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

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:nlm (facet)

Facets


Recent searches

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

110 Results - per page

Show More Columns | Download 110 Result(s)

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Phymm and PhymmBL
 
Resource Report
Resource Website
10+ mentions
Phymm and PhymmBL (RRID:SCR_004751) Phymm, PhymmBL software resource Software for Phylogenetic Classification of Metagenomic Data with Interpolated Markov Models to taxonomically classify DNA sequences and accurately classify reads as short as 100 bp. PhymmBL, the hybrid classifier included in this distribution which combines analysis from both Phymm and BLAST, produces even higher accuracy. metagenome, sequence, taxonomy, classification, phylogenetic classification, genome, short read is listed by: OMICtools
has parent organization: University of Maryland; Maryland; USA
NLM R01-LM006845 PMID:19648916
PMID:21527926
Open-source license OMICS_01461 SCR_004751 2026-09-05 06:25:23 12
NCBI Sequence Read Archive (SRA)
 
Resource Report
Resource Website
5000+ mentions
NCBI Sequence Read Archive (SRA) (RRID:SCR_004891) SRA data or information resource, data repository, database, service resource, storage service resource Repository of raw sequencing data from next generation of sequencing platforms including including Roche 454 GS System, Illumina Genome Analyzer, Applied Biosystems SOLiD System, Helicos Heliscope, Complete Genomics, and Pacific Biosciences SMRT. In addition to raw sequence data, SRA now stores alignment information in form of read placements on reference sequence. Data submissions are welcome. Archive of high throughput sequencing data,part of international partnership of archives (INSDC) at NCBI, European Bioinformatics Institute and DNA Database of Japan. Data submitted to any of this three organizations are shared among them. sequence, blast, next-generation sequence, alignment, read placement, reference sequence, roche 454 gs system, illumina genome analyzer, applied biosystems solid system, helicos heliscope, complete genomics, pacific biosciences smrt, high-throughput sequencing, data analysis service, gold standard is recommended by: National Library of Medicine
is recommended by: NIDDK Information Network (dkNET)
is listed by: OMICtools
is related to: European Nucleotide Archive (ENA)
is related to: RecountDB
is related to: SRAdb
is related to: DDBJ Sequence Read Archive
is related to: Bgee: dataBase for Gene Expression Evolution
is related to: NCBI BioSample
is related to: DDBJ Sequence Read Archive
is related to: METAGENOTE
has parent organization: NCBI
works with: SARS-CoV-2-Sequences
works with: Signaling Pathways Project
NLM PMID:22009675
PMID:21062823
Free, Available for download, Freely available OMICS_01031, nlx_86174, r3d100010775 https://doi.org/10.17616/R31S69 SCR_004891 Sequence Read Archive, , SRA, NCBI SRA 2026-09-05 06:25:26 7247
Protein Data Bank Markup Language
 
Resource Report
Resource Website
1+ mentions
Protein Data Bank Markup Language (RRID:SCR_005085) PDBML data or information resource, interchange format, markup language, narrative resource, standard specification Markup Language that provides a representation of PDB data in XML format. The description of this format is provided in XML schema of the PDB Exchange Data Dictionary. This schema is produced by direct translation of the mmCIF format PDB Exchange Data Dictionary Other data dictionaries used by the PDB have been electronically translated into XML/XSD schemas and these are also presented in the list below. * PDBML data files are provided in three forms: ** fully marked-up files, ** files without atom records ** files with a more space efficient encoding of atom records * Data files in PDBML format can be downloaded from the RCSB PDB website or by ftp. * Software tools for manipulating PDB data in XML format are available. xml is related to: RCSB PDB Software Tools
has parent organization: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
NSF ;
NIGMS ;
DOE ;
NLM ;
NCI ;
NCRR ;
NIBIB ;
NINDS
PMID:15509603 nlx_144096 SCR_005085 PDBML: Protein Data Bank Markup Language 2026-09-05 06:25:29 2
GeneSigDB
 
Resource Report
Resource Website
10+ mentions
GeneSigDB (RRID:SCR_013275) GeneSigDB analysis service resource, data access protocol, data analysis service, data or information resource, data repository, database, production service resource, service resource, software resource, storage service resource, web service Database of traceable, standardized, annotated gene signatures which have been manually curated from publications that are indexed in PubMed. The Advanced Gene Search will perform a One-tailed Fisher Exact Test (which is equivalent to Hypergeometric Distribution) to test if your gene list is over-represented in any gene signature in GeneSigDB. Gene expression studies typically result in a list of genes (gene signature) which reflect the many biological pathways that are concurrently active. We have created a Gene Signature Data Base (GeneSigDB) of published gene expression signatures or gene sets which we have manually extracted from published literature. GeneSigDB was creating following a thorough search of PubMed using defined set of cancer gene signature search terms. We would be delighted to accept or update your gene signature. Please fill out the form as best you can. We will contact you when we get it and will be happy to work with you to ensure we accurately report your signature. GeneSigDB is capable of providing its functionality through a Java RESTful web service. gene, gene signature, curated gene signature, gene expression, gene expression signature, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Dana-Farber Cancer Institute
has parent organization: Computational Biology and Functional Genomics Laboratory at Harvard
Cancer Genome Research Institute ;
Dana-Farber Cancer Institute ;
Women's Cancers Program ;
Claudia Adams Barr Foundation ;
NLM 1R01 LM010129;
NCI 1U19 CA148065;
NHGRI 1P50 HG004233
PMID:22110038 biotools:genesigdb, nlx_149342 https://bio.tools/genesigdb SCR_013275 Gene Signature Data Base, GeneSigDB - Curated Gene Signatures Database 2026-09-05 06:27:34 24
Informatics for Integrating Biology and the Bedside
 
Resource Report
Resource Website
10+ mentions
Informatics for Integrating Biology and the Bedside (RRID:SCR_013629) i2b2 data or information resource, data set, organization portal, portal, software resource, training resource i2b2 (Informatics for Integrating Biology and the Bedside) is an NIH-funded National Center for Biomedical Computing based at Partners HealthCare System. The i2b2 Center is developing a scalable informatics framework that will enable clinical researchers to use existing clinical data for discovery research and, when combined with IRB-approved genomic data, facilitate the design of targeted therapies for individual patients with diseases having genetic origin. For some resources (e.g. software) the use of the resource requires accepting a specific (e.g. OpenSource) license. genetic, biology, biomedical, computing, genomic, health, healthcare, informatic, origin, patient, therapy, predoctoral, postdoctoral is related to: National Centers for Biomedical Computing
is parent organization of: i2b2 Cross-Institutional Clinical Translational Research project
is parent organization of: Smoking NLP Challenge Data
NLM U54LM008748 Free, Public, Acknowledgement requested nif-0000-33133 SCR_013629 2026-09-05 06:27:38 30
PubReader
 
Resource Report
Resource Website
1+ mentions
PubReader (RRID:SCR_013814) software resource, web application A web application which serves as an alternate way to read scientific literature in PubMed Central and Bookshelf. PubReader features an easy-to-read multi-column display, a figure strip for access to figures, and a search function. It is designed especially to support reading on tablets and other smaller devices but is available for reading on laptops and desktops. web application, literature, tablet, mobile device is used by: PubMed Central
is used by: Bookshelf
is listed by: Connected Researchers
is related to: NCBI
is related to: PubMed Central
is related to: Bookshelf
is related to: Connected Researchers
has parent organization: NCBI
NIH ;
NLM ;
United States Department of Health and Human Services ;
U.S. Government
Free, Public SCR_013814 2026-09-05 06:27:41 1
HDBIG
 
Resource Report
Resource Website
HDBIG (RRID:SCR_014120) data processing software, image analysis software, software application, software resource, software toolkit A collection of software tools for high dimensional brain imaging genomics. These tools are designed to perform comprehensive joint analysis of heterogeneous imaging genomics data. HDBIG-SR is an HDBIG toolkit for sparse regression while HDBIG-SCCA is an HDBIG toolkit for sparse association. image analysis software, genomics, imaging, joint analysis, toolkit, sparse association, sparse regression is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: Indiana University; Indiana; USA
NLM R01 LM011360;
NSF IIS-1117335
http://www.iu.edu/~hdbig/ SCR_014120 High Dimensional Brain Imaging Genomics Toolkit 2026-09-05 06:27:43 0
SCORE
 
Resource Report
Resource Website
100+ mentions
SCORE (RRID:SCR_014165) data or information resource, experimental protocol, narrative resource A collection of methods for comparing the performance of different image algorithms. These methods generate quantitative scores that measure divergences to a standard. experiment protocol, method, different image algorithm, quantitative score is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: University of Utah; Utah; USA
NLM HHSN276201000584P;
NIBIB 1R41 EB011796
SCR_014165 2026-09-05 06:27:43 481
HISAT2
 
Resource Report
Resource Website
10000+ mentions
HISAT2 (RRID:SCR_015530) data analysis software, data processing software, sequence analysis software, software application, software resource, source code Graph-based alignment of next generation sequencing reads to a population of genomes. alignment program, mapping reads, population genomics, human genome, bio.tools is used by: Fcirc
is listed by: Debian
is listed by: bio.tools
is related to: TopHat
has parent organization: Johns Hopkins University; Maryland; USA
is required by: SL-quant
is hosted by: GitHub
NLM R01-LM06845;
NIGMS R01-GM083873;
NSF CCF-0347992
PMID:25751142
DOI:10.1038/s41587-019-0201-4
Available for download OMICS_07225, biotools:hisat2 https://github.com/infphilo/hisat2, https://bio.tools/hisat2, https://sources.debian.org/src/hisat2/ SCR_015530 HISAT 2026-09-05 06:27:56 20753
CCPN Data Model
 
Resource Report
Resource Website
CCPN Data Model (RRID:SCR_016982) data or information resource, data processing software, data repository, data storage software, database, service resource, software application, software resource, storage service resource Model to cover data for macromolecular NMR spectroscopy from the initial experimental data to the final validation. Used for the large scale data deposition, data mining and program interoperability. Enables movement from one software package to another without difficulties with data conversion or loss of information. Works with CcpNmr Analysis software for analysis and interactive display, CcpNmr FormatConverter for allowing transfer of data from programs used in NMR to and from the Data Model, and the CLOUDS software for automated structure calculation and assignment. Used within the CCPN software suite for NMR spectroscopy and at the BioMagResBank for converting existing deposited restraint lists to a standard IUPAC nomenclature. data, macromolecular, NMR, spectroscopy, deposition, mining, interoperability, conversion is related to: Biological Magnetic Resonance Data Bank (BMRB)
has parent organization: Collaborative Computing Project for NMR
works with: CCPN Analysis
works with: CCPN Analysis
BBSRC ;
EU ;
NIGMS GM67965;
NLM P41 LM005799
PMID:15815974
PMID:15613391
PMID:21953355
Free, Public SCR_016982 The CCPN Data Model 2026-09-05 06:28:16 0
BECA
 
Resource Report
Resource Website
1+ mentions
BECA (RRID:SCR_015846) BECA data processing software, data visualization software, image analysis software, software application, software resource Visualization and analysis software for interactive visual exploration and mining of fiber-tracts and brain networks with their genetic determinants and functional outcomes. BECA includes an fMRI and Diseases Analysis version as well as a Genome Explorer version. visual exploration, brain, neuroscience, network, genetic determinant, fmri, neuroimaging, genome has parent organization: Indiana University School of Medicine; Indiana; USA NIA P30 AG10133;
NIA R01 AG19771;
NIA RC2 AG036535;
NIA U01 AG024904;
NIBIB R01 EB022574;
NLM R01 LM011360;
NSF IIS-1117335
PMID:27171688 Free, Available for download SCR_015846 Brain Explorer for Connectome Analysis (BECA), BECA - Brain Explorer for Connectome Analysis 2026-09-05 06:28:00 5
SNPs3D
 
Resource Report
Resource Website
100+ mentions
SNPs3D (RRID:SCR_010787) SNPs3D data or information resource, database A website which assigns molecular functional effects of non-synonymous SNPs based on structure and sequence analysis. single nucleotide polymorphism, single nucleotide variation, gene, FASEB list is listed by: OMICtools
has parent organization: University of Maryland; Maryland; USA
NLM The community can contribute to this resource OMICS_00163 SCR_010787 2026-09-05 06:32:00 117
pRESTO
 
Resource Report
Resource Website
50+ mentions
pRESTO (RRID:SCR_001782) pRESTO software resource, software toolkit Software toolkit for processing raw reads from high-throughput sequencing of lymphocyte repertoires. lymphocyte, high throughput sequencing, processing, raw reads, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Yale School of Medicine; Connecticut; USA
EMD/Merck/Serono ;
United States-Israel Binational Science Foundation 2009046;
NCRR RR19895;
NLM T15 LM07056;
NIAAA U19AI089992;
NIAAA U19AI050864
PMID:24618469 Free, Freely available SCR_001782 REpertoire Sequencing TOolkit 2026-09-05 06:32:25 72
Gene functional conservation across cell types and species
 
Resource Report
Resource Website
Gene functional conservation across cell types and species (RRID:SCR_023292) data or information resource, portal, project portal We aligned single-nucleus atlases of middle temporal gyrus (MTG) of 5 primates (human, chimp, gorilla, macaque and marmoset) and identified 57 consensus cell types common to all species. We provide this resource for users to: 1) explore conservation of gene expression across primates at single cell resolution; 2) compare with conservation of gene coexpression across metazoa, and 3) identify genes with changes in expression or connectivity that drive rapid evolution of human brain. Brain Initiative Cell Census Network, single-nucleus atlases, middle temporal gyrus, human, chimp, gorilla, macaque, marmoset, 57 consensus cell types common to all species, 57 consensus cell types identification, is related to: BICCN NARSAD Young Investigator Award ;
NHGRI R01HG009318;
NLM F32MH114501;
NLM R01LM012736;
NLM R01MH113005;
NLM U01MH114812;
NLM U19MH114821
DOI:10.1101/2022.09.20.508736 Free, Freely available SCR_023292 2026-09-05 06:31:01 0
LINCS Data Portal 2.0
 
Resource Report
Resource Website
1+ mentions
LINCS Data Portal 2.0 (RRID:SCR_022566) LDP v2 data or information resource, portal Primary access point for compendium of LINCS data with substantial changes in data architecture and APIs, completely redesigned user interface, and enhanced curated metadata annotations to support more advanced, intuitive and deeper querying, exploration and analysis capabilities. LINCS datasets are accessible at data point level enabling users to directly access and download any subset of signatures across entire library independent from originating source, project or assay. Newly designed query interface enables global metadata search with autosuggest across all annotations associated with perturbations, model systems, and signatures. LINCS Data Portal, Cell, molecules, drug is related to: LINCS Data Portal BD2K-LINCS Data Coordination and Integration Center ;
NCATS U24TR002278;
NHLBI U54HL127624;
NLM U01LM012630
PMID:31701147 Free, Freely available SCR_022566 Library of Integrated Network Based Cellular Signatures 2.0 2026-09-05 06:31:00 2
MUMmerGPU
 
Resource Report
Resource Website
1+ mentions
MUMmerGPU (RRID:SCR_001200) MUMmerGPU data processing software, software application, software resource Software tool as high throughput DNA sequence alignment program that runs on nVidia G80-class GPUs. Aligns sequences in parallel on video card to accelerate widely used serial CPU program MUMmer. parallel computation 4, high-throughput sequencing, sequence alignment, dna, graphics processing unit is listed by: OMICtools
is related to: MUMmer
has parent organization: SourceForge
has parent organization: University of Maryland; Maryland; USA
NIGMS R01 GM083873;
NLM R01 LM006845
PMID:20161021 Free, Available for download, Freely available OMICS_02151 SCR_001200 High-throughput sequence alignment using Graphics Processing Units 2026-09-05 06:30:36 5
NCBI Resource List
 
Resource Report
Resource Website
NCBI Resource List (RRID:SCR_005628) NCBI Resources data or information resource, organization portal, portal The National Center for Biotechnology Information''s listing of resources. Sort by alphabetical character, Databases, Downloads, Submissions, Tools and How-To; or by Topic: Chemicals & Bioassays; Data & Software; DNA & RNA; Domains & Structures; Genes & Expression; Genetics & Medicine; Genomes & Maps; Homology; Literature; Proteins; Sequence Analysis; Taxonomy; Training & Tutorials; Variation. database, download, submission, tool, chemical, bioassay, data, software, dna, rna, domain, structure, gene, expression, genetics, medicine, genomes, map, homology, literature, protein, sequence analysis, taxonomy, training, tutorial, variation, gold standard has parent organization: NCBI NLM nlx_146242 SCR_005628 NCBI Resource Guide, NCBI Resource List (A-Z) 2026-09-05 06:30:41 0
ReBATE
 
Resource Report
Resource Website
ReBATE (RRID:SCR_017139) software resource, software toolkit Open source software Python package to compare relief based feature selection algorithms used in data mining. Used for feature selection in any bioinformatics problem with potentially predictive features and target outcome variable, to detect feature interactions without examination of all feature combinations, to detect features involved in heterogeneous patterns of association such as genetic heterogeneity . compare, relief, feature, algorithm, data, mining, variable, heterogeneous, pattern, genetic has parent organization: University of Pennsylvania; Philadelphia; USA NCATS TR001263;
NEI EY022300;
NHLBI HL134015;
NIAID AI116794;
NIDDK DK112217;
NIEHS ES013508;
NLM LM009012;
NLM LM010098;
NLM LM011360;
Warren Center for Network and Data Science
PMID:30030120 Free, Available for download, Freely available https://epistasislab.github.io/ReBATE/ SCR_017139 Relief Based Algorithm Training Environment 2026-09-05 06:33:02 0
NRG-CING
 
Resource Report
Resource Website
1+ mentions
NRG-CING (RRID:SCR_006079) NRG-CING data or information resource, database NRG-CING presents a complete validation report for all 9,000+ wwPDB NMR entries including remediated experimental data such as chemical shifts from BMRB and restraints from NRG . These CING reports are compiled from internal analyses and those by CCPN, DSSP, PROCHECK-NMR/Aqua, ShiftX, Talos+, Vasco, Wattos, and WHAT_CHECK. The NRG-CING website is a collection of CING reports that has been pre-calculated for all PDB files solved by NMR. (See website for more information on CING.) In case the underlying experimental data is available, these have been cleaned up and made syntactically and semantically correct and homogeneous. For many macromolecular NMR ensembles from the Protein Data Bank (PDB) the experiment-based restraint lists used in the structure calculation are accessible, while other experimental data, mainly chemical shift values, are often available from the BioMagResBank. Assessment of the quality of the structural result is paramount to their usage and a combined, integrated repository of both input data and structural results greatly facilitates such an analysis. In addition, the accuracy and precision of the coordinates in these macromolecular NMR ensembles can be improved by recalculations using the available experimental data and present-day software with improved protocols and force fields. Such efforts, however, generally fail on over half of all deposited structures due to the syntactic and semantic heterogeneity of the data and the wide variety of formats used for their deposition. We have combined the cleaned-up restraints information from the NMR Restraints Grid (NRG) database with available chemical shifts from the BioMagResBank in the weekly updated NRG-CING database. Eleven programs, in addition to CING itself, have been included in the NRG-CING production pipeline to arrive at validation reports that list for each entry the potential inconsistencies between the coordinates and the available restraint and chemical shift data. The longitudinal validation of this data yielded a set of indicators that can be used to judge the quality of every macromolecular structure solved with NMR. The cleaned up NMR experimental datasets and the validation reports are freely available. macromolecular structure, nmr, macromolecule, restraint, chemical shift, validation report, validation, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: Worldwide Protein Data Bank (wwPDB)
is related to: NMR Restraints Grid
is related to: Biological Magnetic Resonance Data Bank (BMRB)
has parent organization: Radboud University; Nijmegen; The Netherlands
Netherlands Organization for Scientific Research (NWO) 700.55.443;
Netherlands Bioinformatics Centre (NBIC) ;
EU FP6 LSHG-CT-2005-018988;
EU FP6 LHSG-CT-2004-512092;
EU FP7 261572;
Brussels Institute for Research and Innovation BB2B 2010-1-12;
NLM LM05799
PMID:22139937 Free nlx_151486, biotools:nrg-cing https://bio.tools/nrg-cing SCR_006079 2026-09-05 06:31:33 1
GO-Module
 
Resource Report
Resource Website
1+ mentions
GO-Module (RRID:SCR_005813) GO-Module analysis service resource, data analysis service, production service resource, service resource GO-Module provides an interface to reduce the dimensionality of GO enrichment results and produce interpretable biomodules of significant GO terms organized by hierarchical knowledge that contain only true positive results. Users can download a text file of GO terms annotated with their significance and identified biomodules, a network visualization of resultant GO IDs or terms in PDF format, and view results in an online table. Platform: Online tool functional similarity, visualization, other analysis, reduce the dimensionality of go enrichment results, produce interpretable biomodules of significant go terms, gene ontology, ontology or annotation visualization, annotation is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: AmiGO
has parent organization: University of Illinois at Chicago; Illinois; USA
NIH ;
Cancer Research Foundation ;
NLM K22 LM008308;
NCI 1U54CA121852;
NCRR UL1 RR024999
PMID:21421553 Free for academic use nlx_149322 SCR_005813 Hierarchical optimization of enriched GO terms 2026-09-05 06:31:32 3

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.