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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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Korea National Institute of Health Resource Report Resource Website 10+ mentions |
Korea National Institute of Health (RRID:SCR_001959) | KNIH | institution | Institute dedicated to medical research to improve biomedical innovation and public health in South Korea. | health research institute, south korea | is parent organization of: Genovar | THIS RESOURCE IS NO LONGER IN SERVICE | grid.415482.e, nlx_156100, ISNI: 0000 0004 0647 4899, Crossref funder ID: 501100003653 | https://ror.org/00qdsfq65 | SCR_001959 | Korea NIH | 2026-08-01 12:01:55 | 11 | ||||||
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SNP Function Portal Resource Report Resource Website 1+ mentions |
SNP Function Portal (RRID:SCR_001954) | SNP Function Portal | data analysis service, data or information resource, database, service resource, production service resource, analysis service resource | Database for exploring the function implication of single nucleotide polymorphism (SNP) alleles. It is designed to be a clearing house for all public domain SNP functional annotation data, as well as in-house functional annotations derived from different data sources. It currently contains SNP functional annotations in six major categories including genomic elements, transcription regulation, protein function, pathway, disease and population genetics. Besides extensive SNP functional annotations, it includes a search engine that accepts different types of genetic markers as input and identifies all genetically related SNPs based on the HapMap Phase II data as well as the relationship of different markers to known genes. As a result, the system allows users to identify the potential biological impact of genetic markers and complex relationships among genetic markers and genes, and it greatly facilitates knowledge discovery in genome-wide SNP scanning experiments. | single nucleotide polymorphism, linkage disequibrilium, functional annotation, function, annotation, genomic element, transcription regulation, protein function, pathway, disease, population genetics |
is listed by: OMICtools has parent organization: University of Michigan; Ann Arbor; USA |
PMID:16873516 | THIS RESOURCE IS NO LONGER IN SERVICE | OMICS_01928 | SCR_001954 | 2026-08-01 12:02:06 | 4 | |||||||
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flowType Resource Report Resource Website 1+ mentions |
flowType (RRID:SCR_001957) | software resource | Software for phenotyping Flow Cytometry assays using multidimentional expansion of single dimentional partitions. | software package, mac os x, unix/linux, windows, r, flow cytometry |
is listed by: OMICtools has parent organization: Bioconductor |
PMID:22383736 | THIS RESOURCE IS NO LONGER IN SERVICE | OMICS_05613 | SCR_001957 | flowType - Phenotyping Flow Cytometry Assays | 2026-08-01 12:01:39 | 9 | |||||||
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Virtual Genetics Education Centre Resource Report Resource Website |
Virtual Genetics Education Centre (RRID:SCR_001958) | VGEC | data or information resource, narrative resource, training material | Hub of evaluated genetics-related teaching resources for teachers and learners in schools and higher education, health professionals and the general public. Suggest or submit a learning resource to the VGEC. Resources include: * simple experiments suitable for all ages * tutorial material * videos on useful techniques * current and relevant links to other evaluated resources The Virtual Genetics Education Centre (VGEC) * Provides information and genetics education resources for higher education, colleges, schools, health professionals and the general public. * Encourages collaboration in the development, evaluation and sharing of genetics education resources * provides links to, and evaluates, sources of information and educational material about genetics. * Explores innovative approaches to teaching and learning in genetics, such as the SWIFT project for example where Second Life is being used to teach some aspects of genetics in a virtual laboratory. | education, genetics, development, teaching, dna, experiment, college student, child, adult, health professional, adolescent, k-12, gene, chromosome, video, evaluation, sharing, learning | has parent organization: University of Leicester; Leicester; United Kingdom | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10529 | SCR_001958 | Virtual Genetics Education Center, GENIE VGEC | 2026-08-01 12:02:06 | 0 | |||||||
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University of Leeds - Computational Biology Group Resource Report Resource Website |
University of Leeds - Computational Biology Group (RRID:SCR_001956) | topical portal, data or information resource, portal | The University of Leeds Computational Biology Group is an interdisciplinary research group based in the Faculty of Biological Sciences, and is part of the Centre for Nonlinear Studies. Research interests are at the interfaces of nonlinear dynamics, computational science and general physiology of excitable tissue (nervous system, cardiac and uterine muscle). A central theme is the reconstruction of tissue and organ physiology and pathologies from networks of intracellular, membrane and cellular models. Sponsors: | biological science, cardiac muscle, cellular model, computational biology, intracellular model, membrane model, nervous system, nonliear study, organ, pathology, physiology, tissue, uterine muscle | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10528 | http://www.cbiol.leeds.ac.uk/ | SCR_001956 | Leeds CBiol | 2026-08-01 12:01:55 | 0 | ||||||||
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Cognitive Neuroscience Society Resource Report Resource Website |
Cognitive Neuroscience Society (RRID:SCR_001990) | data or information resource, portal, meeting resource, community building portal, job resource, training resource, people resource | The Cognitive Neuroscience Society (CNS) is committed to the development of mind and brain research aimed at investigating the psychological, computational, and neuroscientific bases of cognition. Since its founding in 1994, the Society has been dedicated to bringing its 2000 worldwide members the latest research and dialogues in order to facilitate public, professional and scientific discourse. The term cognitive neuroscience has now been with us for almost three decades, and identifies an interdisciplinary approach to understanding the nature of thought. Our members, who are engaged in research focused on elucidating the biological underpinnings of mental processes, form a network of scientists and scholars working at the interface of mind, brain and behavior research. The findings of this research are presented at our member-supported annual scientific conference. The three-day program of plenary speakers, symposia, posters and special events covers all aspects of cognitive neuroscience research. The Society also disseminates information regarding employment opportunities, training fellowships, research grants, and information on related scientific conferences in its monthly newsletter. Our members can receive the Journal of Cognitive Neuroscience at a substantial discount. | behavior, brain, cognition, cognitive neuroscience, computational, human, mind, neuroscientific, psychological, research | nif-0000-10675 | SCR_001990 | CNS | 2026-08-01 12:02:07 | 0 | ||||||||||
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Minimum Information for Biological and Biomedical Investigations Resource Report Resource Website 1+ mentions |
Minimum Information for Biological and Biomedical Investigations (RRID:SCR_002042) | MIBBI | narrative resource, data or information resource, standard specification | A common portal for minimum information (MI) checklists to act as a one-stop shop for those exploring the range of extant projects, foster collaborative development and ultimately promote gradual integration. Goals include * To increase the visibility of projects developing guidance for the reporting of biological and biomedical science. * To encourage appropriate collaborative development between projects to avoid duplication of effort or competition. * To promote the adoption of consensus guidance on reporting by journals and funders. | minimum information, bioscience, metadata standard, MDAR |
lists: MIAPA lists: Minimum Information About a Simulation Experiment is listed by: FORCE11 is related to: Genomic Standards Consortium is related to: MIGen has parent organization: FAIRsharing |
BBSRC BB/E025080/1 | PMID:18688244 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-12075 | http://www.mibbi.org/, http://mibbi.sourceforge.net/, https://www.force11.org/node/4660 | http://www.biosharing.org/mibbi | SCR_002042 | MIBBI: Minimum Information for Biological and Biomedical Investigations | 2026-08-01 12:02:07 | 1 | |||
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BioModels Resource Report Resource Website 100+ mentions |
BioModels (RRID:SCR_001993) | BIOMD | data or information resource, data repository, storage service resource, portal, database, service resource, topical portal | Repository of mathematical models of biological and biomedical systems. Hosts selection of existing literature based physiologically and pharmaceutically relevant mechanistic models in standard formats. Features programmatic access via Web Services. Each model is curated to verify that it corresponds to reference publication and gives proper numerical results. Curators also annotate components of models with terms from controlled vocabularies and links to other relevant data resources allowing users to search accurately for models they need. Models can be retrieved in SBML format and import/export facilities are being developed to extend spectrum of formats supported by resource. | FAIR sharing, mathematical model, computational model, simulation, kinetic model, annotation, web service, data analysis service, systems biology, biological model, biology, molecular biology, nucleotide sequence, gene expression, protein, gene, dna, rna, genetics, gold standard |
is listed by: 3DVC is listed by: re3data.org is listed by: DataCite is related to: SBML is related to: PathCase Pathways Database System has parent organization: European Bioinformatics Institute is parent organization of: Kinetic Simulation Algorithm Ontology |
BBSRC BB/F010516/1; NIGMS R01 GM070923 |
PMID:20587024 PMID:16381960 |
CC0, Public Domain Dedication, Cf. our terms of use. | nif-0000-02609, r3d100010789 | http://www.ebi.ac.uk/biomodels/ | SCR_001993 | BioModels Database - A Database of Annotated Published Models, BioModels Database, BioModels | 2026-08-01 12:01:40 | 249 | ||||
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National Eye Health Education Program Resource Report Resource Website 1+ mentions |
National Eye Health Education Program (RRID:SCR_002049) | data or information resource, portal, narrative resource, training resource, organization portal, training material | NEI established NEHEP to increase awareness among healthcare professionals and the public of scientifically based health information that can be applied to preserving sight and preventing blindness. NEHEP works in partnership with a variety of public and private organizations that conduct eye health education programs. Program activities are designed to promote the importance of early detection and timely treatment of eye disease and the use of vision rehabilitation services using strategies that are culturally appropriate, health-literate, and evidence-based. NEHEP ensures that vision is a health priority by translating eye and vision research into public and professional education programs. NEHEP supports collaboration among eye health professionals, healthcare providers, patients, and the public. NEHEP programs provide healthcare professionals with information, materials, and resources to educate patients and the public about eye health and the importance of comprehensive dilated eye examinations. NEHEP is supported by a Planning Committee and a Partnership, which bring a vast array of knowledge about eye health and experience with populations at higher risk for eye disease. NEHEP Programs *Diabetic Eye Disease: The NEHEP Diabetic Eye Disease (DED) Education Program is designed to increase awareness about DED among people with diabetes, particularly those at higher risk. *Glaucoma: The NEHEP Glaucoma Education Program provides information about glaucoma to people at higher risk as well as those living with the disease. *Low Vision: The NEHEP Low Vision Education Program is designed to create awareness among adults, their families and friends, and the general public about vision rehabilitation services. *Ojo con su Vision: Ojo con su visin or Watch out for your vision is the Spanish-language program of NEHEP that targets the Hispanic/Latino community. Healthy Vision Program Healthy People 2010, the health promotion and disease prevention framework for the Nation, identifies the most significant risks to health and establishes national goals to reduce those risks. Focus area 28 of Healthy People 2010, Vision and Hearing, includes 10 vision objectives known as Healthy Vision. The Healthy Vision objectives identify national eye health concerns, and encourage individuals, organizations, and businesses to help address these concerns in their communities. *Healthy Vision 2010 Focusing on examination and prevention, eye diseases, injury and safety, and vision rehabilitation, Healthy Vision 2010 is designed to help you determine what you can do in your home, community, business, or state to help improve the Nation's eye health. *Healthy Vision Community Awards Program The Healthy Vision Community Awards Program provides awards of up to 10,000 for community-based eye health education programs. The program objectives address examinations and prevention, eye diseases, injury and safety, and vision rehabilitation. *Healthy Vision Month May is Healthy Vision Month, a national eye health observance sponsored by NEI and the National Eye Health Education Program Partnership. Healthy Vision Month is devoted to elevating vision as a public health priority. Each year focuses on a specific eye health topic. *Healthy Vision Community Programs Database The Healthy Vision Community Programs Database is a searchable collection of community-based vision health programs from the different U.S. states and territories. It stimulates ideas for creative eye health education projects and promotes networking among interested groups. Outlook Newsletter: Outlook is the electronic newsletter of the National Eye Health Education Program (NEHEP). Outlook provides quarterly updates on eye health education, disease prevention activities, and NEHEP activities and materials. Related Research: NEHEP represents an extension of the support that NEI provides to vision research, where results are disseminated to health professionals, patients, and the public. | early detection, education, education programs, eye, eye disease, eye health, blindness, diabetic eye disease, glaucoma, hispanic, latino, low vision, prevention, rehabilitation services, spanish-language program, treatment, vision | nif-0000-00576 | http://www.nei.nih.gov/nehep/index.asp | SCR_002049 | NEHEP | 2026-08-01 12:01:58 | 4 | |||||||||
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SHORTY Resource Report Resource Website 1+ mentions |
SHORTY (RRID:SCR_002048) | data analysis software, software application, software resource, sequence analysis software, data processing software | Software for targeted de novo assembly of microreads with mate pair information and sequencing errors. | sequencing, dna, de novo, microreads, assembler, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
PMID:19208115 | Free, Available for download, Freely available | biotools:shorty, OMICS_00030 | https://bio.tools/shorty | SCR_002048 | 2026-08-01 12:02:07 | 3 | |||||||
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ASPGD Resource Report Resource Website 100+ mentions |
ASPGD (RRID:SCR_002047) | ASPGD, ASPGD LOCUS, ASPGD REF | data or information resource, data repository, storage service resource, database, service resource | Database of genetic and molecular biological information about the filamentous fungi of the genus Aspergillus including information about genes and proteins of Aspergillus nidulans and Aspergillus fumigatus; descriptions and classifications of their biological roles, molecular functions, and subcellular localizations; gene, protein, and chromosome sequence information; tools for analysis and comparison of sequences; and links to literature information; as well as a multispecies comparative genomics browser tool (Sybil) for exploration of orthology and synteny across multiple sequenced Sgenus species. Also available are Gene Ontology (GO) and community resources. Based on the Candida Genome Database, the Aspergillus Genome Database is a resource for genomic sequence data and gene and protein information for Aspergilli. Among its many species, the genus contains an excellent model organism (A. nidulans, or its teleomorph Emericella nidulans), an important pathogen of the immunocompromised (A. fumigatus), an agriculturally important toxin producer (A. flavus), and two species used in industrial processes (A. niger and A. oryzae). Search options allow you to: *Search AspGD database using keywords. *Find chromosomal features that match specific properties or annotations. *Find AspGD web pages using keywords located on the page. *Find information on one gene from many databases. *Search for keywords related to a phenotype (e.g., conidiation), an allele (such as veA1), or an experimental condition (e.g., light). Analysis and Tools allow you to: *Find similarities between a sequence of interest and Aspergillus DNA or protein sequences. *Display and analyze an Aspergillus sequence (or other sequence) in many ways. *Navigate the chromosomes set. View nucleotide and protein sequence. *Find short DNA/protein sequence matches in Aspergillus. *Design sequencing and PCR primers for Aspergillus or other input sequences. *Display the restriction map for a Aspergillus or other input sequence. *Find similarities between a sequence of interest and fungal nucleotide or protein sequences. AspGD welcomes data submissions. | function, gene, gene name, annotation, aspergillus, aspergillus nidulans, chromosome, community, dna, genome, genomic, localization, orthology, phenotype, protein, protein-coding genes, s. cerevisiae, sequence, allele, data analysis service, bio.tools, FASEB list |
is used by: NIF Data Federation is listed by: bio.tools is listed by: Debian is related to: Candida Genome Database is related to: AmiGO has parent organization: Stanford University School of Medicine; California; USA has parent organization: Broad Institute |
NIAID R01 AI077599 | PMID:19773420 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-12244, biotools:aspgd | http://www.aspergillusgenome.org/, https://bio.tools/aspgd | SCR_002047 | Aspergillus Genome Database, ASPGD REF, ASPGD LOCUS | 2026-08-01 12:01:41 | 212 | ||||
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Brain and Behavior Research Foundation Resource Report Resource Website 10+ mentions |
Brain and Behavior Research Foundation (RRID:SCR_001992) | topical portal, data or information resource, funding resource, portal |
The Brain and Behavior Research Foundation (formerly NARSAD, the National Alliance for Research on Schizophrenia and Depression) is committed to alleviating the suffering of mental illness by awarding grants that will lead to advances and breakthroughs in scientific research. Additionally, learn about brain and behavior disorders and upcoming events. 100% of all donor contributions for research are invested in NARSAD Grants leading to discoveries in understanding causes and improving treatments of disorders in children and adults, such as depression, bipolar disorder, schizophrenia, autism, attention deficit hyperactivity disorder, and anxiety disorders like obsessive-compulsive and post-traumatic stress disorders. Over a quarter of a century, we have awarded nearly $300 million worldwide to more than 3,000 scientists carefully selected by our prestigious Scientific Council. We receive no government funding. All of our work relies on contributions from families, foundations and other caring donors. |
adult, child, attention deficit-hyperactivity disorder, autism, behavior disorder, bipolar disorder, brain, depressive disorder, human, mental health, research, mental disease, neuropsychiatric illness, proceedings, grant, schizophrenia, post-traumatic stress disorder, anxiety disorder, autism, obsessive-compulsive disorder | nif-0000-12459 | http://www.narsad.org/ | SCR_001992 | National Alliance on Research in Schizophrenia and Depression, NARSAD: The Worlds Leading Charity Dedicated to Mental Health Research, NARSAD: The Brain and Behavior Research Fund, Brain & Behavior Research Foundation, Brain Behavior Research Foundation, National Alliance for Research on Schizophrenia Depression | 2026-08-01 12:01:56 | 26 | |||||||||
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www.brainmapping.org Resource Report Resource Website 1+ mentions |
www.brainmapping.org (RRID:SCR_001987) | data or information resource, training resource, portal, community building portal, knowledge environment, software resource, people resource | This is a topical portal dedicated to the communication of news, science, and information of interest to the brain mapping community, and to sharing and promoting the science of brain mapping. The purpose and goal of brain mapping is to advance the understanding of the relationship between structure and function in the human brain. Scientists in this field seek to gain knowledge of the physical processes that underly human sensation, attention, awareness and cognition. These results are immediately applicable to surgical intervention, to the design of medical interventions and to the treatment of psychological and psychiatric disorders. | function, attention, awareness, brain, brain mapping, cognition, cognitive neuroscience, human, journals, manufacturers, mri, mri safety, scientific societies, sensation, structure, subjects, neuroimaging, video | has parent organization: University of California at Los Angeles; California; USA | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-10669 | SCR_001987 | brainmapping.org | 2026-08-01 12:02:07 | 1 | ||||||||
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International Society for Magnetic Resonance in Medicine Resource Report Resource Website 1+ mentions |
International Society for Magnetic Resonance in Medicine (RRID:SCR_001988) | ISMRM | institution | The International Society for Magnetic Resonance in Medicine is an international, nonprofit, scientific association whose purpose is to promote communication, research, development, and applications in the field of magnetic resonance in medicine and biology and other related topics and to develop and provide channels and facilities for continuing education in the field. In addition to its large scientific meetings, the Society holds workshops and publishes two journals, Magnetic Resonance in Medicine and the Journal of Magnetic Resonance Imaging, and a newsletter, MR Pulse. It also sponsors study groups on specific areas of scientific interest and chapters based on geographical location. Its multidisciplinary membership of over 6,000 consists of clinicians, physicists, engineers, biochemists, and technologists. The ISMRMs inception, on January 1, 1994, resulted from a merger of the Society of Magnetic Resonance in Medicine and the Society of Magnetic Resonance Imaging forming the Society of Magnetic Resonance (now named the International Society for Magnetic Resonance in Medicine). The purposes of the Society are: (A) (i) To promote communication, research, development, applications, and the availability of information on magnetic resonance in medicine and biology and other related topics internationally; (ii) To develop and provide channels and facilities for continuing education and communication in the field, to publish and assist in the publishing of journals and other publications in the field; and (iii) To provide information and advice on those aspects of public policy which are concerned with magnetic resonance in medicine and biology and other related topics, and otherwise perform charitable, scientific and educational functions with respect to magnetic resonance applications in medicine and biology and other related topics. (B) To work with or for, and to co-operate with local, regional and national governments and governmental and private agencies, organizations, firms and institutions in efforts to accomplish one or more of the above purposes. (C) To ensure that scientists and clinicians working in the field have equal and fair opportunities to contribute to it. The site lists a partial list of NMR and MRI resources available on the World Wide Web. The content of these sites is not controlled or endorsed in any way by the ISMRM or SMRT. Sections devoted to MR safety and MRI information for patients is also available. Study groups are established to foster interaction among members with a common interest in topical and active areas of MR. If you are a member of the ISMRM or SMRT, you may become a member of any number of study groups; however, the cost of membership for each study group is US20. Recorded educational presentations, oral presentations, traditional posters, and electronic posters Available only to Meeting registrants - Now online | biology, bookstore, collaboration, journals, magnetic resonance, medicine, mri, mr safety, newsletter, nmr, scientific association, study groups | grid.420361.2, ISNI: 0000 0001 2107 6555, nif-0000-10673 | https://ror.org/038wdy960 | SCR_001988 | ISMRM | 2026-08-01 12:01:56 | 3 | ||||||||
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ISCBFM - International Society for Cerebral Blood Flow and Metabolism Resource Report Resource Website |
ISCBFM - International Society for Cerebral Blood Flow and Metabolism (RRID:SCR_001989) | ISCBFM | data or information resource, portal, narrative resource, meeting resource, k- program resource, topical portal, training resource | The International Society for Cerebral Blood Flow & Metabolism is a corporation operated exclusively for the purpose of promoting the advancement of education in the science of cerebral blood flow and metabolism throughout the world. The ISCBFM produces a quarterly newsletter, an official journal (Journal of Cerebral Blood Flow & Metabolism), have a yearly meeting, opportunities to host summer schools and a job board. ISCBFM members organize summer schools which are courses that have the aim to bring together young and experienced scientists for educational purposes. The biennial Brain Meetings also have a substantial part of the time allocated for educational purposes for young scientists interested in the field of cerebral blood flow and metabolism. Preference will be given to suggestions that are seen as a complement to scheduled courses in connection with the Brain Meetings and to courses that are given in between Brain Meetings. | brain, cerebral blood flow, human, metabolism, newsletter, summer school, k-12 | is related to: Journal of Cerebral Blood Flow and Metabolism | nif-0000-10674 | SCR_001989 | International Society for Cerebral Blood Flow and Metabolism, International Society for Cerebral Blood Flow Metabolism, ISCBFM - International Society for Cerebral Blood Flow Metabolism | 2026-08-01 12:01:40 | 0 | ||||||||
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World Parkinson Congress Resource Report Resource Website 1+ mentions |
World Parkinson Congress (RRID:SCR_002034) | topical portal, data or information resource, disease-related portal, portal | A nonprofit organization dedicated to providing an international forum for the latest scientific discoveries, medical practices and caregiver initiatives related to Parkinson's disease. It hosts the annual World Parkinson Congress, an event which focuses on bringing physicians, scientists, allied health professionals, caregivers and people diagnosed with Parkinson's disease together, in order to create a global dialogue that will help expedite treatment practices and the discovery of a cure . | parkinson's disease, pd, international forum, disease related portal | Parkinson's disease | Free | nif-0000-11855 | SCR_002034 | World Parkinson's Disease Congress | 2026-08-01 12:02:07 | 1 | ||||||||
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ADaCGH2 Resource Report Resource Website |
ADaCGH2 (RRID:SCR_001981) | software resource | Software for analysis and plotting of array comparative genomic hybridization (CGH) data. It allows usage of Circular Binary Segementation, wavelet-based smoothing (both as in Liu et al., and HaarSeg as in Ben-Yaacov and Eldar), HMM, BioHMM, GLAD, CGHseg. Most computations are parallelized (either via forking or with clusters, including MPI and sockets clusters) and use ff for storing data. | standalone software, mac os x, unix/linux, windows, r, copy number variant, microarray, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: Bioconductor |
PMID:24532724 | Free, Available for download, Freely available | biotools:adacgh2, OMICS_03697 | https://bio.tools/adacgh2 | SCR_001981 | ADaCGH2 - Analysis of big data from aCGH experiments using parallel computing and ff objects | 2026-08-01 12:02:07 | 0 | ||||||
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World Parkinson Disease Association Resource Report Resource Website 1+ mentions |
World Parkinson Disease Association (RRID:SCR_002035) | topical portal, data or information resource, disease-related portal, portal | THIS RESOURCE IS NO LONGER IN SERVICE, documented August 23, 2016. The World Parkinson's Disease Association is an alliance of members from all over the world who have come together to share information about Parkinson's disease. In order to further Parkinson's research and better the condition of those diagnosed with the disease, the Association: establishes computerized connections; takes part in and/or finances research activities; urges pharmaceutical companies and government institutions of the various countries to support the guidelines recommended by the associations of Parkinson's patients; and coordinates and promotes interchange of information among its members with the aim of solving problems of mutual interest. | parkinson's disease, research, therapy, pd, topical portal, disease related portal | Parkinson's disease | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-11857 | SCR_002035 | WPDA | 2026-08-01 12:01:57 | 1 | ||||||||
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Wellcome Trust Case Control Consortium Resource Report Resource Website 100+ mentions |
Wellcome Trust Case Control Consortium (RRID:SCR_001973) | WTCCC | data or information resource | Consortium of 50 research groups across the UK to harness the power of newly-available genotyping technologies to improve our understanding of the aetiological basis of several major causes of global disease. The consortium has gathered genotype data for up to 500,000 sites of genome sequence variation (single nucleotide polymorphisms or SNPs) in samples ascertained for the disease phenotypes. Analysis of the genome-wide association data generated has lead to the identification of many SNPs and genes showing evidence of association with disease susceptibility, some of which will be followed up in future studies. In addition, the Consortium has gained important insights into the technical, analytical, methodological and biological aspects of genome-wide association analysis. The core of the study comprised an analysis of 2,000 samples from each of seven diseases (type 1 diabetes, type 2 diabetes, coronary heart disease, hypertension, bipolar disorder, rheumatoid arthritis and Crohn's disease). For each disease, the case samples have been ascertained from sites widely distributed across Great Britain, allowing us to obtain considerable efficiencies by comparing each of these case populations to a common set of 3,000 nationally-ascertained controls also from England, Scotland and Wales. These controls come from two sources: 1,500 are representative samples from the 1958 British Birth Cohort and 1,500 are blood donors recruited by the three national UK Blood Services. One of the questions that the WTCCC study has addressed relates to the relative merits of these alternative strategies for the generation of representative population cohorts. Genotyping for this main Case Control study was conducted by Affymetrix using the (commercial) Affymetrix 500K chip. As part of this study a total of 17,000 samples were typed for 500,000 SNPs. There are two additional components to the study. First, the WTCCC award is part-funding a study of host resistance to infectious diseases in African populations. The same approach has been used to type 2,000 cases of tuberculosis (TB) and 2,000 cases of malaria, as well as 2,000 shared controls. As well as addressing diseases of major global significance, and extending WTCCC coverage into the area of infectious disease, the inclusion of samples of African origin has obvious benefits with respect to methodological aspects of genome-wide association analysis. Second, the WTCCC has, for four additional diseases (autoimmune thyroid disease, breast cancer, ankylosing spondylitis, multiple sclerosis), completed an analysis of 15,000 SNPs designed to represent a large proportion of the known non-synonymous coding SNPs across the genome. This analysis has been performed at the WTSI using a custom Infinium chip (Illumina). Data release The genotypic data of the control samples (1958 British Birth Cohort and UK Blood Service) and from seven diseases analyzed in the main study are now available to qualified researchers. Summary genotype statistics for these collections are available directly from the website. Access to the individual-level genotype data and summary genotype statistics is by application to the Consortium Data Access Committee (CDAC) and approval subject to a Data Access Agreement. WTCCC2: A further round of GWA studies were funded in April 2008. These include 15 WTCCC-collaborative studies and 12 independent studies be supported totaling approximately 120,000 samples. Many of the studies represent major international collaborative networks that have together assembled large sample collections. WTCCC2 will perform genome-wide association studies in 13 disease conditions: Ankylosing spondylitis, Barrett's oesophagus and oesophageal adenocarcinoma, glaucoma, ischaemic stroke, multiple sclerosis, pre-eclampsia, Parkinson's disease, psychosis endophenotypes, psoriasis, schizophrenia, ulcerative colitis and visceral leishmaniasis. WTCCC2 will also investigate the genetics of reading and mathematics abilities in children and the pharmacogenomics of statin response. Over 60,000 samples will be analyzed using either the Affymetrix v6.0 chip or the Illumina 660K chip. The WTCCC2 will also genotype 3,000 controls each from the 1958 British Birth cohort and the UK Blood Service control group, and the 6,000 controls will be genotyped on both the Affymetrix v6.0 and Illumina 1.2M chips. WTCCC3: The Wellcome Trust has provided support for a further round of GWA studies in January 2009. These include 5 WTCCC-collaborative studies to be carried out in WTCCC3 and 5 independent studies, across a range of diseases. Many of the studies represent major international collaborative networks that have together assembled large sample collections. WTCCC3 will perform genome-wide association studies in the following 4 disease conditions: primary biliary cirrhosis, anorexia nervosa, pre-eclampsia in UK subjects, and the interactions between donor and recipient DNA related to early and late renal transplant dysfunction. The WTCCC3 will also carry out a pilot in a study of the genetics of host control of HIV-1 infection. Over 40,000 samples will be analyzed using the Illumina 660K chip. The WTCCC3 will utilize the 6,000 control genotypes generated by the WTCCC2. | gene, genomic, genetics, microarray, genome-wide association study, snp, genome-wide association, blood, dna, genotype, variation, genome, sequence variant, copy number variation, genetic variation, phenotype, disease |
is related to: Psychiatric Genomics Consortium has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom |
Bipolar disorder, Coronary artery disease, Crohn's disease, Rheumatoid arthritis, Type 1 diabetes, Type 2 diabetes, Hypertension, Control, Multiple sclerosis, Breast cancer, Ankylosing spondylitis, Autoimmune thyroid disease, Malaria, Tuberculosis, Inflammatory bowel disease, Barrett's esophagus, Esophageal adenocarcinoma, Glaucoma, Ischemic stroke, Pre-eclampsia, Parkinson's disease, Psychosis endophenotypes, Psoriasis, Schizophrenia, Ulcerative colitis, Visceral leishmaniasis, Primary biliary cirrhosis, Anorexia nervosa, Human immunodeficiency virus, Renal transplant dysfunction, Diabetes | Wellcome Trust ; Bill and Melinda Gates Foundation ; Wellcome Trust Sanger Institute; Hinxton; United Kingdom |
PMID:17554300 | Access to summary data and individual-level genotype data is available by application to the Wellcome Trust Case Control Consortium Data Access Committee. Access to data will be granted to qualified investigators for appropriate use. | nif-0000-10551 | SCR_001973 | Wellcome Trust Case-Control Consortium (WTCCC) | 2026-08-01 12:01:40 | 213 | ||||
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TheBrainMatters.org Resource Report Resource Website |
TheBrainMatters.org (RRID:SCR_002029) | data or information resource, portal, narrative resource, topical portal, video resource, training material, bibliography | THIS RESOURCE IS NO LONGER IN SERVICE, documented on August 18, 2016. TheBrainMatters.org is a comprehensive resource for the public that provides information on on more than 250 neurologic disorders . This site combines important information from such credible sources as the American Academy of Neurology and the National Institute of Neurological Disorders and Stroke websites into one clean, organized, and user-friendly site designed specifically for users to become better informed about neurologic disorders. | clinical trial, clinical trials, discussion forums, donate, neurologic disorder, neurologic disorders, neurologist, neurologists | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-11829 | SCR_002029 | TheBrainMatters.org | 2026-08-01 12:01:41 | 0 |
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