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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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Naturejobs Resource Report Resource Website |
Naturejobs (RRID:SCR_005151) | Naturejobs | data or information resource, job resource, narrative resource | Search for the widest range of science jobs with thousands of vacancies advertised globally on the site. Employers range from top international pharmaceutical and biotechnology companies to highly respected academic and government institutions. Job seekers can find a wide range of scientific career information and news as well as expert advice, all free to access. What''s more, employers can post jobs for free. | employment, science, life science, physical science, applied science, clinical medicine, news, clinical, medicine, database, career |
is used by: NIF Data Federation is listed by: OMICtools is related to: Integrated Jobs has parent organization: Nature Publishing Group |
Free, The community can contribute to this resource | OMICS_01824, nlx_144163 | SCR_005151 | naturejobs.com, naturejobs.com - The premier science jobs recruitment website | 2026-09-12 12:56:22 | 0 | |||||||
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PheKB Resource Report Resource Website 10+ mentions |
PheKB (RRID:SCR_005292) | PheKB | knowledge environment, software repository, software resource | Collaborative environment of building and validating electronic phenotype algorithms using electronic medical records (EMRs) and natural language processing (NLP) for use in genome-wide association studies (GWAS). On this site you can: View existing algorithms, Enter or create new algorithms, Collaborate with others to create or review algorithms, View implementation details for existing algorithms. The Electronic Medical Records and Genomics Network (eMERGE) has investigated whether data captured through routine clinical care using electronic medical records (EMRs) can identify disease phenotypes with sufficient positive and negative predictive values for use in genome-wide association studies (GWAS). Most EMRs captured key information (diagnoses, medications, laboratory tests) used to define phenotypes in a structured format; in addition, natural language processing has also been shown to improve case identification rates. PheKB is an outgrowth of that validation effort. Phenotype algorithms can be viewed by data modalities or methods used: CPT codes, ICD 10 codes, ICD 9 codes, Laboratories, Medications, Vital Signs, Natural Language Processing Algorithms can also be viewed by: * Implementation results (positive predictive value, sensitivity, publications) * Institution * Work Group | phenotype, electronic medical record, medical record, human, clinical, white blood cell, red blood cell, lipid, algorithm, height, cardiac conduction, genome-wide association study, natural language processing |
is related to: eMERGE Network: electronic Medical Records and Genomics has parent organization: Vanderbilt University; Tennessee; USA |
Atrial fibrillation, Crohn''''s disease, Multiple Sclerosis, Rheumatoid arthritis, Type 2 diabetes mellitus, Dementia, Cataracts, Hypothyroidism, Diabetic Retinopathy, High-Density Lipoprotein, Peripheral Arterial Disease | PMID:20362271 | nlx_144339 | SCR_005292 | Phenotype KnowledgeBase, PheKB - a knowledgebase for discovering phenotypes from electronic medical records | 2026-09-12 12:56:24 | 32 | ||||||
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Lurie Center for Autism Resource Report Resource Website |
Lurie Center for Autism (RRID:SCR_005456) | Lurie Center | data or information resource, disease-related portal, patient-support portal, portal, topical portal | The Lurie Center for Autism is a highly successful program designed to evaluate and treat children and adults with a wide variety of developmental and handicapping conditions. Our mission is to provide the highest quality clinical, social and support services to those diagnosed with autism, pervasive developmental disorders and other developmental disabilities. The Lurie Center for Autism is unique because of the population it serves and because it uses a multidisciplinary approach that begins with comprehensive medical evaluations and extends to supporting the well-being of patients and families. Nurses, social workers, speech pathologists, occupational therapists, physical therapists, neuro-psychologists, special education professionals and family members are involved in the treatment processes in addition to physicians. Each has a depth of expertise in his/her respective field. The team, as a unit, plays an integral role in the continuum of care for individuals diagnosed with developmental disabilities. Our services and therapies include: * Extensive diagnostic evaluations * Medical, cognitive and behavioral interventions including speech and language * Speech therapy, occupational therapy, occupational with sensory integration therapy and physical therapy; psychological evaluation and counseling; * Parent skills training and family empowerment * Referral support for additional medical and educational resources at locations near each patient''s home and throughout the New England region The Lurie Center for Autism is committed to improving the medical, social and psychological well-being of children, adolescents, adults and families. To this end, our goals and objectives are to: * Provide a stable, consistent and structured environment within a medical context * Provide opportunities for each individual to achieve * Develop self control, social skills and self esteem in each individual * Support and educate families in order to transfer the learned skills to home, school, work and community environments * Provide teaching to physicians and professionals in training and to pursue research related to the treatment and causes of autism, pervasive developmental disorders and other devlopmental disorders of the central nervous system | autism, pervasive development disorder, asperger syndrome, developmental delay, clinical, human, child, adult, adolescent | Nancy Lurie Marks Family Foundation | nlx_144552 | SCR_005456 | Lurie Family Autism Center | 2026-09-12 12:56:26 | 0 | ||||||||
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UCSF Center for AIDS Prevention Studies (CAPS) Resource Report Resource Website |
UCSF Center for AIDS Prevention Studies (CAPS) (RRID:SCR_005647) | CAPS | data or information resource, disease-related portal, funding resource, portal, service resource, topical portal, training service resource | Established in 1986, the Center for AIDS Prevention Studies (CAPS) at the University California, San Francisco (UCSF) is the world''s largest research center dedicated to social, behavioral, and policy science approaches to HIV. The mission of the CAPS is to conduct research to prevent new HIV infections, improve health outcomes among those infected, and reduce disparities. This is how we do it: * CAPS provides core support for multidisciplinary and high-impact HIV research, enhances the excellence of research projects, trains a new generation of HIV scientists, and assists implementing partners. * Our Administrative Core provides strong leadership and management to stimulate innovative research and ensure scientific rigor and sound fiscal operations. * Our Developmental Core fosters innovative, high-impact, multidisciplinary HIV research by providing funds for innovative pilot work, sponsoring training and education, and ensuring the scientific excellence of research. * Our Methods Core provides comprehensive methodological training and consultation in research design, qualitative and quantitative analysis, and state-of-the-art data collection and management. * Our Policy and Ethics Core stimulates and supports policy-relevant research, identifies and analyzes the policy and ethics implications of research, and ensures the highest ethical conduct of research. * Our Technology and Information Exchange (Domestic Response) Core responds to the domestic epidemic by disseminating information, fostering community collaborative research, providing technical assistance and capacity-building to community-based organizations, and learning from community expertise. * Our Global Response Core responds to the global epidemic by fostering collaborative research with scientists in developing countries, completing and disseminating Cochrane Collaborative scientific reviews, and providing technical assistance, capacity building, and an evidence base to implementing partners. | aids, hiv, clinical, research | has parent organization: University of California at San Francisco; California; USA | AIDS, HIV | nlx_146276 | SCR_005647 | Center for AIDS Prevention Studies, UCSF Center for AIDS Prevention Studies, Center for AIDS Prevention Studies (CAPS) - Responding to the Challenge of HIV | 2026-09-12 12:56:29 | 0 | |||||||
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University of Pittsburgh Alzheimer Disease Research Center Resource Report Resource Website 100+ mentions |
University of Pittsburgh Alzheimer Disease Research Center (RRID:SCR_008084) | ADRC | data or information resource, disease-related portal, portal, topical portal | A research center associated with the University of Pittsburgh that specializes in the diagnosis of Alzheimer's disease and related disorders. The overall objective of the ADRC is to study the pathophysiology of Alzheimer's disease, with the aim of improving the reliability of diagnosis of Alzheimer's and developing effective treatment strategies. Current research foci emphasize neuropsychiatry and neuropsychology, molecular genetics and epidemiology, basic neuroscience, and structural and functional imaging that aid in the diagnosis and treatment of Alzheimer's disease. Specific services at the ADRC include: comprehensive diagnostic evaluation of patients with suspected Alzheimer's disease and other forms of dementia; evaluation of memory, language, judgment, and other cognitive abilities; and education and counseling for patients and families. | african american, alzheimer's disease, assessment, clinical, cognitive, dementia, diagnosis, diagnostic evaluation, human, medical, mild cognitive impairment, neurological, pathophysiology, psychiatric | has parent organization: University of Pittsburgh; Pennsylvania; USA | Alzheimer's disease, Mild Cognitive Impairment, Dementia, Aging | NIA | Public | nif-0000-10750 | SCR_008084 | University of Pittsburgh Alzheimer's Disease Research Center | 2026-09-12 12:56:59 | 494 | |||||
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Affymetrix Power Tools Resource Report Resource Website 10+ mentions |
Affymetrix Power Tools (RRID:SCR_008401) | software resource | Affymetrix Power Tools (APT) are a set of cross-platform command line programs that implement algorithms for analyzing and working with Affymetrix GeneChip arrays. APT programs are intended for power users who prefer programs that can be utilized in scripting environments and are sophisticated enough to handle the complexity of extra features and functionality. APT provides platform for developing and deploying new algorithms without waiting for the GUI implementations. This resource is supported by Affymetrix, Inc. | Affymetrix, Inc., Genomics, Clinical, Study, Bioinformatic, Windows, MacOS, Linux, resource, Data, Normalization, Sequence, Annotation, Gene, Expression, Pattern, Motif, Inference, Toolkit, Model, Fitting, Algorithm |
has parent organization: Affymetrix has parent organization: Affymetrix |
nif-0000-30070 | https://www.affymetrix.com/support/developer/powertools/changelog/install.html, https://media.affymetrix.com/support/developer/powertools/changelog/index.html | http://www.affymetrix.com/partners_programs/programs/developer/tools/powertools.affx | SCR_008401 | APT | 2026-09-12 12:57:03 | 32 | |||||||
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National Institute on Aging, Division of Neuroscience Resource Report Resource Website |
National Institute on Aging, Division of Neuroscience (RRID:SCR_008257) | data or information resource, funding resource, narrative resource, portal, topical portal | A funding resource that supports the research and training for understanding the structure and function of the aging nervous system, with an emphasis on studies involving Alzheimer's disease and age-related dementia. There is an emphasis on brain-behavior relationships. This program is composed of three branches: Neurobiology, Neuropsychology, and Dementias of Aging. The overall aim of this program is to understand the aging nervous system to minimize mental decline and improve the lives of older patients. This resource also includes links to sites for Alzheimer's disease (AD) studies that include: specimen repositories, genetic materials, bio-markers, data, policies on NIA and AD genetics sharing plans, and additional aging or other AD related links. | epidemiological, alzheimer's disease, brain, clinical, dementia, nervous system, neurobiology, neuropsychology, pathological, research, | Aging | R21-Exploratory/Development Grants ; NIH Neuroscience Blueprint initiatives |
nif-0000-22438 | http://www.nia.nih.gov/ResearchInformation/ExtramuralPrograms/NeuroscienceOfAging/ | SCR_008257 | NIA Division of Neuroscience, NIA DN, National Institute on Aging Division of Neuroscience, National Institute on Aging DN | 2026-09-12 12:57:01 | 0 | |||||||
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ConnectomeViewer: Multi-Modal Multi-Level Network Visualization and Analysis Resource Report Resource Website |
ConnectomeViewer: Multi-Modal Multi-Level Network Visualization and Analysis (RRID:SCR_008312) | ConnectomeViewer | d visualization software, data analysis software, data processing software, data visualization software, network analysis software, network graph visualization software, rendering software, software application, software resource | Extensible, scriptable, pythonic software tool for visualization and analysis in structural neuroimaging research on many spatial scales. Employing the Connectome File Format, diverse data such as networks, surfaces, volumes, tracks and metadata are handled and integrated. The field of Connectomics research benefits from recent advances in structural neuroimaging technologies on all spatial scales. The need for software tools to visualize and analyze the emerging data is urgent. The ConnectomeViewer application was developed to meet the needs of basic and clinical neuroscientists, as well as complex network scientists, providing an integrative, extensible platform to visualize and analyze Connectomics data. With the Connectome File Format, interlinking different datatypes such as hierarchical networks, surface data, volumetric data is easy and might provide new ways of analyzing and interacting with data. Furthermore, ConnectomeViewer readily integrates with: * ConnectomeWiki: a semantic knowledge base representing connectomics data at a mesoscale level across various species, allowing easy access to relevant literature and databases. * ConnectomeDatabase: a repository to store and disseminate Connectome files. | extensible, analysis, clinical, data, diverse, metadata, network, neuroscience, neuroscientist, pythonics, research, scriptable, software, structural, surface, technology, tool, track, visualization, volume, neuroimaging |
has parent organization: Ecole Polytechnique Federale de Lausanne; Lausanne; Switzerland has parent organization: University of Lausanne; Lausanne; Switzerland |
nif-0000-24442 | SCR_008312 | 2026-09-12 12:57:02 | 0 | |||||||||
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Clinical and Translational Science Awards Consortium Resource Report Resource Website 1+ mentions |
Clinical and Translational Science Awards Consortium (RRID:SCR_008339) | CTSA | knowledge environment | National consortium of medical research institutions working together to transform the local, regional, and national environment to increase the efficiency and speed of clinical and translational research across the country. Consortium members share a common vision to reduce the time it takes for laboratory discoveries to become treatments for patients, to engage communities in clinical research efforts and to train clinical and translational researchers. This consortium includes 60 medical research institutions located throughout the nation, linking them together to energize the discipline of clinical and translational science. The CTSA consortium has five Strategic Goals: * National Clinical and Translational Research Capability * The Training and Career Development of Clinical and Translational Scientists * Consortium-Wide Collaborations * The Health of our Communities and the Nation * T1 Translational Research | biomedical, clinical, community, consortium, institution, laboratory, medical, patient, research, researcher, science, translational, translational research, treatment |
is related to: REDCap is related to: eBIRT is related to: VIVO is related to: CTSA ShareCenter is related to: CUSP is related to: CDART is related to: cTAKES is related to: CTSA-IP is related to: FURTHeR is related to: HUBzero is related to: ePRISM is related to: ResearchMatch is related to: SPARC Request is related to: Albert Einstein College of Medicine; New York; USA is related to: Clinical Research Resource HUB is related to: Eagle I is related to: CTSAconnect is related to: Boston University; Massachusetts; USA is related to: Case Western Reserve University; Ohio; USA is related to: Columbia University; New York; USA is related to: Duke University; North Carolina; USA is related to: Emory University; Georgia; USA is related to: Morehouse School of Medicine; Georgia; USA is related to: Georgia Institute of Technology; Georgia; USA is related to: Georgetown University; Washington D.C.; USA is related to: Howard University; Washington D.C. is related to: Indiana University School of Medicine; Indiana; USA is related to: Johns Hopkins University; Maryland; USA is related to: Mayo Clinic is related to: Medical College of Wisconsin; Wisconsin; USA is related to: Medical University of South Carolina; South Carolina; USA is related to: Icahn School of Medicine at Mount Sinai; New York; USA is related to: New York University School of Medicine; New York; USA is related to: Northwestern University; Illinois; USA is related to: Oregon Health and Science University; Oregon; USA is related to: Penn State Milton S. Hershey Medical Center; Pennsylvania; USA is related to: Stanford University; Stanford; California is related to: Ohio State University; Ohio; USA is related to: Rockefeller University; New York; USA is related to: Scripps Research Institute is related to: University of Alabama at Birmingham; Alabama; USA is related to: University of North Carolina at Chapel Hill; North Carolina; USA is related to: University of Texas Health Science Center at San Antonio; Texas; USA is related to: University of Utah; Utah; USA is related to: Tufts University; Massachusetts; USA is related to: University of Arkansas for Medical Sciences; Arkansas; USA is related to: University of California at Los Angeles; California; USA is related to: University of California at Davis; California; USA is related to: University of California at Irvine; California; USA is related to: University of California at San Diego; California; USA is related to: University of California at San Francisco; California; USA is related to: University of Chicago; Illinois; USA is related to: University of Cincinnati; Ohio; USA is related to: University of Colorado Denver; Colorado; USA is related to: University of Florida; Florida; USA is related to: University of Illinois at Chicago; Illinois; USA is related to: University of Iowa; Iowa; USA is related to: University of Kansas Medical Center; Kansas; USA is related to: University of Massachusetts Medical School; Massachusetts; USA is related to: University of Miami; Florida; USA is related to: University of Michigan; Ann Arbor; USA is related to: University of Minnesota Twin Cities; Minnesota; USA is related to: University of New Mexico; New Mexico; USA is related to: University of Pennsylvania; Philadelphia; USA is related to: University of Pittsburgh; Pennsylvania; USA is related to: University of Rochester School of Medicine and Dentistry; New York; USA is related to: University of Southern California; Los Angeles; USA is related to: University of Texas Health Science Center at Houston; Texas; USA is related to: University of Texas Medical Branch at Galveston is related to: University of Texas Southwestern Medical Center; Texas; USA is related to: University of Washington; Seattle; USA is related to: University of Wisconsin-Madison; Wisconsin; USA is related to: Vanderbilt University; Tennessee; USA is related to: Meharry Medical College is related to: Virginia Commonwealth University; Virginia; USA is related to: Washington University in St. Louis; Missouri; USA is related to: Weill Cornell Medical College; New York; USA is related to: Hunter College; New York; USA is related to: Yale University; Connecticut; USA has parent organization: Vanderbilt University; Tennessee; USA has parent organization: U.S. Department of Health and Human Services |
National Center for Advancing Translational Sciences 2U54TR000123 | nif-0000-24968 | http://www.ctsaweb.org/ | SCR_008339 | Clinical & Translational Science Awards, Clinical and Translational Science Awards | 2026-09-12 12:57:02 | 6 | ||||||
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Becton Dickinson and Company Resource Report Resource Website 100+ mentions |
Becton Dickinson and Company (RRID:SCR_008418) | commercial organization | A healthcare company that provides biomedical solutions and diagnostic and preclinical systems to life science professionals. | medical, device, laboratory, instrument, antibody, reagent, diagnostic, healthcare, life science, researcher, clinical, pharmaceutical, industry, research | nif-0000-30149 | SCR_008418 | BD | 2026-09-12 12:57:03 | 308 | ||||||||||
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BioBank Central Resource Report Resource Website |
BioBank Central (RRID:SCR_008645) | BioBank Central | biospecimen repository, material storage repository, service resource, storage service resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented on March 27, 2013. Web-based portal to connect all the constituencies in the global biobank community. The project seeks to increase the transparency and accessibility of the scientific research process by connecting researchers with an additional source of funding - microinvestments received from the broader online community. In exchange for these public investments, researchers will maintain research logs detailing the play-by-play progress made in their project, as well as publishing all of their data in a public database under a science commons license. These research projects, in turn, will serve to continually update a research-based neuroscience-based human brain & body curriculum. Biobanks are the meeting point of two major information trends in biomedical research: the generation of huge amounts of genomic and other laboratory data, and the electronic capture and integration of patient clinical records. They are comprised of large numbers of human biospecimens supplemented with clinical data. Biobanks when implemented effectively can harness the power of both genomic and clinical data and serve as a critical bridge between basic and applied research, linking laboratory to patient and getting to cures faster. As science and technology leaders work to address the many challenges facing U.S. biobanks logistical, technical, ethical, financial, intellectual property, and IT BioBank Central will serve as an accurate and timely source of knowledge and news about biorepositories and their role in research and drug development. The Web site also provides a working group venue, patient and public education programs, and a forum for international collaboration and harmonization of best practices. | biobank, community, biomedical, data, genomic, integration, patient, clinical, human, biospecimen, science, technology, biorepository, drug, development, education | has parent organization: Open Source Science Project | FasterCures ; Feinstein Kean Healthcare ; IBM Healthcare and Life Sciences ; Affymetrix ; Bioaccelerate Holdings Inc. ; Invitrogen Corporation |
THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-32933 | SCR_008645 | 2026-09-12 12:57:07 | 0 | |||||||
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NIMH Intramural Research Program Clinical Brain Disorders Branch Resource Report Resource Website 10+ mentions |
NIMH Intramural Research Program Clinical Brain Disorders Branch (RRID:SCR_008728) | CBDB | data or information resource, portal, topical portal | THIS RESOURCE IS NO LONGER IN SERVICE, documented on February 07, 2013. A multidisciplinary neuroscience laboratory in which basic and clinical scientists work side by side exploring neural mechanisms and models of mental and cognitive function and of neuropsychiatric illness. Experiments are performed at many levels of inquiry, from basic molecular biology of the gene to clinical examinations of patients. A major area of investigation of this laboratory is the genetic mechanisms implicated in the pathogenesis of schizophrenia and its treatment. The laboratory is organized as a multi-disciplinary team of investigators with a common mission: to identify and fully characterize basic genetic and neurobiological mechanisms of schizophrenia and related cognitive and emotional disorders. The various components of this effort are centered various different units or divisions represented by groups of investigators, at various levels of training and experience, working on related experiments. The Director of the Branch and of the Genes, Cognition and Psychosis Program (GCAP) is Daniel R. Weinberger, M.D. The CBDB is the principle research laboratory in the created (2003) Genes, Cognition, and Psychosis Program (GCAP) of the NIMH. After twelve years of residing on the pastoral grounds of St. Elizabeths Hospital, in Southeast Washington, CBDB moved back to the main NIH campus in Bethesda, Maryland in 1998. While the unique setting of St. Elizabeths is irreplaceable, we have occupied beautiful new laboratories and clinic spaces that were created for us, and we are in the mainstream of NIH life., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | mental function, cognitive function, gene, clinical, treatment, pathogen |
is related to: Genes Cognition and Psychosis Program has parent organization: NIMH Division of Intramural Research Programs is parent organization of: NIMH Brain Tissue Collection |
Schizophrenia, Neuropsychiatric illness, Cognitive disorder, Emotional disorder | NIMH | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_143685 | SCR_008728 | NIMH Clinical Brain Disorders Branch, Clinical Brain Disorders Branch | 2026-09-12 12:57:08 | 13 | |||||
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PROGENY Resource Report Resource Website 100+ mentions |
PROGENY (RRID:SCR_006647) | Progeny | commercial organization, data management software, software application, software resource | Fully customizable, comprehensive genetic pedigree and clinical data management software including a multi-user relational database with an integrated pedigree drawing component to manage genetic and pedigree data in one database. Manage Pedigrees, Individuals, SNPs, STRs, Samples, Plates, Genotypes and exports to multiple analysis platforms. (entry from Genetic Analysis Software) * LIMS software, providing advanced sample tracking and management (including functionality to generate and record barcodes) and configurable workflows for your specific environment. * Full genotype management gives users the ability to track not only family-based studies, but Whole Genome Association studies containing 1000''s of samples with large arrays. | gene, genetic, genomic, c++, active x control, ms-windows, pedigree, clinical, genotype, data management, drawing, family history, questionnaire, sample, lab management, FASEB list |
is listed by: OMICtools is listed by: Genetic Analysis Software |
nlx_154553, OMICS_00216 | SCR_006647 | Progeny Software LLC, Progeny Software | 2026-09-12 12:56:43 | 416 | ||||||||
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Nex-StoCT Resource Report Resource Website |
Nex-StoCT (RRID:SCR_006777) | Nex-StoCT | data or information resource, knowledge environment, narrative resource, standard specification | National workgroup to define platform-independent approaches for establishing technical process elements of a quality management system (QMS) to assure the analytical validity and compliance of next-generation sequencing (NGS) tests with existing regulatory and professional quality standards. The workgroup identified and addressed gaps in quality practices that could compromise the quality of both clinical laboratory services and translational efforts needed to advance the implementation and utility of NGS in clinical settings. The workgroup was composed of experts with knowledge of and experience with NGS and included clinical laboratory directors, clinicians, platform and software developers and informaticians, as well as individuals actively engaged in NGS guideline development from accreditation bodies and professional organizations. Representatives from US government agencies also participated. These guidelines address four topics that are components of quality management in a clinical environment: (i) test validation, (ii) quality control (QC) procedures to assure and maintain accurate test results, (iii) the independent assessment of test performance through proficiency testing (PT) or alternative approaches and (iv) reference materials (RMs). Discussions were limited to the analytic and informatics processes required for accurate variant calling. The workgroup did not address how variants are prioritized, interpreted or reported. | next-generation sequencing, clinical, testing, test result |
is listed by: OMICtools has parent organization: Centers for Disease Control and Prevention |
PMID:23138292 | OMICS_01787 | SCR_006777 | Next Generation Sequencing: Standardization of Clinical Testing, Nex-StoCT Working Groups, Next Generation Sequencing: Standardization of Clinical Testing Working Groups, Next Generation Sequencing - Standardization of Clinical Testing | 2026-09-12 12:56:45 | 0 | |||||||
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BTRIS: NIH Biomedical Translational Research Information System Resource Report Resource Website 1+ mentions |
BTRIS: NIH Biomedical Translational Research Information System (RRID:SCR_006838) | BTRIS | clinical database, data management software, data repository, service resource, software application, software resource, storage service resource | Provides NIH clinical investigators with access to identifiable data for the subjects on their own active protocols, while providing all NIH investigators with access to de-identified data across all protocols. BTRIS provides users with advanced search, filtering, and aggregation methods to create data sets to support ongoing studies and stimulate ideas for new research. BTRIS is two distinct but interrelated applications, BTRIS Data Access and BTRIS Preferences. * BTRIS Data Access is the data repository where principal investigators or their designee create reports on their active protocols with identified subject data. Reports include the IRB Inclusion Enrollment Report, demographics, patient lists, laboratory and microbiology results, vital signs, medication orders and administration, diagnoses, and radiology reports (with links to images in the CC PACS system). * BTRIS Preferences is a Web based application that allows principal investigators or their designees to verify subject enrollment in their protocol(s). This ensures that reports created in BTRIS Data Access include all subjects. It also allows the principal investigator to designate an alternate investigator from the protocol to manage subject enrollment and create reports in BTRIS Data Access. BTRIS contains subject data from CRIS/MIS (the Clinical Center Medical Information Systems) and research data from NIAID (Crimson), NIAAA, and NCI. Data are available from 1976 to the present. | data management, clinical, data sharing | has parent organization: National Institutes of Health | nif-0000-00577 | SCR_006838 | Biomedical Translational Research Information System | 2026-09-12 12:56:46 | 1 | ||||||||
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AASK Clinical Trial and Cohort Study Resource Report Resource Website |
AASK Clinical Trial and Cohort Study (RRID:SCR_006985) | AASK Cohort Study | clinical trial, data or information resource, disease-related portal, portal, research forum portal, resource, topical portal | Clinical trial investigating whether a specific class of antihypertensive drugs (beta-adrenergic blockers, calcium channel blockers, or angiotensin converting enzyme inhibitors) and/or the level of blood pressure would influence progression of hypertensive kidney disease in African Americans. The initiative consisting of 21 clinical centers and a data-coordinating center is followed by a Continuation of AASK Cohort Study to investigate the environmental, socio-economic, genetic, physiologic, and other co-morbid factors that influence progression of kidney disease in a well-characterized cohort of African Americans with hypertensive kidney disease. Only patients who were previously in the randomized trial are eligible for the cohort study. A significant discovery was made in the treatment strategy for slowing kidney disease caused by hypertension. Angiotensin-converting enzyme (ACE) inhibitors, compared with calcium channel blockers, were found to slow kidney disease progression by 36 percent, and they drastically reduced the risk of kidney failure by 48 percent in patients who had at least one gram of protein in the urine, a sign of kidney failure. ACE inhibitors have been the preferred treatment for hypertension caused by diabetes since 1994; however, calcium channel blockers have been particularly effective in controlling blood pressure in African Americans. The AASK study now recommends ACE inhibitors to protect the kidneys from the damaging effects of hypertension. The Continuation of AASK Cohort Study will be followed at the clinical centers. The patients will be provided with the usual clinical care given to all such patients at the respective centers. Baseline demographic information, selected laboratory tests, and other studies are being obtained at the initiation of the Continuation Study. The patients will be seen quarterly at the centers, and some selected studies done at these visits. Samples will be obtained and stored for additional studies and analyses at a later date. | african american, blood pressure, beta-adrenergic blocker, calcium channel blocker, angiotensin converting enzyme inhibitor, environment, socio-economic, genetic, physiology, co-morbid factor, gene, adult human, antihypertensive drug, clinical, treatment, longitudinal, demographics, laboratory test, biospecimen, biomaterial supply resource |
is listed by: One Mind Biospecimen Bank Listing is related to: NIDDK Information Network (dkNET) is related to: Chronic Renal Insufficiency Cohort Study |
End-stage renal disease, Kidney failure, Kidney disease, Hypertension, Hypertensive kidney disease | NIDDK | nlx_152750 | SCR_006985 | African American Study of Kidney Disease and Hypertension (AASK) Clinical Trial and Cohort Study, African American Study of Kidney Disease and Hypertension Clinical Trial and Cohort Study, Continuation of AASK Cohort Study, African American Study of Kidney Disease and Hypertension | 2026-09-12 12:56:48 | 0 | ||||||
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National Survey on Drug Use and Health Resource Report Resource Website 1+ mentions |
National Survey on Drug Use and Health (RRID:SCR_007031) | NSDUH, NSDUH/NHSDA, NHSDA, NSDUH / NHSDA | data or information resource, data set, portal, topical portal | NSDUH is the primary source of statistical information on the use of illegal drugs, alcohol, and tobacco by the U.S. civilian, noninstitutionalized population aged 12 or older. Conducted by the Federal Government since 1971, the survey collects data through face-to-face interviews with a representative sample of the population at the respondent''s place of residence. Correlates in OAS reports include the following: age, gender, pregnancy status, race / ethnicity, education, employment, geographic area, frequency of use, and association with alcohol, tobacco, & illegal drug use. NSDUH collects information from residents of households and noninstitutional group quarters (e.g., shelters, rooming houses, dormitories) and from civilians living on military bases. The survey excludes homeless persons who do not use shelters, military personnel on active duty, and residents of institutional group quarters, such as jails and hospitals. Most of the questions are administered with audio computer-assisted self-interviewing (ACASI). ACASI is designed to provide the respondent with a highly private and confidential mode for responding to questions in order to increase the level of honest reporting of illicit drug use and other sensitive behaviors. Less sensitive items are administered by interviewers using computer-assisted personal interviewing (CAPI). The 2010 NSDUH employed a State-based design with an independent, multistage area probability sample within each State and the District of Columbia. The eight States with the largest population (which together account for about half of the total U.S. population aged 12 or older) were designated as large sample States (California, Florida, Illinois, Michigan, New York, Ohio, Pennsylvania, and Texas) and had a sample size of about 3,600 each. For the remaining 42 States and the District of Columbia, the sample size was about 900 per State. The design oversampled youths and young adults; each State''s sample was approximately equally distributed among three age groups: 12 to 17 years, 18 to 25 years, and 26 years or older. | substance abuse, data, clinical, mental health, marijuana, cocaine, heroin, hallucinogen, inhalant, psychotherapeutic, alcohol, tobacco, illicit drug, adolescent, early adult, adult | has parent organization: RTI International | Drug Abuse | US Department of Health and Human Services HHSS283200800004C | Public | nlx_146277 | SCR_007031 | National Household Survey on Drug Abuse, SAMHSA National Survey on Drug Use & Health, National Survey on Drug Use Health, National Survey on Drug Use & Health | 2026-09-12 12:56:49 | 2 | |||||
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Alzheimers Association Resource Report Resource Website 100+ mentions |
Alzheimers Association (RRID:SCR_007398) | ALZ | nonprofit organization | A non profit organization dedicated to providing support for patients and families with Alzheimer's disease, to educating the public about the disease, to funding a wide range of Alzheimer's disease related research and to finding ways to treat and eventually to prevent Alzheimer's disease. Resources include: the Alzheimer's Association Green-Field Library, a research grants program, and the Journal of the Alzheimer's Association. | advocacy group, brain, brain health, clinical, dementia, alzheimers disease, community building portal, narrative resource, training material, database, training resource, service resource, FASEB list |
is related to: ADNI - Alzheimer's Disease Neuroimaging Initiative is related to: International Genomics of Alzheimers Project is parent organization of: General Practitioner Assessment of Cognition is parent organization of: Alzheimers Association Research Roundtable is parent organization of: Biomarkers Across Neurodegenerative Diseases is parent organization of: Alzheimer's Association International Research Grant Program is parent organization of: Informant Questionnaire on Cognitive Decline in the Elderly is parent organization of: IADRP is parent organization of: CADRO |
Alzheimer's disease, Aging | Public, Available to the research community | ISNI: 0000 0004 0614 7003, nif-0000-00451, Crossref funder ID: 100000957, Wikidata: Q4738818, grid.422384.b | https://ror.org/0375f4d26 | SCR_007398 | Alzheimers Association, Alzheimer's Association | 2026-09-12 12:56:54 | 128 | |||||
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Centre dEtude du Polymorphisme Humain Resource Report Resource Website 100+ mentions |
Centre dEtude du Polymorphisme Humain (RRID:SCR_008026) | institution | The Centre d''Etude du Polymorphisme Humain (CEPH) is a research laboratory, the main activities of which are the setting up, storage, processing and distribution of DNA collections for the identification of genetic factors conferring susceptibility to complex disorders. These collections are established in partnership and full collaboration with external French or international research groups. The Foundation currently hosts the CEPH reference panel, the HGDP panel (Human genome Diversity Cell Line Panel) and several collections amounting mid-2008 to more than 250 000 samples. The goal of CEPH is to understand complex multifactorial disorders necessitates the establishment of structures facilitating access to large and integrated collection of individuals, characterized by a large number of variables emanating from different technologies and platforms. To achieve this goal, CEPH facilitates the setting up of integrated analyses combining clinical, genetic and environmental data, for the identification of susceptibility factors to complex multifactorial disorders Additionally, CEHP allows the reception, storage, processing and distribution of biological sample collections. At the same time, it promotes and participates in the design and setting up of genetic studies: - in partnership and full collaboration with external research groups - giving access to a large number of variables - in a sufficient number of subjects - allowing large scale integrated analyses | environmental, genome, genetic, analysis, biological, cell, clinical, disorder, distribution, diversity, dna, human, individual, laboratory, polymorphism, process, procession, reception, research, storage, structure, subject, technology, variable | is related to: International AMD Genetics Consortium | Wikidata: Q5464989, nif-0000-10191, ISNI: 0000 0004 0639 125X, grid.417836.f | https://ror.org/01rje3r53 | SCR_008026 | CEPH | 2026-09-12 12:56:59 | 304 | ||||||||
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Wien Center For Alzheimer's Disease and Memory Disorders Resource Report Resource Website |
Wien Center For Alzheimer's Disease and Memory Disorders (RRID:SCR_008755) | data or information resource, disease-related portal, portal, research forum portal, topical portal | A joint program between Mount Sinai Medical Center and the University of Miami Department of Psychiatry that seeks an end to Alzheimer's disease and similar disorders through research, diagnosis, education and treatment. The goals are to improve memory and mental responsiveness of Alzheimer's patients, delay the onset of the disease and, ultimately, find a cure. The Wien Center typically conducts multidisciplinary initiatives utilizing clinical trials. | alzheimer's disease, memory disorder, dementia, clinical, diagnosis, treatment, late adult human |
has parent organization: University of Miami; Florida; USA is parent organization of: Florida Brain Bank |
Aging | NIH | Public | nlx_143957 | SCR_008755 | Wien Center for Alzheimer's Disease and Memory Disorders | 2026-09-12 12:57:08 | 0 |
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