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The Bamberg Surgery: An early European surgical text

November 3, 2015 - 10:51am by Andy Hickner

Monica Green, a scholar of the history of medieval medicine, recently profiled the Bamberg Surgery, which is part of the Medical Historical Library's collection.  The Bamberg Surgery is a surgical text dating from the mid-12th century which was acquired by Dr. Harvey Cushing and subsequently formed part of the original Medical Historical collection at Yale.  Green writes: The Bamberg Surgery doesn’t get a lot of love in histories of surgery, because of its patchwork character. As Corner himself said, “it is a notebook, a partially organized collection of notes, memoranda, prescriptions, and excerpts from other books.” But the Bamberg Surgery merits a closer look to contemplate the question with which we began: how do you begin to build up a body of written surgical knowledge when previously you had none? The Bamberg Surgery draws selectively from the (now complete) translation of (Persian physician​‘Ali ibn al-‘Abbas) al-Majusi’s text, which it fuses with an early medieval text on phlebotomy that circulated under Hippocrates’ name. It then expands on these elements with new pharmaceuticals, new techniques, and elements of anatomical and physiological learning drawn from other texts. For example, al-Majusi’s text had never mentioned marciaton, a compound medicine for a wax-based unguent passed on through the early medieval Latin pharmaceutical tradition. The Chirurgia salernitana had recommended its use, and we find it in the Bamberg Surgery likewise, being recommended for nerve damage from a wound, broken bones, and dislocations. Similarly, the author cites Galen’s Tegni several times, a translation of the foundational handbook of medicine composed by the 2nd-century Greek polymath, used widely in the Islamic world and, increasingly, in Europe as a basic introduction to medical theory and practice.    

The Yale MeSH Analyzer

November 2, 2015 - 1:28pm by Holly Grossetta Nardini

The Yale MeSH Analyzer Two of our librarians, Lei Wang and Holly Grossetta Nardini, have developed a web-based tool to simplify search design and refinement for major, comprehensive database searches. This tool was released at NAHSL’15 in Providence this past October and is primarily for those involved in comprehensive database searching and systematic review research teams. At Yale, based on work by Jan Glover, we have a "best practice" for major searches: creating a MeSH analysis grid. A MeSH analysis grid helps us identify problems in a search strategy by showing how key articles are indexed in the MEDLINE database in an easy-to-scan tabular format. Creating a MeSH analysis grid manually is useful for search validation but time-consuming. The Yale MeSH Analyzer removes the tediousness from the process by automatically retrieving the article metadata and formatting and generating a grid. Using the tool is easy: simply paste a list of up to 20 PMIDs into the text box and click "Go.” You can delimit the PMIDs in any way you like, even pasting in a paragraph that includes text. The Analyzer will scan for PMIDs and attempt to retrieve article data from PubMed, creating a grid in either HTML or Excel for you to manipulate. There are other customizable options, and you can install a browser button on your toolbar to do an analysis in one step. You can then easily scan the grid and identify appropriate MesH terms, term variants, indexing consistency, and the reasons why some articles are retrieved and others are not, a common frustration for expert searchers. This inevitably leads to fresh iterations of the search strategy to include new terms. In addition to MeSH terms, author-assigned keywords, article titles, and abstracts can be included in the analysis display.  We hope that this tool helps you refine your searches and saves you time. We would love to hear your feedback.

Get your omics functional analysis done: upcoming trainings on Ingenuity Pathway Analysis and MetaCore

October 15, 2015 - 4:45pm by Rolando Garcia-Milian

The Yale Medical Library is providing to all Yale affiliates free access to two of the most powerful commercial bioinformatics tools for the analysis of omics data: MetaCore and Ingenuity Pathway Analysis. This is part of a pilot project conducted by the medical library in order to find sustainable and long term access to these tools. Please register for these upcoming trainings if you are interested in learning how to use these tools or if you need a refresher. For questions on how to register for an account or comments please contact Rolando Milian Title: Introduction to Ingenuity Pathway Analysis Description: What is IPA and what questions can it address? Overview of key features in IPA Ingenuity Knowledge Base Search & Pathway Building - Gene/ Chemical, Functions, Drug Targets Advanced Search: Limiting results to a molecule type, family or disease-association. Building pathways: Creating a pathway, pathway navigating, Using Build and Overlay tools Bioprofiler Dataset Analysis: Interpretation of Gene, Transcript, Protein and Metabolite Data Data Upload and Analysis:  Uploading and formatting a dataset, setting analysis parameters and running an analysis Pathway Analysis and Canonical Pathways Downstream Effects Analysis and identifying downstream functions and processes that are likely affected Upstream regulators Analysis Causal Network Analysis and identifying likely root regulators Regulator Effects Analysis to link upstream regulators with downstream functions and processes that are affected Comparison analysis and comparing multiple observations Date & Time:      9:00am - 12:00pm, Tuesday, October 27, 2015 Location:              H-203, Jane Ellen Hope Building, 315 Cedar St, New Haven CT Presenter:          Field Scientist QIAGEN Informatics   Title:      MetaCore: Getting the most from your "omics" analysis (Introductory session) Description: The ability to generate massive amounts of data with "omics" analysis begs the need for a tool to analyze and prioritize the biological relevance of this information. GeneGo provides a solution for using "omics" gene lists to generate and prioritize hypotheses with MetaCore. This tutorial highlights how to work with different types of data (genomics, proteomics, metabolomics and interaction data) beginning with how to upload gene lists and expression data (if available). Here we demonstrate data manager capabilities including how to upload, batch upload, store, share and check data properties and signal distribution. We then focus on how MetaCore uses your gene list to extract functional relevance by determining the most enriched processes across several ontologies. This entails a detailed lesson on how to prioritize your hypothesis using the statistically significance enrichment histograms and associate highly interactive GeneGo Maps and pre-built networks. We further emphasize the role of expression data in your analysis and the ability to visually predict experimental results, associated disease and possible drug targets. Lastly we highlight the benefits of using MetaCore workflows to compare data sets and work with experiment intersections. Date & Time:      10:00am - 12:00pm, Tuesday, November 3, 2015 Location:              C-103 - SHM 333 Cedar St, New Haven CT 06520 Presenter:          Dr. Matthew Wampole, Solution Scientist, IP & Science, Thomson Reuters   Title:      MetaCore: Getting the most from your "omics" analysis (Advanced) Description: In the advanced tutorial, we will explore uses of our network building algorithms and methods for hypothesizing key hubs passed on data. We will begin this session with a discussion on using the Key Pathway Advisor to hypothesize key hubs regulating gene expression data. The session will then review ways of using the 11 network building algorithms in MetaCore. The first example will review how to build a network purely from the curated knowledge within MetaCore. Then we will go through an example of using omics data to build a network of interactions to better understand the relationships within our data. Date & Time:      1:00pm - 3:00pm, Tuesday, November 3, 2015 Location:              C-103 - SHM 333 Cedar St, New Haven CT 06520 Presenter:          Dr. Matthew Wampole, Solution Scientist, IP & Science, Thomson Reuters     Join the End-user Bioinformatics Group and become a member of a community that collaborates on end-user bioinformatics events, training sessions, resources, and tools that support biomedical research at Yale.

October is National Medical Librarians Month!

October 5, 2015 - 2:19pm by Andy Hickner

(Written by John Gallagher, Interim Director) October is National Medical Librarians Month, a month to both celebrate and raise awareness of the important role of the health information professional. Indeed, medical librarians are an integral part of the healthcare team, and research demonstrates that librarian-led information services and resources improve clinical decision making and patient-care outcomes. Librarians also have a direct impact on the quality of research conducted, by helping users stay current about advances in their specialty areas. Librarians teach students and healthcare providers how to find and evaluate information.  The Cushing/Whitney Medical Library has a wonderful team of librarians and staff. While their individual responsibilities and topics of expertise can vary widely, all sincerely share the utmost commitment to helping you save time, and succeed in your patient-care, research, or educational goals.

NCBI's SmartBLAST

August 21, 2015 - 3:52pm by Rolando Garcia-Milian

The National Center for Biotechnology Information is developing a new type of BLAST called SmartBLAST. It process the user query in such a way that presents the three best matches from the non-redundant protein sequence database along with the two best protein matches from well-studied reference species. In addition, it provides results that match the query from the Conserved Domain Database (CDD) SmartBLAST accepts only one query at a time- either as FASTA sequence or protein accession number/GI- and uses a combination of BLAST and a multiple sequence alignment to produce its results. It first uses the query to search the non-redundant (nr) protein database. Then, it searches the reference database with BLASTP, followed by a multiple sequence alignment on the six sequences (the query and five subject sequences) using the COBALT multiple sequence alignment program. Screen capture showing the results of a SmartBLAST for TP53 (GI:187830777). Panel A shows the five matching sequences are represented as a phylogenetic tree and a graphical overview. The matches are color-coded: matches from the reference species are green, matches from the non-redundant protein database are blue, and your query is yellow. Panel B represents the results from the multiple alignments. Join the End-User Bioinformatics Network (EBNET) and become a member of a grass root community that collaborates on end-user bioinformatics events, training sessions, resources, and tools that support biomedical research at Yale.

New discount for Yale authors on article-processing charges

August 20, 2015 - 9:55am by Andy Hickner

Yale is now a “Supporter Member” of the open access publisher BioMed Central. Yale’s membership provides Yale authors with a 15% discount on article-processing charges of all articles accepted for publication in BioMed Central, Chemistry Central or SpringerOpen journals. Yale’s membership in BioMed Central was made possible through funding from Arcadia. BioMed Central publishes more than 100 online journals in biology and medicine. The articles in the journals are open access (no subscription or 'pay-per-view' charges), are indexed in PubMed, and are archived in PubMed Central. Yale’s institutional page on BioMed Central lists Yale authors’ articles and links to more information for authors.

Discovering the Beauty of Science: Call for Entries

April 17, 2015 - 9:51am by Rolando Garcia-Milian

Scientists may not consider themselves artists, however, there are times when science and research experiments lead to incredibly beautiful visual results. We invite Yale biomedical researchers (undergrads, graduate students, postdocs, faculty, associate researchers, etc.) at Yale to “Discover the Beauty of Science” by submitting up to two images per individual. Share with us the visual results of your work where science crosses over to art.  Your images will be reviewed by an interdisciplinary panel of artists, scientists and members of medical community and selected for an YSM exhibition. Contest Deadline Friday, July 31 (deadline extended!), 2015 – 11:59 pm Winners will be notified Monday- August 31st, 2015 Awards Awards will be given to 3 - 1st Honors and 1 - Viewer’s choice and consist of 1 TB USB 3.0 M3 Portable External Hard Drive The images will also be posted online and a print exhibition will be on display in the foyer outside the Medical School Library Fall 2015 Eligibility Yale affiliates including, students, postdocs, faculty, assistants, physicians, etc. working in scientific and biomedical research. Rules of Submission 1.    Individuals may submit up to 2 images. 2.    There is no contest fee. 3.    The submitter must have been involved in the generation of the images and must obtain permission for its use in this contest from any colleagues who also participated. Acknowledgement of collaborators can be credited in the written description. 4.    Images must be submitted electronically USING THIS FORM  5.    In awarding of prizes, images will be judged on esthetics, originality, and composition.   If you have questions or need help, contact Rolando Garcia Milian or Terry Dagradi. 

National Center for Biotechnology Information workshops broadcasted from the University of Michigan Medical Center

March 20, 2015 - 10:53am by Rolando Garcia-Milian

The Yale Medical Library will be hosting a National Center for Biotechnology Information workshop series (broadcasted from the University of Michigan Medical Center). Please register (next to each workshop title) since seating is limited Navigating NCBI Molecular Data through the Integrated Entrez System and BLAST (May 5, 9:00am - 11:30am EDT)  Gene Expression Resources at the NCBI (May 5, 1:00pm - 3:30pm EDT)  Human Genes, Variation, and Medical Genetics Resources (May 6, 9:00am - 11:30am EDT) NCBI Genomes, Assemblies and Annotation Products: Microbiome to Human (May 6, 1:00pm - 3:30pm EDT)  Each workshop consists of four 2.5-hour hands-on sessions emphasizing a different set of NCBI resources. Each session uses specific examples to highlight important features of the resources and tools under study and to demonstrate how to accomplish common tasks. Attendees will learn among others: The content of the sequence databases and uses these as exemplar Entrez molecular databases. The importance of derivative data such as NCBI Reference Sequences (RefSeqs) and sequence-related Entrez information hubs such as Taxonomy, HomoloGene and Gene. Aspects of the Entrez interface to collect and download a specific set of records, to narrow the search, and to use the pre-computed relationships available in the Entrez system to find related sequences, genomic regions, genomic maps, homologous genes and proteins, pathways and expression information. The practical aspects of working with NCBI BLAST, the most popular sequence similarity service in the world. How to use the features of the updated service including direct access from the Entrez sequence databases. The integrated databases to find phenotypes, literature, sequences (genome, mRNA and protein), and variations. How to map variations onto genes, transcripts, proteins, and genomic regions. Gain experience using additional tools and viewers associated with Entrez. These include the Graphical Sequence Viewer, the Variation Viewer, Gene View in dbSNP, and the 1000 Genomes Browser. NCBI's Entrez as a discovery system. Image courtesy of Dr. Peter Cooper, NCBI.

MLA awards 2015 Louise Darling Medal to Yale partner HINARI

March 17, 2015 - 8:37pm by Andy Hickner

Library staff and HINARI collaborators Nathan Rupp, Khadija El-Hazimy, and John Gallagher with the Louise Darling award. The Medical Library Association (MLA) has announced that it has awarded its Louise Darling Medal for Distinguished Achievement in Collection Development in the Health Sciences to the HINARI Access to Research in Health Programme for 2015. HINARI partners with publishers around the world to deliver scholarly health information and content (articles, books, and databases) to developing countries around the world who otherwise could not afford these resources. Under the guidance of Nathan Rupp, the library’s Head of Collection Development and Management, the Cushing/Whitney Medical Library plays and essential role in supporting HINARI by helping update publisher content in the HINARI database. HINARI is headquartered at the World Health Organization in Geneva and is part of the Research4Life (R4L) series of programmes which also includes AGORA (agriculture), ARDI (applied technology), and OARE (environment). Yale University Library is a Founding Partner in Research4Life, starting with the launch of HINARI in 2002. 

New Resources: Bates and Medlantis

January 9, 2015 - 4:10pm by Andy Hickner

The Medical Library has licensed 2 new resources that will be of interest to many users: Bates Visual Guide to Physical Examination features over eight hours of anatomy and system-specific videos, each of which shows a step-by-step examination. Students and faculty appreciate the careful attention to clinical accuracy, as well as the range of patient types profiled in the series. Medlantis provides hundreds of hours of video lectures, plus a wealth of content from Thieme eRadiology and Thieme RadCases: more than 43,000 ebook pages, almost 86,000 images, and over 2,200 case studies.  Users do not need to log in, just scroll down the page for direct access links. In order to access either tool, make sure you are on the Yale network.
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