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

  • Keywords:genetic (facet)

Facets


Recent searches

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

795 Results - per page

Show More Columns | Download 795 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
EDAC
 
Resource Report
Resource Website
1+ mentions
EDAC (RRID:SCR_000829) EDAC software application, software resource THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016. gene, genetic, genomic is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154078 http://www.biostat.wustl.edu/~gc/cgi-bin/calcpwr.cgi SCR_000829 power calculator for Extremely Discordant And Concordant sibpairs 2026-02-15 09:17:59 2
2LD
 
Resource Report
Resource Website
2LD (RRID:SCR_000826) 2LD software application, software resource Software program for calculating linkage disequilibrium (LD) measures between two polymorphic markers. gene, genetic, genomic, c is listed by: Genetic Analysis Software PMID:14871868 THIS RESOURCE IS NO LONGER IN SERVICE nlx_154006 http://www.mrc-epid.cam.ac.uk/Personal/jinghua.zhao/software.htm SCR_000826 2026-02-15 09:17:59 0
SQTL
 
Resource Report
Resource Website
SQTL (RRID:SCR_000827) SQTL software application, software resource Software application (entry from Genetic Analysis Software) gene, genetic, genomic, linux is listed by: Genetic Analysis Software Free, Available for download, Freely available nlx_154032 SCR_000827 Semiparametric QTL mapping in general pedigrees 2026-02-15 09:17:59 0
EIGENSOFT/EIGENSTRAT
 
Resource Report
Resource Website
1+ mentions
EIGENSOFT/EIGENSTRAT (RRID:SCR_001357) EIGENSOFT/EIGENSTRAT software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022. Software application (entry from Genetic Analysis Software) gene, genetic, genomic, linux is listed by: Genetic Analysis Software Free, Available for download, Freely available nlx_154296 http://www.hsph.harvard.edu/faculty/alkes-price/software/ SCR_001357 2026-02-15 09:18:05 1
BIRDSUITE
 
Resource Report
Resource Website
10+ mentions
BIRDSUITE (RRID:SCR_001794) Birdsuite software application, software resource Open-source set of tools to detect and report SNP genotypes, common Copy-Number Polymorphisms (CNPs), and novel, rare, or de novo CNVs in samples processed with the Affymetrix platform. While most of the components of the suite can be run individually (for instance, to only do SNP genotyping), the Birdsuite is especially intended for integrated analysis of SNPs and CNVs. gene, genetic, genomic, snp, genotype, copy number polymorphism, copy number variant, affymetrix is listed by: OMICtools
is listed by: Genetic Analysis Software
has parent organization: Broad Institute
PMID:18776909 Free, Available for download, Freely available OMICS_00705, nlx_154245 SCR_001794 2026-02-15 09:18:10 43
DINDEL
 
Resource Report
Resource Website
10+ mentions
DINDEL (RRID:SCR_001827) Dindel software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on March 7,2024. Software program for calling small indels from short-read sequence data ("next generation sequence data"). It is currently designed to handle only Illumina data. Dindel takes BAM files with mapped Illumina read data and enables researchers to detect small indels and produce a VCF file of all the variant calls. It has been written in C++ and can be used on Linux-based and Mac computers (it has not been tested on Windows operating systems). indel, short-read, next generation sequence, illumina, gene, genetic, genomic, c++, linux, macos, bio.tools is listed by: OMICtools
is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
PMID:20980555
DOI:10.1101/gr.112326.110
THIS RESOURCE IS NO LONGER IN SERVICE , nlx_154283, OMICS_00096, biotools:dindel https://bio.tools/dindel
https://sources.debian.org/src/dindel/
http://www.sanger.ac.uk/resources/software/dindel/ SCR_001827 Dindel: Accurate indel calls from short-read data 2026-02-15 09:18:11 44
SOLAR
 
Resource Report
Resource Website
10+ mentions
SOLAR (RRID:SCR_000850) SOLAR software application, software resource A flexible and extensive software package for genetic variance components analysis, including linkage analysis, quantitative genetic analysis, and covariate screening. Operations are included for calculation of marker-specific or multipoint identity-by-descent (IBD) matrices in pedigrees of arbitrary size and complexity, and for linkage analysis of quantitative traits which may involve multiple loci (oligogenic analysis), dominance effects, and epistasis. (entry from Genetic Analysis Software) gene, genetic, genomic, fortran, c, c++, tcl, unix, (solaris 7-10/solaris x86 8-9/digital unix 4.0e/sg irix), linux, macos, ms-windows is listed by: Genetic Analysis Software nlx_154653 http://www.sfbr.org/Departments/genetics_detail.aspx?p=37 SCR_000850 Sequential Oligogenic Linkage Analysis Routines 2026-02-15 09:18:00 22
PEDIGRAPH
 
Resource Report
Resource Website
10+ mentions
PEDIGRAPH (RRID:SCR_001938) Pedigraph software application, software resource A pedigree visualization program specifically designed to draw large, complex pedigrees. (entry from Genetic Analysis Software) Options include: * Full pedigree * Summarization * Extraction of individual pedigrees * Inbreeding calculation * Coancestry coefficient calculation * Color control * Drawing size * Page size and margins * Drawing styles gene, genetic, genomic, c, c++, ms-windows, linux, pedigree, java, bio.tools is listed by: OMICtools
is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Minnesota Twin Cities; Minnesota; USA
PMID:14986440 Acknowledgement required, Copyrighted biotools:pedigraph, OMICS_00212, nlx_154519 https://bio.tools/pedigraph SCR_001938 2026-02-15 09:18:12 17
MRH
 
Resource Report
Resource Website
MRH (RRID:SCR_000841) MRH software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022. Software application (entry from Genetic Analysis Software) gene, genetic, genomic, ms-windows, unix, solaris is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154493 SCR_000841 Minimum Recombinant Haplotype 2026-02-15 09:18:00 0
QTL CAFE
 
Resource Report
Resource Website
QTL CAFE (RRID:SCR_000844) QTL CAFE software application, software resource Software application providing a user freiendly way to perform QTL analysis. The software currently allows 3 types of QTL analysis: (1) single marker ANOVA. (2) marker regression. (3) interval mapping by regression. (entry from Genetic Analysis Software) gene, genetic, genomic, java is listed by: Genetic Analysis Software nlx_154563 SCR_000844 2026-02-15 09:18:00 0
Italian Institute for Genomic Medicine; Turin; Italy
 
Resource Report
Resource Website
Italian Institute for Genomic Medicine; Turin; Italy (RRID:SCR_017062) IIGM, HuGeF data or information resource, topical portal, portal Private research institute in Turin, Italy. Research programs in immunogenetics, functional genomics, genomic epidemiology, tumour diagnostic and prognostic biomarker research, epigenetic modifications in disease, quantitative biology and computational neuroscience. institute, private, research, human, genetic, genomic, epigenomic, immunogenetic, quantitative, biology, computational, neuroscience is parent organization of: HaTSPiL SCR_017062 2026-02-15 09:21:57 0
University of British Columbia Centre for Molecular Medicine and Therapeutics
 
Resource Report
Resource Website
1+ mentions
University of British Columbia Centre for Molecular Medicine and Therapeutics (RRID:SCR_017241) UBC CMMT data or information resource, topical portal, portal Center is part of University of British Columbia Faculty of Medicine, located at British Columbia Children Hospital Research Institute (BCCHR) in Vancouver, British Columbia, Canada. Research at CMMT is focused on discovering genetic susceptibility to illnesses such as Huntington Disease, Type 2 diabetes and bipolar disorder. genetic, susceptibility, Huntington, disease, type 2 diabetes, bipolar disorder SCR_017241 University of British Columbia (UBC) Centre for Molecular Medicine & Therapeutics, CMMT, Centre for Molecular Medicine and Therapeutics 2026-02-15 09:22:00 9
PEDPLOT
 
Resource Report
Resource Website
PEDPLOT (RRID:SCR_003843) PEDPLOT software application, software resource Pedigree Plotting Program for the Pedfile Format (entry from Genetic Analysis Software) gene, genetic, genomic, c++, postscript, unix, (sparc-solaris 2.5/dec unix 4.0/x86-solaris 2.6) is listed by: Genetic Analysis Software nlx_154526 SCR_003843 2026-02-15 09:18:35 0
PARENTE
 
Resource Report
Resource Website
1+ mentions
PARENTE (RRID:SCR_004717) PARENTE software application, software resource Software application for parentage inference using molecular data from diploid codominant markers (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software nlx_154508 SCR_004717 2026-02-15 09:18:48 2
Multipoint Identical-by-descent Method
 
Resource Report
Resource Website
Multipoint Identical-by-descent Method (RRID:SCR_004676) MIM software application, software resource Software application using multipoint IBD method for partitioning genetic variance of quantitative traits to specific chromosome regions using data on nuclear families. (entry from Genetic Analysis Software) gene, genetic, genomic, c, unix is listed by: Genetic Analysis Software PMID:9433587 nlx_154482 SCR_004676 2026-02-15 09:18:47 0
PEDRAW/WPEDRAW
 
Resource Report
Resource Website
PEDRAW/WPEDRAW (RRID:SCR_004797) PEDRAW/WPEDRAW software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 11, 2023. A pedigree drawing program using LINKAGE data files (entry from Genetic Analysis Software) gene, genetic, genomic, c++, ms-dos, ms-windows, x-window is listed by: Genetic Analysis Software THIS RESOURCE IS NO LONGER IN SERVICE nlx_154527 SCR_004797 Pedigree Drawing/ Window Pedigree Drawing (MS-Window and X-Window version of PEDRAW) 2026-02-15 09:18:54 0
TDTASP
 
Resource Report
Resource Website
1+ mentions
TDTASP (RRID:SCR_004943) TDTASP software application, software resource Software application for power and sample-size calculations for the TDT and ASP tests under a wide variety of ascertainment schemes. Uses the flexible genetic model of McGinnis. Most calculations are exact rather than asymptotic. (entry from Genetic Analysis Software) gene, genetic, genomic, fortran95, unix, ms-windows is listed by: Genetic Analysis Software nlx_154675 SCR_004943 Power and Sample-Size Calculations for the TDT and ASP Tests 2026-02-15 09:18:58 3
TDT/S-TDT
 
Resource Report
Resource Website
1+ mentions
TDT/S-TDT (RRID:SCR_005548) TDT/S-TDT software application, software resource Software program that provides separate results for TDT, S-TDT, and the combined (overall) test, as appropriate. (entry from Genetic Analysis Software) gene, genetic, genomic, java, ms-windows, (95/nt) is listed by: Genetic Analysis Software nlx_154679 SCR_005548 Transmission Disequilibrium Test and Sib Transmission Disequilibrium Test 2026-02-15 09:18:59 3
KI Biobank - KOL
 
Resource Report
Resource Website
KI Biobank - KOL (RRID:SCR_005782) KI Biobank - KOL material resource, biomaterial supply resource Aims to explore heritability for clinically confirmed chronic obstructive lung disease (COPD), estimate the heritability for lung function and investigate interactions between smoking and genes including the genetic effect on smoking habits. Study participants have been recruited from the Swedish Twin Registry. Types of samples * EDTA whole blood * DNA * Plasma * Serum Number of sample donors: 386 (sample collection completed) heritability, lung function, smoking, gene, genetic, nicotine, tobacco is listed by: One Mind Biospecimen Bank Listing
is related to: Swedish Twin Registry
has parent organization: Karolisnka Biobank
Chronic obstructive lung disease, Nicotine Use Disorder nlx_151299 http://ki.se/ki/jsp/polopoly.jsp?d=29354&a=31608&l=en SCR_005782 2026-02-15 09:19:03 0
PEDSCRIPT
 
Resource Report
Resource Website
PEDSCRIPT (RRID:SCR_004571) PEDSCRIPT software application, software resource Software tool that allows scripting of simple modifications to pedigree files. (entry from Genetic Analysis Software) gene, genetic, genomic is listed by: Genetic Analysis Software nlx_154528 SCR_004571 2026-02-15 09:18:50 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. Neuroscience Information Framework Resources

    Welcome to the NIF Resources search. From here you can search through a compilation of resources used by NIF 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 NIF 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 NIF then you can log in from here to get additional features in NIF 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 NIF 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.