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

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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
Track-A-Worm
 
Resource Report
Resource Website
1+ mentions
Track-A-Worm (RRID:SCR_018299) data analysis software, software application, data processing software, software resource Open source system for quantitative assessment of C. Elegans locomotory and bending behavior. Used for quantitative behavioral analyses to understand circuit and gene bases of behavior. Constantly records and analyzes position and body shape of freely moving worm at high magnification. Quantitative assessment, C.Elegans locomotory, bending behavior, behavioral analysis, gene, moving worm position, body shape, automated recording is related to: University of Connecticut; Connecticut; USA NIGMS R01 GM083049;
NIMH R01 MH085927
PMID:23922769 Free, Available for download, Freely available SCR_018299 Tracker-A-Worm version 1.0, Tracker-A-Worm version 2.0 2026-02-17 10:03:03 3
piNET
 
Resource Report
Resource Website
1+ mentions
piNET (RRID:SCR_018693) data access protocol, production service resource, analysis service resource, service resource, software resource, web service Web platform for downstream analysis and visualization of proteomics data. Server that facilitates integrated annotation, analysis and visualization of quantitative proteomics data, with emphasis on PTM networks and integration with LINCS library of chemical and genetic perturbation signatures in order to provide further mechanistic and functional insights. Primary input for server consists of set of peptides or proteins, optionally with PTM sites, and their corresponding abundance values. Analysis, visualization, proteomics data, integrated annotation, quantitative proteomics data, PTM network, LINCS library integration, genetic perturbation signature, peptide, protein, post translational modification site, PTM site, data is related to: LINCS Project NHLBI U54 HL127624;
NIEHS P30 ES006096;
NIMH R01 MH107487;
NCI T32 CA236764;
NCATS UL1 TR001425;
NIGMS U01 GM120953
DOI:10.1093/nar/gkaa436 Free, Freely available SCR_018693 2026-02-17 10:03:50 4
TimeZone
 
Resource Report
Resource Website
1+ mentions
TimeZone (RRID:SCR_018564) data analysis software, software application, data processing software, software resource Software package to detect footprints of positive selection for functionally adaptive point mutations in microbial genomes. Detect footprint, positive selection, functionally adaptive, point mutation, microbial genome NIGMS R01 GM084318;
NIAID RC4 AI092828
PMID:23471110 Free, Available for download, Freely available SCR_018564 2026-02-17 10:03:06 1
Monocle3
 
Resource Report
Resource Website
100+ mentions
Monocle3 (RRID:SCR_018685) software application, data processing software, data analysis software, software resource, software toolkit Software analysis toolkit for single cell RNA-seq. Used for single cell RNA-Seq experiments. Unsupervised algorithm that increases temporal resolution of transcriptome dynamics using single-cell RNA-Seq data collected at multiple time points. Data analysis, singel cell RNAseq data, single cell RNAseq experiment, transcriptome dynamics has parent organization: University of Washington; Seattle; USA NIH Office of the Director DP2 OD00667;
NIGMS P01 GM099117;
NIH Office of the Director DP2 0D008514;
NHGRI P50 HG006193;
Single Cell Genomics initiative
PMID:24658644 Free, Available for download, Freely available https://github.com/cole-trapnell-lab/monocle3 SCR_018685 Monocle, Monocle 3 2026-02-17 10:03:48 270
BpForms
 
Resource Report
Resource Website
BpForms (RRID:SCR_018653) data access protocol, web service, software toolkit, software resource Software toolkit for unambiguously describing molecular structure of DNA, RNA, and proteins, including non-canonical monomeric forms, crosslinks, nicks, and circular topologies. Aims to help epigenomics, transcriptomics, proteomics, systems biology, and synthetic biology researchers share and integrate information about DNA modification, post-transcriptional modification, post-translational modification, expanded genetic codes, and synthetic parts. Molecular structure description, DNA, RNA, protein, modification, epigenetics, transcriptomics, post transcriptional modification, post translational modification, bio.tools uses: BcForms
is used by: ObjTables
is used by: Datanator
is listed by: Debian
is listed by: bio.tools
is related to: BcForms
is related to: ObjTables
NIBIB P41 EB023912;
NSF 1649014;
NIGMS R35 GM119771
PMID:32423472 Free, Freely available biotools:bpforms https://bio.tools/bpforms SCR_018653 2026-02-17 10:03:49 0
ObjTables
 
Resource Report
Resource Website
ObjTables (RRID:SCR_018652) data management software, software application, data processing software, software resource, software toolkit Software toolkit for creating reusable datasets that are both human and machine readable, combining spreadsheets with schemas including classes, their attributes, type of each attribute, and possible relationships between instances of classes.Consists of format for describing schemas for spreadsheets, numerous data types for science, syntax for indicating class and attribute represented by each table and column in workbook, and software for using schemas to rigorously validate, merge, split, compare, and revision datasets. Used for supplementary materials of journal article, as well as for emerging domains which need to quickly build new formats for new types of data and associated software with minimal effort. Creating reusable dataset, combining spreadsheet with schema, spreadsheet, table, supplementary material, schema, object relational map, validation, bio.tools uses: BpForms
uses: BcForms
is listed by: bio.tools
is listed by: Debian
is related to: BpForms
NIBIB P41 EB023912;
NSF 1649014;
NIGMS R35 GM119771
Free, Freely available biotools:objtables https://bio.tools/objtables SCR_018652 2026-02-17 10:03:30 0
MyGene.info
 
Resource Report
Resource Website
10+ mentions
MyGene.info (RRID:SCR_018660) data access protocol, service resource, web service, software resource Web service for querying or retrieving gene annotation data. Querying gene, gene, annotation, gene annotation, annotation data, gene annotation data, retrieving gene annotation data, bio.tools is listed by: Debian
is listed by: bio.tools
NHGRI U01 HG008473;
NIGMS GM083924;
NIGMS U54 GM114833;
NHGRI U01 HG006476;
NCI K22 CA188163;
NCATS UL1 TR001114;
Scripps Translational Science Institute
DOI:10.1186/s13059-016-0953-9 Free, Freely available biotools:mygene.info, BioTools:mygene.info https://bio.tools/mygene.info
https://bio.tools/mygene.info
https://bio.tools/mygene.info
SCR_018660 2026-02-17 10:03:07 20
ROSIE
 
Resource Report
Resource Website
1+ mentions
ROSIE (RRID:SCR_018764) ROSIE data access protocol, application programming interface, web application, software resource Unified web framework for Rosetta applications. Web interface for selected Rosetta protocols. Web front end for Rosetta software suite. Provides common user interface for Rosetta protocols, stable application programming interface for developers to add additional protocols, flexible back-end to allow leveraging of computer cluster resources shared by Rosetta Commons member institutions, and centralized administration by Rosetta Commons to ensure continuous maintenance. Offers general and speedy paradigm for serverification of Rosetta applications. Lowers barriers to Rosetta use for broader biological community. Web interface for Rosetta, Rosetta online server, Rosetta application serverification, Rosetta user interface works with: Rosetta NIGMS R01 GM073151;
NIGMS R01 GM07822;
NIGMS R21 GM102716;
NCRR R00 RR024107;
NCI U54 CA143907;
NEI PN2 EY016586;
NIGMS T32 GM 88118;
Taiwan Governmental Scholarship for Study Abroad ;
Howard Hughes Medical and Institute International Student Research Fellowship ;
NSF
PMID:23717507 Restricted https://rosie.rosettacommons.org/ SCR_018764 Rosetta Online Server that Includes Everyone 2026-02-17 10:03:48 7
GOnet
 
Resource Report
Resource Website
1+ mentions
GOnet (RRID:SCR_018977) data access protocol, production service resource, analysis service resource, service resource, software resource, web service Web tool for interactive Gene Ontology analysis of any biological data sources resulting in gene or protein lists. Gene Ontology, interactive analysis, data, gene, protein, gene list, protein list, analysis, bio.tools is listed by: Debian
is listed by: bio.tools
works with: Gene Ontology
NIH Common Fund ;
NIGMS ;
NHGRI R24 HG010032;
NIAID U19 AI118610;
NIAID U19 AI118626
PMID:30526489 biotools:GOnet https://github.com/mikpom/gonet
https://bio.tools/GOnet
SCR_018977 2026-02-17 10:03:10 3
CAIRN
 
Resource Report
Resource Website
CAIRN (RRID:SCR_019101) data access protocol, software application, data processing software, software resource, web service, data visualization software Web tool to graph all copy number alterations present in segment file. Custom data is permitted. Allows to display copy number alterations which overlap user specified region, to quantify number of amplified CNAs and deleted CNAs. Visualization tool to explore copy number alterations discovered in published cancer datasets. Intended to help oncology community observe of relative rates of amplification, deletion, and mutation of interesting genes and regions. Deleted CNAs quantification, Copy Number Alterations, segment file, data visualization, published cancer datasets CNAs, amplified CNA quantification Nine Girls Ask Foundation ;
NCI CA207729;
NIGMS GM132055;
NCI CA107263;
NCI CA177519;
NCI CA102310;
NIA AG033082;
NCI P30 CA138313
PMID:31923184 Free, Available for download, Freely available https://github.com/jrdelaney/CAIRN SCR_019101 Copy Alterations Intuitive Rendering Navigator 2026-02-17 10:03:52 0
Brain Imaging Data Structure (BIDs)
 
Resource Report
Resource Website
100+ mentions
Brain Imaging Data Structure (BIDs) (RRID:SCR_016124) BIDS data or information resource, narrative resource, portal, standard specification Standard specification for organizing and describing outputs of neuroimaging experiments. Used to organize and describe neuroimaging and behavioral data by neuroscientific community as standard to organize and share data. BIDS prescribes file naming conventions and folder structure to store data in set of already existing file formats. Provides standardized templates to store associated metadata in form of Javascript Object Notation (JSON) and tab-separated value (TSV) files. Facilitates data sharing, metadata querying, and enables automatic data analysis pipelines. System to curate, aggregate, and annotate neuroimaging databases. Intended for magnetic resonance imaging data, magnetoencephalography data, electroencephalography data, and intracranial encephalography data. Data storing structure, neuroimaging, standardized template, data sharing, MRI data, MEG data, EEG data, iEEG data, FASEB list is used by: OpenNeuro
is used by: SPARC Portal
is used by: SPARC Data Standard
is listed by: FAIRsharing
is related to: BIDS-Matlab
is related to: NiPoppy
works with: MNE-BIDS
International Neuroinformatics Coordinating Facility ;
Laura and John Arnold Foundation ;
NIGMS P20 GM103472;
Wellcome Trust ;
NIAAA U01 AA021697;
NIMH Intramural Research Program ;
German federal state of Sachsen-Anhalt ;
European Regional Development Fund ;
Medical Research Council United Kingdom ;
NSF 1429999
PMID:27326542
PMID:29917016
PMID:31239435
PMID:31239438
PMID:37744469
Free, Freely available https://bids-specification.readthedocs.io/en/stable/, https://doi.org/10.25504/FAIRsharing.rd1j6t SCR_016124 Brain Imaging Data Structure, BIDS, Brain Imaging Data Structure (BIDS), Brain Imaging Data Structure v1.4.0 2026-02-17 10:02:58 212
SV-plaudit
 
Resource Report
Resource Website
1+ mentions
SV-plaudit (RRID:SCR_016285) software application, data processing software, data analysis software, software resource, image analysis software Software for rapidly curating structural variant (SVs) predictions. SV-plaudit provides a pipeline for creating image views of genomic intervals, automatically storing them in the cloud, deploying a website to view/score them, and retrieving scores for analysis. genomics, structural, variants, visualization, manual, curation, prediction, image, alignment NHGRI K99 HG009532;
NHGRI R01 HG006693;
NIGMS R01 GM124355;
NCI U24 CA209999
Free, Available for download SCR_016285 2026-02-17 10:03:23 2
star-for-criu
 
Resource Report
Resource Website
1+ mentions
star-for-criu (RRID:SCR_016294) software application, data processing software, software resource, image analysis software, alignment software Software as an Hot Start software container for STAR alignment using CRIU (Checkpoint Restore in Userspace) tool to freeze the running container. Can be deployed to align RNA sequencing data. Used in the processing of biomedical big data for better reproducibility and reliability. hot, start, container, star, aligner, sequencing, data, processing, biomedical, cloud, reproducibility, RNA, analysis, computing, environment is related to: Systems Transcriptional Activity Reconstruction NHLBI U54 HL127624;
AMEDD Advanced Medical Technology Initiative ;
NIGMS R01 GM126019
Free, Freely available, Available for download https://github.com/paizhang/Hotstarting-For-STAR-Alignment SCR_016294 2026-02-17 10:03:23 1
MotionCor2
 
Resource Report
Resource Website
100+ mentions
MotionCor2 (RRID:SCR_016499) data analysis software, software application, data processing software, software resource Software tool for anisotropic correction of beam-induced motion for improved cryo-electron microscopy. Used to describe the sample motion as a local deformation that varies smoothly throughout the exposure. A program running on Linux. anisotropic, correction, beam, induced, motion, cryo, electron, microscopy, exposure, data has parent organization: University of California at San Francisco; California; USA NIH R01 GM031627;
NIGMS P01 GM111126
PMID:28250466 Restricted http://msg.ucsf.edu/em/software/motioncor2.html SCR_016499 MotionCor 2026-02-17 10:03:25 172
Pavian
 
Resource Report
Resource Website
10+ mentions
Pavian (RRID:SCR_016679) web application, production service resource, analysis service resource, service resource, software resource, data analysis service Software R package for interactive analysis of metagenomics classification results with a special focus on infectious disease diagnosis. Used for analyzing and visualization of metagenomics classification results from classifiers such as Kraken, Centrifuge and MetaPhlAn. Provides an alignment viewer for validation of matches to a particular genome. interactive, analysis, metagenomics, classification, result, infectious, disease, diagnosis, data, visualization, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: Centrifuge Classifier
NHGRI R01 HG006677;
NIGMS R01 GM083873;
U. S. Army Research Office W911NF1410490
DOI:10.1101/084715 Free, Freely available biotools:pavian https://fbreitwieser.shinyapps.io/pavian/
https://bio.tools/pavian
SCR_016679 2026-02-17 10:03:04 22
XYalign
 
Resource Report
Resource Website
1+ mentions
XYalign (RRID:SCR_016661) software application, data processing software, data analysis software, software resource, sequence analysis software Software tool for identifying, understanding, and correcting technical biases on the sex chromosomes in next generation sequencing data. correct, technical, bias, sex, chromosome, next, generation, sequencing, data is listed by: OMICtools NIGMS R35 GM124827 DOI:10.1101/346940 Free, Available for download, Freely available SCR_016661 2026-02-17 10:02:44 1
Centrifuge Classifier
 
Resource Report
Resource Website
1+ mentions
Centrifuge Classifier (RRID:SCR_016665) software application, data processing software, data analysis software, software resource, sequence analysis software Software for rapid and sensitive classification of metagenomic sequences. Used for the classification of DNA sequences from microbial samples and analysis of large metagenomics data sets on conventional desktop computers. classification, large, metagenomic, sequence, DNA, microbial, sample, analysis, data, desktop, computer, bio.tools is listed by: bio.tools
is listed by: Debian
is listed by: OMICtools
is related to: Pavian
has parent organization: Center for Computational Biology at JHU
U. S. Army Research Office W911NF1410490;
NSF ABI1356078;
NHGRI R01 HG006677;
NIGMS R01 GM083873
DOI:10.1101/gr.210641.116 Free, Available for download, Freely available biotools:centrifuge, OMICS_12217 https://github.com/infphilo/centrifuge
https://bio.tools/centrifuge
https://sources.debian.org/src/centrifuge/
SCR_016665 2026-02-17 10:02:44 9
trRosetta
 
Resource Report
Resource Website
50+ mentions
trRosetta (RRID:SCR_021181) software application, software resource, simulation software, service resource Software tool for fast and accurate protein structure prediction. Builds protein structure based on direct energy minimizations with restrained Rosetta. Restraints include inter-residue distance and orientation distributions, predicted by deep residual neural network. Homologous templates are included in network prediction to improve accuracy for easy targets. protein structure, restraint-guided structure generation, protein structure prediction uses: Rosetta National Natural Science Foundation of China ;
Fok Ying-Tong Education Foundation ;
Key Laboratory for Medical Data Analysis and Statistical Research of Tianjin ;
Thousand Youth Talents Plan of China ;
China Scholarship Council ;
NIGMS R01 GM092802;
NIH Office of the Director DP5 OD026389
PMID:31896580 Free, Freely available https://github.com/gjoni/trRosetta SCR_021181 transformed restrained Rosetta 2026-02-17 10:03:44 67
Motif Mutation Analysis for Regulatory Genomic Elements
 
Resource Report
Resource Website
500+ mentions
Motif Mutation Analysis for Regulatory Genomic Elements (RRID:SCR_021902) MMARGE software application, data processing software, data analysis software, software resource, software toolkit 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 2026-02-17 10:04:06 608
3DRefine
 
Resource Report
Resource Website
10+ mentions
3DRefine (RRID:SCR_021883) data access protocol, web service, software resource Interactive web server for efficient protein structure refinement with capability to perform web based statistical and visual analysis. efficient protein structure refinement, statistical and visual analysis NIGMS R01 GM093123 DOI:10.1093/nar/gkw336 Free, Freely available SCR_021883 2026-02-17 10:03:55 20

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