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The Serials Crisis and Open Access: a White Paper for the Virginia Tech Commission on Research
The Serials Crisis and Open Access A White Paper for the Virginia Tech Commission on Research Philip Young University Libraries Virginia Tech December 2, 2009 This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License. 1 Introduction This white paper offers an introduction to open access as well as a look at its current development. The open access movement is an attempt to free scholarly communication from restrictions on access, control, and cost, and to enable benefits such as data mining and increased citations. Open access has gained significant momentum through mandates from research funders and universities. While open access can be provided in parallel with traditional publishing, it is increasingly available as a publishing option. While open access is approached here from the problem of subscription inflation, it is important to recognize that open access is not merely a library issue, but affects the availability of research to current and future students and scholars. The Serials Crisis The phrase “serials crisis” has been in use for more than a decade as shorthand for the rise in costs for academic journals and the inability of libraries to bring these costs under control. Price inflation for academic journals significantly exceeds the consumer price index (see graph, next page). The most recent data show that journal prices increased at an average rate of 8% in 2007.1 Because journal subscriptions are a large part of the collections budget at academic libraries, any reduction in funding usually results in a loss of some journals. And the high rate of annual inflation means that academic library budgets must increase every year simply to keep the same resources that students and faculty need. -
Open Science in Archaeology
Marwick, B. et al. (2017) Open science in archaeology. SAA Archaeological Record, 17(4), pp. 8-14. There may be differences between this version and the published version. You are advised to consult the publisher’s version if you wish to cite from it. http://eprints.gla.ac.uk/148887/ Deposited on: 29 September 2017 Enlighten – Research publications by members of the University of Glasgow http://eprints.gla.ac.uk Open Science in Archaeology Ben Marwick*, Jade d’Alpoim Guedes, C. Michael Barton, Lynsey A. Bates, Michael Baxter, Andrew Bevan, Elizabeth A. Bollwerk, R. Kyle Bocinsky, Tom Brughmans, Alison K. Carter, Cyler Conrad, Daniel A. Contreras, Stefano Costa, Enrico R. Crema, Adrianne Daggett, Benjamin Davies, B. Lee Drake, Thomas S. Dye, Phoebe France, Richard Fullagar, Domenico Giusti, Shawn Graham, Matthew D. Harris, John Hawks, Sebastian Heath, Damien Huffer, Eric C. Kansa, Sarah Whitcher Kansa, Mark E. Madsen, Jennifer Melcher, Joan Negre, Fraser D. Neiman, Rachel Opitz, David C. Orton, Paulina Przystupa, Maria Raviele, Julien Riel-Salvatore, Philip Riris, Iza Romanowska, Néhémie Strupler, Isaac I. Ullah, Hannah G. Van Vlack, Ethan C. Watrall, Chris Webster, Joshua Wells, Judith Winters, Colin D. Wren * corresponding author, [email protected] Introduction In archaeology, we are accustomed to investing great effort into collecting data from fieldwork, museum collections, and other sources, followed by detailed description, rigorous analysis, and in many cases ending with publication of our findings in short, highly concentrated reports or journal articles. Very often, these publications are all that is visible of this lengthy process, and even then, most of our journal articles are only accessible to scholars at institutions paying subscription fees to the journal publishers. -
The European Molecular Biology Organization (EMBO) and Nature
The European Molecular Biology Organization (EMBO) and Nature Publishing Group (NPG) are pleased to announce that The EMBO Journal and EMBO reports will accept open-access articles as of January 2007, subject to payment of a publication fee. The journals are moving to a mixed-revenue model of subscription charges and publication fees. The open-access option will be available to all authors submitting original research on or after 1 January 2007. The publication fee will be €2,000 plus VAT (where applicable). Articles published with a publication fee will be clearly identified in the online and print editions of the journal with an open-access icon. Print subscription prices will not be affected and site license prices will be adjusted in line with the amount of subscription content published annually. The journal editors will be blind to the author's choice, avoiding any possibility of a conflict of interest during peer review and acceptance. Authors paying the publication fee will be entitled to self-archive the published version immediately on publication in a repository of their choice, and in any format. Content that an author has decided to make freely available online will be licensed under the Creative Commons Deed 2.5 (http://creativecommons.org/licenses/by-nc-nd/2.5/). The author thereby permits dissemination and re-use of the article, enabling the sharing and re-use of scientific material. This does not however permit commercial exploitation or the creation of derivative works without specific permission. Other articles will continue to be published under NPG’s exclusive License-to-Publish, where its usual self-archiving policy will apply. -
Estimated Costs of Implementing an Open Access Policy at a Private Foundation
bioRxiv preprint doi: https://doi.org/10.1101/128413; this version posted August 17, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Estimated costs of implementing an open access policy at a private foundation 1 2 Carly Strasser and Eesha Khare 1 Gordon and Betty Moore Foundation, Palo Alto, California, USA 2 Harvard University, Cambridge, Massachusetts, USA Corresponding author: Carly Strasser1 Email address: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/128413; this version posted August 17, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Abstract Background: The Gordon and Betty Moore Foundation (GBMF) was interested in understanding the potential effects of a policy requiring open access to peer-reviewed publications resulting from the research the foundation funds. Methods: We collected data on more than 2000 publications in over 500 journals that were generated by GBMF grantees since 2001. We then examined the journal policies to establish how two possible open -
Catalyzed Synthesis of Zinc Clays by Prebiotic Central Metabolites
bioRxiv preprint doi: https://doi.org/10.1101/075176; this version posted September 14, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Catalyzed Synthesis of Zinc Clays by Prebiotic Central Metabolites Ruixin Zhoua, Kaustuv Basub, Hyman Hartmanc, Christopher J. Matochad, S. Kelly Searsb, Hojatollah Valib,e, and Marcelo I. Guzman*,a *Corresponding Author: [email protected] aDepartment of Chemistry, University of Kentucky, Lexington, KY, 40506, USA; bFacility for Electron Microscopy Research, McGill University, 3640 University Street, Montreal, Quebec H3A 0C7, Canada; cEarth, Atmosphere, and Planetary Science Department, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; dDepartment of Plant and Soil Sciences, University of Kentucky, Lexington, KY, 40546, USA; eDepartment of Anatomy & Cell Biology, 3640 University Street, Montreal H3A 0C7, Canada The authors declare no competing financial interest. Number of text pages: 20 Number of Figures: 9 Number of Tables: 0 bioRxiv preprint doi: https://doi.org/10.1101/075176; this version posted September 14, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract How primordial metabolic networks such as the reverse tricarboxylic acid (rTCA) cycle and clay mineral catalysts coevolved remains a mystery in the puzzle to understand the origin of life. -
Downloads Presented on the Abstract Page
bioRxiv preprint doi: https://doi.org/10.1101/2020.04.27.063578; this version posted April 28, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. A systematic examination of preprint platforms for use in the medical and biomedical sciences setting Jamie J Kirkham1*, Naomi Penfold2, Fiona Murphy3, Isabelle Boutron4, John PA Ioannidis5, Jessica K Polka2, David Moher6,7 1Centre for Biostatistics, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom. 2ASAPbio, San Francisco, CA, USA. 3Murphy Mitchell Consulting Ltd. 4Université de Paris, Centre of Research in Epidemiology and Statistics (CRESS), Inserm, Paris, F-75004 France. 5Meta-Research Innovation Center at Stanford (METRICS) and Departments of Medicine, of Epidemiology and Population Health, of Biomedical Data Science, and of Statistics, Stanford University, Stanford, CA, USA. 6Centre for Journalology, Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada. 7School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, Canada. *Corresponding Author: Professor Jamie Kirkham Centre for Biostatistics Faculty of Biology, Medicine and Health The University of Manchester Jean McFarlane Building Oxford Road Manchester, M13 9PL, UK Email: [email protected] Tel: +44 (0)161 275 1135 bioRxiv preprint doi: https://doi.org/10.1101/2020.04.27.063578; this version posted April 28, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. -
Downloaded, Cited, Published, and Discussed Online
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.04.433874; this version posted March 4, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Linguistic Analysis of the bioRxiv Preprint Landscape This manuscript (permalink) was automatically generated from greenelab/annorxiver_manuscript@7744221 on February 26, 2021. Authors David N. Nicholson 0000-0003-0002-5761 · danich1 · dnicholson329 Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine University of Pennsylvania, Philadelphia PA, USA · Funded by The Gordon and Betty Moore Foundation (GBMF4552); The National Institutes of Health (T32 HG000046) Vincent Rubinetti · vincerubinetti · vincerubinetti Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine University of Pennsylvania, Philadelphia PA, USA · Funded by The Gordon and Betty Moore Foundation (GBMF4552); The National Institutes of Health (T32 HG010067) Dongbo Hu · dongbohu Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine University of Pennsylvania, Philadelphia PA, USA · Funded by The Gordon and Betty Moore Foundation (GBMF4552); The National Institutes of Health (T32 HG010067) Marvin Thielk 0000-0002-0751-3664 · MarvinT · TheNeuralCoder Elsevier, Philadelphia PA, USA Lawrence E. Hunter 0000-0003-1455-3370 · LEHunter -
Chromatin and Epigenetics Cross-Journal Focus Chromatin and Epigenetics
EMBO Molecular Medicine cross-journal focus Chromatin and epigenetics cross-journal focus Chromatin and epigenetics EDITORS Esther Schnapp Senior Editor [email protected] | T +49 6221 8891 502 Esther joined EMBO reports in October 2008. She was awarded her PhD in 2005 at the Max Planck Institute for Molecular Cell Biology and Genetics in Dresden, Germany, where she studied tail regeneration in the axolotl. As a post-doc she worked on muscle development in zebrafish and on the characterisation of mesoangioblasts at the Stem Cell Research Institute of the San Raffaele Hospital in Milan, Italy. Anne Nielsen Editor [email protected] | T +49 6221 8891 408 Anne received her PhD from Aarhus University in 2008 for work on miRNA processing in Joergen Kjems’ lab. As a postdoc she then went on to join Javier Martinez’ lab at IMBA in Vienna and focused on siRNA-binding proteins and non-conventional splicing in the unfolded protein response. Anne joined The EMBO Journal in 2012. Maria Polychronidou Editor [email protected] | T +49 6221 8891 410 Maria received her PhD from the University of Heidelberg, where she studied the role of nuclear membrane proteins in development and aging. During her post-doctoral work, she focused on the analysis of tissue-specific regulatory functions of Hox transcription factors using a combination of computational and genome-wide methods. Céline Carret Editor [email protected] | T +49 6221 8891 310 Céline Carret completed her PhD at the University of Montpellier, France, characterising host immunodominant antigens to fight babesiosis, a parasitic disease caused by a unicellular EMBO Apicomplexan parasite closely related to the malaria agent Plasmodium. -
Systems Biology Behind Immunoprotection of Both Sheep and Goats After 2 Sungri/96 PPRV Vaccination
bioRxiv preprint doi: https://doi.org/10.1101/2020.08.14.252056; this version posted August 15, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Systems Biology behind immunoprotection of both Sheep and Goats after 2 Sungri/96 PPRV vaccination 3 Sajad Ahmad Wani1,2#, Manas Ranjan Praharaj3#, Amit R Sahu1, Raja Ishaq Nabi 4 Khan1, Kaushal Kishor Rajak1, Dhanavelu Muthuchelvan4, Aditya Sahoo5, Bina 5 Mishra1, R. K. Singh1*, Bishnu Prasad Mishra1* and Ravi Kumar Gandham3* 6 1 ICAR-Indian Veterinary Research Institute (IVRI), Bareilly, India 7 2 The Ohio State University, Columbus, OH, United States 8 3 DBT-National Institute of Animal Biotechnology, Hyderabad, India 9 4 ICAR-Indian Veterinary Research Institute (IVRI), Mukteswar, India 10 5 ICAR- Directorate of Foot and Mouth Disease, Mukteswar, India 11 # Equal Contributors 12 * Corresponding Authors: Ravi Kumar Gandham, [email protected] 13 Bishnu Prasad Mishra, [email protected] 14 Raj Kumar Singh, [email protected] 15 16 Abstract 17 Immune response is a highly coordinated cascade involving all the subsets of 18 PBMCs. In this study, RNA-Seq analysis of PBMC subsets - CD4+, CD8+, CD14+, 19 CD21+ and CD335+ cells from day 0 and day 5 of Sungri/96 Peste des Petits 20 Ruminants vaccinated sheep and goats was done to delineate the systems biology 21 behind immune - protection of the vaccine in sheep and goats. Assessment of the 22 immune response processes enriched by the differentially expressed genes in all the 23 subsets suggested a strong dysregulation towards development of early inflammatory 24 microenvironment, which is very much required for differentiation of monocytes to 25 macrophages, and for activation and migration of dendritic cells into the draining lymph 26 nodes. -
Total Scicomm: a Strategy for Communicating Open Science
publications Communication Total SciComm: A Strategy for Communicating Open Science Manh-Toan Ho * , Manh-Tung Ho and Quan-Hoang Vuong Centre for Interdisciplinary Social Research, Phenikaa University, Hanoi 100803, Vietnam; [email protected] (M.-T.H.); [email protected] (Q.-H.V.) * Correspondence: [email protected] Abstract: This paper seeks to introduce a strategy of science communication: Total SciComm or all-out science communication. We proposed that to maximize the outreach and impact, scientists should use different media to communicate different aspects of science, from core ideas to methods. The paper uses an example of a debate surrounding a now-retracted article in the Nature journal, in which open data, preprints, social media, and blogs are being used for a meaningful scientific conversation. The case embodied the central idea of Total SciComm: the scientific community employs every medium to communicate scientific ideas and engages all scientists in the process. Keywords: preprints; open science; science communication; social media; Total SciComm 1. Introduction Growing skepticism towards scientific findings makes capturing attention from the public an urgent and serious issue for scientists. The attention will help raise the scien- Citation: Ho, M.-T.; Ho, M.-T.; tists’ profiles and provide scientists a channel to communicate through scientific ideas. Vuong, Q.-H. Total SciComm: A On YouTube, and a new form of radio—podcast—the rise of the Intellectual Dark Web Strategy for Communicating Open group is a prominent example of an effort for good and effective science communication [1]. Science. Publications 2021, 9, 31. -
SCIENCE CITATION INDEX EXPANDED - JOURNAL LIST Total Journals: 8631
SCIENCE CITATION INDEX EXPANDED - JOURNAL LIST Total journals: 8631 1. 4OR-A QUARTERLY JOURNAL OF OPERATIONS RESEARCH 2. AAPG BULLETIN 3. AAPS JOURNAL 4. AAPS PHARMSCITECH 5. AATCC REVIEW 6. ABDOMINAL IMAGING 7. ABHANDLUNGEN AUS DEM MATHEMATISCHEN SEMINAR DER UNIVERSITAT HAMBURG 8. ABSTRACT AND APPLIED ANALYSIS 9. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 10. ACADEMIC EMERGENCY MEDICINE 11. ACADEMIC MEDICINE 12. ACADEMIC PEDIATRICS 13. ACADEMIC RADIOLOGY 14. ACCOUNTABILITY IN RESEARCH-POLICIES AND QUALITY ASSURANCE 15. ACCOUNTS OF CHEMICAL RESEARCH 16. ACCREDITATION AND QUALITY ASSURANCE 17. ACI MATERIALS JOURNAL 18. ACI STRUCTURAL JOURNAL 19. ACM COMPUTING SURVEYS 20. ACM JOURNAL ON EMERGING TECHNOLOGIES IN COMPUTING SYSTEMS 21. ACM SIGCOMM COMPUTER COMMUNICATION REVIEW 22. ACM SIGPLAN NOTICES 23. ACM TRANSACTIONS ON ALGORITHMS 24. ACM TRANSACTIONS ON APPLIED PERCEPTION 25. ACM TRANSACTIONS ON ARCHITECTURE AND CODE OPTIMIZATION 26. ACM TRANSACTIONS ON AUTONOMOUS AND ADAPTIVE SYSTEMS 27. ACM TRANSACTIONS ON COMPUTATIONAL LOGIC 28. ACM TRANSACTIONS ON COMPUTER SYSTEMS 29. ACM TRANSACTIONS ON COMPUTER-HUMAN INTERACTION 30. ACM TRANSACTIONS ON DATABASE SYSTEMS 31. ACM TRANSACTIONS ON DESIGN AUTOMATION OF ELECTRONIC SYSTEMS 32. ACM TRANSACTIONS ON EMBEDDED COMPUTING SYSTEMS 33. ACM TRANSACTIONS ON GRAPHICS 34. ACM TRANSACTIONS ON INFORMATION AND SYSTEM SECURITY 35. ACM TRANSACTIONS ON INFORMATION SYSTEMS 36. ACM TRANSACTIONS ON INTELLIGENT SYSTEMS AND TECHNOLOGY 37. ACM TRANSACTIONS ON INTERNET TECHNOLOGY 38. ACM TRANSACTIONS ON KNOWLEDGE DISCOVERY FROM DATA 39. ACM TRANSACTIONS ON MATHEMATICAL SOFTWARE 40. ACM TRANSACTIONS ON MODELING AND COMPUTER SIMULATION 41. ACM TRANSACTIONS ON MULTIMEDIA COMPUTING COMMUNICATIONS AND APPLICATIONS 42. ACM TRANSACTIONS ON PROGRAMMING LANGUAGES AND SYSTEMS 43. ACM TRANSACTIONS ON RECONFIGURABLE TECHNOLOGY AND SYSTEMS 44. -
Security Implications of Emerging Biotechnologies: Workshop Summary, Analysis, and Recommendations
Security Implications of Emerging Biotechnologies: Workshop Summary, Analysis, and Recommendations Diane DiEuliis and Charles Lutes June 2016 Security Implications of Emerging Biotechnologies Workshop Summary, Analysis, and Recommendations Diane DiEuliis and Charles Lutes On April 26th, 2016, the Center for the Study of Weapons of Mass Destruction (CSWMD) at National Defense University held a workshop to explore “Security Implications of Emerging Biotechnologies.” Participants from government, NGOs and academia discussed opportunities and challenges of a new era of biotechnology, one highlighted by the advancing ease with which the genomes of organisms can be engineered for specific purposes, potentially more rapidly than we are prepared to assess and deal responsibly with its ramifications. Synthetic biology and associated genome editing tools will be essential for addressing the global challenge of resource scarcity, provide unprecedented advances in public health and medicine, and create innovative products that can support national defense, as well as commodities that stimulate the US economy. At the same time, new dual-use technologies will present significant challenges to biosecurity, biosafety, and have already begun to generate ethical and moral dilemmas. Participants stressed the need to address these issues in ways that do not stifle the technology’s advancement nor America’s competitiveness in the global bioeconomy. The workshop was convened to consider the potential biosecurity concerns of emerging biotechnologies and their impact on national security. The dual use problem was discussed in the context of “biosecurity by design,” a concept conceived specifically in preparation for the workshop in which government, industry, academia, national laboratories, and individual users should be mindful of developing potential security solutions at each step of technology development.