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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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Northwestern University Behavioral Phenotyping Core Facility Resource Report Resource Website |
Northwestern University Behavioral Phenotyping Core Facility (RRID:SCR_017765) | BPC | access service resource, core facility, service resource | Facility dedicated to help to determine behavioral effects of genetic manipulations, potential pharmaceuticals, aging, and other manipulations upon normal behavior, and learning and memory capacities of rodents used as model systems. Provides mouse and rat stereotaxic surgery, helps design behavioral studies. | Behavioral, effect, genetic, manipulation, pharmaceutical, aging, rodent, model, mouce, surgery, phenotypin, service, core | Restricted | ABRF_303 | SCR_017765 | Behavioral Phenotyping Core | 2026-02-15 09:21:26 | 0 | ||||||||
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Cancer Therapeutics Response Portal (CTRP) Resource Report Resource Website |
Cancer Therapeutics Response Portal (CTRP) (RRID:SCR_026293) | data or information resource, topical portal, portal | Cancer Therapeutics Response Portal (CTRP) links genetic, lineage, and other cellular features of cancer cell lines to small-molecule sensitivity with the goal of accelerating discovery of patient-matched cancer therapeutics. CTRP can be mined to develop insights into small-molecule mechanisms of action and novel therapeutic hypotheses, and to support future discovery of drugs matched to patients based on predictive biomarkers. | cancer cell lines, genetic, lineage, small-molecule sensitivity, small-molecule mechanisms of action, novel therapeutics, discovery of drugs, predictive biomarkers, | Free, Freely available | SCR_026293 | 2026-02-15 09:23:59 | 0 | |||||||||||
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Genentech Resource Report Resource Website 1000+ mentions |
Genentech (RRID:SCR_003997) | Genentech | commercial organization | A biotechnology corporation that uses human genetic information to discover, develop, manufacture and commercialize medicines to treat patients with serious or life-threatening medical conditions. | drug, genetic, medicine, biotechnology, oncology, immunology, tissue growth, tissue repair, neuroscience, infectious disease, microbiology, medical imaging |
is related to: Alzheimers Disease Genetics Consortium has parent organization: Roche is parent organization of: GMAP |
Infectious disease, Cancer | nlx_158417 | SCR_003997 | Genentech Inc, F. Hoffmann-La Roche Ltd / Genentech | 2026-02-14 02:00:35 | 3306 | |||||||
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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 | 2026-02-14 02:01:28 | 294 | ||||||||
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Australian Center For Plant Functional Genomics PTY LTD Resource Report Resource Website |
Australian Center For Plant Functional Genomics PTY LTD (RRID:SCR_008383) | ACPFG | institution | At the Australian Centre for Plant Functional Genomics (ACPFG), scientists are improving wheat and barley''s tolerance to environmental stresses such as drought, heat, salinity and nutrient toxicities. These stresses known as abiotic stresses, are a major cause of yield and quality loss throughout the world and cause significant problems for cereal growers. These scientists are developing the technologies and resources needed to produce new cereal varieties that allow sustainable farming to generate economic, social and environmental benefits to Australia. ACPFG research is helping to ensure Australia maintains its competitive position in cereal production. - Identify the genetic mechanisms that control tolerance to specific stresses and compare these with those controlling broad range tolerance to abiotic stresses - Use genome-wide analyses to define key cellular processes that enable adapted plants to withstand abiotic stress, and to apply that understanding to the genetic improvement of crops such as wheat and barley - Unravel regulatory networks that control plant growth under abiotic stress - Identify ways of manipulating these networks, through existing genetic diversity or through functional genomics technologies, to deliver tangible industry outcomes, namely cereal varieties better tailored to hostile environments | australian, plant, functional, genomics, scientist, wheat, barley, technology, economic, social, environmental, research, cereal, genetic, mechanism, tolerence, abiotic, stress | Australian Research Council ; Grains Research and Development Corporation ; Department for Environment and Heritage Government of South Australia ; University of Adelaide; Adelaide; Australia ; University of Melbourne; Victoria; Australia ; University of South Australia; Adelaide; Australia ; University of Queensland; Brisbane; Australia |
Wikidata: Q781368, grid.499658.f, ISNI: 0000 0000 8685 1658, nif-0000-30023 | https://ror.org/00xwvfm64 | SCR_008383 | ACPFG | 2026-02-14 02:01:40 | 0 | |||||||
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Cold Spring Harbor Laboratory Resource Report Resource Website 1000+ mentions |
Cold Spring Harbor Laboratory (RRID:SCR_008326) | CSHL | nonprofit organization | Non profit, private research and education institution that performs molecular and genetic research used to generate methods for better diagnostics and treatments for cancer and neurological diseases. Research of cancer causing genes and their respective signaling pathways, mutations and structural variations of the human genome that could cause neurodevelopmental and neurodegenerative illnesses such as autism, schizophrenia, and Alzheimer's and Parkinson's diseases and also research in plant genetics and quantitative biology. | institution, education, genetic, alzheimer's, autism, biological, biotechnology, cancer, diagnostic, dna, genome, molecular, biology, neurodegenerative, neurodevelopmental, neurological, schizophrenia, signaling, structure |
is affiliated with: CyVerse is related to: GenomeScope is parent organization of: RMAP is parent organization of: Cold Spring Harbor Protocols: Collected Resources - Behavioral Assays is parent organization of: Genes to Cognition Online is parent organization of: Gramene is parent organization of: Exonic Splicing Enhancer Finder is parent organization of: bioRxiv is parent organization of: Brain Architecture Project is parent organization of: SCPD - Saccharomyces cerevisiae promoter database is parent organization of: AtProbe is parent organization of: FASTX-Toolkit is parent organization of: Chronux is parent organization of: Learn about SMA website is parent organization of: Transcriptional Regulatory Element Database is parent organization of: CSHL - Hannon Lab is parent organization of: Zebra Finch Song Learning Consortium is parent organization of: SpliceTrap is parent organization of: ESEfinder 3.0 is parent organization of: DNA From The Beginning: AN Animated Primer on the Basics of DNA, Genes, and Heredity is parent organization of: 3D Brain is parent organization of: Alta-Cyclic is parent organization of: WormBase is parent organization of: Reactome is parent organization of: ScanImage is parent organization of: FASTX-Toolkit is parent organization of: Cold Spring Harbor Laboratory Microscopy Shared Resource Core Facility |
nif-0000-24690, grid.225279.9, ISNI: 0000 0004 0387 3667, Wikidata: Q609768 | https://ror.org/02qz8b764 | SCR_008326 | CSHL | 2026-02-14 02:01:39 | 3333 | |||||||
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Oregon National Primate Research Center Resource Report Resource Website 100+ mentions |
Oregon National Primate Research Center (RRID:SCR_008291) | ONPRC | institution | Center that aims to develop biomedical technologies using nonhuman primate (NHP) models. Its goal is to uncover the root causes of various disease and disorders, unlock secrets of the brain, and unleash new methods of diagnostics and treatment. | NPRC, NPRC Consortium, ORIP, enhancement, genetic, aids, animal, biomedical, brain, cancer, cure, delivery, depression, developmental, diabetes, diagnostic, disease, disorder, health, human, model, nonhuman, obesity, premature, primate, reproductive, research, scientific, stem cell, technology, therapy, treatment, vaccine | is listed by: National Primate Research Center Consortium | NIH Office of the Director P51 OD011092; NIH Office of the Director U42 OD023038; NIH Office of the Director U42 OD010426; NIH Office of the Director R24 OD021324 |
Wikidata: Q7101277, Crossref funder ID: 100008143, nif-0000-24358, grid.410436.4, ISNI: 0000 0004 0619 6542 | https://ror.org/05fcfqq67 | SCR_008291 | ONPRC | 2026-02-14 02:01:40 | 108 | ||||||
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tranSMART Resource Report Resource Website 10+ mentions |
tranSMART (RRID:SCR_005586) | tranSMART | software resource | tranSMART is a knowledge management platform that enables scientists to develop and refine research hypotheses by investigating correlations between genetic and phenotypic data, and assessing their analytical results in the context of published literature and other work. tranSMART is licensed through GPL 3. The integration, normalization, and alignment of data in tranSMART permits users to explore data very efficiently to formulate new research strategies. Some of tranSMART''s specific applications include: * Revalidating previous hypotheses * Testing and refining novel hypotheses * Conducting cross-study meta-analysis * Searching across multiple data sources to find associations of concepts, such as a gene''s involvement in biological processes or experimental results * Comparing biological processes and pathways among multiple data sets from related diseases or even across multiple therapeutic areas Data Repository The tranSMART Data Repository combines a data warehouse with access to federated sources of open and commercial databases. tranSMART accommodates: * Phenotypic data, such as demographics, clinical observations, clinical trial outcomes, and adverse events * High content biomarker data, such as gene expression, genotyping, pharmacokinetic and pharmaco-dynamics markers, metabolomics data, and proteomics data * Unstructured text-data, such as published journal articles, conference abstracts and proceedings, and internal studies and white papers * Reference data from sources such as MeSH, UMLS, Entrez, GeneGo, Ingenuity, etc. * Metadata providing context about datasets, allowing users to assess the relevance of results delivered by tranSMART Data in tranSMART is aligned to allow identification and analysis of associations between phenotypic and biomarker data, and it is normalized to conform with CDISC and other standards to facilitate search and analysis across different data sources. tranSMART also enables investigators to search published literature and other text sources to evaluate their analysis in the context of the broader universe of reported research. External data can also be integrated into the tranSMART data repository, either from open data projects like GEO, EBI Array Express, GCOD, or GO, or from commercially available data sources. Making data accessible in tranSMART enables organizations to leverage investments in manual curation, development costs of automated ETL tools, or commercial subscription fees across multiple research groups. Dataset Explorer tranSMART''s Dataset Explorer provides flexible, powerful search and analysis capabilities. The core of the Dataset Explorer integrates and extends the open source i2b2 application, Lucene text indexing, and GenePattern analytical tools. Connections to other open source and commercial analytical tools such as Galaxy, Integrative Genomics Viewer, Plink, Pathway Studio, GeneGo, Spotfire, R, and SAS can be established to expand tranSMART''s capabilities. tranSMART''s design allows organizations flexibility in selecting analytical tools accessible through the Dataset Explorer, and provides file export capabilities to enable researchers to use tools not accessible in the tranSMART portal. | source code, genetic, phenotype, gene, data storage repository, data analysis service |
is used by: eTRIKS is used by: RanchoBiosciences |
nlx_146211 | http://www.transmartproject.org/ | SCR_005586 | 2026-02-14 02:00:57 | 13 | ||||||||
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Illumina Resource Report Resource Website 1000+ mentions |
Illumina (RRID:SCR_010233) | Illumina, Inc. | commercial organization | American company incorporated that develops, manufactures and markets integrated systems for the analysis of genetic variation and biological function. Provides a line of products and services that serve the sequencing, genotyping and gene expression and proteomics markets. Its headquarters are located in San Diego, California. | Commercial, organization, develope, manufacture, system, analysis, genetic, sequencing, genotyping, gene, expression, proteomic |
is related to: fermi-lite is related to: Illumina NextSeq 2000 system is parent organization of: Strelka is parent organization of: Tk-GO is parent organization of: BaseSpace is parent organization of: Illumina iSeq 100 Sequencing System |
nlx_156846, grid.185669.5, Wikidata: Q2068984, ISNI: 0000 0004 0507 3954 | https://ror.org/05k34t975 | SCR_010233 | Inc., Illumina | 2026-02-14 02:01:54 | 2340 | |||||||
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TAIR Resource Report Resource Website 5000+ mentions |
TAIR (RRID:SCR_004618) | TAIR, AGI LocusCode | data or information resource, database | Database of genetic and molecular biology data for the model higher plant Arabidopsis thaliana. Data available includes the complete genome sequence along with gene structure, gene product information, metabolism, gene expression, DNA and seed stocks, genome maps, genetic and physical markers, publications, and information about the Arabidopsis research community. Gene product function data is updated every two weeks from the latest published research literature and community data submissions. Gene structures are updated 1-2 times per year using computational and manual methods as well as community submissions of new and updated genes. TAIR also provides extensive linkouts from data pages to other Arabidopsis resources. The data can be searched, viewed and analyzed. Datasets can also be downloaded. Pages on news, job postings, conference announcements, Arabidopsis lab protocols, and useful links are provided. | genetic, molecular biology, gene, genome, structure, product, metabolism, gene expression, dna, seed stock, genome map, genetic marker, physical marker, genome sequence, gene product, blast, experimental protocol, gold standard |
is used by: NIF Data Federation is listed by: OMICtools is listed by: re3data.org is listed by: DataCite is related to: AmiGO is related to: Saskatoon Arabidopsis T-DNA mutant population SK Collection is related to: CLENCH has parent organization: Carnegie Institution for Science is parent organization of: TAIR Keyword Browser is parent organization of: PubSearch |
NSF DBI-0850219; corporate and nonprofit organizations |
PMID:22140109 PMID:17986450 PMID:12444417 PMID:12519987 PMID:18287693 |
r3d100010185, nlx_61477, OMICS_01662 | https://doi.org/10.17616/R3QW21 | SCR_004618 | AGI LocusCode, The Arabidopsis Information Resource | 2026-02-14 02:00:59 | 7421 | |||||
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University of Leicester; Leicester; United Kingdom Resource Report Resource Website |
University of Leicester; Leicester; United Kingdom (RRID:SCR_004900) | university | Public research university based in Leicester, England. Famous for the discovery of genetic fingerprinting and contributing to the discovery and identification of the remains of King Richard III. | public, research, university, England, discovery, genetic, fingerprinting |
is related to: Predict-TB is related to: GetReal is related to: READNA is related to: EMIF is related to: Collaborative Computing Project for NMR is parent organization of: Virtual Genetics Education Centre is parent organization of: CCLG is parent organization of: cafe variome is parent organization of: GWAS Central is parent organization of: Database of Osteogenesis Imperfecta and Type III Collagen Variants is parent organization of: GWAS Central is parent organization of: CCLG Tissue Bank is parent organization of: University of Leicester Advanced Imaging Facility |
nlx_20502 | SCR_004900 | The University of Leicester, University of Leicester | 2026-02-14 02:01:00 | 0 | |||||||||
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Gramene Resource Report Resource Website 500+ mentions |
Gramene (RRID:SCR_002829) | GR | data or information resource, database | Curated, open-source, integrated data resource for comparative functional genomics in crops and model plant species to facilitate the study of cross-species comparisons using information generated from projects supported by public funds. It currently hosts annotated whole genomes in over two dozen plant species and partial assemblies for almost a dozen wild rice species in the Ensembl browser, genetic and physical maps with genes, ESTs and QTLs locations, genetic diversity data sets, structure-function analysis of proteins, plant pathways databases (BioCyc and Plant Reactome platforms), and descriptions of phenotypic traits and mutations. The web-based displays for phenotypes include the Genes and Quantitative Trait Loci (QTL) modules. Sequence based relationships are displayed in the Genomes module using the genome browser adapted from Ensembl, in the Maps module using the comparative map viewer (CMap) from GMOD, and in the Proteins module displays. BLAST is used to search for similar sequences. Literature supporting all the above data is organized in the Literature database. In addition, Gramene now hosts a variety of web services including a Distributed Annotation Server (DAS), BLAST and a public MySQL database. Twice a year, Gramene releases a major build of the database and makes interim releases to correct errors or to make important updates to software and/or data. Additionally you can access Gramene through an FTP site. | crop, plant genome, genetic, blast, gene, genome, genetic diversity, pathway, protein, marker, quantitative trait locus, comparative map, phenotype, genomics, physiology, comparative, grain, expressed sequence tag, trait, mutation, environment, taxonomy, web service, bio.tools, FASEB list |
is used by: NIF Data Federation is listed by: re3data.org is listed by: bio.tools is listed by: Debian is related to: AmiGO is related to: Gene Ontology is related to: Plant Ontology is related to: Trait Ontology is related to: EnvO is related to: BioCyc has parent organization: Cold Spring Harbor Laboratory has parent organization: Cornell University; New York; USA is parent organization of: Trait Ontology is parent organization of: Plant Environmental Conditions is parent organization of: Plant Trait Ontology is parent organization of: Cereal Plant Development Ontology is parent organization of: Cereal Plant Gross Anatomy Ontology |
USDA IFAFS 00-52100-9622; USDA 58-1907-0-041; USDA 1907-21000-030; NSF 0321685; NSF 0703908; NSF 0851652 |
PMID:21076153 PMID:17984077 PMID:16381966 |
Free, Freely available | r3d100010856, nif-0000-02926, nlx_65829, biotools:gramene | https://bio.tools/gramene https://doi.org/10.17616/R3GG7M |
SCR_002829 | GR PROTEIN, RiceGenes, GR REF, GR GENE, Gramene: A Resource for Comparative Grass Genomics, GR QTL | 2026-02-14 02:00:19 | 778 | ||||
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MONARCH Initiative Resource Report Resource Website 10+ mentions |
MONARCH Initiative (RRID:SCR_000824) | Monarch | data or information resource, database | Repository of information about model organisms, in vitro models, genes, pathways, gene expression, protein and genetic interactions, orthology, disease, phenotypes, publications, and authors, and ability to navigate multi-scale spatial and temporal phenotypes across in vivo and in vitro model systems in context of genetic and genomic data, using semantics and statistics. Discovery system provides basic and clinical science researchers, informaticists, and medical professionals with integrated interface and set of discovery tools to reveal genetic basis of disease, facilitate hypothesis generation, and identify novel candidate drug targets. Database that indexes authoritative information on experimental models of disease from MGI, RGD and ZFIN. | disease, animal model, phenotype, model organism, in vitro model, gene, pathway, gene expression, protein interaction, genetic interaction, orthology, disease, publication, author, genetic, genomic, model system, genotype, drug, in vivo model |
uses: Animal QTLdb uses: Ensembl Variation uses: Human Phenotype Ontology is used by: NIF Data Federation is related to: Mouse Genome Informatics (MGI) is related to: Rat Genome Database (RGD) is related to: Zebrafish Information Network (ZFIN) is related to: openSNP is related to: Ancora is related to: PhenoGen Informatics is related to: Lifespan Observations Database has parent organization: Oregon Health and Science University; Oregon; USA is parent organization of: monarch-ontologies |
NIH Office of the Director R24 OD011883 | PMID:26269093 | Free, Freely available | r3d100011594, nlx_152525, SCR_001373, nlx_152748 | https://orip.nih.gov/comparative-medicine/programs/genetic-biological-and-information-resources https://doi.org/10.17616/R31M09 |
SCR_000824 | MONARCH Integrated Disease Model, MONARCH Integrated Disease Models View, MONARCH Disease Models View, The MONARCH Initiative | 2026-02-14 01:59:54 | 12 | ||||
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Duke Model System Genomics Resource Report Resource Website |
Duke Model System Genomics (RRID:SCR_001051) | access service resource, service resource | Portal to the Duke University Model Systems Genomics facility equipped to perform molecular genetic research in Drosophilia. Equipment includes stereo microscopes for fly pushing and microdissection, a compound microscope and a microscope equipped to view GFP and RFP as well as two inverted microscopes for embryo injections. | molecular, genetic, drosophilia, microdissection, fly pushing, embryo injections, model system genetics |
is listed by: ScienceExchange is related to: Duke University Labs and Facilities has parent organization: Duke University; North Carolina; USA |
THIS RESOURCE IS NO LONGER IN SERVICE | SciEx_586 | SCR_001051 | Duke University Model System Genomics | 2026-02-14 01:59:58 | 0 | ||||||||
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Asper Biotech Resource Report Resource Website 10+ mentions |
Asper Biotech (RRID:SCR_000700) | instrument resource | A genetic testing company for rare and complex disorders and syndromes. The company specializes in retinal disorders, reproductive medicine and oncology. They also offer custom genotyping services. | genetic, test, syndrome, disorder, retinal, reproductive, medicine, oncology, genotyping, genotype, dna, blood, saliva, microarray, primer | nif-0000-30125 | SCR_000700 | AsperBio | 2026-02-14 01:59:49 | 10 | ||||||||||
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TIDE BC Resource Report Resource Website 10+ mentions |
TIDE BC (RRID:SCR_003924) | TIDE | data or information resource, portal | A collaborative care and research initiative with a focus on prevention and treatment of Intellectual disability (ID) that is due to inborn errors of metabolism (IEM), which can be treated with diet or drugs. Health care policy and institutional culture is still operating under the old premise that all ID is incurable and thus, many children born with treatable ID are at risk of not being treated. To acknowledge the multidisciplinary scope and the ways in which health care professionals and researchers will collaborate, the goals of the TIDE BC project are demonstrated within a framework of 7 Work Packages: * Implementation of a new Protocol for diagnostic evaluation of ID, focusing of treatable conditions; * Development of infrastructure to facilitate implementation, evaluation and sustainability of the Protocol; * Investments into next generation genomic technologies; * Improving evidence of and access to treatments; * Evaluation and health economy; * Knowledge dissemination; * Education and Mentoring. The objectives addressed in all Work Packages reflect a highly integrated cluster combining clinical care, research, evaluation, and knowledge dissemination. | child, prevention, treatment, pediatric, genetic | Intellectual disability, Inborn error of metabolism | BC Childrens Hospital Foundation | nlx_158289 | SCR_003924 | TIDE-BC, Treatable Intellectual Disability Endeavor in B.C. | 2026-02-14 02:05:27 | 27 | |||||||
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Compilation of Genetics Resource Databases Resource Report Resource Website 10+ mentions |
Compilation of Genetics Resource Databases (RRID:SCR_017501) | data or information resource, portal | Portal provides list of genetic resources such as Brain Atlases and genomes for various species provided by National Institute of Drug Abuse. | Genetic, data, brain, atlas, information, National, Institute, Drug, Abuse, FASEB list | Restricted | SCR_017501 | 2026-02-14 02:05:35 | 49 | |||||||||||
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Rice Proteome Database Resource Report Resource Website 1+ mentions |
Rice Proteome Database (RRID:SCR_000743) | data or information resource, database |
THIS RESOURCE IS NO LONGER IN SERVICE, documented July 22, 2016. A database on the proteome of rice that contains reference maps based on two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) of proteins from rice tissues and subcellular compartments. |
rice, proteome, gene, genetic, eleoctrophoresis, 2d-page, tissue, subcellular compartments | has parent organization: National Institute of Agrobiological Sciences; Ibaraki; Japan | PMID:16217611 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-03409 | http://dbarchive.biosciencedbc.jp/en/rpd/desc.html | SCR_000743 | 2026-02-14 02:05:33 | 2 | |||||||
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Wiring the Brain Resource Report Resource Website |
Wiring the Brain (RRID:SCR_005528) | Wiring the Brain | data or information resource, narrative resource, blog | This blog highlights and comments on current research and hypotheses relating to how the brain wires itself up during development, how the end result can vary in different people and what happens when it goes wrong. It includes discussions of the genetic and neurodevelopmental bases of traits such as intelligence and personality characteristics, as well as of conditions such as schizophrenia, autism, dyslexia, epilepsy, synaesthesia and others. | research, brain, development, genetic, wiring, neurodevelopment, trait, intelligence, personality, schizophrenia, autism, dyslexia, epilepsy, synaesthesia | Schizophrenia, Autism, Dyslexia, Epilepsy, Synaesthesia, Etc. | nlx_144622 | SCR_005528 | 2026-02-14 02:05:52 | 0 | |||||||||
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Epilepsy Genetic Association Database Resource Report Resource Website 1+ mentions |
Epilepsy Genetic Association Database (RRID:SCR_006840) | data or information resource, database | 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. | epilepsy, gene, genome, genetic, bias, disease, interleukin-1-beta, meta-analysis, pharmacogenetic, pharmacogenetics, published, repository, research, researcher, studies, study, temporal lobe epilepsy (tle), tool, unpublished | nif-0000-10221 | SCR_006840 | epiGAD | 2026-02-14 02:06:27 | 5 |
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