International Partnerships in Large Science Projects (July 1995)
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Suitcase Fusion 8 Getting Started
Copyright © 2014–2018 Celartem, Inc., doing business as Extensis. This document and the software described in it are copyrighted with all rights reserved. This document or the software described may not be copied, in whole or part, without the written consent of Extensis, except in the normal use of the software, or to make a backup copy of the software. This exception does not allow copies to be made for others. Licensed under U.S. patents issued and pending. Celartem, Extensis, LizardTech, MrSID, NetPublish, Portfolio, Portfolio Flow, Portfolio NetPublish, Portfolio Server, Suitcase Fusion, Type Server, TurboSync, TeamSync, and Universal Type Server are registered trademarks of Celartem, Inc. The Celartem logo, Extensis logos, LizardTech logos, Extensis Portfolio, Font Sense, Font Vault, FontLink, QuickComp, QuickFind, QuickMatch, QuickType, Suitcase, Suitcase Attaché, Universal Type, Universal Type Client, and Universal Type Core are trademarks of Celartem, Inc. Adobe, Acrobat, After Effects, Creative Cloud, Creative Suite, Illustrator, InCopy, InDesign, Photoshop, PostScript, Typekit and XMP are either registered trademarks or trademarks of Adobe Systems Incorporated in the United States and/or other countries. Apache Tika, Apache Tomcat and Tomcat are trademarks of the Apache Software Foundation. Apple, Bonjour, the Bonjour logo, Finder, iBooks, iPhone, Mac, the Mac logo, Mac OS, OS X, Safari, and TrueType are trademarks of Apple Inc., registered in the U.S. and other countries. macOS is a trademark of Apple Inc. App Store is a service mark of Apple Inc. IOS is a trademark or registered trademark of Cisco in the U.S. and other countries and is used under license. Elasticsearch is a trademark of Elasticsearch BV, registered in the U.S. -
Mapping Our Genes—Genome Projects: How Big? How Fast?
Mapping Our Genes—Genome Projects: How Big? How Fast? April 1988 NTIS order #PB88-212402 Recommended Citation: U.S. Congress, Office of Technology Assessment, Mapping Our Genes-The Genmne Projects.’ How Big, How Fast? OTA-BA-373 (Washington, DC: U.S. Government Printing Office, April 1988). Library of Congress Catalog Card Number 87-619898 For sale by the Superintendent of Documents U.S. Government Printing Office, Washington, DC 20402-9325 (order form can be found in the back of this report) Foreword For the past 2 years, scientific and technical journals in biology and medicine have extensively covered a debate about whether and how to determine the function and order of human genes on human chromosomes and when to determine the sequence of molecular building blocks that comprise DNA in those chromosomes. In 1987, these issues rose to become part of the public agenda. The debate involves science, technol- ogy, and politics. Congress is responsible for ‘(writing the rules” of what various Federal agencies do and for funding their work. This report surveys the points made so far in the debate, focusing on those that most directly influence the policy options facing the U.S. Congress, The House Committee on Energy and Commerce requested that OTA undertake the project. The House Committee on Science, Space, and Technology, the Senate Com- mittee on Labor and Human Resources, and the Senate Committee on Energy and Natu- ral Resources also asked OTA to address specific points of concern to them. Congres- sional interest focused on several issues: ● how to assess the rationales for conducting human genome projects, ● how to fund human genome projects (at what level and through which mech- anisms), ● how to coordinate the scientific and technical programs of the several Federal agencies and private interests already supporting various genome projects, and ● how to strike a balance regarding the impact of genome projects on international scientific cooperation and international economic competition in biotechnology. -
FY 1982 Submission Provided
DRAFT DOE/FE-0033 Previous No. DOE/ER-0102 ENERGY MATERIALS COORDINATING COMMITTEE (EMACC) Fiscal Year 1982 March 1983 ANNUAL TECHNICAL REPORT U.S. Department of Energy Washington, D.C. 20545 DRAFT DOE/FE-0033 Previous No. DOE/ER-0102 ENERGY MATERIALS COORDINATING COMMITTEE (EMACC) Fiscal Year 1982 March 1983 ANNUAL TECHNICAL REPORT U.S. Department of Energy TABLE OF CONTENTS Page No. INTRODUCTION ........................................................ 1 Fiscal Year 1982 Activities ....................................... 2 Materials Funding Trends in the Department of Energy .............. 6 PROGRAM DESCRIPTIONS ................................................ 11 - Office of Conservation and Renewable Systems .................... 14 * Office of Building Energy Research Development .............. 14 * Energy Conversion and Utilization Technologies .............. 15 * Division of Energy Storage Technology - Electrochemical Storage Branch .............................. 16 * Office of Vehicle and Engine R&D ............................ 17 * Office of Industrial Programs ............................... 18 * Biomass Energy Technology Division - Biological Hydrogen Program .......................................... 18 * Division of Ocean Energy Technology - Ocean Thermal Energy Conversion Program ................................. 19 * Office of Solar Energy/Photovoltaics Energy - Technology - Materials Research ........................... 20 * Wind Energy Technology Division - Large Wind Turbine Research and Technology Development ........................ -
Windows & Mirrors
THE HOMETOWN NEWSPAPER FOR MENLO PARK, ATHERTON, PORTOLA VALLEY AND WOODSIDE APRIL 26, 2017 | VOL. 52 NO. 34 WWW.ALMANACNEWS.COM Windows & mirrors KitaabWorld aims to give kids glimpses and reflections of different cultures PageP20 20 ERS’ CH D O I A C E E Pick your favorite restaurants, R shops and services | Page 9 2017 / / Alain Pinel Realtors® HOME STARTS HERE Atherton $12,800,000 Woodside $12,395,000 Menlo Park $4,988,000 489 Fletcher Drive | 6bd/7.5ba 835 La Honda Road | 4bd/3.5ba 1158 Windsor Way | 4bd/3.5ba Mary & Brent Gullixson | 650.462.1111 Judy Citron | 650.462.1111 Monica Corman & Mandy Montoya | 650.462.1111 By Appointment By Appointment By Appointment Atherton $5,250,000 Mountain View $3,498,000 Atherton $3,400,000 9 Valley Road | 5bd/3.5ba 278 Carmelita Drive | 5bd/5ba 390 Greenoaks Drive | 3bd/3ba Mary & Brent Gullixson | 650.462.1111 Keri Nicholas | 650.304.3100 Carol & Nicole | 650.462.1111 By Appointment By Appointment By Appointment Atherton $3,000,000 Menlo Park $1,949,000 Palo Alto $1,495,000 73 Watkins Avenue | 5bd/4ba 211 Pearl Lane | 3bd/2.5ba 548 Everett Avenue | 2bd/2ba Demetrius Tam | 650.462.1111 Janise Taylor | 650.462.1111 Brendan Callahan | 650.304.3100 By Appointment By Appointment By Appointment San Carlos $1.299.000 San Carlos $1,995,000 Redwood City $799,000 438 Portofino Drive #101 | 3bd/3ba 3189 La Mesa Drive | 3bd/2ba 111 Wellesley Crescent #2S | 2bd/3ba Zach Trailer | 650.304.3100 Courtney Charney | 650.462.1111 Shane Stent | 650.304.3100 Open Sat & Sun 1:30-4:30 By Appointment Open Sat & Sun 1:00-4:00 -
2019-2020 Catalog an Independent, Coeducational Institution of Higher Learning
2019-2020 Catalog An Independent, Coeducational Institution of Higher Learning Menlo College is VISION accredited by the Menlo College’s vision is to redefine undergraduate business education to be dynamically Western Association of Schools and Colleges adaptive, innovative, and relevant so that students can recognize opportunities and apply Senior College and 21st century skills to make a positive impact on the world. University Commission* and The Association to Advance Collegiate MISSION Schools of Business** At Menlo College, we ignite potential and educate students to make meaningful *WASC Senior College and contributions in the innovation economy. University Commission Our students thrive in an environment that values the following: small class sizes, 985 Atlantic Ave., Ste. 100 Alameda, CA 94501 experiential learning, engaged and student-centered faculty, holistic advising, exceptional 510.748.9001 student success resources, robust athletics programs and student leadership activities, www.wscuc.org and opportunities to engage in the Silicon Valley environment. Our graduates are able to **AACSB International 777 South Harbour Island learn throughout their lives and to think analytically, creatively, and responsibly in order Boulevard, Suite 750 to drive positive change in organizations and communities. Our faculty members mentor Tampa, FL 33602 813.769.6500 students by identifying potential, cultivating students’ individual talents, and helping www.aacsb.edu them build a roadmap to support their success. We support our faculty in -
US Neutron Facility Development in the Last Half-Century: a Cautionary Tale
Phys. Perspect. Ó 2015 The Author(s). This article is published with open access at Springerlink.com DOI 10.1007/s00016-015-0158-8 Physics in Perspective US Neutron Facility Development in the Last Half-Century: A Cautionary Tale John J. Rush* Large multi-user facilities serve many thousands of researchers in fields from particle physics to fundamental biology. The great expense—up to billions of current-day dollars— and the complexity of such facilities required access to extensive engineering and research infrastructures, most often found at national laboratories and the largest research univer- sities. Although the development of such facilities has been largely successful and the research results unique and often spectacular, the processes for choosing, funding, and locating them were complex and not always productive. In this review, I describe the troubled efforts over the past fifty years to develop neutron research facilities in the United States. During this period, the US has moved from a preeminent position in neutron-based science to a lesser status with respect to Europe. Several major US centers of excellence have been shut down and replaced with more focused capabilities. I compare the US efforts in neutron facilities with parallel developments in Europe and Asia, discuss the reasons for this state of affairs, and make some suggestions to help prevent similar consequences in the future. Key words: neutron research; national laboratories; Department of Energy; National Institute of Standards and Technology; research reactors; spallation neutron sources; Institut Laue-Langevin; National Academy of Sciences. Introduction A major element in the great expansion both of US and international science since the Second World War has been the development of large multi-user facilities to serve many thousands of researchers around the world with applications in almost all fields, ranging from particle physics to fundamental biology. -
Exascale Workshop Panel Report Meeting
DISCLAIMER This report was prepared as an account of a workshop sponsored by the U.S. Department of Energy. Neither the United States Government nor any agency thereof, nor any of their employees or officers, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of document authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof. Copyrights to portions of this report (including graphics) are reserved by original copyright holders or their assignees, and are used by the Government’s license and by permission. Requests to use any images must be made to the provider identified in the image credits. On the cover: Oak Ridge National Laboratory’s Cray XT5TM supercomputer. The computer, dubbed Jaguar, is the largest in the U.S. Department of Energy’s Office of Science. The Jaguar’s computing power makes it among the most powerful open scientific systems in the world. Future reports in the Scientific Grand Challenges workshop series will feature different Office of Science computers on their covers. EXASCALE WORKSHOP PANEL MEETING REPORT Report from the Meeting Held January 19-20, 2010 Sponsored by the U.S. -
The Global Optima HIV Allocative Efficiency Model
Targeting of resources in efforts to end AIDS: the global Optima HIV allocative efficiency model Sherrie L Kelly, Rowan Martin-Hughes, Robyn M Stuart, Xiao F Yap, David J Kedziora, Kelsey L Grantham, S Azfar Hussain, Iyanoosh Reporter, Andrew J Shattock, Laura Grobicki, Hassan Haghparast-Bidgoli, Jolene Skordis-Worrall, Zofia Baranczuk, Olivia Keiser, Janne Estill, Janka Petravic, Richard T Gray, Clemens J Benedikt, Nicole Fraser, Marelize Gorgens, David Wilson, Cliff C Kerr, David P Wilson Burnet Institute, Melbourne, Australia (S L Kelly MSc, R Martin-Hughes PhD, R M Stuart PhD, X F Yap MSc, D J Kedziora PhD, S A Hussain MSc, I Reporter MSc, J Petravic PhD, C Kerr PhD, Prof D P Wilson PhD) Monash University, Melbourne, Australia (S L Kelly MSc, D J Kedziora PhD, K L Grantham MAppStat, J Petravic PhD, Prof David P Wilson PhD) Department of Mathematical Sciences, University of Copenhagen, Copenhagen, Denmark (R M Stuart PhD) The Kirby Institute, UNSW Sydney, Sydney, Australia (A J Shattock PhD, R T Gray PhD) Institute for Global Health, University College London, London, UK (L Grobicki MSc, H Haghparast-Bidgoli PhD, J Skordis-Worrall PhD) Institute of Global Health, University of Geneva, Geneva, Switzerland (Z Baranczuk PhD, O Keiser PhD, J Estill PhD) Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland (Z Baranczuk PhD, O Keiser PhD, J Estill PhD) Institute of Mathematics, University of Zurich, Zurich, Switzerland (Z Baranczuk PhD) Institute of Mathematical Statistics and Actuarial Science, University of -
Does Mla Require Times New Roman
Does Mla Require Times New Roman Valvar and well-made Gordan intercalated, but Davie purringly jugging her Ramadan. Jean-Paul still baptizes unpleasantly evilly.while enchanting Corwin disturb that plebeians. Composed Flinn never hesitating so voluptuously or shoehorn any podsol Your coverage should be centered. Fontchoose an proceed to read font such as Times New Roman. How will Use MLA Style Writing in Essays Education. Why does not require one from mla does mla require times new roman to mla? Learn more than the mla? Formatting double after one inch margins 12 pt font in Times New Roman page area in the. Requirements Printed on standard 5 x 11-inch paper Legible text typically Times New Roman at least 12 pt 1 inch margins on each experience of the document The. Here then the guidelines for formatting a paper according to MLA style. In title does not professionally designed and times new page at the edit header in mls style does mla require times new roman, they are often get advanced writing center your paper? The vertical distance between lines of headlight on about page. What damage the easiest way would create MLA citations? Is gift a Verb? They climb the ones who developed the MLA formatting commonly used today. When finished, so we sure many take tax time should read cancel the assignment carefully. First page in mla does mla require times new roman? In discourse text of the canopy or paper, Hollywood did put on quite and few. In mla requires that appears at the new roman numerals, you have times new roman? Your mla does not needed to. -
Articles the Global Optima HIV Allocative Efficiency Model
17TLHIV0277 THELANCETHIV-D-17-00277 0094 S2352-3018(18)30024-9 Articles Embargo: March 9, 2018—23:30 (GMT) JG Doctopic: Primary Research This version saved: 17:34, 07-Mar-18 The global Optima HIV allocative efficiency model: targeting resources in efforts to end AIDS Sherrie L Kelly, Rowan Martin-Hughes, Robyn M Stuart, Xiao F Yap, David J Kedziora, Kelsey L Grantham, S Azfar Hussain, Iyanoosh Reporter, Andrew J Shattock, Laura Grobicki, Hassan Haghparast-Bidgoli, Jolene Skordis-Worrall, Zofia Baranczuk, Olivia Keiser, Janne Estill, Janka Petravic, Richard T Gray, Clemens J Benedikt, Nicole Fraser, Marelize Gorgens, David Wilson, Cliff C Kerr, David P Wilson Summary Background To move towards ending AIDS by 2030, HIV resources should be allocated cost-effectively. We used the Lancet HIV 2018 Optima HIV model to estimate how global HIV resources could be retargeted for greatest epidemiological effect and Published Online how many additional new infections could be averted by 2030. March 9, 2018 http://dx.doi.org/10.1016/ S2352-3018(18)30024-9 Methods We collated standard data used in country modelling exercises (including demographic, epidemiological, See Online/Comment behavioural, programmatic, and expenditure data from Jan 1, 2000, to Dec 31, 2015) for 44 countries, capturing 80% http://dx.doi.org/10.1016/ of people living with HIV worldwide. These data were used to parameterise separate subnational and national models S2352-3018(18)30041-9 within the Optima HIV framework. To estimate optimal resource allocation at subnational, national, regional, and Burnet Institute, Melbourne, global levels, we used an adaptive stochastic descent optimisation algorithm in combination with the epidemic VIC, Australia (S L Kelly MSc, models and cost functions for each programme in each country. -
Adobe Type 1 Font Format Adobe Systems Incorporated
Type 1 Specifications 6/21/90 final front.legal.doc Adobe Type 1 Font Format Adobe Systems Incorporated Addison-Wesley Publishing Company, Inc. Reading, Massachusetts x Menlo Park, California x New York Don Mills, Ontario x Wokingham, England x Amsterdam Bonn x Sydney x Singapore x Tokyo x Madrid x San Juan Library of Congress Cataloging-in-Publication Data Adobe type 1 font format / Adobe Systems Incorporated. p. cm Includes index ISBN 0-201-57044-0 1. PostScript (Computer program language) 2. Adobe Type 1 font (Computer program) I. Adobe Systems. QA76.73.P67A36 1990 686.2’2544536—dc20 90-42516 Copyright © 1990 Adobe Systems Incorporated. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without the prior written permission of Adobe Systems Incorporated and Addison-Wesley, Inc. Printed in the United States of America. Published simultaneously in Canada. The information in this book is furnished for informational use only, is subject to change without notice, and should not be construed as a commitment by Adobe Systems Incorporated. Adobe Systems Incorporated assumes no responsibility or liability for any errors or inaccuracies that may appear in this book. The software described in this book is furnished under license and may only be used or copied in accordance with the terms of such license. Please remember that existing font software programs that you may desire to access as a result of information described in this book may be protected under copyright law. -
Human Genome Project
Human Genome Project The Human Genome Project (HGP) was an international scientific research project with the goal of determining the sequence of nucleotide base pairs that make up human DNA, and of identifying and mapping all of the genes of the human genome from both a physical and a functional standpoint.[1] It remains the world's largest collaborative biological project.[2] After the idea was picked up in 1984 by the US government when the planning started, the project formally launched in 1990 and was declared complete in 2003[3]. Funding came from the US government through the National Institutes of Health (NIH) as well as numerous other groups from around the world. A parallel project was conducted outside government by the Celera Corporation, or Celera Genomics, which was formally launched in 1998. Most of the government-sponsored sequencing was performed in twenty universities and research centers in the United States, the United Kingdom, Japan, France, Logo HGP; Vitruvian Man, Leonardo Germany, Spain and China.[4] da Vinci The Human Genome Project originally aimed to map the nucleotides contained in a human haploid reference genome (more than three billion). The "genome" of any given individual is unique; mapping the "human genome" involved sequencing a small number of individuals and then assembling these together to get a complete sequence for each chromosome. Therefore, the finished human genome is a mosaic, not representing any one individual. Contents Human Genome Project History State of completion Applications and proposed