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

  • Funding Agency:nci (facet)

Facets


Recent searches

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

346 Results - per page

Show More Columns | Download 346 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
Physician Data Query
 
Resource Report
Resource Website
1+ mentions
Physician Data Query (RRID:SCR_006833) PDQ clinical trial, ontology, data or information resource, people resource, registry, controlled vocabulary, database NCI''s comprehensive cancer database that contains summaries on a wide range of cancer topics; a registry of 8,000+ open and 19,000+ closed cancer clinical trials from around the world; a directory of professionals who provide genetics services; the NCI Dictionary of Cancer Terms, with definitions for 6,800+ cancer and medical terms; and the NCI Drug Dictionary, which has information on 2,300+ agents used in the treatment of cancer or cancer-related conditions. The PDQ cancer information summaries are peer reviewed and updated monthly by six editorial boards comprised of specialists in adult treatment, pediatric treatment, supportive care, screening and prevention, genetics, and complementary and alternative medicine. The Boards review current literature from more than 70 biomedical journals, evaluate its relevance, and synthesize it into clear summaries. Many of the summaries are also available in Spanish. adult, pediatric, child, alternative, breast, clinical trial, colorectal, hypercalcemia, legal, lung, medicine, medullary, nausea, ovarian, pain, pathophysiology, pediatric, pharmaceutical, physician, prevention, prognosis, prostate, psychosocial, query, risk factor, screening, social, syndrome, thyroid, treatment, umls, genetics, medical, drug, peer review is listed by: BioPortal
has parent organization: National Cancer Institute
Cancer, Cancer-related condition NCI nif-0000-21318 SCR_006833 PDQ - NCI''s Comprehensive Cancer Database 2026-02-17 10:01:07 2
Synapse
 
Resource Report
Resource Website
1000+ mentions
Synapse (RRID:SCR_006307) Synapse storage service resource, data or information resource, database, service resource, data repository A cloud-based collaborative platform which co-locates data, code, and computing resources for analyzing genome-scale data and seamlessly integrates these services allowing scientists to share and analyze data together. Synapse consists of a web portal integrated with the R/Bioconductor statistical package and will be integrated with additional tools. The web portal is organized around the concept of a Project which is an environment where you can interact, share data, and analysis methods with a specific group of users or broadly across open collaborations. Projects provide an organizational structure to interact with data, code and analyses, and to track data provenance. A project can be created by anyone with a Synapse account and can be shared among all Synapse users or restricted to a specific team. Public data projects include the Synapse Commons Repository (SCR) (syn150935) and the metaGenomics project (syn275039). The SCR provides access to raw data and phenotypic information for publicly available genomic data sets, such as GEO and TCGA. The metaGenomics project provides standardized preprocessed data and precomputed analysis of the public SCR data. data sharing, collaboration, data management, analysis, genome, phenotype, crowd sourcing, open data, provenance, resource management, annotation, authoring, markup, r, python, java, command-line, cloud, FASEB list is used by: NF Data Portal
is listed by: FORCE11
is listed by: DataCite
is listed by: re3data.org
is related to: clearScience
is related to: Exemplar Microscopy Images of Tissues
has parent organization: Sage Bionetworks
Cancer, Normal, Cardiovascular disease, Floppy hat syndrome Life Sciences Discovery Fund ;
NCI ;
NHLBI ;
Alfred P. Sloan Foundation
The community can contribute to this resource nlx_151983, DOI:10.17616/R3B934, r3d100011894, DOI:10.7303 https://doi.org/10.17616/R3B934
https://doi.org/10.48550/arxiv.1506.00272
https://doi.org/10.7303/
https://dx.doi.org/10.7303
https://doi.org/10.17616/R3B934
SCR_006307 2026-02-17 10:01:06 1002
FairSubset
 
Resource Report
Resource Website
FairSubset (RRID:SCR_019102) data access protocol, web service, software resource Web tool to choose representative subsets of data for use with replicates or groups of different sample sizes. Used to retain distribution information at single datum level and may be considered for standardized use in fair publishing practices. Representative data subsets, different sample sizes groups, different sample sizes replicates, retaining distribution information, fair publishing NCI CA207729;
Polish government grant
PMID:31583263 Free, Freely available SCR_019102 2026-02-17 10:03:36 0
ArchR
 
Resource Report
Resource Website
100+ mentions
ArchR (RRID:SCR_020982) software application, data processing software, data analysis software, software resource, software toolkit Software R package for processing and analyzing single-cell ATAC-seq data. Used for integrative single cell chromatin accessibility analysis.Provides intuitive, user focused interface for complex single cell analysis, including doublet removal, single cell clustering and cell type identification, unified peak set generation, cellular trajectory identification, DNA element-to-gene linkage, transcription factor footprinting, mRNA expression level prediction from chromatin accessibility and multi-omic integration with single-cell RNA sequencing. single-cell ATAC-seq data analysis, single-cell ATAC-seq data processing, single cell chromatin accessibility analysis, doublet removal, single cell clustering, cell type identification, unified peak set generation, cellular trajectory identification, transcription factor footprinting NHGRI RM1 HG007735;
NHGRI UM1 HG009442;
NCI R35 CA209919;
NHGRI UM1 HG009436;
NCI U2C CA233311;
NIAID U19 AI057266;
NIA K99 AG059918;
American Society of Hematology Scholar Award ;
International Collaborative Award ;
Defense Advanced Research Project Agency ;
Ray and Dagmar Dolby Family Fund ;
Stanford Cancer Institute-Goldman Sachs Foundation Cancer Research Award
PMID:33633365 Free, Available for download, Freely available https://github.com/GreenleafLab/ArchR
https://www.archrproject.com/
https://github.com/GreenleafLab/ArchR_2020
SCR_020982 2026-02-17 10:03:55 358
GSVA
 
Resource Report
Resource Website
100+ mentions
GSVA (RRID:SCR_021058) GSVA software application, data processing software, data analysis software, software resource, software toolkit Open source software R package for assaying variation of gene set enrichment over sample population.Used for microarray and RNA-seq data analysis. Gene set enrichment method that estimates variation of pathway activity over sample population in unsupervised manner. Gene set enrichment, variation estimation, pathway activity, sample population, microarray, RNA-seq, data analysis is listed by: Bioconductor ISCIII COMBIOMED ;
Spanish MINECO ;
NCI U54 CA149237
PMID:23323831 Free, Available for download, Freely available SCR_021058 Gene Set Variation Analysis 2026-02-17 10:03:18 256
CyLinter
 
Resource Report
Resource Website
1+ mentions
CyLinter (RRID:SCR_021157) software application, data processing software, software resource, segmentation software, image analysis software Open source software tool as interactive image segmentation filter for multiplex microscopy that aids in identification and removal of cell segmentation instances corrupted by optical and image processing artifacts. multiplex microscopy, quality control, single-cell data, Interactive Image Segmentation Filter NCI U2C CA233262;
NCI U54 CA225088
Free, Available for download, Freely available SCR_021157 2026-02-17 10:03:44 3
MCMICRO
 
Resource Report
Resource Website
10+ mentions
MCMICRO (RRID:SCR_021048) image processing software, software application, data processing software, software resource Open source software tool as multiple choice microscopy pipeline for multiplexed whole slide imaging and tissue microarrays. Scalable, modular image processing pipeline for multiplexed tissue imaging. Used for performing sequential steps needed to transform large, multi channel whole slide images into single cell data. NCI U54 CA225088;
Harvard Medical School ;
Ludwig Cancer Research Foundation ;
University of Zurich BioEntrepreneur Fellowship ;
Swiss National Science Foundation Early Postdoc Mobility fellowship
DOI:10.1101/2021.03.15.435473 Free, Available for download, Freely available https://github.com/labsyspharm/mcmicro SCR_021048 2026-02-17 10:04:00 11
StringTie
 
Resource Report
Resource Website
1000+ mentions
StringTie (RRID:SCR_016323) software application, data processing software, data analysis software, software resource, sequence analysis software Software application for assembling of RNA-Seq alignments into potential transcripts. It enables improved reconstruction of a transcriptome from RNA-seq reads. This transcript assembling and quantification program is implemented in C++ . assembling, RNA, sequence, transcript, gene, alignment, reconstruction, read, analysis, process, bio.tools is listed by: bio.tools
is listed by: Debian
is listed by: OMICtools
the Cancer Prevention and Research Institute of Texas ;
NHGRI R01 HG006677;
NIGMS R01 GM105705;
NHGRI R01 HG006102;
NCI R01 CA120185;
NCI R01 CA134292
PMID:25690850
DOI:10.1038/nbt.3122
Open source, Free, Freely available, Available for download biotools:stringtie, OMICS_07226 https://github.com/gpertea/stringtie
https://bio.tools/stringtie
https://sources.debian.org/src/stringtie/
SCR_016323 2026-02-17 10:03:23 4072
DESeq2
 
Resource Report
Resource Website
10000+ mentions
DESeq2 (RRID:SCR_015687) software application, data processing software, software tool, data analysis software, software resource Software package for differential gene expression analysis based on the negative binomial distribution. Used for analyzing RNA-seq data for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates. differential, gene, expression, analysis, binominal, distribution, RNA-seq data, Bioconductor, bio.tools is used by: Glimma
is used by: TEtranscripts
is listed by: Bioconductor
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: SARTools
works with: tximport
International Max Planck Research School for Computational Biology and Scientific Computing ;
NCI T32 CA009337;
European Union’s 7th Framework Programme
Free, Available for download, Freely available biotools:deseq2 https://github.com/mikelove/DESeq2
https://bio.tools/deseq2
SCR_015687 2026-02-17 10:02:36 43994
Markov Affinity based Graph Imputation of Cells
 
Resource Report
Resource Website
50+ mentions
Markov Affinity based Graph Imputation of Cells (RRID:SCR_022371) MAGIC data analysis software, software application, data processing software, software resource Software tool for imputing missing values restoring structure of large biological datasets.Method that shares information across similar cells, via data diffusion, to denoise cell count matrix and fill in missing transcripts. imputing missing values, restoring structure, shares information across similar cells, denoise cell count matrix, fill in missing transcripts NICHD DP1 HD084071;
NCI R01 CA164729;
NCI P30 CA008748;
American Cancer Society ;
Simons SFARI grants
PMID:29961576 Free, Available for download, Freely available SCR_022371 2026-02-17 10:04:03 83
Differential Gene Correlation Analysis
 
Resource Report
Resource Website
1+ mentions
Differential Gene Correlation Analysis (RRID:SCR_020964) DGCA data analysis software, software application, data processing software, software resource Software R package to perform differential gene correlation analysis. Performs differential correlation analysis on input matrices, with multiple conditions specified by design matrix. Differential gene, gene, gene correlation, correlation analysis, input matrices, differential correlations, identifier pairs, gene expression data, calculate differential correlations is listed by: CRAN NIA F30 AG052261;
NIA R01 AG046170;
NCI R01 CA163772;
NIAID U01 AI111598
PMID:27846853 Free, Available for download, Freely available https://github.com/andymckenzie/DGCA SCR_020964 2026-02-17 10:03:55 1
Minimum Information about Tissue Imaging
 
Resource Report
Resource Website
Minimum Information about Tissue Imaging (RRID:SCR_022830) MITI narrative resource, organization portal, data or information resource, consortium, standard specification, portal Consortium provides guidelines for highly multiplexed tissue images. Standard that applies best practices developed for genomics and other microscopy data to highly multiplexed tissue images and traditional histology. Data and metadata standards consistent with Findable, Accessible, Interoperable, and Reusable (FAIR) standards that guide data deposition, curation and release. Data and metadata standards, FAIR, tissue imaging, minimum information standard, guidelines for highly multiplexed tissue images NCI U2C CA233262;
NCI U54 CA225088;
NCI U2C CA233280;
NCI U2C CA233195;
NCI U2C CA233291;
NCI U2C CA233311;
NCI U2C CA233238;
NCI U2C CA233285;
NCI U2C CA233303;
NCI U2C CA233284;
NCI U2C CA233254
PMID:35277708 Free, Freely available https://github.com/miti-consortium/MITI SCR_022830 MITI Consortium 2026-02-17 10:04:26 0
miQC
 
Resource Report
Resource Website
1+ mentions
miQC (RRID:SCR_022697) data analysis software, software application, data processing software, software resource Software tool as flexible, probablistic metrics for quality control of scRNA-seq data. Adaptive probabilistic framework for quality control of single-cell RNA-sequencing data. Data driven QC metric that jointly models proportion of reads mapping to mtDNA and number of detected genes with mixture models in probabilistic framework to predict which cells are low quality in given dataset. scRNA-seq data quality control, QC metric, low quality data prediction, single cell RNA-sequencing data NCI CA237170;
NHGRI HG009007;
European Union Horizon 2020 research and innovation program ;
Academy of Finland ;
Cancer Foundation Finland
PMID:34428202 Free, Available for download, Freely available SCR_022697 2026-02-17 10:03:43 2
caHUB
 
Resource Report
Resource Website
caHUB (RRID:SCR_009657) caHUB data or information resource, narrative resource, standard specification THIS RESOURCE IS NO LONGER IN SERVICE. Documented July 5, 2018. A national center for biospecimen science and standards to advance cancer research and treatment. It was created in response to the critical and growing need for high-quality, well-documented biospecimens for cancer research. The initiative builds on resources already developed by the NCI, including the Biospecimen Research Network and the NCI Best Practices for Biospecimen Resources, both of which were developed to address challenges around standardization of the collection and dissemination of quality biospecimens. caHUB will develop the infrastructure for collaborative biospecimen research and the production of evidence-based biospecimen standard operating procedures. biospecimen, clinical, biomaterial supply resource, tissue is listed by: NIDDK Information Network (dkNET)
is related to: Biorepositories and Biospecimens Research Branch
has parent organization: National Cancer Institute
Cancer NCI ;
ARRA
THIS RESOURCE IS NO LONGER IN SERVICE nlx_156094 SCR_009657 The Cancer Human Biobank, cancer Human Biobank 2026-02-17 10:01:15 0
SPRING
 
Resource Report
Resource Website
10+ mentions
SPRING (RRID:SCR_023578) data access protocol, web service, software resource Interactive web tool to visualize single cell data using force directed graph layouts. Kinetic interface for visualizing high dimensional single cell expression data. Collection of pre-processing scripts and web browser based tool for visualizing and interacting with high dimensional data. visualizing high dimensional single cell expression data, single cell expression data visualization, high dimensional data, has parent organization: Harvard University; Cambridge; United States NIGMS 5T32GM080177;
NCI 1R33CA212697;
Burroughs-Wellcome Career Award at the Scientific Interface ;
Edward J Mallinckrodt Foundation Fellowship
PMID:29228172 Free, Available for download, Freely available https://github.com/AllonKleinLab/SPRING/
https://github.com/AllonKleinLab/SPRING_dev
SCR_023578 2026-02-17 10:04:25 24
Hetnet Connectivity Search
 
Resource Report
Resource Website
1+ mentions
Hetnet Connectivity Search (RRID:SCR_023630) Hetnet data access protocol, web service, software resource Web app that allows users to search for the most important paths connecting any two nodes in Hetionet. Hetionet, paths connection, paths search, paths connecting any two nodes in Hetionet, Pfizer Inc ;
NHGRI T32 HG000046;
NHGRI R01 HG010067;
NCI R01 CA237170;
Gordon and Betty Moore Foundation
PMID:36711546 Free, Freely available SCR_023630 , Heterogeneous network Connectivity Search, heterogeneous network 2026-02-17 10:03:58 1
Kinase Enrichment Analysis 3
 
Resource Report
Resource Website
10+ mentions
Kinase Enrichment Analysis 3 (RRID:SCR_023623) KEA3 data access protocol, web service, software resource Web server application that infers overrepresentation of upstream kinases whose putative substrates are in user inputted list of proteins. Used to analyze data from phosphoproteomics and proteomics studies to predict upstream kinases responsible for observed differential phosphorylations. overrepresentation of upstream kinases, upstream kinases, upstream kinases substrates, user inputted list of proteins, has parent organization: Icahn School of Medicine at Mount Sinai; New York; USA NHLBI U54 HL127624;
NCI U24 CA224260;
NIGMS T32 GM062754;
NIH Office of the Director OT3 OD025467
PMID:34019655 Free, Freely available SCR_023623 2026-02-17 10:04:25 11
GeneRanger
 
Resource Report
Resource Website
GeneRanger (RRID:SCR_023622) data access protocol, web service, software resource Web server application that provides access to processed data about expression of human genes and proteins across human cell types, tissues, and cell lines from several atlases. Used to explore single gene expression across tissues and cell types. explore single gene expression, gene expression across tissues and cell types, gene expression, is related to: TargetRanger
has parent organization: Icahn School of Medicine at Mount Sinai; New York; USA
NCI U24CA264250;
NCI U24CA224260;
NIDDK R01DK131525;
NIH Office of the Director OT2OD030160;
NIDDK RC2DK131995;
NCI U24CA271114
PMID:37166966 Free, Freely available SCR_023622 2026-02-17 10:04:29 0
TargetRanger
 
Resource Report
Resource Website
1+ mentions
TargetRanger (RRID:SCR_023621) data access protocol, web service, software resource Web server application that identifies targets from user inputted RNA-seq samples collected from cells we wish to target. By comparing inputted samples with processed RNA-seq and proteomics data from several atlases, TargetRanger identifies genes that are highly expressed in target cells while lowly expressed across normal human cell types, tissues, and cell lines. identify targets, identify genes, user inputted RNA-seq samples, target cells, proteomics data, human cells, is related to: GeneRanger
has parent organization: Icahn School of Medicine at Mount Sinai; New York; USA
NCI U24CA264250;
NCI U24CA224260;
NIDDK R01DK131525;
NIH Office of the Director OT2OD030160;
NIDDK RC2DK131995;
NCI U24CA271114
PMID:37166966 Free, Freely available https://maayanlab.github.io/Workshop.io/generanger SCR_023621 2026-02-17 10:03:57 2
HemOnc Knowledgebase
 
Resource Report
Resource Website
1+ mentions
HemOnc Knowledgebase (RRID:SCR_023436) data or information resource, topical portal, portal, disease-related portal Medical wiki of interventions, regimens, and general information relevant to fields of hematology and oncology. Knowledge base for hematology and oncology providers, containing details about hematology/oncology drugs and treatment regimens. Any healthcare professional can sign up to contribute. Acuracy and completeness of content is overseen by Editorial Board. Hematology and oncology knowledge base, hematology providers, oncology providers, hematology reference, oncology reference, hematology, oncology, drug interventions, treatment regimens, reference, healthcare professional, cancer NCI U24 CA265879 Free, Freely available https://hemonc.org/wiki/ SCR_023436 , HemOnc, Free Hematology/Oncology Reference, HemOnc.org 2026-02-17 10:03:54 4

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. Neuroscience Information Framework Resources

    Welcome to the NIF Resources search. From here you can search through a compilation of resources used by NIF 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 NIF 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 NIF then you can log in from here to get additional features in NIF 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 NIF 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.