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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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European Mouse Phenotyping Resource of Standardised Screens Resource Report Resource Website 50+ mentions |
European Mouse Phenotyping Resource of Standardised Screens (RRID:SCR_003087) | EMPReSS | data or information resource, data set, narrative resource, standard specification | Database of validated Standard Operating Procedures (SOPs) for screens to determine the phenotype of a mouse, developed by the EUMORPHIA consortium. The SOP's cover all of the main body systems including: clinical chemistry, hormonal and metabolic systems, cardiovascular, allergy and infection, renal function, sensory function, neurological and behavioral function, cancer, bone and cartilage, and respiratory function. In addition, there are generic SOPs in histology, necropsy, pathology and gene expression. EMPReSS is a platform of individual tests. These can be performed as individual tests or grouped together in sequences, recommended in the EMPReSS database, to give more information on particular phenotype. Quick List of Current Pipelines: * EUMODIC Pipeline 1 * EUMODIC Pipeline 2 * GMC Pipeline * MGP Pipeline * Additional Tests * EUMODIC Pipeline 3 | phenotype, phenotyping, dysmorphology, body weight, blood pressure, calorimetry, ipgtt, dexa, x-ray, chemistry, clinical, heart weight, tibia length, standard operating procedure, FASEB list |
is related to: Understanding Human Disease Through Mouse Genetics is related to: Europhenome Mouse Phenotyping Resource is related to: Impress is related to: Europhenome Mouse Phenotyping Resource has parent organization: MRC Mammalian Genetics Unit |
PMID:17905814 | Free, Freely available | nif-0000-30492 | https://academic.oup.com/bioinformatics/article/21/12/2930/268092 | SCR_003087 | European Mouse Phenotyping Resource of Standardized Screens | 2026-09-12 12:55:51 | 78 | |||||
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XNAT - The Extensible Neuroimaging Archive Toolkit Resource Report Resource Website 50+ mentions |
XNAT - The Extensible Neuroimaging Archive Toolkit (RRID:SCR_003048) | XNAT | data management software, data processing software, software application, software resource, source code | Software platform designed to facilitate common management and productivity tasks for neuroimaging and associated data. | analyze, client application, collaboration, data archive, data management, data sharing, data store, informatics, metadata, middleware, middleware engine, neuroinformatics, open source, productivity task, quality control, sharing, software platform, user interface, workflow, xml schema, neuroimaging, mri, processing, image, clinical, dicom, anonymization, clinical assessment, application, ct, database application, eeg, meg, ecog, java, magnetic resonance, nifti-1, os independent, pet, spect, platform, web environment, FASEB list |
is used by: studyforrest.org is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC) is listed by: Debian is related to: MIRIAD is related to: pyxnat is related to: XNAT Extras is related to: XNAT Central is related to: NUNDA is related to: CardioVascular Research Grid (CVRG) is related to: ConnectomeDB is related to: NA-MIC Kit has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA |
NIBIB R01 EB009352; NIBIB U54 EB005149 |
PMID:17426351 | Free, Available for download, Freely available | nif-0000-00531 | http://www.nitrc.org/projects/xnat, https://sources.debian.org/src/xnat/ | SCR_003048 | Extensible Neuroimaging Archive Toolkit, Extensible Neuroimaging Archive Toolkit (XNAT) | 2026-09-12 12:55:50 | 66 | ||||
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Viral Immunology Center Resource Report Resource Website |
Viral Immunology Center (RRID:SCR_001089) | data or information resource, disease-related portal, laboratory portal, organization portal, portal, research forum portal, topical portal | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 18,2025. The National B Virus Resource Center is located in the Viral Immunology Center of Georgia State Universitys Department of Biology. Their laboratory is studying viruses that directly affect the central nervous system of infected hosts. Current projects in the laboratory are focused on the molecular biology of human and nonhuman primate alphaherpesviruses and the diseases they cause, immune response characterization, antiviral strategies, including drug discovery and high-throughput drug screening within unique, high containment laboratory suites. They are also actively engaged in the study of unique reoviruses that have the capacity to infect the central nervous systems of non human primates, langur viruses, and a newly isolated mangaby herpesvirus. Alphaherpesviruses target the central nervous system of susceptible hosts, and subsequently establish latent infections generally without severely damaging the host. There may be an initial acute phase when the virus successfully replicates in peripheral tissue of the host. This replication, when it occurs, induces a series of specific immune functions that can serve as markers of infection. We use these markers to design, develop and implement diagnostic assays that will be useful during the management of clinical disease. Each herpesvirus coexists peacefully with the natural host in which it has co-evolved, but when the viruses for any reason find themselves no longer in the natural host, the usual host:parasite relationship may change dramatically. In some closely related hosts the virus can replicate and, in some cases, pathogenesis of the infection is radically more severe than that which occurs in the natural host. For example, this can be seen when New World monkeys are infected with humans herpesviruses, e.g., HSV-1 or HSV-2, or when humans are infected with B virus from a macaque, a member of the Old World monkey family. Their studies focus on the mechanisms by which virus kills the host and how that process can be circumvented with early identification, appropriate antiviral drugs, and in the future, effective vaccines. We continually screen the efficacy of existing as well as novel antiviral agents to inhibit the growth of viruses that can potentially cross into the human population, either through occupational exposure or through more subtle contact. Their laboratory provides a global resource funded by National Institutes of Healths National Center for Research Resources to assist in the identification of zoonotic disease transmissions and develop enhanced strategies to detect virus in macaques. They particularly focus on the transmission of B virus from Asian monkeys to humans who come in contact with them. Members of the genus Macaca include rhesus monkeys, cynomolgus macaques, snow macaques, as well as all other macaques. If the macaque is in the midst of the acute or recurrent infection with B, virus can be transmitted to people who handle these monkeys through cuts, scratches, splashes, bites, or even contaminated equipment or surfaces, i.e., fomites. To counter the effects of this virus, the NIH and Centers for Disease Control and Prevention have instituted a critical set of guidelines for institutions to follow in the event of exposures. Their laboratory provides immediate support to these cases to assist in the rapid diagnosis of B virus infections and to determine the efficacy of selected treatment. Lifetime patient monitoring is provided to identify possible reactivation disease and to better track this unique herpesvirus as it has begun its existence in the human populations. Sponsors: The viral immunology center is funded by National Institutes of Healths National Center for Research Resources. | drug, acute, agent, alphaherpesvirus, antiviral, biology, b virus, center, central, clinical, cynomolgus, disease, herpes, host, hsv-1, hsv-2, human, immune, immunology, infect, infection, langur, macaque, mangaby, molecular, monkey, nervous system, nonhuman, parasite, pathogenesis, population, primate, reovirus, replicate, response, screening, snow, viral, virus | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-24367 | SCR_001089 | Viral Immunology Center | 2026-09-12 12:55:19 | 0 | |||||||||
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Vanderbilt University Medical Center Pharmacology Resource Report Resource Website |
Vanderbilt University Medical Center Pharmacology (RRID:SCR_001450) | Vanderbilt Pharmacology | data or information resource, department portal, organization portal, portal | At the Department of Pharmacology at Vanderbilt University Medical Center we engage in scientific discovery to elucidate biological mechanisms and develop novel therapeutics. We provide training focused on critical thinking to promote innovation, scholarship and integrity. To this end, we foster creativity, collegiality, and leadership. The Department is one of the most distinguished Pharmacology departments in the country and have placed in the top two NIH ranking positions for sixteen of the last twenty years. Research interests in the Department include five major areas: signal transduction, neuroscience, bioactive lipid metabolism, genetic basis of cardiovascular dysfunction, and drug metabolism. Molecules under investigation include G-protein coupled receptors (rhodopsin, adrenergic, serotonin and receptors), heterotrimeric G-proteins, ion channels, transporters and regulatory proteins such as arrestins, protein kinases and protein phosphatases. A strength in our research and training environment is that Vanderbilt University has a world-acclaimed Division of Clinical Pharmacology, which links the Department of Medicine with the Department of Pharmacology. Faculty members in the Division of Clinical Pharmacology focus on human disease and clinical enigmas as the origin of their questions for research. Basic scientists who pursue their inquiries in this environment are continually informed by their colleagues of the pathophysiological and potential therapeutic relevance that can be achieved by appropriate focus of their efforts. We have created one of the first programs in the country to answer the call from the National Institutes of Health (NIH) for more scientists trained in the area of drug discovery and development. A unique feature of the department is our outstanding Ph.D. training program. Almost 60 scientists in training are addressing important issues in fields such neuroscience, cardiovascular development, receptor signaling, and drug metabolism. Scientists in these areas are linked by a common interest in, and understanding of, the basic principles of drug action and design. This perspective makes our trainees ideally suited for a wide range of careers and our program is committed to developing leaders in academia, industry, and regulatory affairs. Postdoctoral and other positions are available. | pharmacology, clinical, signal transduction, neuroscience, bioactive lipid metabolism, cardiovascular dysfunction, drug metabolism, g-protein coupled receptor, rhodopsin, adrenergic, serotonin, receptor, heterotrimeric g-protein, ion channel, transporter, regulatory protein, arrestins, protein kinase, protein phosphatase, disease, drug discovery, drug development |
has parent organization: Vanderbilt University School of Medicine; Tennessee; USA has parent organization: Vanderbilt University Medical Center; Tennessee; USA |
Free, Freely Available | nif-0000-02295 | http://www.mc.vanderbilt.edu/vumcdept/pharm/ | SCR_001450 | Vanderbilt Department of Pharmacology | 2026-09-12 12:55:25 | 0 | ||||||
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PD-DOC Resource Report Resource Website |
PD-DOC (RRID:SCR_001596) | PD-DOC | data or information resource, data repository, database, portal, service resource, storage service resource, topical portal | THIS RESOURCE IS NO LONGER IN SERVICE, documented on December 02, 2011. Notice: This domain name expired on 10/29/11 and is pending renewal or deletion PD-DOC is a portal and a database resource, hosting a database and linking to other databases and data sets of clinical and translational data. PD-DOC functions to organize and facilitate clinical and translational research in Parkinson's disease. The PD-DOC Database contains standardized data collected by user institutions on large numbers of patients with Parkinsons disease and other parkinsonian disorders. In some cases, data is obtained at a single point in time, while in others data is collected repeatedly over time. The PD-DOC Database is composed of the Core Data Set (CDS) which consists of those variables required to be gathered for each subject whose data is entered into the PD-DOC database. In 2005, working groups of Udall Center and invited experts deliberated to establish the components of each CDS section (e.g. General Clinical, Cognitive/Behavioral, Postmortem Brain Neuropathological Findings). The PD-DOC CDS was established and designed to optimize data analyses and data mining for large numbers of subjects participating in a variety of research studies. In most cases corresponding DNA samples are available form the NINDS Human Genetic Repository (at Coriell). Much of the website is publicly available for viewing. To request access to sections of the website dealing with downloading or requesting data, requesting a consultation, or submitting data or other information you will need to register. Before registering, you should read the PD-DOC Policies. Note that PD-DOC data can be used for research purposes only. Once your registration is successfully completed you will be automatically logged into the website. | data, parkinson's disease, translational research, clinical, gds-15, cowat, dna, hoehn and yahr, idiopathic pd, lnst, merq, mmse, npi-q, parkinsonism, se/adl, updrs |
is related to: NINDS Repository has parent organization: University of Rochester; New York; USA |
NINDS U01NS050095 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10109 | SCR_001596 | The Parkinson's Disease Data and Organizing Center (PD-DOC), Parkinson's Disease Data and Organizing Center, The Parkinson's Disease Data and Organizing Center | 2026-09-12 12:55:28 | 0 | ||||||
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Epidemiology of Diabetes Interventions and Complications Resource Report Resource Website 1+ mentions |
Epidemiology of Diabetes Interventions and Complications (RRID:SCR_001468) | EDIC | bibliography, clinical trial, data or information resource, database, resource | Publications from a multi-center, longitudinal, observational study examining the risk factors associated with the long-term complications of type 1 diabetes. The study began in 1994 and follows the 1441 participants previously enrolled in the Diabetes Control and Complications Trial (DCCT), http://diabetes.niddk.nih.gov/dm/pubs/control/index.aspx. The primary aim of EDIC is to examine the long-term effects of conventional vs. intensive diabetes treatment received during the DCCT on the subsequent development and progression of microvascular, neuropathic and cardiovascular complications. This involves studying the influence of genetic factors and other factors such as HbA1c, blood pressure, lipid levels, and treatment modalities on the development and progression of these complications. Annual or biennial measurements (using DCCT methods, standardized protocols and central laboratories) of vascular events, albumin excretion, GFR, ECG, ankle-brachial BP index, serum lipids and HbA1c allows the following analyses: 1) continuation of intention-to-treat analyses to determine long-term effects of prior separation of glycemic levels; 2) risk factors for macrovascular outcomes; 3) correlation of progression of micro- and macrovascular outcomes. The current updated version of the EDIC Protocol is available for download. EDIC is made up of 28 clinical centers, one data coordinating center and one clinical coordinating center. | longitudinal, observational, nephropathy, macrovascular, complication, risk factor, clinical, genetic factor, hba1c, blood pressure, lipid level, treatment modality, complication |
is listed by: ClinicalTrials.gov is listed by: NIDDK Information Network (dkNET) is listed by: NIDDK Central Repository is related to: Diabetes Control and Complications Trial is related to: Diabetes Control and Complications Trial has parent organization: George Washington University; Washington D.C.; USA |
Type 1 diabetes, Diabetes | NIDDK 4U01DK094157 | Free, Freely Available | nlx_152698 | SCR_001468 | 2026-09-12 12:55:26 | 1 | ||||||
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Adult to Adult Living Donor Liver Transplantation Cohort Study Resource Report Resource Website |
Adult to Adult Living Donor Liver Transplantation Cohort Study (RRID:SCR_001494) | A2ALL | data or information resource, disease-related portal, portal, research forum portal, resource, topical portal | Study consisting of nine liver transplant centers with expertise in adult living-donor liver transplantation (LDLT) and a central data coordinating center to provide valuable information on the outcomes of adult to adult living donor liver transplantation (AALDLT) to aid decisions made by physicians, patients, and potential donors. The study will establish and maintain the infrastructure required to accrue and follow sufficient numbers of patients being considered for and undergoing AALDLT to provide generalizable data from adequately powered studies. The major aims of A2ALL are as follows: * Quantify the impact of choosing LDLT on the candidate for transplantation * Characterize the difference between LDLT and deceased donor liver transplant (DDLT) in terms of post-transplant outcomes, including patient and graft survival, surgical morbidity, and resource utilization on the recipient of a transplant * Determine the short- and long-term health and quality of life (QOL) impact of donation, including (a) morbidity after liver donation and (b) long-term health-related QOL of donors. * Standardize and assess the role of informed consent in affecting the decision to donate and satisfaction after living liver donation * Other aims include comparison of the severity of recurrence of hepatocellular carcinoma for DDLT versus LDLT, the systematic characterization of liver regeneration and function in donors and recipients, the evaluation of the differences in the immune response to LDLT versus DDLT, and the establishment of a robust data and sample repository on liver transplantation that may be used to study clinical and biological questions as new technologies and resources become available. Patients enrolled in the study will be followed and managed in a standardized fashion. | transplant, liver, adult human, risk factor, surgery, outcome, quality of life, clinical |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Michigan; Ann Arbor; USA |
Liver transplant, Liver disease | NIDDK 1U01DK62498 | PMID:18976306 PMID:18756453 PMID:16135918 |
Free, Freely available | nlx_152749 | http://www.nih-a2all.org/ | SCR_001494 | A2ALL: The Adult to Adult Living Donor Liver Transplantation Cohort Study | 2026-09-12 12:55:26 | 0 | |||
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Behavior Enhances Drug Reduction of Incontinence Resource Report Resource Website |
Behavior Enhances Drug Reduction of Incontinence (RRID:SCR_001495) | BE-DRI | bibliography, clinical trial, data or information resource, resource | Multi-center randomized clinical trial to determine if the addition of behavioral treatment to drug therapy for the treatment of urge incontinence will make it possible to discontinue the drug and still maintain a reduced number of accidents. The most popular treatments for urge incontinence are drug therapy and behavior therapy, each with its own limitations. In this clinical study, the Urinary Incontinence Treatment Network (UITN) aims to determine differences with the addition of behavioral treatment to drug therapy alone. | drug therapy, behavioral therapy, female, urinary incontinence, overactive bladder, combined modality therapy, quality of life, pelvic floor muscle exercise, tolterodine, clinical |
is listed by: ClinicalTrials.gov is listed by: NIDDK Information Network (dkNET) has parent organization: Urinary Incontinence Treatment Network |
Urge incontinence, Urinary Incontinence | NIDDK U01DK58225; NIDDK U01DK58234; NIDDK U01DK58229; NIDDK U01DK58231; NIDDK U01DK60397; NIDDK U01DK60401; NIDDK U01DK60395; NIDDK U01DK60393; NIDDK U01DK60380; NIDDK U01DK60379 |
PMID:16919506 | Free, Freely available | nlx_152752 | http://www.uitn.net/bedri.asp | SCR_001495 | 2026-09-12 12:55:26 | 0 | ||||
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Standardization of C-peptide measurements Resource Report Resource Website |
Standardization of C-peptide measurements (RRID:SCR_001499) | Standardization of c-peptide | data or information resource, narrative resource, resource, standard specification | Standardization of c-peptide by calibrating C-peptide measurement to a reference method can increase comparability between laboratories. The C-peptide standardization program is supported to establish reliability in results and facilitate the conduct of international clinical trials. For c-peptide, purified or processed material shows significant matrix effects and cannot be used for calibration. The C-peptide program has evaluated the use of single donor and pooled specimens for use by manufacturers in the calibration of these assays and determined that this strategy will reduce C-peptide variability among different assay methods. The standardization process through manufacturer re-calibration is ongoing. | c-peptide, insulin secretion, clinical, calibration |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Missouri School of Medicine; Missouri; USA |
Diabetes | NIDDK 200200409985 | PMID:18420730 | Free, Freely available | nlx_152766 | SCR_001499 | C-peptide Standardization | 2026-09-12 12:55:26 | 0 | ||||
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Diabetic Retinopathy Clinical Research Network Resource Report Resource Website 1+ mentions |
Diabetic Retinopathy Clinical Research Network (RRID:SCR_001514) | DRCR.net, DRCRnet | bibliography, clinical trial, data or information resource, data set, disease-related portal, portal, research forum portal, slide, topical portal | A collaborative network to facilitate multicenter clinical research of diabetic retinopathy, diabetic macular edema and associated conditions. It supports the identification, design, and implementation of multicenter clinical research initiatives focused on diabetes-induced retinal disorders. Principal emphasis is placed on clinical trials, but epidemiologic outcomes and other research may be supported as well. It currently includes over 109 participating sites (offices) with over 320 physicians throughout the United States. Closed and active studies are listed along with the associated protocols, public datasets, and publications. | eye, retina, clinical, clinical trial, epidemiology, outcome, ophthalmic, ophthalmology, experimental protocol |
is listed by: NIDDK Information Network (dkNET) has parent organization: Jaeb Center for Health Research |
Diabetic retinopathy, Diabetic macular edema, Diabetes, Retinopathy, Macular edema, Diabetes-induced retinal disorder | NEI EY14231; NEI EY018817 |
Public, Registration required, To download data sets | nlx_152816 | SCR_001514 | Diabetic Retinopathy Clinical Research Network (DRCR.net), DRCR Network | 2026-09-12 12:55:26 | 1 | |||||
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Longitudinal Assessment of Bariatric Surgery Resource Report Resource Website 1+ mentions |
Longitudinal Assessment of Bariatric Surgery (RRID:SCR_001536) | LABS | data or information resource, disease-related portal, narrative resource, portal, research forum portal, resource, topical portal | Consortium comprised of six clinical centers and a data coordinating center to facilitate coordinated clinical, epidemiological, and behavioral research in the field of bariatric surgery, through the cooperative development of common clinical protocols and a bariatric surgery database that will collect information from participating clinical centers. LABS will help pool the necessary clinical expertise and administrative resources to facilitate the conduct of multiple clinical studies in a timely, efficient manner. Also, the use of standardized definitions, clinical protocols, and data-collection instruments will enhance the investigator's ability to provide meaningful evidence-based recommendations for patient evaluation, selection, and follow-up care. The consortium was funded in September 2003. The investigators have collaboratively developed a core database and clinical protocols, and subject enrollment began in early 2005. A repository of data and biological specimens for future research also will be collected by the centers participating in LABS. These will provide valuable resources for future study of obesity and its complications. | clinical, epidemiology, behavior, longitudinal, risk, benefit, surgical procedure, clinical outcome, database, clinical trial, experimental protocol, biomaterial supply resource |
is listed by: NIDDK Information Network (dkNET) is listed by: NIDDK Research Resources has parent organization: University of Pittsburgh; Pennsylvania; USA |
Bariatric surgery, Obesity | NIDDK 5U01DK066557 | nlx_152842 | SCR_001536 | Longitudinal Assessment of Bariatric Surgery Consortium, LABS consortium, Longitudinal Assessment of Bariatric Surgery (LABS) Consortium | 2026-09-12 12:55:27 | 1 | ||||||
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Grinder Resource Report Resource Website 1+ mentions |
Grinder (RRID:SCR_000168) | Grinder | software resource | An open-source bioinformatic tool to create simulated omic shotgun and amplicon sequence libraries for all main sequencing platforms. The tool is available through multiple interfaces like GUI, CLI and API. It is useful for simulating clinical or environmental microbial communities and complements the use of in vitro mock communities. | simulation, amplicon, shotgun, genomic sequencing, clinical, metagenomic, transcriptomic and metatranscriptomic |
is listed by: OMICtools is listed by: Debian has parent organization: SourceForge |
PMID:22434876 DOI:10.1093/nar/gks251 |
Free, Available for download, Freely available | OMICS_01508 | https://sources.debian.org/src/grinder/ | SCR_000168 | 2026-09-12 12:55:04 | 3 | ||||||
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World Health Organization: The Global Health Library Resource Report Resource Website 1+ mentions |
World Health Organization: The Global Health Library (RRID:SCR_000391) | bibliography, data or information resource, portal, topical portal | The Global Health Library assembles health data, readable in many languages. The GHL aims to: * point to reliable information collections and systems, in which different users and user groups (ministries of health, policy makers, health workers, information providers, patients and their families, general public) can focus on the knowledge that best meets their health information needs; * act as a facilitator enabling access to information contents produced by numerous key providers - be they commercial companies, government institutions, civil society, not-for-profit organizations, and regional or international bodies; and * strive for universality, with focus on developing countries, and will act as a resource locator for print materials essential to areas that do not have access to electronic content. | clinical, health, human, people | has parent organization: World Health Organization | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10556 | http://www.who.int/ghl/en/ | SCR_000391 | GHL | 2026-09-12 12:55:08 | 2 | |||||||
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ALS Association Resource Report Resource Website 10+ mentions |
ALS Association (RRID:SCR_000442) | ALS Association | nonprofit organization | Established in 1985, The ALS Association is the only national non-profit organization fighting Lou Gehrig's Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure. As the preeminent ALS organization, The Association leads the way in research, care services, public education, and public policy giving help and hope to those facing the disease. The Association's nationwide network of chapters provides comprehensive patient services and support to the ALS community. The mission of The ALS Association is to lead the fight to treat and cure ALS through global research and nationwide advocacy, while also empowering people with Lou Gehrig's Disease and their families to live fuller lives by providing them with compassionate care and support. The ALS Association has committed more than $58 million to find effective treatments and a cure for Lou Gehrig's Disease. Our global research effort has helped increase the number of scientists working on ALS, advanced new discoveries and treatments, and has shed light on the complex genetic and environmental factors involved in ALS. Diversity exemplifies The ALS Association's research philosophy. The Association spearheads investigator-initiated projects that originate from the minds of scientists. It also has ALS Association-initiated projects in which research ideas come from a small, blue ribbon committee of scientists who reach out with specific projects for designated scientists in the field. The ALS Association offers multi-year grants to established investigators, as well as one-year starter research awards. The Association is proud to administer The Milton Safenowitz Post-Doctoral Fellowship for ALS Research, which is the only post-doctoral fellowship for ALS research. In addition, The ALS Association's Sheila Essey Award, the premier ALS award, recognizes achievement in research. The ALS Association holds workshops each year that bring together scientists researching ALS and other neurodegenerative diseases to generate new research suggestions and fresh insight. In addition, our TREAT ALS (Transitional Research Advancing Therapy for ALS) initiative combines efficient new drug discovery with priorities set for existing drug candidates to accelerate clinical testing of compounds with promise for the disease. Our Clinical Management Research Program focuses on managing the care of people with ALS in such areas as nutrition, respiration, mobility and psychosocial needs. Since 1998, The Association has funded 21 clinical management research projects representing a total commitment of $750,000. The Association produces a series of manuals and videos as well as a DVD, called Living with ALS, that educate patients about all aspects of the disease. | research, clinical care center, treatment, cure, care service, public education, public policy, post-doctoral fellowship, clinical, grant, award | Amyotrophic Lateral Sclerosis | nif-0000-00449, Wikidata: Q4652439, grid.430438.8, ISNI: 0000 0004 0590 7963, Crossref funder ID: 100000971 | https://ror.org/00mwp5989 | SCR_000442 | Amyotrophic Lateral Sclerosis Association, ALS Association - Fighting Lou Gehrig's Disease, ALS Association | 2026-09-12 12:55:09 | 11 | |||||||
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Jefferson Hospital for Neuroscience Alzheimers Disease and Dementia Center Resource Report Resource Website |
Jefferson Hospital for Neuroscience Alzheimers Disease and Dementia Center (RRID:SCR_000579) | Jefferson Alzheimer's Disease and Dementia Center | data or information resource, disease-related portal, patient-support portal, portal, topical portal | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 6,2023. If you or someone you love has been diagnosed with dementia caused by Alzheimer's disease, you'll be in good hands at Jefferson. Our neurologists and psychiatrists are dedicated to: Compassionate care for individuals with Alzheimer's disease; Supporting families; Advancing care through research into the epidemiology and treatment of neurodegenerative diseases. We interact with patients very early in the disease progression, when impairment is typically mild; deliver state-of-the-art care; provide information; build care-giving skills; and help caregivers connect with community support and plan for the future. | alzheimer's disease, late adult human, neurodegenerative disease, dementia, brain bank, clinical trial, clinical | has parent organization: Thomas Jefferson University; Pennsylvania; USA | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_144497 | http://www.jeffersonhospital.org/departments-and-services/alzheimers-disease-dementia-center.aspx | SCR_000579 | Jefferson Hospital for Neuroscience Alzheimers Disease Dementia Center, Jefferson Hospital for Neuroscience Alzheimer's Disease Dementia Center, Jefferson Hospital for Neuroscience Alzheimer's Disease and Dementia Center | 2026-09-12 12:55:11 | 0 | ||||||
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VariantMaster Resource Report Resource Website |
VariantMaster (RRID:SCR_000569) | VariantMaster | software resource | Software program that extracts causative variants in familial and sporadic genetic diseases. The algorithm takes into account predicted variants (SNPs and indels) in affected individuals or tumor samples and utilizes the row (BAM) data to robustly estimate the conditional probability of segregation in a family, as well as the probability of it being de novo or somatic. In familial cases, various modes of inheritance are considered: X-linked, autosomal dominant, and recessive (homozygosity or compound heterozygosity). Moreover, it integrates phenotypes and genotypes, and employs Annovar to produce additional information as allelic frequencies in general population and damaging scores. | unix/linux, clinical, genetics, high throughput sequencing, monogenic disease, variant, snp, indel |
is listed by: OMICtools has parent organization: SourceForge |
Genetic disease, Tumor | PMID:24389049 | Free, Available for download, Freely available, | OMICS_02261 | SCR_000569 | VariantMaster - Extract causative variants for monogenic and sporadic genetic diseases | 2026-09-12 12:55:11 | 0 | |||||
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Cystic Fibrosis Mutation Database Resource Report Resource Website 10+ mentions |
Cystic Fibrosis Mutation Database (RRID:SCR_000685) | CFTR1, CFMDB | data or information resource, data repository, database, service resource, storage service resource | Collection of mutations in CFTR gene for international cystic fibrosis genetics research community. Provides up to date information about individual mutations in CFTR gene. All known CFTR mutations and sequence variants have been converted to standard nomenclature recommended by Human Genome Variation Society. On line process for submission of new mutations has been added.While they continue to ensure quality of data, they urge international community to give them feedback and suggestions. Clinical information in this database relates only to details of discovery of specific mutations. As part of 2010 upgrade, CFTR1 joined new project called CFTR2 - Clinical and Functional TRanslation of CFTR. Links to CFTR2 for many mutations in CFTR1 will provide up-to-date summaries of genotype-phenotype information from patient registries around the world. | Gene, genetic, amino acid, clinical, cystic fibrosis, mutation, phenotype, genotype-phenotype, genotype, dna sequence, mouse, sequence, genetic variation, polymorphism, translation, function, sequence variation, metadata standard, cftr2, FASEB list | is related to: CFTR2 | Cystic fibrosis | Free, Freely available | nif-0000-21105, r3d100012093 | https://doi.org/10.17616/R38356 | SCR_000685 | 2026-09-12 12:55:13 | 42 | ||||||
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NIH - Rapid Access to Interventional Development Resource Report Resource Website 1+ mentions |
NIH - Rapid Access to Interventional Development (RRID:SCR_000713) | analysis service resource, biomaterial analysis service, biomaterial manufacture, funding resource, material analysis service, material service resource, production service resource, service resource | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 14, 2025.NIH-RAID makes available at no cost to researchers and organizations certain critical resources needed for the development of new therapeutic agents. This program, part of the Translational Research component of Reengineering the Clinical Research Enterprise, uses resources of NCI's Developmental Therapeutics Program and the National Heart Lung and Blood Institutes (NHLBI) Gene Therapy Resource Program. The services provided will depend upon the stage of the project and the strength of the preliminary data. Services available include: production, bulk supply, GMP manufacturing, formulation, development of an assay suitable for pharmacokinetic testing, and animal toxicology. Assistance also will be provided in the regulatory process, through access to independent product development planning expertise. Proposals in support of animal efficacy studies or synthesis and formulation of recombinant proteins or monoclonal antibodies will not be accepted. NIH-RAID is not a grant program. Successful projects will gain access to the governments contract resources, as well as the assistance of the NIH in establishing and implementing a product development plan. Funds to support individual projects will come both from the Roadmap and from individual Institutes, with Institutes assuming the bulk of support in the specific disease areas germane to their mission. This co-sponsorship is critical because of the resource and expertise needs and because NIH-RAID cannot support the full developmental pipeline; an Institute partnership may therefore be important for subsequent translational efforts. To obtain access to NIH-RAID resources, applications must be submitted electronically through Grants.gov using SF424. Applications are initially screened to determine whether the resources requested are appropriate for this program. Then they are reviewed by the NIH Center for Scientific Research. The results of that evaluation along with supplemental information from the lead investigator will guide final Institute and Roadmap resource allocation. The services provided will depend upon the stage of the project and the strength of the preliminary data. When a lead therapeutic agent has been selected and proposed for preclinical development, the following services are available: For small molecules, natural products, peptides, oligonucleotides, and gene vectors: Synthesis, Scale-up production, Development of analytical methods, Development of suitable formulations, Isolation and purification of natural products, Pharmacokinetic/ADME studies including bioanalytical method development, Range-finding initial toxicology, IND-directed toxicology, Manufacture of clinical trial supplies, Product development planning and advice in IND preparation For recombinant proteins and monoclonal antibodies: Pharmacokinetic/ADME studies including bioanalytical method development, Range-finding initial toxicology, IND-directed toxicology, Product development planning and advice in IND preparation When a lead therapeutic agent has not yet been selected and proposed for preclinical development, the following services are available: For small molecules, natural products, peptides, oligonucleotides, and gene vectors: Synthesis, Development of analytical methods, Isolation and purification of natural products, Preliminary Pharmacokinetic/ADME studies, including bioanalytical method development, Preliminary toxicology For recombinant proteins and monoclonal antibodies, Preliminary Pharmacokinetic/ADME studies, including bioanalytical method development, Preliminary toxicology In some cases the NIH-RAID program will support only one or two key steps for preclinical development, while in other cases it may be possible to provide assistance with most of the development tasks needed to file an Investigational New Drug (IND) application to the Food and Drug Administration (FDA). When the NIH-RAID program does not provide all of the remaining services required for IND submission, it is expected that other resources will be in place to complete development steps not supported by NIH-RAID. Funding Resource,. | adme, applied, biomaterial method development, clinical, pharmacology, student, toxicology | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-00543 | http://nihroadmap.nih.gov/raid/ | SCR_000713 | NIH-RAID | 2026-09-12 12:55:14 | 1 | ||||||||
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Online Education for the International Research Community: AboutIntroduction to Clinical Drug and Substance Abuse Research Methods Resource Report Resource Website |
Online Education for the International Research Community: AboutIntroduction to Clinical Drug and Substance Abuse Research Methods (RRID:SCR_000802) | certificate program, continuing medical education, short course, training resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented on November 07, 2012. Decemeber 15, 2011 - Thank you for your interest in DrugAbuseResearchTraining.org. The site, courses, and resources are no longer available. Please send an email to inquiry (at) md-inc.com if you would like to be notified if the site or courses become available again. Introduction to Clinical Drug and Substance Abuse Research Methods is an online training program intended to introduce clinicians and substance abuse professionals to basic clinical research methods. The program is divided into four modules. Each module covers an entire topic and includes self-assessment questions, references, and online resources: * The Neurobiology of Drug Addiction * Biostatistics for Drug and Substance Abuse Research * Evaluating Drug and Substance Abuse Programs * Designing and Managing Drug and Substance Abuse Clinical Trials The learning objectives of this program are to help you: * Evaluate the benefits of alternative investigative approaches for answering important questions in drug abuse evaluation and treatment. * Define the proper levels of measurement and appropriate statistical methods for a clinical study. * Address common problems in data collection and analysis. * Anticipate key human subjects and ethical issues that arise in drug abuse studies. * Interpret findings from the drug abuse research literature and prepare a clinical research proposal. * Prepare research findings for internal distribution or publication in the peer reviewed literature. * Recognize drug addiction as a cyclical, chronic disease. * Understand and describe the brain circuits that are affected by addicting drugs, and explain to others the effects of major classes of addicting drugs on brain neurotransmitters. * Utilize new pharmacologic treatments to manage persons with drug addiction. Physicians can earn AMA PRA Category 1 Credit and purchase a high resolution printable electronic CME certificate(view sample); non-physicians can purchase high resolution printable electronic certificate of course participation that references AMA PRA Category 1 credit (view sample). This program does not offer printed certificates. | clinical, drug, substance abuse, research, course, clinician, neurobiology, addiction, literature, disease, brain, circuit, neurotransmitter, pharmacologic, treatment, education, training | NIDA | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-37940 | SCR_000802 | Neurobiology of Addiction Online Course | 2026-09-12 12:55:15 | 0 | ||||||||
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Undiagnosed Diseases Network Resource Report Resource Website 1+ mentions |
Undiagnosed Diseases Network (RRID:SCR_014415) | training resource | A network of clinical sites and core laboratories to accelerate discovery and innovate the way medical professionals diagnose and treat patients with previously undiagnosed diseases. It will serve to test whether this type of cross-disciplinary approach to disease diagnosis is feasible to implement in academic medical centers. It also provides clinical training of contemporary genomic approaches in diagnosing disease. | network, clinical, undiagnosed disease, rare disease | has parent organization: National Human Genome Research Institute | Available to the research community | SCR_014415 | NIH Undiagnosed Diseases Network | 2026-09-12 12:58:16 | 1 |
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