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

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

  • Keywords:gene (facet)

Facets


Recent searches

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

1,737 Results - per page

Show More Columns | Download Top 1000 Results

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
SEQUENCE LD/SEQUENCE LDHOT
 
Resource Report
Resource Website
SEQUENCE LD/SEQUENCE LDHOT (RRID:SCR_009379) software application, software resource Software program that analyzes sequence data. It obtains an approximation to the likelihood of a summary of the data (as such it can be thought of as a marginal likelihood approach). It does not use all the information in the data, but computationally it can be substantially more efficient than the full-likelihood methods (and hence able to analyze larger data sets). (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software nlx_154614 http://www.maths.lancs.ac.uk/~fearnhea/Software.html SCR_009379 2026-08-04 09:42:22 0
SDMINP
 
Resource Report
Resource Website
SDMINP (RRID:SCR_009377) SDMINP software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 24,2023. Software program for fast calculation of empirical and adjusted p-values for correlated and uncorrelated hypotheses in multiple testing experiments. It is based on the Free Step-Down Resampling Method for controlling the Family Wise Error Rate, originally proposed by Westfall and Young (1993), and implements a variation of the efficient algorithm of Ge et al. (2003), in which the originally necessary re-sampling effort was reduced considerably and the method made computationally more feasible. The program is independent of the underlying test statistic and works with provided observed and permutation test statistics. (entry from Genetic Analysis Software) gene, genetic, genomic, python 2.3.5, unix, linux, ms-windows is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154612 http://www.dkfz.de/SDMinP/ SCR_009377 Step-Down MIN P-value 2026-08-04 09:42:21 0
R/SNP.PLOTTER
 
Resource Report
Resource Website
1+ mentions
R/SNP.PLOTTER (RRID:SCR_009376) software application, software resource An R package that creates publishable-quality plots of p-values using single SNP and/or haplotype data. Main features of the package include options to display a linkage disequilibrium (LD) plot and the ability to plot multiple sets of results simultaneously. Plots can be created using global and/or individual haplotype p-values along with single SNP p-values. Images are created as either Portable Document Format (PDF) or Encapsulated (EPS) files. (entry from Genetic Analysis Software) gene, genetic, genomic, r is listed by: Genetic Analysis Software nlx_154599, SCR_009405, nlx_154649 https://github.com/cannin/snp_plotter http://cbdb.nimh.nih.gov/~kristin/snp.plotter.html SCR_009376 SNP.PLOTTER 2026-08-04 09:42:22 2
R/METASIM
 
Resource Report
Resource Website
1+ mentions
R/METASIM (RRID:SCR_009370) software application, software resource An R package that uses an individual-based approach to simulate distributions of genotypes that result from arbitrary within and among population demographies (including extinction/recolonization). These distributions can be used to test new or existing population-genetics summary statistics or develop null distributions under various demographies. (entry from Genetic Analysis Software) gene, genetic, genomic, r, c++, unix, ms-windows, macos is listed by: Genetic Analysis Software nlx_154592 http://linum.cofc.edu/software.html SCR_009370 METApopulation SIMulation 2026-08-04 09:42:22 1
ROSATTA SYLLEGO SYSTEM
 
Resource Report
Resource Website
ROSATTA SYLLEGO SYSTEM (RRID:SCR_009363) Syllego system software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on August 2, 2014. A genetic data management and analysis system designed to advance your whole genome association, linkage, and eQTL studies, providing you with an easy-to-use project workspace so that you can organize, analyze, and share your genotype and phenotype data along with your analysis results. With the Syllego system, generating high quality analysis data and meaningful results becomes simple. The Syllego system automates all tedious data management and data formatting tasks so that you can streamline your genetic analysis workflows using your analysis methods of choice. Managing all your genetic data and reference information is straightforward. The Syllego system converts public and private genotype data sets and reference annotations, such as dbSNP and HapMap, as well as individual (sample) information into a single, consistent repository for fast, convenient access. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154578 SCR_009363 2026-08-04 09:42:22 0
ROMPREV
 
Resource Report
Resource Website
ROMPREV (RRID:SCR_009361) ROMPREV software application, software resource Software tool for testing for association between polymorphisms and quantitative traits, as well as estimating trait heritability and locus-specific heritability using family data. (entry from Genetic Analysis Software) gene, genetic, genomic, r, any with r installation, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
nlx_154577, biotools:romprev https://bio.tools/romprev SCR_009361 Regression of Offspring on Mid-Parent (REVised) 2026-08-04 09:42:21 0
PASS PEDIGREE
 
Resource Report
Resource Website
PASS PEDIGREE (RRID:SCR_009315) PASS PEDIGREE software application, software resource Software application to draw the most complex family trees in a matter of minutes instead of hours of work. The basis of this is an algorithm for automatically builing a family tree. Of course, manual adjustments in the family tree can be made for your specific requirements. PASS Pedigree meets all international conventions concerning the drawing of pedigrees. A converter can convert historical Cyrillic pedigrees automatically to PASS Pedigree. Unlike before, all your family trees are stored in one single database. PASS Pedigree can intelligently connect to many genetic centers (e.g. three genetic centers in the Netherlands) with the existing patient information, via the lab system HELIX based on HL7 techniques. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software nlx_154509 SCR_009315 2026-08-04 09:42:21 0
OSIRIS
 
Resource Report
Resource Website
100+ mentions
OSIRIS (RRID:SCR_009313) OSIRIS software application, software resource Software tool for the retrieval of articles from MEDLINE related to the sequence variants reported for a human gene. The variations considered are single nucleotide polymorphisms (SNPs), insertion/deletion polymorphisms (indel), microsatellite, and named variations (e.g. Alu sequences). (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_154505 SCR_009313 2026-08-04 09:42:21 218
P ACT
 
Resource Report
Resource Website
1+ mentions
P ACT (RRID:SCR_009314) P_ACT software application, software resource An R program that adjusts sets of up to 1000 p-values from association tests between correlated traits and SNPs for multiple testing, accounting for the correlation between tests. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software nlx_154506 SCR_009314 P-values: Adjustment for Correlated Tests 2026-08-04 09:42:20 4
MARGARITA
 
Resource Report
Resource Website
1+ mentions
MARGARITA (RRID:SCR_009279) MARGARITA software application, software resource Software application that infers genealogies from population genotype data and uses these to map disease loci. These genealogies take the form of the Ancestral Recombination Graph (ARG). The ARG defines a genealogical tree for each locus, and as one moves along the chromosome the topologies of consecutive trees shift according to the impact of historical recombination events. (entry from Genetic Analysis Software) gene, genetic, genomic, java is listed by: Genetic Analysis Software nlx_154460 SCR_009279 2026-08-04 09:42:21 2
MAPINSPECT
 
Resource Report
Resource Website
100+ mentions
MAPINSPECT (RRID:SCR_009277) MAPINSPECT software application, software resource Software application that can be used to compare linkage maps obtained from different sources/populations/etc.. It will draw the linkage maps and look for common marker names, these are then connected in the drawing with dashed lines. All neighboring maps are compared in this way. Images can be printed and saved. Orders of the MAPs (ie which map is compared with which other map) can be changed and maps can be flipped (right mouse button). remark: MapComp bears close relationships with the GGT software package (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic, delphi pascal, ms-window (32-bit) is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154458 SCR_009277 GGT 2026-08-04 09:42:20 324
NOCOM
 
Resource Report
Resource Website
1+ mentions
NOCOM (RRID:SCR_009310) NOCOM software application, software resource Software application to estimate parameters for mixture of normal distributions (entry from Genetic Analysis Software) gene, genetic, genomic, fortran, ms-dos, os2 is listed by: Genetic Analysis Software nlx_154500 SCR_009310 2026-08-04 09:42:20 8
MAPDISTO
 
Resource Report
Resource Website
100+ mentions
MAPDISTO (RRID:SCR_009275) MAPDISTO software application, software resource Software program for mapping genetic markers in experimental segregating populations like backcross, doubled haploids, single-seed descent. Its specificity is to propose recombination fraction estimates in case of segregation distortion. It can (1) compute and draw genetic maps easily and quickly through a graphical interface; (2) facilitate the analysis of marker data showing segregation distortion due to differential viability of gametes or zygotes. (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic, ms-excel is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154456 SCR_009275 2026-08-04 09:42:20 115
MAP/MAP+/MAP+H/MAP2000
 
Resource Report
Resource Website
MAP/MAP+/MAP+H/MAP2000 (RRID:SCR_009272) MAP/MAP+/MAP+H/MAP2000 software application, software resource Software application for multiple pairwise linkage analysis under interference (entry from Genetic Analysis Software) gene, genetic, genomic, fortran, unix, sunos is listed by: Genetic Analysis Software nlx_154453 SCR_009272 (MAP+H is the radiation Hybrid module of MAP+) 2026-08-04 09:42:20 0
MANTEL-STRUCT
 
Resource Report
Resource Website
1+ mentions
MANTEL-STRUCT (RRID:SCR_009271) MANTEL-STRUCT software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application that tests for population structure through the use of Mantel tests (entry from Genetic Analysis Software) gene, genetic, genomic, ms-windows is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154451 SCR_009271 2026-08-04 09:42:20 4
MULTISIM
 
Resource Report
Resource Website
10+ mentions
MULTISIM (RRID:SCR_009308) MULTISIM software application, software resource Software application to analyze the numbers of individuals that founded new populations following a bottleneck or founding event (entry from Genetic Analysis Software) gene, genetic, genomic, ms-dos is listed by: Genetic Analysis Software nlx_154498 SCR_009308 2026-08-04 09:42:21 12
MALDSOFT
 
Resource Report
Resource Website
MALDSOFT (RRID:SCR_009269) MALDSOFT software application, software resource Software program for admixture mapping of complex trait loci, using case-control data. The samples should come from a recently-admixed population; additional ''learning'' samples from the parental populations are helpful. (entry from Genetic Analysis Software) gene, genetic, genomic, unix, linux, ms-windows, (dos/window...) is listed by: Genetic Analysis Software nlx_154449 SCR_009269 2026-08-04 09:42:20 0
SAGE
 
Resource Report
Resource Website
1000+ mentions
SAGE (RRID:SCR_009302) SAGE software application, software resource Software application that provides researchers with the tools necessary for various types of statistical genetic analysis of human family data. (entry from Genetic Analysis Software) gene, genetic, genomic, c, version 4.0 will be in c++, unix, (dec unix/solaris), ms-windows, (95/nt), linux is listed by: Genetic Analysis Software
is listed by: SoftCite
nlx_154606 SCR_009302 Statistical Analysis for Genetic Epidemiology 2026-08-04 09:42:21 1029
PEDMANAGER
 
Resource Report
Resource Website
PEDMANAGER (RRID:SCR_009300) PEDMANAGER software application, software resource Software application (entry from Genetic Analysis Software) gene, genetic, genomic, c, unix is listed by: Genetic Analysis Software nlx_154491 SCR_009300 2026-08-04 09:42:20 0
SIBERROR
 
Resource Report
Resource Website
SIBERROR (RRID:SCR_009380) software application, software resource Software application that identifies pedigree errors in sibship data. Examples include half siblings, unrelated individuals, identical twins, and parental exclusions. The test statistic is based on the summation of the number of alleles shared by a pair of relatives for a large number of markers and the number of alleles and allele frequencies for those markers. (entry from Genetic Analysis Software) gene, genetic, genomic, c, unix is listed by: Genetic Analysis Software nlx_154615 SCR_009380 SibError 2026-08-04 09:42:21 0

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. RRID Portal Resources

    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.

  2. Navigation

    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.

  3. Logging in and Registering

    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.

  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 RRID 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.