phasing, characterize short indels and complex structural variants, and establish the rate of de novo mutational events. GoNL will also serve as a reference panel for imputation in the available genome-wide association studies in Dutch and other cohorts to refine association signals and uncover population-specific variants. GoNL will create a catalog of human genetic variation in this sample that is uniquely characterized with respect to micro-geographic location and a wide range of phenotypes. The resource will be made available to the research and medical community to guide the interpretation of sequencing projects. The present paper summarizes the global characteristics of the project.</p
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Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands'
Although genome-wide association studies (GWAS) have identified many common variants associated with complex traits, low-frequency and rare variants have not been interrogated in a comprehensive manner. Imputation from dense reference panels, such as the 1000 Genomes Project (1000G), enables testing of ungenotyped variants for association. Here we present the results of imputation using a large, new population-specific panel: the Genome of The Netherlands (GoNL). We benchmarked the performance of the 1000G and GoNL reference sets by comparing imputation genotypes with ‘true' genotypes typed on ImmunoChip in three European populations (Dutch, British, and Italian). GoNL showed significant improvement in the imputation quality for rare variants (MAF 0.05–0.5%) compared with 1000G. In Dutch samples, the mean observed Pearson correlation, r2, increased from 0.61 to 0.71. We also saw improved imputation accuracy for other European populations (in the British samples, r2 improved from 0.58 to 0.65, and in the Italians from 0.43 to 0.47). A combined reference set comprising 1000G and GoNL improved the imputation of rare variants even further. The Italian samples benefitted the most from this combined reference (the mean r2 increased from 0.47 to 0.50). We conclude that the creation of a large population-specific reference is advantageous for imputing rare variants and that a combined reference panel across multiple populations yields the best imputation results
WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene
Telomere length (TL) regulation is an important factor in ageing, reproduction and cancer development. Genetic, hereditary and environmental factors regulating TL are currently widely investigated, however, their relative contribution to TL variability is still understudied. We have used whole genome sequencing data of 250 family trios from the Genome of the Netherlands project to perform computational measurement of TL and a series of regression and genome-wide association analyses to reveal TL inheritance patterns and associated genetic factors. Our results confirm that TL is a largely heritable trait, primarily with mother’s, and, to a lesser extent, with father’s TL having the strongest influence on the offspring. In this cohort, mother’s, but not father’s age at conception was positively linked to offspring TL. Age-related TL attrition of 40 bp/year had relatively small influence on TL variability. Finally, we have identified TL-associated variations in ribonuclease reductase catalytic subunit M1 (RRM1 gene), which is known to regulate telomere maintenance in yeast. We also highlight the importance of multivariate approach and the limitations of existing tools for the analysis of TL as a polygenic heritable quantitative trait
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