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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
DiProGB
 
Resource Report
Resource Website
1+ mentions
DiProGB (RRID:SCR_005651) DiProGB software resource Genome browser that encodes the genome sequence by physico-chemical dinucleotide properties such as stacking energy, melting temperature or twist angle. Analyses can be performed for the + and ?, as well as for the double strand. genome, browser, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Dinucleotide Property Database
PMID:19605418 Free, Freely available biotools:diprogb, OMICS_00880 https://bio.tools/diprogb SCR_005651 DiProGB - The Dinucleotide Properties Genome Browser, Dinucleotide Properties Genome Browser 2026-02-14 02:00:58 4
MagicViewer
 
Resource Report
Resource Website
10+ mentions
MagicViewer (RRID:SCR_005648) MagicViewer software resource Software to easily visualize the short reads alignment, identify the genetic variation and associate with the annotation information of reference genome. MagicViewer provides a user-friendly interface in which large-scale short reads and sequencing depth can be easily visualized in zoomable images under user definable color scheme through an operating system-independent manner with the implement of Java language. Meanwhile, it holds a versatile genetic variation annotation and visualization interface, providing details of the query options, functional classifications, subset selection, sequence association and primer design. dna methylation, bisulfite sequencing is listed by: OMICtools
has parent organization: Wenzhou Medical University; Zhejiang; China
PMID:20444865 Free, Public OMICS_00887 SCR_005648 MagicViewer: Integrated Solution for Next-generation Sequencing Data Visualization and Genetic Variation Detection and Annotation 2026-02-14 02:01:09 16
MATRICS - Measurement And Treatment Research to Improve Cognition in Schizophrenia
 
Resource Report
Resource Website
1+ mentions
MATRICS - Measurement And Treatment Research to Improve Cognition in Schizophrenia (RRID:SCR_005644) MATRICS knowledge environment Cognitive deficits -- including impairments in areas such as memory, attention, and executive function -- are a major determinant and predictor of long-term disability in schizophrenia. Unfortunately, available antipsychotic medications are relatively ineffective in improving cognition. Scientific discoveries during the past decade suggest that there may be opportunities for developing medications that will be effective for improving cognition in schizophrenia. The NIMH has identified obstacles that are likely to interfere with the development of pharmacological agents for treating cognition in schizophrenia. These include: (1) a lack of a consensus as to how cognition in schizophrenia should be measured; (2) differing opinions as to the pharmacological approaches that are most promising; (3) challenges in clinical trial design; (4) concerns in the pharmaceutical industry regarding the US Food and Drug Administration''s (FDA) approaches to drug approval for this indication; and (5) issues in developing a research infrastructure that can carry out clinical trials of promising drugs. The MATRICS program will bring together representatives of academia, industry, and government in a consensus process for addressing all of these obstacles. Specific goals of the NIMH MATRICS are: * To catalyze regulatory acceptance of cognition in schizophrenia as a target for drug registration. * To promote development of novel compounds to enhance cognition in schizophrenia. * Leverage economic research power of industry to focus on important but neglected clinical targets. * Identify lead compounds and if deemed feasible, support human proof of concept trials for cognition in schizophrenia. schizophrenia, cognitive deficit, memory, attention, executive function, disability, cognition, clinical has parent organization: University of California at Los Angeles; California; USA Schizophrenia NIMH nlx_146271 SCR_005644 Measurement And Treatment Research to Improve Cognition in Schizophrenia, Measurement Treatment Research to Improve Cognition in Schizophrenia 2026-02-14 02:00:56 6
WISECONDOR
 
Resource Report
Resource Website
10+ mentions
WISECONDOR (RRID:SCR_005646) WISECONDOR software resource A set of python scripts that detects fetal chromosomal and subchromosomal duplications and deletions in maternal blood samples., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. is listed by: OMICtools
has parent organization: Netherlands Bioinformatics Centre
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00354 SCR_005646 WIthin-SamplE COpy Number aberration DetectOR 2026-02-14 02:01:08 12
COBrA
 
Resource Report
Resource Website
1000+ mentions
COBrA (RRID:SCR_005677) COBrA software resource COBrA is a Java-based ontology editor for bio-ontologies that distinguishes itself from other editors by supporting the linking of concepts between two ontologies, and providing sophisticated analysis and verification functions. In addition to the Gene Ontology and Open Biology Ontologies formats, COBrA can import and export ontologies in the Semantic Web formats RDF, RDFS and OWL. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. ontology, anatomy, browser, ontology or annotation browser is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: OBO
has parent organization: University of Edinburgh; Scotland; United Kingdom
BBSRC 15/BEP 17046 PMID:15513995 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149117 SCR_005677 COBrA - An Ontology Browser for Anatomy, COBrA: a bio-ontology editor 2026-02-14 02:00:59 1396
DMRforPairs
 
Resource Report
Resource Website
1+ mentions
DMRforPairs (RRID:SCR_005702) software resource Software for identifying differentially methylated regions between unique samples using array based methylation profiles. It allows researchers to compare n greater than or equal to 2 unique samples with regard to their methylation profile. The (pairwise) comparison of n unique single samples distinguishesit from other existing pipelines as these often compare groups of samples in either single CpG locus or region based analysis. DMRforPairs defines regions of interest as genomic ranges with sufficient probes located in close proximity to each other. Probes in one region are optionally annotated to the same functional class(es). Differential methylation is evaluated by comparing the methylation values within each region between individual samples and (if the difference is sufficiently large), testing this difference formally for statistical significance. standalone software, mac os x, unix/linux, windows, r, annotation, dna methylation, differential methylation, microarray, report writing, visualization, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:24884391 GNU General Public License, v2 or greater biotools:dmrforpairs, OMICS_04059 https://bio.tools/dmrforpairs SCR_005702 DMR2+, DMRforPairs: identifying Differentially Methylated Regions between unique samples using array based methylation profiles 2026-02-14 02:01:09 4
Principe Felipe Research Centre; Valencia; Spain
 
Resource Report
Resource Website
1+ mentions
Principe Felipe Research Centre; Valencia; Spain (RRID:SCR_005691) CIPF institution The Pr��ncipe Felipe Research Centre (CIPF), which was inaugurated by their Royal Highnesses the Prince and Princess of Asturias on 17th March 2005, is a centre dedicated to biomedical research, with the aim of taking on new challenges in the field of basic research and encouraging scientific works of excellence. The construction of the Centre was carried out thanks to the Regional Development Funds from the European Union, and from the Regional Government (Generalitat Valenciana) through its Ministry of Health. The current financing of the CIPF comes mainly from the investment made by the Generalitat Valenciana through the Ministry of Health, as well as the Regenerative Medicine Programme, the fruit of an agreement between the Institute of Health Carlos III and the Ministry of Health for basic and translation research in this field. The CIPF takes the research tradition from the then Valencian Cytological Research Institute and the Valencian Biomedical Research Foundation, with the aim of consolidating and expanding this research. Therefore the activity in the CIPF can be divided into three main strategic work areas: The Regenerative Medicine area focuses its research on cellular therapy and interdisciplinary research in human embryonic and adult stem cells, with the aim of regenerating damaged organs to improve human health. The Chemical and Quantative Biology area aims to understand, through the application of (bio) chemical, genetic, and bioinformatic methods, to understand the molecular mechanisms that control the biological processes and alterations that lead to pathological conditions. The Biomedicine area focuses on understanding the molecular bases of human pathologies that require new diagnostic and clinical procedures for their identification and treatment, pathologies such as cancer, neurological pathologies and rare illnesses. is parent organization of: QualiMap
is parent organization of: VARIANT
is parent organization of: CIPF Bioinformatics and Genomics Department
is parent organization of: Blast2GO
is parent organization of: Gene Expression Profile Analysis Suite
nlx_149142, grid.418274.c, ISNI: 0000 0004 0399 600X https://ror.org/05xr2yq54 SCR_005691 Centro de Investigaci��n Pr��ncipe Felipe, Centro de Investigacion Principe Felipe, Principe Felipe Research Center, Pr��ncipe Felipe Research Centre 2026-02-14 02:01:10 2
VAGUE
 
Resource Report
Resource Website
1+ mentions
VAGUE (RRID:SCR_005607) VAGUE software resource An open-source de novo genome assembly software tool, which is run from the Unix command line, providing a multi-platform graphical front-end for the Velvet de novo assembler. VAGUE is implemented in JRuby and targets the Java Virtual Machine. command line, assembler is listed by: OMICtools
has parent organization: Monash University; Melbourne; Australia
PMID:23162059 GNU General Public License, v2, Acknowledgement requested OMICS_00897 SCR_005607 Velvet Assembler Graphical Front End 2026-02-14 02:00:58 5
Bismark
 
Resource Report
Resource Website
1000+ mentions
Bismark (RRID:SCR_005604) Bismark software resource Software tool to map bisulfite converted sequence reads and determine cytosine methylation states. Flexible aligner and methylation caller for Bisulfite-Seq applications. Used to map bisulfite treated sequencing reads to genome of interest and perform methylation calls in single step. Map bisulfite treated sequence reads, determine cytosine methylation states, genome, sequence reads, perform methylation calls, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Babraham Institute
PMID:21493656
DOI:10.1093/bioinformatics/btr167
Free, Available for download, Freely available biotools:bismark, OMICS_00575 https://github.com/FelixKrueger/Bismark
https://bio.tools/bismark
https://sources.debian.org/src/bismark/ SCR_005604 2026-02-14 02:01:09 1123
jMHC
 
Resource Report
Resource Website
10+ mentions
jMHC (RRID:SCR_005605) jMHC software resource Software for analyzing and visualization of the results of deep amplicon sequencing. matlab is listed by: OMICtools
has parent organization: Google Code
PMID:21676201 GNU General Public License, v3, Acknowledgement requested OMICS_00300 SCR_005605 jmhc - software for analyzing and visualization of the results of deep amplicon sequencing 2026-02-14 02:00:56 10
TMA-Combiner
 
Resource Report
Resource Website
1+ mentions
TMA-Combiner (RRID:SCR_005600) TMA-Combiner software resource A Simple Software Tool to Permit Analysis of Replicate Cores on Tissue Microarrays., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. tissue microarray is listed by: OMICtools
is related to: Stanford TMA Software
has parent organization: Stanford University; Stanford; California
PMID:16258508 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00822 SCR_005600 2026-02-14 02:01:09 1
TMAJ
 
Resource Report
Resource Website
10+ mentions
TMAJ (RRID:SCR_005601) TMAJ software resource Open-source software to support information and images related to tissue micro-arrays. It contains support for multiple organ systems, multiple users, image analysis, and is designed to be compliant with HIPPA regulations. Patients, specimens, blocks, slides, cores, images, and scores can all be stored and viewed. Features include advanced security, custom dynamic fields, and an image analysis program. tissue microarray, java, java swing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Johns Hopkins University; Maryland; USA
has parent organization: SourceForge
GNU General Public License, v3 biotools:tmaj, OMICS_00823 https://bio.tools/tmaj SCR_005601 TMAJ Software Project 2026-02-14 02:00:56 10
GOProfiler
 
Resource Report
Resource Website
1+ mentions
GOProfiler (RRID:SCR_005683) GOProfiler service resource Service that provides a summary of GO annotations available for each species. The user provides a taxon id and GOProfiler displays the number of GO associations and the number of annotated proteins for that species. The results are listed by evidence code and a separate list of unannotated proteins is also provided. ontology or annotation browser, annotation, protein, gene ontology is listed by: Gene Ontology Tools
is listed by: OMICtools
is related to: Gene Ontology
has parent organization: AgBase
PMID:16961921 Free for academic use OMICS_02269, nlx_149127 SCR_005683 2026-02-14 02:00:59 2
National Hellenic Research Foundation
 
Resource Report
Resource Website
1+ mentions
National Hellenic Research Foundation (RRID:SCR_005719) NHRF institution The National Hellenic Research Foundation (NHRF) is a multidisciplinary Research Centre established by Royal Decree on 9th October 1958. Its purpose is the organisation, finance and support of high-level research projects in the humanities and the natural sciences. The Humanities Institute cover a wide spectrum of study and research fields in Greek history and culture, contributing substantially and critically to the knowledge and promotion of Greek identity. The Natural Sciences Institutes perform basic and applied research in leading edge areas of science such as health, pharmaceuticals, environment, biotechnology and new materials. They develop innovative methods for solving complex problems facing Greek industry and they provide specialised services and know-how both to the public and private sector. The NHRF is governed by the Board of Directors and the Central Administration under the Director/Chairman of the Board. humanities, natural sciences is parent organization of: StRAnGER ISNI: 0000 0001 2232 6894, grid.22459.38, Wikidata: Q1248816, nlx_149177 https://ror.org/033m02g29 SCR_005719 National Hellenic Research Foundation 2026-02-14 02:01:09 4
Stanford TMA Software
 
Resource Report
Resource Website
1+ mentions
Stanford TMA Software (RRID:SCR_005598) Stanford TMA software resource Software Tools for High-Throughput Analysis and Archiving of Immunohistochemistry Staining Data Obtained with Tissue Microarrays. tissue microarray is listed by: OMICtools
is related to: TMA-Combiner
has parent organization: Stanford University; Stanford; California
PMID:12414504 OMICS_00819 SCR_005598 Stanford TMA Software website, Stanford Tissue Microarray Software 2026-02-14 02:00:58 1
OXBench
 
Resource Report
Resource Website
1+ mentions
OXBench (RRID:SCR_005591) OXBench software resource A suite of programs aimed at developers of alignment methods rather than end-users to assess the accuracy of multiple sequence alignment methods. It includes a reference database of protein multiple sequence alignments that were generated by consideration of protein three-dimensional structure. alignment, linux, protein, sequence alignment is listed by: OMICtools
has parent organization: University of Dundee; Scotland; United Kingdom
PMID:14552658 Acknowledgement requested OMICS_00983 http://www.compbio.dundee.ac.uk/Software/Oxbench/oxbench.html Alt. URL: http://www.compbio.dundee.ac.uk/software.html SCR_005591 2026-02-14 02:00:57 2
Staden Package
 
Resource Report
Resource Website
50+ mentions
Staden Package (RRID:SCR_005629) software resource A fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin) for Unix, Linux, MacOSX and MS Windows. c, unix/linux, sequence assembly, dna/protein analysis, spin, sequence alignment, genome, genome viewer, c++, fortran, tcl, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:20513662
DOI:10.1093/bioinformatics/btq268
BSD License OMICS_00894, biotools:staden https://bio.tools/staden
https://sources.debian.org/src/staden/
SCR_005629 Staden Package 2026-02-14 02:01:09 79
Chromaseq
 
Resource Report
Resource Website
1+ mentions
Chromaseq (RRID:SCR_005587) Chromaseq software resource A software package in Mesquite that processes chromatograms, makes contigs, base calls, etc., using in part the programs Phred and Phrap. chromatogram, sequence, mesquite is listed by: OMICtools
has parent organization: Oregon State University; Oregon; USA
NSF EF-0531754 Acknowledgement required OMICS_01017 SCR_005587 Chromaseq: a package for processing chromatograms and sequence data in Mesquite 2026-02-14 02:01:09 7
MAGENTA
 
Resource Report
Resource Website
100+ mentions
MAGENTA (RRID:SCR_003422) MAGENTA software resource A computational tool that tests for enrichment of genetic associations in predefined biological processes or sets of functionally related genes, using genome-wide genetic data as input. is listed by: OMICtools
has parent organization: Broad Institute
PMID:20714348 Free, Available for download, Freely available OMICS_00236 SCR_003422 Meta-Analysis Gene-set Enrichment of variaNT Associations 2026-02-14 02:00:27 140
NAPPA
 
Resource Report
Resource Website
10+ mentions
NAPPA (RRID:SCR_003419) NAPPA software resource Software that enables the processing and normalization of the standard mRNA data output from the Nanostring nCounter software. normalization, processing, nanostring, mirna, mrna, os x, windows is listed by: OMICtools GNU General Public License, v3 OMICS_02310 SCR_003419 NAPPA: Performs the processing and normalisation of Nanostring miRNA and mRNA data 2026-02-14 02:00:48 12

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