检索结果-内蒙古大学图书馆

arXiv 2020年

作者： Shoeibi, Afshin Khodatars, Marjane Jafari, Mahboobeh Ghassemi, Navid Sadeghi, Delaram Moridian, Parisa Khadem, Ali Alizadehsani, Roohallah Hussain, Sadiq Zare, Assef Sani, Zahra Alizadeh Khozeimeh, Fahime Nahavandi, Saeid Rajendra Acharya, U. Gorriz, Juan M. The Data Science and Computational Intelligence Institute University of Granada Spain The Computer Engineering Department Ferdowsi University of Mashhad Mashhad Iran Deakin University VIC3217 Australia The Faculty of Electrical Engineering K. N. Toosi University of Technology Tehran Iran System Administrator at Dibrugarh University Assam786004 India Faculty of Electrical Engineering Gonabad Branch Islamic Azad University Gonabad Iran Rajaie Cardiovascular Medical and Research Center Iran University of Medical Sciences Tehran Iran The School of Mathematics Physics and Computing University of Southern Queensland Springfield Australia Dept. of Psychiatry University of Cambridge United Kingdom

Coronavirus, or COVID-19, is a hazardous disease that has endangered the health of many people around the world by directly affecting the lungs. COVID-19 is a medium-sized, coated virus with a single-stranded RNA, and also has one of the largest RNA genomes and is approximately 120 nm. The X-Ray and computed tomography (CT) imaging modalities are widely used to obtain a fast and accurate medical diagnosis. Identifying COVID-19 from these medical images is extremely challenging as it is time-consuming and prone to human errors. Hence, artificial intelligence (AI) methodologies can be used to obtain consistent high performance. Among the AI methods, deep learning (DL) networks have gained popularity recently compared to conventional machine learning (ML). Unlike ML, all stages of feature extraction, feature selection, and classification are accomplished automatically in DL models. In this paper, a complete survey of studies on the application of DL techniques for COVID-19 diagnostic and segmentation of lungs is discussed, concentrating on works that used X-Ray and CT images. Additionally, a review of papers on the forecasting of coronavirus prevalence in different parts of the world with DL is presented. Lastly, the challenges faced in the detection of COVID-19 using DL techniques and directions for future research are discussed. © 2020, CC BY-NC-ND.

关键词： COVID-19

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Genomic basis for RNA alterations in cancer (vol 578, pg 129, 2020)

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NATURE 2023年第7948期614卷 E37-E37页

作者： Calabrese, Claudia Davidson, Natalie R. Demircioglu, Deniz Fonseca, Nuno A. He, Yao Lehmann, Kjong-Van Liu, Fenglin Shiraishi, Yuichi Soulette, Cameron M. Urban, Lara Greger, Liliana Li, Siliang Liu, Dongbing Perry, Marc D. Xiang, Qian Zhang, Fan Zhang, Junjun Bailey, Peter Erkek, Serap Hoadley, Katherine A. Hou, Yong Huska, Matthew R. Kilpinen, Helena Korbel, Jan O. Marin, Maximillian G. Markowski, Julia Nandi, Tannistha Pan-Hammarstrom, Qiang Pedamallu, Chandra Sekhar Siebert, Reiner Stark, Stefan G. Su, Hong Tan, Patrick Waszak, Sebastian M. Yung, Christina Zhu, Shida Awadalla, Philip Creighton, Chad J. Meyerson, Matthew Ouellette, B. F. Francis Wu, Kui Yang, Huanming Brazma, Alvis Brooks, Angela N. Goke, Jonathan Ratsch, Gunnar Schwarz, Roland F. Stegle, Oliver Zhang, Zemin European Molecular Biology Laboratory European Bioinformatics Institute Hinxton UK European Molecular Biology Laboratory European Bioinformatics Institute (EMBL-EBI) Cambridge UK Genome Biology Unit European Molecular Biology Laboratory (EMBL) Heidelberg Germany CIBIO/InBIO - Research Center in Biodiversity and Genetic Resources Universidade do Porto Vairão Portugal Berlin Institute for Medical Systems Biology Max Delbruck Center for Molecular Medicine Berlin Germany German Cancer Consortium (DKTK) partner site Berlin Germany German Cancer Research Center (DKFZ) Heidelberg Germany Berlin Institute for Medical Systems Biology Max Delbrück Center for Molecular Medicine Berlin Germany German Cancer Consortium (DKTK) Partner site Berlin Berlin Germany European Molecular Biology Laboratory Genome Biology Unit Heidelberg Germany Division of Computational Genomics and Systems Genetics German Cancer Research Center (DKFZ) Heidelberg Germany ETH Zurich Zurich Switzerland Memorial Sloan Kettering Cancer Center New York NY USA Weill Cornell Medical College New York NY USA SIB Swiss Institute of Bioinformatics Lausanne Switzerland University Hospital Zurich Zurich Switzerland Computational Biology Center Memorial Sloan Kettering Cancer Center New York NY USA Department of Biology ETH Zurich Zürich Switzerland Department of Computer Science ETH Zurich Zurich Switzerland Korea University Seoul South Korea Computational and Systems Biology Program Memorial Sloan Kettering Cancer Center New York NY USA Department of Physiology and Biophysics Weill Cornell Medicine New York NY USA Institute for Computational Biomedicine Weill Cornell Medicine New York NY USA Controlled Department and Institution New York NY USA Englander Institute for Precision Medicine Weill Cornell Medicine New York NY USA National University of Singapore Singapore Singapore Genome Institute of Singapore Singapore Singapore Computational and Systems Biology Genome Institute of Singap

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Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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Nature 2024年第8003期627卷 347-357页

作者： Ken Suzuki Konstantinos Hatzikotoulas Lorraine Southam Henry J Taylor Xianyong Yin Kim M Lorenz Ravi Mandla Alicia Huerta-Chagoya Giorgio E M Melloni Stavroula Kanoni Nigel W Rayner Ozvan Bocher Ana Luiza Arruda Kyuto Sonehara Shinichi Namba Simon S K Lee Michael H Preuss Lauren E Petty Philip Schroeder Brett Vanderwerff Mart Kals Fiona Bragg Kuang Lin Xiuqing Guo Weihua Zhang Jie Yao Young Jin Kim Mariaelisa Graff Fumihiko Takeuchi Jana Nano Amel Lamri Masahiro Nakatochi Sanghoon Moon Robert A Scott James P Cook Jung-Jin Lee Ian Pan Daniel Taliun Esteban J Parra Jin-Fang Chai Lawrence F Bielak Yasuharu Tabara Yang Hai Gudmar Thorleifsson Niels Grarup Tamar Sofer Matthias Wuttke Chloé Sarnowski Christian Gieger Darryl Nousome Stella Trompet Soo-Heon Kwak Jirong Long Meng Sun Lin Tong Wei-Min Chen Suraj S Nongmaithem Raymond Noordam Victor J Y Lim Claudia H T Tam Yoonjung Yoonie Joo Chien-Hsiun Chen Laura M Raffield Bram Peter Prins Aude Nicolas Lisa R Yanek Guanjie Chen Jennifer A Brody Edmond Kabagambe Ping An Anny H Xiang Hyeok Sun Choi Brian E Cade Jingyi Tan K Alaine Broadaway Alice Williamson Zoha Kamali Jinrui Cui Manonanthini Thangam Linda S Adair Adebowale Adeyemo Carlos A Aguilar-Salinas Tarunveer S Ahluwalia Sonia S Anand Alain Bertoni Jette Bork-Jensen Ivan Brandslund Thomas A Buchanan Charles F Burant Adam S Butterworth Mickaël Canouil Juliana C N Chan Li-Ching Chang Miao-Li Chee Ji Chen Shyh-Huei Chen Yuan-Tsong Chen Zhengming Chen Lee-Ming Chuang Mary Cushman John Danesh Swapan K Das H Janaka de Silva George Dedoussis Latchezar Dimitrov Ayo P Doumatey Shufa Du Qing Duan Kai-Uwe Eckardt Leslie S Emery Daniel S Evans Michele K Evans Krista Fischer James S Floyd Ian Ford Oscar H Franco Timothy M Frayling Barry I Freedman Pauline Genter Hertzel C Gerstein Vilmantas Giedraitis Clicerio González-Villalpando Maria Elena González-Villalpando Penny Gordon-Larsen Myron Gross Lindsay A Guare Sophie Hackinger Liisa Hakaste Sohee Han Andrew T Hattersley Christian Herder Momoko Horikoshi Annie-Green Howard Willa Centre for Genetics and Genomics Versus Arthritis Centre for Musculoskeletal Research Division of Musculoskeletal and Dermatological Sciences University of Manchester Manchester UK. Department of Diabetes and Metabolic Diseases Graduate School of Medicine University of Tokyo Tokyo Japan. Department of Statistical Genetics Osaka University Graduate School of Medicine Suita Japan. Institute of Translational Genomics Helmholtz Zentrum München German Research Center for Environmental Health Neuherberg Germany. konstantinos.hatzikotoulas@helmholtz-munich.de. Institute of Translational Genomics Helmholtz Zentrum München German Research Center for Environmental Health Neuherberg Germany. Center for Precision Health Research National Human Genome Research Institute National Institutes of Health Bethesda MD USA. British Heart Foundation Cardiovascular Epidemiology Unit Department of Public Health and Primary Care University of Cambridge Cambridge UK. Heart and Lung Research Institute University of Cambridge Cambridge UK. Department of Epidemiology School of Public Health Nanjing Medical University Nanjing China. Department of Biostatistics and Center for Statistical Genetics University of Michigan Ann Arbor MI USA. Corporal Michael J. Crescenz VA Medical Center Philadelphia PA USA. Department of Systems Pharmacology and Translational Therapeutics University of Pennsylvania Perelman School of Medicine Philadelphia PA USA. Department of Genetics University of Pennsylvania Perelman School of Medicine Philadelphia PA USA. Programs in Metabolism and Medical and Population Genetics Broad Institute of Harvard and MIT Cambridge MA USA. Diabetes Unit and Center for Genomic Medicine Massachusetts General Hospital Boston MA USA. TIMI Study Group Division of Cardiovascular Medicine Brigham and Women's Hospital Harvard Medical School Boston MA USA. William Harvey Research Institute Barts and the London School of Medicine and Dentistry Queen Mary University of London L

Type 2 diabetes (T2D) is a heterogeneous disease that develops through diverse pathophysiological processes and molecular mechanisms that are often specific to cell type. Here, to characterize the genetic contribution to these processes across ancestry groups, we aggregate genome-wide association study data from 2,535,601 individuals (39.7% not of European ancestry), including 428,452 cases of T2D. We identify 1,289 independent association signals at genome-wide significance (P < 5 × 10) that map to 611 loci, of which 145 loci are, to our knowledge, previously unreported. We define eight non-overlapping clusters of T2D signals that are characterized by distinct profiles of cardiometabolic trait associations. These clusters are differentially enriched for cell-type-specific regions of open chromatin, including pancreatic islets, adipocytes, endothelial cells and enteroendocrine cells. We build cluster-specific partitioned polygenic scores in a further 279,552 individuals of diverse ancestry, including 30,288 cases of T2D, and test their association with T2D-related vascular outcomes. Cluster-specific partitioned polygenic scores are associated with coronary artery disease, peripheral artery disease and end-stage diabetic nephropathy across ancestry groups, highlighting the importance of obesity-related processes in the development of vascular outcomes. Our findings show the value of integrating multi-ancestry genome-wide association study data with single-cell epigenomics to disentangle the aetiological heterogeneity that drives the development and progression of T2D. This might offer a route to optimize global access to genetically informed diabetes care.

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Where do stars explode in the ISM? - The distribution of dense gas around massive stars and supernova remnants in M33

arXiv

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arXiv 2023年

作者： Sarbadhicary, Sumit K. Wagner, Jordan Koch, Eric W. Chen, Ness Mayker Leroy, Adam K. Lahén, Natalia Rosolowsky, Erik Neugent, Kathryn F. Kim, Chang-Goo Chomiuk, Laura Dalcanton, Julianne J. Lopez, Laura A. Pingel, Nickolas M. Indebetouw, Remy Williams, Thomas G. Tarantino, Elizabeth Meyer, Jennifer Donovan Skillman, Evan D. Smercina, Adam Kepley, Amanda A. Murphy, Eric J. Strader, Jay Wong, Tony Stanimirović, Snežana Villanueva, Vicente Walter, Fabian Ott, Juergen Darling, Jeremy Roman-Duval, Julia Murray, Claire E. Department of Physics The Ohio State University ColumbusOH43210 United States Center for Cosmology & Astro-Particle Physics The Ohio State University ColumbusOH43210 United States Department of Astronomy The Ohio State University ColumbusOH43210 United States Center for Astrophysics Harvard & Smithsonian 60 Garden St. CambridgeMA02138 United States Max-Planck-Institute für Astrophysik Karl-Schwarzschild-Straße 1 GarchingD-85740 Germany Department of Physics University of Alberta EdmontonABT6G 2E1 Canada Department of Astrophysical Sciences Princeton University PrincetonNJ08544 United States Center for Data Intensive and Time Domain Astronomy Department of Physics and Astronomy Michigan State University East LansingMI48824 United States Department of Astronomy University of Washington Box 351580 SeattleWA98195-1580 United States Center for Computational Astrophysics Flatiron Institute 162 Fifth Ave New YorkNY10010 United States Department of Astronomy University of Wisconsin-Madison 475 North Charter St. MadisonWI53706-15821 United States University of Virginia Astronomy Dept. 530 McCormick Road CharlottesvilleVA22904-4325 United States National Radio Astronomy Observatory 520 Edgemont Road CharlottesvilleVA22903-2475 United States Sub-department of Astrophysics Department of Physics University of Oxford Keble Road OxfordOX1 3RH United Kingdom Space Telescope Science Institute 3700 San Martin Drive BaltimoreMD21218 United States Department of Astronomy University of Maryland College ParkMD20742 United States Minnesota Institute for Astrophysics University of Minnesota MinneapolisMN55455 United States Department of Astronomy University of Illinois UrbanaIL61801 United States Max Planck Institute for Astronomy Königstuhl 17 HeidelbergD-69117 Germany National Radio Astronomy Observatory Pete V. Domenici Array Science Center P.O. Box O SocorroNM87801 United States New Mexico Institute of Mining and Technology 801

Star formation in galaxies is regulated by turbulence, outflows, gas heating and cloud dispersal - processes which depend sensitively on the properties of the interstellar medium (ISM) into which supernovae (SNe) explode. Unfortunately, direct measurements of ISM environments around SNe remain scarce, as SNe are rare and often distant. Here we demonstrate a new approach: mapping the ISM around the massive stars that are soon to explode. This provides a much larger census of explosion sites than possible with only SNe, and allows comparison with sensitive, high-resolution maps of the atomic and molecular gas from the Jansky VLA and ALMA. In the well-resolved Local Group spiral M33, we specifically observe the environments of red supergiants (RSGs, progenitors of Type II SNe), Wolf-Rayet stars (WRs, tracing stars >30M☉, and possibly future stripped-envelope SNe), and supernova remnants (SNRs, locations where SNe have exploded). We find that massive stars evolve not only in dense, molecular-dominated gas (with younger stars in denser gas), but also a substantial fraction (∼45% of WRs;higher for RSGs) evolve in lower-density, atomic-gas-dominated, inter-cloud media. We show that these measurements are consistent with expectations from different stellar-age tracer maps, and can be useful for validating SN feedback models in numerical simulations of galaxies. Along with the discovery of a 20-pc diameter molecular gas cavity around a WR, these findings reemphasize the importance of pre-SN/correlated-SN feedback evacuating the dense gas around massive stars before explosion, and the need for high-resolution (down to pc-scale) surveys of the multi-phase ISM in nearby galaxies. © 2023, CC BY.

关键词： Supernovae

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Federated variance-reduced stochastic gradient descent with robustness to Byzantine attacks

arXiv

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arXiv 2019年

作者： Wu, Zhaoxian Ling, Qing Chen, Tianyi Giannakis, Georgios B. School of Data and Computer Science Guangdong Province Key Laboratory of Computational Science Sun Yat-Sen University GuangzhouGuangdong510006 China Department of Electrical Computer and Systems Engineering Rensselaer Polytechnic Institute TroyNY12180 United States Department of Electrical and Computer Engineering Digital Technology Center University of Minnesota MinneapolisMN55455 United States

This paper deals with distributed finite-sum optimization for learning over networks in the presence of malicious Byzantine attacks. To cope with such attacks, most resilient approaches so far combine stochastic gradient descent (SGD) with different robust aggregation rules. However, the sizeable SGD-induced stochastic gradient noise makes it challenging to distinguish malicious messages sent by the Byzantine attackers from noisy stochastic gradients sent by the 'honest' workers. This motivates us to reduce the variance of stochastic gradients as a means of robustifying SGD in the presence of Byzantine attacks. To this end, the present work puts forth a Byzantine attack resilient distributed (Byrd-) SAGA approach for learning tasks involving finite-sum optimization over networks. Rather than the mean employed by distributed SAGA, the novel Byrd-SAGA relies on the geometric median to aggregate the corrected stochastic gradients sent by the workers. When less than half of the workers are Byzantine attackers, the robustness of geometric median to outliers enables Byrd-SAGA to attain provably linear convergence to a neighborhood of the optimal solution, with the asymptotic learning error determined by the number of Byzantine workers. Numerical tests corroborate the robustness to various Byzantine attacks, as well as the merits of Byrd-SAGA over Byzantine attack resilient distributed SGD. Copyright © 2019, The Authors. All rights reserved.

关键词： Optimization

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Synergy of Binary Substitutions for Improving the Cycle Performance in LiNiO2 Revealed by Ab Initio Materials Informatics

arXiv

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arXiv 2020年

作者： Yoshida, Tomohiro Maezono, Ryo Hongo, Kenta Department of Computer-Aided Engineering and Development Sumitomo Metal Mining Co. Ltd. 3-5 Sobiraki-cho NiihamaEhime792-0001 Japan School of Information Science JAIST Asahidai 1-1 IshikawaNomi923-1292 Japan Computational Engineering Applications Unit RIKEN 2-1 Hirosawa SaitamaWako351-0198 Japan Research Center for Advanced Computing Infrastructure JAIST Asahidai 1-1 NomiIshikawa923-1292 Japan Center for Materials Research by Information Integration Research and Services Division of Materials Data and Integrated System National Institute for Materials Science 1-2-1 Sengen TsukubaIbaraki305-0047 Japan PRESTO Japan Science and Technology Agency 4-1-8 Honcho SaitamaKawaguchi-shi322-0012 Japan

We explore LiNiO2-based cathode materials with two-element substitutions by an ab initio simulation based materials informatics (AIMI) approach. According to our previous study, a higher cycle performance strongly correlates with less structural change during charge–discharge cycles;the latter can be used for evaluating the former. However, if we target the full substitution space, full simulations are infeasible even for all binary combinations. To circumvent such an exhaustive search, we rely on Bayesian optimization. Actually, by searching only 4% of all the combinations, our AIMI approach discovered two promising combinations, Cr-Mg and Cr-Re, whereas each atom itself never improved the performance. We conclude that the synergy never emerges from a common strategy restricted to combinations of "good" elements that individually improve the performance. In addition, we propose a guideline for the binary substitutions by elucidating the mechanism of crystal structure change. Copyright © 2020, The Authors. All rights reserved.

关键词： Binary alloys

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Chemical identification and indexing in full-text articles: an overview of the NLM-Chem track at BioCreative VII

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database 2023年第2023期2023卷 baad005-baad005页

作者： Leaman, Robert Islamaj, Rezarta Adams, Virginia Alliheedi, Mohammed A. Almeida, João Rafael Antunes, Rui Bevan, Robert Chang, Yung-Chun Erdengasileng, Arslan Hodgskiss, Matthew Ida, Ryuki Kim, Hyunjae Li, Keqiao Mercer, Robert E. Mertová, Lukrécia Mobasher, Ghadeer Shin, Hoo-Chang Sung, Mujeen Tsujimura, Tomoki Yeh, Wen-Chao Lu, Zhiyong National Center for Biotechnology Information (NCBI) National Library of Medicine National Institutes of Health 8600 Rockville Pike Bethesda 20894 MD United States Nvidia 2788 San Tomas Expressway Santa Clara 95051 CA United States Department of Computer Science Al Baha University 4781 King Fahd Rd Al Aqiq 65779 Saudi Arabia Department of Electronics Telecommunications and Informatics (DETI) Institute of Electronics and Informatics Engineering of Aveiro (IEETA) University of Aveiro Campus Universitário de Santiago Aveiro 3810-193 Portugal Department of Information and Communications Technologies University of A Coruña Camiño Do Lagar de Castro A Coruña 15008 Spain Informatics Department Medicines Discovery Catapult Alderley Park Block 35 Mereside Macclesfield SK10 4ZF United Kingdom Graduate Institute of Data Science Taipei Medical University No. 172-1 Section 2 Keelung Rd Da’an District Taipei City 106 Taiwan Department of Statistics Florida State University 117 N. Woodward Ave Tallahassee 32306 FL United States Computational Intelligence Laboratory Toyota Technological Institute 2-12-1 Hisakata Tempaku-ku Nagoya Aichi 468-8511 Japan Department of Computer Science and Engineering Korea University 145 Anam-ro Seongbuk-gu Seoul 02841 South Korea Department of Computer Science The University of Western Ontario Middlesex College Room 355 London N6A 5B7 ON Canada Scientific Databases and Visualization Group Heidelberg Institute for Theoretical Studies (HITS GGmbH) Schloss-Wolfsbrunnenweg 35 Heidelberg 69118 Germany Institute of Computer Science Heidelberg University Im Neuenheimer Feld 205 Heidelberg 69120 Germany Institute of Information Systems and Applications National Tsing Hua University No. 101 Section 2 Kuang-Fu Road Hsinchu 30013 Taiwan

The BioCreative National Library of Medicine (NLM)-Chem track calls for a community effort to fine-tune automated recognition of chemical names in the biomedical literature. Chemicals are one of the most searched biomedical entities in PubMed, and - as highlighted during the coronavirus disease 2019 pandemic - their identification may significantly advance research in multiple biomedical subfields. While previous community challenges focused on identifying chemical names mentioned in titles and abstracts, the full text contains valuable additional detail. We, therefore, organized the BioCreative NLM-Chem track as a community effort to address automated chemical entity recognition in full-text articles. The track consisted of two tasks: (i) chemical identification and (ii) chemical indexing. The chemical identification task required predicting all chemicals mentioned in recently published full-text articles, both span [i.e. named entity recognition (NER)] and normalization (i.e. entity linking), using Medical Subject Headings (MeSH). The chemical indexing task required identifying which chemicals reflect topics for each article and should therefore appear in the listing of MeSH terms for the document in the MEDLINE article indexing. This manuscript summarizes the BioCreative NLM-Chem track and post-challenge experiments. We received a total of 85 submissions from 17 teams worldwide. The highest performance achieved for the chemical identification task was 0.8672 F-score (0.8759 precision and 0.8587 recall) for strict NER performance and 0.8136 F-score (0.8621 precision and 0.7702 recall) for strict normalization performance. The highest performance achieved for the chemical indexing task was 0.6073 F-score (0.7417 precision and 0.5141 recall). This community challenge demonstrated that (i) the current substantial achievements in deep learning technologies can be utilized to improve automated prediction accuracy further and (ii) the chemical indexing task is substanti

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The repertoire of mutational signatures in human cancer (vol 578, pg 94, 2020)

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NATURE 2023年第7948期614卷 E41-E41页

作者： Alexandrov, Ludmil B. Kim, Jaegil Haradhvala, Nicholas J. Huang, Mi Ni Ng, Alvin Wei Tian Wu, Yang Boot, Arnoud Covington, Kyle R. Gordenin, Dmitry A. Bergstrom, Erik N. Islam, S. M. Ashiqul Lopez-Bigas, Nuria Klimczak, Leszek J. McPherson, John R. Morganella, Sandro Sabarinathan, Radhakrishnan Wheeler, David A. Mustonen, Ville Getz, Gad Rozen, Steven G. Stratton, Michael R. Department of Cellular and Molecular Medicine Department of Bioengineering Moores Cancer Center University of California San Diego CA USA Wellcome Sanger Institute Wellcome Genome Campus Hinxton UK Department of Cellular and Molecular Medicine and Department of Bioengineering University of California San Diego La Jolla CA USA UC San Diego Moores Cancer Center San Diego CA USA University of California San Diego San Diego CA USA Broad Institute of MIT and Harvard Cambridge MA USA Center for Cancer Research Massachusetts General Hospital Boston MA USA Massachusetts General Hospital Boston MA USA Department of Pathology Massachusetts General Hospital Boston MA USA Harvard Medical School Boston MA USA Laboratory for Medical Science Mathematics RIKEN Center for Integrative Medical Sciences Yokohama Japan Computational Biology Program Ontario Institute for Cancer Research Toronto ON Canada Programme in Cancer & Stem Cell Biology Duke-NUS Medical School Singapore Singapore Centre for Computational Biology Duke-NUS Medical School Singapore Singapore Programme in Cancer and Stem Cell Biology Duke-NUS Medical School Singapore Singapore Programme in Cancer and Stem Cell Biology Centre for Computational Biology Duke-NUS Medical School Singapore Singapore SingHealth Duke-NUS Institute of Precision Medicine National Heart Centre Singapore Singapore Singapore Cancer Science Institute of Singapore National University of Singapore Singapore Singapore Institute of Molecular and Cell Biology Singapore Singapore Laboratory of Cancer Epigenome Division of Medical Science National Cancer Centre Singapore Singapore Singapore Duke-NUS Medical School Singapore Singapore Human Genome Sequencing Center Baylor College of Medicine Houston TX USA Dan L. Duncan Cancer Center Baylor College of Medicine Houston TX USA Department of Molecular and Human Genetics Baylor College of Medicine Houston TX USA Genome Integrity and Structural Biology Laboratory National Ins

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Spintronic superconductor in a bulk layered material with natural spin-valve structure

arXiv

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arXiv 2020年

作者： Sakuragi, Shunsuke Sasaki, S. Akashi, R. Sakagami, R. Kuroda, K. Bareille, C. Hashimoto, T. Nagashima, T. Kinoshita, Y. Hirata, Y. Shimozawa, M. Asai, S. Yajima, T. Doi, S. Tsujimoto, N. Kunisada, S. Noguchi, R. Kurokawa, K. Azuma, N. Hirata, K. Yamasaki, Y. Nakao, H. Kim, T.K. Cacho, C. Masuda, T. Tokunaga, M. Wadati, H. Okazaki, K. Shin, S. Kamihara, Y. Yamashita, Minoru Kondo, Takeshi Institute for Solid State Physics University of Tokyo Kashiwa Chiba Japan Department of Physics University of Tokyo Tokyo Japan Department of Applied Physics and Phisico-Informatics Keio University Yokohama Japan Department of Applied Physics National Defense Academy of Japan Yokosuka Japan Division of Materials Physics Graduate School of Engineering Science Osaka University Toyonaka Japan Research Center for Computational Design of Advanced Functional Materials National Institute of Advanced Industrial Science and Technology Tsukuba Japan Research and Services Division of Materials Data and Integrated System National Institute for Materials Science Tsukuba Japan RIKEN Center for Emergent Matter Science Wako Japan PRESTO Japan Science and Technology Agency Kawaguchi Japan Condensed Matter Research Center and Photon Factory Institute of Materials Structure Science High Energy Accelerator Research Organization Tsukuba Japan Diamond Light Source Harwell Campus Didcot United Kingdom Graduate School of Material Science University of Hyogo Hyogo Japan TheUniversity of Tokyo Kashiwa Chiba277-8581 Japan Center for Spintronics Research Network Keio University Yokohama Japan

Multi-layered materials provide fascinating platforms to realize various functional properties, possibly leading to future electronic devices controlled by external fields. In particular, layered magnets coupled with conducting layers have been extensively studied recently for possible control of their transport properties via the spin structure. Successful control of quantum-transport properties in the materials with antiferromagnetic (AFM) layers, so-called natural spin-valve structure, has been reported for the Dirac Fermion and topological/axion materials [1-11]. However, a bulk crystal in which magnetic and superconducting layers are alternately stacked has not been realized until now, and the search for functional properties in it is an interesting yet unexplored field in material science. Here, we discover superconductivity providing such an ideal platform in EuSn2As2 with the van der Waals stacking of magnetic Eu layers and superconducting Sn-As layers, and present the first demonstration of a natural spin-valve effect on the superconducting current. Below the superconducting transition temperature (Tc), the electrical resistivity becomes zero in the in-plane direction. In contrast, it, surprisingly, remains finite down to the lowest temperature in the out-of-plane direction, mostly due to the structure of intrinsic magnetic Josephson junctions in EuSn2As2. The magnetic order of the Eu layers (or natural spin-valve) is observed to be extremely soft, allowing one to easy control of the out-of-plane to in-plane resistivities ratio from 1 to ∞ by weak external magnetic fields. The concept of multi-functional materials with stacked magnetic-superconducting layers will open a new pathway to develop novel spintronic devices with magnetically controllable superconductivity. Copyright © 2020, The Authors. All rights reserved.

关键词： Europium compounds

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The evolutionary history of 2,658 cancers (vol 578, pg 122, 2020)

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NATURE 2023年第7948期614卷 E42-E42页

作者： Gerstung, Moritz Jolly, Clemency Leshchiner, Ignaty Dentro, Stefan C. Gonzalez, Santiago Rosebrock, Daniel Mitchell, Thomas J. Rubanova, Yulia Anur, Pavana Yu, Kaixian Tarabichi, Maxime Deshwar, Amit Wintersinger, Jeff Kleinheinz, Kortine Vazquez-Garcia, Ignacio Haase, Kerstin Jerman, Lara Sengupta, Subhajit Macintyre, Geoff Malikic, Salem Donmez, Nilgun Livitz, Dimitri G. Cmero, Marek Demeulemeester, Jonas Schumacher, Steven Fan, Yu Yao, Xiaotong Lee, Juhee Schlesner, Matthias Boutros, Paul C. Bowtell, David D. Zhu, Hongtu Getz, Gad Imielinski, Marcin Beroukhim, Rameen Sahinalp, S. Cenk Ji, Yuan Peifer, Martin Markowetz, Florian Mustonen, Ville Yuan, Ke Wang, Wenyi Morris, Quaid D. Spellman, Paul T. Wedge, David C. Van Loo, Peter European Molecular Biology Laboratory European Bioinformatics Institute (EMBL-EBI) Cambridge UK European Molecular Biology Laboratory Genome Biology Unit Heidelberg Germany Wellcome Sanger Institute Cambridge UK Genome Biology Unit European Molecular Biology Laboratory (EMBL) Heidelberg Germany University of Ljubljana Ljubljana Slovenia The Francis Crick Institute London UK Big Data Institute University of Oxford Oxford UK Wellcome Sanger Institute Wellcome Genome Campus Hinxton UK Big Data Institute Li Ka Shing Centre University of Oxford Oxford UK University of Cambridge Cambridge UK Cambridge University Hospitals NHS Foundation Trust Cambridge UK Department of Applied Mathematics and Theoretical Physics Centre for Mathematical Sciences University of Cambridge Cambridge UK Department of Epidemiology and Biostatistics Memorial Sloan Kettering Cancer Center New York NY USA Department of Statistics Columbia University New York NY USA Department of Haematology University of Cambridge Cambridge UK University of Leuven Leuven Belgium Broad Institute of MIT and Harvard Cambridge MA USA Center for Cancer Research Massachusetts General Hospital Charlestown MA USA Department of Pathology Massachusetts General Hospital Boston MA USA Harvard Medical School Boston MA USA Center for Cancer Research Massachusetts General Hospital Boston MA USA Dana-Farber Cancer Institute Boston MA USA Department of Medical Oncology Dana-Farber Cancer Institute Boston MA USA Department of Cancer Biology Dana-Farber Cancer Institute Boston MA USA Oxford NIHR Biomedical Research Centre Oxford UK Oxford NIHR Biomedical Research Centre University of Oxford Oxford UK University of Toronto Toronto Ontario Canada Vector Institute Toronto Ontario Canada Vector Institute Toronto ON Canada Department of Computer Science University of Toronto Toronto ON Canada Ontario Institute for Cancer Research Toronto Ontario Canada University of California Los Angeles

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