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
CEM
 
Resource Report
Resource Website
1+ mentions
CEM (RRID:SCR_013241) CEM software resource An algorithm to assemble transcripts and estimate their expression levels from RNA-Seq reads. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of California at Riverside; California; USA
OMICS_01271, biotools:cem https://bio.tools/cem SCR_013241 CEM: Transcriptome Assembly and Isoform Expression Level Estimation from Biased RNA-Seq Reads 2026-08-01 12:04:46 1
SeqSite
 
Resource Report
Resource Website
SeqSite (RRID:SCR_013243) SeqSite software resource Software for detecting transcription factor binding sites from ChIP-seq data. is listed by: OMICtools OMICS_00493 SCR_013243 SeqSite: ChIP-Seq Binding Site Identification 2026-08-01 12:04:47 0
Repitools
 
Resource Report
Resource Website
10+ mentions
Repitools (RRID:SCR_013242) Repitools software resource Software tools for the analysis of enrichment-based epigenomic data. is listed by: OMICtools
has parent organization: Bioconductor
OMICS_00619 SCR_013242 2026-08-01 12:04:57 21
SmashCommunity
 
Resource Report
Resource Website
1+ mentions
SmashCommunity (RRID:SCR_013245) SmashCommunity software resource A stand-alone metagenomic annotation and analysis pipeline suitable for data from Sanger and 454 sequencing technologies. is listed by: OMICtools
has parent organization: EMBL - Bork Group
OMICS_01482 SCR_013245 2026-08-01 12:04:46 8
miRSeqNovel
 
Resource Report
Resource Website
1+ mentions
miRSeqNovel (RRID:SCR_013257) miRSeqNovel software resource An R/Bioconductor based workflow for novel miRNA prediction from deep sequencing data. is listed by: OMICtools
has parent organization: SourceForge
Free, Public, Non-commercial OMICS_00381 SCR_013257 2026-08-01 12:04:46 2
AutoMap
 
Resource Report
Resource Website
50+ mentions
AutoMap (RRID:SCR_013095) AutoMap software resource A tool for structural biology and drug design. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01596 SCR_013095 2026-08-01 12:04:45 92
DynamicProg
 
Resource Report
Resource Website
DynamicProg (RRID:SCR_013217) DynamicProg software resource A model-based statistical methods for base calling in Illumina''s next-generation sequencing platforms. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01150 SCR_013217 2026-08-01 12:04:57 0
muliAlignFree
 
Resource Report
Resource Website
muliAlignFree (RRID:SCR_013188) muliAlignFree software resource R package intended to implement a program for multiple alignment-free sequence comparison based on long genome sequence or NGS data. is listed by: OMICtools
has parent organization: University of Southern California; Los Angeles; USA
PMID:23990418 Free OMICS_00981 SCR_013188 muliAlignFree: Multiple Alignment-free Sequence Comparison 2026-08-01 12:04:46 0
CancerMutationAnalysis
 
Resource Report
Resource Website
CancerMutationAnalysis (RRID:SCR_013181) CancerMutationAnalysis software resource Software package that implements gene and gene-set level analysis methods for somatic mutation studies of cancer. is listed by: OMICtools
has parent organization: Bioconductor
Cancer OMICS_00141 SCR_013181 2026-08-01 12:04:46 0
BEADS
 
Resource Report
Resource Website
10+ mentions
BEADS (RRID:SCR_013229) BEADS software resource Software for a normalization scheme that corrects nucleotide composition bias, mappability variations and differential local DNA structural effects in deep sequencing data. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
has parent organization: University of Cambridge; Cambridge; United Kingdom
PMID:21646344 OMICS_00466, biotools:beads https://bio.tools/beads SCR_013229 BEADS: Bias Elimination Algorithm for Deep Sequencing, Bias Elimination Algorithm for Deep Sequencing 2026-08-01 12:04:47 37
CongrPE
 
Resource Report
Resource Website
1+ mentions
CongrPE (RRID:SCR_013190) CongrPE software resource A de novo assembly algorithm for Next-Generation Sequencing technology. is listed by: OMICtools
has parent organization: SourceForge
OMICS_00011 SCR_013190 2026-08-01 12:04:56 1
CallSim
 
Resource Report
Resource Website
CallSim (RRID:SCR_013192) CallSim software resource A software application that provides evidence for the validity of base calls believed to be sequencing errors and it is applicable to Ion Torrent and 454 data. matlab is listed by: OMICtools
has parent organization: SourceForge
Apache License OMICS_01098 SCR_013192 CallSim - Low-volume read processing base corrector 2026-08-01 12:04:46 0
SAPAS
 
Resource Report
Resource Website
50+ mentions
SAPAS (RRID:SCR_013195) SAPAS software resource A RNA-seq method for polyA research. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01413 SCR_013195 2026-08-01 12:04:56 66
HMMSplicer
 
Resource Report
Resource Website
1+ mentions
HMMSplicer (RRID:SCR_013315) HMMSplicer software resource An accurate and efficient algorithm for discovering canonical and non-canonical splice junctions in short read datasets. is listed by: OMICtools
has parent organization: University of California at San Francisco; California; USA
OMICS_01241 SCR_013315 2026-08-01 12:04:47 3
Trans-ABySS
 
Resource Report
Resource Website
50+ mentions
Trans-ABySS (RRID:SCR_013322) Trans-ABySS software resource A software pipeline for analyzing ABySS-assembled contigs from shotgun transcriptome data. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
OMICS_01326, biotools:trans-abyss https://bio.tools/trans-abyss/ SCR_013322 2026-08-01 12:04:58 69
NEUMA
 
Resource Report
Resource Website
1+ mentions
NEUMA (RRID:SCR_013324) NEUMA software resource Software for estimating mRNA abundances from the whole transcriptome shotgun sequencing (RNA-Seq) data based on effective length normalization using uniquely mappable areas of gene and mRNA isoform models. Using the known transcriptome sequence model such as RefSeq, NEUMA pre-computes the numbers of all possible gene-wise and isoform-wise informative reads: the former being sequences mapped to all mRNA isoforms of a single gene exclusively and the latter uniquely mapped to a single mRNA isoform. The results are used to estimate the effective length of genes and transcripts, taking experimental distributions of fragment size into consideration. NEUMA covers a large proportion of genes and mRNA isoforms and offers a measure of consistency (''consistency coefficient'') for each gene between an independently measured gene-wise level and the sum of the isoform levels. NEUMA is applicable to both paired-end and single-end RNA-Seq data. is listed by: OMICtools
has parent organization: Korea Research Institute of Bioscience and Biotechnology; Daejeon; South Korea
PMID:21059678 OMICS_01281 SCR_013324 Normalization by Expected Uniquely Mappable Area 2026-08-01 12:04:48 5
chimerascan
 
Resource Report
Resource Website
50+ mentions
chimerascan (RRID:SCR_013298) chimerascan software resource Software package that detects gene fusions in paired-end RNA sequencing (RNA-Seq) datasets. Used for detection of chimeric transcripts in high-throughput sequencing data. Gene fusion detection, paired-end RNA sequencing data, RNA sequencing data, chimeric transcripts detection, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Free, Available for download, Freely available biotools:chimerascan, OMICS_01343 https://bio.tools/chimerascan SCR_013298 2026-08-01 12:04:58 53
wapRNA
 
Resource Report
Resource Website
1+ mentions
wapRNA (RRID:SCR_013292) wapRNA software resource A free web-based application for the processing of high-throughput RNA-Seq data from next generation sequencing (NGS) platforms, such as Genome Analyzer of Illumina Inc. (Solexa) and SOLiD of Applied Biosystems (SOLiD). is listed by: OMICtools PMID:21896507 OMICS_00370 SCR_013292 2026-08-01 12:04:47 1
RosettaDock
 
Resource Report
Resource Website
100+ mentions
RosettaDock (RRID:SCR_013393) RosettaDock software resource Predicts the structure of a protein-protein complex from the individual structures of the monomer components. is listed by: OMICtools
has parent organization: Johns Hopkins University; Maryland; USA
OMICS_01604 SCR_013393 2026-08-01 12:04:48 118
ArrayOligoSelector
 
Resource Report
Resource Website
10+ mentions
ArrayOligoSelector (RRID:SCR_013494) ArrayOligoSelector software resource Software program to systematically design gene specific long oligonucleotide probes for entire genomes, for the purpose of developing whole genome microarrays. For each open reading frame, the program optimizes the oligo selection based upon several parameters, including uniqueness in the genome, sequence complexity, lack of self-binding, GC content and proximity to the 3''end of the gene. is listed by: OMICtools
has parent organization: University of California at San Francisco; California; USA
has parent organization: SourceForge
PMID:12620119 Free, Public, Commercial requires license, Use of the blat or gfclient options requires license OMICS_00826 SCR_013494 2026-08-01 12:04:48 13

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.