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
aCGH.Spline
 
Resource Report
Resource Website
aCGH.Spline (RRID:SCR_002927) software resource An R package for array comparative genomic hybridization (aCGH) dye bias normalization. standalone software, mac os x, unix/linux, windows, r is listed by: OMICtools
has parent organization: CRAN
PMID:21357574 Free, Available for download, Freely available OMICS_02607 http://cran.r-project.org/web/packages/aCGH.Spline/ SCR_002927 2026-02-07 02:06:06 0
StreamingTrim
 
Resource Report
Resource Website
1+ mentions
StreamingTrim (RRID:SCR_002922) software resource A DNA reads trimming software, written in Java, with which researchers are able to analyse the quality of DNA sequences in fastq files and to search for low-quality zones in a very conservative way. standalone software, java, 16s rrna, sequence is listed by: OMICtools PMID:24128146 Free, Available for download, Freely available OMICS_05196 SCR_002922 2026-02-07 02:06:06 8
pLabel
 
Resource Report
Resource Website
10+ mentions
pLabel (RRID:SCR_002923) software resource Mass spectral peak labeling software developed for proteomics research., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. mass spectrometry, proteomics is listed by: OMICtools
has parent organization: Chinese Academy of Sciences; Beijing; China
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02469 SCR_002923 2026-02-07 02:05:52 28
hot scan
 
Resource Report
Resource Website
1+ mentions
hot scan (RRID:SCR_002840) software resource A free software to detect genomic regions unusually rich in translocation breakpoints. More generally, it may be used to detect a region that is unusually rich in a given character of a binary sequence. software package, perl, r, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:24860160 Free, Freely available, Available for download biotools:hot_scan, OMICS_05200 https://bio.tools/hot_scan SCR_002840 hot_scan 2026-02-07 02:05:50 6
rDock
 
Resource Report
Resource Website
100+ mentions
rDock (RRID:SCR_002838) software resource A fast and versatile Open Source docking software program that can be used to dock small molecules against proteins and nucleic acids. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:24722481 Free, Freely available, Available for download OMICS_03835 SCR_002838 2026-02-07 02:05:51 107
Basic4Cseq
 
Resource Report
Resource Website
1+ mentions
Basic4Cseq (RRID:SCR_002836) software resource An R/Bioconductor package for basic filtering, analysis and subsequent near-cis visualization of 4C-seq data. Virtual fragment libraries can be created for any BSGenome package, and filter functions for both reads and fragments and basic quality controls are included. Fragment data in the vicinity of the experiment's viewpoint can be visualized as a coverage plot based on a running median approach and a multi-scale contact profile. software package, unix/linux, mac os x, windows, r, quality control, visualization is listed by: OMICtools
has parent organization: Bioconductor
PMID:25078398 Free, Freely available, Available for download OMICS_05202 SCR_002836 Basic4Cseq: an R/Bioconductor package for analyzing 4C-seq data 2026-02-07 02:05:50 5
SMRT-Analysis
 
Resource Report
Resource Website
100+ mentions
SMRT-Analysis (RRID:SCR_002942) software resource Open-source bioinformatics software suite for analyzing single molecule, real-time DNA sequencing data. Users can choose from a variety of analysis protocols that utilize PacBio and third-party tools. Analysis protocols include de novo genome assembly, cDNA mapping, DNA base-modification detection, and long-amplicon analysis to determine phased consensus sequences. software suite is listed by: OMICtools
is listed by: Debian
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_05142 http://www.pacb.com/devnet/
https://sources.debian.org/src/smrtanalysis/
SCR_002942 SMRT Analysis 2026-02-07 02:05:52 130
mzR
 
Resource Report
Resource Website
mzR (RRID:SCR_002856) software resource Software that provides a unified API to the common file formats and parsers available for mass spectrometry data. It comes with a wrapper for the ISB random access parser for mass spectrometry mzXML, mzData and mzML files. standalone software, mac os x, unix/linux, windows, r, data import, infrastructure, mass spectrometry, metabolomics, proteomics is listed by: OMICtools
has parent organization: Bioconductor
Free, Freely available, Available for download OMICS_02654 SCR_002856 mzR - parser for netCDF mzXML mzData and mzML and mzIdentML files 2026-02-07 02:05:50 0
BiGGR
 
Resource Report
Resource Website
BiGGR (RRID:SCR_002854) software resource Software package that provides an interface to simulate metabolic reconstruction from the BiGG database and other metabolic reconstruction databases. The package facilitates flux balance analysis (FBA) and the sampling of feasible flux distributions. Metabolic networks and estimated fluxes can be visualized with hypergraphs. standalone software, mac os x, unix/linux, windows, r, metabolomics, network, visualization, metabolic reconstruction, model uses: BiGG Database
is listed by: OMICtools
has parent organization: Bioconductor
PMID:25806817 Free, Freely available, Available for download OMICS_02655 SCR_002854 BiGGR - Constraint based modeling in R using metabolic reconstruction databases 2026-02-07 02:06:04 0
PAPi
 
Resource Report
Resource Website
50+ mentions
PAPi (RRID:SCR_002857) software resource An R package for predicting the activity of metabolic pathways based solely on a metabolomics data set containing a list of metabolites identified and their respective abundances in different biological samples. PAPi generates hypothesis that improves the final biological interpretation. standalone software, mac os x, unix/linux, windows, r, mass spectrometry, metabolomics is listed by: OMICtools
has parent organization: Bioconductor
PMID:20929912 Free, Freely available, Available for download OMICS_02653 SCR_002857 PAPi - Predict metabolic pathway activity based on metabolomics data, Pathway Activity Profiling 2026-02-07 02:06:04 53
CNVassoc
 
Resource Report
Resource Website
1+ mentions
CNVassoc (RRID:SCR_002901) software resource Software package that carries out association analysis of common copy number variants in population-based studies. It includes functions for analysing association under a series of study designs (case-control, cohort, etc), using several dependent variables (class status, censored data, counts) as response, adjusting for covariates and considering various inheritance models. It also includes functions for inferring copy number (CNV genotype calling). Various classes and methods for generic functions (print, summary, plot, anova, ... ) have been created to facilitate the analysis. standalone software, mac os x, unix/linux, windows, r is listed by: OMICtools
has parent organization: CRAN
PMID:21609482 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02609 SCR_002901 CNVassoc: Association analysis of CNV data 2026-02-07 02:05:52 1
CoRAL - Classification of RNAs by Analysis of Length
 
Resource Report
Resource Website
1+ mentions
CoRAL - Classification of RNAs by Analysis of Length (RRID:SCR_010828) CoRAL software resource A machine learning software package that can predict the precursor class of small RNAs present in a high-throughput RNA-sequencing dataset. In addition to classification, it also produces information about the features that are most important for discriminating different populations of small non-coding RNAs. is listed by: OMICtools
has parent organization: University of Pennsylvania; Philadelphia; USA
PMID:23700308 Acknowledgement requested OMICS_00372 SCR_010828 Classification of RNAs by Analysis of Length 2026-02-07 02:07:53 7
PriVar
 
Resource Report
Resource Website
1+ mentions
PriVar (RRID:SCR_010784) PriVar software resource A toolkit for prioritizing SNVs and indels from next-generation sequencing data. is listed by: OMICtools OMICS_00160 SCR_010784 2026-02-07 02:07:52 1
CNVer
 
Resource Report
Resource Website
1+ mentions
CNVer (RRID:SCR_010820) CNVer software resource A method for CNV detection that supplements the depth-of-coverage with paired-end mapping information, where matepairs mapping discordantly to the reference serve to indicate the presence of variation. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
biotools:cnver, OMICS_00341 https://bio.tools/cnver SCR_010820 2026-02-07 02:07:53 8
CNVnator
 
Resource Report
Resource Website
100+ mentions
CNVnator (RRID:SCR_010821) CNVnator software resource An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. is listed by: OMICtools OMICS_00343 SCR_010821 2026-02-07 02:08:02 498
Diplotyper
 
Resource Report
Resource Website
Diplotyper (RRID:SCR_010789) Diplotyper software resource A fully automated software tool which is available for Linux to investigate associations between a diplotype group and a phenotype in linear or logistic regression. is listed by: OMICtools
has parent organization: Google Code
OMICS_00195 SCR_010789 2026-02-07 02:08:04 0
Control-FREEC
 
Resource Report
Resource Website
100+ mentions
Control-FREEC (RRID:SCR_010822) Control-FREEC software resource Prediction of copy number alterations and loss of heterozygosity using deep-sequencing data. is listed by: OMICtools OMICS_00344 SCR_010822 2026-02-07 02:07:53 315
readDepth
 
Resource Report
Resource Website
10+ mentions
readDepth (RRID:SCR_010824) readDepth software resource This package for R can detect copy number aberrations by measuring the depth of coverage obtained by massively parallel sequencing of the genome. is listed by: OMICtools OMICS_00350 SCR_010824 2026-02-07 02:08:02 21
HapCUT
 
Resource Report
Resource Website
10+ mentions
HapCUT (RRID:SCR_010791) HapCUT software resource A max-cut based algorithm for haplotype assembly using sequence reads from the two chromosomes of an individual. is listed by: OMICtools OMICS_00198 SCR_010791 2026-02-07 02:07:52 17
Relate
 
Resource Report
Resource Website
10+ mentions
Relate (RRID:SCR_010794) Relate software resource Software providing a method that estimates the probability of sharing alleles identity by descent (IBD) across the genome and can also be used for mapping disease loci using distantly related individuals. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:19025785 biotools:relateadmix, OMICS_00207 https://bio.tools/relateadmix SCR_010794 2026-02-07 02:08:04 41

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.