Pattern recognition techniques to reduce backgrounds in the search for the 136Xe double beta decay with gaseous TPCs

The observation of the neutrinoless double beta decay may provide essential information on the nature of neutrinos. Among the current experimental approaches, a high pressure gaseous TPC is an attractive option for the search of double beta decay due to its good energy resolution and the detailed topological information of each event. We present in this talk a detailed study of the ionization topology of the 136Xe double beta decay events in a High Pressure Xenon TPC, as well as that of the typical competing backgrounds. We define some observables based on graph theory concepts to develop automated discrimination algorithms. Our criteria are able to reduce the background level by about three orders of magnitude in the region of interest of the 136Xe Qbb for a signal acceptance of 40%. This result provides a quantitative assessment of the benefit of topological information offered by gaseous TPCs for double beta decay search, and proves that it is a promising feature in view of future experiments in the field. Possible ideas for further improvement in the discrimination algorithms and the dependency of these results with the gas diffusion and readout granularity will be also discussed.Comment: Proceedings of the Low Radioactivity Techniques Conference (LRT2013), Gran Sasso (Italy). To be published in AIP Conf. Pro

Radiopurity control in the NEXT-100 double beta decay experiment: procedures and initial measurements

We have investigated the possibility of calibrating the PMTs of scintillation detectors, using the primary scintillation produced by X-rays to induce single photoelectron response of the PMT. The high-energy tail of this response, can be approximated to an exponential function, under some conditions. In these cases, it is possible to determine the average gain for each PMT biasing voltage from the inverse of the exponent of the exponential fit to the tail, which can be done even if the background and/or noise cover-up most of the distribution. We have compared our results with those obtained by the commonly used single electron response (SER) method, which uses a LED to induce a single photoelectron response of the PMT and determines the peak position of such response, relative to the pedestal peak (the electronic noise peak, which corresponds to 0 photoelectrons). The results of the exponential fit method agree with those obtained by the SER method when the average number of photoelectrons reaching the first dynode per light/scintillation pulse is around 1.0. The SER method has higher precision, while the exponential fit method has the advantage of being useful in situations where the PMT is already in situ, being difficult or even impossible to apply the SER method, e.g. in sealed scintillator/PMT devices

Characterization of a medium size Xe/TMA TPC instrumented with microbulk Micromegas, using low-energy gamma-rays

NEXT-MM is a general-purpose high pressure (10 bar, ~ 25 l active volume) Xenon-based TPC, read out in charge mode with an 0.8 cm × 0.8 cm-segmented 700 cm2 plane (1152 ch) of the latest microbulk-Micromegas technology. It has been recently commissioned at University of Zaragoza as part of the R&D of the NEXT 0νββ experiment, although the experiment's first stage is currently being built based on a SiPM/PMT-readout concept relying on electroluminescence. Around 2 million events were collected during the last months, stemming from the low energy γ-rays emitted by a 241Am source when interacting with the Xenon gas (Eγ = 26, 30, 59.5 keV). The localized nature of such events around atmospheric pressure, the long drift times, as well as the possibility to determine their production time from the associated α particle in coincidence, allow the extraction of primordial properties of the TPC filling gas, namely the drift velocity, diffusion and attachment coefficients. In this work we focus on the little explored combination of Xe and trimethylamine (TMA) for which, in particular, such properties are largely unknown. This gas mixture offers potential advantages over pure Xenon when aimed at Rare Event Searches, mainly due to its Penning characteristics, wave-length shifting properties and reduced diffusion, and it is being actively investigated by our collaboration. The chamber is currently operated at 2.7 bar, as an intermediate step towards the envisaged 10 bar. We report here its performance as well as a first implementation of the calibration procedures that have allowed the extension of the previously reported energy resolution to the whole readout plane (10.6% FWHM@30 keV)

Is there an orthographic boost for ambiguous words during their processing?

The present study explores the issue of why ambiguous words are recognized faster than unambiguous ones during word recognition. To this end we contrasted two different hypotheses: the semantic feedback hypothesis (Hino and Lupker in J Exp Psychol Hum Percept Perform 22:1331-1356, 1996. https://doi.org/10.1037/0096-1523.22.6.1331 ), and the hypothesis proposed by Borowsky and Masson (J Exp Psychol Learn Mem Cognit 22:63-85, 1996. https://doi.org/10.1037/0278-7393.22.1.63 ). Although both hypotheses agree that ambiguous words benefit during recognition in that they engage more semantic activation, they disagree as to whether or not this greater semantic activation feeds back to the orthographic level, hence speeding up the orthographic coding of ambiguous words. Participants were presented with ambiguous and unambiguous words in two tasks, a lexical decision task (LDT) and a two-alternative forced-choice task (2AFC). We found differences between ambiguous and unambiguous words in both the LDT and the 2AFC tasks. These results suggest that the orthographic coding of ambiguous words is boosted during word processing. This finding lends support to the semantic feedback hypothesis.This research was funded by the Spanish Ministry of Economy and Competitiveness (PSI2015-63525-P) and by the Research Promotion Program of the Universitat Rovira i Virgili (2016PFR-URV-B2-37). This has also been partially supported by the FCT (Foundation for Science and Technology) through the state budget with Reference IF/00784/2013/CP1158/CT0013. The first author also holds a grant from the Universitat Rovira i Virgili (2015PMF-PIPF-16)

Caracterización de la púrpura trombótica trombocitopénica congénita mediante técnicas inmunológicas y moleculares: resultados de la colección nacional del GEPTT

CO-093 Introducción: La Púrpura Trombótica Trombocitopénica congénita (PTTc) es una enfermedad ultra-rara caracterizada por un déficit severo de la enzima ADAMTS13 como consecuencia de mutaciones heredadas de forma autosómica recesiva en el gen ADAMTS13 (9q34). En este estudio, desarrollado dentro del Grupo Cooperativo Español de PTT (GEPTT), se ha llevado a cabo la creación de una colección centralizada de muestras biológicas y su caracterización inmunológica y molecular para mejorar el diagnóstico y el manejo clínico de los pacientes. Métodos: Se incluyeron en este estudio seis pacientes con diagnóstico clínico o sospecha de PTTc de diferentes hospitales españoles. Se estudió la actividad de ADAMTS13 e inhibidores mediante la técnica ELISA con el kit “TECHNOZYM® ADAMTS-13 Activity e INH” (Technoclone). Además, se realizó test Bethesda para descartar la presencia de inhibidores no IgG. Para el estudio genético, se implementó un panel de captura (SureSelect, Agilent) dirigido a la región genómica completa, incluyendo también las regiones no codificantes, del gen ADAMTS13 (chr9: 136278459 - 136325025, hg19). Las librerías de DNA se secuenciaron con la plataforma MiSeq (Illumina®) y el posible efecto patogénico de las variantes identificadas se estudió a nivel de i) proteína, utilizando predictores de cambio de aminoácido (SIFT) y de estructura de la proteína (SwissModel) y ii) splicing, con herramientas de análisis in silico (HSF) y validación funcional in vitro mediante minigenes. En 3 casos se realizó un cariotipo molecular utilizando array de SNPs (CytoScan HD, Affymetrix) para detectar regiones de pérdida de material genético y/o de heterocigosidad (LOH). Resultados: La mediana de actividad de ..

A systematic review of studies measuring health-related quality of life of general injury populations

Background. It is important to obtain greater insight into health-related quality of life (HRQL) of injury patients in order to document people's pathways to recovery and to quantify the impact of injury on population health over time. We performed a systematic review of studies measuring HRQL in general injury populations with a generic health state measure to summarize existing knowledge. Methods. Injury studies (1995-2009) were identified with main inclusion criteri

Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

\ua9 2021, The Author(s).Acute myeloid leukemia (AML) is a hematological malignancy with an undefined heritable risk. Here we perform a meta-analysis of three genome-wide association studies, with replication in a fourth study, incorporating a total of 4018 AML cases and 10488 controls. We identify a genome-wide significant risk locus for AML at 11q13.2 (rs4930561; P = 2.15 7 10−8; KMT5B). We also identify a genome-wide significant risk locus for the cytogenetically normal AML sub-group (N = 1287) at 6p21.32 (rs3916765; P = 1.51 7 10−10; HLA). Our results inform on AML etiology and identify putative functional genes operating in histone methylation (KMT5B) and immune function (HLA)

Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

Acute myeloid leukemia (AML) is a hematological malignancy with an undefined heritable risk. Here we perform a meta-analysis of three genome-wide association studies, with replication in a fourth study, incorporating a total of 4018 AML cases and 10488 controls. We identify a genome-wide significant risk locus for AML at 11q13.2 (rs4930561; P = 2.15 × 10-8; KMT5B). We also identify a genome-wide significant risk locus for the cytogenetically normal AML sub-group (N = 1287) at 6p21.32 (rs3916765; P = 1.51 × 10-10; HLA). Our results inform on AML etiology and identify putative functional genes operating in histone methylation (KMT5B) and immune function (HLA)