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


Facets


Recent searches

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

27,138 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 Authority Synonyms Record Last Update Mentions Count
Jmosaics
 
Resource Report
Resource Website
Jmosaics (RRID:SCR_001094) data analysis software, data processing software, sequence analysis software, software application, software resource R software that detects enriched regions of ChIP-seq data sets jointly. chip seq, data, genomics, sequencing, r, sequence analysis software is listed by: OMICtools
is hosted by: Bioconductor
Free, Available for download, Freely available OMICS_00445 SCR_001094 SciCrunch Registry 2026-09-26 02:12:54 0
AutoAssemblyD
 
Resource Report
Resource Website
AutoAssemblyD (RRID:SCR_001087) data analysis software, data processing software, sequence analysis software, software application, software resource Software which performs local and remote genome assembly by several assemblers based on an XML Template which can replace the large command lines required by most assemblers. genome, genome assembly, xml, sequence analysis software, local genome assembly, remote genome assembly, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:24143057 Free, Available for download, Freely available biotools:autoassemblyd, OMICS_00874 https://bio.tools/autoassemblyd SCR_001087 SciCrunch Registry 2026-09-26 02:12:54 0
Howard University; Washington D.C.
 
Resource Report
Resource Website
Howard University; Washington D.C. (RRID:SCR_001084) HU university A federally chartered, private, coeducational, nonsectarian, historically black university in Washington, D.C. Howard University has graduate schools in many fields, including business, nursing, engineering, and medicine. undergraduate, graduate, master's, doctoral, phD, institution, university, nonsectarian is related to: Clinical and Translational Science Awards Consortium
is parent organization of: Howard Flow Cytometry Core
is parent organization of: Howard Imaging Core Facility: Molecular Imaging Laboratory
is parent organization of: Howard Biobehavioral Core Laboratory
is parent organization of: Howard Biostatistics Core
is parent organization of: Howard University Center for Computational Biology and Bioinformatics Core Facility
is parent organization of: Howard Molecular Genetics Core
is parent organization of: Howard Nanoscale Science and Engineering Facility
is parent organization of: Howard RCMI Proteomics Facility
nlx_152178 SCR_001084 SciCrunch Registry Howard, Howard University, Howard U 2026-09-26 02:12:54 0
University of Florida College of Medicine Neuroscience
 
Resource Report
Resource Website
University of Florida College of Medicine Neuroscience (RRID:SCR_001081) data or information resource, department portal, organization portal, portal A department at the University of Florida's College of Medicine that offers programs of study on neural function and how it changes with injury and disease. The institution's research ranges from fundamental discovery to clinical application. These neuroscience programs are offered at the undergraduate, graduate, postdoctoral and resident level. neuroscience, neural function, undergraduate, graduate, postdoctoral, resident, clinical, injury, disease nif-0000-02172 SCR_001081 SciCrunch Registry UFL 2026-09-26 02:12:54 0
Simpleaffy
 
Resource Report
Resource Website
50+ mentions
Simpleaffy (RRID:SCR_001302) Simpleaffy data analysis software, data processing software, software application, software resource Software package that provides high level functions for reading Affy .CEL files, phenotypic data, and then computing simple things with it, such as t-tests, fold changes and the like. It makes heavy use of the affy library. It also has some basic scatter plot functions and mechanisms for generating high resolution journal figures. affymetrix, annotation, data import, differential expression, microarray, one channel, preprocessing, quality control, report writing, transcription, visualization is listed by: OMICtools
has parent organization: Bioconductor
PMID:16076888 GNU General Public License, v2 or newer OMICS_02034 SCR_001302 SciCrunch Registry Simpleaffy - Very simple high level analysis of Affymetrix data 2026-09-26 02:12:58 85
BSSim
 
Resource Report
Resource Website
1+ mentions
BSSim (RRID:SCR_001212) BSSim software resource Software to mimic various methylation level and bisulfite conversion rate in CpG, CHG and CHH context, respectively. It can also simulate genetic variations that are divergent from the reference sequence along with the sequencing error and quality distributions. In the output, both directional/non-directional, various read length, single/paired-end reads and alignment data in the SAM format can be generated. BSSim is a cross-platform BS-seq simulator offers output read datasets not only suitable for Illumina's Solexa, but also for Roche's 454 and Applied Biosystems' SOLiD. bisulfite sequencing, simulator, next-generation sequencing, python, dna methylation, snp, read quality is listed by: OMICtools THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02130 SCR_001212 SciCrunch Registry BSSim: Bisulfite sequencing simulator for next-generation sequencing 2026-09-26 02:12:56 1
sim4cc
 
Resource Report
Resource Website
sim4cc (RRID:SCR_001204) alignment software, data processing software, image analysis software, software application, software resource Software tool as cross species spliced alignment program.Heuristic sequence alignment tool for comparing cDNA sequence with genomic sequence containing homolog of gene in another species. Cross species spliced alignment, unix, sequence alignment, cdna sequence, genomic sequence, homolog, gene, splice, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Johns Hopkins University; Maryland; USA
NLM R01 LM006845;
NSF CLS20163A;
Sloan Research Fellowship
PMID:19429899 Free, Available for download, Freely available biotools:sim4cc, OMICS_02145 https://bio.tools/sim4cc SCR_001204 SciCrunch Registry 2026-09-26 02:12:56 0
QualiMap
 
Resource Report
Resource Website
10+ mentions
QualiMap (RRID:SCR_001209) QualiMap software resource Software application written in Java and R that provides both a Graphical User Inteface (GUI) and a command-line interface to facilitate the quality control of alignment sequencing data. It examines sequencing alignment data in SAM / BAM files according to the features of the mapped reads and provides an overall view of the data that helps to the detect biases in the sequencing and/or mapping of the data and eases decision-making for further analysis. next-generation sequencing, alignment, linux, macos, windows, quality control, sam, bam, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Principe Felipe Research Centre; Valencia; Spain
Spanish Ministry of Economy and Competitiveness BIO2009-10799;
EU funded program ERA-NET PathoGenoMics BIO2008-05266-E
PMID:22914218
DOI:10.1093/bioinformatics/bts503
Free, Available for download, Freely available OMICS_02133, biotools:qualimap https://bio.tools/qualimap https://sources.debian.org/src/qualimap/ SCR_001209 SciCrunch Registry QualiMap - Evaluating next generation sequencing alignment data 2026-09-26 02:12:56 48
Omixon Target Data Analysis
 
Resource Report
Resource Website
Omixon Target Data Analysis (RRID:SCR_001207) Omixon Target commercial organization, data analysis software, data processing software, software application, software resource, software toolkit Software application suite to help clinical labs adopt next generation sequencing for the analysis of diagnostic gene targets. next-generation sequencing, gene target, windows, linux, mac, gene, diagnostic is listed by: OMICtools
is parent organization of: Omixon Target HLA Typing
License required OMICS_02141 SCR_001207 SciCrunch Registry 2026-09-26 02:12:56 0
North Dakota State University; North Dakota; USA
 
Resource Report
Resource Website
1+ mentions
North Dakota State University; North Dakota; USA (RRID:SCR_001110) NDSU university Public research university in North Dakota, USA. It is a land-grant university that focuses on agriculture and the applied sciences. In addition, it offers undergraduate and graduate degrees in a wide variety of areas including engineering, science and mathematics, health professions, business, and agriculture and food systems studies. public, research, land grant, agriculture, applied sciences, food systems, health profession is parent organization of: NDSU Center for Protease Research
is parent organization of: North Dakota State University Labs and Facilities
is parent organization of: North Dakota State University School of Pharmacy; North Dakota; USA
Wikidata:Q2000624, grid.261055.5, nlx_71768, ISNI:0000 0001 2293 4611, Crossref funder ID:100007518 https://ror.org/05h1bnb22 SCR_001110 SciCrunch Registry North Dakota State University 2026-09-26 02:12:55 1
Genome Trax
 
Resource Report
Resource Website
1+ mentions
Genome Trax (RRID:SCR_001234) Genome Trax service resource Service that provides a comprehensive compilation of variant knowledge that allows you to identify pathogenic variants in human whole genome or exome sequences. It makes it easy to upload a complete genome?s worth of variations and identify the biologically relevant subset of known mutations, mutations that are novel and appear in a candidate disease genes, or mutations that are predicted to have a deleterious effect. The database includes a comprehensive collection of disease causing mutations from HGMD Professional, regulatory sites from TRANSFAC , and disease genes, drug targets and pathways from PROTEOME, as well as pharmacogenomic variants. It integrates the best public data-sets on somatic mutations, allele frequencies and clinical variants, in their most up-to-date version, for a total of more than 165 million annotations. It is possible to identify known pathogenic variants, remove harmless common variants, and obtain deleterious predictions for novel variants. With family data, it is possible to identify variants that are de novo, compound heterozygous only in the offspring. All of the results can be downloaded to Excel for further review. For core facilities and bioinformaticians, the complete underlying data is made available for download and easy integration into custom analysis pipelines. Genome Trax data is optimized to work with many other software packages, such as ANNOVARTM, CLC bio, Alamut, SimulConsult, and Cartagenia. next-generation sequencing, genome, exome, sequence, variation, mutation, pathogenic, database, bio.tools, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: BIOBASE Corporation
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02109, biotools:genome_trax https://bio.tools/genome_trax SCR_001234 SciCrunch Registry Genome Trax for Next Generation Sequencing 2026-09-26 02:12:56 2
Speech Perception
 
Resource Report
Resource Website
Speech Perception (RRID:SCR_001114) data or information resource, portal, topical portal An entry of the Cognitive Atlas which defines the term speech perception. cognitive science, language, processing language is related to: Cognitive Atlas THIS RESOURCE IS NO LONGER IN SERVICE nlx_145380 SCR_001114 SciCrunch Registry 2026-09-26 02:12:55 0
PHACCS
 
Resource Report
Resource Website
1+ mentions
PHACCS (RRID:SCR_001232) software resource Software that gives estimates of the structure and diversity of uncultured viral communities using metagenomic information. matlab is listed by: OMICtools
has parent organization: SourceForge
PMID:15743531 Free, Available for download, Freely available OMICS_03529 SCR_001232 SciCrunch Registry 2026-09-26 02:12:56 1
QUAST
 
Resource Report
Resource Website
1000+ mentions
QUAST (RRID:SCR_001228) QUAST software resource Quality assessment software tool for evaluating and comparing genome assemblies. It works both with and without a given reference genome. It produces many reports, summary tables and plots. genome assembly, genomics, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Saint Petersburg Academic University; Saint Petersburg; Russia
has parent organization: SourceForge
PMID:23422339 biotools:quast, OMICS_02115 https://bio.tools/quast, https://sources.debian.org/src/quast/ SCR_001228 SciCrunch Registry QUAST: Quality Assessment Tool for Genome Assemblies 2026-09-26 02:12:56 3293
R453Plus1Toolbox
 
Resource Report
Resource Website
1+ mentions
R453Plus1Toolbox (RRID:SCR_001105) data analysis software, data processing software, sequence analysis software, software application, software resource, software toolkit R software toolbox of functions for the analysis of data generated by Roche's 454 sequencing platform. Additional functions are included for quality assurance, annotation and visualization of detected variants, complementing the software tools shipped by Roche with their product. A pipeline for the detection of structural variants is provided. genome, sequence, visualization, structural variants, r, sequence analysis software is listed by: OMICtools
is hosted by: Bioconductor
PMID:21349869 Free, Available for download, Freely available OMICS_01354 SCR_001105 SciCrunch Registry 2026-09-26 02:12:55 4
Academy Biomedical Company
 
Resource Report
Resource Website
Academy Biomedical Company (RRID:SCR_001108) commercial organization Commercial antibody supply company that focuses on providing antibodies for research in cardiovascular and atherosclerosis. antibody, cardiovascular, athersclerosis, antibody supplier nlx_152249 SCR_001108 SciCrunch Registry Academy Bio-Medical Company, Academy Biomedical Company Inc. 2026-09-26 02:12:55 0
TileQC
 
Resource Report
Resource Website
TileQC (RRID:SCR_001229) TileQC software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May,10, 2021.Software providing a visually oriented tile based approach to error detection for Solexa next-gen sequencing data. It is written in R and has both qualitative and quantitative error detection features. This software was written with the idea that the researcher's visual pattern recognition is the best way to detect novel errors and contains variety of ways to visualize that data. Once a new type of error is identified the data extraction features of the program may then be used as a starting point for the programmatic detection and/or filtration of similar errors. A supplementary role of tileQC is to convert the Eland and Q-score data contained within the Solexa "*_prb.txt" and "*_eland_results.txt" text files to a more flexible database form. Once in database form, tileQC simplifies the mechanics of interacting with that data and supplements standard SQL with an expression subsitution mechanism that allows R to be easily comingled with SQL. This system requires access to a mySQL server and the R package RMySQL as well as a few standard UNIX tools (also available on Windows and Macintosh). next-generation sequencing, quality control, solexa, r, tile, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Oregon State University; Oregon; USA
PMID:18507856 THIS RESOURCE IS NO LONGER IN SERVICE biotools:tileqc, OMICS_02114 https://bio.tools/tileqc SCR_001229 SciCrunch Registry TileQC: A tile based approached to quality control 2026-09-26 02:12:56 0
ChanTest
 
Resource Report
Resource Website
10+ mentions
ChanTest (RRID:SCR_001220) CT commercial organization An ion channel focused Contract Research Organization (CRO) that does safety testing and screening for global pharma and biotech companies. ChanTest has developed a complete library of validated human ion channel-expressing cell lines to serve all the ion channel needs of its pharmaceutical and biotech customers. Services range from early functional screens for profiling drug candidates or ranking within profiles during the drug-discovery process to a complete set of in vitro GLP service products for cardiac risk assessment. ChanTest works in partnership with customers to speed the drug-development process, save time and money, and ultimately to help make better, safer drugs. ion channel, safety testing, screening, drug, drug development nlx_152331 http://chantest.com SCR_001220 SciCrunch Registry ChanTest.com 2026-09-26 02:12:56 12
BreakFusion
 
Resource Report
Resource Website
1+ mentions
BreakFusion (RRID:SCR_001102) BreakFusion software resource Software package written in Perl and C++ that provides a computational pipeline for identifying gene fusions from RNA-seq data. computational pipeline, gene fusions, rna, sequence, data, perl, c++ is listed by: OMICtools
has parent organization: University of Texas MD Anderson Cancer Center
PMID:22563071
DOI:10.1093/bioinformatics/bts272
Free, Available for download, Freely available OMICS_01342 SCR_001102 SciCrunch Registry 2026-09-26 02:12:55 3
Body System Terms from ICD11
 
Resource Report
Resource Website
Body System Terms from ICD11 (RRID:SCR_001252) ICD11-BODYSYSTEM controlled vocabulary, data or information resource, ontology Ontology of a set of body-system terms used in the ICD (International Classification of Diseases) 11 revision owl is listed by: BioPortal THIS RESOURCE IS NO LONGER IN SERVICE nlx_157339 SCR_001252 SciCrunch Registry 2026-09-26 02:12:57 0

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.