107 research outputs found

    RSK tableaux and the weak order on fully commutative permutations

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    For each fully commutative permutation, we construct a "boolean core," which is the maximal boolean permutation in its principal order ideal under the right weak order. We partition the set of fully commutative permutations into the recently defined crowded and uncrowded elements, distinguished by whether or not their RSK insertion tableaux satisfy a sparsity condition. We show that a fully commutative element is uncrowded exactly when it shares the RSK insertion tableau with its boolean core. We present the dynamics of the right weak order on fully commutative permutations, with particular interest in when they change from uncrowded to crowded. In particular, we use consecutive permutation patterns and descents to characterize the minimal crowded elements under the right weak order.Comment: 20 pages, 2 figure

    Runs and RSK tableaux of boolean permutations

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    We define and construct the "canonical reduced word" of a boolean permutation, and show that the RSK tableaux for that permutation can be read off directly from this reduced word. We also describe those tableaux that can correspond to boolean permutations, and enumerate them. In addition, we generalize a result of Mazorchuk and Tenner, showing that the "run" statistic influences the shape of the RSK tableau of arbitrary permutations, not just of those that are boolean.Comment: 18 pages, 3 figure

    What Disease does this Patient Have? A Large-scale Open Domain Question Answering Dataset from Medical Exams

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    Open domain question answering (OpenQA) tasks have been recently attracting more and more attention from the natural language processing (NLP) community. In this work, we present the first free-form multiple-choice OpenQA dataset for solving medical problems, MedQA, collected from the professional medical board exams. It covers three languages: English, simplified Chinese, and traditional Chinese, and contains 12,723, 34,251, and 14,123 questions for the three languages, respectively. We implement both rule-based and popular neural methods by sequentially combining a document retriever and a machine comprehension model. Through experiments, we find that even the current best method can only achieve 36.7\%, 42.0\%, and 70.1\% of test accuracy on the English, traditional Chinese, and simplified Chinese questions, respectively. We expect MedQA to present great challenges to existing OpenQA systems and hope that it can serve as a platform to promote much stronger OpenQA models from the NLP community in the future.Comment: Submitted to AAAI 202

    Ī³Ī“ T Cells Provide an Early Source of Interferon Ī³ in Tumor Immunity

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    Interferon (IFN)-Ī³ is necessary for tumor immunity, however, its initial cellular source is unknown. Because Ī³Ī“ T cells primarily produce this cytokine upon activation, we hypothesized that they would provide an important early source of IFN-Ī³ in tumor immunosurveillance. To address this hypothesis, we first demonstrated that Ī³Ī“ T cellā€“deficient mice had a significantly higher incidence of tumor development after challenge with a chemical carcinogen methylcholanthrene (MCA) or inoculation with the melanoma cell line B16. In wild-type mice, Ī³Ī“ T cells were recruited to the site of tumor as early as day 3 after inoculation, followed by Ī±Ī² T cells at day 5. We then used bone marrow chimeras and fetal liver reconstitutions to create mice with an intact Ī³Ī“ T cell repertoire but one that was specifically deficient in the capacity to produce IFN-Ī³. Such mice had a higher incidence of tumor development, induced either with MCA or by inoculation of B16 melanoma cells, compared with mice with IFN-Ī³ā€“competent Ī³Ī“ T cells. Moreover, genetic deficiency of Ī³Ī“ T cells resulted in impaired IFN-Ī³ production by tumor antigen-triggered Ī±Ī² T cell upon immunization with tumor lysate. These results demonstrate that Ī³Ī“ T cells can play a necessary role in tumor immunity through provision of an early source of IFN-Ī³ that in turn may regulate the function of tumor-triggered Ī±Ī² T cells

    Riverine Carbon Cycling Over The Past Century in the Midā€Atlantic Region of the United States

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    The lateral transport and degassing of carbon in riverine ecosystems is difficult to quantify on large spatial and long temporal scales due to the relatively poor representation of carbon processes in many models. Here, we coupled a scaleā€adaptive hydrological model with the Dynamic Land Ecosystem Model to simulate key riverine carbon processes across the Chesapeake and Delaware Bay Watersheds from 1900 to 2015. Our results suggest that throughout this time period riverine CO2 degassing and lateral dissolved inorganic carbon fluxes to the coastal ocean contribute nearly equally to the total riverine carbon outputs (mean Ā± standard deviation: 886 Ā± 177 Gg Cāˆ™yrāˆ’1 and 883 Ā± 268 Gg Cāˆ™yrāˆ’1, respectively). Following in order of decreasing importance are the lateral dissolved organic carbon flux to the coastal ocean (293 Ā± 81 Gg Cāˆ™yrāˆ’1), carbon burial (118 Ā± 32 Gg Cāˆ™yrāˆ’1), and lateral particulate organic carbon flux (105 Ā± 35 Gg Cāˆ™yrāˆ’1). In the early 2000s, carbon export to the coastal ocean from both the Chesapeake and Delaware Bay watersheds was only 15%ā€“20% higher than it was in the early 1900s (decade), but it showed a twofold increase in standard deviation. Climate variability (changes in temperature and precipitation) explains most (225 Gg Cāˆ™yrāˆ’1) of the increase since 1900, followed by changes in atmospheric CO2 (82 Gg Cāˆ™yrāˆ’1), atmospheric nitrogen deposition (44 Gg Cāˆ™yrāˆ’1), and applications of nitrogen fertilizer and manure (27 Gg Cāˆ™yrāˆ’1); in contrast, land conversion has resulted in a 188 Gg Cāˆ™yrāˆ’1 decrease in carbon export

    Impacts of Multiple Environmental Changes on Longā€Term Nitrogen Loading From the Chesapeake Bay Watershed

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    Excessive nutrient inputs from land, particularly nitrogen (N), have been found to increase the occurrence of hypoxia and harmful algal blooms in coastal ecosystems. To identify the main contributors of increased N loading and evaluate the efficacy of water pollution control policies, it is essential to quantify and attribute the longā€term changes in riverine N export. Here, we use a stateā€ofā€theā€art terrestrialā€“aquatic interface model to examine how multiple environmental factors may have affected N export from the Chesapeake Bay watershed since 1900. These factors include changes in climate, carbon dioxide, land use, and N inputs (i.e., atmospheric N deposition, animal manure, synthetic N fertilizer use, and wastewater discharge). Our results estimated that ammonium (NH4+) and nitrate (NO3āˆ’) export increased substantially (66% for NH4+ and 123% for NO3āˆ’) from the 1900s to the 1990s and then declined (32% for NH4+ and 14% for NO3āˆ’) since 2000. The temporal trend of dissolved organic nitrogen (DON) export paralleled that of dissolved inorganic N, while particulate organic nitrogen export was relatively constant during 1900ā€“2015. Precipitation was the primary driver of interannual variability in N export to the Bay. Wastewater discharge explained most of the longā€term change in riverine NH4+ and DON fluxes from 1900 to 2015. The changes in atmospheric deposition, wastewater, and synthetic fertilizer were responsible for the trend of riverine NO3āˆ’. In light of our modelā€based attribution analysis, terrestrial nonā€point source nutrient management will play an important role in achieving water quality goals

    Impacts of Multiple Environmental Changes on Longā€Term Nitrogen Loading From the Chesapeake Bay Watershed

    Get PDF
    Excessive nutrient inputs from land, particularly nitrogen (N), have been found to increase the occurrence of hypoxia and harmful algal blooms in coastal ecosystems. To identify the main contributors of increased N loading and evaluate the efficacy of water pollution control policies, it is essential to quantify and attribute the longā€term changes in riverine N export. Here, we use a stateā€ofā€theā€art terrestrialā€“aquatic interface model to examine how multiple environmental factors may have affected N export from the Chesapeake Bay watershed since 1900. These factors include changes in climate, carbon dioxide, land use, and N inputs (i.e., atmospheric N deposition, animal manure, synthetic N fertilizer use, and wastewater discharge). Our results estimated that ammonium (NH4+) and nitrate (NO3āˆ’) export increased substantially (66% for NH4+ and 123% for NO3āˆ’) from the 1900s to the 1990s and then declined (32% for NH4+ and 14% for NO3āˆ’) since 2000. The temporal trend of dissolved organic nitrogen (DON) export paralleled that of dissolved inorganic N, while particulate organic nitrogen export was relatively constant during 1900ā€“2015. Precipitation was the primary driver of interannual variability in N export to the Bay. Wastewater discharge explained most of the longā€term change in riverine NH4+ and DON fluxes from 1900 to 2015. The changes in atmospheric deposition, wastewater, and synthetic fertilizer were responsible for the trend of riverine NO3āˆ’. In light of our modelā€based attribution analysis, terrestrial nonā€point source nutrient management will play an important role in achieving water quality goals

    Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center

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    BACKGROUND & AIMS: A proportion of infants and young children with inflammatory bowel diseases (IBDs) have subtypes associated with a single gene variant (monogenic IBD). We aimed to determine the prevalence of monogenic disease in a cohort of pediatric patients with IBD. METHODS: We performed whole-exome sequencing analyses of blood samples from an unselected cohort of 1005 children with IBD, aged 0-18 years (median age at diagnosis, 11.96 years) at a single center in Canada and their family members (2305 samples total). Variants believed to cause IBD were validated using Sanger sequencing. Biopsies from patients were analyzed by immunofluorescence and histochemical analyses. RESULTS: We identified 40 rare variants associated with 21 monogenic genes among 31 of the 1005 children with IBD (including 5 variants in XIAP, 3 in DOCK8, and 2 each in FOXP3, GUCY2C, and LRBA). These variants occurred in 7.8% of children younger than 6 years and 2.3% of children aged 6-18 years. Of the 17 patients with monogenic Crohn\u27s disease, 35% had abdominal pain, 24% had nonbloody loose stool, 18% had vomiting, 18% had weight loss, and 5% had intermittent bloody loose stool. The 14 patients with monogenic ulcerative colitis or IBD-unclassified received their diagnosis at a younger age, and their most predominant feature was bloody loose stool (78%). Features associated with monogenic IBD, compared to cases of IBD not associated with a single variant, were age of onset younger than 2 years (odds ratio [OR], 6.30; P = .020), family history of autoimmune disease (OR, 5.12; P = .002), extra-intestinal manifestations (OR, 15.36; P \u3c .0001), and surgery (OR, 3.42; P = .042). Seventeen patients had variants in genes that could be corrected with allogeneic hematopoietic stem cell transplantation. CONCLUSIONS: In whole-exome sequencing analyses of more than 1000 children with IBD at a single center, we found that 3% had rare variants in genes previously associated with pediatric IBD. These were associated with different IBD phenotypes, and 1% of the patients had variants that could be potentially corrected with allogeneic hematopoietic stem cell transplantation. Monogenic IBD is rare, but should be considered in analysis of all patients with pediatric onset of IBD
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