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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
Appyters
 
Resource Report
Resource Website
1+ mentions
Appyters (RRID:SCR_021245) software resource, web application Collection of web-based software applications that enable users to execute bioinformatics workflows without coding. Turns Jupyter notebooks into fully functional standalone web-based bioinformatics applications. Each Appyter application introduces data entry form for uploading or fetching data, as well as for selecting options for various settings. Once user presses Submit, Appyter is executed in cloud and user is presented with Jupyter Notebook report that contain results. Report includes markdown text, interactive and static figures, and source code. Appyter users can share the link to the output report, as well as download the fully executable notebook for execution on other platforms. Jupyter Notebooks, data-driven web apps collection, Jupyter Notebook results report is used by: Hypothesis Center
has parent organization: Icahn School of Medicine at Mount Sinai; New York; USA
NCI U24 CA224260;
NHLBI U54 HL127624;
NIH Office of the Director OT2 OD030160
DOI:10.1016/j.patter.2021.100213 Free, Available for download, Freely available https://github.com/MaayanLab/appyter
https://github.com/MaayanLab/appyter-catalog
SCR_021245 2026-02-14 02:04:12 9
Atherosclerosis Risk in Communities
 
Resource Report
Resource Website
10+ mentions
Atherosclerosis Risk in Communities (RRID:SCR_021769) ARIC disease-related portal, data or information resource, portal, topical portal Platform for prospective epidemiologic study conducted in four U.S. communities. One of most significant and longest running heart health studies and is the largest study of heart health in African Americans. ARIC investigates risk factors for heart disease and stroke, and connections between cardiovascular and cognitive health. ARIC includes two parts: Cohort Component and Community Surveillance Component. Cohort Component began in 1987, and each ARIC field center randomly selected and recruited cohort sample of individuals aged 45-64 from defined population in their community, to receive extensive examinations, including medical, social, and demographic data. In Community Surveillance Component, four communities are investigated to determine long term trends in hospitalized myocardial infarction and coronary heart disease deaths in men and women aged 35-84 years. Heart health studies, epidemiologic study, heart disease risk factors, stroke risk factors, cardiovascular and cognitive health connection, atherosclerosis risk coronary heart disease, stroke, myocardial infarction, atherosclerosis NHLBI PMID:2646917
PMID:34112321
Free, Freely available SCR_021769 The Atherosclerosis Risk in Communities (ARIC) Study 2026-02-14 02:04:21 35
Motif Mutation Analysis for Regulatory Genomic Elements
 
Resource Report
Resource Website
500+ mentions
Motif Mutation Analysis for Regulatory Genomic Elements (RRID:SCR_021902) MMARGE data processing software, data analysis software, software toolkit, software application, software resource Software package that integrates genome wide genetic variation with epigenetic data to identify collaborative transcription factor pairs. Optimized to work with chromatin accessibility assays such as ATAC-seq or DNase I hypersensitivity, as well as transcription factor binding data collected by ChIP-seq. Used to identify combinations of cell type specific transcription factors while simultaneously interpreting functional effects of non-coding genetic variation. genome wide genetic variation, epigenetic data, identify collaborative transcription factor pairs, interpreting functional effects, non-coding genetic variation NCI CA173903;
NIGMS GM085764;
NIDDK DK091183;
NHLBI R00 123485
PMID:29893919 Free, Available for download, Freely available SCR_021902 2026-02-14 02:04:24 608
Polysolver
 
Resource Report
Resource Website
10+ mentions
Polysolver (RRID:SCR_022278) data analysis software, software resource, data processing software, software application Software tool for HLA typing based on whole exome sequencing data and infers alleles for three major MHC class I genes. Enables accurate inference of germline alleles of class I HLA-A, B and C genes and subsequent detection of mutations in these genes using inferred alleles as reference. HLA typing, whole exome sequencing data, accurate inference of germline alleles, high precision HLA-typing, alleles of class I HLA-A, B and C genes, detection of mutations, inferred alleles has parent organization: Broad Institute Blavatnik Family Foundation ;
NHLBI 1RO1HL103532;
NCI 1R01CA155010;
AACR
PMID:26372948 Free, Available for download, Freely available SCR_022278 POLYmorphic loci reSOLVER, POLYSOLVER 2026-02-14 02:04:42 30
SigCom LINCS
 
Resource Report
Resource Website
1+ mentions
SigCom LINCS (RRID:SCR_022275) data access protocol, software resource, web service Web server that serves over million gene expression signatures processed, analyzed, and visualized from LINCS, GTEx, and GEO. Data and metadata search engine for gene expression signatures. FAIR data, data and metadata search engine, gene expression signatures, gene expression signature processed, analyzed, and visualized, LINCS, GTEx, GEO, gene expression signatures, NHLBI U54HL127624;
NIDDK R01DK131525;
NIH Office of the Director OT2OD030160
PMID:35524556 Free, Freely available https://github.com/MaayanLab/sigcom-lincs SCR_022275 SigCom Library of Integrated Network-based Cellular Signatures 2026-02-14 02:04:38 7
sei
 
Resource Report
Resource Website
1+ mentions
sei (RRID:SCR_022571) data access protocol, software resource, web service Web server for systematically predicting sequence regulatory activities and applying sequence information to human genetics data. Provides global map from any sequence to regulatory activities, as represented by sequence classes, and each sequence class integrates predictions for chromatin profiles like transcription factor, histone marks, and chromatin accessibility profiles across wide range of cell types. systematically predicting sequence regulatory activities, applying sequence information, human genetics data, sequence class predictions National Science Foundation Graduate Research Fellowship Program ;
NHGRI R01HG005998;
NHLBI U54HL117798;
NIGMS R01GM071966
PMID:35817977 Free, Available for download, Freely available https://hb.flatironinstitute.org/sei SCR_022571 2026-02-14 02:05:02 6
Sleep Heart Health Study
 
Resource Report
Resource Website
50+ mentions
Sleep Heart Health Study (RRID:SCR_016559) SHHS disease-related portal, data or information resource, portal, topical portal Portal for a multi-cohort study focused on sleep-disordered breathing and cardiovascular outcomes implemented by the National Heart Lung and Blood Institute. Recorded signals are: EEG, ECG, EOG, SaO2, HR, EOG, EMG, respiratory inductance plethysmography, respiration (thermistor), position, light. dataset, analysis, sleep, apnea, breathing, disorder, cardiovascular, disease, EEG, ECG, respiration, PSG is listed by: National Sleep Research Resource (NSRR) sleep disorder, sleep apnea, cardiovascular disease NHLBI U01 HL53916;
NHLBI U01 HL53931;
NHLBI U01 HL53934;
NHLBI U01 HL53937;
NHLBI U01 HL64360;
NHLBI U01 HL53938;
NHLBI U01 HL53941
PMID:9493915 Free, Freely available, Registration required for membership SCR_016559 Sleep Heart Health Study 2026-02-14 02:03:14 76
SINCERA Pipeline
 
Resource Report
Resource Website
1+ mentions
SINCERA Pipeline (RRID:SCR_016563) SINCERA data processing software, data analysis software, data analytics software, software application, software resource Software tool implemented in R S4 as an analytic pipeline for processing single-cell RNA-seq data from a whole organ or sorted cells. Used for Single Cell RNA-Seq profiling analysis. single, cell, RNA seq, data, sorted, whole, organ, profiling, analysis NHLBI U01 HL110964;
NHLBI U01 HL122642;
NHLBI R01 HL105433
PMID:26600239 Free, Available for download, Freely available https://research.cchmc.org/pbge/sincera.html SCR_016563 SINCERA, SINgle CEll RNA seq profiling Analysis 2026-02-14 02:03:14 5
Drug Gene Budger
 
Resource Report
Resource Website
Drug Gene Budger (RRID:SCR_016489) DGB data access protocol, software resource, web service, service resource Web based application to assist researchers with identifying drugs and small molecules that are predicted to maximally influence expression of mammalian gene of interest. Used to identify drugs and small molecules to regulate expression of target genes for research purpose only. Application for ranking drugs to modulate specific gene based on transcriptomic signatures. identify, drug, small, molecule, predict, influence, expression, mammalian, gene, regulate, target is related to: LINCS Project
has parent organization: Icahn School of Medicine at Mount Sinai; New York; USA
works with: CMAP
works with: Gene Expression Omnibus (GEO)
BD2K-LINCS Data Coordination and Integration Center Mount Sinai Knowledge Management Center for IDG ;
NHLBI U54 HL127624;
NCI U24 CA224260
PMID:30169739 Restricted SCR_016489 Drug Gene Budger 2026-02-14 02:03:05 0
Apnea, Bariatric surgery, and CPAP study
 
Resource Report
Resource Website
Apnea, Bariatric surgery, and CPAP study (RRID:SCR_016575) ABC study disease-related portal, data or information resource, portal, topical portal Portal for randomized controlled trial to compare effectiveness of bariatric surgery versus continuous positive airway pressure (CPAP) therapy for obstructive sleep apnea. Signals included in the polysomnography (PSG) montage are EEG, EMG, EOG, ECG, SpO2, airflow, CPAP pressure, CPAP flow, plethysmography, position, pulse, light, respiratory effort, snore. dataset, bariatric, surgery, continuous, positive, airway, pressure, therapy, sleep, apnea, obesity II is listed by: National Sleep Research Resource (NSRR) class II obesity, obstructive sleep apnea NHLBI R01 HL106410;
NHLBI K24 HL127307
DOI:10.1164/rccm.201708-1637LE Free, Available for public download, Registration required SCR_016575 and Cpap study, Bariatric surgery, Apnea 2026-02-14 02:03:06 0
Best Apnea Interventions for Research (BestAIR) sleep study
 
Resource Report
Resource Website
1+ mentions
Best Apnea Interventions for Research (BestAIR) sleep study (RRID:SCR_016583) BestAIR disease-related portal, data or information resource, portal, topical portal Portal for sleep study to address challenges in conducting future large-scale trials of sleep apnea treatment. Includes data from sleep apnea patients with cardiovascular disease or risk factors. Signals included in the polysomnography (PSG) montage are ECG, SpO2, airflow, nasal pressure, position, pulse, respiratory effort, snore, tidal volume. data, analysis, sleep, apnea, treatment, cardiovascular, disease, risk, factor, polysomnography, ECG, SpO2 is listed by: National Sleep Research Resource (NSRR) sleep apnea, cardiovascular disease ResMed Foundation ;
Philips Respironics ;
NHLBI U34 HL105277
DOI:10.5665/sleep.4266 SCR_016583 bestair, , Best Apnea Interventions for Research, Bestair 2026-02-14 02:03:17 2
LINCS Data Portal
 
Resource Report
Resource Website
10+ mentions
LINCS Data Portal (RRID:SCR_014939) data or information resource, portal Portal which provides a unified interface for searching LINCS dataset packages and reagents. Users can use the portal to access datasets, small molecules, cells, genes, proteins and peptides, and antibodies. portal, assay, lincs, kinome, dataset, small molecule, cell, gene, protein, peptide, and antibodies. is related to: LINCS Data Portal 2.0
has parent organization: University of Miami; Florida; USA
is parent organization of: CycIF.org
NIH Common Fund ;
NHLBI 1U01HL111561;
NHLBI 3U01HL111561-01S1;
NHLBI 3U01HL111561-02S1;
NHGRI U54HG006097;
NHGRI U54 HG006093
Freely available SCR_014939 2026-02-14 02:05:13 13
HMS LINCS Center
 
Resource Report
Resource Website
10+ mentions
HMS LINCS Center (RRID:SCR_016370) HMS LINCS data or information resource, organization portal, portal Center that is part of the NIH Library of Integrated Network-based Cellular Signatures (LINCS) Program. Its goals are to collect and disseminate data and analytical tools needed to understand how human cells respond to perturbation by drugs, the environment, and mutation. LINCS, Program, library, network, cell, signature, analysis, drugs, human, research is related to: HMS LINCS Database
has parent organization: Harvard Medical School; Massachusetts; USA
NHLBI U54 HL127365 PMID:29199020 SCR_016370 LINCS Center, Harvard Medical School LINCS Center, Harvard Medical School LINCS, Harvard Medical School (HMS) LINCS Center 2026-02-14 02:05:40 15
LINCS Information Framework
 
Resource Report
Resource Website
1+ mentions
LINCS Information Framework (RRID:SCR_003937) data or information resource, database LIFE search engine contains data generated from LINCS Pilot Phase, to integrate LINCS content leveraging semantic knowledge model and common LINCS metadata standards. LIFE makes LINCS content discoverable and includes aggregate results linked to Harvard Medical School and Broad Institute and other LINCS centers, who provide more information including experimental conditions and raw data. Please visit LINCS Data Portal. bioassay, cell, small molecule, kinase protein, compound, cell, gene, metadata standard, cell line, primary cell, rnai reagent, rnai, reagent, protein reagent, protein, antibody reagent, antibody, perturbagen, growth factor, ligand, linked data, organ, disease, data set uses: HMS LINCS Database
uses: Bioassay Ontology
uses: Molecular Libraries Program
is related to: Broad Institute
is related to: Harvard Medical School; Massachusetts; USA
is related to: Columbia University; New York; USA
is related to: Yale University; Connecticut; USA
is related to: Arizona State University; Arizona; USA
has parent organization: University of Miami; Florida; USA
NHLBI U01 HL111561;
NHGRI
PMID:29140462 Free, Freely available nlx_158348 http://dev3.ccs.miami.edu:8080/datasets-beta/ http://lifekb.org/ SCR_003937 lifekb, LIFE LINCS Information Framework 2026-02-14 02:06:16 1
Poly Peak Parser
 
Resource Report
Resource Website
1+ mentions
Poly Peak Parser (RRID:SCR_023776) data access protocol, software resource, web service THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 25,2025. Web tool to parse Sanger sequencing chromatograms with double peaks into wildtype and alternative allele sequences. Used to separate chromatogram data containing ambiguous base calls into wildtype and mutant allele sequences.Used for identification of unknown indels using sanger sequencing of polymerase chain reaction products. unknown indels identification, parse Sanger sequencing chromatograms, chromatograms with double peaks, separate chromatogram data, ambiguous base calls, wildtype sequences, mutant allele sequences, alternative allele sequences, NHLBI U01HL0981;
NHLBI U01HL098188;
NHLBI 1F32HL115881
PMID:25160973 THIS RESOURCE IS NO LONGER IN SERVICE http://yosttools.genetics.utah.edu/PolyPeakParser/ SCR_023776 2026-02-14 02:05:00 5
Body Mass Index Calculator
 
Resource Report
Resource Website
Body Mass Index Calculator (RRID:SCR_000122) BMI Calculator data analysis service, production service resource, service resource, analysis service resource Body Mass Index (BMI) for adults can be calculated using only height and weight. Body mass index (BMI) is a measure of body fat based on height and weight that applies to adult men and women. adult human, body mass, male, female is listed by: NIDDK Information Network (dkNET)
is listed by: Genetic Analysis Software
has parent organization: National Heart Lung and Blood Institute
NHLBI Free, Public nlx_152731 SCR_000122 Calculate Your Body Mass Index 2026-02-14 02:05:31 0
NeuroPedia
 
Resource Report
Resource Website
10+ mentions
NeuroPedia (RRID:SCR_001551) NeuroPedia data or information resource, database A neuropeptide encyclopedia of peptide sequences (including genomic and taxonomic information) and spectral libraries of identified MS/MS spectra of homolog neuropeptides from multiple species. proteomics, peptide, neuropeptide, mass spectrometry assay, peptide sequence, spectrum, homolog has parent organization: Center for Computational Mass Spectrometry NCRR P41-RR024851;
NIDA 5K01DA23065;
NINDS R01 NS24553;
NIDA R01 DA04271;
NIMH R01 MH077305;
NHLBI P01 HL58120
PMID:21821666 Free, Freely available nlx_152894 SCR_001551 NeuroPedia: Neuropeptide database and spectra library 2026-02-14 02:05:35 12
UniProt
 
Resource Report
Resource Website
10000+ mentions
UniProt (RRID:SCR_002380) UniProt data or information resource, database Collection of data of protein sequence and functional information. Resource for protein sequence and annotation data. Consortium for preservation of the UniProt databases: UniProt Knowledgebase (UniProtKB), UniProt Reference Clusters (UniRef), and UniProt Archive (UniParc), UniProt Proteomes. Collaboration between European Bioinformatics Institute (EMBL-EBI), SIB Swiss Institute of Bioinformatics and Protein Information Resource. Swiss-Prot is a curated subset of UniProtKB. collection, protein, sequence, annotation, data, functional, information is used by: LIPID MAPS Proteome Database
is used by: ChannelPedia
is used by: Open PHACTS
is used by: DisGeNET
is used by: Smart Dictionary Lookup
is used by: MitoMiner
is used by: Cytokine Registry
is used by: MobiDB
is used by: Pathway Analysis Tool for Integration and Knowledge Acquisition
is used by: Phospho.ELM
is used by: GEROprotectors
is used by: SwissLipids
is recommended by: NIDDK Information Network (dkNET)
is recommended by: National Library of Medicine
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: re3data.org
is listed by: LabWorm
is related to: Clustal W2
is related to: UniProt DAS
is related to: UniParc at the EBI
is related to: ProDom
is related to: LegumeIP
is related to: Pathway Commons
is related to: NIH Data Sharing Repositories
is related to: FlyMine
is related to: IMEx - The International Molecular Exchange Consortium
is related to: 3D-Interologs
is related to: Biomine
is related to: EBIMed
is related to: STOP
is related to: Coremine Medical
is related to: BioExtract
is related to: STRAP
is related to: GOTaxExplorer
is related to: GoAnnotator
is related to: IT-GOM: Integrated Tool for IC-based GO Semantic Similarity Measures
is related to: Whatizit
is related to: MOPED - Model Organism Protein Expression Database
is related to: Polbase
is related to: PredictSNP
is related to: PSICQUIC Registry
is related to: IntAct
is related to: p300db
is related to: UniProt Proteomes
is related to: SARS-CoV-2 mutation effects and 3D structure prediction from sequence covariation
has parent organization: European Bioinformatics Institute
has parent organization: SIB Swiss Institute of Bioinformatics
has parent organization: Protein Information Resource
is parent organization of: UniProtKB
is parent organization of: NEWT
is parent organization of: UniParc
is parent organization of: UniProt Chordata protein annotation program
is parent organization of: UniRef
works with: Genotate
works with: CellPhoneDB
works with: MOLEonline
works with: MiMeDB
NHGRI U41 HG006104;
NHGRI P41 HG02273;
NIGMS 5R01GM080646;
NIGMS R01 GM080646;
NLM G08 LM010720;
NCRR P20 RR016472;
NSF DBI-0850319;
British Heart Foundation ;
NEI ;
NHLBI ;
NIA ;
NIAID ;
NIDDK ;
NIMH ;
NCI ;
EMBL ;
PDUK ;
ARUK ;
NHGRI U24 HG007722
PMID:19843607
PMID:18836194
PMID:18045787
PMID:17142230
PMID:16381842
PMID:15608167
PMID:14681372
nif-0000-00377, SCR_018750, r3d100010357 http://www.ebi.uniprot.org
http://www.uniprot.org/uniprot/
http://www.pir.uniprot.org
ftp://ftp.uniprot.org
https://doi.org/10.17616/R3BW2M
SCR_002380 , The Universal Protein Resource, Universal Protein Resource, UNIPROT Universal Protein Resource 2026-02-14 02:05:47 17565
MITOMAP - A human mitochondrial genome database
 
Resource Report
Resource Website
100+ mentions
MITOMAP - A human mitochondrial genome database (RRID:SCR_002996) MITOMAP data or information resource, database Database of polymorphisms and mutations of the human mitochondrial DNA. It reports published and unpublished data on human mitochondrial DNA variation. All data is curated by hand. If you would like to submit published articles to be included in mitomap, please send them the citation and a pdf. gene, genome, diabetes, disease, disease-association, high resolution screening, human, inversion, metabolism, mitochondrial dna, mutation, phenotype, polymorphism, polypeptide assignment, pseudogene, restriction site, rna, sequence, trna, unpublished, variation, mitochondria, dna, insertion, deletion, FASEB list is used by: HmtVar
is listed by: OMICtools
is related to: Hereditary Hearing Loss Homepage
has parent organization: Childrens Hospital of Philadelphia - Research Institute; Pennsylvania; USA
has parent organization: Emory University School of Medicine; Atlanta; Georgia; USA
NIH ;
Muscular Dystrophy Foundation ;
Ellison Foundation ;
Diputacion General de Aragon Grupos consolidados B33 ;
NIGMS GM46915;
NINDS NS21328;
NHLBI HL30164;
NIA AG10130;
NIA AG13154;
NINDS NS213L8;
NHLBI HL64017;
NIH Biomedical Informatics Training Grant T15 LM007443;
NSF EIA-0321390;
Spanish Fondo de Investigacion Sanitaria PI050647;
Ciber Enfermedades raras CB06/07/0043
PMID:17178747
PMID:15608272
PMID:9399813
PMID:9016535
PMID:8594574
Except where otherwise noted, Creative Commons Attribution License, The community can contribute to this resource nif-0000-00511, OMICS_01641 SCR_002996 2026-02-14 02:05:42 368
mgatk
 
Resource Report
Resource Website
1+ mentions
mgatk (RRID:SCR_021159) data processing software, software resource, software toolkit, software application Software python-based command line interface for processing .bam files with mitochondrial reads and generating high-quality heteroplasmy estimation from sequencing data. This package places a special emphasis on mitochondrial genotypes generated from single-cell genomics data, primarily mtscATAC-seq, but is generally applicable across other assays. processing .bam files, mitochondrial reads, heteroplasmy estimation, sequencing data, mitochondrial genotypes, mtscATAC-seq NCI F31 CA232670;
NCI R01 CA208756;
NCI P01 CA206978;
NCI U10 CA180861;
NIDDK R01 DK103794;
NHLBI R33 HL120791
DOI:10.1038/s41587-020-0645-6 Free, Available for download, Freely available SCR_021159 mitochondrial genome analysis toolkit 2026-02-14 02:05:42 2

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