Presentation by Dr Steve McEachern, ADA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Hugo Leroux and Liming Zhu, CSIRO, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Investigator-initiated clinical trials: a community perspectiveARDC
Presentation by Miranda Cumpston, ACTA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Kelly Hart, ONDC in PM&C, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
International perspective for sharing publicly funded medical research dataARDC
Presentation by Olivier Salvado, CSIRO, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Prof Lisa Askie, ANZCTR, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
This presentation was provided by Dr. Paul Burton of the University of Bristol during the NISO Symposium, Privacy Implications of Research Data, held on September 11, 2016, in conjunction with the International Data Week in Denver, Colorado.
Presentation by Hugo Leroux and Liming Zhu, CSIRO, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Investigator-initiated clinical trials: a community perspectiveARDC
Presentation by Miranda Cumpston, ACTA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Kelly Hart, ONDC in PM&C, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
International perspective for sharing publicly funded medical research dataARDC
Presentation by Olivier Salvado, CSIRO, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Prof Lisa Askie, ANZCTR, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
This presentation was provided by Dr. Paul Burton of the University of Bristol during the NISO Symposium, Privacy Implications of Research Data, held on September 11, 2016, in conjunction with the International Data Week in Denver, Colorado.
BioSHaRE: The DataSHIELD Legal Analysis Template - Susan Wallace - University...Lisette Giepmans
BioSHaRE conference July 28th, 2015, Milan - Latest tools and services for data sharing
Stream 2: ELSI approaches and services
An ethico-legal analysis was conducted at ULEIC that examined each step of the DataSHIELD process from the perspective of UK case law, regulations, and guidance. In order to facilitate a similar analysis for other countries/ jurisdictions, a ‘DataSHIELD Legal Analysis Template’ is being made. Contact: sew40@leicester.ac.uk
DataSHIELD was born of the requirement in the biomedical and social sciences to co-analyse individual patient data (micro data) from different sources, without disclosing identity or sensitive information. Under DataSHIELD, raw data never leave the data provider and no micro data or disclosive information can be seen by the researcher. The analysis is taken to the data – not the data to the analysis. It provides a flexible, modular, open-source solution ideally placed to serve a broad user and development community and to circumvent barriers related to ethical-legal restrictions, intellectual property and physical size of the data as a limiting factor.
Data sharing promotes many goals of the NIH research endeavor. It is particularly important for unique data that cannot be readily replicated. Data sharing allows scientists to expedite the translation of research results into knowledge, products, and procedures to improve human health. Do you know what a data sharing plan should include? Are you aware of common practices and standards for data sharing? Do you know what services are available to help share your data responsibly? This workshop will begin to address these questions. Q&A will follow the presentation. Anyone interested in or planning to apply for NIH funding should attend. Note: The NIH data-sharing policy applies to applicants seeking $500,000 or more in direct costs in any year of the proposed research.
David Van Enckevort - FAIR sample and data access DataSciSIG
David van Enckevort from the University of Groningen describes FAIR Sample and Data Access in Biobanking and Biorepositories.
This talk was sponsored by the NIH Data Science Special Interest Group and part of a webinar panel on June 23, 2017 on Global Biobanking and Access to Specimens.
This presentation was provided by Helen Henderson of Ringgold, during the NISO at NASIG Pre-conference "Metadata in a Digital Age: New Models of Creation, Discovery, and Use," held on June 4, 2008.
Stop press: should embargo conditions apply to metadata?Jisc RDM
Sarah Middle of Cambridge University discusses whether embargo conditions should apply to metadata. Session held at the Research Data Network event in May 2016, Cardiff University.
Research information management: making sense of it allDigital Science
"Research information management: making sense of it all" - Julia Hawks, VP North America, Symplectic
Slides from Shaking It Up: Challenges and Solutions in Scholarly Information Management, San Francisco, April 22, 2015
Practical applications for altmetrics in a changing metrics landscapeDigital Science
"Practical applications for altmetrics in a changing metrics landscape" - Sara Rouhi, Altmetric product specialist, and Anirvan Chatterjee, Director Data Strategy for CTSI at UCSF
FAIR Data - A is for Accessible
David Fitzgerald, Data Manager for the Australian Longitudinal Study of Women’s Health (ALSWH) presented on how ALSWH makes a nationally significant longitudinal study with highly sensitive data accessible for others to reuse.
Full webinar recording: https://youtu.be/me27whU8GG8
RDAP 16 Poster: Measuring adoption of Electronic Lab Notebooks and their impa...ASIS&T
Research Data Access and Preservation Summit, 2016
Atlanta, GA
May 4-7, 2016
Poster session (Wednesday, May 4)
Presenters:
Jan Cheetham, University of Wisconsin-Madison
Wendy Kozlowski, Cornell University
CINECA webinar slides: Making cohort data FAIRCINECAProject
Cohort studies, which recruit groups of individuals who share common characteristics and follow them over a period of time, are a robust and essential method in biomedical research for understanding the links between risk factors and diseases. Through questionnaires, medical assessments, and other interactions, voluminous and complex data are collected about the study participants. While cohort studies present a treasure trove of data, the data is often not FAIR (findable, accessible, interoperable and reusable). First, due to the sensitive and private nature of medical information, cohort data are often access controlled. Due to the lack of information about the studies (metadata), often one needs to dig deep to know what data is available in a cohort study. Therefore, many cohort datasets suffer from the findable and accessible issues. Second, often data collection is performed with instruments and data specifications tailored to the study. As a result, combining data across cohorts, even ones with similar characteristics, is difficult, making interoperability and reusability a challenge. In this presentation, we will explore several informatics techniques, such as the use of ontology, to make cohort data more FAIR. We will also consider the implications of making cohort data more open and the ethical and governance issues associated with open science benefit sharing.
This webinar is part of the “How FAIR are you” webinar series and hackathon, which aim at increasing and facilitating the uptake of FAIR approaches into software, training materials and cohort data, to facilitate responsible and ethical data and resource sharing and implementation of federated applications for data analysis.
The CINECA webinar series aims to discuss ways to address common challenges and share best practices in the field of cohort data analysis, as well as distribute CINECA project results. All CINECA webinars include an audience Q&A session during which attendees can ask questions and make suggestions. Please note that all webinars are recorded and available for posterior viewing. CINECA webinars include an audience Q&A session during which attendees can ask questions and make suggestions.
This webinar took place on 17th February 2021 and is part of the CINECA webinar series.
For previous and upcoming CINECA webinars see:
https://www.cineca-project.eu/webinars
This presentation was provided by Melissa Levine of the University of Michigan during a NISO Virtual Conference on the topic of data curation, held on Wednesday, August 31, 2016
Managing provenance in the Social Sciences: the Data Documentation Initiative...ARDC
Slides from webinar: Provenance and social science data. Presented on 15 March 2017. Presenter was Dr Steve McEachern, Director Australian Data Archive
FULL webinar recording: https://youtu.be/elPcKqWoOPg
1. Dr Steve McEachern (Director, Aust Data Archive) Data Documentation Initiative (DDI: http://www.ddialliance.org/): A free, international standard for describing data produced by surveys and other observational methods in the social, behavioral, economic, and health sciences. It can document and manage different stages in the research data lifecycle, eg conceptualization, collection, processing, distribution, discovery, and archiving. Documenting data with DDI facilitates understanding, interpretation, and use -- by people, software systems, and computer networks.
Steven McEachern - ADA, DDI (metadata standard) and the Data LifecycleSteve Androulakis
Dr. McEachern is Director of the Australian Data Archive at the Australian National University, and has research interests in data management and archiving, community and social attitude surveys, new data collection methods, and reproducible research methods.
This talk was given for the Monthly Tech Talks event hosted by Australian data infrastructure groups ANDS, NeCTAR, RDS and others.
BioSHaRE: The DataSHIELD Legal Analysis Template - Susan Wallace - University...Lisette Giepmans
BioSHaRE conference July 28th, 2015, Milan - Latest tools and services for data sharing
Stream 2: ELSI approaches and services
An ethico-legal analysis was conducted at ULEIC that examined each step of the DataSHIELD process from the perspective of UK case law, regulations, and guidance. In order to facilitate a similar analysis for other countries/ jurisdictions, a ‘DataSHIELD Legal Analysis Template’ is being made. Contact: sew40@leicester.ac.uk
DataSHIELD was born of the requirement in the biomedical and social sciences to co-analyse individual patient data (micro data) from different sources, without disclosing identity or sensitive information. Under DataSHIELD, raw data never leave the data provider and no micro data or disclosive information can be seen by the researcher. The analysis is taken to the data – not the data to the analysis. It provides a flexible, modular, open-source solution ideally placed to serve a broad user and development community and to circumvent barriers related to ethical-legal restrictions, intellectual property and physical size of the data as a limiting factor.
Data sharing promotes many goals of the NIH research endeavor. It is particularly important for unique data that cannot be readily replicated. Data sharing allows scientists to expedite the translation of research results into knowledge, products, and procedures to improve human health. Do you know what a data sharing plan should include? Are you aware of common practices and standards for data sharing? Do you know what services are available to help share your data responsibly? This workshop will begin to address these questions. Q&A will follow the presentation. Anyone interested in or planning to apply for NIH funding should attend. Note: The NIH data-sharing policy applies to applicants seeking $500,000 or more in direct costs in any year of the proposed research.
David Van Enckevort - FAIR sample and data access DataSciSIG
David van Enckevort from the University of Groningen describes FAIR Sample and Data Access in Biobanking and Biorepositories.
This talk was sponsored by the NIH Data Science Special Interest Group and part of a webinar panel on June 23, 2017 on Global Biobanking and Access to Specimens.
This presentation was provided by Helen Henderson of Ringgold, during the NISO at NASIG Pre-conference "Metadata in a Digital Age: New Models of Creation, Discovery, and Use," held on June 4, 2008.
Stop press: should embargo conditions apply to metadata?Jisc RDM
Sarah Middle of Cambridge University discusses whether embargo conditions should apply to metadata. Session held at the Research Data Network event in May 2016, Cardiff University.
Research information management: making sense of it allDigital Science
"Research information management: making sense of it all" - Julia Hawks, VP North America, Symplectic
Slides from Shaking It Up: Challenges and Solutions in Scholarly Information Management, San Francisco, April 22, 2015
Practical applications for altmetrics in a changing metrics landscapeDigital Science
"Practical applications for altmetrics in a changing metrics landscape" - Sara Rouhi, Altmetric product specialist, and Anirvan Chatterjee, Director Data Strategy for CTSI at UCSF
FAIR Data - A is for Accessible
David Fitzgerald, Data Manager for the Australian Longitudinal Study of Women’s Health (ALSWH) presented on how ALSWH makes a nationally significant longitudinal study with highly sensitive data accessible for others to reuse.
Full webinar recording: https://youtu.be/me27whU8GG8
RDAP 16 Poster: Measuring adoption of Electronic Lab Notebooks and their impa...ASIS&T
Research Data Access and Preservation Summit, 2016
Atlanta, GA
May 4-7, 2016
Poster session (Wednesday, May 4)
Presenters:
Jan Cheetham, University of Wisconsin-Madison
Wendy Kozlowski, Cornell University
CINECA webinar slides: Making cohort data FAIRCINECAProject
Cohort studies, which recruit groups of individuals who share common characteristics and follow them over a period of time, are a robust and essential method in biomedical research for understanding the links between risk factors and diseases. Through questionnaires, medical assessments, and other interactions, voluminous and complex data are collected about the study participants. While cohort studies present a treasure trove of data, the data is often not FAIR (findable, accessible, interoperable and reusable). First, due to the sensitive and private nature of medical information, cohort data are often access controlled. Due to the lack of information about the studies (metadata), often one needs to dig deep to know what data is available in a cohort study. Therefore, many cohort datasets suffer from the findable and accessible issues. Second, often data collection is performed with instruments and data specifications tailored to the study. As a result, combining data across cohorts, even ones with similar characteristics, is difficult, making interoperability and reusability a challenge. In this presentation, we will explore several informatics techniques, such as the use of ontology, to make cohort data more FAIR. We will also consider the implications of making cohort data more open and the ethical and governance issues associated with open science benefit sharing.
This webinar is part of the “How FAIR are you” webinar series and hackathon, which aim at increasing and facilitating the uptake of FAIR approaches into software, training materials and cohort data, to facilitate responsible and ethical data and resource sharing and implementation of federated applications for data analysis.
The CINECA webinar series aims to discuss ways to address common challenges and share best practices in the field of cohort data analysis, as well as distribute CINECA project results. All CINECA webinars include an audience Q&A session during which attendees can ask questions and make suggestions. Please note that all webinars are recorded and available for posterior viewing. CINECA webinars include an audience Q&A session during which attendees can ask questions and make suggestions.
This webinar took place on 17th February 2021 and is part of the CINECA webinar series.
For previous and upcoming CINECA webinars see:
https://www.cineca-project.eu/webinars
This presentation was provided by Melissa Levine of the University of Michigan during a NISO Virtual Conference on the topic of data curation, held on Wednesday, August 31, 2016
Managing provenance in the Social Sciences: the Data Documentation Initiative...ARDC
Slides from webinar: Provenance and social science data. Presented on 15 March 2017. Presenter was Dr Steve McEachern, Director Australian Data Archive
FULL webinar recording: https://youtu.be/elPcKqWoOPg
1. Dr Steve McEachern (Director, Aust Data Archive) Data Documentation Initiative (DDI: http://www.ddialliance.org/): A free, international standard for describing data produced by surveys and other observational methods in the social, behavioral, economic, and health sciences. It can document and manage different stages in the research data lifecycle, eg conceptualization, collection, processing, distribution, discovery, and archiving. Documenting data with DDI facilitates understanding, interpretation, and use -- by people, software systems, and computer networks.
Steven McEachern - ADA, DDI (metadata standard) and the Data LifecycleSteve Androulakis
Dr. McEachern is Director of the Australian Data Archive at the Australian National University, and has research interests in data management and archiving, community and social attitude surveys, new data collection methods, and reproducible research methods.
This talk was given for the Monthly Tech Talks event hosted by Australian data infrastructure groups ANDS, NeCTAR, RDS and others.
An introduction to the FAIR principles and a discussion of key issues that must be addressed to ensure data is findable, accessible, interoperable and re-usable. The session explored the role of the CDISC and DDI standards for addressing these issues.
Presented by Gareth Knight at the ADMIT Network conference, organised by the Association for Data Management in the Tropics, in Antwerp, Belgium on December 1st 2015.
Agencies such as the NSF and NIH require data management plans as part of research proposals and the Office of Science and Technology Policy (OSTP) is requiring federal agencies to develop plans to increase public access to results of federally funded scientific research. These slides explore sustainable data sharing models, including models for sharing restricted-use data. Demos of these models and tips for accessing public data access services are provided as well as resources for creating data management plans for grant applications.
Data Management Lab: Session 4 Slides (more details at http://ulib.iupui.edu/digitalscholarship/dataservices/datamgmtlab)
What you will learn:
1. Build awareness of research data management issues associated with digital data.
2. Introduce methods to address common data management issues and facilitate data integrity.
3. Introduce institutional resources supporting effective data management methods.
4. Build proficiency in applying these methods.
5. Build strategic skills that enable attendees to solve new data management problems.
Presentation by Prof Chris Rowe, ADNet, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Dr Merran Smith, PHRN, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Dr Davina Ghersi, NHMRC, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Dr Adrian Burton, ARDC, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
FAIR for the future: embracing all things dataARDC
FAIR for the future: embracing all things data - Natasha Simons, Keith Russell and Liz Stokes, presented at Taylor & Francis Scholarly Summits in Sydney 11 Feb 2019 and Melbourne 14 Feb 2019.
How to make your data count webinar, 26 Nov 2018ARDC
Slides from the 26 Nov Make your data count webinar. The research community has long grappled with the problem of assessing and tracking the results of scholarship. Research data is no exception. The Make Data Count (MDC) project (https://makedatacount.org/), funded by the Sloan Foundation, has delivered a data usage metric standard (Code of Practice) and a workflow for the retrieval and display of standardised usage and citation metrics in your repository interface.
Listen to this webinar to learn more about the Make Data Count project and the 5 steps you can take to make the data in your repository count. Hear from MDC project team members who have already implemented MDC in the dash (https://dash.ucop.edu) and DataOne (https://search.dataone.org/data) repositories. Learn from their experience, see the results.
Our international speaker line-up includes Daniella Lowenberg (California Digital Library) and Patricia Cruse (DataCite).
Recording available: https://youtu.be/Lkysz0Mc7fo
A Strategic Approach: GenAI in EducationPeter Windle
Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
Operation “Blue Star” is the only event in the history of Independent India where the state went into war with its own people. Even after about 40 years it is not clear if it was culmination of states anger over people of the region, a political game of power or start of dictatorial chapter in the democratic setup.
The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
Biological screening of herbal drugs: Introduction and Need for
Phyto-Pharmacological Screening, New Strategies for evaluating
Natural Products, In vitro evaluation techniques for Antioxidants, Antimicrobial and Anticancer drugs. In vivo evaluation techniques
for Anti-inflammatory, Antiulcer, Anticancer, Wound healing, Antidiabetic, Hepatoprotective, Cardio protective, Diuretics and
Antifertility, Toxicity studies as per OECD guidelines
Model Attribute Check Company Auto PropertyCeline George
In Odoo, the multi-company feature allows you to manage multiple companies within a single Odoo database instance. Each company can have its own configurations while still sharing common resources such as products, customers, and suppliers.
Macroeconomics- Movie Location
This will be used as part of your Personal Professional Portfolio once graded.
Objective:
Prepare a presentation or a paper using research, basic comparative analysis, data organization and application of economic information. You will make an informed assessment of an economic climate outside of the United States to accomplish an entertainment industry objective.
Normal Labour/ Stages of Labour/ Mechanism of LabourWasim Ak
Normal labor is also termed spontaneous labor, defined as the natural physiological process through which the fetus, placenta, and membranes are expelled from the uterus through the birth canal at term (37 to 42 weeks
Francesca Gottschalk - How can education support child empowerment.pptxEduSkills OECD
Francesca Gottschalk from the OECD’s Centre for Educational Research and Innovation presents at the Ask an Expert Webinar: How can education support child empowerment?
4. ADA in Brief
• The ADA was set up in 1981, with a mission to collect
and preserve Australian research data on behalf of the
social science research community
• The Archive holds over data from over 1500 datasets,
including national election studies; public opinion polls;
social attitudes surveys, major longitudinal studies,
censuses, aggregate statistics, administrative data and
selected international collections
• Covers social sciences, population health, business
and economics and humanities
• Data holdings are sourced from academic, government
and private sectors
5. ADA Dataverse
http://dataverse.ada.edu.au
• Redevelopment of our database and website infrastructure (completed
late 2018)
– New website
– New data catalogue (including DOIs for datasets)
– Open data access
– API access (both for deposit and access, e.g. through R)
• New functionality (in development):
– Self-deposit of data
– Behavioural trials registry
– ORCID and Shibboleth authentication
– Secure data facility
– Qualitative data archive
7. Metadata and catalogue pages
Study information is based on the DDI-C (Data Documentation Initiative)
standard, and includes:
• Files
– Data files
– Related Materials: additional documentation (reports, questionnaires, technical
information), links and other related studies (eg. others in the series) that may
interest you
– Request forms
• Metadata
– Study: information including the investigators, abstract, sample, data collection
methods, and access requirements.
– Variables: a list of variables available in a quantitative dataset
• Terms
– Terms and conditions of use
– Restrictions
– …
• Versions
– Version control
15. Business rules
• ADA approves “standard” requests, subject to
business rules (based on the contents of the user
request)
• ADA refers “non-standard” requests (e.g. from
commercial organisations) to owner for review
• ADA or owner reviews and approves/rejects non-
standard requests
• Approvals are managed in Dataverse
• Communications between users, ADA and owners
regarding requests is managed via email, and
logged in the ADA ticketing system
15