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

26,885 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
WEBQTL
 
Resource Report
Resource Website
10+ mentions
WEBQTL (RRID:SCR_009072) WEBQTL software application, software resource An interactive web site useful for exploring the genetic modulation of thousands of phenotypes gathered over a 30-year period by hundreds of investigators using reference panels of recombinant inbred strains of mice. WebQTL includes dense error-checked genetic maps, as well as extensive gene expression data sets (Affymetrix) acquired across more than 35 strains of mice. WebQTL accepts user-entered traits for BXD, AXB/BXA, CXB, BXH, AKXD recombinant inbred strains. (entry from Genetic Analysis Software) gene, genetic, genomic, c++, and, python, all via internet is listed by: Genetic Analysis Software nlx_154066 http://www.webqtl.org/search.html SCR_009072 2026-08-09 09:05:08 46
genehunter-imprinting
 
Resource Report
Resource Website
1+ mentions
genehunter-imprinting (RRID:SCR_009104) GENEHUNTER-TWOLOCUS software application, software resource Resource no longer in service. Documented on February 23,2021.Software tool as modification of GENEHUNTER software package . Allows for parametric multi-marker linkage analysis of dichotomous traits caused by imprinted genes. By specification of two heterozygote penetrance parameters, paternal and maternal origin of the disease allele can be treated differently in terms of probability of expression of the trait. gene, genetic, genomic, c, unix, sunos, solaris, osf, hpux, aix, ultrix, linux, ms-windows, bio.tools is listed by: Genetic Analysis Software
is listed by: Debian
is listed by: bio.tools
DOI:10.1086/302911 Resource no longer in service. Documented on February 23,2021 nlx_154199, biotools:genehunter-imprinting https://bio.tools/genehunter-imprinting http://www.staff.uni-marburg.de/~strauchk/software.html SCR_009104 GENEHUNTER-MODSCORE, GENEHUNTER-PLUS, GENEHUNTER, GENEHUNTER-IMPRINTING 2026-08-09 09:05:08 1
GENEHUNTER-MODSCORE
 
Resource Report
Resource Website
1+ mentions
GENEHUNTER-MODSCORE (RRID:SCR_009069) GENEHUNTER-MODSCORE software application, software resource Software application that is an extension of GENEHUNTER-IMPRINTING, based on the original GENEHUNTER version 2.1 release 6, that allows for a MOD-score analysis, in which parametric LOD scores are maximized over the parameters of the trait model, i.e., the penetrances and disease allele frequency. As of version 2.0, it is possible to use sex-specific recombination frequencies. The genetic positions of markers can be automatically read from a publicly available genetic map. (entry from Genetic Analysis Software) gene, genetic, genomic, c, unix, sunos, solaris, osf, hpux, aix, ultrix, linux, ms-windows is listed by: Genetic Analysis Software nlx_154061 http://www.staff.uni-marburg.de/~strauchk/software.html SCR_009069 2026-08-09 09:05:07 1
MAREYMAP
 
Resource Report
Resource Website
10+ mentions
MAREYMAP (RRID:SCR_009066) MAREYMAP software application, software resource Software application that is a meiotic recombination rate estimation program. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic, r, tcl/tk is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154056 SCR_009066 2026-08-09 09:05:07 41
ASSOCIATIONVIEWER
 
Resource Report
Resource Website
ASSOCIATIONVIEWER (RRID:SCR_009063) ASSOCIATIONVIEWER software application, software resource A Java application used to display SNPs in a genetic context. Supplementary data (such as genes or LD plots) is downloaded from various public data sources on the fly and saved locally in a cache. Custom data can be added as supplementary tracks. (entry from Genetic Analysis Software) gene, genetic, genomic, java, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
nlx_154050, biotools:association_viewer https://bio.tools/association_viewer SCR_009063 2026-08-09 09:05:07 0
WHICHRUN
 
Resource Report
Resource Website
WHICHRUN (RRID:SCR_009064) WHICHRUN software application, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application that uses multilocus genotypic data to allocate individuals to their most likely source population. gene, genetic, genomic, c++, ms-windows, (95/98/nt) is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154051 http://www.bml.ucdavis.edu/whichrun.htm SCR_009064 2026-08-09 09:04:56 0
MAP MANAGER QTX
 
Resource Report
Resource Website
1+ mentions
MAP MANAGER QTX (RRID:SCR_009061) MAP MANAGER QTX software application, software resource A graphic, interactive program to map quantitative trait loci using intercrosses, backcrosses or recombinant inbred strains in experimental plants or animals. A completely rewritten cross-platform version of Map Manager QT with enhanced analysis functions. (entry from Genetic Analysis Software) gene, genetic, genomic, c++, and cross-platform code from xvt, ms-windows, macos is listed by: Genetic Analysis Software nlx_154046 SCR_009061 2026-08-09 09:04:56 4
G-MENDEL
 
Resource Report
Resource Website
G-MENDEL (RRID:SCR_009062) G-MENDEL software application, software resource Software tool for construction of genetic linkage maps and analyzing Mendelian phenotypes. (entry from Genetic Analysis Software) gene, genetic, genomic, unix, ms-windows is listed by: Genetic Analysis Software nlx_154049 http://cropandsoil.oregonstate.edu/G-mendel SCR_009062 2026-08-09 09:05:04 0
BQTL
 
Resource Report
Resource Website
1+ mentions
BQTL (RRID:SCR_009137) BQTL software application, software resource Software application for the mapping of genetic traits from line crosses and recombinant inbred lines. It performs (1) maximum likelihood estimation of multi-gene models; (2) Bayesian estimation of multi-gene models via Laplace Approximations; and (3) interval mapping and composite interval mapping of genetic loci (entry from Genetic Analysis Software) gene, genetic, genomic, s, c, fortran, the software is engineered to work in conjunction with r., unix, ms-windows, macos is listed by: Genetic Analysis Software nlx_154252 http://hacuna.ucsd.edu/bqtl/ SCR_009137 Bayesian Quantitative Trait Locus mapping 2026-08-09 09:05:10 1
DNABASER
 
Resource Report
Resource Website
10+ mentions
DNABASER (RRID:SCR_009138) DNABASER software application, software resource Software tool for manual and automatic DNA sequence assembly, DNA sequence analysis, automatic sample processing, contig editing, metadata integration, file format conversion and mutation detection. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154256 SCR_009138 2026-08-09 09:04:57 45
BPPH
 
Resource Report
Resource Website
BPPH (RRID:SCR_009136) BPPH software application, software resource Software application for inferring haplotypes from genotypes to determine if there are resulting haplotypes that fit a tree model (i.e. a perfect phylogeny, a coalescent). In population genetic terms, BPPH determines whether a set of SNP genotypes can be explained by haplotype pairs that could have evolved on a coalescent under the no-recombination, infinite sites model. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software nlx_154251 SCR_009136 Berkeley method for Perfect Phylogeney Haplotyping 2026-08-09 09:05:06 0
BLOCK
 
Resource Report
Resource Website
100+ mentions
BLOCK (RRID:SCR_009133) BLOCK software application, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application that performs general pedigree analysis on a general pedigree with any number of loops. It also allows users to perform two-point linkage analysis on a general pedigree with an arbitrary number of alleles., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic, ms-dos, linux, unix, solaris, irix 64, aix 3.2.5, dec alpha is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154247 SCR_009133 Blocking Gibbs sampler for pedigree analysis 2026-08-09 09:05:06 134
FastTree
 
Resource Report
Resource Website
5000+ mentions
FastTree (RRID:SCR_015501) source code, software resource Source code that infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences. It uses the Jukes-Cantor or generalized time-reversible (GTR) models of nucleotide evolution and the JTT, WAG, or LG models of amino acid evolution. phylogenetic tree, phylogenetic tree creation, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
is related to: VeryFastTree
PMID:19377059
DOI:10.1371/journal.pone.0009490
biotools:fasttree, OMICS_14703 https://bio.tools/fasttree, https://sources.debian.org/src/fasttree/ SCR_015501 2026-08-09 09:06:25 6279
MSM
 
Resource Report
Resource Website
1+ mentions
MSM (RRID:SCR_015500) source code, software resource Source code for fitting continuous-time Markov and hidden Markov multi-state models to longitudinal data. It was originally designed for processes observed at arbitrary times in continuous time but some other observation schemes are supported. Both Markov transition rates and the hidden Markov output process can be modelled in terms of covariates, which may be constant or piecewise-constant in time. markov, continuous time markov, hidden markov multi state model is hosted by: CRAN DOI:10.18637/jss.v038.i08 Available for download https://www.jstatsoft.org/article/view/v038i08 SCR_015500 Multi-State Markov and Hidden Markov Models in Continuous Time (MSM), Multi-State Markov and Hidden Markov Models in Continuous Time 2026-08-09 09:06:53 1
phytools
 
Resource Report
Resource Website
500+ mentions
phytools (RRID:SCR_015502) source code, software resource Software R package for phylogenetic comparative biology. The package contains various functions for phylogenetic analysis of comparative data from species. r package, phylogenetic comparison, phylogenetic analysis is listed by: Debian
is listed by: OMICtools
is hosted by: GitHub
DOI:10.1111/j.2041-210X.2011.00169.x Available for download, Acknowledgement requested OMICS_12499 https://github.com/liamrevell/phytools, https://sources.debian.org/src/r-cran-phytools/ SCR_015502 2026-08-09 09:06:41 718
Mikado
 
Resource Report
Resource Website
50+ mentions
Mikado (RRID:SCR_016159) source code, software resource Mikado is a lightweight Python3 pipeline whose purpose is to facilitate the identification of expressed loci from RNA-Seq data * and to select the best models in each locus. annotation, rna-seq, genomics, transcriptomics is related to: Portcullis BBSRC BB/J004669/1;
BBSRC BB/J010375/1;
BBSRC BB/CSP17270/1;
BBSRC BB/CCG1720/1
DOI:10.1101/216994 Free, Available for download http://mikado.readthedocs.io/ SCR_016159 2026-08-09 09:06:59 93
CUDAICA
 
Resource Report
Resource Website
1+ mentions
CUDAICA (RRID:SCR_015630) source code, software resource Software that implements Infomax ICA, which is an algorithm to perform Independent Component Analysis, in CUDA (a parallel computing platform and programming model). infomax ica, ica, independent component analysis, eeg PMID:22811699 Free, Available for download https://liaa.dc.uba.ar/node/10 SCR_015630 2026-08-09 09:06:27 3
regist custom genome
 
Resource Report
Resource Website
1+ mentions
regist custom genome (RRID:SCR_015999) source code, software resource One stop platform for NGS big data from analysis to visualization. There are about 400 analysis pipelines integrated on Maser. List of all analysis pipelines, including descriptions and approximate execution times, can be found on page for ‘All pipelines’ in the User Guide.. Regist custom genome software registers custom genomes to Genome Explorer (IN: FASTA). analysis, pipeline, maser, genome, explorer, fasta, custom, register Ministry of Education ;
Culture ;
Sports ;
Science and Technology ;
Japan
Restricted http://cell-innovation.nig.ac.jp/maser_cgi/cip-pl_list_violin_en.cgi SCR_015999 Management and Analysis System for Enormous Reads: regist custom genome 2026-08-09 09:06:33 1
kCSD-python
 
Resource Report
Resource Website
1+ mentions
kCSD-python (RRID:SCR_015777) source code, software resource Source code for the Python implementation of the kernel Current Source Density method. The method operates in one-, two-, and three-dimensional space to perform nonparametric estimation of transmembrane current sources from local field potentials recorded from arbitrarily distributed electrodes. kernel current source density, 1d, 2d, 3d, python, local field potential, transmembrane current source uses: Python Programming Language PMID:22091662 Free, Available for download SCR_015777 kernel current source density method - python, kCSD inverse method, Kernel Current Source Density Method 2026-08-09 09:06:29 7
lme4
 
Resource Report
Resource Website
100+ mentions
lme4 (RRID:SCR_015654) source code, software resource Software R package. Fit linear and generalized linear mixed-effects models. The models and their components are represented using S4 classes and methods. The core computational algorithms are implemented using the 'Eigen' C++ library for numerical linear algebra and 'RcppEigen' "glue." linear mixed-effects model, s4 class, eigen c++ library, r package, r, bio.tools is listed by: CRAN
is listed by: bio.tools
is listed by: Debian
works with: R package: lmerTest
Free, Available for download biotools:lme4 https://cran.r-project.org/package=lme4, https://github.com/lme4/lme4/, https://bio.tools/lme4 SCR_015654 lme4, lme4.0, lme4: Linear Mixed-Effects Models using 'Eigen' and S4, lme4: Linear Mixed-Effects Models, R package: lme4 2026-08-09 09:06:54 411

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.