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Institution

Sandia National Laboratories

FacilityLivermore, California, United States
About: Sandia National Laboratories is a facility organization based out in Livermore, California, United States. It is known for research contribution in the topics: Laser & Combustion. The organization has 21501 authors who have published 46724 publications receiving 1484388 citations. The organization is also known as: SNL & Sandia National Labs.


Papers
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Journal ArticleDOI
TL;DR: This review covers advances in the MOF field from the past three years, focusing on applications, including gas separation, catalysis, drug delivery, optical and electronic applications, and sensing.
Abstract: Metal-organic frameworks (MOFs) represent a new class of hybrid organic-inorganic supramolecular materials comprised of ordered networks formed from organic electron donor linkers and metal cations. They can exhibit extremely high surface areas, as well as tunable pore size and functionality, and can act as hosts for a variety of guest molecules. Since their discovery, MOFs have enjoyed extensive exploration, with applications ranging from gas storage to drug delivery to sensing. This review covers advances in the MOF field from the past three years, focusing on applications, including gas separation, catalysis, drug delivery, optical and electronic applications, and sensing. We also summarize recent work on methods for MOF synthesis and computational modeling.

1,193 citations

Journal ArticleDOI
Joshua Quick1, Nicholas J. Loman1, Sophie Duraffour2, Jared T. Simpson3, Jared T. Simpson4, Ettore Severi5, Ettore Severi6, Lauren A. Cowley, Joseph Akoi Bore2, Raymond Koundouno2, Gytis Dudas7, Amy Mikhail, Nobila Ouedraogo8, Babak Afrough, Amadou Bah9, Jonathan H.J. Baum2, Beate Becker-Ziaja2, Jan Peter Boettcher8, Mar Cabeza-Cabrerizo2, Álvaro Camino-Sánchez2, Lisa L. Carter10, Juliane Doerrbecker2, Theresa Enkirch11, Isabel García-Dorival12, Nicole Hetzelt8, Julia Hinzmann8, Tobias Holm2, Liana E. Kafetzopoulou13, Liana E. Kafetzopoulou6, Michel Koropogui, Abigael Kosgey14, Eeva Kuisma6, Christopher H. Logue6, Antonio Mazzarelli, Sarah Meisel2, Marc Mertens15, Janine Michel8, Didier Ngabo, Katja Nitzsche2, Elisa Pallasch2, Livia Victoria Patrono2, Jasmine Portmann, Johanna Repits16, Natasha Y. Rickett12, Andreas Sachse8, Katrin Singethan17, Inês Vitoriano, Rahel L. Yemanaberhan2, Elsa Gayle Zekeng12, Trina Racine18, Alexander Bello18, Amadou A. Sall19, Ousmane Faye19, Oumar Faye19, N’Faly Magassouba, Cecelia V. Williams20, Victoria Amburgey20, Linda Winona20, Emily Davis21, Jon Gerlach21, Frank Washington21, Vanessa Monteil, Marine Jourdain, Marion Bererd, Alimou Camara, Hermann Somlare, Abdoulaye Camara, Marianne Gerard, Guillaume Bado, Bernard Baillet, Déborah Delaune, Koumpingnin Yacouba Nebie22, Abdoulaye Diarra22, Yacouba Savane22, Raymond Pallawo22, Giovanna Jaramillo Gutierrez23, Natacha Milhano24, Natacha Milhano5, Isabelle Roger22, Christopher Williams, Facinet Yattara, Kuiama Lewandowski, James E. Taylor, Phillip A. Rachwal25, Daniel J. Turner, Georgios Pollakis12, Julian A. Hiscox12, David A. Matthews, Matthew K. O'Shea, Andrew Johnston, Duncan W. Wilson, Emma Hutley, Erasmus Smit6, Antonino Di Caro, Roman Wölfel26, Kilian Stoecker26, Erna Fleischmann26, Martin Gabriel2, Simon A. Weller25, Lamine Koivogui, Boubacar Diallo22, Sakoba Keita, Andrew Rambaut27, Andrew Rambaut7, Pierre Formenty22, Stephan Günther2, Miles W. Carroll 
11 Feb 2016-Nature
TL;DR: This paper presents sequence data and analysis of 142 EBOV samples collected during the period March to October 2015 and shows that real-time genomic surveillance is possible in resource-limited settings and can be established rapidly to monitor outbreaks.
Abstract: A nanopore DNA sequencer is used for real-time genomic surveillance of the Ebola virus epidemic in the field in Guinea; the authors demonstrate that it is possible to pack a genomic surveillance laboratory in a suitcase and transport it to the field for on-site virus sequencing, generating results within 24 hours of sample collection. This paper reports the use of nanopore DNA sequencers (known as MinIONs) for real-time genomic surveillance of the Ebola virus epidemic, in the field in Guinea. The authors demonstrate that it is possible to pack a genomic surveillance laboratory in a suitcase and transport it to the field for on-site virus sequencing, generating results within 24 hours of sample collection. The Ebola virus disease epidemic in West Africa is the largest on record, responsible for over 28,599 cases and more than 11,299 deaths1. Genome sequencing in viral outbreaks is desirable to characterize the infectious agent and determine its evolutionary rate. Genome sequencing also allows the identification of signatures of host adaptation, identification and monitoring of diagnostic targets, and characterization of responses to vaccines and treatments. The Ebola virus (EBOV) genome substitution rate in the Makona strain has been estimated at between 0.87 × 10−3 and 1.42 × 10−3 mutations per site per year. This is equivalent to 16–27 mutations in each genome, meaning that sequences diverge rapidly enough to identify distinct sub-lineages during a prolonged epidemic2,3,4,5,6,7. Genome sequencing provides a high-resolution view of pathogen evolution and is increasingly sought after for outbreak surveillance. Sequence data may be used to guide control measures, but only if the results are generated quickly enough to inform interventions8. Genomic surveillance during the epidemic has been sporadic owing to a lack of local sequencing capacity coupled with practical difficulties transporting samples to remote sequencing facilities9. To address this problem, here we devise a genomic surveillance system that utilizes a novel nanopore DNA sequencing instrument. In April 2015 this system was transported in standard airline luggage to Guinea and used for real-time genomic surveillance of the ongoing epidemic. We present sequence data and analysis of 142 EBOV samples collected during the period March to October 2015. We were able to generate results less than 24 h after receiving an Ebola-positive sample, with the sequencing process taking as little as 15–60 min. We show that real-time genomic surveillance is possible in resource-limited settings and can be established rapidly to monitor outbreaks.

1,187 citations

Journal ArticleDOI
TL;DR: Sampling-based methods for uncertainty and sensitivity analysis are reviewed and special attention is given to the determination of sensitivity analysis results.

1,179 citations

Proceedings ArticleDOI
08 Dec 1995
TL;DR: A multilevel algorithm for graph partitioning in which the graph is approximated by a sequence of increasingly smaller graphs, and the smallest graph is then partitioned using a spectral method, and this partition is propagated back through the hierarchy of graphs.
Abstract: The graph partitioning problem is that of dividing the vertices of a graph into sets of specified sizes such that few edges cross between sets. This NP-complete problem arises in many important scientific and engineering problems. Prominent examples include the decomposition of data structures for parallel computation, the placement of circuit elements and the ordering of sparse matrix computations. We present a multilevel algorithm for graph partitioning in which the graph is approximated by a sequence of increasingly smaller graphs. The smallest graph is then partitioned using a spectral method, and this partition is propagated back through the hierarchy of graphs. A variant of the Kernighan-Lin algorithm is applied periodically to refine the partition. The entire algorithm can be implemented to execute in time proportional to the size of the original graph. Experiments indicate that, relative to other advanced methods, the multilevel algorithm produces high quality partitions at low cost.

1,162 citations

Journal ArticleDOI
TL;DR: This paper presents a method of using deep neural networks to learn a model for the Reynolds stress anisotropy tensor from high-fidelity simulation data and proposes a novel neural network architecture which uses a multiplicative layer with an invariant tensor basis to embed Galilean invariance into the predicted anisotropic tensor.
Abstract: There exists significant demand for improved Reynolds-averaged Navier–Stokes (RANS) turbulence models that are informed by and can represent a richer set of turbulence physics. This paper presents a method of using deep neural networks to learn a model for the Reynolds stress anisotropy tensor from high-fidelity simulation data. A novel neural network architecture is proposed which uses a multiplicative layer with an invariant tensor basis to embed Galilean invariance into the predicted anisotropy tensor. It is demonstrated that this neural network architecture provides improved prediction accuracy compared with a generic neural network architecture that does not embed this invariance property. The Reynolds stress anisotropy predictions of this invariant neural network are propagated through to the velocity field for two test cases. For both test cases, significant improvement versus baseline RANS linear eddy viscosity and nonlinear eddy viscosity models is demonstrated.

1,159 citations


Authors

Showing all 21652 results

NameH-indexPapersCitations
Lily Yeh Jan16246773655
Jongmin Lee1502257134772
Jun Liu13861677099
Gerbrand Ceder13768276398
Kevin M. Smith114171178470
Henry F. Schaefer111161168695
Thomas Bein10967742800
David Chandler10742452396
Stephen J. Pearton104191358669
Harold G. Craighead10156940357
Edward Ott10166944649
S. Das Sarma10095158803
Richard M. Crooks9741931105
David W. Murray9769943372
Alán Aspuru-Guzik9762844939
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202340
2022245
20211,510
20201,580
20191,535
20181,514