184 research outputs found

    Progress toward Monte Carlo–thermal hydraulic coupling using low-order nonlinear diffusion acceleration methods

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    A new approach for coupled Monte Carlo (MC) and thermal hydraulics (TH) simulations is proposed using low-order nonlinear diffusion acceleration methods. This approach uses new features such as coarse mesh finite difference diffusion (CMFD), multipole representation for fuel temperature feedback on microscopic cross sections, and support vector machine learning algorithms (SVM) for iterations between CMFD and TH equations. The multipole representation method showed small differences of about 0.3% root mean square (RMS) error in converged assembly source distribution compared to a conventional MC simulation with ACE data at the same temperature. This is within two standard deviations of the real uncertainty. Eigenvalue differences were on the order of 10 pcm. Support vector machine regression was performed on-the-fly during MC simulations. Regression results of macroscopic cross sections parametrized by coolant density and fuel temperature were successful and eliminated the need of partial derivative tables generated from lattice codes. All of these new tools were integrated together to perform MC-CMFD-TH-SVM iterations. Results showed that inner iterations between CMFD-TH-SVM are needed to obtain a stable solution

    Progress and Status of the Openmc Monte Carlo Code

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    The present work describes the latest advances and progress in the development of the OpenMC Monte Carlo code, an open-source code originating from the Massachusetts Institute of Technology. First, an overview of the development workflow of OpenMC is given. Various enhancements to the code such as real-time XML input validation, state points, plotting, OpenMP threading, and coarse mesh finite difference acceleration are described.United States. Department of Energy. Naval Reactors Division (Rickover Fellowship Program in Nuclear Engineering)United States. Department of Energy (Consortium for Advanced Simulation of Light Water Reactors. Contract DE-AC05-00OR22725)United States. Department of Energy. Office of Advanced Scientific Computing Research (Contract DE-AC02-06CH11357

    A Chandra HETG Observation of the Quasar H 1821+643 and Its Surrounding Cluster

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    We present the high-resolution X-ray spectrum of the low-redshift quasar H 1821+643 and its surrounding hot cluster observed with the Chandra High Energy Transmission Grating Spectrometer (HETGS). An iron emission line attributed to the quasar at ~6.43 keV (rest frame) is clearly resolved, with an equivalent width of ~100 eV. Although we cannot rule out contributions to the line from a putative torus, the diskline model provides an acceptable fit to this iron line. We also detect a weak emission feature at ~6.9 keV (rest frame). We suggest that both lines could originate in an accretion disk comprised of a highly ionized optically thin atmosphere sitting atop a mostly neutral disk. We search for absorption features from a warm/hot component of the intergalactic medium along the ~1.5Gpc/h line of sight to the quasar. No absorption features are detected at or above the 3 sigma level while a total of six OVI intervening absorption systems have been detected with HST and FUSE. Based on the lack of OVII and OVIII absorption lines and by assuming collisionally ionization, we constrain the gas temperature of a typical OVI absorber to 10^5 < T < 10^6 K, which is consistent with the results from hydrodynamic simulations of the intergalactic medium. The zeroth order image reveals the extended emission from the surrounding cluster. We have been able to separate the moderate CCD X-ray spectrum of the surrounding cluster from the central quasar and find that this is a hot cluster with a temperature of ~10 keV and a metal abundance of ~0.3 Zo. We also independently obtain the redshift of the cluster, which is consistent with the optical results. We estimate that the cluster makes negligible contributions to the 6.9 keV iron K line flux.Comment: 33 pages, 9 figures (2 color). Accepted for publication in the Astrophysical Journa

    Studying the Salt Dependence of the Binding of σ70 and σ32 to Core RNA Polymerase Using Luminescence Resonance Energy Transfer

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    The study of protein-protein interactions is becoming increasingly important for understanding the regulation of many cellular processes. The ability to quantify the strength with which two binding partners interact is desirable but the accurate determination of equilibrium binding constants is a difficult process. The use of Luminescence Resonance Energy Transfer (LRET) provides a homogeneous binding assay that can be used for the detection of protein-protein interactions. Previously, we developed an LRET assay to screen for small molecule inhibitors of the interaction of σ70 with theβ' coiled-coil fragment (amino acids 100–309). Here we describe an LRET binding assay used to monitor the interaction of E. coli σ70 and σ32 with core RNA polymerase along with the controls to verify the system. This approach generates fluorescently labeled proteins through the random labeling of lysine residues which enables the use of the LRET assay for proteins for which the creation of single cysteine mutants is not feasible. With the LRET binding assay, we are able to show that the interaction of σ70 with core RNAP is much more sensitive to NaCl than to potassium glutamate (KGlu), whereas the σ32 interaction with core RNAP is insensitive to both salts even at concentrations >500 mM. We also find that the interaction of σ32 with core RNAP is stronger than σ70 with core RNAP, under all conditions tested. This work establishes a consistent set of conditions for the comparison of the binding affinities of the E.coli sigma factors with core RNA polymerase. The examination of the importance of salt conditions in the binding of these proteins could have implications in both in vitro assay conditions and in vivo function

    A pipeline for high throughput detection and mapping of SNPs from EST databases

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    Single nucleotide polymorphisms (SNPs) represent the most abundant type of genetic variation that can be used as molecular markers. The SNPs that are hidden in sequence databases can be unlocked using bioinformatic tools. For efficient application of these SNPs, the sequence set should be error-free as much as possible, targeting single loci and suitable for the SNP scoring platform of choice. We have developed a pipeline to effectively mine SNPs from public EST databases with or without quality information using QualitySNP software, select reliable SNP and prepare the loci for analysis on the Illumina GoldenGate genotyping platform. The applicability of the pipeline was demonstrated using publicly available potato EST data, genotyping individuals from two diploid mapping populations and subsequently mapping the SNP markers (putative genes) in both populations. Over 7000 reliable SNPs were identified that met the criteria for genotyping on the GoldenGate platform. Of the 384 SNPs on the SNP array approximately 12% dropped out. For the two potato mapping populations 165 and 185 SNPs segregating SNP loci could be mapped on the respective genetic maps, illustrating the effectiveness of our pipeline for SNP selection and validation

    Trauma-related emotions and radical acceptance in dialectical behavior therapy for posttraumatic stress disorder after childhood sexual abuse

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    Background: Posttraumatic Stress Disorder (PTSD) related to childhood sexual abuse (CSA) is often associated with a wide range of trauma-related aversive emotions such as fear, disgust, sadness, shame, guilt, and anger. Intense experience of aversive emotions in particular has been linked to higher psychopathology in trauma survivors. Most established psychosocial treatments aim to reduce avoidance of trauma-related memories and associated emotions. Interventions based on Dialectical Behavior Therapy (DBT) also foster radical acceptance of the traumatic event. Methods: This study compares individual ratings of trauma-related emotions and radical acceptance between the start and the end of DBT for PTSD (DBT-PTSD) related to CSA. We expected a decrease in trauma-related emotions and an increase in acceptance. In addition, we tested whether therapy response according to the Clinician Administered PTSD-Scale (CAPS) for the DSM-IV was associated with changes in trauma-related emotions and acceptance. The data was collected within a randomized controlled trial testing the efficacy of DBT-PTSD, and a subsample of 23 women was included in this secondary data analysis. Results: In a multilevel model, shame, guilt, disgust, distress, and fear decreased significantly from the start to the end of the therapy whereas radical acceptance increased. Therapy response measured with the CAPS was associated with change in trauma-related emotions. Conclusions: Trauma-related emotions and radical acceptance showed significant changes from the start to the end of DBT-PTSD. Future studies with larger sample sizes and control group designs are needed to test whether these changes are due to the treatment. Trial registration: ClinicalTrials.gov, number NCT0048100

    GpaXItarl originating from Solanum tarijense is a major resistance locus to Globodera pallida and is localised on chromosome 11 of potato

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    Resistance to Globodera pallida Rookmaker (Pa3), originating from wild species Solanum tarijense was identified by QTL analysis and can be largely ascribed to one major QTL. GpaXItarl explained 81.3% of the phenotypic variance in the disease test. GpaXItarl is mapped to the long arm of chromosome 11. Another minor QTL explained 5.3% of the phenotypic variance and mapped to the long arm of chromosome 9. Clones containing both QTL showed no lower cyst counts than clones with only GpaXItarl. After Mendelising the phenotypic data, GpaXItarl could be more precisely mapped near markers GP163 and FEN427, thus anchoring GpaXItarl to a region with a known R-gene cluster containing virus and nematode resistance genes

    Hypermethylation of the DLC1 CpG island does not alter gene expression in canine lymphoma

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    <p>Abstract</p> <p>Background</p> <p>This study is a comparative epigenetic evaluation of the methylation status of the <it>DLC1 </it>tumor suppressor gene in naturally-occurring canine lymphoma. Canine non-Hodgkin's lymphoma (NHL) has been proposed to be a relevant preclinical model that occurs spontaneously and may share causative factors with human NHL due to a shared home environment. The canine <it>DLC1 </it>mRNA sequence was derived from normal tissue. Using lymphoid samples from 21 dogs with NHL and 7 normal dogs, the methylation status of the promoter CpG island of the gene was defined for each sample using combined bisulfite restriction analysis (COBRA), methylation-specific PCR (MSP), and bisulfite sequencing methods. Relative gene expression was determined using real-time PCR.</p> <p>Results</p> <p>The mRNA sequence of canine <it>DLC1 </it>is highly similar to the human orthologue and contains all protein functional groups, with 97% or greater similarity in functional regions. Hypermethylation of the 5' and 3' flanking regions of the promoter was statistically significantly associated with the NHL phenotype, but was not associated with silencing of expression or differences in survival.</p> <p>Conclusion</p> <p>The canine <it>DLC1 </it>is constructed highly similarly to the human gene, which has been shown to be an important tumor suppressor in many forms of cancer. As in human NHL, the promoter CpG island of <it>DLC1 </it>in canine NHL samples is abnormally hypermethylated, relative to normal lymphoid tissue. This study confirms that hypermethylation occurs in canine cancers, further supporting the use of companion dogs as comparative models of disease for evaluation of carcinogenesis, biomarker diagnosis, and therapy.</p
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