The Westermo test results data set

There is a growing body of knowledge in the computer science, software engineering, software testing and software test automation disciplines. However, there is a challenge for researchers to evaluate their research findings, innovations and tools due to lack of realistic data. This paper presents the Westermo test results data set, more than one million verdicts from testing of embedded systems, from more than five hundred consecutive days of nightly testing. The data also contains information on code changes in both the software under test and the test framework used for testing. This data set can support the research community in particular with respect to the regression test selection problem, flaky tests, test results visualization, etc

SEPIA345: A 345 GHz dual polarization heterodyne receiver channel for SEPIA at the APEX telescope

Context. We describe the new SEPIA345 heterodyne receiver channel installed at the Atacama Pathfinder EXperiment (APEX) telescope, including details of its configuration, characteristics, and test results on sky. SEPIA345 is designed and built to be a part of the Swedish ESO PI Instrument for the APEX telescope (SEPIA). This new receiver channel is suitable for very high-resolution spectroscopy and covers the frequency range 272- 376 GHz. It utilizes a dual polarization sideband separating (2SB) receiver architecture, employing superconductor-isolator-superconductor mixers (SIS), and provides an intermediate frequency (IF) band of 4- 12 GHz for each sideband and polarization, thus covering a total instantaneous IF bandwidth of 4 \uc3\uc2 - 8 = 32 GHz. Aims. This paper provides a description of the new receiver in terms of its hardware design, performance, and commissioning results. Methods. The methods of design, construction, and testing of the new receiver are presented. Results. The achieved receiver performance in terms of noise temperature, sideband rejection, stability, and other parameters are described. Conclusions. SEPIA345 is a commissioned APEX facility instrument with state-of-the-art wideband IF performance. It has been available on the APEX telescope for science observations since July 2021

A Swedish heterodyne facility instrument for the APEX telescope

In March 2008, the APEX facility instrument was installed on the telescope at the site of Lliano Chajnantor in northern Chile. The main objective of the paper is to introduce the new instrument to the radio astronomical community. It describes the hardware configuration and presents some initial results from the on-sky commissioning. The heterodyne instrument covers frequencies between 211 GHz and 1390 GHz divided into four bands. The first three bands are sideband-separating mixers operating in a single sideband mode and based on superconductor-insulator-superconductor (SIS) tunnel junctions. The fourth band is a hot-electron bolometer, waveguide balanced mixer. All bands are integrated in a closedcycle temperature-stabilized cryostat and are cooled to 4 K. We present results from noise temperature, sideband separation ratios, beam, and stability measurements performed on the telescope as a part of the receiver technical commissioning. Examples of broad extragalactic lines are also included

Auxilin is a novel susceptibility gene for congenital heart block which directly impacts fetal heart function

Objective: Neonatal lupus erythematosus (NLE) may develop after transplacental transfer of maternal autoantibodies with cardiac manifestations (congenital heart block, CHB) including atrioventricular block, atrial and ventricular arrhythmias, and cardiomyopathies. The association with anti-Ro/SSA antibodies is well established, but a recurrence rate of only 12%–16% despite persisting maternal autoantibodies suggests that additional factors are required for CHB development. Here, we identify fetal genetic variants conferring risk of CHB and elucidate their effects on cardiac function. Methods: A genome-wide association study was performed in families with at least one case of CHB. Gene expression was analysed by microarrays, RNA sequencing and PCR and protein expression by western blot, immunohistochemistry, immunofluorescence and flow cytometry. Calcium regulation and connectivity were analysed in primary cardiomyocytes and cells induced from pleuripotent stem cells. Fetal heart performance was analysed by Doppler/echocardiography. Results: We identified DNAJC6 as a novel fetal susceptibility gene, with decreased cardiac expression of DNAJC6 associated with the disease risk genotype. We further demonstrate that fetal cardiomyocytes deficient in auxilin, the protein encoded by DNAJC6, have abnormal connectivity and Ca2+ homoeostasis in culture, as well as decreased cell surface expression of the Cav1.3 calcium channel. Doppler echocardiography of auxilin-deficient fetal mice revealed cardiac NLE abnormalities in utero, including abnormal heart rhythm with atrial and ventricular ectopias, as well as a prolonged atrioventricular time intervals. Conclusions: Our study identifies auxilin as the first genetic susceptibility factor in NLE modulating cardiac function, opening new avenues for the development of screening and therapeutic strategies in CHB.publishedVersio

The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia : design, results and future prospects

The impact of many unfavorable childhood traits or diseases, such as low birth weight and mental disorders, is not limited to childhood and adolescence, as they are also associated with poor outcomes in adulthood, such as cardiovascular disease. Insight into the genetic etiology of childhood and adolescent traits and disorders may therefore provide new perspectives, not only on how to improve wellbeing during childhood, but also how to prevent later adverse outcomes. To achieve the sample sizes required for genetic research, the Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia were established. The majority of the participating cohorts are longitudinal population-based samples, but other cohorts with data on early childhood phenotypes are also involved. Cohorts often have a broad focus and collect(ed) data on various somatic and psychiatric traits as well as environmental factors. Genetic variants have been successfully identified for multiple traits, for example, birth weight, atopic dermatitis, childhood BMI, allergic sensitization, and pubertal growth. Furthermore, the results have shown that genetic factors also partly underlie the association with adult traits. As sample sizes are still increasing, it is expected that future analyses will identify additional variants. This, in combination with the development of innovative statistical methods, will provide detailed insight on the mechanisms underlying the transition from childhood to adult disorders. Both consortia welcome new collaborations. Policies and contact details are available from the corresponding authors of this manuscript and/or the consortium websites.Peer reviewe