Result for 03CBB98C50BBE87C5E1207CB0EAD5563E19AF86B

Query result

Key Value
FileName./usr/lib/R/site-library/qtl/contrib/bin/test/regression/t24out.txt
FileSize73222
MD5076F23F188360CA130A7C4CF428EF4F6
SHA-103CBB98C50BBE87C5E1207CB0EAD5563E19AF86B
SHA-256D21EC2D58DA4DB4B0F114E0B299169190C50E9C351AD1CCF424CA9788493CE2C
SSDEEP1536:hy3YGNLNOm+gY4MfGSCq3hnReamQRTa+uwAdq8HP7LbqLmooypJzheywuwmV9a+Z:RCq3hnReamQRTa+uwAdq8HP7LbqLmoo6
TLSHT1796378FEECCEA582A934444572B7757C0221B01F14CE7C03F628B1518DA69DAFFA7A25
hashlookup:parent-total48
hashlookup:trust100

Network graph view

Parents (Total: 48)

The searched file hash is included in 48 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
FileSize4202324
MD599686B1BD763235E671CBBB2E30D1BBE
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 Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.40-8-1
SHA-1012F6E3BB53279E9B6AABD81E2BC50BBF1E2FF8F
SHA-256660B67D4C1B29086E127E03045A7292F1AA49F0B1B72BF9DF2DCB973D7B813FD
Key Value
FileSize5512124
MD5C300B6A622E3E70B72373E196A71AE51
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
PackageVersion1.44-9-1
SHA-10E17D939F22C3DB6A41069624595EF4204B80D4B
SHA-2561BA3FC9194A6409F75539F371E21FBF8C55A8543C1B363371F5D19FE637C475E
Key Value
FileSize5515160
MD5C3DC3AF48D24EE23D47621165BAE2D05
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
PackageVersion1.50-1
SHA-114243A7D65A38B9D9FDD01FE23CA8198E37E7194
SHA-256D384B40D18182758C1229BC6FF90481DA48F8755E1DEA9D5A3A68DAAC3B3AFB5
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
FileSize4186496
MD506AC5EF798721B67DF8FD918AFC7E904
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 Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.40-8-1
SHA-12BCF1023028031488B29CD16190CB57C5B8C069D
SHA-256F1CE284F9B0980FEB5592FDE04B6A4052423E11AFE9A5DA663F9609114E6A105
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
FileSize5507028
MD52D389C7C2EF21D2D7F410E554D6131C3
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
PackageVersion1.44-9-1
SHA-1314FF5C657535EC140F5BFC76253C7C4F4F91A88
SHA-2563BEB9C22DEE2FE76BD5AE0404C4E92AED3FC77B127C1F7993E789D2025886529
Key Value
FileSize5486588
MD50ECBFD01AAEDA7EE987566A28EFA1F71
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
PackageVersion1.42-8-1
SHA-13C3226FF90EE54F40FA89E86BB8C24AD6DC37C83
SHA-256E857F7C88E48D710E62357902008641DF1EC96AD408FC3E89FEB1125093DEE14
Key Value
FileSize5505408
MD52E897D29C8A94EE12F14AC903EF8AC47
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
PackageVersion1.50-1
SHA-1416DB0E26B81A09429A27FD410E55361B7C38C48
SHA-2561A0F79A3974410E95F44D29C11D0AEE61B3A870437C8C8E0F78D4BF6C63E9052
Key Value
FileSize4200908
MD5504FD99AFB59CC68A1779D35028DE0B3
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 Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
PackageNamer-cran-qtl
PackageSectiongnu-r
PackageVersion1.40-8-1
SHA-142131E75034242647E4F10158EEFB723B07F0A41
SHA-2569FEBD061F3D411E26F8AB032B598DD60CF5B3E40D66E88EA786F151F8A9587A1