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 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
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 | 2026-02-07 02:14:25 | 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 | 2026-02-07 02:14:35 | 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 | 2026-02-07 02:14:26 | 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 | 2026-02-07 02:14:24 | 1 | ||||||||
|
BQTL Resource Report Resource Website |
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 | 2026-02-07 02:14:36 | 0 | |||||||
|
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 | 2026-02-07 02:14:28 | 45 | ||||||||
|
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 | 2026-02-07 02:14:28 | 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 | 2026-02-07 02:14:36 | 134 | |||||||
|
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 | 2026-02-07 02:14:26 | 1 | |||||||
|
BLADE Resource Report Resource Website 100+ mentions |
BLADE (RRID:SCR_009132) | BLADE | software resource, software application | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154246 | SCR_009132 | Bayesian LinkAge DisEquilibrium mapping | 2026-02-07 02:14:28 | 110 | ||||||||
|
STEPC Resource Report Resource Website |
STEPC (RRID:SCR_009096) | STEPC | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 6, 2016. Software application (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154114 | SCR_009096 | STatistical Explanation for Positional Cloning | 2026-02-07 02:14:26 | 0 | |||||||
|
RECORD Resource Report Resource Website 1000+ mentions |
RECORD (RRID:SCR_009097) | RECORD | software resource, software application | Software application that can be used for the ordering of loci on genetic linkage maps. The method is based on minimisation of the total number of recombination events. Since the criterion does not require intensive calculations, the algorithm rapidly produces an optimal ordering as well as a series of near-optimal ones. The latter provides insight into the local certainty of ordering along the map. RECORD can deal with the following types of mapping populations: BC1, F2, F3, RILs (in fact any generation obtained by repeated selfing of a hybrid between homozygous parents). Data files are .LOC JoinMap format. Mapping populations from non-inbreds should be split into BC1 or HAP data that represent the maternal and paternal gametes. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, ms-windows, (win98, xp) and ms-dos | is listed by: Genetic Analysis Software | nlx_154153 | SCR_009097 | REcombination Counting and ORDering | 2026-02-07 02:14:22 | 1289 | ||||||||
|
TDT-AE Resource Report Resource Website 1+ mentions |
TDT-AE (RRID:SCR_009094) | TDT-AE | software resource, software application | Software program that computes a likelihood-based transmission disequilibrium test. The data are genotypes on trios (father, mother, affected child) in which random genotyping errors leading to Mendelian inconsistencies may or may not have occurred. This program computes the TDT-AE statistic on all trios (whether Mendelianly consistent or not) and thereby maintains a correct type I error rate in the presence of random genotyping errors. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, ms-windows, (2000/dos), unix, (sun solaris), linux, (redhat) | is listed by: Genetic Analysis Software | PMID:11443542 | nlx_154112 | ftp://linkage.rockefeller.edu/software/tdtae2 | SCR_009094 | Transmission Disequilibrium Test Allowing for Errors | 2026-02-07 02:14:26 | 2 | ||||||
|
GENOMIZER Resource Report Resource Website 1+ mentions |
GENOMIZER (RRID:SCR_009127) | GENOMIZER | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 6, 2016. A platform independent Java program for the analysis of genome wide association experiments. (entry from Genetic Analysis Software). | gene, genetic, genomic, java, ms-windows, linux | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154349 | http://www.ikmb.uni-kiel.de/genomizer/ | SCR_009127 | 2026-02-07 02:14:23 | 3 | |||||||
|
GENEPOOL Resource Report Resource Website 10+ mentions |
GENEPOOL (RRID:SCR_009087) | GENEPOOL | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. Software application that provides analysis tools for the detection of shifts in relative allele frequency between pooled genomic DNA from cases and controls using SNP-based genotyping microarrays. GenePool supports genotyping platforms from Affymetrix and Illumina. | gene, genetic, genomic, c/c++/perl, linux, macos, (should compile on most unix systems with gcc) | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154104 | SCR_009087 | 2026-02-07 02:14:22 | 48 | ||||||||
|
ANALYZE Resource Report Resource Website 1000+ mentions |
ANALYZE (RRID:SCR_009120) | ANALYZE | software resource, software application | A set of useful accessory programs to the LINKAGE package. It simplifies the performance of a large array of parametric and nonparametric tests for linkage and association on data entered in LINKAGE format pedigree and parameter files. (entry from Genetic Analysis Software) | gene, genetic, genomic, pascal, unix, sunos, solaris, osf1 |
is listed by: Genetic Analysis Software is listed by: SoftCite |
nlx_154223 | SCR_009120 | 2026-02-07 02:14:27 | 1094 | |||||||||
|
EPISTACY Resource Report Resource Website 1+ mentions |
EPISTACY (RRID:SCR_009088) | EPISTACY | software resource, software application | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic, sas | is listed by: Genetic Analysis Software | nlx_154105 | SCR_009088 | 2026-02-07 02:14:26 | 1 | |||||||||
|
R/QTL Resource Report Resource Website 500+ mentions |
R/QTL (RRID:SCR_009085) | R/QTL | software resource, software application | Software program for mapping quantitative trait loci in experimental crosses. (entry from Genetic Analysis Software) | gene, genetic, genomic, c and r, unix, ms-windows, macos |
is listed by: Genetic Analysis Software is listed by: Debian is listed by: OMICtools |
DOI:10.1093/bioinformatics/btg112 | OMICS_07093, nlx_154097 | https://sources.debian.org/src/r-cran-qtl/ | SCR_009085 | 2026-02-07 02:14:35 | 976 | |||||||
|
QUANTO Resource Report Resource Website 500+ mentions |
QUANTO (RRID:SCR_009084) | QUANTO | software resource, software application | Software program that computes sample size or power for association studies of genes, environmental factors, gene-environment interaction, or gene-gene interaction. Available study designs for a disease (binary) outcome include the unmatched case-control, matched case-control, case-sibling, case-parent, and case-only designs. Study designs for a quantitative tra it include independent individuals and case parent designs. Quanto is a 32-bit Windows application requiring Windows 95, 98, NT, 2000, ME or XP to run. The graphical user interface allows th e user to easily change the model and view the results without having to edit an input file and rerun the program for every model. The results of a session are stored to a log file. This log can be printed or saved to a file for reviewing at a later date. An option is included to create a text file of the log that can be imported into other documents. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, ms-windows, (98/nt/2000/..) |
is listed by: Genetic Analysis Software is listed by: SoftCite |
nlx_154095 | SCR_009084 | 2026-02-07 02:14:25 | 908 | |||||||||
|
BOTTLENECK Resource Report Resource Website 100+ mentions |
BOTTLENECK (RRID:SCR_009082) | BOTTLENECK | software resource, software application | Software application for detecting recent effective population size reductions from allele data frequencies (entry from Genetic Analysis Software) | gene, genetic, genomic, ms-windows, (95) | is listed by: Genetic Analysis Software | nlx_154093 | SCR_009082 | 2026-02-07 02:14:25 | 470 |
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.