Result for 0E6435EAF77EEAA6AA7AB3BA34A03CF0F152B08A

Query result

Key Value
FileName./usr/lib/R/site-library/qtl/help/AnIndex
FileSize7698
MD58AF7C918C3159798D507083A18B8C96D
SHA-10E6435EAF77EEAA6AA7AB3BA34A03CF0F152B08A
SHA-2562730DBB6528CD2C291A6A3BC7A1EF1D7E48A6E17714BD04A54AB1E88EE44915D
SSDEEP96:GQw7L3HDYL15eRJeZUPXWZQQ667ennDsnyeCFgs4JxNNFn8ef50HW/qKLfc:5WzHDYL1508UuKFDsu0xNb8ef5b/rfc
TLSHT1EFF1FE366156180AEFE9478D4BB95BC0673C5E922EFBC10B160D866A12E3C4FC51D3CC
hashlookup:parent-total30
hashlookup:trust100

Network graph view

Parents (Total: 30)

The searched file hash is included in 30 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
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
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
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
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
MD5D41702ED918A105184033810F5119CE3
PackageArchx86_64
PackageDescriptionAnalysis of experimental crosses to identify genes (called quantitative trait loci, QTLs) contributing to variation in quantitative traits. Broman et al. (2003) <doi:10.1093/bioinformatics/btg112>.
PackageNameR-qtl
PackageReleaselp154.1.1
PackageVersion1.50
SHA-167E5AA70FD7C79E2C3E136349BCD3C5D518F39C1
SHA-256B82F44AE845C19B098824C19F99B51E2326C75FA9AD3B660CA8813D3EF3E6BFE
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
MD5BCA1C362AC99A7649FD1F77496F55125
PackageArchx86_64
PackageDescriptionAnalysis of experimental crosses to identify genes (called quantitative trait loci, QTLs) contributing to variation in quantitative traits. Broman et al. (2003) <doi:10.1093/bioinformatics/btg112>.
PackageNameR-qtl
PackageReleaselp152.1.2
PackageVersion1.50
SHA-16E1997E8C21A5932A4D4FF5A28F5D53FE70F7015
SHA-2566EB77E9FFFE81EF2853AEA965D4C15B4DBD691493FCEDB97EA12C5F9292BA940