Archive for the ‘Announcements’ Category
Since the last REMM update in August, 2016, the following important US government document have been incorporated into the resource. Additional information is available by visiting What’s New on REMM?
An update to Mobile REMM is also coming soon!
The National Library of Medicine has just released a new design for its main Web site search engine results page. The new design is responsive and is a result of usability testing, analytics, and user feedback. Searches for health topics will feature a MedlinePlus result on the right side of the screen. Search results from PubMed and the LocatorPlus catalog record will display separately, also on the right. Searches for an NLM product or service will highlight a curated result in the “NLM Recommended Resources” box. The facets have been combined into four basic categories and now can be found above the results display. They include:
- Health Information: MedlinePlus encyclopedia pages, drug monographs, health topic pages, supplement pages, and MedlinePlus Magazine pages.
- Programs and Services: NLM main Web site pages including NCBI and SIS.
- Exhibits and Collections: History of Medicine Division exhibition sites and the Digital Collections records.
- Web Archives: Older Web pages from the NLM main Web site.
Further details about the redesigned web site are available in the NLM Technical Bulletin.
The National Institutes of Health has just issued a Request for Information (RFI) seeking public comment on the data submission and access processes for the NIH National Center for Biotechnology (NCBI) database of Genotypes and Phenotypes (dbGaP). The RFI also seeks comment on the management of data in dbGaP in order to consider options to improve and streamline these processes and to maximize the use and utility of dbGaP. The complete RFI, as well as instructions on how to comment, are available on the NIH website. Electronic responses will be accepted through April 7, 2017. NIH will consider all public comments before taking next steps. No proprietary, classified, confidential, or sensitive information should be included in responses. Comments received, including any personal information, will be posted without change after the close of the comment period to the NIH Genomic Data Sharing website.
Additional information about the importance of this RFI is included in a new Under the Poliscope blog posting, published by Dr. Carrie D. Wolinetz. For more information or additional questions, please contact the NIH Office of Science Policy.
The National Library of Medicine Board of Regents welcomed three new members at its recent meeting:
- Jane Blumenthal, MSLS, the associate university librarian for health sciences and director of the Taubman Health Sciences Library at the University of Michigan, Ann Arbor. A past-president of the Medical Library Association, she has more than 30 years of experience in information and library services.
- Eric Horvitz, MD, PhD, managing director and technical fellow at Microsoft Research. His research focuses on principles of machine intelligence and leveraging the complementarities of human and machine reasoning.
- Gary Puckrein, PhD, executive director of the National Minority Quality Forum (NMQF), in Washington, DC. The NMQF strengthens efforts to use evidence-based, data-driven initiatives to eliminate premature death and preventable illness for racial and ethnic minorities and other special populations. Dr. Puckrein created and launched Minority Health Today, which served clinicians practicing in minority communities.
The National Library of Medicine seeks applications for novel informatics and data science approaches that can help individuals gather, manage and use data and information about their personal health. A goal of this program is to advance research and application by patients and the research community through broadly sharing the results via publication, and through open source mechanisms for data or resource sharing. To bring the benefits of big data research to consumers and patients, new biomedical informatics and data science approaches are needed, shaped to meet the needs of consumers and patients, whose health literacy, language skills, technical sophistication, education and cultural traditions affect how they find, understand and use personal health information. Data science approaches are needed to help individuals at every step, from harvesting to storing to using data and information in a personal health library.
Application deadlines are May 1, 2017, and March 19, 2018. Eligible applicants include higher education institutions, government entities, faith-based or community-based organizations, and other institutions. Applicants must base their proposed work on an informed profile of the intended users, and, the work should be developed through interaction with the user. The strongest projects will provide approaches that incorporate health data and information from more than one source, such as diagnostic images and links to full-text articles or genome sequence data linked to a family health history. An application should be centered on the problem area being addressed and the intended audience, propose a possible solution that employs novel data science or informatics, and undertake a pilot that will result in evidence of the degree of success and/or needed next steps. Applicants should expect to involve the intended users in their work. The number of awards will be contingent upon NIH appropriations and the submission of a sufficient number of meritorious applications. Up to $250,000 direct costs may be requested in any single year. The total project period may not exceed four years.
A major milestone was recently reached as MedlinePlus.gov launched its 1,000th health topic page about “Eye Care.” Created and maintained by the National Library of Medicine, MedlinePlus is the National Institutes of Health’s website providing trusted health information to the public. The winner of multiple awards and a consistent top scorer among federal websites, MedlinePlus debuted in 1998 with 22 health topic pages, which bring together information on a particular disease, condition, or wellness issue. Each health topic page provides a description of the condition or issue and directs users to vetted information from the NIH and other trusted sources. All content on MedlinePlus is reviewed and must meet strict quality guidelines.
MedlinePlus has steadily added new topics to respond to the growing needs of the public for reliable, up-to-date health information. The demand for additional health topics grew with the 2010 launch of MedlinePlus Connect, a service that links Electronic Health Records and other Health IT systems to targeted information from MedlinePlus. Today, over a million people visit MedlinePlus daily and benefit from the health topic pages, a medical encyclopedia, health news, surgery videos, a medical dictionary and much more. A Spanish language version of the site, MedlinePlus en español, premiered in 2002.
The Medical Library Association Guide to Data Management for Librarians, edited by Lisa Federer, provides a background from theoretical foundations to practical applications for librarians who are new to data management, as well as new ideas and approaches for experienced data librarians. It highlights the many ways that librarians are addressing researchers’ changing needs at a variety of institutions, including academic, hospital, and government libraries. Each chapter ends with “pearls of wisdom,” a bulleted list of 5-10 takeaway messages from the chapter that will help readers quickly put the ideas from the chapter into practice. This new publication supports librarians with exciting new opportunities to use their expertise and skills in the development of services and programs to help researchers meet the demands of the data-driven research enterprise!
The National Institutes of Health has announced a new funding opportunity for organizations interested in helping engage volunteers in the All of Us Research Program, part of the Precision Medicine Initiative. This opportunity is open to national and regional organizations, as well as local community groups, and will support activities to promote enrollment and retention in the All of Us Research Program across diverse communities. All of Us is an ambitious effort to gather data over time from 1 million or more people living in the United States, with the ultimate goal of accelerating research and improving health. Unlike research studies that are focused on a specific disease or population, All of Us will serve as a national research resource to inform thousands of studies, covering a wide variety of health conditions. Researchers will use data from the program to learn more about how individual differences in lifestyle, environment and biological make-up can influence health and disease. By taking part, people will be able to learn more about their own health and contribute to an effort that will advance the health of generations to come. NIH plans to launch the program later this year.
Pending available funds, NIH is designating up to $5 million per year over the next three years to support these community-led outreach efforts, to complement the program’s existing research and engagement infrastructure. Eligible organizations include nonprofits, other community- and faith-based organizations, minority-serving institutions and local governments, among others. Applicants must submit their proposed strategy for helping educate community members or health care providers about All of Us, whether through special events, trainings, communication programs or other activities. Applicants must also include a funding proposal tied to specific outreach goals. In addition to conducting their engagement activities, awardees will provide input on program plans and share feedback about community needs. Applications are due on March 24, 2017, and NIH plans to issue awards in May 2017.
Love Your Data week is an online event coming up on February 13-17, 2017! This year’s theme is emphasizing data quality for researchers at any stage in their career. Follow the activities on Twitter to gain inspiration, share ideas, and find new ways to promote data services and resources at your library and beyond! More details will be available soon!
The NN/LM South Central Region is sponsoring the webinar series, Pieces of Systematic Review, featuring guest speaker Margaret Foster, on the first Thursday of every month from Febuary – July at 8:00-9:00am PT. The first session will be held Thursday, February 2. Systematic reviews are well-documented as contributing to evidence-based healthcare by, in part, revealing gaps in the literature or illustrating the effectiveness of health interventions. They are common practice, but they can often be fraught with issues in how they’re conducted, leaving a constant need for education and discussion. Margaret Foster is an Associate Professor at Texas A&M University and serves as the Systematic Reviews Coordinator at the Medical Sciences Library with a joint position at the School of Public Health and the College of Medicine of the Texas A&M University Health Sciences Center. The series will highlight the following topics:
- February 2, 2017 – How do you determine if a research question is right for a systematic review?
- March 2, 2017 – What searches beyond the typical databases should be done?
- April 6, 2017 – What happens after the search?
- May 4, 2017 – What free software is useful for conducting review?
- June 1, 2017 – How can a librarian support other types of reviews (scoping, integrative, rapid)?
- July 6, 2017 – What are the new developments in review methods?