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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 Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
AbbVie
 
Resource Report
Resource Website
500+ mentions
AbbVie (RRID:SCR_010484) ABBV commercial organization A research-based biopharmaceutical company that develops advanced therapies to address global health problems. pharmaceutical, advanced therapy, biopharmaceutical, research, global health, commercial organization is related to: Kidney Health Initiative
is related to: Structural Genomics Consortium
is related to: Alzheimers Association Research Roundtable
is related to: Abbott
is related to: Abbott
is related to: NEWMEDS
is related to: ORBITO
is related to: PREDECT
nlx_158067, grid.472726.2 https://ror.org/024e28c54 SCR_010484 AbbVie Inc., AbbVie Deutschland GmbH & Co KG, AbbVie Deutschland GmbH and Co KG 2026-09-12 12:57:20 916
HMCan
 
Resource Report
Resource Website
10+ mentions
HMCan (RRID:SCR_010858) HMCan software resource A Hidden Markov Model based software tool that is developed to detect histone modification in cancer ChIP-seq data. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: King Abdullah University of Science and Technology; Makkah Province; Saudi Arabia
PMID:24021381 biotools:hmcan, OMICS_00443 https://bio.tools/hmcan SCR_010858 Histone Modification in Cancer 2026-09-12 12:57:24 14
DFLAT
 
Resource Report
Resource Website
1+ mentions
DFLAT (RRID:SCR_010738) DFLAT data or information resource, data set, narrative resource, standard specification We are an interdisciplinary team dedicated to annotating gene function related to human fetal development. We are contributing new functional annotation to the Gene Ontology, curating and mining gene sets suitable for the interpretation of developmental genomic data, and creating the computational tools needed to apply genomics for better understanding the molecular mechanisms of human development. Our GO annotation is in the process of being incorporated into the GOA public release. The GONE (Gene Ontology Non-Eligible) database is where we store annotations relevant to our research but that don''t quite meet GOA''s standards. Usually an annotation falls into this category because either the gene/protein described is a family of genes/proteins rather than a specific one, there is no UniProt ID to identify the gene/protein in the system, a GO term does not yet exist to describe the particular function, process, or location of the gene/protein, the species is not clearly identifiable in the paper, or the evidence is not as reliable (GO evidence codes TAS and NAS). As individual annotations these are more suspect than current GO annotation. However, for functional analysis of expression data, these gene sets can be valuable even with a certain amount of noise. We also include here a link to the supplementary data from our forthcoming PSB 2011 paper on gene set mining. human, fetal, development has parent organization: Tufts University; Massachusetts; USA NICHD R01 HD058880 PMID:21121032 nlx_95610 SCR_010738 Developmental FunctionaL Annotation at Tufts 2026-09-12 12:57:22 2
TESS: Transcription Element Search System
 
Resource Report
Resource Website
100+ mentions
TESS: Transcription Element Search System (RRID:SCR_010739) TESS analysis service resource, data analysis service, data or information resource, database, production service resource, service resource TESS is a web tool for predicting transcription factor binding sites in DNA sequences. It can identify binding sites using site or consensus strings and positional weight matrices from the TRANSFAC, JASPAR, IMD, and our CBIL-GibbsMat database. You can use TESS to search a few of your own sequences or for user-defined CRMs genome-wide near genes throughout genomes of interest. Search for CRMs Genome-wide: TESS now has the ability to search whole genomes for user defined CRMs. Try a search in the AnGEL CRM Searches section of the navigation bar.. You can search for combinations of consensus site sequences and/or PWMs from TRANSFAC or JASPAR. Search DNA for Binding Sites: TESS also lets you search through your own sequence for TFBS. You can include your own site or consensus strings and/or weight matrices in the search. Use the Combined Search under ''Site Searches'' in the menu or use the box for a quick search. TESS assigns a TESS job number to all sequence search jobs. The job results are stored on our server for a period of time specified in the search submit form. During this time you may recall the search results using the form on this page. TESS can also email results to you as a tab-delimited file suitable for loading into a spreadsheet program. Query for Transcription Factor Info: TESS also has data browsing and querying capabilities to help you learn about the factors that were predicted to bind to your sequence. Use the Query TRANSFAC or Query Matrices links above or use the search interface provided from the home page. transcription factor, dna sequence, genome, promoter, gene regulation, FASEB list has parent organization: University of Pennsylvania; Philadelphia; USA PMID:18428685 nlx_97404 http://www.pcbi.upenn.edu/tess SCR_010739 Transcription Element Search System 2026-09-12 12:57:22 191
miRTar
 
Resource Report
Resource Website
50+ mentions
miRTar (RRID:SCR_010851) miRTar analysis service resource, data analysis service, data or information resource, data set, production service resource, service resource An integrated web server for identifying miRNA-target interactions in human. The tool enables biologists easily to identify the biological functions and regulatory relationships between a group of known/putative miRNAs and protein coding genes. It also provides perspective of information on the miRNA targets on alternatively spliced transcripts. is listed by: OMICtools
has parent organization: National Chiao Tung University; Hsinchu; Taiwan
OMICS_00410 SCR_010851 MicroRNA Target prediction 2026-09-12 12:57:24 55
COPS
 
Resource Report
Resource Website
100+ mentions
COPS (RRID:SCR_010852) COPS software resource Software for detecting Co-Occurrence and Spatial Arrangement of Transcription Factor Binding Motifs in Genome-Wide Datasets. is listed by: OMICtools
has parent organization: Heidelberg University; Baden-Wurttemberg; Germany
PMID:23272209 OMICS_00479 SCR_010852 COPS: Detecting Co-Occurrence and Spatial Arrangement of Transcription Factor Binding Motifs in Genome-Wide Datasets 2026-09-12 12:57:24 273
E-RANGE
 
Resource Report
Resource Website
E-RANGE (RRID:SCR_010856) E-RANGE software resource A Python package for doing RNA-seq and ChIP-seq (hence the dual-use). is listed by: OMICtools OMICS_00439 SCR_010856 2026-09-12 12:57:24 0
SRS
 
Resource Report
Resource Website
1+ mentions
SRS (RRID:SCR_010736) SRS analysis service resource, data analysis service, data or information resource, database, production service resource, service resource THIS RESOURCE IS NO LONGER IN SERVICE, documented August 29, 2016. The EBI SRS server is a primary gateway to major databases in the field of molecular biology produced and supported at EBI as well as European public access point to the MEDLINE database provided by US National Library of Medicine (NLM). It is a reference server for latest developments in data and application integration. Features include: concept of virtual databases, integration of XML databases like the Integrated Resource of Protein Domains and Functional Sites (InterPro), Gene Ontology (GO), MEDLINE, Metabolic pathways, etc., user friendly data representation in ''Nice views'', SRSQuickSearch bookmarklets. Quick Searches allow users to make a number of searches without needing to learn how to use SRS in depth. The searches query some of the common databanks without having to go and select them explicitly and without the need to understand the SRS Query Forms. Quick Searches can be performed from either the Start page (when you first open SRS) or the SRS Quick Search page (when you are already in a project). SRS also has the ability to search for links between your current results and related information in other databanks. Additionally, it is able to analyze the results of your search using many bioinformatics analysis tools or applications. This enables you to seek out further information that may be relevant to your initial search. data set, gold standard is listed by: 3DVC
has parent organization: European Bioinformatics Institute
PMID:11847095
PMID:12176845
PMID:8435768
THIS RESOURCE IS NO LONGER IN SERVICE nlx_95251 SCR_010736 EBI SRS, EBI SRS server, Sequence Retrieval System 2026-09-12 12:57:22 1
FindPeaks
 
Resource Report
Resource Website
100+ mentions
FindPeaks (RRID:SCR_010857) FindPeaks software resource Software application that can be used for converting Eland, Maq (.map), BED or other files into WIG files and identifying areas of enrichment (ChIP-Seq analysis). chip-seq is listed by: OMICtools
has parent organization: SourceForge
BC Cancer Agency ;
Michael Smith Foundation for Health Research
OMICS_00440 SCR_010857 2026-09-12 12:57:24 348
CoRAL - Classification of RNAs by Analysis of Length
 
Resource Report
Resource Website
10+ mentions
CoRAL - Classification of RNAs by Analysis of Length (RRID:SCR_010828) CoRAL software resource A machine learning software package that can predict the precursor class of small RNAs present in a high-throughput RNA-sequencing dataset. In addition to classification, it also produces information about the features that are most important for discriminating different populations of small non-coding RNAs. is listed by: OMICtools
has parent organization: University of Pennsylvania; Philadelphia; USA
PMID:23700308 Acknowledgement requested OMICS_00372 SCR_010828 Classification of RNAs by Analysis of Length 2026-09-12 12:57:24 11
PriVar
 
Resource Report
Resource Website
1+ mentions
PriVar (RRID:SCR_010784) PriVar software resource A toolkit for prioritizing SNVs and indels from next-generation sequencing data. is listed by: OMICtools OMICS_00160 SCR_010784 2026-09-12 12:57:23 2
CNVer
 
Resource Report
Resource Website
1+ mentions
CNVer (RRID:SCR_010820) CNVer software resource A method for CNV detection that supplements the depth-of-coverage with paired-end mapping information, where matepairs mapping discordantly to the reference serve to indicate the presence of variation. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
biotools:cnver, OMICS_00341 https://bio.tools/cnver SCR_010820 2026-09-12 12:57:24 8
CNVnator
 
Resource Report
Resource Website
500+ mentions
CNVnator (RRID:SCR_010821) CNVnator software resource An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. is listed by: OMICtools OMICS_00343 SCR_010821 2026-09-12 12:57:24 547
Diplotyper
 
Resource Report
Resource Website
Diplotyper (RRID:SCR_010789) Diplotyper software resource A fully automated software tool which is available for Linux to investigate associations between a diplotype group and a phenotype in linear or logistic regression. is listed by: OMICtools
has parent organization: Google Code
OMICS_00195 SCR_010789 2026-09-12 12:57:23 0
Control-FREEC
 
Resource Report
Resource Website
100+ mentions
Control-FREEC (RRID:SCR_010822) Control-FREEC software resource Prediction of copy number alterations and loss of heterozygosity using deep-sequencing data. is listed by: OMICtools OMICS_00344 SCR_010822 2026-09-12 12:57:24 346
readDepth
 
Resource Report
Resource Website
10+ mentions
readDepth (RRID:SCR_010824) readDepth software resource This package for R can detect copy number aberrations by measuring the depth of coverage obtained by massively parallel sequencing of the genome. is listed by: OMICtools OMICS_00350 SCR_010824 2026-09-12 12:57:24 23
HapCUT
 
Resource Report
Resource Website
10+ mentions
HapCUT (RRID:SCR_010791) HapCUT software resource A max-cut based algorithm for haplotype assembly using sequence reads from the two chromosomes of an individual. is listed by: OMICtools OMICS_00198 SCR_010791 2026-09-12 12:57:23 17
Relate
 
Resource Report
Resource Website
10+ mentions
Relate (RRID:SCR_010794) Relate software resource Software providing a method that estimates the probability of sharing alleles identity by descent (IBD) across the genome and can also be used for mapping disease loci using distantly related individuals. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:19025785 biotools:relateadmix, OMICS_00207 https://bio.tools/relateadmix SCR_010794 2026-09-12 12:57:23 47
National Institute of Genetics; Shizuoka; Japan
 
Resource Report
Resource Website
National Institute of Genetics; Shizuoka; Japan (RRID:SCR_010836) institution Institute for genetics, through National BioResource Project, collects, preserves, and provides bio-resources (strains, populations, tissues, cells, genes of animals, plants and microorganisms, and information on these materials for R&D use) that are essential for life science research. RIN, Resource Information Network, strains, populations, tissues, cells, genes of animals, plants and microorganisms, RRID Community Authority is listed by: Resource Information Network
is parent organization of: Genome Network Platform
is parent organization of: DNA DataBank of Japan (DDBJ)
is parent organization of: NEXTDB
is parent organization of: RAP-DB
is parent organization of: Alternate Splicing - induced ALteration of Protein Structure
is parent organization of: GTOP - Genomes To Protein structures
is parent organization of: Protein Mutant Database
works with: International Mouse Strain Resource
nlx_92390 SCR_010836 NIG 2026-09-12 12:57:24 0
RNAsnp
 
Resource Report
Resource Website
10+ mentions
RNAsnp (RRID:SCR_010837) RNAsnp analysis service resource, data analysis service, production service resource, service resource, software resource Software / Web Server to predict the effect of SNPs on local RNA secondary structure based on the RNA folding algorithms implemented in the Vienna RNA package. is listed by: OMICtools
has parent organization: University of Copenhagen; Copenhagen; Denmark
PMID:23630321 OMICS_00392 SCR_010837 RNAsnp Web Server, RNAsnp Web Server: Predicting SNP effects on local RNA secondary structure 2026-09-12 12:57:24 34

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