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http://www.cerner.com/

A global health company contributing to the systemic improvement of health care delivery and the health of communities. We are transforming health care by eliminating error, variance and waste for health care providers and consumers around the world. Our solutions optimize processes for health care organizations ranging from single-doctor practices to entire countries, for the pharmaceutical and medical device industries, and for the field of health care as a whole. Our solutions are licensed by more than 9,000 facilities worldwide. We invite you to join us in our quest to make health care become all it should be. Since our company began, we have been committed to transformational change in the vital task of keeping people well. Now more than ever, our focus is on developing the innovations that will help improve the entire health care system. Ultimately, as our CEO Neal Patterson has said, health care is personal. Because in the end, nothing matters more than our health and our families. We''re changing the way people: * Use and share information ** We empower providers to base decisions on best clinical evidence. ** We coordinate care across traditionally fragmented health care systems. ** We provide clinical organizations with the reliability, flexibility and continuous innovation available through cloud-based intelligence. ** We provide contextually relevant information to the right people at the right time. * Pay for health and care ** We believe IT investment must be matched with innovative payment models that are much easier to navigate. ** We are replacing the current, claims-based system with streamlined electronic payments. ** We develop ways to reward people and their providers for proactively achieving positive health goals. * Think about health ** We empower people to actively engage in their health by providing them with a standards-based, lifetime Personal Health Record. ** We are replacing the reactive sick care model with a proactive, personalized plan for health.

Proper citation: Cerner Millenium (RRID:SCR_013581) Copy   

•   Source: SciCrunch Registry

https://www.readcube.com

A software resource application which organizes research literature. Users can import PDF articles into the application and create a searchable library. ReadCube enables users to perform keyword searches and provides references as well as note-taking tools. ReadCube also recommends articles to users based on library contents. For publishers, ReadCube enables interactive PDF versions of articles with tools for readers to make notes or perform author and keyword searches.

Proper citation: ReadCube (RRID:SCR_013777) Copy   

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http://www.harvard.edu/

Institution of higher education in the United States. Private Ivy League research university in Cambridge, Massachusetts.

Proper citation: Harvard University; Cambridge; United States (RRID:SCR_011273) Copy   

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http://www.gsu.edu/

Public research university in downtown Atlanta, Georgia, United States. Founded in 1913. One of the University System of Georgia's four research universities.

Proper citation: Georgia State University; Georgia; USA (RRID:SCR_011234) Copy   

•   Source: SciCrunch Registry

https://catalog.data.gov/dataset?groups=research9385#topic=research_navigation

A catalog of high-value public science and research data sets from across the Federal Government.

Proper citation: Data.gov Science and Research Data Catalog (RRID:SCR_003927) Copy   

•   Source: SciCrunch Registry

http://www.fraxa.org

FRAXA's mission is to accelerate progress toward effective treatments and ultimately a cure for Fragile X, by directly funding the most promising research. FRAXA also supports families affected by Fragile X and raises awareness of this important but relatively unknown disease. FRAXA was founded in 1994 by three parents of children with Fragile X, Katie Clapp, Michael Tranfaglia MD, and Kathy May, to support scientific research aimed at finding a treatment and a cure for Fragile X. Fragile X research is drastically underfunded, considering its high prevalence, prospects for a cure, and the promise that this research holds for advancing understanding of other disorders like autism, Alzheimer's disease, and X-linked mental retardation. FRAXA funds grants and fellowships at universities all over the world. We have funded more than $17 million dollars in top-notch science. FRAXA's management expenses have always been just 4% or less of income, as we have just one full-time staff, three part time staff, and hundreds of volunteer parents. Since FRAXA was founded, the Fragile X field has grown tremendously, due in large part to our grass-roots efforts. You can help us accomplish much more. FRAXA is a 501c3 tax-exempt organization; Tax ID 04-3222167

Proper citation: FRAXA Research Foundation (RRID:SCR_003125) Copy   

•   Source: SciCrunch Registry

http://bioinformatics.aecom.yu.edu/index.htm

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 6, 2023. Primary informatics resource for joint research efforts of the Albert Einstein College of Medicine and Montefiore Medical Center to facilitate the study and understanding of biological processes, clinical disorders, pathologic abnormalities, and the relationships among them, using a wide variety of informatics techniques, applications, and user training. Their services include: * Collaboration on research design to enable effective data management throughout all phases of a project * Provision of management capability for large volumes of data generated by microarrays and related technologies * Provision and supports a software toolchest for data capture, retrieval, and analysis * Design and implementation of custom interfaces to incorporate existing or separately designed databases into the central data management architecture * Support for data management for the Biorepository, to enhance specimen storage, identification, and linkage with clinical data * Ensuring conformity of data elements and structures to national standards via participation in standards organizations, facilitating intramural and extramural collaboration * Providing individualized support to end-users with bioinformatics training needs * Serving as a bioinformatics liaison to other research institutes and organizations * Providing data management support for clinical research * Providing a common, secure repository for clinical, experimental, and biosample storage data

Proper citation: Einstein-Montefiore ICTR Research Informatics Core (RRID:SCR_003451) Copy   

•   Source: SciCrunch Registry

http://www.thesciencejobs.com/

An international career website for vacancies in academic, research and related professions in Science, Technology and Engineering. Announcements on upcoming conferences, workshops, training courses, etc are also available in the site. Job seekers can subscribe for email alerts on latest jobs/event postings. Employers can post jobs free of cost. The site can be viewed in about 35 world languages. About 500 jobs, fellowships and conference announcements are made available to the site every month. Users belong to more than 120 countries.

Proper citation: TheScienceJobs.com (RRID:SCR_005160) Copy   

•   Source: SciCrunch Registry

http://www.utsouthwestern.edu/education/medical-school/departments/neurology/programs/alzheimers-disease-center/brain-tissue-donation-program.html

Brain tissue donation program at the UT Southwestern Memory Clinic that aims to utilize these contributions for research on Alzheimer's. Diagnosis of Alzheimer's disease or other dementias are made through autopsy, the results of which are available to family members.

Proper citation: UT Southwestern ADC Brain Tissue Donation Program (RRID:SCR_008837) Copy   

•   Source: SciCrunch Registry

http://accelrys.com/products/collaborative-science/biovia-pipeline-pilot/

Software used to automate the process of accessing, analyzing and reporting scientific data. This software can be used by a person with little or no software development experience can create scientific protocols that can be executed through a variety of interfaces including: BIOVIA Web Port, other BIOVIA solutions such as BIOVIA Electronic Lab Notebook, Isentris, Chemical Registration and third-party applications such as Microsoft SharePoint. The protocols aggregate and provide immediate access to volumes of research data, they automate the scientific analysis of data and allow researchers to explore, visualize and report results.

Proper citation: Pipeline Pilot (RRID:SCR_014917) Copy   

•   Source: SciCrunch Registry

http://www.anim.med.kyoto-u.ac.jp/nbr/default.aspx

NBRP-Rat was established to overcome limitations associated with properly utilizing existing rat resources. The collection of existing strains and genetic sub strains, phenotypic and genotypic characterization, cryopreservation of embryos, distribution of the collected rat strains, and a publicly accessible database of all assembled data are the major goals of this project. Once achieved, this unique database including the unique rat strains will become a powerful tool for biomedical research. A catalog of comparable, standardized and well characterized rat strains will lead to new and more precise research topics as well as it will facilitate biomedical sciences, drug discovery, advanced chemical research, and contributes to life sciences worldwide. As mentioned before, the major goals of NBRP-Rat are the collection, preservation and supply of rat strains. The repository includes strains from Japan and abroad, spontaneous mutants, congenic and recombinant strains as well as transgenic and mutagenized rats. Deposited rat strains are not only conserved as cryopreserved embryos and sperm. Many reference and frequently used rat strains are also maintained as living animals under SPF conditions. Furthermore, NBRP-rat provides a unique database on various rat strain phenotypes accompanied with basic genetic information. This allows scientists the selection of standardized and research specific strains. The animals themselves are provided free of charge to the research community (except for shipping costs). Sponsors: This project is one part of the National BioResource Projects (NBRP) in Japan for more than 20 species including animals, plants, microbes, tissues and DNAs. It is founded by the Japanese Ministry of Education, Culture, Sports, Science and Technology (Monkasho) and started in 2002.

Proper citation: National Bio Resource Project for the Rat. (RRID:SCR_012774) Copy   

•   Source: SciCrunch Registry

http://databib.org/

Tool for helping people identify and locate online repositories of research data. Users and bibliographers create and curate records that describe data repositories that users can search. * What repositories are appropriate for a researcher to submit his or her data to? * How do users find appropriate data repositories and discover datasets that meet their needs? * How can librarians help patrons locate and integrate data into their research or learning? Databib attempts to address these needs for the research community, including: * data users * data producers * publishers and professional societies * librarians * research funding agencies Are you familiar with a data repository that isn''t included in Databib? Please consider submitting a new record. You can suggest a repository for us to catalog by simply entering its title, URL, authority, and a subject for it... and we''ll do the rest!

Proper citation: Databib (RRID:SCR_005831) Copy   

•   Source: SciCrunch Registry

http://bps-research-digest.blogspot.com/

The British Psychological Society''s award-winning Research Digest blog provides original, authoritative reports on the latest psychology research papers. Plus we publish a few other fun features too. The Digest doesn''t just pick up on the same studies covered by the mainstream media. The editor trawls hundreds of peer-reviewed journals looking for the latest findings from across the breadth of psychological science. The aim is to write accessible, accurate reports on those studies that make an important contribution, that are relevant to real life, timely, novel or thought-provoking. We want to demonstrate how interesting and useful psychological science can be, whilst also casting a critical eye over the methods used. We also hope you''ll use the comments function to have your say on the new research reported here. There are also ''Extras'' posts with links to eye-catching studies that didn''t make the final cut, and the ''Special Issue Spotter'' with links to the latest journal special issues in psychology. Over the years there have also been a number of special guest features - look out for more in the future. In 2010 the Digest was voted best psychology blog in the inaugural Research Blogging awards.

Proper citation: Research Digest (RRID:SCR_006621) Copy   

•   Source: SciCrunch Registry

http://rucore.libraries.rutgers.edu/

Repository of digital research and educational materials created and used by the Rutgers University community and its strategic collaborators. The goal of the repository is to advance research and learning at Rutgers, to foster interdisciplinary collaboration, and to contribute to the development of new knowledge through the archiving, preservation, and presentation of digital resources. Original research products and papers of the faculty and administrators and the unique resources of the libraries will be permanently preserved and made accessible with tools developed to facilitate and encourage their continued use. RUcore''s developing collection includes * Primary source materials-manuscripts, photographs, maps, and multimedia, from the libraries'' special collections. * Resources about New Jersey, from the state''s libraries, museums, archives and historical societies from the New Jersey Digital Highway collection. * Electronic theses and dissertations, in collaboration with the Rutgers University graduate schools. * Faculty and Departmental publications: pre-prints, postprints, presentations, technical reports, etc.

Proper citation: RUcore (RRID:SCR_006382) Copy   

•   Source: SciCrunch Registry

http://lawneuro.org/blog/

Blog that provides an on-line forum where the members of the MacArthur Foundation Research Network on Law and Neuroscience can share their ideas and interact with not only other researchers but also with the interested public more generally. One of the main goals of the blog is to provide a resource with information about cutting edge research at the cross-roads of neuroscience, law, and philosophy.

Proper citation: Law and Neuroscience (RRID:SCR_006155) Copy   

•   Source: SciCrunch Registry

http://report.nih.gov/

A database of federally funded biomedical research projects conducted at universities, hospitals, and other research institutions that provides a central point of access to reports, data, and analyses of NIH research. The RePORTER has replaced the CRISP database. The database, maintained by the Office of Extramural Research at the National Institutes of Health, includes projects funded by the National Institutes of Health (NIH), Substance Abuse and Mental Health Services (SAMHSA), Health Resources and Services Administration (HRSA), Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDCP), Agency for Health Care Research and Quality (AHRQ), and Office of Assistant Secretary of Health (OASH).

Proper citation: National Institutes of Health Research Portfolio Online Reporting Tool (RRID:SCR_006874) Copy   

•   Source: SciCrunch Registry

http://www.epilepsygenes.org/page/show/homepage

The Epilepsy Genetic Association Database (epiGAD) is an online repository of data relating to genetic association studies in the field of epilepsy. It summarizes the results of both published and unpublished studies, and is intended as a tool for researchers in the field to keep abreast of recent studies, providing a bird''s eye view of this research area. The goal of epiGAD is to collate all association studies in epilepsy in order to help researchers in this area identify all the available gene-disease associations. Finally, by including unpublished studies, it hopes to reduce the problem of publication bias and provide more accurate data for future meta-analyses. It is also hoped that epiGAD will foster collaboration between the different epilepsy genetics groups around the world, and faciliate formation of a network of investigators in epilepsy genetics. There are 4 databases within epiGAD: - the susceptibility genes database - the epilepsy pharmacogenetics database - the meta-analysis database - the genome-wide association studies (GWAS) database The susceptibility genes database compiles all studies related to putative epilepsy susceptibility genes (eg. interleukin-1-beta in TLE), while the pharmacogenetics studies in epilepsy (eg. ABCB1 studies) are stored in ''phamacogenetics''. The meta-analysis database compiles all existing published epilepsy genetic meta-analyses, whether for susceptibility genes, or pharmacogenetics. The GWAS database is currently empty, but will be filled once GWAS are published. Sponsors: The epiGAD website is supported by the ILAE Genetics Commission.

Proper citation: Epilepsy Genetic Association Database (RRID:SCR_006840) Copy   

•   Source: SciCrunch Registry

http://cmckb.cellmigration.org

It is a database of keys facts about proteins, families, and complexes involved in cell migration. This ongoing project provides a large amount of automated and curated data, collected from numerous online resources that are updated monthly. These data include names, synonyms, sequence information, summaries, CMC research data, reagents, structures, as well as protein family and complex details. CMKB''s ultimate goal is to create a database that will enable the cell migration community to conveniently access significant information about molecules of interest. This will also serve as a stepping stone to pathway analysis and demonstrate how these molecules coordinate with one another during cell adhesion and movement. Sponsors: This resource is supported by the Cell Migration Consortium.

Proper citation: CMKB (RRID:SCR_007229) Copy   

•   Source: SciCrunch Registry

http://www.nimh.nih.gov/about/director/index.shtml

Blog by the NIMH Director, Thomas R. Insel, M.D. Users may sort posts by topic and/or subsribe to the RSS Feed, http://www.nimh.nih.gov/site-info/feed-directors-blog.atom

Proper citation: NIMH Director's Blog (RRID:SCR_008841) Copy   

•   Source: SciCrunch Registry

http://www.phylo.org/sub_sections/portal/

This database is a public resource for inference of large phylogenetic trees. It is designed to provide all researchers with access to large computational resources of the NSF TeraGrid through a simple browser interface. The CIPRES Science Gateway provides new hybrid parallel versions of RAxML (7.2.7) and MrBayes (3.1.2), as well as parallel GARLI (1.0) code to insure the fastest possible run times for submitted jobs. Through a collaboration with Alexandros Stamatakis and Wayne Pfeiffer, they now offer the fastest hybrid versions of RAxML and MrBayes currently available. Sponsors: The CIPRES project is a multi-site collaboration funded by the NSF Information Technology Research (ITR) program grant entitled BUILDING THE TREE OF LIFE: A National Resource for Phyloinformatics and Computational Phylogenetics.

Proper citation: CIPRES Science Gateway (RRID:SCR_008439) Copy   

•   Source: SciCrunch Registry