Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
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.
| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GMCHECK Resource Report Resource Website |
GMCHECK (RRID:SCR_009213) | GMCHECK | software resource, software application | Software application that finds the posterior probabilities for data errors for genotypes and phenotypes in pedigree data (entry from Genetic Analysis Software) | gene, genetic, genomic, java | is listed by: Genetic Analysis Software | nlx_154362 | http://episun7.med.utah.edu/~alun/gmcheck/ | SCR_009213 | 2026-02-13 10:56:21 | 0 | ||||||||
|
GLIDERS Resource Report Resource Website 1+ mentions |
GLIDERS (RRID:SCR_009210) | GLIDERS | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 6, 2016. | gene, genetic, genomic | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154359 | SCR_009210 | Genome-wide LInkage DisEquilibrium Repository and Search engine | 2026-02-13 10:56:21 | 1 | |||||||
|
MLD Resource Report Resource Website |
MLD (RRID:SCR_009298) | MLD | software resource, software application | Software application performing a shuffling version of the exact conditional tests for different combinations of allelic and genotypic disequilibrium on haploid and diploid data, or their combination. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, unix, ms-windows, (95) | is listed by: Genetic Analysis Software | nlx_154489 | SCR_009298 | 2026-02-13 10:56:22 | 0 | |||||||||
|
MLBGH Resource Report Resource Website 1+ mentions |
MLBGH (RRID:SCR_009297) | MLBGH | software resource, software application | Software application that is an extension of the GENEHUNTER program to perform sib-pair and sib-ship linkage analysis using the Maximum Likelihood Binomial (MLB) method. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix | is listed by: Genetic Analysis Software | nlx_154488 | SCR_009297 | Maximum-Likelihood-Binomial analysis of affected sib-pair and sibship data extended from the GENEHUNTER program | 2026-02-13 10:56:22 | 1 | ||||||||
|
MITPENE Resource Report Resource Website |
MITPENE (RRID:SCR_009294) | MITPENE | software resource, software application | Software program for analysis of mitochondrial diseases (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154485 | SCR_009294 | 2026-02-13 10:56:22 | 0 | |||||||||
|
MKGST Resource Report Resource Website 1+ mentions |
MKGST (RRID:SCR_009295) | MKGST | software resource, software application | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154486 | SCR_009295 | including ASP (power calculator for gene mapping using a sibpair design), with given infants or parent-infant duos), child and putative father), MUTPROF/MUTCOMP (comparison of mutation profiles), Michael Krawczak''s Genetics Software Tools, typed at single locus DNA markers, PATERN (calculation of paternity probabilities from the multilocus DNA profiles of trios, comparing specific types of simple hypotheses regarding the familial relationships involved), ASPSHARE (rapid calculation of the expected ibd sharing at the trait locus, FINDSIRE (identify mothers or sires by means of the comparison of a large number of potential parents, EASYPAT (calculation of likelihood ratios for single locus data, comprising mother, based upon the model) | 2026-02-13 10:56:22 | 2 | ||||||||
|
MINIMAC Resource Report Resource Website 100+ mentions |
MINIMAC (RRID:SCR_009292) | MINIMAC | software resource, software application | Software application that is a low memory, computationally efficient implementation of the MaCH algorithm for genotype imputation. It is designed to work on phased genotypes and can handle very large reference panels with hundreds or thousands of haplotypes. The name has two parts. The first, mini, refers to the modest amount of computational resources it requires. The second, mac, is short hand for MaCH, our widely used algorithm for genotype imputation. (entry from Genetic Analysis Software) | gene, genetic, genomic |
is listed by: Genetic Analysis Software is listed by: Debian is listed by: OMICtools is related to: Michigan Imputation Server |
DOI:10.1038/ng.3656 | nlx_154483, OMICS_08953 | https://sources.debian.org/src/minimac4/ | SCR_009292 | MACH | 2026-02-13 10:56:22 | 187 | ||||||
|
MFLINK Resource Report Resource Website |
MFLINK (RRID:SCR_009290) | MFLINK | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application (entry from Genetic Analysis Software) | gene, genetic, genomic, c | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154477 | SCR_009290 | (nearly) model-free linkage analysis | 2026-02-13 10:56:22 | 0 | |||||||
|
GEVALT Resource Report Resource Website 1+ mentions |
GEVALT (RRID:SCR_009207) | GEVALT | software resource, software application | Software application designed to simplify and expedite the process of genotype analysis and disease association tests by providing a common interface to several common tasks relating to such analyses. It is aimed for analysis of unrelated individuals as well as two-generation families. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154354 | SCR_009207 | GEnotype Visualization and ALgorithmic Tool | 2026-02-13 10:56:21 | 6 | ||||||||
|
GGT Resource Report Resource Website 1+ mentions |
GGT (RRID:SCR_009208) | GGT | software resource, software application | Software application that combines genetic map data and locus data to display Graphical Genotypes. Data can be viewed by individual or by linkage group, and sorted on markers. Statistics are calculated and simultaneous filtering/selection on multiple linkage groups is possible. Output of hi-res genotype drawings directly to printer or to emf/jpeg/bitmap image. A module for constructing GGT-datafiles from common mapmaker/joinmap style formatted data is available. (entry from Genetic Analysis Software) | gene, genetic, genomic, delphi, (pascal), ms-windows, (95/98/2000/xp) | is listed by: Genetic Analysis Software | nlx_154356 | http://www.dpw.wau.nl/pv/PUB/ggt/ | SCR_009208 | Graphical GenoTyping package MAPCOMP | 2026-02-13 10:56:21 | 1 | |||||||
|
GENOCHECK Resource Report Resource Website 1+ mentions |
GENOCHECK (RRID:SCR_009203) | GENOCHECK | software resource, software application | Software application designed to identify genotypes that are likely to be errors. The statistical method was designed to identify typing error rather than pedigree errors, but is general enough to pinpoint any unlikely genotype still consistent with Mendelian inheritance. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix | is listed by: Genetic Analysis Software | nlx_154345 | SCR_009203 | GenoCheck | 2026-02-13 10:56:20 | 7 | ||||||||
|
MERLIN Resource Report Resource Website 500+ mentions |
MERLIN (RRID:SCR_009289) | MERLIN | software resource, software application | Software application that carries out single-point and multipoint analyses of pedigree data, including IBD and kinship calculations, nonparametric and variance component linkage analyses, error detection and information content mapping. For multipoint analyses in dense maps, Merlin allows the user to impose constraints on the number of recombinants between consecutive markers. Merlin estimates haplotypes by finding the most likely path of gene flow or by sampling paths of gene flow at all markers jointly. It can also list all possible nonrecombinant haplotypes within short regions. Finally, Merlin provides swap-file support for handling very large numbers of markers as well as gene-dropping simulations for estimating empirical significance levels. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, unix. linux | is listed by: Genetic Analysis Software | nlx_154475 | SCR_009289 | Multipoint Engine for Rapid Likelihood INference | 2026-02-13 10:56:22 | 910 | ||||||||
|
GENEWEAVER Resource Report Resource Website 10+ mentions |
GENEWEAVER (RRID:SCR_009202) | GENEWEAVER | software resource, software application | Software application for charting family medical/health history (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic, ms-windows, (95/98/2000/nt/xp) | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154343 | SCR_009202 | 2026-02-13 10:56:20 | 39 | ||||||||
|
GENOOM Resource Report Resource Website |
GENOOM (RRID:SCR_009200) | GENOOM | software resource, software application | Software application that implements a virtual computer world where biological entities are digital objects. In this world, each individual of a population is represented by a set of chromosomes with genetic elements (markers, genes, Quantitative Traits Loci, etc.) and attributes (phenotype, age, fertility, living status, exposure, etc.). It comes with a built-in model allowing basic genetic studies by simulations, performed according to parameter values such a penetrance matrix (phenotype probabilities for each genotype), exposure, between-relative mating probabilities, and a probability of migration in a two-dimensional migration process. The simulated populations could be analysed with different packages for statistical or genetical analysis (e.g., SAS, S-PLUS, Linkage, Mapmaker/sibs, Genehunter). Pedigrees can also be simulated according to a pedigree file at the LINKAGE format. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, unix, linux | is listed by: Genetic Analysis Software | nlx_154350 | http://www.genoom.com/ | SCR_009200 | GENetic Object Oriented Modeling in population genetics | 2026-02-13 10:56:21 | 0 | |||||||
|
MENDEL Resource Report Resource Website 500+ mentions |
MENDEL (RRID:SCR_009288) | MENDEL | software resource, software application | Software application for genetic analysis of human pedigree data under models involving a small number of loci. MENDEL is useful for segregation analysis, linkage calculations, genetic counseling, allele frequency estimation, and related kinds of problems. (entry from Genetic Analysis Software) | gene, genetic, genomic, fortran77 | is listed by: Genetic Analysis Software | nlx_154473 | SCR_009288 | 2026-02-13 10:56:22 | 554 | |||||||||
|
MEGA2 Resource Report Resource Website 100+ mentions |
MEGA2 (RRID:SCR_009286) | MEGA2 | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application that uses as input a trio of files: 1) a LINKAGE-format locus file modified to contain locus name information; 2) a LINKAGE-format pedigree file; and 3) a map file. Mega2 then takes this trio of input files and, via a menu-driven interface, transforms them into various other file formats, thus greatly facilitating a variety of different analyses. In addition, for many of these options, it also sets up a C-shell script that then can automatically run these analyses (if you are using Mega2 in a Unix environment that supports C-shell scripts). (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix, (solaris, silicon graphics, osf1, macos x), linux, ms-windows, macos, (x) | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154471 | SCR_009286 | a Manipulation Environment for Genetic Analyses | 2026-02-13 10:56:22 | 114 | |||||||
|
MAPQTL Resource Report Resource Website 100+ mentions |
MAPQTL (RRID:SCR_009284) | MAPQTL | software resource, software application | Software application for mapping of quantitative trait loci (QTLs) for several types of mapping populations: BC1, F2, RILs, (doubled) haploids, full-sib family of outbreeders. Analyses: interval mapping, composite interval mapping, nonparametric mapping, automatic cofactor selection, permutation test for interval mapping. QTL charts. Everything available in an intuitive MS-Windows user interface. (entry from Genetic Analysis Software) | gene, genetic, genomic, ansi c, delphi, ms-windows, (95/98/me/nt4.0/2000) | is listed by: Genetic Analysis Software | nlx_154468 | SCR_009284 | Software for the calculation of QTL positions on genetic maps | 2026-02-13 10:56:22 | 392 | ||||||||
|
MAPMAKER/EXP Resource Report Resource Website 100+ mentions |
MAPMAKER/EXP (RRID:SCR_009281) | MAPMAKER/EXP | software resource, software application | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix, vms, ms-dos, macos | is listed by: Genetic Analysis Software | nlx_154462 | SCR_009281 | MMDRAWER | 2026-02-13 10:56:22 | 282 | ||||||||
|
MAPMAKER/HOMOZ Resource Report Resource Website 1+ mentions |
MAPMAKER/HOMOZ (RRID:SCR_009282) | MAPMAKER/HOMOZ | software resource, software application | Software application that calculates multipoint lod scores in pedigrees with inbreeding loops (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix | is listed by: Genetic Analysis Software | nlx_154463 | ftp://ftp-genome.wi.mit.edu/distribution/software/homoz | SCR_009282 | homozygosity mapping | 2026-02-13 10:56:22 | 1 | |||||||
|
HPLUS Resource Report Resource Website 10+ mentions |
HPLUS (RRID:SCR_009239) | HPLUS | software resource, software application | An analysis tool for performing haplotype estimation on genetic markers such as SNPs and microsatellites. It is able to handle datasets that include case-control status as well as covariates and marker location variables (such as gene name, chromosome location, etc). (entry from Genetic Analysis Software) | gene, genetic, genomic, ms-windows, linux | is listed by: Genetic Analysis Software | nlx_154400 | SCR_009239 | 2026-02-13 10:56:21 | 12 |
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.
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.
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.
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.
Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:
If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the facets that you can filter the data by.
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.