Biomedical Informatics Research Network
Encyclopedia
The Biomedical Informatics Research Network (BIRN) is a national initiative to assist biomedical research through data sharing and online collaboration. BIRN provides data-sharing infrastructure, software tools and techniques, and advisory services from a single source. The effort is funded by the National Center for Research Resources (NCRR), a component of the United States National Institutes of Health
(NIH).
BIRN is designed to serve the biomedical research community’s data-intensive sharing and analysis needs, which are particularly evident in fields such as biomedical imaging and genetics. All data transfer is designed to be consistent with Health Insurance Portability and Accountability Act of 1996 (HIPAA) privacy and security guidelines
BIRN's user-driven, software-based framework enables research teams to share significant quantities of data across geographic distance or incompatible computing systems. Participants may transfer data securely and privately. Groups may choose whether to share data with internal or external audiences.
BIRN also offers documented best practices, expert advice, and data-sharing, query and analysis software tools specific to biomedical research. Its researchers develop new data-sharing tools, authorization capability, and engineering tools to help biomedical researchers make sense of information in new ways.
BIRN is a collaborative effort between the NCRR and a nationwide leadership consortium: the Information Sciences Institute
(ISI) at the University of Southern California
, the University of Chicago
, Massachusetts General Hospital
, the University of California at Irvine, and the University of California at Los Angeles.
Its interdisciplinary team consists of computer scientists, engineers, physicians, biomedical researchers and other technical experts, including grid computing developers Carl Kesselman of USC ISI, and Ian Foster
of Argonne National Laboratories. Co-Principal Investigators are:
By using BIRN's capabilities both to access data and perform research, groups can can conduct large-scale data analysis while maximizing their existing technical infrastructure and expertise. Users also can participate in BIRN Working Groups, which develop and support operations, data-sharing requirements, security and other key functions.
BIRN offers a website, wiki and mailing lists to help users stay current on news, best practices and topics related directly to their data-sharing considerations. Its experts can help biomedical teams select software, data and metadata community standards; set up security mechanisms and sharing protocols; and create multi-institutional policies from a potentially overwhelming range of options.
BIRN's mission also has shifted from a repository of users' data to a means of supporting efficient data transfer.
As a result, BIRN no longer provides hardware, offers or maintain servers (previously called “racks”) for storing user information, or uses participants’ computers as network nodes.
The user-driven, software-based approach instead supports data sharing on participants’ existing hardware and software. Each user group retains control over, and responsibility for, its own hardware -- and for the security and privacy of its own information. Data is stored on users' systems rather than in a central repository, making possible storage of, and access to, vastly greater data quantities than was possible with BIRN “racks” alone.
Among the characteristics of groups likely to get the most out of BIRN: the need to exchange data between multiple sites on an ongoing basis, not just from one site to another or for a one-time-only project, and/or to make data from multiple sites publicly available.
On a social level, BIRN looks for groups that understand users’ data-sharing problems and can articulate how those issues affect them in day-to-day, real-world ways. Groups aren't expected to be technical wizards, but do need to be able to articulate specific data-sharing needs and problems.
BIRN contributes technical expertise, while users provide the knowledge specific to their fields. For instance, BIRN can advise on how to go about defining user needs and requirements, but only users can determine specifically what those factors should be. Because BIRN isn't a plug-and-play, off-the-shelf product, the network seeks prospective users who are committed to conceiving, designing, building and implementing the best solution for their circumstances.
To become members, groups begin by filling out a contact form on the BIRN website. A BIRN team member responds, and if its services appear to be a good match, s/he typically refers questioners to a BIRN member or WG for more in-depth conversations.
WGs typically discuss whether BIRN’s capabilities will address the group's data usage requirements, which BIRN tools and areas of expertise would fit best, and related issues. BIRN strongly encourages inquiries from biomedical research groups nationwide.
National Institutes of Health
The National Institutes of Health are an agency of the United States Department of Health and Human Services and are the primary agency of the United States government responsible for biomedical and health-related research. Its science and engineering counterpart is the National Science Foundation...
(NIH).
BIRN is designed to serve the biomedical research community’s data-intensive sharing and analysis needs, which are particularly evident in fields such as biomedical imaging and genetics. All data transfer is designed to be consistent with Health Insurance Portability and Accountability Act of 1996 (HIPAA) privacy and security guidelines
BIRN's user-driven, software-based framework enables research teams to share significant quantities of data across geographic distance or incompatible computing systems. Participants may transfer data securely and privately. Groups may choose whether to share data with internal or external audiences.
BIRN also offers documented best practices, expert advice, and data-sharing, query and analysis software tools specific to biomedical research. Its researchers develop new data-sharing tools, authorization capability, and engineering tools to help biomedical researchers make sense of information in new ways.
BIRN is a collaborative effort between the NCRR and a nationwide leadership consortium: the Information Sciences Institute
Information Sciences Institute
The Information Sciences Institute is a research and development unit of the University of Southern California's Viterbi School of Engineering which focuses on computer and communications technology and information processing...
(ISI) at the University of Southern California
University of Southern California
The University of Southern California is a private, not-for-profit, nonsectarian, research university located in Los Angeles, California, United States. USC was founded in 1880, making it California's oldest private research university...
, the University of Chicago
University of Chicago
The University of Chicago is a private research university in Chicago, Illinois, USA. It was founded by the American Baptist Education Society with a donation from oil magnate and philanthropist John D. Rockefeller and incorporated in 1890...
, Massachusetts General Hospital
Massachusetts General Hospital
Massachusetts General Hospital is a teaching hospital and biomedical research facility in the West End neighborhood of Boston, Massachusetts...
, the University of California at Irvine, and the University of California at Los Angeles.
Its interdisciplinary team consists of computer scientists, engineers, physicians, biomedical researchers and other technical experts, including grid computing developers Carl Kesselman of USC ISI, and Ian Foster
Ian Foster
Ian Foster is a Distinguished Fellow and the Associate Division Director in the Mathematics and Computer Science Division at Argonne National Laboratory, where he leads the Distributed Systems Laboratory, and he is a Professor in the Department of Computer Science at the University of Chicago...
of Argonne National Laboratories. Co-Principal Investigators are:
- Carl Kesselman, Ph.D., a professor in the University of Southern California (USC) Daniel J. Epstein Department of Industrial and Systems Engineering, and a Fellow of the Information Sciences Institute (ISI), its highest honor;
- Ian Foster, Ph.D., Director of the Computation Institute, a joint project between the University of Chicago and Argonne National Laboratory, and Associate Director of Argonne’s Mathematics and Computer Science Division;
- Steven G. Potkin, M.D., a professor in the Department of Psychiatry and Human Behavior at the University of California at Irvine (UCI) and Director of UCI’s Brain Imaging Center;
- Bruce R. Rosen, M.D., Ph.D., a professor of Radiology at Harvard Medical School and Health Sciences and Technology at the Harvard-MIT Division of Health Sciences and Technology, and Director of the Athinoula A. Martinos Center for Biomedical Imaging at the Massachusetts General Hospital in Boston, MA;
- Jonathan C. Silverstein, M.D., Associate Director and senior fellow at the University of Chicago-Argonne National Laboratory Computation Institute, and an associate professor of Surgery, Radiology and Biological Sciences at UC;
- Arthur Toga, Ph.D., a professor in the University of California at Los Angeles (UCLA) Department of Neurology, associate dean of the Geffen School of Medicine, and Director of the UCLA Laboratory of Neuro Imaging; and
- Liming Yang, Ph.D., a health scientist administrator for NCRR’s Biomedical Technology Division, where he manages a portfolio of grants on computational biology, software development and genetic studies.
Member tools
Users range from small research groups to large, national consortia such as the Nonhuman Primate Research Consortium (NHPRC) and the Cardiovascular Research Grid (CVRG), both funded by NIH.By using BIRN's capabilities both to access data and perform research, groups can can conduct large-scale data analysis while maximizing their existing technical infrastructure and expertise. Users also can participate in BIRN Working Groups, which develop and support operations, data-sharing requirements, security and other key functions.
BIRN offers a website, wiki and mailing lists to help users stay current on news, best practices and topics related directly to their data-sharing considerations. Its experts can help biomedical teams select software, data and metadata community standards; set up security mechanisms and sharing protocols; and create multi-institutional policies from a potentially overwhelming range of options.
History
BIRN began as an NCRR initiative built around several "testbeds," or select projects, in neurology research. In 2008, its mandate expanded significantly to include data-sharing support across the biomedical research community. The network is now open to all biomedical research groups that BIRN believes will benefit from its services, regardless of a group's specialty, mandate, size or U.S. location.BIRN's mission also has shifted from a repository of users' data to a means of supporting efficient data transfer.
As a result, BIRN no longer provides hardware, offers or maintain servers (previously called “racks”) for storing user information, or uses participants’ computers as network nodes.
The user-driven, software-based approach instead supports data sharing on participants’ existing hardware and software. Each user group retains control over, and responsibility for, its own hardware -- and for the security and privacy of its own information. Data is stored on users' systems rather than in a central repository, making possible storage of, and access to, vastly greater data quantities than was possible with BIRN “racks” alone.
Membership
BIRN seeks to aid university- and institute-based researchers with complex, distributed projects -- either technologically or geographically -- such as multi-site clinical trials. Working Groups (WGs) evaluate candidate projects based on their unique characteristics and use cases. There are no specific project criteria or required sizes, although WGs may consider factors such as research goals, potential impact, technical challenges, host institution and sponsor funding.Among the characteristics of groups likely to get the most out of BIRN: the need to exchange data between multiple sites on an ongoing basis, not just from one site to another or for a one-time-only project, and/or to make data from multiple sites publicly available.
On a social level, BIRN looks for groups that understand users’ data-sharing problems and can articulate how those issues affect them in day-to-day, real-world ways. Groups aren't expected to be technical wizards, but do need to be able to articulate specific data-sharing needs and problems.
BIRN contributes technical expertise, while users provide the knowledge specific to their fields. For instance, BIRN can advise on how to go about defining user needs and requirements, but only users can determine specifically what those factors should be. Because BIRN isn't a plug-and-play, off-the-shelf product, the network seeks prospective users who are committed to conceiving, designing, building and implementing the best solution for their circumstances.
To become members, groups begin by filling out a contact form on the BIRN website. A BIRN team member responds, and if its services appear to be a good match, s/he typically refers questioners to a BIRN member or WG for more in-depth conversations.
WGs typically discuss whether BIRN’s capabilities will address the group's data usage requirements, which BIRN tools and areas of expertise would fit best, and related issues. BIRN strongly encourages inquiries from biomedical research groups nationwide.