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

  • Related Resources:bio.tools (facet)

Facets


Recent searches

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

1,660 Results - per page

Show More Columns | Download Top 1000 Results

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
AgBase
 
Resource Report
Resource Website
100+ mentions
AgBase (RRID:SCR_007547) AgBase data or information resource, database A curated, open-source, web-accessible resource for functional analysis of agricultural plant and animal gene products. Our long-term goal is to serve the needs of the agricultural research communities by facilitating post-genome biology for agriculture researchers and for those researchers primarily using agricultural species as biomedical models. AgBase provides tools designed to assist with the analysis of proteomics data and tools to evaluate experimental datasets using the GO. Additional tools for sequence analysis are also provided. We use controlled vocabularies developed by the Gene Ontology (GO) Consortium to describe molecular function, biological process, and cellular component for genes and gene products in agricultural species. AgBase will also accept annotations from any interested party in the research communities. AgBase develops freely available tools for functional analysis, including tools for using GO. We appreciate any and all questions, comments, and suggestions. AgBase uses the NCBI Blast program for searches for similar sequences. And the Taxonomy Browser allows users to find the NCBI defined taxon ID for or taxon name for different organisms. gene ontology, agricultural species, biological process, cellular component for genes, molecular function, protein identification, animals, plants, microbes, parasites, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is related to: IntAct
has parent organization: Mississippi State University; Mississippi; USA
is parent organization of: GORetriever
is parent organization of: GOSlimViewer
is parent organization of: GOProfiler
is parent organization of: GOanna
Mississippi State University; Mississippi; USA ;
USDA Agriculture and Food Research Initiative Competitive Grant 2011-67015-30332;
National Research Initiative of the USDA Cooperative State Research Education and Extension Service 2007-35205-17941;
NIGMS project 07111084;
NSF EPS 0903787
PMID:21075795 nif-0000-02537, biotools:agbase, r3d100012427 https://bio.tools/agbase, https://doi.org/10.17616/R3P772 SCR_007547 2026-09-12 01:01:47 112
HubMed
 
Resource Report
Resource Website
1+ mentions
HubMed (RRID:SCR_007296) data or information resource, database HubMed provides an interface to PubMed. Quick access to searches with a Firefox search plugin or a HubMed bookmarklet (drag to your browser''s bookmarks toolbar). Export citations in RIS, BibTeX, RDF and MODS formats, or directly to RefWorks. Unzip HubMed''s import filter into Endnote''s Filters folder for direct import into Endnote, or install the RIS Export plugin for direct import into ProCite, RefMan and older versions of Endnote. Use the Citation Finder to convert reference lists from PDFs into search results. Create lists of closely related papers using Rank Relations, then visualise and browse clusters of related papers using TouchGraph (requires Java). Graph occurrences of keywords in published papers over time. Tag and store annotated metadata for articles of interest. bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: National Center for Integrative Biomedical Informatics
nif-0000-00111, biotools:hubmed https://bio.tools/hubmed SCR_007296 HubMed 2026-09-12 01:01:46 9
COGEME Phytopathogenic Fungi and Oomycete EST Database
 
Resource Report
Resource Website
1+ mentions
COGEME Phytopathogenic Fungi and Oomycete EST Database (RRID:SCR_007604) data or information resource, database COGEME is an ongoing BBSRC-funded study to construct a relational database of genomic information from phytopathogenic fungi. This site also hosts microarray data for Blumeria graminis. Expressed sequence tags (ESTs) obtained from eighteen species of plant pathogenic fungi, two species of phytopathogenic oomycete and three species of saprophytic fungi are included here. Hierarchical clustering software was used to classify together ESTs representing the same gene and produce a single contig, or consensus sequence. The unisequence set for each pathogen therefore represents a set of unique gene sequences, each one consisting of either a single EST or a contig sequence made from a group of ESTs. Unisequences were annotated based on top hits against the NCBI non-redundant protein database using blastx. blumeria graminis, phytopathogen, phytopathogen est, phytopathogenic fungi, phytopathogenic oomycete, plant pathogenic fungi, saprophytic fungi, bio.tools is listed by: bio.tools
is listed by: Debian
nif-0000-02673, biotools:cogeme https://bio.tools/cogeme SCR_007604 COGEME 2026-09-12 01:01:48 5
Atlas of Genetics and Cytogenetics in Oncology and Haematology
 
Resource Report
Resource Website
10+ mentions
Atlas of Genetics and Cytogenetics in Oncology and Haematology (RRID:SCR_007199) atlas, data or information resource, database Online journal and database devoted to genes, cytogenetics, and clinical entities in cancer, and cancer-prone diseases. Its aim is to cover the entire field under study and it presents concise and updated reviews (cards) or longer texts (deep insights) concerning topics in cancer research and genomics. gene, cytogenetic, cancer, cancer research, genomic, online journal, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
PMID:23161685 Freely available, Available to the scientific community nif-0000-30129, biotools:atlasgeneticsoncology https://bio.tools/atlasgeneticsoncology SCR_007199 Genetics and Cytogenetics Atlas 2026-09-12 01:01:46 43
CATH: Protein Structure Classification
 
Resource Report
Resource Website
100+ mentions
CATH: Protein Structure Classification (RRID:SCR_007583) data or information resource, database CATH is a hierarchical classification of protein domain structures, which clusters proteins at four major levels: Class (C), Architecture (A), Topology (T) and Homologous superfamily (H). The boundaries and assignments for each protein domain are determined using a combination of automated and manual procedures which include computational techniques, empirical and statistical evidence, literature review and expert analysis Users can search CATH by ID/Sequence/text. They can also browse CATH from the top of the hierarchy, or download CATH data. architecture, class, homologous superfamily, protein cluster, protein domain structure, topology, bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
is related to: FunTree
has parent organization: University College London; London; United Kingdom
nif-0000-02640, r3d100012629, biotools:cath https://bio.tools/cath, https://doi.org/10.17616/R32Z1F SCR_007583 CATH 2026-09-12 01:01:48 306
Hyper Cell Line Database
 
Resource Report
Resource Website
Hyper Cell Line Database (RRID:SCR_007730) HyperCLDB biomaterial supply resource, material resource, tissue bank Hypertext on cell culture availability extracted from the Cell Line Data Base of the Interlab Project. HyperCLDB includes links to records of OMIM, the Online Mendelian Inheritance in Man Catalogue, and now also links to the PubMed, database of bibliographic biomedical references, which are drawn primarily from MEDLINE and PREMEDLINE. cell, cell line, tumor, tissue, organ, blood, bodily fluid, ascitic fluid, brain, bone marrow, cancer, transforming agent, software, bio.tools is listed by: One Mind Biospecimen Bank Listing
is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
is related to: ATCC
is related to: Cell Line Knowledge Base
has parent organization: IST National Institute for Cancer Research; Genoa; Italy
Cancer, Etc. PMID:18927105 nif-0000-03004, biotools:hypercldb https://bio.tools/hypercldb SCR_007730 2026-09-12 01:01:51 0
Genome Reviews
 
Resource Report
Resource Website
1+ mentions
Genome Reviews (RRID:SCR_007685) data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE, documented April 24, 2017. The Genome Reviews database provides an up-to-date, standardized and comprehensively annotated view of the genomic sequence of organisms with completely deciphered genomes. Currently, Genome Reviews contains the genomes of archaea, bacteria, bacteriophages and selected eukaryota. Genome Reviews is available as a MySQL relational database, or a flat file format derived from that in the EMBL Nucleotide Sequence Database. An Ensembl-style browser is now available for Genome Reviews, providing a zoomable graphical view of all chromosomes and plasmids represented in the database. The location and structure of all genes is shown and the distribution of features throughout the sequence is displayed. complete genome sequence, genome sequence, nucleotides, gold standard, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: European Bioinformatics Institute
European Union FELICS contract 021902 (RII3);
European Union TEMBLOR contract QLRI- CT-2001000015
PMID:16901215
PMID:15608201
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02899, biotools:genomereviews https://bio.tools/genomereviews SCR_007685 Genome Reviews Database 2026-09-12 01:01:50 4
FireDB
 
Resource Report
Resource Website
1+ mentions
FireDB (RRID:SCR_007655) FireDB data or information resource, database A database of Protein Data Bank structures, ligands and annotated functional site residues. The database can be accessed by PDB codes or UniProt accession numbers as well as keywords. FireDB contains information on every chemical compound in the PDB, including their descriptions, the PDB structures in which the compounds are found and the amino acids that are in contact with the ligand. protein, protein structure, pdb, bio.tools uses: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is listed by: bio.tools
is listed by: Debian
has parent organization: Spanish National Cancer Research Center
nif-0000-02839, biotools:firedb https://bio.tools/firedb SCR_007655 2026-09-12 01:01:49 7
MfunGD - MIPS Mouse Functional Genome Database
 
Resource Report
Resource Website
50+ mentions
MfunGD - MIPS Mouse Functional Genome Database (RRID:SCR_007783) MfunGD data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 16, 2019.Database for annotated mouse proteins and their occurrence in protein networks. It contains cDNA and protein sequences, annotation, gene models and mapping, FunCat, UCSC Genome Viewer, SIMAP, pseudogenes (Genome Viewer Track), InterPro, and splice variants. Protein function annotation is performed using the Functional Catalogue (FunCat) annotation scheme, which is a hierarchically structured classification system. To provide up-to-date similarity search results and InterPro domain analyses, the protein entries are interconnected with the SIMAP database. The gene models are based on the RefSeq mouse cDNAs. The work of our group is focussed on the annotation of biological systems. Therefore, results from the Mammalian Protein-Protein Interaction Database and the Comprehensive Resource of Mammalian Protein Complexes are linked to the MfunGD dataset. Links to external resources are also provided. MfunGD is implemented in GenRE, a J2EE based component oriented multi-tier architecture. bio.tools is listed by: Debian
is listed by: bio.tools
GSF National Research Center for Environment and Health ;
German Federal Ministry of Research and Education
PMID:16381934 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-03121, biotools:mfungd https://bio.tools/mfungd SCR_007783 Mouse Functional Genome Database 2026-09-12 01:01:52 90
IRESite
 
Resource Report
Resource Website
50+ mentions
IRESite (RRID:SCR_007753) data or information resource, database Database of experimentally verified IRES structures. Presents information about experimentally studied Internal Ribosome Entry Site segments. bio.tools, experimentally verified IRES structures, Internal Ribosome Entry Site segments, IRES structures, IRES segments is listed by: bio.tools
is listed by: Debian
has parent organization: Charles University; Prague; Czech Republic
nif-0000-03047, nif-0000-03046, SCR_007754, biotools:iresite https://bio.tools/iresite http://ifr31w3.toulouse.inserm.fr/IRESdatabase/ SCR_007753 IRESdb, , IRESdb - the Internal Ribosome Entry Site database, Internal Ribosome Entry Site 2026-09-12 01:01:52 52
Integr8 : Access to complete genomes and proteomes
 
Resource Report
Resource Website
50+ mentions
Integr8 : Access to complete genomes and proteomes (RRID:SCR_007740) data or information resource, database The Integr8 web portal provides easy access to integrated information about deciphered genomes and their corresponding proteomes. Available data includes DNA sequences (from databases including the EMBL Nucleotide Sequence Database, Genome Reviews, and Ensembl); protein sequences (from databases including the UniProt Knowledgebase and IPI); statistical genome and proteome analysis (performed using InterPro, CluSTr, and GOA); and information about orthology, paralogy, and synteny. bio.tools is listed by: bio.tools
is listed by: Debian
is related to: InteroPorc
has parent organization: European Bioinformatics Institute
nif-0000-03027, biotools:intergr8 https://bio.tools/intergr8 SCR_007740 Integr8 2026-09-12 01:01:51 52
BamView
 
Resource Report
Resource Website
10+ mentions
BamView (RRID:SCR_004207) BamView software resource, source code A free interactive display of read alignments in BAM data files that can be launched with Java Web Start or downloaded. This interactive Java application for visualizing the large amounts of data stored for sequence reads which are aligned against a reference genome sequence can be used in a number of contexts including SNP calling and structural annotation. It has been integrated into Artemis so that the reads can be viewed in the context of the nucleotide sequence and genomic features. The source code is available as part of the Artemis code which can be downloaded from GitHub. bam, next-generation sequencing, java, snp calling, structural annotation, macosx, unix, windows, visualize, analyze, sequence read, reference sequence, single nucleotide polymorphism, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
PMID:22253280
PMID:20071372
GNU General Public License biotools:bamview, OMICS_00878, nlx_22933 https://bio.tools/bamview SCR_004207 2026-09-12 01:03:14 21
Genomedata
 
Resource Report
Resource Website
1+ mentions
Genomedata (RRID:SCR_004544) Genomedata software resource, source code A format for efficient storage of multiple tracks of numeric data anchored to a genome. The format allows fast random access to hundreds of gigabytes of data, while retaining a small disk space footprint. They have also developed utilities to load data into this format. Retrieving data from this format is more than 2900 times faster than a naive approach using wiggle files. A reference implementation in Python and C components is available here under the GNU General Public License. The software has only been tested on Linux and Mac systems. genome, data, format, linux, mac, functional genomics, function, bio.tools is listed by: OMICtools
is listed by: 3DVC
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Washington; Seattle; USA
PMID:20435580 GNU General Public License nlx_53677, biotools:genomedata, OMICS_02148 https://bio.tools/genomedata SCR_004544 2026-09-12 01:03:15 1
Strelka2
 
Resource Report
Resource Website
100+ mentions
Strelka2 (RRID:SCR_005109) software resource, source code Software for somatic single nucleotide variant (SNV) and small indel detection from sequencing data of matched tumor-normal samples. Strelka2 germline and somatic small variant caller. single nucleotide variant, indel, somatic snv, next-generation sequencing, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
has parent organization: Illumina
Cancer, Tumor, Normal PMID:22581179
PMID:30013048
Free, Available for download, Freely available biotools:strelka https://bio.tools/strelka, https://sources.debian.org/src/strelka/ http://bioinformatics.oxfordjournals.org/content/early/2012/05/10/bioinformatics.bts271.full.pdf SCR_005109 Strelka 2026-09-12 01:03:15 283
ALCHEMY
 
Resource Report
Resource Website
1+ mentions
ALCHEMY (RRID:SCR_005761) ALCHEMY software resource, source code ALCHEMY is a genotype calling algorithm for Affymetrix and Illumina products which is not based on clustering methods. Features include explicit handling of reduced heterozygosity due to inbreeding and accurate results with small sample sizes. ALCHEMY is a method for automated calling of diploid genotypes from raw intensity data produced by various high-throughput multiplexed SNP genotyping methods. It has been developed for and tested on Affymetrix GeneChip Arrays, Illumina GoldenGate, and Illumina Infinium based assays. Primary motivations for ALCHEMY''s development was the lack of available genotype calling methods which can perform well in the absence of heterozygous samples (due to panels of inbred lines being genotyped) or provide accurate calls with small sample batches. ALCHEMY differs from other genotype calling methods in that genotype inference is based on a parametric Bayesian model of the raw intensity data rather than a generalized clustering approach and the model incorporates population genetic principles such as Hardy-Weinberg equilibrium adjusted for inbreeding levels. ALCHEMY can simultaneously estimate individual sample inbreeding coefficients from the data and use them to improve statistical inference of diploid genotypes at individual SNPs. The main documentation for ALCHEMY is maintained on the sourceforge-hosted MediaWiki system. Features * Population genetic model based SNP genotype calling * Simultaneous estimation of per-sample inbreeding coefficients, allele frequencies, and genotypes * Bayesian model provides posterior probabilities of genotype correctness as quality measures * Growing number of scripts and supporting programs for validation of genotypes against control data and output reformating needs * Multithreaded program for parallel execution on multi-CPU/core systems * Non-clustering based methods can handle small sample sets for empirical optimization of sample preparation techniques and accurate calling of SNPs missing genotype classes ALCHEMY is written in C and developed on the GNU/Linux platform. It should compile on any current GNU/Linux distribution with the development packages for the GNU Scientific Library (gsl) and other development packages for standard system libraries. It may also compile and run on Mac OS X if gsl is installed. diploid, genotype, snp, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
has parent organization: Cornell University; New York; USA
NSF 0606461 PMID:20926420 GNU General Public License biotools:alchemy, nlx_149227 https://bio.tools/alchemy SCR_005761 ALCHEMY - An automated population genetic model driven SNP genotype calling method 2026-09-12 01:03:15 5
ProteomeXchange
 
Resource Report
Resource Website
5000+ mentions
ProteomeXchange (RRID:SCR_004055) catalog, consortium, data or information resource, data repository, database, organization portal, portal, service resource, storage service resource A data repository for proteomic data sets. The ProteomeExchange consortium, as a whole, aims to provide a coordinated submission of MS proteomics data to the main existing proteomics repositories, as well as to encourage optimal data dissemination. ProteomeXchange provides access to a number of public databases, and users can access and submit data sets to the consortium's PRIDE database and PASSEL/PeptideAtlas. consortium, database, proteomics, MS proteomics, protein, mass spectrometry, bio.tools, FASEB list uses: Proteomics Identifications (PRIDE)
uses: PeptideAtlas
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: bio.tools
is listed by: Debian
is affiliated with: Omics Discovery Index
is related to: Proteomics Identifications (PRIDE)
is related to: PeptideAtlas
is related to: SIB Swiss Institute of Bioinformatics
is related to: Mass spectrometry Interactive Virtual Environment (MassIVE)
is related to: European Bioinformatics Institute
is related to: ProteomeTools
is related to: Integrated Proteome Resources
has parent organization: European Bioinformatics Institute
European Union 260558 Public, The community can contribute to this resource r3d100012122, nlx_158620, biotools:proteomexchange http://proteomecentral.proteomexchange.org, https://bio.tools/proteomexchange, https://doi.org/10.17616/R32D29 SCR_004055 , ProteomeXchange, Proteome Exchange 2026-09-12 01:00:10 6107
ngLOC
 
Resource Report
Resource Website
10+ mentions
ngLOC (RRID:SCR_003150) ngLOC analysis service resource, data analysis service, production service resource, service resource, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 5, 2023.An n-gram-based Bayesian classifier that predicts subcellular localization of proteins both in prokaryotes and eukaryotes. The downloadable version of this software with source code is freely available for academic use under the GNU General Public License. subcellular localization, protein, eukaryote, prokaryote, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:22780965
PMID:17472741
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01629, biotools:ngloc https://bio.tools/ngloc SCR_003150 ngLOC - A Bayesian method for predicting protein subcellular localization 2026-09-12 01:00:09 22
ImaGene
 
Resource Report
Resource Website
100+ mentions
ImaGene (RRID:SCR_002178) data analysis software, data processing software, software application, software resource Software tool as convolutional neural network to quantify natural selection from genomic data.Supervised machine learning algorithm to predict natural selection and estimate selection coefficients from population genomic data. Can be used to estimate any parameter of interest from evolutionary population genetics model., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. microarray analysis, machine vision, convolutional neural network, quantify natural selection, genomic data, population genomic data, evolutionary population, genetics model, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Imperial College London ;
Politecnico di Milano
PMID:31757205 THIS RESOURCE IS NO LONGER IN SERVICE biotools:ImaGene, OMICS_00841 https://github.com/mfumagalli/ImaGene, https://bio.tools/ImaGene http://www.biodiscovery.com/software/imagene/ SCR_002178 2026-09-12 01:00:07 405
QualitySNPng
 
Resource Report
Resource Website
1+ mentions
QualitySNPng (RRID:SCR_002479) data processing software, data visualization software, software application, software resource, standalone software Software for the detection and visualization of single nucleotide polymorphisms (SNPs) from next generation sequencing data that uses a haplotype-based strategy. single nucleotide polymorphism, haplotype strategy, next generation sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:23632165 Free, Available for download, Freely available biotools:qualitysnpng, OMICS_00070 https://bio.tools/qualitysnpng SCR_002479 2026-09-12 01:00:08 7
VIRsiRNAdb
 
Resource Report
Resource Website
1+ mentions
VIRsiRNAdb (RRID:SCR_006108) VIRsiRNAdb analysis service resource, data analysis service, data or information resource, data repository, database, production service resource, service resource, storage service resource VIRsiRNAdb is a curated database of experimentally validated viral siRNA / shRNA targeting diverse genes of 42 important human viruses including influenza, SARS and Hepatitis viruses. Submissions are welcome. Currently, the database provides detailed experimental information of 1358 siRNA/shRNA which includes siRNA sequence, virus subtype, target gene, GenBank accession, design algorithm, cell type, test object, test method and efficacy (mostly quantitative efficacies). Further, wherever available, information regarding alternative efficacies of above 300 siRNAs derived from different assays has also been incorporated. The database has facilities like search, advance search (using Boolean operators AND, OR) browsing (with data sorting option), internal linking and external linking to other databases (Pubmed, Genbank, ICTV). Additionally useful siRNA analysis tools are also provided e.g. siTarAlign for aligning the siRNA sequence with reference viral genomes or user defined sequences. virsiRNAdb would prove useful for RNAi researchers especially in siRNA based antiviral therapeutics development. virus, sirna, shrna, gene, influenza, sars, hepatitis, sirna sequence, virus subtype, target gene, genbank accession, design algorithm, cell type, efficacy, target genome region, target object, experimental assay, off-target, sirna matching, reference viral sequence, influenza virus, hepatitis b virus, hpv, sars corona virus, viral genome, reference genome, align, sirna sequence, fasta, blast, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Institute of Microbial Technology; Chandigarh; India
Influenza, SARS, Hepatitis, Infectious disease Council of Scientific and Industrial Research; New Delhi; India PMID:22139916 Open unspecified license / Freely available nlx_151610, biotools:virsirnadb https://bio.tools/virsirnadb SCR_006108 VIRsiRNAdb - Database of Viral siRNA / shRNA, Viral siRNA Database, Viral siRNA Database (VIRsiRNAdb) 2026-09-12 01:00:11 4

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. NIDDK Information Network Resources

    Welcome to the dkNET Resources search. From here you can search through a compilation of resources used by dkNET 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 dkNET 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 dkNET then you can log in from here to get additional features in dkNET 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 dkNET 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.