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:omictools (facet)

Facets


Recent searches

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

2,818 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
HeurAA
 
Resource Report
Resource Website
HeurAA (RRID:SCR_013212) HeurAA software resource Software for accurate and fast detection of genetic variations with a novel heuristic amplicon aligner program for next generation sequencing. unix/linux, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:23349847 OMICS_00097, biotools:heuraa https://bio.tools/heuraa SCR_013212 heurAA - NGS multiplexed amplicon aligner 2026-08-08 12:00:20 0
bisReadMapper
 
Resource Report
Resource Website
bisReadMapper (RRID:SCR_013171) bisReadMapper software resource Fast and lightweight package for mapping bisulfite converted DNA sequencing reads from the Illumina platform. illumina is listed by: OMICtools
has parent organization: SourceForge
OMICS_00576 SCR_013171 bisReadMapper - Software for dealing with DNA methylation sequencing data 2026-08-08 12:00:20 0
mGOASVM
 
Resource Report
Resource Website
1+ mentions
mGOASVM (RRID:SCR_013098) mGOASVM production service resource, web service, software resource, data access protocol, data analysis service, analysis service resource, service resource Data analysis service for the prediction of multi-label protein subcellular localization based on gene ontology and support vector machines. Web services are also available. subcellular localization, gram-negative protein, virus, protein is listed by: OMICtools
has parent organization: Hong Kong Polytechnic University; Hong Kong; China
PMID:23130999 OMICS_01627 SCR_013098 2026-08-08 11:59:52 4
CEDER
 
Resource Report
Resource Website
10+ mentions
CEDER (RRID:SCR_013255) CEDER software resource R package intended to implement a program for detecting differentially expressed genes (DEG) using RNA-Seq by combining significance of exons within a gene. is listed by: OMICtools
has parent organization: University of Southern California; Los Angeles; USA
OMICS_01301 SCR_013255 2026-08-08 12:00:20 11
QuantiSNP
 
Resource Report
Resource Website
50+ mentions
QuantiSNP (RRID:SCR_013091) QuantiSNP software resource THIS RESOURCE IS NO LONGER IN SERVICE, documented May 10, 2017. A pilot effort that has developed a centralized, web-based biospecimen locator that presents biospecimens collected and stored at participating Arizona hospitals and biospecimen banks, which are available for acquisition and use by researchers. Researchers may use this site to browse, search and request biospecimens to use in qualified studies. The development of the ABL was guided by the Arizona Biospecimen Consortium (ABC), a consortium of hospitals and medical centers in the Phoenix area, and is now being piloted by this Consortium under the direction of ABRC. You may browse by type (cells, fluid, molecular, tissue) or disease. Common data elements decided by the ABC Standards Committee, based on data elements on the National Cancer Institute''s (NCI''s) Common Biorepository Model (CBM), are displayed. These describe the minimum set of data elements that the NCI determined were most important for a researcher to see about a biospecimen. The ABL currently does not display information on whether or not clinical data is available to accompany the biospecimens. However, a requester has the ability to solicit clinical data in the request. Once a request is approved, the biospecimen provider will contact the requester to discuss the request (and the requester''s questions) before finalizing the invoice and shipment. The ABL is available to the public to browse. In order to request biospecimens from the ABL, the researcher will be required to submit the requested required information. Upon submission of the information, shipment of the requested biospecimen(s) will be dependent on the scientific and institutional review approval. Account required. Registration is open to everyone.Software to detect rare or de novo copy number alterations in normal DNA samples. Please note that QuantiSNP is no longer under active development. matlab, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:17341461 THIS RESOURCE IS NO LONGER IN SERVICE biotools:quantisnp, OMICS_00730 https://bio.tools/quantisnp SCR_013091 2026-08-08 11:59:52 83
Celera Genome Browser
 
Resource Report
Resource Website
Celera Genome Browser (RRID:SCR_013093) Celera Genome Browser software resource Software developed at Celera Genomics as part of Celera''s sequencing and annotation of the human genome, and released as open source in 2006. matlab is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v3 OMICS_00904 SCR_013093 2026-08-08 12:00:07 0
GPSeq
 
Resource Report
Resource Website
1+ mentions
GPSeq (RRID:SCR_013250) GPSeq software resource A software tool to analyze RNA-seq data to estimate gene and exon expression, identify differentially expressed genes, and differentially spliced exons., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. is listed by: OMICtools
has parent organization: University of Southern California; Los Angeles; USA
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01333 SCR_013250 2026-08-08 11:59:54 6
MAP
 
Resource Report
Resource Website
1+ mentions
MAP (RRID:SCR_013216) software resource This resource is out of service. Documented on February 23,2021. Software for de novo metagenomic assembly program for shotgun DNA reads., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Peking University; Beijing; China
PMID:22495746 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01424, biotools:MAP https://bio.tools/MAP SCR_013216 Metagenomic Assembly Program 2026-08-08 12:00:20 1
DiffSplice
 
Resource Report
Resource Website
10+ mentions
DiffSplice (RRID:SCR_013215) DiffSplice software resource The Genome-Wide Detection of Differential Splicing Events with RNA-seq. is listed by: OMICtools
has parent organization: University of Kentucky; Kentucky; USA
PMID:23155066 OMICS_01330 SCR_013215 2026-08-08 12:00:09 15
genCAT
 
Resource Report
Resource Website
1+ mentions
genCAT (RRID:SCR_013220) genCAT software resource Software designed as an open platform that allows users to incorporate as many datasets (concepts) as possible to annotate the input gene list, as long as these datasets are prepared in bigwig, BED, BAM/SAM formats. is listed by: OMICtools
has parent organization: Google Code
GNU General Public License, v2 OMICS_01416 SCR_013220 gencat - Gene''s Comprehensive Annotation Tool 2026-08-08 12:00:20 6
SOCS
 
Resource Report
Resource Website
50+ mentions
SOCS (RRID:SCR_013223) SOCS software resource Performs ungapped alignment of SOLiD (color space) sequencing reads against reference sequences. is listed by: OMICtools
has parent organization: SourceForge
OMICS_00590 SCR_013223 2026-08-08 11:59:53 91
PolyPhen: Polymorphism Phenotyping
 
Resource Report
Resource Website
1000+ mentions
PolyPhen: Polymorphism Phenotyping (RRID:SCR_013189) PolyPhen, PolyPhen-2, POLYPHEN software resource, software application, simulation software, data analysis software, data processing software Software tool which predicts possible impact of amino acid substitution on structure and function of human protein using straightforward physical and comparative considerations. PolyPhen-2 is new development of PolyPhen tool for annotating coding nonsynonymous SNPs. annotate, nonsynonymous, SNP, predict, coding, damaging, effect, missense, mutation, sequence, variant, phenotype, genetic, disease, exon, protein, coding, fraction, genome, bio.tools is listed by: Genetic Analysis Software
is listed by: Debian
is listed by: bio.tools
is related to: OMICtools
has parent organization: Harvard University; Cambridge; United States
PMID:20354512
PMID:23315928
SCR_013200, OMICS_00136, nlx_154540, nif-0000-21329, biotools:polyphen, SCR_013238 https://bio.tools/polyphen http://www.bork.embl-heidelberg.de/PolyPhen/ SCR_013189 PolyPhen, POLYPHEN, PolyPhen-2, Polymorphism Phenotyping, Polymorphism Phenotyping v2 2026-08-08 12:00:08 4723
aCGH
 
Resource Report
Resource Website
100+ mentions
aCGH (RRID:SCR_013232) aCGH software resource Software functions for reading aCGH data from image analysis output files and clone information files, creation of aCGH S3 objects for storing these data. Basic methods for accessing/replacing, subsetting, printing and plotting aCGH objects. is listed by: OMICtools
has parent organization: Bioconductor
OMICS_00698 SCR_013232 2026-08-08 11:59:53 136
DSP
 
Resource Report
Resource Website
DSP (RRID:SCR_013114) DSP software resource Pipeline for small genome assembly using SOLiD sequencing technology. is listed by: OMICtools
has parent organization: SourceForge
Apache License, v2 OMICS_00013 SCR_013114 denovo_solid_pipeline 2026-08-08 12:00:07 0
RepeatSeq
 
Resource Report
Resource Website
10+ mentions
RepeatSeq (RRID:SCR_013235) RepeatSeq software resource Software that determines genotypes for microsatellite repeats in high-throughput sequencing data. is listed by: OMICtools PMID:23090981 OMICS_00112 SCR_013235 2026-08-08 12:00:20 18
Tuxedo
 
Resource Report
Resource Website
100+ mentions
Tuxedo (RRID:SCR_013194) Tuxedo software resource Software that manages the RNA-sequencing pipeline based on the TopHat suite of software automatically. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01415 SCR_013194 Tuxedo: Automated RNA-sequencing Pipeline Script 2026-08-08 12:00:20 103
MicroRazerS
 
Resource Report
Resource Website
1+ mentions
MicroRazerS (RRID:SCR_013316) MicroRazerS software resource A software tool optimized for mapping short RNAs onto a reference genome. is listed by: OMICtools
has parent organization: Free University of Berlin; Berlin; Germany
PMID:19880369 OMICS_00371 SCR_013316 2026-08-08 12:00:10 5
FusionSeq
 
Resource Report
Resource Website
1+ mentions
FusionSeq (RRID:SCR_013329) FusionSeq software resource A modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data. is listed by: OMICtools OMICS_01351 SCR_013329 2026-08-08 12:00:21 7
MACS
 
Resource Report
Resource Website
1000+ mentions
MACS (RRID:SCR_013291) MACS software resource, software application, data analysis software, data processing software Software Python package for identifying transcript factor binding sites. Used to evaluate significance of enriched ChIP regions. Improves spatial resolution of binding sites through combining information of both sequencing tag position and orientation. Can be used for ChIP-Seq data alone, or with control sample with increase of specificity. identify, transcript, factor, binding, site, model, based, analysis, CHIP Seq, short, read, sequencer, protein, DNA, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
has parent organization: Dana-Farber Cancer Institute
NHGRI HG004069;
NHGRI HG004270;
NIDDK DK074967
PMID:18798982
DOI:10.1186/gb-2008-9-9-r137
Free, Available for download, Freely available OMICS_00446, biotools:macs https://bio.tools/macs, https://sources.debian.org/src/macs/ SCR_013291 MACS - Model-based Analysis for ChIP-Seq, Model-based Analysis for ChIP-Seq, MACS2 2026-08-08 11:59:54 1418
SeqTRACS
 
Resource Report
Resource Website
SeqTRACS (RRID:SCR_013294) SeqTRACS software resource Software for a Laboratory Information Management System (LIMS) for tracking, organizing, and accessing sequencing requests and ABI trace files produced by a centralized sequencing core facility. matlab is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v3 OMICS_01013 SCR_013294 SeqTRACS: LIMS for sequencing core facilities 2026-08-08 11:59:54 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. RRID Portal Resources

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