Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Condition:normal (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

85 Results - per page

Show More Columns | Download 85 Result(s)

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
QuadGT
 
Resource Report
Resource Website
1+ mentions
QuadGT (RRID:SCR_000073) QuadGT software resource Software package for calling single-nucleotide variants in four sequenced genomes comprising a normal-tumor pair and the two parents. Genotypes are inferred using a joint model of parental variant frequencies, de novo germline mutations, and somatic mutations. The model quantifies the descent-by-modification relationships between the unknown genotypes by using a set of parameters in a Bayesian inference setting. Note that you can use it on any subset of the four related genomes, including parent-offspring trios, and normal-tumor pairs without parental samples. single-nucleotide variant, sequenced genome, genotype, genome is listed by: OMICtools
has parent organization: University of Montreal; Quebec; Canada
Normal, Tumor, Cancer Terry Fox Research Institute ;
Canadian Institutes for Health Research ;
Canada National Sciences and Engineering Research Council
PMID:23734724 Free, Available for download, Freely available OMICS_02108 SCR_000073 2026-02-07 02:05:16 1
ABSOLUTE
 
Resource Report
Resource Website
100+ mentions
ABSOLUTE (RRID:SCR_005198) ABSOLUTE software resource Software to estimate purity / ploidy, and from that compute absolute copy-number and mutation multiplicities. When DNA is extracted from an admixed population of cancer and normal cells, the information on absolute copy number per cancer cell is lost in the mixing. The purpose of ABSOLUTE is to re-extract these data from the mixed DNA population. This process begins by generation of segmented copy number data, which is input to the ABSOLUTE algorithm together with pre-computed models of recurrent cancer karyotypes and, optionally, allelic fraction values for somatic point mutations. The output of ABSOLUTE then provides re-extracted information on the absolute cellular copy number of local DNA segments and, for point mutations, the number of mutated alleles. is listed by: OMICtools
has parent organization: Broad Institute
Cancer, Normal PMID:22544022 Account required OMICS_00217 SCR_005198 2026-02-07 02:07:06 246
mutationSeq
 
Resource Report
Resource Website
10+ mentions
mutationSeq (RRID:SCR_006815) mutationSeq software resource A software suite using feature-based classifiers for somatic mutation prediction from paired tumour/normal next-generation sequencing data. mutationSeq has the advantages of integrating different features (e.g., base qualities, mapping qualities, strand bias, and tailed distance features), and validated somatic mutations to make predictions. Given paired normal/tumour bam files, mutationSeq will output the probability of each candidate site being somatic. next-generation sequencing, somatic mutation, tumor, normal is listed by: OMICtools
is related to: JointSNVMix
has parent organization: BC Cancer Agency
Tumor, Normal PMID:22084253 OMICS_00086 SCR_006815 2026-02-07 02:07:34 24
Internet Brain Volume Database
 
Resource Report
Resource Website
1+ mentions
Internet Brain Volume Database (RRID:SCR_002060) IBVD data or information resource, database A database of brain neuroanatomic volumetric observations spanning various species, diagnoses, and structures for both individual and group results. A major thrust effort is to enable electronic access to the results that exist in the published literature. Currently, there is quite limited electronic or searchable methods for the data observations that are contained in publications. This effort will facilitate the dissemination of volumetric observations by making a more complete corpus of volumetric observations findable to the neuroscience researcher. This also enhances the ability to perform comparative and integrative studies, as well as metaanalysis. Extensions that permit pre-published, non-published and other representation are planned, again to facilitate comparative analyses. Design strategy: The principle organizing data structure is the "publication". Publications report on "groups" of subjects. These groups have "demographic" information as well as "volume" information for the group as a whole. Groups are comprised of "individuals", which also have demographic and volume information for each of the individuals. The finest-grained data structure is the "individual volume record" which contains a volume observation, the units for the observation, and a pointer to the demographic record for individual upon which the observation is derived. A collection of individual volumes can be grouped into a "group volume" observation; the group can be demographically characterized by the distribution of individual demographic observations for the members of the group. anatomy, volume, dsm-iv, normal, schizophrenia, autistic disorder, bipolar disorder, major depressive disorder, alzheimer's disease, attention deficit-hyperactivity disorder, alcohol dependence, dementia, traumatic brain injury, borderline personality disorder, obsessive-compulsive disorder, asperger syndrome, brain, brain structure, in vivo, ex vivo, male, female, gorilla beringei beringei, pongo pygmaeus, volumetric analysis is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: NIF Data Federation
is related to: Integrated Manually Extracted Annotation
has parent organization: Harvard Medical School; Massachusetts; USA
Normal, Alzheimers disease, Seizure, Complex febrile seizure, Holoprosencephaly, Alcohol dependence, Bipolar Disorder, Traumatic brain injury, Schizophrenia The Human Brain Project ;
NINDS NS034189
PMID:21931990 Free, Available for download, Freely available nif-0000-00033 http://www.nitrc.org/projects/ibvd http://www.cma.mgh.harvard.edu/ibvd/ SCR_002060 2026-02-11 10:56:22 4
Open Access Series of Imaging Studies
 
Resource Report
Resource Website
100+ mentions
Open Access Series of Imaging Studies (RRID:SCR_007385) OASIS data or information resource, database Project aimed at making neuroimaging data sets of brain freely available to scientific community. By compiling and freely distributing neuroimaging data sets, future discoveries in basic and clinical neuroscience are facilitated. early, stage, alzheimer, disease, mri, fmri, image, brain, dicom, magnetic, resonance, collection, data, FASEB list is used by: NIF Data Federation
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: Automatic Registration Toolbox
is related to: 2012 MICCAI Multi-Atlas Labeling Challenge Data
has parent organization: Howard Hughes Medical Institute
has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA
has parent organization: Biomedical Informatics Research Network
is parent organization of: Cover Pages
Alzheimer's disease, Dementia, Normal, Nondemented, Aging NIA P50 AG05681;
NIA P01 AG03991;
NIA R01 AG021910;
NIMH P50 MH071616;
NCRR U24 RR021382;
NIMH R01 MH56584
Free, Acknowledgement required r3d100012182, nif-0000-00387 http://www.nitrc.org/projects/oasis
https://doi.org/10.17616/R3RS8K
SCR_007385 The Open Access Series of Imaging Studies, Open Access Series of Imaging Studies, OASIS 2026-02-11 10:57:34 299
UMKC Neuroscience Brain Tissue Bank and Research Laboratory
 
Resource Report
Resource Website
UMKC Neuroscience Brain Tissue Bank and Research Laboratory (RRID:SCR_005148) UMKC Brain Tissue Bank biomaterial supply resource, tissue bank, material resource, brain bank THIS RESOURCE IS NO LONGER IN SERVICE, documented August 31, 2016. The UMKC Neuroscience Brain Tissue Bank and Research Laboratory has been established to obtain, process, and distribute human brain tissue to qualified scientists and clinicians dedicated to neuroscience research. No other living organ approaches the human brain in complexity or capacity. Healthy, it astounds and inspires miracles. Diseased, it confounds and diminishes hope. The use of human brain tissue for research will provide insight into the anatomical and neurochemical aspects of diseased and non-diseased brains. While animal models are helpful and necessary in understanding disease, certain disorders can be more efficiently studied using human brain tissue. Also, modern research techniques are often best applied to human tissue. We also need samples of brain tissue that have not been affected by disease. They help us to compare a 'normal' brain with a diseased one. Also, we have a critical need for brain donations from relatives who have genetically inherited disorders. Tissue preparation consists of fresh quick-frozen tissue blocks or coronal slices (nitrogen vapor frozen; custom dissection of specific anatomic regions) or formalin-fixed coronal slices (custom dissection of specific anatomic regions). brain tissue, brain, tissue, fresh quick-frozen, block, nitrogen vapor frozen, frozen, formalin-fixed, disease, normal, genetically inherited disorder, normal control, matched control, neuroscience, post-mortem, coronal slice is listed by: One Mind Biospecimen Bank Listing
has parent organization: University of Missouri-Kansas City School of Medicine; Missouri; USA
Disease, Normal, Genetically inherited disorder, Normal control, Matched control THIS RESOURCE IS NO LONGER IN SERVICE nlx_144161 SCR_005148 UMKC Neuroscience Brain Tissue Bank Research Laboratory, University of Missouri-Kansas City Neuroscience Brain Tissue Bank & Research Laboratory, UMKC Neuroscience Brain Tissue Bank & Research Laboratory 2026-02-11 10:57:08 0
Internet Brain Segmentation Repository
 
Resource Report
Resource Website
10+ mentions
Internet Brain Segmentation Repository (RRID:SCR_001994) IBSR data or information resource, data set Data set of manually-guided expert segmentation results along with magnetic resonance brain image data. Its purpose is to encourage the development and evaluation of segmentation methods by providing raw test and image data, human expert segmentation results, and methods for comparing segmentation results. Please see the MediaWiki for more information. This repository is meant to contain standard test image data sets which will permit a standardized mechanism for evaluation of the sensitivity of a given analysis method to signal to noise ratio, contrast to noise ratio, shape complexity, degree of partial volume effect, etc. This capability is felt to be essential to further development in the field since many published algorithms tend to only operate successfully under a narrow range of conditions which may not extend to those experienced under the typical clinical imaging setting. This repository is also meant to describe and discuss methods for the comparison of results. 3d model, anatomy, brainstem, cerebellum, cortex, gray matter, imaging, morphology, mri, segmentation, volume, white matter, adult human, male, child, image collection, application, magnetic resonance, os independent, php, quality metrics, segmentation, test data, web service is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: Harvard Medical School; Massachusetts; USA
Normal, Tumor NINDS 1 R01 NS34189-01 Free, Available for download, Freely available nif-0000-00032 http://www.cma.mgh.harvard.edu/ibsr/ SCR_001994 2026-02-11 10:56:21 24
EEG time series Data Sets
 
Resource Report
Resource Website
1+ mentions
EEG time series Data Sets (RRID:SCR_001579) EEG time series data data or information resource, data set Five data sets containing quasi-stationary, artifact-free EEG signals both in normal subjects and epileptic patients were put in the web by Ralph Andrzejak from the Epilepsy center in Bonn, Germany. Each data set contains 100 single channel EEG segments of 23.6 sec duration. eeg, time series, brain, electrical activity, eyes closed, eyes open, intracranial, eeg recording, epileptic seizure is related to: Neural Cipher
has parent organization: Pompeu Fabra University; Barcelona; Spain
Epilepsy, Normal PMID:11736210 Free, Available for download, Freely available nlx_153816 http://epileptologie-bonn.de/cms/front_content.php?idcat=193&lang=3&changelang=3 SCR_001579 2026-02-11 10:56:15 1
ABIDE
 
Resource Report
Resource Website
100+ mentions
ABIDE (RRID:SCR_003612) ABIDE data or information resource, data set Resting state functional magnetic resonance imaging (R-fMRI) datasets from 539 individuals with autism spectrum disorder (ASD) and 573 typical controls. This initiative involved 16 international sites, sharing 20 samples yielding 1112 datasets composed of both MRI data and an extensive array of phenotypic information common across nearly all sites. This effort is expected to facilitate discovery science and comparisons across samples. All datasets are anonymous, with no protected health information included. phenotype, resting state functional magnetic resonance imaging, mri, image, fmri is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: 1000 Functional Connectomes Project
has parent organization: NeuroImaging Tools and Resources Collaboratory (NITRC)
Autism spectrum disorder, Normal Leon Levy Foundation ;
Joseph P. Healy ;
Stavros Niarchos Foundation ;
NIMH K23MH087770;
NIMH R03MH096321
Account required, Creative Commons Attribution-NonCommercial-ShareAlike License, v3 nlx_157761 SCR_003612 Autism Brain Imaging Data Exchange 2026-02-11 10:56:46 212
Kawasaki Disease Dataset2
 
Resource Report
Resource Website
Kawasaki Disease Dataset2 (RRID:SCR_008839) KD Data data or information resource, data set Dataset from an investigation of biochemical evidence of myocardial strain, oxidative stress, and cardiomyocyte injury in 55 acute KD subjects (30 with paired convalescent samples), 54 febrile control (FC), and 50 healthy control (HC) children by measuring concentrations of cardiovascular biomarkers. NT-proBNP and sST2 were elevated in acute KD subjects and correlated with impaired myocardial relaxation. These findings, combined with elevated levels of cTnI, suggest that both cardiomyocyte stress and cell death are associated with myocardial inflammation in acute KD. kawasaki disease, nt-probnp, sst2, copeptin, ct-proet-1, mr-proadm, mr-proanp, pct, troponin i cardiac muscle, cardiovascular biomarker, cardiovascular, biomarker, child, acute, convalescent, febrile, ctni, myocardial inflammation, pediatric is used by: NIF Data Federation
has parent organization: University of California at San Diego; California; USA
Kawasaki disease, Normal PMID:21777987 nlx_144644 http://neuinfo.org/nif/nifgwt.html?query=kawasaki&category=Data%20Type:Dataset SCR_008839 2026-02-11 10:57:57 0
Cancer Methylome System
 
Resource Report
Resource Website
1+ mentions
Cancer Methylome System (RRID:SCR_012013) CMS data or information resource, database Datbase and web-based system for visualization and analysis of genome-wide methylation data of human cancers. gene, methylation, visualization is listed by: OMICtools
has parent organization: University of Texas Health Science Center at San Antonio; Texas; USA
Cancer, Normal NCI PMID:22035855 Acknowledgement requested OMICS_01836 SCR_012013 2026-02-11 10:58:29 8
HeadIT
 
Resource Report
Resource Website
1+ mentions
HeadIT (RRID:SCR_005657) HeadIT data repository, service resource, storage service resource, data or information resource, data set Platform for sharing, download, and re-analysis or meta-analysis of sophisticated, fully annotated, human electrophysiological data sets. It uses EEG Study Schema (ESS) files to provide task, data collection, and subject metadata, including Hierarchical Event Descriptor (HED) tag descriptions of all identified experimental events. Visospatial task data also available from, http://sccn.ucsd.edu/eeglab/data/headit.html: A 238-channel, single-subject EEG data set recorded at the Swartz Center, UCSD, by Arnaud Delorme, Julie Onton, and Scott Makeig is al. electrophysiology, data sharing, eeg, visual-auditory cued attention shift paradigm, adult, early adult human, late adult human, memory task, modified sternberg working memory task, visual, auditory, auditory oddball, memory, task uses: HED Tags
is related to: EEGLAB
has parent organization: University of California at San Diego; California; USA
Normal, Healthy, Others possible NIMH R01-MH084819;
NINDS R01-NS047293
Public, Must agree to Data Use Agreement and Terms of Use., Account required for collaboration and to upload data. nlx_149081 http://headit-beta.ucsd.edu/
http://sccn.ucsd.edu/eeglab/data/headit.html
http://HeadIT.org SCR_005657 Human Electrophysiology Anatomic Data & Integrated Tools (HeadIT) Resource, Human Electrophysiology Anatomic Data & Integrated Tools Resource, Human Electrophysiology Anatomic Data & Integrated Tools, Human Electrophysiology Anatomic Data and Integrated Tools (HeadIT) Resource 2026-02-12 09:44:08 5
USC Multimodal Connectivity Database
 
Resource Report
Resource Website
10+ mentions
USC Multimodal Connectivity Database (RRID:SCR_012809) UMCD data repository, service resource, storage service resource, database, data or information resource Web-based repository and analysis site for connectivity matrices that have been derived from neuroimaging data including different imaging modalities, subject groups, and studies. Users can analyze connectivity matrices that have been shared publicly and upload their own matrices to share or analyze privately. fmri, dti, dsi, mri, eeg, meg, data set, image, computational hosting, connectivity, neuroimaging, data sharing, brain, rendering, diffusion-weighted mri, functional connectivity, graph theory, resting-state fmri, structural connectivity, image display, magnetic resonance, python, rendering, visualization, connectivity matrix, network, brain network, matrix, de-identified, male, female, apoe, child, adult is used by: NIF Data Federation
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: MGH-USC Human Connectome Project
Normal, Lesioned, Attention deficit-hyperactivity disorder, Autism Spectrum Disorder, Obsessive-Compulsive Disorder, BDD, APOE 4/4, APOE 3/4, APOE 3/3, Alzheimer's disease NRSA ;
NIH Blueprint for Neuroscience Research ;
NIA F31AG035438-01;
NIDA HHSN271200800035C
PMID:23226127
PMID:20850551
The community can contribute to this resource, Some features require an account nlx_83091 http://www.nitrc.org/projects/umcd http://jessebrown.webfactional.com/welcome/default/index SCR_012809 UCLA Connectivity Database, UCLA Multimodal Connectivity Database: Web-based brain network analysis and data sharing, UCLA Multimodal Connectivity Database 2026-02-12 09:46:05 25
Mutascope
 
Resource Report
Resource Website
1+ mentions
Mutascope (RRID:SCR_001265) Mutascope software resource, software application, data analysis software, data processing software Software suite to analyze data from high throughput sequencing of PCR amplicons, with an emphasis on normal-tumor comparison for the accurate and sensitive identification of low prevalence mutations. high throughput sequencing, pcr amplicon, pcr, mutation, amplicon, sequencing, somatic variant is listed by: OMICtools
has parent organization: SourceForge
Tumor, Normal PMID:23712659 Free, Public OMICS_02074 SCR_001265 Mutascope - Analysis software designed for PCR-amplicon sequencing data 2026-02-12 09:43:07 4
Mouse Biomedical Informatics Research Network
 
Resource Report
Resource Website
Mouse Biomedical Informatics Research Network (RRID:SCR_003392) MouseBIRN, mBIRN data or information resource, atlas, reference atlas, data set Animal model data primarily focused on mice including high resolution MRI, light and electron microscopic data from normal and genetically modified mice. It also has atlases, and the Mouse BIRN Atlasing Toolkit (MBAT) which provides a 3D visual interface to spatially registered distributed brain data acquired across scales. The goal of the Mouse BIRN is to help scientists utilize model organism databases for analyzing experimental data. Mouse BIRN has ended. The next phase of this project is the Mouse Connectome Project (https://www.nitrc.org/projects/mcp/). The Mouse BIRN testbeds initially focused on mouse models of neurodegenerative diseases. Mouse BIRN testbed partners provide multi-modal, multi-scale reference image data of the mouse brain as well as genetic and genomic information linking genotype and brain phenotype. Researchers across six groups are pooling and analyzing multi-scale structural and functional data and integrating it with genomic and gene expression data acquired from the mouse brain. These correlated multi-scale analyses of data are providing a comprehensive basis upon which to interpret signals from the whole brain relative to the tissue and cellular alterations characteristic of the modeled disorder. BIRN's infrastructure is providing the collaborative tools to enable researchers with unique expertise and knowledge of the mouse an opportunity to work together on research relevant to pre-clinical mouse models of neurological disease. The Mouse BIRN also maintains a collaborative Web Wiki, which contains announcements, an FAQ, and much more. electron microscopy, expression, functional, gene, 3-dimentional, brain, cellular, disorder, genomic, genotype, mouse, neurodegenerative disease, phenotype, molecular neuroanatomy resource, mri, light microscopy, model organism, gene expression, atlas data, imaging genomics, magnetic resonance is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: Mouse BIRN Atlasing Toolkit
is related to: Mouse Connectome Project
has parent organization: Biomedical Informatics Research Network
Normal, Neurodegenerative disease, Multiple Sclerosis, Alzheimer's disease, Parkinson's disease NIH ;
Collaborative Tools Support Network Award ;
NCRR 1U24-RR025736;
NCRR U24-RR021992;
NCRR U24-RR021760;
NCRR 1U24-RR026057-01
Free, Available for download, Freely available nif-0000-00200 https://loni.usc.edu/research/software?name=MBATWA http://www.loni.ucla.edu/BIRN/Projects/Mouse/index.shtml SCR_003392 Mouse BIRN 2026-02-12 09:43:36 0
CNSforum: Image Bank
 
Resource Report
Resource Website
CNSforum: Image Bank (RRID:SCR_002718) data or information resource, image collection A collection of downloadable central nervous system (CNS) images for teaching, presentations, articles, and other purposes. The following major categories of images are as follows: Brain anatomy, Brain physiology, Anxiety, Depression, Schizophrenia, Dementia, Parkinson's disease, Stroke, and Others. image collection, human brain, brain anatomy, brain physiology, anxiety, depression, schizophrenia, dementia, parkinson's disease, stroke, brain has parent organization: CNS Forum Anxiety, Depressive Disorder, Schizophrenia, Dementia, Parkinson's disease, Stroke, Normal Free, Freely available nif-0000-23576 SCR_002718 CNS Forum Image Bank, Lundbeck Institute CNSforum Image Bank 2026-02-12 09:43:26 0
SumsDB
 
Resource Report
Resource Website
10+ mentions
SumsDB (RRID:SCR_002759) SumsDB, WebCaret analysis service resource, data repository, service resource, image repository, production service resource, storage service resource, database, atlas, data analysis service, data or information resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on May 11, 2016. Repository of brain-mapping data (surfaces and volumes; structural and functional data) derived from studies including fMRI and MRI from many laboratories, providing convenient access to a growing body of neuroimaging and related data. WebCaret is an online visualization tool for viewing SumsDB datasets. SumsDB includes: * data on cerebral cortex and cerebellar cortex * individual subject data and population data mapped to atlases * data from FreeSurfer and other brainmapping software besides Caret SumsDB provides multiple levels of data access and security: * Free (public) access (e.g., for data associated with published studies) * Data access restricted to collaborators in different laboratories * Owner-only access for work in progress Data can be downloaded from SumsDB as individual files or as bundles archived for offline visualization and analysis in Caret WebCaret provides online Caret-style visualization while circumventing software and data downloads. It is a server-side application running on a linux cluster at Washington University. WebCaret "scenes" facilitate rapid visualization of complex combinations of data Bi-directional links between online publications and WebCaret/SumsDB provide: * Links from figures in online journal article to corresponding scenes in WebCaret * Links from metadata in WebCaret directly to relevant online publications and figures segmentation, volume, neuroimaging, brain, fmri, stereotaxic foci, stereotaxic coordinate, brain-mapping, foci, structural mri, mri, cerebral cortex, cerebellar cortex, afni brik, analyze, atlas, nifti, registration, rendering, spatial transformation, surface analysis, surface rendering, visualization, volume rendering, brain mapping, neuroanatomy is used by: NIF Data Federation
is listed by: Biositemaps
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: re3data.org
is related to: Computerized Anatomical Reconstruction and Editing Toolkit
is related to: Integrated Manually Extracted Annotation
has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA
Mental disease, Neurological disorder, Normal Human Brain Project ;
NSF ;
NCI ;
NLM ;
NASA ;
National Partnership for Advanced Computational Infrastructure ;
NIMH R01 MH60974-06
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-00016, r3d100010169 http://brainvis.wustl.edu/wiki/index.php/Sums:About http://www.nitrc.org/projects/sumsdb
https://doi.org/10.17616/R3JC76
SCR_002759 SumsDB WebCaret, SumsDB Database, Web Caret, WebCaret Online Visualization, Surface Management System Database and WebCaret Online Visualization, SumsDB and WebCaret, Sums database, SumsDB (Surface Management System Database) and WebCaret Online Visualization, Sums DB, SumsDB (Surface Management System Database) WebCaret Online Visualization, Surface Management System Database 2026-02-12 09:43:26 13
Cancer Genome Anatomy Project
 
Resource Report
Resource Website
100+ mentions
Cancer Genome Anatomy Project (RRID:SCR_003072) CGAP data or information resource, portal, topical portal Project to determine the gene expression profiles of normal, precancer, and cancer cells, whose generated resources are available to the cancer community. Interconnected modules provide access to all CGAP data, bioinformatic analysis tools, and biological resources allowing the user to find in silico answers to biological questions in a fraction of the time it once took in the laboratory. * Genes * Tissues * Pathways * RNAi * Chromosomes * SAGE Genie * Tools gene, gene expression, normal cell, precancer cell, cancer cell, cell, genome, anatomy, gene expression profile, tissue, pathway, rnai, chromosome, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: National Cancer Institute
is parent organization of: CGAP GO Browser
Cancer, Normal, Precancer NCI Free, download Freely available biotools:cgap, nif-0000-30468 https://mitelmandatabase.isb-cgc.org/mb_search SCR_003072 Cancer Genome Anatomy Project (CGAP) 2026-02-12 09:43:31 107
NIMH Stem Cell Center
 
Resource Report
Resource Website
10+ mentions
NIMH Stem Cell Center (RRID:SCR_006682) NIMH Stem Cell Center material resource, cell repository, biomaterial supply resource Induced Pluripotent Stem Cell (iPSC) and Source Cells available for distribution for postnatal-to-adult human control and patient-derived cells and their reprogrammed derivatives in support of stem cell research relevant to mental disorders. This includes but is not limited to anxiety disorders, attention deficit hyperactivity disorder, autism spectrum disorders, bipolar disorder, borderline personality disorder, depression, eating disorders, obsessive-compulsive disorder, panic disorder, post-traumatic stress disorder, and schizophrenia. The capabilities of the repository range from derivation and banking of primary source cells from postnatal through adult human subject tissue to more comprehensive banking and validation of induced pluripotent stem cells (iPSCs) or similar reprogrammed / de-differentiated cells. Please send a message with the Contact page if you wish to contribute source cells or iPSC. stem cell, cell, induced pluripotent stem cell, mental disease, anxiety disorder, attention deficit-hyperactivity disorder, autism spectrum disorder, bipolar disorder, borderline personality disorder, depressive disorder, eating disorder, obsessive-compulsive disorder, panic disorder, post-traumatic stress disorder, depression, schizophrenia, adult, postnatal, adolescent, normal is listed by: One Mind Biospecimen Bank Listing
is related to: NIMH Repository and Genomics Resources
has parent organization: Rutgers Cell and DNA Repository
Mental disease, Anxiety Disorder, Attention deficit-hyperactivity disorder, Autism spectrum disorder, Bipolar Disorder, Borderline personality disorder, Depressive Disorder, Eating disorder, Obsessive-Compulsive Disorder, Panic Disorder, Post-Traumatic Stress Disorder, Schizophrenia, Normal NIMH Registration required nlx_143795 SCR_006682 2026-02-12 09:44:17 11
Stem Cell Commons
 
Resource Report
Resource Website
1+ mentions
Stem Cell Commons (RRID:SCR_004415) Stem Cell Commons analysis service resource, source code, software resource, data repository, service resource, production service resource, storage service resource, database, data or information resource, data set Open source environment for sharing, processing and analyzing stem cell data bringing together stem cell data sets with tools for curation, dissemination and analysis. Standardization of the analytical approaches will enable researchers to directly compare and integrate their results with experiments and disease models in the Commons. Key features of the Stem Cell Commons * Contains stem cell related experiments * Includes microarray and Next-Generation Sequencing (NGS) data from human, mouse, rat and zebrafish * Data from multiple cell types and disease models * Carefully curated experimental metadata using controlled vocabularies * Export in the Investigation-Study-Assay tabular format (ISA-Tab) that is used by over 30 organizations worldwide * A community oriented resource with public data sets and freely available code in public code repositories such as GitHub Currently in development * Development of Refinery, a novel analysis platform that links Commons data to the Galaxy analytical engine * ChIP-seq analysis pipeline (additional pipelines in development) * Integration of experimental metadata and data files with Galaxy to guide users to choose workflows, parameters, and data sources Stem Cell Commons is based on open source software and is available for download and development. therapeutic target, blood, stem cell, self-renewal, embryonic stem cell, hematopoietic stem cell, leukemia stem cell, gene, protein, phenotype, therapeutic, annotate, share, analyze, data sharing, statistics, visualize, analyze, microarray, next-generation sequencing, statistics, transcription profiling, genome, genome browser, disease model is related to: Galaxy
is related to: ISA Infrastructure for Managing Experimental Metadata
has parent organization: Harvard Stem Cell Institute
Normal, Acute Myelogenous Leukemia, Glioblastoma, Primitive Neuroectodermal Tumor, Etc. PMID:24303302 Open unspecified license nlx_42085 http://bloodprogram.hsci.harvard.edu/ SCR_004415 HSCI Blood Genomics, Harvard Stem Cell Institute Blood Genomics, Harvard Stem Cell Institute Blood Program, HSCI Blood Program 2026-02-12 09:43:48 2

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. NIDM Terminology Resources

    Welcome to the nidm-terms Resources search. From here you can search through a compilation of resources used by nidm-terms and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that nidm-terms has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on nidm-terms then you can log in from here to get additional features in nidm-terms such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into nidm-terms you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.