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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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EAGLET Resource Report Resource Website 1+ mentions |
EAGLET (RRID:SCR_009166) | EAGLET | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software package that provides a number of improved statistics for detecting linkage and estimating trait location. EAGLET uses multiple subsamples of dense SNP data to detect linkage with increased power, and to construct sharp 95% confidence intervals for the true trait location. | gene, genetic, genomic, perl, c, linux, macos | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154288 | SCR_009166 | Efficient Analysis of Genetic Linkage: Testing and Estimation | 2026-02-14 02:07:08 | 1 | |||||||
|
EASYLINKAGE/EASYLINKAGE-PLUS Resource Report Resource Website 1+ mentions |
EASYLINKAGE/EASYLINKAGE-PLUS (RRID:SCR_009167) | EASYLINKAGE/EASYLINKAGE-PLUS | software resource, software application | Software application that combines automated setup and performance of linkage analyses and simulation. The program package supports currently single-point linkage analyses, multi-point linkage analyses, and the simulation package SLink, and provides genome-wide as well as chromosomal postscript plots of LOD scores, NPL scores, P values, and other parameters. The software can analyze STRPs as well as SNP chip data from Affymetrix, Illumina, or self-defined SNP data. The program performs single- and multi-point simulation studies. | gene, genetic, genomic, perl, v5.8 (program can be provided as perl script or as a compiled exe for the use in windows), ms-windows, (2000/xp), linux | is listed by: Genetic Analysis Software | nlx_154289 | https://omictools.com/easylinkage-tool | http://compbio.charite.de/genetik/hoffmann/easyLINKAGE/ | SCR_009167 | 2026-02-14 02:07:00 | 5 | |||||||
|
DPPH Resource Report Resource Website 1000+ mentions |
DPPH (RRID:SCR_009164) | DPPH | software resource, software application | Software application that is similar to the BPPH program (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic, linux, macos | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154287 | SCR_009164 | Direct method for Perfect Phylogeney Haplotyping | 2026-02-14 02:07:14 | 1148 | |||||||
|
GREGOR Resource Report Resource Website 10+ mentions |
GREGOR (RRID:SCR_009165) | GREGOR | software resource, software application | Software program that allows students and scientists to explore potential manifestations of genetic models and stochastic processes. It also provides a means to evaluate the effectiveness of statistical procedures such as linkage analysis or QTL detection. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic, ms-dos | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154364 | http://gnome.agrenv.mcgill.ca/tinker/gregor.htm | SCR_009165 | 2026-02-14 02:06:46 | 47 | |||||||
|
MAKEPED Resource Report Resource Website 1+ mentions |
MAKEPED (RRID:SCR_009162) | MAKEPED | software resource, software application | Software application - part of the LINKAGE auxiliary programs (entry from Genetic Analysis Software) | gene, genetic, genomic, c and pascal, unix, vms, ms-dos, os2 | is listed by: Genetic Analysis Software | nlx_154285 | SCR_009162 | MAKE PEDfiles | 2026-02-14 02:07:08 | 1 | ||||||||
|
DOLINK Resource Report Resource Website |
DOLINK (RRID:SCR_009163) | DOLINK | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application that manage genetic data (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, ms-dos, ms-windows | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154286 | SCR_009163 | WDLINK | 2026-02-14 02:07:00 | 0 | |||||||
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DISENTANGLER Resource Report Resource Website 1+ mentions |
DISENTANGLER (RRID:SCR_009161) | DISENTANGLER | software resource, software application | Software application that is a visualization technique for linkage disequilibrium mapping and haplotype analysis of multiple multi-allelic genetic markers. (entry from Genetic Analysis Software) | gene, genetic, genomic, java/jre1.5, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
nlx_154284, bIotools:disentangler | https://bio.tools/disentangler | SCR_009161 | 2026-02-14 02:06:46 | 4 | ||||||||
|
ALOHOMORA Resource Report Resource Website 1+ mentions |
ALOHOMORA (RRID:SCR_009117) | ALOHOMORA | software resource, software application | Software application designed to facilitate genome-wide linkage studies performed with high-density single nucleotide polymorphism (SNP) marker panels such as the Affymetrix GeneChip(R) Human Mapping 10K Array. (entry from Genetic Analysis Software) | gene, genetic, genomic, perl, ms-window, linux, unix, solaris, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
nlx_154219, biotools:alohomora | https://bio.tools/alohomora | SCR_009117 | 2026-02-14 02:06:45 | 8 | ||||||||
|
ALP Resource Report Resource Website |
ALP (RRID:SCR_009118) | ALP | software resource, software application | Microsoft Windows application designed to analyze microsatellite DNA fragments separated on an Automated Laser Fluorescence sequencer. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, ms-windows, (3.1/95/nt) | is listed by: Genetic Analysis Software | nlx_154220 | SCR_009118 | Automated Linkage Preprocessor | 2026-02-14 02:07:07 | 0 | ||||||||
|
SIMULAPLOT Resource Report Resource Website |
SIMULAPLOT (RRID:SCR_009079) | SIMULAPLOT | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. A tool designed to help visualize the joint effect of genes and continuous environmental covariates on complex human disease simulation models. | gene, genetic, genomic, r | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154089 | http://www.chg.duke.edu/research/simlaplot.html | SCR_009079 | 2026-02-14 02:07:12 | 0 | |||||||
|
TUNA Resource Report Resource Website 1+ mentions |
TUNA (RRID:SCR_009112) | TUNA | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVICE, documented September 22, 2016. Free software package for estimating allele frequencies for all the SNPs available in a population reference panel (e.g. HapMap data base) based on genotype data from a subset of markers (e.g. the Illumina HumanHap300 BeadChip SNP set) in a group of subjects (e.g. the cases in a case-control sample)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic | is listed by: Genetic Analysis Software | PMID:18057020 | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154211 | SCR_009112 | Testing UNtyped Alleles | 2026-02-14 02:06:45 | 2 | ||||||
|
CASPAR Resource Report Resource Website 50+ mentions |
CASPAR (RRID:SCR_009074) | CASPAR | software resource, software application | Software application who''s main novel feature is conditional linkage analyses, in which the population can be subdivided according to criteria at some loci and analyzed for linkage at other loci. CASPAR uses simulation to overcome the problems inherent in such multiple testing. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
biotools:caspar, nlx_154071 | https://bio.tools/caspar | SCR_009074 | Computerized Affected Sibling Pair Analyzer and Reporter | 2026-02-14 02:07:12 | 52 | |||||||
|
WEBQTL Resource Report Resource Website 10+ mentions |
WEBQTL (RRID:SCR_009072) | WEBQTL | software resource, software application | An interactive web site useful for exploring the genetic modulation of thousands of phenotypes gathered over a 30-year period by hundreds of investigators using reference panels of recombinant inbred strains of mice. WebQTL includes dense error-checked genetic maps, as well as extensive gene expression data sets (Affymetrix) acquired across more than 35 strains of mice. WebQTL accepts user-entered traits for BXD, AXB/BXA, CXB, BXH, AKXD recombinant inbred strains. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, and, python, all via internet | is listed by: Genetic Analysis Software | nlx_154066 | http://www.webqtl.org/search.html | SCR_009072 | 2026-02-14 02:07:07 | 46 | ||||||||
|
genehunter-imprinting Resource Report Resource Website 1+ mentions |
genehunter-imprinting (RRID:SCR_009104) | GENEHUNTER-TWOLOCUS | software resource, software application | Resource no longer in service. Documented on February 23,2021.Software tool as modification of GENEHUNTER software package . Allows for parametric multi-marker linkage analysis of dichotomous traits caused by imprinted genes. By specification of two heterozygote penetrance parameters, paternal and maternal origin of the disease allele can be treated differently in terms of probability of expression of the trait. | gene, genetic, genomic, c, unix, sunos, solaris, osf, hpux, aix, ultrix, linux, ms-windows, bio.tools |
is listed by: Genetic Analysis Software is listed by: Debian is listed by: bio.tools |
DOI:10.1086/302911 | Resource no longer in service. Documented on February 23,2021 | nlx_154199, biotools:genehunter-imprinting | https://bio.tools/genehunter-imprinting | http://www.staff.uni-marburg.de/~strauchk/software.html | SCR_009104 | GENEHUNTER-MODSCORE, GENEHUNTER-PLUS, GENEHUNTER, GENEHUNTER-IMPRINTING | 2026-02-14 02:07:13 | 1 | ||||
|
GENEHUNTER-MODSCORE Resource Report Resource Website 1+ mentions |
GENEHUNTER-MODSCORE (RRID:SCR_009069) | GENEHUNTER-MODSCORE | software resource, software application | Software application that is an extension of GENEHUNTER-IMPRINTING, based on the original GENEHUNTER version 2.1 release 6, that allows for a MOD-score analysis, in which parametric LOD scores are maximized over the parameters of the trait model, i.e., the penetrances and disease allele frequency. As of version 2.0, it is possible to use sex-specific recombination frequencies. The genetic positions of markers can be automatically read from a publicly available genetic map. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix, sunos, solaris, osf, hpux, aix, ultrix, linux, ms-windows | is listed by: Genetic Analysis Software | nlx_154061 | http://www.staff.uni-marburg.de/~strauchk/software.html | SCR_009069 | 2026-02-14 02:06:57 | 1 | ||||||||
|
BQTL Resource Report Resource Website 1+ mentions |
BQTL (RRID:SCR_009137) | BQTL | software resource, software application | Software application for the mapping of genetic traits from line crosses and recombinant inbred lines. It performs (1) maximum likelihood estimation of multi-gene models; (2) Bayesian estimation of multi-gene models via Laplace Approximations; and (3) interval mapping and composite interval mapping of genetic loci (entry from Genetic Analysis Software) | gene, genetic, genomic, s, c, fortran, the software is engineered to work in conjunction with r., unix, ms-windows, macos | is listed by: Genetic Analysis Software | nlx_154252 | http://hacuna.ucsd.edu/bqtl/ | SCR_009137 | Bayesian Quantitative Trait Locus mapping | 2026-02-14 02:07:14 | 1 | |||||||
|
DNABASER Resource Report Resource Website 10+ mentions |
DNABASER (RRID:SCR_009138) | DNABASER | software resource, software application | Software tool for manual and automatic DNA sequence assembly, DNA sequence analysis, automatic sample processing, contig editing, metadata integration, file format conversion and mutation detection. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154256 | SCR_009138 | 2026-02-14 02:06:45 | 45 | ||||||||
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BPPH Resource Report Resource Website |
BPPH (RRID:SCR_009136) | BPPH | software resource, software application | Software application for inferring haplotypes from genotypes to determine if there are resulting haplotypes that fit a tree model (i.e. a perfect phylogeny, a coalescent). In population genetic terms, BPPH determines whether a set of SNP genotypes can be explained by haplotype pairs that could have evolved on a coalescent under the no-recombination, infinite sites model. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154251 | SCR_009136 | Berkeley method for Perfect Phylogeney Haplotyping | 2026-02-14 02:06:59 | 0 | ||||||||
|
BLOCK Resource Report Resource Website 100+ mentions |
BLOCK (RRID:SCR_009133) | BLOCK | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application that performs general pedigree analysis on a general pedigree with any number of loops. It also allows users to perform two-point linkage analysis on a general pedigree with an arbitrary number of alleles., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic, ms-dos, linux, unix, solaris, irix 64, aix 3.2.5, dec alpha | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154247 | SCR_009133 | Blocking Gibbs sampler for pedigree analysis | 2026-02-14 02:07:13 | 134 | |||||||
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QUTIE Resource Report Resource Website 1+ mentions |
QUTIE (RRID:SCR_009098) | QUTIE | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application for enabling the analysis of rare variants in large-scale case control and quantitative trait association studies. CCRaVAT (Case-Control Rare Variant Analysis Tool) and QuTie (Quantitative Trait) are software packages that enable efficient large-scale analysis of rare variants across specific regions or genome-wide. These programs implement a rare variant super-locus or collapsing method that investigates the accumulation of rare variant alleles in either a case-control or quantitative trait study design. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154191 | SCR_009098 | Case-Control RAre Variant Analysis Tool CCRAVAT | 2026-02-14 02:07:07 | 1 |
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