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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 | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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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 | SciCrunch Registry | 2026-10-24 12:51:34 | 0 | |||||||||
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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 | SciCrunch Registry | 2026-10-24 12:51:32 | 12 | |||||||||
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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 | SciCrunch Registry | Bayesian Analysis of Multilocus Association | 2026-10-24 12:51:32 | 98 | |||||||
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SNPHARVESTER Resource Report Resource Website 1+ mentions |
SNPHARVESTER (RRID:SCR_008536) | SNPHARVESTER | software application, software resource | Software tool for detecting epistatic interactions in genome-wide association studies (entry from Genetic Analysis Software) | gene, genetic, genomic, java | is listed by: Genetic Analysis Software | nlx_154643 | SCR_008536 | SciCrunch Registry | 2026-10-24 12:51:32 | 6 | |||||||||
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BDGEN Resource Report Resource Website 1+ mentions |
BDGEN (RRID:SCR_008811) | BDGEN | software application, software resource | 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) | gene, genetic, genomic, ms-windows | is listed by: Genetic Analysis Software | nlx_154237 | SCR_008811 | SciCrunch Registry | 2026-10-24 12:51:30 | 1 | |||||||||
|
HELIXTREE Resource Report Resource Website 10+ mentions |
HELIXTREE (RRID:SCR_009067) | HELIXTREE | software application, software resource | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. | gene, genetic, genomic, c++, ms-windows, linux, macos x | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154059 | http://www.goldenhelix.com/SNP_Variation/HelixTree | SCR_009067 | SciCrunch Registry | HelixTree Genetic Association Software | 2026-10-24 12:51:32 | 24 | ||||||
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SVCC Resource Report Resource Website 1+ mentions |
SVCC (RRID:SCR_009068) | SVCC | software application, software resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented September 29, 2016. | gene, genetic, genomic, linux | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154060 | http://www.bios.unc.edu/~lin/software/SVCC/ | SCR_009068 | SciCrunch Registry | Semiparametric Variance-Component for Censored data | 2026-10-24 12:51:32 | 3 | ||||||
|
GENECLASS Resource Report Resource Website 50+ mentions |
GENECLASS (RRID:SCR_009065) | GENECLASS | software application, software resource | Software application employing multilocus genotypes to select or exclude populations as origins of individuals (Assignment and Migrants Detection). (entry from Genetic Analysis Software) | gene, genetic, genomic, delphi, ms-windos, unix | is listed by: Genetic Analysis Software | nlx_154053 | SCR_009065 | SciCrunch Registry | 2026-10-24 12:51:34 | 88 | |||||||||
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CHIP2SPELL Resource Report Resource Website 1+ mentions |
CHIP2SPELL (RRID:SCR_009060) | CHIP2SPELL | software application, software resource | Software application that aims to speed up the preparation of linkage data files passed on to the Alohomora software for data from the Affymetrix or Illumina assays. Chip2Spell gathers the information necessary to supplement the genotype data (such as the genetic map of the markers and the population-specific allele frequencies) from publicly available annoation files from Affymetrix and Illumina. The program formats the genotype data for input into the Alohomora program. (entry from Genetic Analysis Software) | gene, genetic, genomic, perl, linux, ms-windows | is listed by: Genetic Analysis Software | nlx_154045 | SCR_009060 | SciCrunch Registry | 2026-10-24 12:51:31 | 1 | |||||||||
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EASYPOP Resource Report Resource Website 10+ mentions |
EASYPOP (RRID:SCR_008961) | EASYPOP | software application, software resource | 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. | gene, genetic, genomic, ms-windows, (95/98/nt/2000/xp), macos, (x) | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154012 | http://www.unil.ch/dee/page36926_fr.html | SCR_008961 | SciCrunch Registry | 2026-10-24 12:51:30 | 16 | |||||||
|
CARTHAGENE Resource Report Resource Website 10+ mentions |
CARTHAGENE (RRID:SCR_009013) | CARTHAGENE | software application, software resource | 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) | gene, genetic, genomic, c++, tcl/tk, ms-windows, unix, solaris, linux, sources are available for other operating systems (gpl/qpl). | is listed by: Genetic Analysis Software | nlx_154008 | SCR_009013 | SciCrunch Registry | 2026-10-24 12:51:31 | 42 | |||||||||
|
SNP-HWE Resource Report Resource Website 1+ mentions |
SNP-HWE (RRID:SCR_008555) | SNP-HWE | software application, software resource | Software application for a fast exact Hardy-Weinberg Equilibrium test for SNPs (entry from Genetic Analysis Software) | gene, genetic, genomic, fortran, c, c++, r | is listed by: Genetic Analysis Software | nlx_154645 | SCR_008555 | SciCrunch Registry | 2026-10-24 12:51:30 | 4 | |||||||||
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PEDPEEL Resource Report Resource Website |
PEDPEEL (RRID:SCR_008436) | PEDPEEL | software application, software resource | 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) | gene, genetic, genomic, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
nlx_154524, biotools:pedpeel | https://bio.tools/pedpeel | SCR_008436 | SciCrunch Registry | 2026-10-24 12:51:29 | 0 | ||||||||
|
GENOME Resource Report Resource Website 50+ mentions |
GENOME (RRID:SCR_008949) | GENOME | software application, software resource | 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) | gene, genetic, genomic, c++, unix, solaris, linux, ms-windows | is listed by: Genetic Analysis Software | nlx_154347 | SCR_008949 | SciCrunch Registry | 2026-10-24 12:51:33 | 63 | |||||||||
|
FASTMAP (1) Resource Report Resource Website |
FASTMAP (1) (RRID:SCR_008346) | FASTMAP (1) | software application, software resource, software toolkit | Fluorescent allele-calling software toolkit: a computer software for fully automated microsatellite genotyping. (entry from Genetic Analysis Software) | gene, genetic, genomic, unix, macos, matlab, programming environment is required. | is listed by: Genetic Analysis Software | nlx_154310 | SCR_008346 | SciCrunch Registry | Fluorescent Allele-calling Software Toolkit: Microsatellite Automation Package | 2026-10-24 12:51:30 | 0 | ||||||||
|
TAGSNP Resource Report Resource Website 50+ mentions |
TAGSNP (RRID:SCR_008623) | TAGSNP | software application, software resource | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic, fortran90 | is listed by: Genetic Analysis Software | nlx_154671 | SCR_008623 | SciCrunch Registry | 2026-10-24 12:51:30 | 71 | |||||||||
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2DMAP Resource Report Resource Website |
2DMAP (RRID:SCR_009036) | 2DMAP | software application, software resource | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application for constructing 2-d crossover-based map. | gene, genetic, genomic, ms-dos | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154001 | SCR_009036 | SciCrunch Registry | 2026-10-24 12:51:33 | 0 | ||||||||
|
ADMIXMAP Resource Report Resource Website 10+ mentions |
ADMIXMAP (RRID:SCR_009035) | ADMIXMAP | software application, software resource | General-purpose program for modelling admixture, using marker genotypes and trait data on a sample of individuals from an admixed population (such as African-Americans), where the markers have been chosen to have extreme differentials in allele frequencies between two or more of the ancestral populations between which admixture has occurred. The main difference between ADMIXMAP and classical programs for estimation of admixture such as ADMIX is that ADMIXMAP is based on a multilevel model for the distribution of individual admixture in the population and the stochastic variation of ancestry on hybrid chromosomes. This makes it possible to model the associations of ancestry between linked marker loci, and the association of a trait with individual admixture or with ancestry at a linked marker locus. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, linux, ms-windows, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
biotools:admixmap, nlx_153999 | https://bio.tools/admixmap | SCR_009035 | SciCrunch Registry | Admixture mapping | 2026-10-24 12:51:31 | 20 | |||||||
|
FINETTI Resource Report Resource Website 100+ mentions |
FINETTI (RRID:SCR_009179) | FINETTI | software application, software resource | Software application that tests for deviation from Hardy-Weinberg equilibrium and tests for association in case controls studies; Plot genotype frequencies graphically using a de Finetti diagram. (entry from Genetic Analysis Software) | gene, genetic, genomic, pascal, (web implementation: perl, c, php), web-based, ms-dos, ms-windows, (32), linux, (for stand-alone version) | is listed by: Genetic Analysis Software | nlx_154316 | SCR_009179 | SciCrunch Registry | de FINETTI generator | 2026-10-24 12:51:37 | 299 | ||||||||
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FBAT Resource Report Resource Website 50+ mentions |
FBAT (RRID:SCR_009178) | FBAT | software application, software resource | Software application that allows the user to test for association/linkage between disease phenotypes and haplotypes by utilizing family-based controls. The method extends the approach for testing described in Rabinowitz and Laird (2000) to handle multiple tightly linked markers. It is robust to population admixture, yet efficient in the sense that it utilizes data from families where phase cannot be completely resolved in all individuals by using weights, which are estimated from the sample. However, the method remains robust to population stratification and population admixture. The method can handle any type of phenotype, including multiple phenotypes and missing parents, marker data, and/or phase, and provides both bi-allelic and multi-allelic tests. PowerFBAT is a tool for power simulation of association analysis using FBAT with binary outcomes. XWXW is an extension to the Haseman-Elston method for non-parametric linkage test with quantitative traits. XDT is a software that performs classical TDT, SDT and Rabinowitz TDT for nuclear families (not supported anymore). (entry from Genetic Analysis Software) | gene, genetic, genomic, unix, solaris, linux, ms-windows, mac, macos x, darwin | is listed by: Genetic Analysis Software | nlx_154315 | SCR_009178 | SciCrunch Registry | (haplotype) Family Based Association Test PBAT | 2026-10-24 12:51:34 | 82 |
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