Diagnostic Kits/Commons based cases in Kits: Difference between revisions
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**three categories: | **three categories: | ||
***Genetic Inherited Disease & Pharmacogenetics | ***Genetic Inherited Disease & Pharmacogenetics | ||
****"information about cell lines, DNA, and other samples that can be used as reference materials for various inherited diseases (including cystic fibrosis, fragile X, Huntington disease, and Ashkenazi Jewish-related diseases), pharmacogenetic loci, and biochemical genetics." ([http://wwwn.cdc.gov/dls/genetics/rmmaterials/default.aspx GeT-RM]) | |||
***Molecular Oncology | |||
****"information about commercially available cell lines, DNA, and other kinds of materials that could be used as reference materials for various types of cancers, including leukemia/lymphoma and solid tumors." ([http://wwwn.cdc.gov/dls/genetics/rmmaterials/default.aspx GeT-RM]) | ****"information about commercially available cell lines, DNA, and other kinds of materials that could be used as reference materials for various types of cancers, including leukemia/lymphoma and solid tumors." ([http://wwwn.cdc.gov/dls/genetics/rmmaterials/default.aspx GeT-RM]) | ||
***Infectious Disease | ***Infectious Disease | ||
****"information about commercially available cell lines, DNA, and other kinds of materials that could be used as reference materials for various infectious disease pathogens including viruses, bacteria, and protozoa." ([http://wwwn.cdc.gov/dls/genetics/rmmaterials/default.aspx GeT-RM]) | ****"information about commercially available cell lines, DNA, and other kinds of materials that could be used as reference materials for various infectious disease pathogens including viruses, bacteria, and protozoa." ([http://wwwn.cdc.gov/dls/genetics/rmmaterials/default.aspx GeT-RM]) | ||
*[http://www.biomarkersconsortium.org/ Biomarkers Consortium] | *[http://www.biomarkersconsortium.org/ Biomarkers Consortium] |
Revision as of 13:56, 6 November 2009
Answer the questions:
- Commons based cases (the cases that we know will appear in the right part of the quadrants)
- Identify cases
- Correlate them with their main outputs (Data. Narratives. Tools)
- How and in what extent they are “experimenting” or “adopting” commons-based approach. Are they adopting OA policies, for instance? Are they adopting Social Responsible License approaches?
- Identify these cases and treat them as entities that will also be placed in our mapping device (the quadrants)
- Identify what actors are participating on this and what actors are just observers (Use the questionnaire to guide your research when appropriate - Carol will select specific relevant and helpful questions)
Specific Examples
- Genetic Testing Reference Materials Coordination Program (GeT-RM) (associated with the CDC)
- the project provides reference materials for molecular genetic testing
- three categories:
- Genetic Inherited Disease & Pharmacogenetics
- "information about cell lines, DNA, and other samples that can be used as reference materials for various inherited diseases (including cystic fibrosis, fragile X, Huntington disease, and Ashkenazi Jewish-related diseases), pharmacogenetic loci, and biochemical genetics." (GeT-RM)
- Molecular Oncology
- "information about commercially available cell lines, DNA, and other kinds of materials that could be used as reference materials for various types of cancers, including leukemia/lymphoma and solid tumors." (GeT-RM)
- Infectious Disease
- "information about commercially available cell lines, DNA, and other kinds of materials that could be used as reference materials for various infectious disease pathogens including viruses, bacteria, and protozoa." (GeT-RM)
- Genetic Inherited Disease & Pharmacogenetics
- Biomarkers Consortium
- members include many major pharmaceutical firms
- participants are entitled to nonexclusive license to all intellectual property created from that project
- Launched by:
- The Foundation for the National Institutes of Health (FNIH)
- The National Institutes of Health (NIH)
- The Food and Drug Administration (FDA)
- The Pharmaceutical Research and Manufacturers of America (PhRMA)
- About the Biomarkers Consortium
- General Intellectual Property and Data Sharing Principles (pdf)
- Old Data: participants pre-existing Data and Intellectual Property remains with participants
- New Data: New Data and Consortium Inventions
- participants have a right to protect the inventions but must grant to all other participants (this includes inventions made under a Federal governmental grant or contract) subject to the Bayh-Dole Act
- a non-exclusive, remuneration-free license
- a non-exclusive research license
- participants have a right to protect the inventions but must grant to all other participants (this includes inventions made under a Federal governmental grant or contract) subject to the Bayh-Dole Act
- Licensing is not limited to members
- Open Educational Resources for Cancer
- The OERC Mission Statement (bullet points are quotes from the website)
- To create an open resource repository of cancer educational materials covering diverse aspects of oncology.
- To promote global sharing of cancer educational resources (WHO 2007 Cancer Report).
- To utilize knowledge sharing to assist countries develop cancer control strategies.
- To provide educational resources to enhance the capacities of physicians, nurses and care givers in developing countries to diagnose and treat cancer patients.
- To provide free access to advances in basic and clinical cancer research information in user friendly format.
- To contribute to the development of a research infrastructure and a research ethos for cancer care and prevention at a global level.
- The OERC Mission Statement (bullet points are quotes from the website)
- [Biological Material Transfer Agreement]
- used to facilitate the easy exchange of research tools
General Examples
- The Biological Innovation for Open Society (BIOS) license
- This specifically aims to provide open access to patented DNA sequences.
- Resources:
- Wired Magazine Open-Source Biology Evolves
- Geertrui Van Overwalle et al., 2005. Models for facilitating access to patents on genetic inventions. Available at: http://www.nature.com/nrg/journal/v7/n2/full/nrg1765.html [Accessed August 10, 2009].
- BiOS site
- Article describing the commons created by BiOS: Synthetic Biology: Caught between Property Rights, the Public Domain, and the Commons
- MIT Registry of Standard Biological Parts
- "A collection of ~3200 genetic parts that can be mixed and matched to build synthetic biology devices and systems. Founded in 2003 at MIT, the Registry is part of the Synthetic Biology community's efforts to make biology easier to engineer."
- The proposed BioBricks Foundation (BBF) license for BioBrick-standard biological "parts"
- More information here: http://openwetware.org/wiki/The_BioBricks_Foundation:Legal
- Drew Endy from the BBF has been increasingly focused on developing the license, organizing legal workshops and spending more time talking about it in lectures, but I couldn't find much online describing progress the BBF has made recently (they have been spending significant time working on it for at least the last 12 months).
- We could touch base with the BBF to find out of there are any publications in preparation or an expert who could provide more information in an interview by subscribing to and emailing legal@biobricks.org. If that doesn't work, contacting someone from the recent BBF + Berkeley Law Samuelson Clinic would probably be effective.
- Example set of parts: http://partsregistry.org
- Janet Hope covers the BBF & CAMBIA in her book, Biobazaar, on pages 316-317: here's a scan (and here's a google book search)
- http://bbf.openwetware.org/
- MIT Registry of Standard Biological Parts
- DNA Patent Database
- http://dnapatents.georgetown.edu/
- Updated weekly, the DPD contains over 51,000 DNA-based patents issued from 1971 to the present and over 73,000 patent applications published from 2001 to the present.
- The science commons in health research: structure, function, and value
- http://www.springerlink.com/content/782310p623282449/
- "early algorithms for interpreting DNA sequenceâsuch as the BLAST and Smith-Waterman algorithmsâwere developed by individuals committed to open science."
- National Center for Biotechnology Information: GeneTests
- http://www.ncbi.nlm.nih.gov/sites/GeneTests/?db=GeneTests
- "A publicly funded medical genetics information resource developed for physicians, other healthcare providers, and researchers, available at no cost to all interested persons."
- The site offers:
- peer-reviewed disease descriptions
- An international directory of genetic testing laboratories
- An international directory of genetics and prenatal diagnosis clinics
- A compilation of educational materials