154 research outputs found
Variational Multiscale Stabilization and the Exponential Decay of Fine-scale Correctors
This paper addresses the variational multiscale stabilization of standard
finite element methods for linear partial differential equations that exhibit
multiscale features. The stabilization is of Petrov-Galerkin type with a
standard finite element trial space and a problem-dependent test space based on
pre-computed fine-scale correctors. The exponential decay of these correctors
and their localisation to local cell problems is rigorously justified. The
stabilization eliminates scale-dependent pre-asymptotic effects as they appear
for standard finite element discretizations of highly oscillatory problems,
e.g., the poor approximation in homogenization problems or the pollution
effect in high-frequency acoustic scattering
Reduced basis isogeometric mortar approximations for eigenvalue problems in vibroacoustics
We simulate the vibration of a violin bridge in a multi-query context using
reduced basis techniques. The mathematical model is based on an eigenvalue
problem for the orthotropic linear elasticity equation. In addition to the nine
material parameters, a geometrical thickness parameter is considered. This
parameter enters as a 10th material parameter into the system by a mapping onto
a parameter independent reference domain. The detailed simulation is carried
out by isogeometric mortar methods. Weakly coupled patch-wise tensorial
structured isogeometric elements are of special interest for complex geometries
with piecewise smooth but curvilinear boundaries. To obtain locality in the
detailed system, we use the saddle point approach and do not apply static
condensation techniques. However within the reduced basis context, it is
natural to eliminate the Lagrange multiplier and formulate a reduced eigenvalue
problem for a symmetric positive definite matrix. The selection of the
snapshots is controlled by a multi-query greedy strategy taking into account an
error indicator allowing for multiple eigenvalues
A standardized framing for reporting protein identifications in mzIdentML 1.2
Inferring which protein species have been detected in bottom-up proteomics experiments has been a challenging problem for which solutions have been maturing over the past decade. While many inference approaches now function well in isolation, comparing and reconciling the results generated across different tools remains difficult. It presently stands as one of the greatest barriers in collaborative efforts such as the Human Proteome Project and public repositories such as the PRoteomics IDEntifications (PRIDE) database. Here we present a framework for reporting protein identifications that seeks to improve capabilities for comparing results generated by different inference tools. This framework standardizes the terminology for describing protein identification results, associated with the HUPO-Proteomics Standards Initiative (PSI) mzIdentML standard, while still allowing for differing methodologies to reach that final state. It is proposed that developers of software for reporting identification results will adopt this terminology in their outputs. While the new terminology does not require any changes to the core mzIdentML model, it represents a significant change in practice, and, as such, the rules will be released via a new version of the mzIdentML specification (version 1.2) so that consumers of files are able to determine whether the new guidelines have been adopted by export software
Community structures of actively growing bacteria shift along a north-south transect in the western North Pacific
Bacterial community structures and their activities in the ocean are tightly coupled with organic matter fluxes and thus control ocean biogeochemical cycles. Bromodeoxyuridine (BrdU), halogenated nucleoside and thymidine analogue, has been recently used to monitor actively growing bacteria (AGB) in natural environments. We labelled DNA of proliferating cells in seawater bacterial assemblages with BrdU and determined community structures of the bacteria that were possible key species in mediating biochemical reactions in the ocean. Surface seawater samples were collected along a north-south transect in the North Pacific in October 2003 and subjected to BrdU magnetic beads immunocapture and PCR-DGGE (BUMP-DGGE) analysis. Change of BrdU-incorporated community structures reflected the change of water masses along a north-south transect from subarctic to subtropical gyres in the North Pacific. We identified 25 bands referred to AGB as BrdU-incorporated phylotypes, belonging to Alphaproteobacteria (5 bands), Betaproteobacteria (1 band), Gammaproteobacteria (4 bands), Cytophaga-Flavobacterium-Bacteroides (CFB) group bacteria (5 bands), Gram-positive bacteria (6 bands), and Cyanobacteria (4 bands). BrdU-incorporated phylotypes belonging to Vibrionales, Alteromonadales and Gram-positive bacteria appeared only at sampling stations in a subtropical gyre, while those belonging to Roseobacter-related bacteria and CFB group bacteria appeared at the stations in both subarctic and subtropical gyres. Our result revealed phylogenetic affiliation of AGB and their dynamic change along with north-south environmental gradients in open oceans. Different species of AGB utilize different amount and kinds of substrates, which can affect the change of organic matter fluxes along transect
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood (vol 6, 92, 2021)
Genetics of disease, diagnosis and treatmen
Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020
We show the distribution of SARS-CoV-2 genetic clades over time and between countries and outline potential genomic surveillance objectives. We applied three available genomic nomenclature systems for SARS-CoV-2 to all sequence data from the WHO European Region available during the COVID-19 pandemic until 10 July 2020. We highlight the importance of real-time sequencing and data dissemination in a pandemic situation. We provide a comparison of the nomenclatures and lay a foundation for future European genomic surveillance of SARS-CoV-2.Peer reviewe
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