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.
http://mga.bionet.nsc.ru/soft/index.html
Software application that allows drawing pedigrees with a difficult structure, those containing consanguinity loops, and those individuals with multiple mates or several related families (entry from Genetic Analysis Software)
Proper citation: PEDIGREEQUERY (RRID:SCR_009041) Copy
http://genapha.icapture.ubc.ca/PathTutorial/
Web application to investigate gene-gene interactions in genetic association studies designed to: 1. Interface your SNP data with biological information from several online bioinformatics databases. 2. Generate biologically plausible hypotheses for testing gene-gene interactions. 3. Select a subset of SNPs and conduct SNP-SNP interaction tests. 4. Store analysis results. 5. Explore analysis results through interactive plots and summary tables. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.
Proper citation: PATH (RRID:SCR_009042) Copy
https://varscan.sourceforge.net/
Platform-independent, technology-independent software tool for identifying SNPs and indels in massively parallel sequencing of individual and pooled samples. Given data for a single sample, VarScan identifies and filters germline variants based on read counts, base quality, and allele frequency. Given data for a tumor-normal pair, VarScan also determines the somatic status of each variant (Germline, Somatic, or LOH) by comparing read counts between samples. (entry from Genetic Analysis Software).
Proper citation: VarScan (RRID:SCR_006849) Copy
The record is no longer available at this source.
Software application that is part of the LINKAGE auxiliary programs (entry from Genetic Analysis Software)
Proper citation: LSP (RRID:SCR_007059) Copy
http://watson.hgen.pitt.edu/register/soft_doc.html
Software application that is a faster version of SLINK (entry from Genetic Analysis Software)
Proper citation: FASTSLINK (RRID:SCR_008664) Copy
http://bios.ugr.es/~mabad/rTDT/index.html
Software application (entry from Genetic Analysis Software)
Proper citation: RTDT (RRID:SCR_007336) Copy
http://www.hpcf.upr.edu/~humberto/software/TkMap/
Software program for drawing genetic maps (entry from Genetic Analysis Software)
Proper citation: TKMAP (RRID:SCR_007457) Copy
https://github.com/gaow/genetic-analysis-software/blob/master/pages/GENEPI.JAR.md
A set of Java programs for genetic epidemiology analysis (entry from Genetic Analysis Software)
Proper citation: GENEPI.JAR (RRID:SCR_008782) Copy
http://bioinformatics.ust.hk/SNPHarvester.html
Software tool for detecting epistatic interactions in genome-wide association studies (entry from Genetic Analysis Software)
Proper citation: SNPHARVESTER (RRID:SCR_008536) Copy
http://www.simedic.com.ar/bdgen.htm
Powerful database software with improvement tools for paternity testing, database searching (like CODIS) and NRC II recommendations based formulae for investigating likelyhood ratios in putative contributors to crime evidences. Additional genetic population parameters estimations are added in this version. Only spanish version available. (entry from Genetic Analysis Software)
Proper citation: BDGEN (RRID:SCR_008811) Copy
https://www.ncbi.nlm.nih.gov/CBBresearch/Schaffer/fastlink.html
FASTLINK is significantly modified and improved version of main programs of LINKAGE that runs much faster sequentially, can run in parallel, allows the user to recover gracefully from a computer crash, and provides abundant new documentation.
Proper citation: FASTLINK (RRID:SCR_007042) Copy
https://www.unil.ch/dee/en/home/menuinst/softwares--dataset/softwares/easypop.html
Software application allowing to simulate population genetics datasets. It allows generating genetic data for haploid, diploid, and haplodiploid organisms under a variety of mating systems. It includes various migration and mutation models. Output can be generated for the FSTAT, GENEPOP, and ARLEQUIN genetic analysis packages. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.
Proper citation: EASYPOP (RRID:SCR_008961) Copy
http://www.inra.fr/mia/T/CarthaGene/
A genetic/radiation hybrid mapping software that looks for multiple populations maximum likelihood consensus maps using a fast EM algorithm for maximum likelihood estimation and powerful ordering algorithms inspired from TSP (Traveling Salesman Problem) technology. It can handle large data sets made up of different populations (either F2 backcross, recombinant inbred lines, F2 intercross, phase known outbreds, haploid/diploid radiation hybrids). It can also exploit existing syntenic relationships between the organism mapped and a reference (sequenced) organism for accurate dense RH mapping. (entry from Genetic Analysis Software)
Proper citation: CARTHAGENE (RRID:SCR_009013) Copy
http://www.sph.umich.edu/csg/abecasis/Exact/index.html
Software application for a fast exact Hardy-Weinberg Equilibrium test for SNPs (entry from Genetic Analysis Software)
Proper citation: SNP-HWE (RRID:SCR_008555) Copy
http://mga.bionet.nsc.ru/soft/pedpeel/
Software program that prepares pedigree data for calculation of Elston-Stewarts'' likelihood function. It finds an optimal way to peel a pedigree and returns text file containing 7 description arrays (entry from Genetic Analysis Software)
Proper citation: PEDPEEL (RRID:SCR_008436) Copy
http://www.sph.umich.edu/csg/liang/genome/
Software application to simulate sequences drawn from a population under the Wright-Fisher neutral model. The purpose of this program is to simulate sequences on the whole genome scale within practical time. (entry from Genetic Analysis Software)
Proper citation: GENOME (RRID:SCR_008949) Copy
http://www.stat.cmu.edu/~roeder/=ettdt/
Software application (entry from Genetic Analysis Software)
Proper citation: ET-TDT (RRID:SCR_007657) Copy
http://www.cs.cmu.edu/~genome/FAST-MAP.html
Fluorescent allele-calling software toolkit: a computer software for fully automated microsatellite genotyping. (entry from Genetic Analysis Software)
Proper citation: FASTMAP (1) (RRID:SCR_008346) Copy
http://www-rcf.usc.edu/~stram/tagSNPs.html
Software application (entry from Genetic Analysis Software)
Proper citation: TAGSNP (RRID:SCR_008623) Copy
http://www.people.fas.harvard.edu/~junliu/BEAM/
Software application that treats the disease-associated markers and their interactions via a bayesian partitioning model and computes, via Markov chain Monte Carlo, the posterior probability that each marker set is associated with the disease. (entry from Genetic Analysis Software)
Proper citation: BEAM (RRID:SCR_007258) 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.