Magnetic Tunnel Junction Performance Under Mechanical Strain

In this work we investigate the effect of the mechanical stress on the performance of magnetic tunnel junctions (MTJ) with perpendicular magnetic anisotropy. We developed a 4-point bending setup, that allows us to apply a constant stress over a large substrate area with access to electrical measurements and external magnetic field. This setup enables us to measure key device performance parameters, such as tunnel magnetoresistance (TMR), switching current ($I_c^{50\%}$) and thermal stability ($\Delta$), as a function of applied stress. We find that variations in these parameters are negligible: less than \SI{2}{\percent} over the entire measured range between the zero stress condition and the maximum stress at the point of wafer breakage.Comment: 4 pages, 4 figure

Äärellisen kytkennän korjauksia kuuman QCD:n holografisiin ennusteisiin

Finite ’t Hooft coupling corrections to multiple physical observables in strongly coupled N=4 supersymmetric Yang-Mills plasma are examined, in an attempt to assess the stability of the expansion in inverse powers of the ’t Hooft coupling λ. Observables considered include thermodynamic quantities, transport coefficients, and quasinormal mode frequencies. Although large λ expansions for quasinormal mode frequencies are notably less well behaved than the expansions of other quantities, we find that a partial resummation of higher order corrections can significantly reduce the sensitivity of the results to the value of λ.Finite 't Hooft coupling corrections to multiple physical observables in strongly coupled N = 4 supersymmetric Yang-Mills plasma are examined, in an attempt to assess the stability of the expansion in inverse powers of the 't Hooft coupling lambda. Observables considered include thermodynamic quantities, transport coefficients, and quasinormal mode frequencies. Although large lambda expansions for quasinormal mode frequencies are notably less well behaved than the expansions of other quantities, we find that a partial resummation of higher order corrections can significantly reduce the sensitivity of the results to the value of lambda.Peer reviewe

Comprehensive Validation of the Regeneration Workload Forecast for Complex Capital Goods Using Data Mining

Capacity planning in the regeneration of complex capital goods faces major challenges because it is affected by a high level of uncertain workload information. A methodology is developed here to predict the regeneration workload on the basis of the CRISP-DM model using Bayesian networks. The forecasts are validated for the different capacity planning levels. The results support the conclusion that capacity planning can gain permanent benefits from the methodology developed

Dominance is common in mammals and is associated with trans-acting gene expression and alternative splicing

Background: Dominance and other non-additive genetic effects arise from the interaction between alleles, and historically these phenomena play a major role in quantitative genetics. However, most genome-wide association studies (GWAS) assume alleles act additively. // Results: We systematically investigate both dominance—here representing any non-additive within-locus interaction—and additivity across 574 physiological and gene expression traits in three mammalian stocks: F2 intercross pigs, rat heterogeneous stock, and mice heterogeneous stock. Dominance accounts for about one quarter of heritable variance across all physiological traits in all species. Hematological and immunological traits exhibit the highest dominance variance, possibly reflecting balancing selection in response to pathogens. Although most quantitative trait loci (QTLs) are detectable as additive QTLs, we identify 154, 64, and 62 novel dominance QTLs in pigs, rats, and mice respectively that are undetectable as additive QTLs. Similarly, even though most cis-acting expression QTLs are additive, gene expression exhibits a large fraction of dominance variance, and trans-acting eQTLs are enriched for dominance. Genes causal for dominance physiological QTLs are less likely to be physically linked to their QTLs but instead act via trans-acting dominance eQTLs. In addition, thousands of eQTLs are associated with alternatively spliced isoforms with complex additive and dominant architectures in heterogeneous stock rats, suggesting a possible mechanism for dominance. // Conclusions: Although heritability is predominantly additive, many mammalian genetic effects are dominant and likely arise through distinct mechanisms. It is therefore advantageous to consider both additive and dominance effects in GWAS to improve power and uncover causality

Primary care management for optimized antithrombotic treatment [PICANT]: study protocol for a cluster-randomized controlled trial

Background: Antithrombotic treatment is a continuous therapy that is often performed in general practice and requires careful safety management. The aim of this study is to investigate whether a best practice model that applies major elements of case management, including patient education, can improve antithrombotic management in primary health care in terms of reducing major thromboembolic and bleeding events. Methods: This 24-month cluster-randomized trial will be performed in 690 adult patients from 46 practices. The trial intervention will be a complex intervention involving general practitioners, health care assistants and patients with an indication for oral anticoagulation. To assess adherence to medication and symptoms in patients, as well as to detect complications early, health care assistants will be trained in case management and will use the Coagulation-Monitoring-List (Co-MoL) to regularly monitor patients. Patients will receive information (leaflets and a video), treatment monitoring via the Co-MoL and be motivated to perform self-management. Patients in the control group will continue to receive treatment-as-usual from their general practitioners. The primary endpoint is the combined endpoint of all thromboembolic events requiring hospitalization, and all major bleeding complications. Secondary endpoints are mortality, hospitalization, strokes, major bleeding and thromboembolic complications, severe treatment interactions, the number of adverse events, quality of anticoagulation, health-related quality of life and costs. Further secondary objectives will be investigated to explain the mechanism by which the intervention is effective: patients' assessment of chronic illness care, self-reported adherence to medication, general practitioners' and health care assistants' knowledge, patients' knowledge and satisfaction with shared decision making. Practice recruitment is expected to take place between July and December 2012. Recruitment of eligible patients will start in July 2012. Assessment will occur at three time points: baseline (T0), follow-up after 12 (T1) and after 24 months (T2). Discussion: The efficacy and effectiveness of individual elements of the intervention, such as antithrombotic interventions, self-management concepts in orally anticoagulated patients and the methodological tool, case-management, have already been extensively demonstrated. This project foresees the combination of several proven instruments, as a result of which we expect to profit from a reduction in the major complications associated with antithrombotic treatment

Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes

Background: Untranslated regions (UTRs) are important mediators of post-transcriptional regulation. The length of UTRs and the composition of regulatory elements within them are known to vary substantially across genes, but little is known about the reasons for this variation in humans. Here, we set out to determine whether this variation, specifically in 5’UTRs, correlates with gene dosage sensitivity. Results: We investigate 5’UTR length, the number of alternative transcription start sites, the potential for alternative splicing, the number and type of upstream open reading frames (uORFs) and the propensity of 5’UTRs to form secondary structures. We explore how these elements vary by gene tolerance to loss-of-function (LoF; using the LOEUF metric), and in genes where changes in dosage are known to cause disease. We show that LOEUF correlates with 5’UTR length and complexity. Genes that are most intolerant to LoF have longer 5’UTRs, greater TSS diversity, and more upstream regulatory elements than their LoF tolerant counterparts. We show that these differences are evident in disease gene-sets, but not in recessive developmental disorder genes where LoF of a single allele is tolerated. Conclusions: Our results confirm the importance of post-transcriptional regulation through 5'UTRs in tight regulation of mRNA and protein levels, particularly for genes where changes in dosage are deleterious and lead to disease. Finally, to support gene-based investigation we release a web-based browser tool, VuTR, that supports exploration of the composition of individual 5'UTRs and the impact of genetic variation within them