2,342 research outputs found

    Les sis estratègies clau per al suport de la inclusió a l'escola i a la classe

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    Diatoms as Indicators of Water-level Change in Freshwater Lakes

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    Water-level changes result from a variety of geological, biological, and/or climatic processes. Many of these changes occur over long periods; others may be rapid or result from catastrophic events. In aquatic environments, diatoms are highly sensitive indicator organisms and their microfossils, deposited in lake sediments, can be used to infer environmental changes (Smol, 2008). Unambiguous diatom signals can be reconstructed from lakes isolated from marine or brackish waters (e.g. Fritz et al., this volume; Horton & Sawai, this volume). However, in freshwater systems lake-level changes are often recorded as increases in planktonic (free-floating) diatoms – although as discussed below, interpretation of this signal should be supported by additional evidence

    Anomaly Inflow for Gauge Defects

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    Topological defects constructed out of scalar fields and possessing chiral fermion zero modes are known to exhibit an anomaly inflow mechanism which cancels the anomaly in the effective theory of the zero modes through an inflow of current from the space in which the defect is embedded. We investigate the analog of this mechanism for defects constructed out of gauge fields in higher dimensions. In particular we analyze this mechanism for string (one-brane) defects in six dimensions and for fivebranes in ten dimensions.}Comment: 23 pp (harvmac l

    A family-based probabilistic method for capturing de novo mutations from high-throughput short-read sequencing data

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    Recent advances in high-throughput DNA sequencing technologies and associated statistical analyses have enabled in-depth analysis of whole-genome sequences. As this technology is applied to a growing number of individual human genomes, entire families are now being sequenced. Information contained within the pedigree of a sequenced family can be leveraged when inferring the donors' genotypes. The presence of a de novo mutation within the pedigree is indicated by a violation of Mendelian inheritance laws. Here, we present a method for probabilistically inferring genotypes across a pedigree using high-throughput sequencing data and producing the posterior probability of de novo mutation at each genomic site examined. This framework can be used to disentangle the effects of germline and somatic mutational processes and to simultaneously estimate the effect of sequencing error and the initial genetic variation in the population from which the founders of the pedigree arise. This approach is examined in detail through simulations and areas for method improvement are noted. By applying this method to data from members of a well-defined nuclear family with accurate pedigree information, the stage is set to make the most direct estimates of the human mutation rate to date

    The Impact of State Mandated Healthcare-Associated Infection Reporting on Infection Prevention and Control Departments in Acute Care Hospitals: Results from a National Survey

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    Background: In addition to federally mandated reporting, most US states have adopted legislation requiring hospitals to submit healthcare-associated infection (HAI) data. Evidence that state HAI laws have increased patient safety and reduced HAI rates is inconsistent, however, and resources needed to comply are considerable. We evaluated the impact of state HAI laws on infection prevention and control departments (IPCD). Methods: Web-based survey of a national sample of hospital IPCD was conducted in Fall 2011; all non-VA hospitals enrolled in the National Healthcare Safety Network were eligible to participate. States with HAI laws effective prior to Fall 2011 were identified using systematic legal review. Variations in IPCD resources and characteristics in states with and without laws were compared using χ2or Wilcoxon-Mann-Whitney tests. Multinomial logistic regression was used to identify increases or decreases, vs no change, in resources and characteristics. Results: 1,038 IPCD provided complete data (30% response rate); 756 (73%) were located in states with laws. When asked how mandatory reporting affected their IPCD, more respondents in states with laws reported differences in resources (42% vs 33%, p \u3c 0.01), time for routine activities other than for mandatory reporting (79% vs 71%, p \u3c 0.01), influence in hospital decision making (55% vs 48%, p \u3c 0.05), and visibility of their department (75% vs 65%, p \u3c 0.001); they also spent more hours per week fulfilling mandatory reporting requirements (17 vs 13, p \u3c 0.0001). Based on regression analysis, respondents in states with laws were more likely to report increased resources (p = 0.02) and influence (p = 0.04) and decreased time for routine activities (p \u3c 0.01). Perception of visibility in the hospital was mixed with reports of both increased (p \u3c 0.001) and decreased (p = 0.01) visibility vs the same. Conclusion: Respondents in states with laws reported a significantly higher burden to their IPCD, beyond what was required by federally mandated HAI reporting alone. However, they also reported receiving increased resources to offset demands on time for routine activities and fulfilling reporting requirements. Further research is needed to investigate resources necessary to comply with state HAI laws, and to evaluate their unintended consequences

    Spectroscopic distance, mass, and age estimations for APOGEE DR17

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    We derive distances and masses of stars from the Sloan Digital Sky Survey (SDSS) Apache Point Observatory Galactic Evolution Experiment (APOGEE) Data Release 17 (DR17) using simple neural networks. Training data for distances comes from Gaia EDR3, supplemented by literature distances for star clusters. For masses, the network is trained using asteroseismic masses for evolved stars and isochrone masses for main sequence stars. The models are trained on effective temperature, surface gravity, metallicity and carbon and nitrogen abundances. We found that our distance predictions have median fractional errors that range from ≈20%\approx 20\% at low log g and ≈10%\approx 10\% at higher log g with a standard deviation of ≈11%\approx 11\%. The mass predictions have a standard deviation of ±12%\pm 12\%. Using the masses, we derive ages for evolved stars based on the correspondence between mass and age for giant stars given by isochrones. The results are compiled into a Value Added Catalog (VAC) called DistMass that contains distances and masses for 733901 independent spectra, plus ages for 396548 evolved stars.Comment: 23 pages, 18 figure

    State law mandates for reporting of healthcare-associated Clostridium difficile infections in hospitals.

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    US state and territorial laws were reviewed to identify Clostridium difficile infection reporting mandates. Twenty states require reporting either under state law or by incorporating federal Centers for Medicare & Medicaid Services\u27 reporting requirements. Although state law mandates are more common, the incorporation of federal reporting requirements has been increasing

    An improved zebrafish transcriptome annotation for sensitive and comprehensive detection of cell type-specific genes

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    The zebrafish is ideal for studying embryogenesis and is increasingly applied to model human disease. In these contexts, RNA-sequencing (RNA-seq) provides mechanistic insights by identifying transcriptome changes between experimental conditions. Application of RNA-seq relies on accurate transcript annotation for a genome of interest. Here, we find discrepancies in analysis from RNA-seq datasets quantified using Ensembl and RefSeq zebrafish annotations. These issues were due, in part, to variably annotated 3\u27 untranslated regions and thousands of gene models missing from each annotation. Since these discrepancies could compromise downstream analyses and biological reproducibility, we built a more comprehensive zebrafish transcriptome annotation that addresses these deficiencies. Our annotation improves detection of cell type-specific genes in both bulk and single cell RNA-seq datasets, where it also improves resolution of cell clustering. Thus, we demonstrate that our new transcriptome annotation can outperform existing annotations, providing an important resource for zebrafish researchers
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