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.
Software application that is a graphic way of organizing the mass of information gathered during a family assessment and finding patterns in the family system (entry from Genetic Analysis Software)
Proper citation: GENOGRAM-MAKER (RRID:SCR_008751) Copy
Software application to reduce family members so the families can be used in GENEHUNTER program. FASTER eliminates the most redundant individuals according to the set of weights (preferences) (Age, Information about genetic Markers, etc.) The program has several features such as automatical reducement of branches without any affected individuals, etc. (entry from Genetic Analysis Software)
Proper citation: FASTER (RRID:SCR_009045) Copy
Software application that integrates a broad spectrum of data mining, statistical analysis, interactive visualization and modeling tools that allow QTL analysis based on advanced and sophisticated methods for maximum extraction of the mapping information from data. (entry from Genetic Analysis Software)
Proper citation: MULTIQTL (RRID:SCR_009043) Copy
http://galton.uchicago.edu/~mcpeek/software/spermseg
Software application for analysis of segregation in single-sperm data (entry from Genetic Analysis Software)
Proper citation: SPERMSEG (RRID:SCR_009044) Copy
http://cedar.genetics.soton.ac.uk/pub/PROGRAMS/ALLASS
Software application (entry from Genetic Analysis Software)
Proper citation: ALLASS (RRID:SCR_009040) Copy
http://cooke.gsf.de/wjst/download.cfm
Software application that allows pedigree entry and retrieval from an internet browser into a distant MS ACCESS database. Includes IP access restriction, automatic numbering of families and individuals and database consistency checks. (entry from Genetic Analysis Software)
Proper citation: PEDJAVA (RRID:SCR_008429) Copy
http://www.nhgri.nih.gov/DIR/IDRB/GASP/
Software tool for testing and investigating methods in statistical genetics by generating samples of family data based on user specified models. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.
Proper citation: GASP (RRID:SCR_008703) Copy
A set of programs for performing multipoint exclusion mapping of affected sibling pair data for discrete traits. (entry from Genetic Analysis Software)
Proper citation: ASPEX (RRID:SCR_008414) Copy
http://mlemire.freeshell.org/software.html
THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 12,2023. Software application with implementation of the Sad statistic, more robust to transmission ratio distortion in the context of allele sharing (entry from Genetic Analysis Software)
Proper citation: GENEHUNTER++SAD (RRID:SCR_008777) Copy
http://pbil.univ-lyon1.fr/software/mareymap/
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.
Proper citation: MAREYMAP (RRID:SCR_009066) Copy
http://associationviewer.vital-it.ch/
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)
Proper citation: ASSOCIATIONVIEWER (RRID:SCR_009063) Copy
https://github.com/gaow/genetic-analysis-software/blob/master/pages/WHICHRUN.md
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.
Proper citation: WHICHRUN (RRID:SCR_009064) Copy
http://www.mapmanager.org/mmQTX.html
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)
Proper citation: MAP MANAGER QTX (RRID:SCR_009061) Copy
https://github.com/gaow/genetic-analysis-software/blob/master/pages/G-MENDEL.md
Software tool for construction of genetic linkage maps and analyzing Mendelian phenotypes. (entry from Genetic Analysis Software)
Proper citation: G-MENDEL (RRID:SCR_009062) Copy
http://gaow.github.io/genetic-analysis-software/t-1.html#tlinkage
Software programs that are extensions of the LINKAGE programs that allow the disease phenotype to be under the control of disease two loci. (entry from Genetic Analysis Software)
Proper citation: TLINKAGE (RRID:SCR_008838) Copy
http://research.nhgri.nih.gov/software/TRAP/
Software tool for determining a regression model of quantitative or binary trait variation when the number of possible genetic predictors is very large, considering only a moderate number of predictors at one time, using unrelated or family data. (entry from Genetic Analysis Software)
Proper citation: TRAP (RRID:SCR_009002) Copy
https://github.com/gaow/genetic-analysis-software/blob/master/pages/2SNP.md
THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. An algorithm resource for scalable phasing method for trios and unrelated individuals.
Proper citation: 2SNP (RRID:SCR_009038) Copy
https://github.com/gaow/genetic-analysis-software/blob/master/pages/AGEINF.md
THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application used to infer the age of a rare, selectively-neutral mutation.
Proper citation: AGEINF (RRID:SCR_009039) Copy
http://www.stat.washington.edu/thompson/Genepi/Albert/albert.shtml
Software application that estimates genotype relative risks, genotyping error rates and population risk allele frequencies from marker genotype data in case-parent trios. ALBERT uses the distribution of trio marker genotypes to compute maximum likelihood estimates for the parameters. (entry from Genetic Analysis Software)
Proper citation: ALBERT (RRID:SCR_009037) Copy
http://www.epigenetic.org/Linkage/act.html,
Software application that contains the following modules: ibd, calculates the proportion of gene shared identical by decent for a nuclear family; ibdn, (modified program of ERPA), which implements a method for assessing increased-allele sharing between all pairs of affected relatives within a pedigree; multic, multivariate analysis for complex traits; ml, estimation of variance components using maximum likelihood; ql, estimation of variance components using quasi likelihood; relcov, generates first degree relationship coefficients for extended families; sim2s, the simulation program that was used to test ACT; cage, Cohort Analysis for Genetic Epidemiology; gh: GeneHunter, heavily modified to assist multipoint calculation using multic; TDT: TDT programs written in SAS; gcc and f77 compilers are necessary. Executable programs are included for compatible operating systems, i.e., Solaris2.6. (entry from Genetic Analysis Software)
Proper citation: ACT (RRID:SCR_009033) Copy
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:
You can save any searches you perform for quick access to later from here.
We recognized your search term and included synonyms and inferred terms along side your term to help get the data you are looking for.
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 sources that were queried against in your search that you can investigate further.
Here are the categories present within RRID that you can filter your data on
Here are the subcategories present within this category that you can filter your data on
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.