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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

(last updated: Sep 14, 2019)

Physical Resource or Software Tool Software

16,796 Results - per page

Resource NameResource TypeDescriptionKeywordsResource IDProper CitationParent OrganizationRelated ConditionFunding AgencyRelationReferenceWebsite StatusAlternate IDsAlternate URLsOld URLs
(at)NoteResource, software resource, software application, text-mining softwareTHIS RESOURCE IS NO LONGER AVAILABLE. Documented September 18, 2017. Text Mining platform that copes with major Information Retrieval and Information Extraction tasks and promotes multi-disciplinary research. It aims to provide support to three different usage roles: biologists, text miners and application developers. The workbench supports the retrieval, processing and annotation of documents as well as their analysis at different, java swt, text, miningSCR_005342((at)Note, RRID:SCR_005342)SourceForge , University of Minho; Braga; Portugal listed by: OMICtoolsPMID:19393341Last checked upOMICS_01167
100, 000 Genomes ProjectResource, data or information resource, databaseThe project will focus on patients with a rare disease and their families and patients with cancer. The first samples for sequencing are being taken from patients living in England with discussions taking place with Scotland, Wales and Northern Ireland about potential future involvement. Genomics England, a company wholly owned and funded by the Department of Health, was set up to deliver this flagship project which will sequence 100,000 whole genomes from NHS patients by 2017. Its four main aims are; to create an ethical and transparent programme based on consent; to bring benefit to patients and set up a genomic medicine service for the NHS; to enable new scientific discovery and medical insights; and to kick start the development of a UK genomics industry.cancer, autonomic rare diseaseSCR_010502(100, 000 Genomes Project, RRID:SCR_010502)UK Department of HealthLast checked upnlx_158734
1000 Functional Connectomes ProjectResource, database, image collection, catalog, service resource, storage service resource, image repository, data repository, data or information resourceDatabase of resting state fMRI (R-fMRI) datasets collected from sites around the world. It demonstrates open sharing of R-fMRI data and aims to emphasize the aggregation and sharing of well-phenotyped datasets.resting state functional mri, fmri, brain, neuroimaging, phenotype, function, data sharing, human, mri, r-fmri, rs-fmri, fc-fmri, rs--fcmri, resting-state, dicom, dti, child, adolescent, brain imaging, neuroinformatics, adult human, phenotype, data setSCR_005361(1000 Functional Connectomes Project, RRID:SCR_005361)NeuroImaging Tools and Resources Collaboratory (NITRC) related to: Spanish Resting State Network, NITRC-IR, NIH Data Sharing Repositories, BASH4RfMRI, International Neuroimaging Data-Sharing Initiative, used by: NIF Data Federation, DataLad, Integrated Datasets, MetaSearch, listed by: NITRC-IR, NeuroImaging Tools and Resources Collaboratory (NITRC), NIH Data Sharing Repositories, affiliated with: Preprocessed Connectomes ProjectReferences (2)Last checked downnlx_144428
1000 Fungal Genome ProjectResource, topical portal, data access protocol, database, web service, organism-related portal, portal, software resource, project portal, data or information resourceWeb application to provide genomic information for fungi. Includes sequenced fungal genomes, those in progress, and selected nominations. Nomination of new species for genome sequencing in the families or only one reference genome possible after providing DNA/RNA samples for their sequencing. Used to explore the diversity of fungi important for energy and the environment.project, genomic, information, fungi, data, sequence, energy, environmentSCR_016463(1000 Fungal Genome Project, RRID:SCR_016463)DOE Joint Genome Institute the DOE Office of Biological and Environmental Research (BER)related to: MycoCosm, Lawrence Berkeley National Laboratory, submitted by: Resource Identification PortalLast checked down
1000 Genomes: A Deep Catalog of Human Genetic VariationResource, organization portal, database, consortium, data set, portal, data or information resourceInternational collaboration producing an extensive public catalog of human genetic variation, including SNPs and structural variants, and their haplotype contexts, in an effort to provide a foundation for investigating the relationship between genotype and phenotype. The genomes of about 2500 unidentified people from about 25 populations around the world were sequenced using next-generation sequencing technologies. Redundant sequencing on various platforms and by different groups of scientists of the same samples can be compared. The results of the study are freely and publicly accessible to researchers worldwide. The consortium identified the following populations whose DNA will be sequenced: Yoruba in Ibadan, Nigeria; Japanese in Tokyo; Chinese in Beijing; Utah residents with ancestry from northern and western Europe; Luhya in Webuye, Kenya; Maasai in Kinyawa, Kenya; Toscani in Italy; Gujarati Indians in Houston; Chinese in metropolitan Denver; people of Mexican ancestry in Los Angeles; and people of African ancestry in the southwestern United States. The goal Project is to find most genetic variants that have frequencies of at least 1% in the populations studied. Sequencing is still too expensive to deeply sequence the many samples being studied for this project. However, any particular region of the genome generally contains a limited number of haplotypes. Data can be combined across many samples to allow efficient detection of most of the variants in a region. The Project currently plans to sequence each sample to about 4X coverage; at this depth sequencing cannot provide the complete genotype of each sample, but should allow the detection of most variants with frequencies as low as 1%. Combining the data from 2500 samples should allow highly accurate estimation (imputation) of the variants and genotypes for each sample that were not seen directly by the light sequencing. All samples from the 1000 genomes are available as lymphoblastoid cell lines (LCLs) and LCL derived DNA from the Coriell Cell Repository as part of the NHGRI Catalog. The sequence and alignment data generated by the 1000genomes project is made available as quickly as possible via their mirrored ftp sites. variation, gene, next-generation sequencing, sequence, alignment, genome, single-nucleotide polymorphism, structural variant, haplotype, genome-wide association study, pharmacology, genetics, biomarker, consortium, data sharing, genotype, phenotypeSCR_006828(1000 Genomes: A Deep Catalog of Human Genetic Variation, RRID:SCR_006828) European Bioinformatics Institute , NCBI , Broad Institute , Harvard Medical School; Massachusetts; USA , National Human Genome Research Institute , Wellcome Trust Sanger Institute; Hinxton; United Kingdom 454 Life Sciences Roche, Beijing Genomics Institute; Shenzhen; China, Illumina, Life Technologies, NHGRI, Wellcome Trust Sanger Institute; Hinxton; United Kingdomrelated to: MOSAIK, ART, SNAP - SNP Annotation and Proxy Search, used by: BioSample Database at EBI, uses: NHGRI Sample Repository for Human Genetic Research, listed by: OMICtools,, Consortia-pediaLast checked upnlx_143819, OMICS_00261
1000 Genomes Project and AWSResource, data set, data or information resourceA dataset containing the full genomic sequence of 1,700 individuals, freely available for research use. The 1000 Genomes Project is an international research effort coordinated by a consortium of 75 companies and organizations to establish the most detailed catalogue of human genetic variation. The project has grown to 200 terabytes of genomic data including DNA sequenced from more than 1,700 individuals that researchers can now access on AWS for use in disease research free of charge. The dataset containing the full genomic sequence of 1,700 individuals is now available to all via Amazon S3. The data can be found at: The 1000 Genomes Project aims to include the genomes of more than 2,662 individuals from 26 populations around the world, and the NIH will continue to add the remaining genome samples to the data collection this year. Public Data Sets on AWS provide a centralized repository of public data hosted on Amazon Simple Storage Service (Amazon S3). The data can be seamlessly accessed from AWS services such Amazon Elastic Compute Cloud (Amazon EC2) and Amazon Elastic MapReduce (Amazon EMR), which provide organizations with the highly scalable compute resources needed to take advantage of these large data collections. AWS is storing the public data sets at no charge to the community. Researchers pay only for the additional AWS resources they need for further processing or analysis of the data. All 200 TB of the latest 1000 Genomes Project data is available in a publicly available Amazon S3 bucket. You can access the data via simple HTTP requests, or take advantage of the AWS SDKs in languages such as Ruby, Java, Python, .NET and PHP. Researchers can use the Amazon EC2 utility computing service to dive into this data without the usual capital investment required to work with data at this scale. AWS also provides a number of orchestration and automation services to help teams make their research available to others to remix and reuse. Making the data available via a bucket in Amazon S3 also means that customers can crunch the information using Hadoop via Amazon Elastic MapReduce, and take advantage of the growing collection of tools for running bioinformatics job flows, such as CloudBurst and Crossbow.genomic data, genome, cloud computing, cloud, human, gene, genetic variation, research, dnaSCR_008801(1000 Genomes Project and AWS, RRID:SCR_008801)Amazon Web Services used by: HmtVarLast checked upnlx_144340
16p_resource CodeResource, software resource, source codeSoftware tool as a code to support figure generation for the manuscript by Roth, Muench et al. Used to perform analysis.code, support, figure, generation, analysis, manuscript, Roth, MuenchSCR_016845(16p_resource Code, RRID:SCR_016845)Last checked up
1DegreeBioResource, software resourceA registry which provides links and reviews for material resources such as reagents, equipment, digital tools, and providers, as well as the companies that sell them. Users can search for specific materials or search by vendor, product, or service type.registry, reagents, equipment, digital tool, marketplace, service provider, reviewSCR_011994(1DegreeBio, RRID:SCR_011994)related to: Connected Researchers, listed by: OMICtools, Connected ResearchersLast checked upOMICS_01765
2009 Grantees MeetingResource, meeting resource, training resourceThis project is meant for planning the NITRC Grantee meetings. The meetings introduce NITRC participants to one another, promote discussion of common interests, and identify opportunities for collaboration and interoperability. The 2009 meeting for NITRC enhancement grant awardees was held on June 18, 2009 (8:00 AM - 5:00 PM) in San Francisco at the San Francisco Marriott.SCR_014081(2009 Grantees Meeting, RRID:SCR_014081)listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)Last checked up
2012 MICCAI Multi-Atlas Labeling Challenge DataResource, 3d spatial image, data set, 3d t1 weighted mri scan, mri 3d image, atlas, image, data or information resourceManually created neuroanatomically labeled MRI brain scans with unique subjects, 5 subjects scanned twice.neuroanatomy, MRI, brain, scan, segmentation, parcellation, atlas, imageSCR_017008(2012 MICCAI Multi-Atlas Labeling Challenge Data, RRID:SCR_017008)related to: Neuromorphometrics, Open Access Series of Imaging StudiesLast checked up
2100 Expert SoftwareResource, data analytics software, software application, software resourceA software for analyzing digital assay data. The software performs RNA quality control, comparison between multiple chips, smear analysis, and data export in multiple analysis, digital assay, RNA quality control, smear analysis, data exportSCR_014466(2100 Expert Software, RRID:SCR_014466)submitted by: Resource Identification PortalLast checked up
2200 TapeStation InstrumentResource, resourceHardware system which automates RNA, DNA, and protein sample QC, including sample loading, separation, and imaging.rna, dna, protein sample qc, quality control, agilent, hardware, instrument, equipmentSCR_014994(2200 TapeStation Instrument, RRID:SCR_014994)Last checked up
2DMAPResource, software resource, software applicationTHIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application for constructing 2-d crossover-based map.gene, genetic, genomic, ms-dosSCR_009036(2DMAP, RRID:SCR_009036)listed by: Genetic Analysis SoftwareLast checked downnlx_154001
2LDResource, software resource, software applicationTHIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software program for calculating linkage disequilibrium (LD) measures between two polymorphic markers.gene, genetic, genomic, cSCR_000826(2LD, RRID:SCR_000826)listed by: Genetic Analysis SoftwareLast checked downnlx_154006
2SNPResource, software resource, software applicationTHIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. An algorithm resource for scalable phasing method for trios and unrelated individuals.gene, genetic, genomicSCR_009038(2SNP, RRID:SCR_009038)listed by: Genetic Analysis SoftwarePMID:18451440Last checked downnlx_154003
3DBarResource, production service resource, analysis service resource, reference atlas, software resource, service resource, atlas, data or information resourceSoftware package for reconstructing three-dimensional models of brain structures from 2-D delineations using a customizable and reproducible workflow. 3dBAR also works as an on-line service ( offering a variety of functions for the hosted datasets: * downloading reconstructions of desired brain structures in predefined quality levels in various supported formats as well as created using customizable settings, * previewing models as bitmap thumbnails and (for webGL enabled browsers) interactive manipulation (zooming, rotating, etc.) of the structures, * downloading slides from available datasets as SVG drawings. 3dBAR service can also be used by other websites or applications to enhance their functionality. * Operating System: Linux * Programming Language: Python * Supported Data Format: NIfTI-1, Other Format, VRML3d, reconstruction, brain structure, brain, algorithm or reusable library, web service, atlas application, three dimensional display, spinal cord, sensory system, waxholm spaceSCR_008896(3DBar, RRID:SCR_008896)Nencki Institute of Experimental Biology; Warsaw; Poland related to: Scalable Brain Atlas, Allen Mouse Brain Atlas, Waxholm Space Atlas, listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)PMID:22227717Last checked upnlx_151380,,,
3D BrainResource, software application, narrative resource, training material, software resource, mobile app, data or information resourceiPhone and iPad app that provides a good overview of the brain and its structures allowing you to rotate and zoom around 29 interactive structures with your touch screen. Discover how each brain region functions, what happens when it is injured, and how it is involved in mental illness. Each detailed structure comes with information on functions, disorders, brain damage, case studies, and links to modern research. Compatible with iPhone, iPod touch and iPad. Requires iOS 3.0 or later.neuroanatomy, brain, gross neuroanatomySCR_013138(3D Brain, RRID:SCR_013138)Cold Spring Harbor Laboratory Hewlett Foundation, The Dana Foundationrelated to: Genes to Cognition OnlineLast checked upnlx_152078
3D de novo assemblyResource, software resource, software application, data analysis software, data processing softwareSoftware tool as 3D de novo assembly (3D DNA) pipeline. Used to help generate HI-C novo, assembly, 3D, DNA, HI-C, data, scaffold, pipeline, chromosome, genomeSCR_017227(3D de novo assembly, RRID:SCR_017227)DOI:10.1126/science.aal3327Last checked up
3D DTI Atlas of the Rat Brain In Postnatal Day 5 14 and AdulthoodResource, atlas, reference atlas, data or information resource3D DTI anatomical rat brain atlases have been created by the UNC- Chapel Hill Department of Psychiatry and the CAMID research collaboration. There are three age groups, postnatal day 5, postnatal day 14, and postnatal day 72. The subjects were Sprague-Dawley rats that were controls in a study on cocaine abuse and development. The P5 and P14 templates were made from scans of twenty rats each (ten female, ten male); the P72, from six females. The individual cases have been resampled to isotropic resolution, manually skull-stripped, and deformably registered via an unbiased atlas building method to create a template for each age group. Each template was then manually segmented using itk-SNAP software. Each atlas is made up of 3 files, a template image, a segmentation, and a label file.magnetic resonance, adult rat, newborn rat, infant rat, young rat, sprague dawley, male, femaleSCR_009437(3D DTI Atlas of the Rat Brain In Postnatal Day 5 14 and Adulthood, RRID:SCR_009437)University of North Carolina at Chapel Hill; North Carolina; USA Control, NormalNICHD, NIDA, NINDS, UNC Neurodevelopment Disorders Research Centerlisted by: NeuroImaging Tools and Resources Collaboratory (NITRC)Last checked upnlx_155577
3D Facial Norms DatabaseResource, data or information resource, databaseDatabase of high-quality craniofacial anthropometric normative data for the research and clinical community based on digital stereophotogrammetry. Unlike traditional craniofacial normative datasets that are limited to measures obtained with handheld calipers and tape measurers, the anthropometric data provided here are based on digital stereophotogrammetry, a method of 3D surface imaging ideally suited for capturing human facial surface morphology. Also unlike more traditional normative craniofacial resources, the 3D Facial Norms Database allows users to interact with data via an intuitive graphical interface and - given proper credentials - gain access to individual-level data, allowing users to perform their own analyses.face, phenotype, genotype, facial landmark, coordinate, anthropometric, facial measurementSCR_005991(3D Facial Norms Database, RRID:SCR_005991)FaceBase NIDCRLast checked upnlx_151373
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