Result for 0063D212E13D1E1973831926292E1DE0F10D7228

Query result

Key Value
FileName./usr/lib/R/site-library/qtl/data/listeria.RData
FileSize6906
MD588495D8B2C2EFE8C951876A6A739670B
SHA-10063D212E13D1E1973831926292E1DE0F10D7228
SHA-25683FE0C881D5E90BB9BF7FFCE465DE0C1223DC10033401705438332BBEE4BCB80
SSDEEP96:jTUxsGATHDmuMG7+0PsX2SGU0uUDOgExlebtYvwNaqVi6MGVbm6DUMmcFKLl9qUU:jTNGAp7+fdWox4qvgViQlW9bMO4Slvdo
TLSHT1B0E1BF8F8F4C3B32FC996BBF215E51621D7A4CA5D967483F6E00243A242F8355C6B118
hashlookup:parent-total16
hashlookup:trust100

Network graph view

Parents (Total: 16)

The searched file hash is included in 16 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
MD57F0EAE861B694463414031C1E3A0D919
PackageArchx86_64
PackageDescriptionR-qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. Our goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. We have implemented the main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses. The current version of R-qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation and Haley-Knott regression.
PackageMaintainerFedora Project
PackageNameR-qtl
PackageRelease1.fc34
PackageVersion1.48.1
SHA-104395CD09440B0BCCC7F0934EDFD8791E3FC2B2D
SHA-2565BBDAF293CDA5CF7AEA02B07FDD7B8D7059477AC542276CE0AAA5C25163AE21B
Key Value
FileSize5508644
MD59C2AC17C6B1E7E7C6CE177CDBFC512E4
PackageDescriptionGNU R package for genetic marker linkage analysis R/qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. It is implemented as an add-on-package for the freely available and widely used statistical language/software R (see http://www.r-project.org). . The development of this software as an add-on to R allows one to take advantage of the basic mathematical and statistical functions, and powerful graphics capabilities, that are provided with R. Further, the user will benefit by the seamless integration of the QTL mapping software into a general statistical analysis program. The goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. . A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. The main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses were implemented. . The current version of R/qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation.
PackageMaintainerDebian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.47-9-1
SHA-12222AC44AF4EA9F4E14297CCEB4845A5C256E38F
SHA-2563117A2FA50B30102E28392B3554AF656434701BC85165E5627EB77E27448DC88
Key Value
FileSize5520592
MD5DA984ED7C6B9D226E38D69A05E335E91
PackageDescriptionGNU R package for genetic marker linkage analysis R/qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. It is implemented as an add-on-package for the freely available and widely used statistical language/software R (see http://www.r-project.org). . The development of this software as an add-on to R allows one to take advantage of the basic mathematical and statistical functions, and powerful graphics capabilities, that are provided with R. Further, the user will benefit by the seamless integration of the QTL mapping software into a general statistical analysis program. The goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. . A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. The main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses were implemented. . The current version of R/qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation.
PackageMaintainerUbuntu Developers <ubuntu-devel-discuss@lists.ubuntu.com>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.47-9-1
SHA-12D338FBCA48566735C4DB1CB76CA07EAEB273DC1
SHA-256F7B69E894F0A7B79C87F96BE99FA408BD749E6FAEE0844E21466588942BB449B
Key Value
MD54315C3C736B523E162A885B59678B1B1
PackageArcharmv7hl
PackageDescriptionR-qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. Our goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. We have implemented the main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses. The current version of R-qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation and Haley-Knott regression.
PackageMaintainerFedora Project
PackageNameR-qtl
PackageRelease1.fc34
PackageVersion1.48.1
SHA-149CF0EB687C7C50AF90520C3F408E80A6664FF6E
SHA-25620C249291F36AECD15A5878EA108CBB3BB7984F3AEB251F0EACCC5F337C9DD09
Key Value
FileSize5509276
MD5746B6EBD3654BABF1630B60EB3E89EA3
PackageDescriptionGNU R package for genetic marker linkage analysis R/qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. It is implemented as an add-on-package for the freely available and widely used statistical language/software R (see http://www.r-project.org). . The development of this software as an add-on to R allows one to take advantage of the basic mathematical and statistical functions, and powerful graphics capabilities, that are provided with R. Further, the user will benefit by the seamless integration of the QTL mapping software into a general statistical analysis program. The goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. . A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. The main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses were implemented. . The current version of R/qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation.
PackageMaintainerDebian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.47-9-1
SHA-161A7F299095D30700F3F099D6FB1F1D651BC3FA8
SHA-256CC0D44FBEF4A6014BA2818C8127621AB3750DDCC6972D8516222E6DA7775AC9D
Key Value
FileSize5522628
MD546AEAFEDF5016726B4CC696A9115943A
PackageDescriptionGNU R package for genetic marker linkage analysis R/qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. It is implemented as an add-on-package for the freely available and widely used statistical language/software R (see http://www.r-project.org). . The development of this software as an add-on to R allows one to take advantage of the basic mathematical and statistical functions, and powerful graphics capabilities, that are provided with R. Further, the user will benefit by the seamless integration of the QTL mapping software into a general statistical analysis program. The goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. . A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. The main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses were implemented. . The current version of R/qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation.
PackageMaintainerDebian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.47-9-1
SHA-168DB7DBC0F16B23F43D54D15EBDDDE025A96D426
SHA-256A35FF9C91972E833C4A33993218B3B3BD18AAEA6C4152BAE344A1C5520A3522D
Key Value
FileSize5526312
MD5CC0C55CD7FD4281802ACB69EA01F059B
PackageDescriptionGNU R package for genetic marker linkage analysis R/qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. It is implemented as an add-on-package for the freely available and widely used statistical language/software R (see http://www.r-project.org). . The development of this software as an add-on to R allows one to take advantage of the basic mathematical and statistical functions, and powerful graphics capabilities, that are provided with R. Further, the user will benefit by the seamless integration of the QTL mapping software into a general statistical analysis program. The goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. . A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. The main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses were implemented. . The current version of R/qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation.
PackageMaintainerDebian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.47-9-1
SHA-17B8134941D49D7B8242A2573A44E3ABE2E4E1A2C
SHA-2560423335539F4EC4524A5A033F2D9266C1EDBD96708F2FDDD7D0AFE2FE176B17E
Key Value
FileSize5517356
MD579948065B9A1BE663A5B4E8B1D2220D3
PackageDescriptionGNU R package for genetic marker linkage analysis R/qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. It is implemented as an add-on-package for the freely available and widely used statistical language/software R (see http://www.r-project.org). . The development of this software as an add-on to R allows one to take advantage of the basic mathematical and statistical functions, and powerful graphics capabilities, that are provided with R. Further, the user will benefit by the seamless integration of the QTL mapping software into a general statistical analysis program. The goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. . A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. The main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses were implemented. . The current version of R/qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation.
PackageMaintainerDebian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.47-9-1
SHA-19312399CDC5AD3537140913352DB93D8EA1FB92B
SHA-256F34069DD82759D7BCC27524F2A895BBE74D45BF983E0217F9902D43F1650BC9D
Key Value
FileSize5509528
MD5B6E94842C30747E5A12EA0D9AC93E86D
PackageDescriptionGNU R package for genetic marker linkage analysis R/qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. It is implemented as an add-on-package for the freely available and widely used statistical language/software R (see http://www.r-project.org). . The development of this software as an add-on to R allows one to take advantage of the basic mathematical and statistical functions, and powerful graphics capabilities, that are provided with R. Further, the user will benefit by the seamless integration of the QTL mapping software into a general statistical analysis program. The goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. . A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. The main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses were implemented. . The current version of R/qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation.
PackageMaintainerDebian R Packages Maintainers <r-pkg-team@alioth-lists.debian.net>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.47-9-1
SHA-19D1C600AFB150AB862CB0267A5AE4CE6FF790D66
SHA-256C9AFE54BBD66CE5E04F60A2C83FBBC5DD9C21FBB5D6FA424B496939711E579AF
Key Value
MD59193E7242FEAA900A4B427A11B23D7E3
PackageArchs390x
PackageDescriptionR-qtl is an extensible, interactive environment for mapping quantitative trait loci (QTLs) in experimental crosses. Our goal is to make complex QTL mapping methods widely accessible and allow users to focus on modeling rather than computing. A key component of computational methods for QTL mapping is the hidden Markov model (HMM) technology for dealing with missing genotype data. We have implemented the main HMM algorithms, with allowance for the presence of genotyping errors, for backcrosses, intercrosses, and phase-known four-way crosses. The current version of R-qtl includes facilities for estimating genetic maps, identifying genotyping errors, and performing single-QTL genome scans and two-QTL, two-dimensional genome scans, by interval mapping (with the EM algorithm), Haley-Knott regression, and multiple imputation. All of this may be done in the presence of covariates (such as sex, age or treatment). One may also fit higher-order QTL models by multiple imputation and Haley-Knott regression.
PackageMaintainerFedora Project
PackageNameR-qtl
PackageRelease3.el8
PackageVersion1.48.1
SHA-1A7D6889ADAEDF8284B0A0762BF261B6F6EF52EBD
SHA-256EA036F89098591048E558A34D80DFE54A92F0D007B7FC33CD4C66B566E0A8BEC