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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.

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On page 9 showing 161 ~ 180 out of 795 results
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  • RRID:SCR_009144

http://cedar.genetics.soton.ac.uk/pub/PROGRAMS/ceph2map

Software application developed from crimap v2.4 for use with the map suite of programs. (entry from Genetic Analysis Software)

Proper citation: CEPH2MAP (RRID:SCR_009144) Copy   


  • RRID:SCR_009145

    This resource has 1+ mentions.

http://www.sanger.ac.uk/resources/software/evoker/

A graphical tool for visualizing genotype intensity data in order to assess genotype calls as part of quality control procedures for genome-wide association studies. It provides a solution to the computational and storage problems related to being able to work with the huge volumes of data generated by such projects by implementing a compact, binary format that allows rapid access to data, even with hundreds of thousands of observations. (entry from Genetic Analysis Software)

Proper citation: EVOKER (RRID:SCR_009145) Copy   


  • RRID:SCR_009142

http://www.stat.auckland.ac.nz/~browning/ccrel/ccrel.htm

Software program for case-control genetic analysis that takes relatedness between individuals into account. It will perform single-marker and haplotypic tests, however it will only work with SNP or other biallelic markers. (entry from Genetic Analysis Software)

Proper citation: CCREL (RRID:SCR_009142) Copy   


  • RRID:SCR_009218

http://theory.stanford.edu/~xuying/hapar/

Software application to infer haplotype from genotype data. It uses the parsimony principle, i.e. try to find the minimum number of haplotypes that can reconstruct the input genotypes. (entry from Genetic Analysis Software)

Proper citation: HAPAR (RRID:SCR_009218) Copy   


  • RRID:SCR_009217

http://www.mrc-epid.cam.ac.uk/Personal/jinghua.zhao/software/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application (entry from Genetic Analysis Software)

Proper citation: HAP 2 (RRID:SCR_009217) Copy   


  • RRID:SCR_009215

    This resource has 10+ mentions.

http://www.stats.ox.ac.uk/~marchini/software/gwas/gtool.html

Software application for transforming sets of genotype data for use with the programs SNPTEST and IMPUTE. (entry from Genetic Analysis Software)

Proper citation: GTOOL (RRID:SCR_009215) Copy   


  • RRID:SCR_009213

http://genepi.med.utah.edu/~alun/software/docs/index.html?GMCheck.html

Software application that finds the posterior probabilities for data errors for genotypes and phenotypes in pedigree data (entry from Genetic Analysis Software)

Proper citation: GMCHECK (RRID:SCR_009213) Copy   


  • RRID:SCR_009210

    This resource has 1+ mentions.

http://mather.well.ox.ac.uk/GLIDERS/

THIS RESOURCE IS NO LONGER IN SERVCE, documented September 6, 2016.

Proper citation: GLIDERS (RRID:SCR_009210) Copy   


  • RRID:SCR_009298

http://ftp://statgen.ncsu.edu/pub/zaykin/

Software application performing a shuffling version of the exact conditional tests for different combinations of allelic and genotypic disequilibrium on haploid and diploid data, or their combination. (entry from Genetic Analysis Software)

Proper citation: MLD (RRID:SCR_009298) Copy   


  • RRID:SCR_009297

    This resource has 1+ mentions.

http://ftp://ftp.biomath.jussieu.fr/pub/mlbgh (not available)

Software application that is an extension of the GENEHUNTER program to perform sib-pair and sib-ship linkage analysis using the Maximum Likelihood Binomial (MLB) method. (entry from Genetic Analysis Software)

Proper citation: MLBGH (RRID:SCR_009297) Copy   


  • RRID:SCR_009294

http://mga.bionet.nsc.ru/soft/mitpene/mitpene.html (in Russian)

Software program for analysis of mitochondrial diseases (entry from Genetic Analysis Software)

Proper citation: MITPENE (RRID:SCR_009294) Copy   


  • RRID:SCR_009295

    This resource has 1+ mentions.

http://www.uni-kiel.de/medinfo/mitarbeiter/krawczak/download/index.html

Software application (entry from Genetic Analysis Software)

Proper citation: MKGST (RRID:SCR_009295) Copy   


  • RRID:SCR_009292

    This resource has 100+ mentions.

http://genome.sph.umich.edu/wiki/Minimac

Software application that is a low memory, computationally efficient implementation of the MaCH algorithm for genotype imputation. It is designed to work on phased genotypes and can handle very large reference panels with hundreds or thousands of haplotypes. The name has two parts. The first, mini, refers to the modest amount of computational resources it requires. The second, mac, is short hand for MaCH, our widely used algorithm for genotype imputation. (entry from Genetic Analysis Software)

Proper citation: MINIMAC (RRID:SCR_009292) Copy   


  • RRID:SCR_009290

http://www.mds.qmw.ac.uk/statgen/dcurtis/software.html

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software application (entry from Genetic Analysis Software)

Proper citation: MFLINK (RRID:SCR_009290) Copy   


  • RRID:SCR_009207

    This resource has 1+ mentions.

http://acgt.cs.tau.ac.il/gevalt/

Software application designed to simplify and expedite the process of genotype analysis and disease association tests by providing a common interface to several common tasks relating to such analyses. It is aimed for analysis of unrelated individuals as well as two-generation families. (entry from Genetic Analysis Software)

Proper citation: GEVALT (RRID:SCR_009207) Copy   


  • RRID:SCR_009208

    This resource has 1+ mentions.

https://github.com/gaow/genetic-analysis-software/blob/master/pages/GGT.md

Software application that combines genetic map data and locus data to display Graphical Genotypes. Data can be viewed by individual or by linkage group, and sorted on markers. Statistics are calculated and simultaneous filtering/selection on multiple linkage groups is possible. Output of hi-res genotype drawings directly to printer or to emf/jpeg/bitmap image. A module for constructing GGT-datafiles from common mapmaker/joinmap style formatted data is available. (entry from Genetic Analysis Software)

Proper citation: GGT (RRID:SCR_009208) Copy   


  • RRID:SCR_009203

    This resource has 1+ mentions.

http://softlib.rice.edu/geno.html

Software application designed to identify genotypes that are likely to be errors. The statistical method was designed to identify typing error rather than pedigree errors, but is general enough to pinpoint any unlikely genotype still consistent with Mendelian inheritance. (entry from Genetic Analysis Software)

Proper citation: GENOCHECK (RRID:SCR_009203) Copy   


  • RRID:SCR_009289

    This resource has 500+ mentions.

http://www.sph.umich.edu/csg/abecasis/Merlin

Software application that carries out single-point and multipoint analyses of pedigree data, including IBD and kinship calculations, nonparametric and variance component linkage analyses, error detection and information content mapping. For multipoint analyses in dense maps, Merlin allows the user to impose constraints on the number of recombinants between consecutive markers. Merlin estimates haplotypes by finding the most likely path of gene flow or by sampling paths of gene flow at all markers jointly. It can also list all possible nonrecombinant haplotypes within short regions. Finally, Merlin provides swap-file support for handling very large numbers of markers as well as gene-dropping simulations for estimating empirical significance levels. (entry from Genetic Analysis Software)

Proper citation: MERLIN (RRID:SCR_009289) Copy   


  • RRID:SCR_009202

    This resource has 10+ mentions.

http://www.geneweaveronline.com/

Software application for charting family medical/health history (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: GENEWEAVER (RRID:SCR_009202) Copy   


  • RRID:SCR_009200

https://github.com/gaow/genetic-analysis-software/blob/master/pages/GENOOM.md

Software application that implements a virtual computer world where biological entities are digital objects. In this world, each individual of a population is represented by a set of chromosomes with genetic elements (markers, genes, Quantitative Traits Loci, etc.) and attributes (phenotype, age, fertility, living status, exposure, etc.). It comes with a built-in model allowing basic genetic studies by simulations, performed according to parameter values such a penetrance matrix (phenotype probabilities for each genotype), exposure, between-relative mating probabilities, and a probability of migration in a two-dimensional migration process. The simulated populations could be analysed with different packages for statistical or genetical analysis (e.g., SAS, S-PLUS, Linkage, Mapmaker/sibs, Genehunter). Pedigrees can also be simulated according to a pedigree file at the LINKAGE format. (entry from Genetic Analysis Software)

Proper citation: GENOOM (RRID:SCR_009200) Copy   



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