The HS/HSL will be closed Saturday 9/29 – Monday 9/1 in observance of the Labor Day holiday. Regular hours will resume Tuesday 9/2.
HS/HSL Closed Labor Day Weekend
NIH Issues Finalized Policy on Genomic Data Sharing
The National Institutes of Health has issued a final NIH Genomic Data Sharing (GDS) policy to promote data sharing as a way to speed the translation of data into knowledge, products and procedures that improve health while protecting the privacy of research participants. The final policy was posted in the Federal Register Aug. 26, 2014 and published in the NIH Guide for Grants and Contracts Aug. 27, 2014.
Click here for full details.
NLM Launches Emergency Access Initiative Granting Free Access to Books and Journals for Healthcare Professionals Fighting Ebola Outbreak
The National Library of Medicine (NLM) Emergency Access Initiative (EAI) has been activated to support healthcare professionals working on the Ebola public health emergency in West Africa.
The EAI is a collaborative partnership between NLM and participating publishers to provide free access to full-text from over 650 biomedical journals and over 4,000 reference books and online databases to healthcare professionals and libraries affected by disasters. It serves as a temporary collection replacement and/or supplement for libraries affected by disasters that need to continue to serve medical staff and affiliated users. It is also intended for medical personnel responding to the specified disaster. EAI is not an open access collection. It is only intended for those affected by the disaster or assisting the affected population. If you know of a library or organization involved in healthcare efforts in response to the Ebola outbreak, please let them know of this service. EAI was activated four times in the past, including following the earthquake and subsequent cholera epidemic in Haiti, flooding in Pakistan and the earthquake and tsunami in Japan.
ILLiad System Downtime
The ILLiad system for requesting articles and books will be unavailable from August 15, 4 p.m. to August 25 as we prepare for the new UMID login.
A-Z Journal List Back Up
We were temporarily experiencing problems accessing the A-Z journal list. The problems have been cleared up and the A-Z list is now working correctly.
A-Z List of Journals Down
We are currently experiencing problems with the A-Z journal list. Please access journals through the Library Catalog while we work to resolve the issue.
ILLiad System Downtime
The ILLiad system for requesting articles and books will be unavailable from August 15, 4 p.m. to August 25 as we prepare for the new UMID login.
New Ebola Virus Disease Subject Guide
Check out the HS/HSL’s new Ebola Virus Disease (EVD) subject guide for trustworthy information resources and the latest headlines from the CDC, WHO, New York Times and others.
Essential Science Indicators Cancellation
For the past year the MPower Virtual Research Library initiative has licensed Essential Science Indicators for researchers and students at UMB,UMCP, and the Universities at Shady Grove. Unfortunately, the MPower Virtual Research Library budget was reduced this year to the point where we can no longer support this resource. The last day of availability will be August 31, 2014. Please send any comments or concerns to M.J. Tooey, Associate Vice President, Academic Affairs and Executive Director, HS/HSL at mjtooey@hshsl.umaryland.edu.
NCBI Webinar August 13th: Using the New NCBI Variation Viewer to Explore Human Genetic Variation
On August 13th, NCBI will host a webinar entitled “Using the New NCBI Variation Viewer to Explore Human Genetic Variation”. This presentation will show you how to find human sequence variants by chromosome position, gene, disease names and database identifiers (RefSNP, Variant region IDs) using NCBI’s new Variation Viewer (http://www.ncbi.nlm.nih.gov/variation/view).
This presentation will show you how to find human sequence variants by chromosome position, gene, disease names, and database identifiers(RefSNP, Variant region ids) using NCBI’s new Variation Viewer (http://www.ncbi.nlm.nih.gov/variation/view). You will learn how to browse the genome, navigate by gene or exon, filter results by one or more categories including allele frequencies from 1000 Genomes or GO-ESP, and link to related information in NCBI’s molecular databases and medical genetics resources such as ClinVar, MedGen and GTR. You will also be shown how to upload your own data to add to the display, and download results. Anyone who works with clinical or research variation data will find that the Variation Viewer provides a convenient and powerful way to access human variation data in a genomic context that is fully integrated with all other NCBI tools and databases.
To register, please go to: https://attendee.gotowebinar.com/register/2762824590748330498.