Patricia L. Whetzel
Stanford University
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Featured researches published by Patricia L. Whetzel.
Nucleic Acids Research | 2009
Natalya Fridman Noy; Nigam H. Shah; Patricia L. Whetzel; Benjamin Dai; Michael Dorf; Nicholas Griffith; Clement Jonquet; Daniel L. Rubin; Margaret-Anne D. Storey; Christopher G. Chute; Mark A. Musen
Biomedical ontologies provide essential domain knowledge to drive data integration, information retrieval, data annotation, natural-language processing and decision support. BioPortal (http://bioportal.bioontology.org) is an open repository of biomedical ontologies that provides access via Web services and Web browsers to ontologies developed in OWL, RDF, OBO format and Protégé frames. BioPortal functionality includes the ability to browse, search and visualize ontologies. The Web interface also facilitates community-based participation in the evaluation and evolution of ontology content by providing features to add notes to ontology terms, mappings between terms and ontology reviews based on criteria such as usability, domain coverage, quality of content, and documentation and support. BioPortal also enables integrated search of biomedical data resources such as the Gene Expression Omnibus (GEO), ClinicalTrials.gov, and ArrayExpress, through the annotation and indexing of these resources with ontologies in BioPortal. Thus, BioPortal not only provides investigators, clinicians, and developers ‘one-stop shopping’ to programmatically access biomedical ontologies, but also provides support to integrate data from a variety of biomedical resources.
Nucleic Acids Research | 2011
Patricia L. Whetzel; Natalya Fridman Noy; Nigam H. Shah; Paul R. Alexander; Csongor Nyulas; Tania Tudorache; Mark A. Musen
The National Center for Biomedical Ontology (NCBO) is one of the National Centers for Biomedical Computing funded under the NIH Roadmap Initiative. Contributing to the national computing infrastructure, NCBO has developed BioPortal, a web portal that provides access to a library of biomedical ontologies and terminologies (http://bioportal.bioontology.org) via the NCBO Web services. BioPortal enables community participation in the evaluation and evolution of ontology content by providing features to add mappings between terms, to add comments linked to specific ontology terms and to provide ontology reviews. The NCBO Web services (http://www.bioontology.org/wiki/index.php/NCBO_REST_services) enable this functionality and provide a uniform mechanism to access ontologies from a variety of knowledge representation formats, such as Web Ontology Language (OWL) and Open Biological and Biomedical Ontologies (OBO) format. The Web services provide multi-layered access to the ontology content, from getting all terms in an ontology to retrieving metadata about a term. Users can easily incorporate the NCBO Web services into software applications to generate semantically aware applications and to facilitate structured data collection.
Nucleic Acids Research | 2003
Amit Bahl; Brian P. Brunk; Jonathan Crabtree; Martin Fraunholz; Bindu Gajria; Gregory R. Grant; Hagai Ginsburg; Dinesh Gupta; Jessica C. Kissinger; Philip Labo; Li Li; Matthew D. Mailman; Arthur J. Milgram; David Pearson; David S. Roos; Jonathan Schug; Christian J. Stoeckert; Patricia L. Whetzel
PlasmoDB (http://PlasmoDB.org) is the official database of the Plasmodium falciparum genome sequencing consortium. This resource incorporates the recently completed P. falciparum genome sequence and annotation, as well as draft sequence and annotation emerging from other Plasmodium sequencing projects. PlasmoDB currently houses information from five parasite species and provides tools for intra- and inter-species comparisons. Sequence information is integrated with other genomic-scale data emerging from the Plasmodium research community, including gene expression analysis from EST, SAGE and microarray projects and proteomics studies. The relational schema used to build PlasmoDB, GUS (Genomics Unified Schema) employs a highly structured format to accommodate the diverse data types generated by sequence and expression projects. A variety of tools allow researchers to formulate complex, biologically-based, queries of the database. A stand-alone version of the database is also available on CD-ROM (P. falciparum GenePlot), facilitating access to the data in situations where internet access is difficult (e.g. by malaria researchers working in the field). The goal of PlasmoDB is to facilitate utilization of the vast quantities of genomic-scale data produced by the global malaria research community. The software used to develop PlasmoDB has been used to create a second Apicomplexan parasite genome database, ToxoDB (http://ToxoDB.org).
Bioinformatics | 2006
Patricia L. Whetzel; Helen Parkinson; Helen C. Causton; Liju Fan; Jennifer Fostel; Gilberto Fragoso; Mervi Heiskanen; Norman Morrison; Philippe Rocca-Serra; Susanna-Assunta Sansone; Chris F. Taylor; Joseph White; Christian J. Stoeckert
MOTIVATION The generation of large amounts of microarray data and the need to share these data bring challenges for both data management and annotation and highlights the need for standards. MIAME specifies the minimum information needed to describe a microarray experiment and the Microarray Gene Expression Object Model (MAGE-OM) and resulting MAGE-ML provide a mechanism to standardize data representation for data exchange, however a common terminology for data annotation is needed to support these standards. RESULTS Here we describe the MGED Ontology (MO) developed by the Ontology Working Group of the Microarray Gene Expression Data (MGED) Society. The MO provides terms for annotating all aspects of a microarray experiment from the design of the experiment and array layout, through to the preparation of the biological sample and the protocols used to hybridize the RNA and analyze the data. The MO was developed to provide terms for annotating experiments in line with the MIAME guidelines, i.e. to provide the semantics to describe a microarray experiment according to the concepts specified in MIAME. The MO does not attempt to incorporate terms from existing ontologies, e.g. those that deal with anatomical parts or developmental stages terms, but provides a framework to reference terms in other ontologies and therefore facilitates the use of ontologies in microarray data annotation. AVAILABILITY The MGED Ontology version.1.2.0 is available as a file in both DAML and OWL formats at http://mged.sourceforge.net/ontologies/index.php. Release notes and annotation examples are provided. The MO is also provided via the NCICBs Enterprise Vocabulary System (http://nciterms.nci.nih.gov/NCIBrowser/Dictionary.do). CONTACT [email protected] SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.
BMC Bioinformatics | 2006
Tim F. Rayner; Philippe Rocca-Serra; Paul T. Spellman; Helen C. Causton; Anna Farne; Ele Holloway; Rafael A. Irizarry; Junmin Liu; Donald Maier; Michael R. Miller; Kjell Petersen; John Quackenbush; Gavin Sherlock; Christian J. Stoeckert; Joseph White; Patricia L. Whetzel; Farrell Wymore; Helen Parkinson; Ugis Sarkans; Catherine A. Ball; Alvis Brazma
BackgroundSharing of microarray data within the research community has been greatly facilitated by the development of the disclosure and communication standards MIAME and MAGE-ML by the MGED Society. However, the complexity of the MAGE-ML format has made its use impractical for laboratories lacking dedicated bioinformatics support.ResultsWe propose a simple tab-delimited, spreadsheet-based format, MAGE-TAB, which will become a part of the MAGE microarray data standard and can be used for annotating and communicating microarray data in a MIAME compliant fashion.ConclusionMAGE-TAB will enable laboratories without bioinformatics experience or support to manage, exchange and submit well-annotated microarray data in a standard format using a spreadsheet. The MAGE-TAB format is self-contained, and does not require an understanding of MAGE-ML or XML.
Journal of the American Medical Informatics Association | 2012
Mark A. Musen; Natalya Fridman Noy; Nigam H. Shah; Patricia L. Whetzel; Christopher G. Chute; Margaret Anne Story; Barry Smith
The National Center for Biomedical Ontology is now in its seventh year. The goals of this National Center for Biomedical Computing are to: create and maintain a repository of biomedical ontologies and terminologies; build tools and web services to enable the use of ontologies and terminologies in clinical and translational research; educate their trainees and the scientific community broadly about biomedical ontology and ontology-based technology and best practices; and collaborate with a variety of groups who develop and use ontologies and terminologies in biomedicine. The centerpiece of the National Center for Biomedical Ontology is a web-based resource known as BioPortal. BioPortal makes available for research in computationally useful forms more than 270 of the worlds biomedical ontologies and terminologies, and supports a wide range of web services that enable investigators to use the ontologies to annotate and retrieve data, to generate value sets and special-purpose lexicons, and to perform advanced analytics on a wide range of biomedical data.
Nature | 2002
Jessica C. Kissinger; Brian P. Brunk; Jonathan Crabtree; Martin Fraunholz; Bindu Gajria; Arthur J. Milgram; David Pearson; Jonathan Schug; Amit Bahl; Sharon J. Diskin; Hagai Ginsburg; Gregory R. Grant; Dinesh Gupta; Philip Labo; Li Li; Matthew D. Mailman; Shannon K. McWeeney; Patricia L. Whetzel; Christian J. Stoeckert; David S. Roos
Designing and mining a eukaryotic genomics resource.
Nature Biotechnology | 2007
Andrew R. Jones; Michael R. Miller; Ruedi Aebersold; Rolf Apweiler; Catherine A. Ball; Alvis Brazma; James DeGreef; Nigel Hardy; Henning Hermjakob; Simon J. Hubbard; Peter Hussey; Mark Igra; Helen Jenkins; Randall K. Julian; Kent Laursen; Stephen G. Oliver; Norman W. Paton; Susanna-Assunta Sansone; Ugis Sarkans; Christian J. Stoeckert; Chris F. Taylor; Patricia L. Whetzel; Joseph White; Paul T. Spellman; Angel Pizarro
The Functional Genomics Experiment data model (FuGE) has been developed to facilitate convergence of data standards for high-throughput, comprehensive analyses in biology. FuGE models the components of an experimental activity that are common across different technologies, including protocols, samples and data. FuGE provides a foundation for describing entire laboratory workflows and for the development of new data formats. The Microarray Gene Expression Data society and the Proteomics Standards Initiative have committed to using FuGE as the basis for defining their respective standards, and other standards groups, including the Metabolomics Standards Initiative, are evaluating FuGE in their development efforts. Adoption of FuGE by multiple standards bodies will enable uniform reporting of common parts of functional genomics workflows, simplify data-integration efforts and ease the burden on researchers seeking to fulfill multiple minimum reporting requirements. Such advances are important for transparent data management and mining in functional genomics and systems biology.
Journal of Biomedical Semantics | 2011
Joanne S. Luciano; Bosse Andersson; Colin R. Batchelor; Olivier Bodenreider; Timothy W.I. Clark; Christine Denney; Christopher Domarew; Thomas Gambet; Lee Harland; Anja Jentzsch; Vipul Kashyap; Peter Kos; Julia Kozlovsky; Timothy Lebo; Scott M Marshall; James P. McCusker; Deborah L. McGuinness; Chimezie Ogbuji; Elgar Pichler; Robert L Powers; Eric Prud’hommeaux; Matthias Samwald; Lynn M. Schriml; Peter J. Tonellato; Patricia L. Whetzel; Jun Zhao; Susie Stephens; Michel Dumontier
BackgroundTranslational medicine requires the integration of knowledge using heterogeneous data from health care to the life sciences. Here, we describe a collaborative effort to produce a prototype Translational Medicine Knowledge Base (TMKB) capable of answering questions relating to clinical practice and pharmaceutical drug discovery.ResultsWe developed the Translational Medicine Ontology (TMO) as a unifying ontology to integrate chemical, genomic and proteomic data with disease, treatment, and electronic health records. We demonstrate the use of Semantic Web technologies in the integration of patient and biomedical data, and reveal how such a knowledge base can aid physicians in providing tailored patient care and facilitate the recruitment of patients into active clinical trials. Thus, patients, physicians and researchers may explore the knowledge base to better understand therapeutic options, efficacy, and mechanisms of action.ConclusionsThis work takes an important step in using Semantic Web technologies to facilitate integration of relevant, distributed, external sources and progress towards a computational platform to support personalized medicine.AvailabilityTMO can be downloaded from http://code.google.com/p/translationalmedicineontology and TMKB can be accessed at http://tm.semanticscience.org/sparql.
Database | 2011
Pascale Gaudet; Amos Marc Bairoch; Dawn Field; Susanna-Assunta Sansone; Chris Taylor; Teresa K. Attwood; Alex Bateman; Judith A. Blake; J. Michael Cherry; Rex L. Chrisholm; Guy Cochrane; Charles E. Cook; Janan T. Eppig; Michael Y. Galperin; Robert Gentleman; Carole A. Goble; Takashi Gojobori; John M. Hancock; Douglas G. Howe; Tadashi Imanishi; Janet Kelso; David Landsman; Suzanna E. Lewis; Ilene Karsch Mizrachi; Sandra Orchard; B. F. Francis Ouellette; Shoba Ranganathan; Lorna Richardson; Philippe Rocca-Serra; Paul N. Schofield
The present article proposes the adoption of a community-defined, uniform, generic description of the core attributes of biological databases, BioDBCore. The goals of these attributes are to provide a general overview of the database landscape, to encourage consistency and interoperability between resources; and to promote the use of semantic and syntactic standards. BioDBCore will make it easier for users to evaluate the scope and relevance of available resources. This new resource will increase the collective impact of the information present in biological databases.