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What's a guide? And how can Yale library guides help me?

January 11, 2016 - 3:12pm by Andy Hickner

Librarians at Yale have developed numerous online guides for Yale users.  Here at Yale, our guides can provide a number of things, including: Research guidance for a particular Yale course; Instructions on how to research a subject; Documentation for a research tool or service; or Instructions on accessing and using collections or resources. You might find different guides of particular interest based on your role and field, for example: NIH Public Access Policy, for researchers who receive NIH funding and the staff who support them. Get started exploring our full list of guides in the field of medicine, or browse all Yale guides including on topics outside the health sciences. 

DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources (DECIPHER)

January 6, 2016 - 1:41pm by Rolando Garcia-Milian

Many genetic variants are novel or rare which makes difficult their clinical interpretation. The DECIPHER Consortium was initiated in 2004 as a community of academic centers of Clinical Genetics who submit consented, anonymized  genotype  and  phenotype  data  from  patients  with  rare  genomic  disorders for sharing with other clinicians and researchers. The identification of patients sharing variants in a given locus with common phenotypic features leads to greater certainty in the clinical interpretation of these variants. As of January 6, 2015, there are 18 539 publicly available patient record, 51 496 phenotype observation in these patients, and 27 175 publicly available copy-number variants in this database. DECIPHER can be search by phenotype, by genomic position, band, gene, pathogenicity, variant consequence, etc. Results are presented as a table or can be visualized in a browser. This browser contains different tracks where variants can be visualized in the context of other data. Learn more on DECIPHER and how to use it to make sense of genetic variants at the workshop “Making Sense of Variation”.  You can also contact Rolando Garcia-Milian with questions on this or any other variation tool, References DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources. Firth, H.V. et al (2009). Am.J.Hum.Genet 84, 524-533 (DOI: dx.doi.org/10/1016/j.ajhg.2009.03.010)

YSM theses now available through EliScholar

December 15, 2015 - 11:37am by Andy Hickner

(by Nathan Rupp and Melissa Grafe) Nearly 900 Yale School of Medicine theses are now available through Yale University’s online institutional repository known as EliScholar. These include “current” theses published in the last decade that have come out of embargo as well as several YSM alumni theses published as far back as 1952. These theses document the rich research done by Yale’s medical students, and can provide a starting point for current medical students embarking on their projects.  We’re also pleased to make this part of our collection more openly accessible to researchers in general, as the print theses are stored in locked stacks at the Medical Library.  Current YSM students can browse this collection for examples of what a YSM thesis looks like. For more information about accessing theses at the Medical Library, please see https://library.medicine.yale.edu/collections/thesis.

Great American Smokeout: Key Info Resources

November 18, 2015 - 12:27pm by Andy Hickner

Thursday, November 19 is the American Cancer Society's annual "Great American Smokeout," encouraging smokers to quit, even if it's only for one day.  What better time than to round up a few key information resources on tobacco cessation? Smokers may find the American Cancer Society's website helpful, in particular its "Stay Away from Tobacco" section.  For help finding more evidence on tobacco and smoking cessation, you can always contact your department's librarian.   

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.
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