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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 38 showing 741 ~ 760 out of 795 results
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  • RRID:SCR_009364

    This resource has 1+ mentions.

http://www.mrc-epid.cam.ac.uk/~jinghua.zhao/r-progs.htm

An integrated software package for genetic data analysis of both population and family data. Currently it contains functions for sample size calculations of both population-based and family-based designs, classic twin ACE/ADE/AE/CE models, probability of familial disease aggregation, kinship calculation, some statistics in linkage analysis, and association analysis involving one or more genetic markers including haplotype analysis with or without environmental covariates (entry from Genetic Analysis Software)

Proper citation: R/GAP (RRID:SCR_009364) Copy   


  • RRID:SCR_009365

https://cran.r-project.org/web/packages/hapassoc/index.html

Software application using a likelihood approach to inference of haplotype and nongenetic effects and their interactions in generalized linear models of disease penetrance, when haplotype phase is unknown for some subjects. Parameter estimates are obtained by use of an expectation-maximization (EM) algorithm and standard errors are calculated using Louis'' formula. (entry from Genetic Analysis Software)

Proper citation: R/HAPASSOC (RRID:SCR_009365) Copy   


  • RRID:SCR_009360

    This resource has 1+ mentions.

http://csg.sph.umich.edu/boehnke/rhmap.php

Software application (entry from Genetic Analysis Software)

Proper citation: RHMAP (RRID:SCR_009360) Copy   


  • RRID:SCR_009319

    This resource has 1+ mentions.

http://www.chg.duke.edu/software/pdt.html

Software analysis program to evaluate evidence of linkage disequilibrium (LD) in general pedigree data. All family data may be used without nullifying the validity of the association test, even when there is more than one affected in a family. The PDT program performs both allele-specific and genotype-specific LD analysis of individual markers. Version 5.1 adds the ability to perform genotype-specific analysis over marker sets. (entry from Genetic Analysis Software)

Proper citation: PDT (RRID:SCR_009319) Copy   


  • RRID:SCR_009317

http://www.ibms.sinica.edu.tw/~csjfann/first%20flow/programlist.htm

Software tool for analyses of pooled DNA data (entry from Genetic Analysis Software)

Proper citation: PDA (RRID:SCR_009317) Copy   


  • RRID:SCR_009318

http://cougar.fhcrc.org/software.php

Software application that is a Windows-based system designed for pedigree data management, providing a graphical interface for pedigree construction and output. (entry from Genetic Analysis Software)

Proper citation: PDPSYS (RRID:SCR_009318) Copy   


  • RRID:SCR_009316

    This resource has 10+ mentions.

http://linkage.rockefeller.edu/pawe/

Software application for power and sample size calculations for genetic case-control association studies allowing for errors (entry from Genetic Analysis Software)

Proper citation: PAWE (RRID:SCR_009316) Copy   


  • RRID:SCR_009311

http://mlemire.freeshell.org/software.html

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 16,2023. Software program that splits extended pedigrees into nuclear families, with the option of recoding all sibs as half-sibs with distinct mothers of fathers. (entry from Genetic Analysis Software)

Proper citation: NUCULAR (RRID:SCR_009311) Copy   


  • RRID:SCR_000388

https://github.com/wtsi-npg/Illuminus

A fast and accurate algorithm for assigning single nucleotide polymorphism (SNP) genotypes to microarray data from the Illumina BeadArray technology.

Proper citation: ILLUMINUS (RRID:SCR_000388) Copy   


  • RRID:SCR_000839

http://cedar.genetics.soton.ac.uk/pub/PROGRAMS/ldb;

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022. Software application that integrate genetic linkage map and physical map (entry from Genetic Analysis Software)

Proper citation: LDB/LDB+ (RRID:SCR_000839) Copy   


  • RRID:SCR_000837

    This resource has 1+ mentions.

http://research.calit2.net/hap/

Software application (entry from Genetic Analysis Software)

Proper citation: HAP 1 (RRID:SCR_000837) Copy   


  • RRID:SCR_000835

http://www.biostat.harvard.edu/complab/dchip/snp.htm

THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016.

Proper citation: DCHIP LINKAGE (RRID:SCR_000835) Copy   


  • RRID:SCR_000836

http://faculty.washington.edu/browning/floss/floss.htm

Software application that performs ordered subset analysis using MERLIN's ouput .lod file created with the --perFamily option. Ordered subset analysis uses covariate information to identify a more homogenous subset of families for linkage analysis. The homogeneous subset of families does not need to be specified a priori, and the covariates can include environmental exposures, quantitative traits, or linkage scores at another locus in the genome. The evidence for linkage is evaluated with a permutation test. (entry from Genetic Analysis Software)

Proper citation: FLOSS (RRID:SCR_000836) Copy   


  • RRID:SCR_000828

http://null

Software application for calculating the heterozygosity, PIC, and LIC values for polymorphic markers (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: POLYMORPHISM (RRID:SCR_000828) Copy   


  • RRID:SCR_000829

    This resource has 1+ mentions.

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

THIS RESOURCE IS NO LONGER IN SERVCE, documented September 22, 2016.

Proper citation: EDAC (RRID:SCR_000829) Copy   


  • RRID:SCR_000826

https://github.com/gaow/genetic-analysis-software/blob/master/pages/2LD.md

Software program for calculating linkage disequilibrium (LD) measures between two polymorphic markers.

Proper citation: 2LD (RRID:SCR_000826) Copy   


  • RRID:SCR_000827

http://www.bios.unc.edu/~lin/software/SQTL/

Software application (entry from Genetic Analysis Software)

Proper citation: SQTL (RRID:SCR_000827) Copy   


  • RRID:SCR_000850

    This resource has 10+ mentions.

http://solar-eclipse-genetics.org

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)

Proper citation: SOLAR (RRID:SCR_000850) Copy   


  • RRID:SCR_000841

http://www-rcf.usc.edu/~gqian/software.htm (not available)

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022. Software application (entry from Genetic Analysis Software)

Proper citation: MRH (RRID:SCR_000841) Copy   


  • RRID:SCR_000844

http://www.biosciences-labs.bham.ac.uk/Kearsey/

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)

Proper citation: QTL CAFE (RRID:SCR_000844) Copy   



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