We support boolean queries, use +,-,<,>,~,* to alter the weighting of terms
A collection of small sequence processing utilities that are modeled after the Unix command line text processing utilities so every utility tries to perform a specific task and most of them take a sequence file as input and create a new processed sequence file as output. This design encourages the assembly of the seq_crumbs utilities with Unix pipes to create complex pipelines.
The COLT-Cancer database is a collection of shRNA dropout signatures profiles, covering ~16000 human genes, and derived from more than 70 Pancreatic, Ovarian and Breast human cancer cell-lines using the microarray detection platform developed in the COLT (CCBR-OICR Lentiviral Technology) facility at the Moffat Lab. All shRNA dropout profiles are freely available through download or queries via this website.
THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 23,2023. Software tool developed for ArrayTrack that takes a list of genes and identifies terms in Gene Ontology associated with those genes. GOFFA provides tools to view/access the following: GO term hierarchy, full listing of GO terms annotated with the genes associated with a given term, Fisher's exact test p-value providing the probability of identifying that many genes for a given term by chance alone, and relative enrichment factor (E-value) giving the enrichment of a GO term for genes in the submitted list relative to the frequency of genes assigned to that term from the full set of GOFFA annotated genes for a particular species.
A private, coeducational, liberal arts college with the distinction of being the only historically black Roman Catholic institution of higher education located in the Gert Town section of New Orleans, Louisiana, USA.
Pathpedia.com is web-based wiki on human anatomical, clinical, and experimental pathology created for pathologists. This collaborative portal includes news, education, jobs, meetings, forums and links. The Education tab includes access to journals, books, CME / SAM/ CMIL, WikiBooks, eAtlas, etc. The eAtlas module allows you post unusual and difficult pathology cases to be reviewed by other pathologists across the globe. This module may help in identifying previously unreported entities and unusual / variant examples of known entities. Categories include Histopathology, Gross pathology, Normal histology, Image quiz and Case sharing. Immunopedia - A clinically useful web-based database on the immunohistochemical and flow cytometric evaluation of neoplasms. 1. Large database 2. Regular updates 3. Quality citations 4. Exquisite modules *Data included for both neoplastic & non-neoplastic tissues/cells *Clones indicated wherever applicable along with their markers *References cited for each piece of data on markers or diseases *Option provided to merge data of discrete disease categories Online case sharing *Share unusual cases with pathology community *Help identify previously unreported entities *Get expert reviews and comments from your peers
One of the world''s largest digital research libraries that changed the ways that faculty, students, and researchers discover and access information using innovative technology to connect content and communities in ways that enhance teaching, learning, and research. In partnership with the UC libraries, the CDL has continually broken new ground by developing systems linking their users to the vast print and online collections within UC and beyond. Building on the foundations of the Melvyl Catalog, they developed one of the largest online library catalogs in the country. They saved the University millions of dollars by facilitating the co-investment and sharing of materials and services used by libraries across the UC system. They work in partnership with campuses to bring the treasures of their libraries, museums, and cultural heritage organizations to the world. And they continue to explore how services such as digital curation, scholarly publishing, archiving and preservation support research throughout the information lifecycle.
Software that finds and displays approximate tandem repeats in DNA sequences.
Wired Science Blogs is new network of all-star science bloggers.
CurePSP+ is an organization dedicated to increasing awareness of progressive supranuclear palsy, corticobasal degeneration, and related disorders, advancing research toward a cure, educating health professionals, and providing support, education and hope for persons with PSP, CBD and their families. PSP provides a number of resources, including a research grants/funding program, support for patients and families, educational materials, and PSP-related events. Patient and family support services include an online magazine, a resources guide, an educational center that provides The Guide for Persons with PSP, videos, support group meetings, and outreach and education brochures and conferences. In addition, CurePSP offers ART2CURE, a program of CurePSP (The Society for Progressive Supranuclear Palsy) that helps to generate essential revenue for research, advocacy, outreach, education and operating through the promotion and sale of artwork provided by various artists throughout the country. CurePSP is located in Hunt Valley, Maryland. :NIF thanks the :<A TARGET=_blank HREF=http://www.pdf.org> :<U>Parkinson''s Disease FoundationU> :A> :<A TARGET=_blank HREF=http://www.pdf.org> A> :for their referral of this resource to us.
The BATB is open to individuals who are involved or interested in Tissue Banking, research, clinical or donor-related activities. Corporate membership is available for organizations that supply technology/services to tissue banks (or have an interest in the use of human tissue for research, bio-engineering or other medical purposes). The Association is instituted for the advancement of tissue banking: * to contribute to the preparation and maintenance of professional standards for the practice of tissue banking in the United Kingdom * to facilitate the interchange of information between members * to provide opportunities for the discussion of all aspects of tissue banking practice * to encourage relevant research and development: to provide informed comment to external agencies * to foster education and training in tissue banking: to maintain national and international links with relevant bodies * to make knowledge in the field of tissue banking available to any person for the general good of the community
Scientific society whose members conduct basic and clinical pharmacological research in academia, industry and the government developing disease-fighting medicines and therapeutic agents. ASPET publishes five journals: Drug Metabolism and Disposition, Journal of Pharmacology and Experimental Therapeutics, Molecular Pharmacology, Pharmacological Reviews, and Molecular Interventions. ASPET''s membership newsletter is The Pharmacologist. ASPET''s annual meeting is part of Experimental Biology. There are numerous career opportunities in the field of pharmacology available to graduates of advanced training programs. The Society''s web site lists university departments of pharmacology that have established Web sites describing their graduate study programs but it is unlikely that their listing will be complete. ASPET supports nine Divisions, each of which is governed by an Executive Committee. * Division for Behavioral Pharmacology * Division for Cardiovascular Pharmacology * Division for Drug Discovery and Development * Division for Drug Metabolism * Division for Integrative Systems, Translational and Clinical Pharmacology * Division for Molecular Pharmacology * Division for Neuropharmacology * Division for Pharmacology Education * Division for Toxicology
Current Topics in Genome Analysis lecture series consists of 13 lectures on successive Wednesdays, with a mixture of local and outside speakers covering the major areas of genomics. In this tenth edition of the series, rather than splitting the lectures into laboratory-based and computationally-based blocks, we have intermingled the lectures by general subject area. We hope that this approach conveys the idea that both laboratory- and computationally-based approaches are necessary in order to do cutting-edge biological research in the future. The lectures are geared at the level of first year graduate students, are practical in nature, and are intended for a diverse audience. Handouts will be provided for each lecture, and time will be available at the end of each lecture for questions and discussion. All lectures are held on Wednesday mornings from 9:30 a.m. to 11:00 a.m. in the Lipsett Amphitheatre of the National Institutes of Health Clinical Center (Building 10). Course Directors: Andy Baxevanis, Ph.D., Eric Green, M.D., Ph.D., Tyra Wolfsberg, Ph.D. Lectures in this series will be available on the GenomeTV channel of YouTube viewing shortly after the live lecture and also includes all of the handouts. Lectures will not be Webcast live. The lecture series archives (available from 2005-) covers important milestones in genetics. CME Credits: This activity has been approved for AMA PRA Category 1 Credits. The intended audience includes clinicians, clinical geneticists, social and behavioral scientists, genetic counselors, those involved with genetics and public policy, health educators, and other biomedical and clinical scientists with an interest in genetics, genomics and personalized medicine. No prior expertise on the part of the audience will be required and the lecturers will be instructed to provide any relevant background as part of their lectures.
The Autism Chromosome Rearrangement Database is a collection of hand curated breakpoints and other genomic features, including phenotypes, organized by chromosome, related to autism, taken from publicly available literature: databases and unpublished data. The database welcomes submission of data and comments regarding the database from the research community. The database is continuously updated with information from in-house experimental data as well as data from published research studies.
A production service that gives researchers the ability to create and manage long-term identifiers so that they can to track usage, get credit for their work, share their data, and have the data reused for additional research. As a result, EZID identifiers also make it possible to increase citations, to build on previous work, to conduct new research, and avoid duplicating previous efforts. EZID identifiers provide a simple but powerful way to track research materials, including datasets, throughout their life cycle. In this way, researchers can share their data, get more citations, and track their results.
A portal to biomedical and genomic information. NCBI creates public databases, conducts research in computational biology, develops software tools for analyzing genome data, and disseminates biomedical information for the better understanding of molecular processes affecting human health and disease.
A listing of all current openings across the NIH. You may search for NIH Jobs, browse job descriptions, view all descriptions or use the quick links.
THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 4th,2023. It was integrated with Antibody Registry. The JCN antibody database is a listing of all antibodies used in JCN papers from 2006 onward. The catalog numbers and vendor information is included for all antibodies listed, and with a new collaboration with NIF''''s AntibodyRegistry, a unique identifier is also listed for each antibody. The Journal of Comparative Neurology requires rigorous characterization for all antibodies that are used in JCN papers. The antibodies in the The Journal of Comparative Neurology antibody database have in nearly all cases been described and characterized adequately according to the provided guidelines. This information can be used to identify a particular target immunohistochemically or to design an experiment using the antibody information. If you are looking for an antibody to identify a particular target immunohistochemically, this list is a good place to begin your search. We suggest you then look up the paper in which the antibody was used, to make sure that it will meet your needs and to verify its characterization. (The characterization of antibodies in JCN papers often goes well beyond the material published by the manufacturer, so that examining this information before you order an antibody can be very useful.) While we do not guarantee that these antibodies will identify only the intended target (that is a function of the actual experiment and controls), this is the most carefully verified list of antibodies that we are aware of, and we wanted to share this resource with our readers and authors.
Overview of the genetics of hereditary hearing impairment for researchers and clinicians. The site lists data and references for all known gene localizations and identifications for nonsyndromic hearing impairment, and several for syndromic hearing loss. For syndromic hearing impairment, only a few of the most frequent forms are covered. An atlas of cochlea with genes listed can be accessed from this site.
THIS RESOURCE IS NO LONGER IN SERVCE, documented on August, 19, 2021. Antibody supplier.
Online repository of information about Australian plants, animals, and fungi. Development started in 2006. The Commonwealth Scientific and Industrial Research Organisation is organisation significantly involved in development of ALA.