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
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

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

2,819 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 Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
CHANCE
 
Resource Report
Resource Website
10+ mentions
CHANCE (RRID:SCR_005330) CHANCE software resource A standalone software package for ChIP-seq quality control and protocol optimization. is listed by: OMICtools OMICS_00429 SCR_005330 CHiP-seq ANalytics and Confidence Estimation 2026-02-14 02:01:06 12
NCBO Annotator
 
Resource Report
Resource Website
1+ mentions
NCBO Annotator (RRID:SCR_005329) NCBO Annotator web service, production service resource, service resource, data access protocol, software resource A Web service that annotates textual metadata (e.g. journal abstract) with relevant ontology concepts. NCBO uses this Web service to annotate resources in the NCBO Resource Index. They also provide this Web service as a stand-alone service for users. This Web service can be accessed through BioPortal or used directly in your software. Currently, the annotation workflow is based on syntactic concept recognition (using concept names and synonyms) and on a set of semantic expansion algorithms that leverage the semantics in ontologies (e.g., is_a relations). Their service methodology leverages ontologies to create annotations of raw text and returns them using semantic web standards. ontology, annotation, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: STOP
has parent organization: BioPortal
has parent organization: National Centers for Biomedical Computing
has parent organization: Stanford University; Stanford; California
NHGRI U54 HG004028 PMID:19483092 biotools:bioportal, nlx_144389, OMICS_01172 https://bio.tools/bioportal SCR_005329 Open Biomedical Annotator, NCBO BioPortal Annotator 2026-02-14 02:00:54 6
Assembly Likelihood Estimator
 
Resource Report
Resource Website
Assembly Likelihood Estimator (RRID:SCR_005326) ALE software resource Software using a probabalistic framework for determining the likelihood of an assembly given the data (raw reads) used to assemble it. It allows for the rapid discovery of errors and comparisons between similar assemblies. standalone software, c, python is listed by: OMICtools
has parent organization: DOE Joint Genome Institute
has parent organization: Cornell University; New York; USA
PMID:23303509 Open-source license OMICS_04067 https://github.com/sc932/ALE SCR_005326 ALE: Assembly Likelihood Estimator 2026-02-14 02:01:06 0
CoPub
 
Resource Report
Resource Website
1+ mentions
CoPub (RRID:SCR_005327) CoPub data access protocol, software resource, web service, service resource Text mining tool that detects co-occuring biomedical concepts in abstracts from the MedLine literature database. It allows batch input of multiple human, mouse or rat genes and produces lists of keywords from several biomedical thesauri that are significantly correlated with the set of input genes. These lists link to Medline abstracts in which the co-occurring input genes and correlated keywords are highlighted. Furthermore, CoPub can graphically visualize differentially expressed genes and over-represented keywords in a network, providing detailed insight in the relationships between genes and keywords, and revealing the most influential genes as highly connected hubs. microarray, gene, literature, enrich, annotate, network, database, differential expression, bio.tools uses: MEDLINE
uses: Gene Ontology
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Netherlands Bioinformatics Centre
Netherlands Bioinformatics Centre PMID:18442992 Free, Public, Acknowledgement requested OMICS_01178, biotools:copub https://bio.tools/copub http://services.nbic.nl/cgi-bin/copub/CoPub.pl SCR_005327 2026-02-14 02:00:52 5
FaBox
 
Resource Report
Resource Website
100+ mentions
FaBox (RRID:SCR_005350) FaBox software resource Tools for splitting, joining and otherwise manipulating FASTA format sequence files. The first tools in the toolbox is for manipulating fasta headers, cropping alignments and doing some sequence comparison allowing users to combine the description of data (often in excel spreadsheets) with the actual data (often DNA sequences). Also, producing correct input files for a range of programs seems to be problematic for the average user. Hence, some converters in some of the services have been included as well as some stand-alone converters. The converters are not necessarily meant to provide the final input file, but you''ll get a valid input file for Arlequin, MrBayes etc. - that you may further edit so it suit your needs. This means that you may need to combine several of the tools to finish your handling - but it keeps it relatively simple to use. Please note that FaBox is written in PHP and ONLY RUNS ON A WEBSERVER. fasta, dna, protein sequence, dna sequence, protein, sequence, php is listed by: OMICtools
has parent organization: Aarhus University; Aarhus; Denmark
Acknowledgement requested OMICS_01165 SCR_005350 FaBox - an online fasta sequence toolbox 2026-02-14 02:01:06 116
PeakSeq
 
Resource Report
Resource Website
10+ mentions
PeakSeq (RRID:SCR_005349) PeakSeq software resource A software program for identifying and ranking peak regions in ChIP-Seq experiments. It takes as input, mapped reads from a ChIP-Seq experiment, mapped reads from a control experiment and outputs a file with peak regions ranked with increasing Q-values. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Yale University; Connecticut; USA
PMID:19122651 biotools:peakseq, OMICS_00453 https://bio.tools/peakseq SCR_005349 2026-02-14 02:00:54 39
Anne O'Tate
 
Resource Report
Resource Website
1+ mentions
Anne O'Tate (RRID:SCR_005340) Anne O'Tate service resource A web based search tool to help you gain an overview of the set of articles (up to 25,000 most recent articles) retrieved by a PubMed query. Once you enter a query, you can select different types of summary information to view: Important words, Topics, Authors, Affiliations, Journals, Year, Clustered by topic. database is listed by: OMICtools
is related to: PubMed
has parent organization: University of Illinois at Chicago; Illinois; USA
PMID:18279519 OMICS_01171 SCR_005340 2026-02-14 02:01:05 1
GEM
 
Resource Report
Resource Website
10+ mentions
GEM (RRID:SCR_005339) GEM software resource Java software for studying protein-DNA interaction using ChIP-seq / ChIP-exo data. It links binding event discovery and motif discovery with positional priors in the context of a generative probabilistic model of ChIP data and genome sequence, resolves ChIP data into explanatory motifs and binding events at unsurpassed spatial resolution. GEM reciprocally improves motif discovery using binding event locations, and binding event predictions using discovered motifs. chip-seq, chip-exo, genome, event, motif, protein-dna interaction, java, transcription factor, genome sequence, motif discovery, binding event calling is listed by: OMICtools
has parent organization: Massachusetts Institute of Technology; Massachusetts; USA;
PMID:22912568 OMICS_00441 SCR_005339 Genome wide Event finding and Motif discovery, GEM: ChIP-Seq and ChIP-exo analysis tool 2026-02-14 02:00:52 12
Hiclib
 
Resource Report
Resource Website
10+ mentions
Hiclib (RRID:SCR_005535) Hiclib software resource An Software resource is listed by: OMICtools OMICS_00521 SCR_005535 2026-02-14 02:01:08 21
SHRiMP
 
Resource Report
Resource Website
100+ mentions
SHRiMP (RRID:SCR_005496) SHRiMP software resource A software package for aligning genomic reads against a target genome. next generation sequencing, alignment is used by: Jambalaya
is listed by: OMICtools
is related to: Jambalaya
is related to: Proovread
has parent organization: University of Toronto; Ontario; Canada
PMID:21278192 OMICS_00685 SCR_005496 SHRiMP - SHort Read Mapping Package 2026-02-14 02:00:54 207
PAZAR
 
Resource Report
Resource Website
10+ mentions
PAZAR (RRID:SCR_005410) PAZAR data repository, storage service resource, data or information resource, service resource, software resource, database Database that unites independently created and maintained data collections of transcription factor and regulatory sequence annotation. The flexible PAZAR schema permits the representation of diverse information derived from experiments ranging from biochemical protein-DNA binding to cellular reporter gene assays. Data collections can be made available to the public, or restricted to specific system users. The data ''boutiques'' within the shopping-mall-inspired system facilitate the analysis of genomics data and the creation of predictive models of gene regulation., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. transcription factor, target gene, regulatory sequence, transcription factor profile, annotation, sequence, profile, transcription factor binding profile, chip, chip-seq, gene, cis-regulatory element, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of British Columbia; British Columbia; Canada
has parent organization: SourceForge
PMID:18971253 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00540, biotools:pazar https://bio.tools/pazar SCR_005410 2026-02-14 02:01:06 32
SMALT
 
Resource Report
Resource Website
500+ mentions
SMALT (RRID:SCR_005498) SMALT software resource Software that aligns DNA sequencing reads with a reference genome. Reads from a wide range of sequencing platforms, for example Illumina, Roche-454, Ion Torrent, PacBio or ABI-Sanger, can be processed including paired reads. is listed by: OMICtools
is related to: Sequence Search and Alignment by Hashing Algorithm
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
OMICS_00686 SCR_005498 2026-02-14 02:00:56 507
TIGRFAMS
 
Resource Report
Resource Website
100+ mentions
TIGRFAMS (RRID:SCR_005493) JCVI TIGRFAMS, TIGRFAM data set, data or information resource, database Consists curated multiple sequence alignments, Hidden Markov Models (HMMs) for protein sequence classification, and associated information designed to support automated annotation of (mostly prokaryotic) proteins. Starting with release 10.0, TIGRFAMs models use HMMER3, which provides excellent search speed as well as exquisite search sensitivity. See the "TIGRFAMs Complete Listing" page to review the accession, protein name, model type, and EC number (if assigned) of all models. TIGRFAMs is a member database in InterPro. The HMM libraries and supporting files are available to download and use for free from our FTP site. sequence alignment, hidden markov model, protein sequence, classification, protein, protein family, sequence homology, sequence, homology, function, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: InterPro
is related to: InterPro
has parent organization: J. Craig Venter Institute
PMID:23197656 Free nif-0000-03560, OMICS_01700, biotools:tigrfams https://bio.tools/tigrfams http://www.tigr.org/TIGRFAMs SCR_005493 TIGRFAMs 2026-02-14 02:01:06 135
Segemehl
 
Resource Report
Resource Website
10+ mentions
Segemehl (RRID:SCR_005494) Segemehl software resource A software to map short sequencer reads to reference genomes. It is able to detect not only mismatches but also insertions and deletions. Furthermore, it is not limited to a specific read length and is able to mapprimer- or polyadenylation contaminated reads correctly. segemehl implements a matching strategy based on enhanced suffix arrays (ESA). Segemehl now supports the SAM format, reads gziped queries to save both disk and memory space and allows bisulfite sequencing mapping and split read mapping. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: ANNOgesic
has parent organization: University of Leipzig; Saxony; Germany
PMID:24512684
PMID:22581174
PMID:19750212
DOI:10.1371/journal.pcbi.1000502
Acknowledgement requested, Free, Public biotools:segemehl, OMICS_00683 https://bio.tools/segemehl
https://sources.debian.org/src/segemehl/
SCR_005494 segemehl - short read mapping with gaps 2026-02-14 02:00:56 45
PASS
 
Resource Report
Resource Website
1000+ mentions
PASS (RRID:SCR_005490) PASS software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on October 19, 2020.A program to align short sequences that has been developed with an innovative strategy to perform fast gapped and ungapped alignment onto a reference sequence. It supports several data formats and allows the user to modulate very finely the sensitivity of the alignments. The program is designed to handle huge amounts of short reads generated by ILLUMINA, SOLiD and Roche-454 technology. The optimization of the internal data structure and a filter based on precomputed short-word alignments allow the program to skip false positives in the extension phase, thus reducing the execution time without loss of sensitivity. The final alignment is performed by dynamic programming., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is related to: PASS-bis
has parent organization: University of Padua; Padua; Italy
PMID:19218350 THIS RESOURCE IS NO LONGER IN SERVICE biotools:pass, OMICS_00673 https://bio.tools/pass SCR_005490 PASS: a program to align short sequences 2026-02-14 02:01:08 2085
pyDNase
 
Resource Report
Resource Website
10+ mentions
pyDNase (RRID:SCR_005406) pyDNase software resource A software library for analyzing DNase-seq data. is listed by: OMICtools OMICS_00518 SCR_005406 2026-02-14 02:01:07 41
NeuroLex
 
Resource Report
Resource Website
10+ mentions
NeuroLex (RRID:SCR_005402) NeuroLex narrative resource, data or information resource, wiki A freely editable semantic wiki for community-based curation of the terms used in Neuroscience. Entries are curated and eventually incorporated into the formal NIFSTD ontology. NeuroLex also includes a Resource branch for community members to freely add neuroscience relevant resources that do not become part of NIFSTD ontology but rather make up the NIF Registry. As part of the NIF, we provide a simple search interface to many different sources of neuroscience information and data. To make this search more effective, we are constructing ontologies to help organize neuroscience concepts into category hierarchies, e.g., neuron is a cell. These categories provide the means to perform more effective searches and also to organize and understand the information that is returned. But an important adjunct to this activity is to clearly define all of the terms that we use to describe our data, e.g., anatomical terms, techniques, organism names. Because wikis provide an easy interface for communities to contribute their knowledge, we started the NeuroLex. behavioral activity, behavioral paradigm, brain region, cell, neuron, disease, molecule, nervous system function, subcellular part, resource type, quality, brain, neuroscience, biological process, cellular anatomy, anatomy, subcellular, subcellular anatomy, organism, neurological disorder, neurologic disease, dysfunction, atlas application, knowledge environment, php, web service, rdf, knowledge management, neuroanatomy, ontology, semantics, lexicon is used by: MicroDraw
is listed by: OMICtools
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: Program on Ontologies of Neural Structures
is related to: NIFSTD
is related to: neuroelectro
is related to: Whole Brain Catalog
is related to: Linked Neuron Data
is related to: SciCrunch Registry
is related to: InterLex
has parent organization: Neuroscience Information Framework
has parent organization: International Neuroinformatics Coordinating Facility
is parent organization of: Integrated
is parent organization of: Common Upper Mammalian Brain Ontology
is parent organization of: SciCrunch Registry
Neuroscience Information Framework PMID:24009581 Creative Commons Attribution License, v3 Unported OMICS_01703, nlx_144511 http://www.nitrc.org/projects/incf_neurolex-w SCR_005402 NeuroLex.org 2026-02-14 02:00:55 17
Fulcrum
 
Resource Report
Resource Website
1+ mentions
Fulcrum (RRID:SCR_005523) Fulcrum software resource Software to collapse identical and near-identical Illumina and 454 reads (such as those from PCR clones) into single error-corrected sequences; it can process paired-end as well as single-end reads. Fulcrum is customizable and can be deployed on a single machine, a local network or a commercially available MapReduce cluster, and it has been optimized to maximize ease-of-use, cross-platform compatibility and future scalability. Sequence datasets have been collapsed by up to 71%, and the reduced number and improved quality of the resulting sequences allow assemblers to produce longer contigs while using less memory. illumina, 454, read, paired-end read, single-end read, high-throughput sequencing, redundant read, genome, transcriptome, ultra high throughput sequencing is listed by: OMICtools
has parent organization: Stanford University School of Medicine; California; USA
PMID:22419786 BSD-like license OMICS_01049 http://pringlelab.stanford.edu/protocols.html SCR_005523 Fulcrum Read Collapser 2026-02-14 02:01:08 4
Maq
 
Resource Report
Resource Website
50+ mentions
Maq (RRID:SCR_005485) Maq software resource A set of programs that map and assemble fixed-length Solexa/SOLiD reads in a fast and accurate way. command-line, curses/ncurses, opengl, c, c++, perl, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
has parent organization: SourceForge
DOI:10.1101/gr.078212.108 GNU General Public License, v2 biotools:maq, OMICS_00668 https://bio.tools/maq
https://sources.debian.org/src/maq/
SCR_005485 mapass2, Mapping and Assembly with Quality, Mapping and Assembly with Qualities, Maq: Mapping and Assembly with Qualities 2026-02-14 02:00:56 69
MOSAIK
 
Resource Report
Resource Website
50+ mentions
MOSAIK (RRID:SCR_005486) MOSAIK software resource A reference-guided assembler comprising of two main modular programs: MosaikBuild and MosaikAligner. MosaikBuild converts various sequence formats into Mosaik?s native read format. MosaikAligner pairwise aligns each read to a specified series of reference sequences and produces BAMs as outputs. At this time, the workflow consists of supplying sequences in FASTA, FASTQ, Illumina Bustard & Gerald, or SRF file formats and producing results in the BAM format. Unlike many current read aligners, MOSAIK produces gapped alignments using the Smith-Waterman algorithm. MOSAIK is written in highly portable C++ and currently targetted for the following platforms: Microsoft Windows, Apple Mac OS X, FreeBSD, and Linux operating systems. Other platforms can easily be supported upon request. MOSAIK is multithreaded. If you have a machine with 8 processors, you can use all 8 processors to align reads faster while using the same memory footprint as when using one processor. MOSAIK supports multiple sequencing technologies. In addition to legacy technologies such as Sanger capillary sequencing, our program supports next generation technologies such as Roche 454, Illumina, AB SOLiD, and experimental support for the Helicos Heliscope. next-generation sequencing, alignment, smith-waterman algorithm, c++, computational biology, reference guided aligner is listed by: OMICtools
is listed by: Debian
is related to: 1000 Genomes: A Deep Catalog of Human Genetic Variation
has parent organization: Google Code
Free, Freely available OMICS_00669 https://sources.debian.org/src/mosaik-aligner/ SCR_005486 mosaik-aligner 2026-02-14 02:01:08 86

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.