73 research outputs found
Recent progress on univariate and multivariate polynomial and spline quasi-interpolants
Polynomial and spline quasi-interpolants (QIs) are practical and effective approximation operators. Among their remarkable properties, let us cite for example: good shape properties, easy computation and evaluation (no linear system to solve), uniform boundedness independently of the degree (polynomials) or of the partition (splines), good approximation order. We shall emphasize new results on various types of univariate and multivariate polynomial or spline QIs, depending on the nature of coefficient functionals, which can be differential, discrete or integral. We shall also present some applications of QIs to numerical methods
On the solution of Fredholm integral equations based on spline quasi-interpolating projectors
Polynomial cubic splines with tension properties
In this paper we present a new class of spline functions with tension properties. These splines are composed by polynomial cubic pieces and therefore are conformal to the standard, NURBS based CAD/CAM systems
C2 piecewise cubic quasi-interpolants on a 6-direction mesh
We study two kinds of quasi-interpolants (abbr. QI) in the space of C2 piecewise cubics in the plane, or in a rectangular domain, endowed with the highly symmetric triangulation generated by a uniform 6-direction mesh. It has been proved recently that this space is generated by the integer translates of two multi-box splines. One kind of QIs is of differential type and the other of discrete type. As those QIs are exact on the space of cubic polynomials, their approximation order is 4 for sufficiently smooth functions. In addition, they exhibit nice superconvergent properties at some specific points. Moreover, the infinite norms of the discrete QIs being small, they give excellent approximations of a smooth function and of its first order partial derivatives. The approximation properties of the QIs are illustrated by numerical examples
A study on spline quasi-interpolation based quadrature rules for the isogeometric Galerkin BEM
Two recently introduced quadrature schemes for weakly singular integrals
[Calabr\`o et al. J. Comput. Appl. Math. 2018] are investigated in the context
of boundary integral equations arising in the isogeometric formulation of
Galerkin Boundary Element Method (BEM). In the first scheme, the regular part
of the integrand is approximated by a suitable quasi--interpolation spline. In
the second scheme the regular part is approximated by a product of two spline
functions. The two schemes are tested and compared against other standard and
novel methods available in literature to evaluate different types of integrals
arising in the Galerkin formulation. Numerical tests reveal that under
reasonable assumptions the second scheme convergences with the optimal order in
the Galerkin method, when performing -refinement, even with a small amount
of quadrature nodes. The quadrature schemes are validated also in numerical
examples to solve 2D Laplace problems with Dirichlet boundary conditions
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients
The cause of Huntington disease (HD) is a polyglutamine repeat expansion of more than 36 units in the huntingtin protein, which is inversely correlated with the age at onset of the disease. However, additional genetic factors are believed to modify the course and the age at onset of HD. Recently, we identified the V471A polymorphism in the autophagy-related gene ATG7, a key component of the autophagy pathway that plays an important role in HD pathogenesis, to be associated with the age at onset in a large group of European Huntington disease patients. To confirm this association in a second independent patient cohort, we analysed the ATG7 V471A polymorphism in additional 1,464 European HD patients of the “REGISTRY” cohort from the European Huntington Disease Network (EHDN). In the entire REGISTRY cohort we could not confirm a modifying effect of the ATG7 V471A polymorphism. However, analysing a modifying effect of ATG7 in these REGISTRY patients and in patients of our previous HD cohort according to their ethnic origin, we identified a significant effect of the ATG7 V471A polymorphism on the HD age at onset only in the Italian population (327 patients). In these Italian patients, the polymorphism is associated with a 6-years earlier disease onset and thus seems to have an aggravating effect. We could specify the role of ATG7 as a genetic modifier for HD particularly in the Italian population. This result affirms the modifying influence of the autophagic pathway on the course of HD, but also suggests population-specific modifying mechanisms in HD pathogenesis
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
Background Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT. Age at onset has been used as a quantitative phenotype in genetic analysis looking for Huntington's disease modifiers, but is hard to define and not always available. Therefore, we aimed to generate a novel measure of disease progression and to identify genetic markers associated with this progression measure. Methods We generated a progression score on the basis of principal component analysis of prospectively acquired longitudinal changes in motor, cognitive, and imaging measures in the 218 indivduals in the TRACK-HD cohort of Huntington's disease gene mutation carriers (data collected 2008–11). We generated a parallel progression score using data from 1773 previously genotyped participants from the European Huntington's Disease Network REGISTRY study of Huntington's disease mutation carriers (data collected 2003–13). We did a genome-wide association analyses in terms of progression for 216 TRACK-HD participants and 1773 REGISTRY participants, then a meta-analysis of these results was undertaken. Findings Longitudinal motor, cognitive, and imaging scores were correlated with each other in TRACK-HD participants, justifying use of a single, cross-domain measure of disease progression in both studies. The TRACK-HD and REGISTRY progression measures were correlated with each other (r=0·674), and with age at onset (TRACK-HD, r=0·315; REGISTRY, r=0·234). The meta-analysis of progression in TRACK-HD and REGISTRY gave a genome-wide significant signal (p=1·12 × 10−10) on chromosome 5 spanning three genes: MSH3, DHFR, and MTRNR2L2. The genes in this locus were associated with progression in TRACK-HD (MSH3 p=2·94 × 10−8 DHFR p=8·37 × 10−7 MTRNR2L2 p=2·15 × 10−9) and to a lesser extent in REGISTRY (MSH3 p=9·36 × 10−4 DHFR p=8·45 × 10−4 MTRNR2L2 p=1·20 × 10−3). The lead single nucleotide polymorphism (SNP) in TRACK-HD (rs557874766) was genome-wide significant in the meta-analysis (p=1·58 × 10−8), and encodes an aminoacid change (Pro67Ala) in MSH3. In TRACK-HD, each copy of the minor allele at this SNP was associated with a 0·4 units per year (95% CI 0·16–0·66) reduction in the rate of change of the Unified Huntington's Disease Rating Scale (UHDRS) Total Motor Score, and a reduction of 0·12 units per year (95% CI 0·06–0·18) in the rate of change of UHDRS Total Functional Capacity score. These associations remained significant after adjusting for age of onset. Interpretation The multidomain progression measure in TRACK-HD was associated with a functional variant that was genome-wide significant in our meta-analysis. The association in only 216 participants implies that the progression measure is a sensitive reflection of disease burden, that the effect size at this locus is large, or both. Knockout of Msh3 reduces somatic expansion in Huntington's disease mouse models, suggesting this mechanism as an area for future therapeutic investigation
Pi, Archimedes and circular splines
In the present paper, we give approximate values of π deduced from the areas of inscribed and circumscribed quadratic and cubic circular splines. Similar results on circular splines of higher degrees and higher approximation orders can be obtained in the same way. We compare these values to those obtained by computing the perimeters of those circular splines. We observe that the former are much easier to compute than the latter and give results of the same order. It also appears that Richardson extrapolation is very efficient on sequences of areas and give very good approximations of π. Finally, we also consider circular curves obtained by two subdivision algorithms. 1 Introduction: Archimede
- …