Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Resources:genetic analysis software (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

585 Results - per page

Show More Columns | Download 585 Result(s)

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
EMLD
 
Resource Report
Resource Website
1+ mentions
EMLD (RRID:SCR_009171) EMLD software resource, software application Software application to calculate pair-wise linkage disequilibrium based on SNP genotype data from unrelated individuals. EM algorithm is used to estimate pair-wise haplotype frequencies. The output file is in the format of input file for GOLD program, thus it can be directly plug into GOLD to get LD plots. (entry from Genetic Analysis Software) gene, genetic, genomic, java, unix, ms-windows is listed by: Genetic Analysis Software nlx_154298 http://epi.mdanderson.org/~qhuang/Software/pub.htm SCR_009171 EM estimation of haplotype frequencies and LD calculation 2026-02-14 02:07:00 4
EPDT
 
Resource Report
Resource Website
1+ mentions
EPDT (RRID:SCR_009172) EPDT software resource, software application THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application that for detecting linkage/disequilibrium signals # between genetic markers and disease loci, particularly if only one # or a few large pedigrees are available. The strategy differs from # conventional approaches that require at least a moderate number of # families to attain adequate statistical power. The proposed testing # procedure is advantageous in that it provides high statistical power # coupled with reduced sample collection. Furthermore, the proposed # method avoids problems such as potential population stratification # and genetic heterogeneity, and is robust with respect to misspecification # of phenotype. (entry from Genetic Analysis Software) gene, genetic, genomic, unix is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154301 SCR_009172 Extended Pedigree Disequilibrium Test 2026-02-14 02:07:14 1
EH
 
Resource Report
Resource Website
EH (RRID:SCR_009168) EH software resource, software application Software application (entry from Genetic Analysis Software) gene, genetic, genomic, pascal, ms-dos, unix is listed by: Genetic Analysis Software nlx_154291 SCR_009168 FASTEHPLUS, EHP, Estimating Haplotype-frequencies EHPLUS 2026-02-14 02:07:14 0
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
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

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.

Can't find the RRID you're searching for? X
X
  1. SPARC Anatomical Working Group Resources

    Welcome to the SPARC SAWG Resources search. From here you can search through a compilation of resources used by SPARC SAWG and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that SPARC SAWG 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.

  3. Logging in and Registering

    If you have an account on SPARC SAWG then you can log in from here to get additional features in SPARC SAWG such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into SPARC SAWG you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    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.