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

  • Keywords:genomic (facet)

Facets


Recent searches

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

828 Results - per page

Show More Columns | Download 828 Result(s)

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
JENTI
 
Resource Report
Resource Website
JENTI (RRID:SCR_009053) JENTI software application, software resource An efficient tool for mining complex inbred genealogies that identify clusters of individuals sharing the same expected amount of relatedness is described. Additionally it allows for the reconstruction of sub-pedigrees suitable for genetic mapping in a systematic way. (entry from Genetic Analysis Software) gene, genetic, genomic, java is listed by: Genetic Analysis Software nlx_154033 SCR_009053 2026-08-04 09:42:17 0
COMBIN
 
Resource Report
Resource Website
COMBIN (RRID:SCR_009050) COMBIN software application, software resource Software application designed for the construction of highly saturated linkage maps, based on BC1, DH, Radiation Hybrid or CP (CrossPollinators) data sets. F2 is not supported. (entry from Genetic Analysis Software) gene, genetic, genomic, visual basic 5, ms-windows, (95/98/nt) is listed by: Genetic Analysis Software nlx_154025 http://www.dpw.wau.nl/pv/pub/combin/ SCR_009050 2026-08-04 09:42:17 0
ARLEQUIN
 
Resource Report
Resource Website
5000+ mentions
ARLEQUIN (RRID:SCR_009051) ARLEQUIN software application, software resource An exploratory population genetics software environment able to handle large samples of molecular data (RFLPs, DNA sequences, microsatellites), while retaining the capacity of analyzing conventional genetic data (standard multi-locus data or mere allele frequency data). (entry from Genetic Analysis Software) gene, genetic, genomic, ms-windows, (95/98/nt/2000/xp) is listed by: Genetic Analysis Software nlx_154029 SCR_009051 this software is about the study of genetic polymorphism.), a character of the Italian Commedia dell''Arte. He has many aspects, but can switch among them very easily according to needs and necessities. Similarly, (French translation of Arlecchino 2026-08-04 09:42:18 5536
GRONLOD
 
Resource Report
Resource Website
GRONLOD (RRID:SCR_009049) GRONLOD software application, software resource Conversion programs from LINKAGE files are available. The program uses peeling and can employ nested conditioning. There is an automatic peeling program that will unravel (multiple) loops. Alleles do not need to be recoded, so real allele sizes can be used. Genotype probabilities for a chosen person can be calculated for purposes of genetic risk calculation. Later versions include one for calculations using linked markers and mutations and mosaicism, made by Martin van der Meulen. A symbolic versions will generate the formula to compute the pedigree likelihood. (entry from Genetic Analysis Software) gene, genetic, genomic, prolog, ms-windows, (3.1/95/nt) is listed by: Genetic Analysis Software nlx_154024 SCR_009049 GRONingen university LOR score calculation 2026-08-04 09:42:16 0
SNP ASSISTANT
 
Resource Report
Resource Website
SNP ASSISTANT (RRID:SCR_009048) SNP ASSISTANT software application, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application for SNP data managing, import & export from linkage format, data validation, pairwise LD calculation and visualisation, case-control and TDT tests, visual comparison of two datasets, relationships testing. Suitable for large projects. gene, genetic, genomic, c++, ms-windows, (95 and newer) is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154023 SCR_009048 2026-08-04 09:42:18 0
DHSMAP
 
Resource Report
Resource Website
1+ mentions
DHSMAP (RRID:SCR_009160) DHSMAP software application, software resource Software application for fine-mapping of qualitative traits by linkage disequilibrium. Given a set of marker haplotypes or genotypes from affected individuals, haplotypes or genotypes from appropriately selected controls, and a genetic map of the markers at which both sets of individuals are typed, DHSMAP estimates the location of the trait-associated variant by maximum likelihood or maximum quasi-likelihood. (entry from Genetic Analysis Software) gene, genetic, genomic, c++, unix, solaris, linux is listed by: Genetic Analysis Software nlx_154282 SCR_009160 Decay of Haplotype Sharing MAPping software 2026-08-04 09:42:18 1
AMELIA
 
Resource Report
Resource Website
100+ mentions
AMELIA (RRID:SCR_009119) AMELIA software application, software resource Software application that employs allele matching to analyse the effects of rare variants within a specific locus. There is increasing evidence that rare variants play a role in some complex traits, but their analysis is not straightforward. Locus-based tests become necessary due to low power in rare variant single-point association analyses. In addition, variant quality scores are available for sequencing data, but are rarely taken into account. To enable this analysis, AMELIA has been developed as an allele-matching approach that is robust to the presence of both directions of effect for variants within the locus analysed. (entry from Genetic Analysis Software) gene, genetic, genomic, r, unix, linux is listed by: Genetic Analysis Software nlx_154222 SCR_009119 Allele Matching Empirical Locus-specific Integrated Association test 2026-08-04 09:42:19 121
ALLEGRO
 
Resource Report
Resource Website
50+ mentions
ALLEGRO (RRID:SCR_009116) ALLEGRO software application, software resource Software application that is a faster version of GENEHUNTER and Allegro 1.2 (several degrees of increase of speed, can handle bigger families, up to 50 bits) (entry from Genetic Analysis Software) gene, genetic, genomic, c++ is listed by: Genetic Analysis Software nlx_154217 SCR_009116 2026-08-04 09:42:19 63
SIBSIM
 
Resource Report
Resource Website
SIBSIM (RRID:SCR_009113) SIBSIM software application, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application that simulates either genotype and/or quantitative phenotype data in family structures in a modern, easy to use and highly scalable way. It is based on XML, completely written in C++ and published under the GNU General Public License. gene, genetic, genomic, c++, xml, unix is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154212 SCR_009113 2026-08-04 09:42:19 0
IGG
 
Resource Report
Resource Website
1+ mentions
IGG (RRID:SCR_009114) IGG software application, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. gene, genetic, genomic, java, web-based is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154214 http://bioinfo.hku.hk:13080/iggweb/ SCR_009114 Integrate Genotypes for genome-wide Genetic studies 2026-08-04 09:42:17 2
QTLNetwork
 
Resource Report
Resource Website
50+ mentions
QTLNetwork (RRID:SCR_009078) software application, software resource Software package for mapping and visualizing the genetic architecture underlying complex traits for experimental populations derived from a cross between two inbred lines. (entry from Genetic Analysis Software). QTLNetwork-2.0 for mapping quantitative trait loci (QTL) with epistatic effects and QE interaction effects in DH, RI, BC, F2, IF2 and BxFy populations, and for graphical presentation of QTL mapping results. gene, genetic, genomic is listed by: Genetic Analysis Software PMID:18202029
PMID:20593516
nlx_154076 SCR_009078 , QTLNetwork, QTL network 2, QTLNetwork 2.0 2026-08-04 09:42:18 50
TREELD
 
Resource Report
Resource Website
TREELD (RRID:SCR_009111) TREELD software application, software resource Free software tool for mapping complex trait loci. TreeLD performs a multipoint LD-analysis by inferring the ancestry of a genomic region and analyzing this ancestry for signals of disease mutations. The generated likelihoods can be used to test for the presence of a disease locus and to fine-map its location, providing a point estimate and a credible region. Furthermore, the package provides a novel way of visualizing the association signal in a sample. TreeLD is designed for high-density SNP haplotypes and can be applied to case-control data, TDT trio data and quantitative trait data. (entry from Genetic Analysis Software) gene, genetic, genomic, unix, solaris, linux, ms-windows, (95/98/nt/2000/xp) is listed by: Genetic Analysis Software Free nlx_154210 SCR_009111 2026-08-04 09:42:17 0
MIXSCORE
 
Resource Report
Resource Website
1+ mentions
MIXSCORE (RRID:SCR_009076) MIXSCORE software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application using a method for combining SNP association and admixture association statistics to increase power in GWAS in admixed populations. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154074 SCR_009076 2026-08-04 09:42:17 6
POWQ
 
Resource Report
Resource Website
POWQ (RRID:SCR_009077) POWQ software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 9, 2023. A user-friendly, graphical package for power evaluation and enhancement planning through variance component linkage analysis in a multipoint framework. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software PMID:16585065 THIS RESOURCE IS NO LONGER IN SERVICE nlx_154075 SCR_009077 2026-08-04 09:42:17 0
STRAT
 
Resource Report
Resource Website
10+ mentions
STRAT (RRID:SCR_009110) STRAT software application, software resource Software application that is a companion program to STRUCTURE that is a structured association method, for use in association mapping, enabling valid case-control studies even in the presence of population structure. (entry from Genetic Analysis Software) gene, genetic, genomic, ms-dos, ms-windows, unix, solaris, linux is listed by: Genetic Analysis Software
is related to: STRUCTURE
is related to: STRUCTURE
nlx_154208 SCR_009110 2026-08-04 09:42:19 12
HAPLOVISUAL
 
Resource Report
Resource Website
HAPLOVISUAL (RRID:SCR_009073) HAPLOVISUAL software application, software resource Software application (entry from Genetic Analysis Software) gene, genetic, genomic, java is listed by: Genetic Analysis Software nlx_154068 SCR_009073 2026-08-04 09:42:16 0
FAMHAP
 
Resource Report
Resource Website
10+ mentions
FAMHAP (RRID:SCR_009070) FAMHAP software application, software resource Software application for haplotype association analysis of unphased genotype data. It can be used both for population data (case-control) and nuclear family data. The program is optimized for haplotype frequency estimation with the EM-algorithm for many markers. FAMHAP provides a method which searches for potential genotyping errors and several tests for haplotype-based association analysis. Particular emphasis is on Monte-Carlo simulations, which are necessary in the context of haplotype association, where asymptotic theory often fails, and in the context of multiple testing problems. (entry from Genetic Analysis Software) gene, genetic, genomic, c, unix, ms-windows, macos is listed by: Genetic Analysis Software nlx_154064 SCR_009070 2026-08-04 09:42:16 12
BAMA
 
Resource Report
Resource Website
50+ mentions
BAMA (RRID:SCR_009071) BAMA software application, software resource Software application to select a trait-associated subset of markers among many candidates. The program is based on Bayesian modeling/estimation and it suits for both quantitative and qualitative traits. It can handle bi- and multiallelic markers as well as applied in situations where part of the marker genotypes may be missing. As an output of the program, one obtains posterior estimate of number and positions of trait-associated markers. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic, c, linux is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154065 SCR_009071 Bayesian Analysis of Multilocus Association 2026-08-04 09:42:17 98
HARDY
 
Resource Report
Resource Website
5000+ mentions
HARDY (RRID:SCR_009107) HARDY software application, software resource Markov chain Monte Carlo program for association in two-dimensional contingency tables, and for testing Hardy-Weinberg equilibrium. (entry from Genetic Analysis Software) gene, genetic, genomic, c, unix, (dec-unix/..) is listed by: Genetic Analysis Software nlx_154205 SCR_009107 PANGAEA 2026-08-04 09:42:18 7329
PBAT
 
Resource Report
Resource Website
50+ mentions
PBAT (RRID:SCR_009105) PBAT software application, software resource An interactive software package that provides tools for the design and the data analysis of family-based association studies. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software nlx_154203 SCR_009105 Power calculation of family-Based Association Tests FBAT 2026-08-04 09:42:17 75

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.