Result for 02B52B8F9BCD21F33508AFACABF3CDD7C2AE9290

Query result

Key Value
FileName./usr/lib/R/site-library/qtl/STATUS.txt
FileSize147377
MD58F6449842C9796BB28BAC48155CBA91E
SHA-102B52B8F9BCD21F33508AFACABF3CDD7C2AE9290
SHA-256889C4458B65EF175625647752BCD8C5D7FE14BD40FAB25794B1D405F86D3B3A2
SSDEEP1536:cqiK/sUJ3JJkKCDsLVl63FRnaxc6Nhb9K3TFdSxa4sSTIVJ1yMsK:cqhJkKFLV0zefW4sSTUJ8k
TLSHT14FE3B5177A09237741420AB566EF62D5F72CD6BDB721598834AEC0AC271287F023FBD9
hashlookup:parent-total7
hashlookup:trust85

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Parents (Total: 7)

The searched file hash is included in 7 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
MD5B84FCB1EFE45BF81C3C358FC5D5F85B6
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
PackageRelease1.fc23
PackageVersion1.37.11
SHA-1B96E6936F6EBB196CEC8FB83F846A64A000D8485
SHA-2560E48AFF1EA0A7AC09C86ADEB1E307B6F270520BD0D06F8FA3E7FF6340F8334C8
Key Value
MD55A7519C77B459350B12DF2E0344E02EC
PackageArchs390
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.fc23
PackageVersion1.37.11
SHA-15597AB1C35636F9329E4A723930636FB0C608171
SHA-2568AADF7AF4CF9C4ABE90FEF44E6923AF742DBB8ACCB026315D5AABA000AA36733
Key Value
FileSize5022684
MD5994F37C529B630C00FF8CE7C540C28B5
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
PackageVersion1.37-11-1
SHA-10765EF32CCED8DFFBE9D15F85B426C96ACC089CF
SHA-25656C37B4EE4F9A10B11445CCD5433525A616C972DEC9552E2E31A1AB067B3D457
Key Value
MD57BC63886C8405050D8FC53A4F5231E63
PackageArchppc64le
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.fc23
PackageVersion1.37.11
SHA-16A26D1509A5C28C6901261C47E33B51F2C90D2FA
SHA-256F36992A11E07767B39738F17172E2D164F55B701AD2EA16BDF0C3F8CCA87ACF6
Key Value
FileSize5022486
MD539EE8384121F9B92017413545BB75057
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
PackageVersion1.37-11-1
SHA-17406E4D5A17C1F06FE9D44EA3752F48A64AA0D1C
SHA-256D8D780F0FC201FAB7B7EBD04ACB064A504DC0134F3190AF7310CBBC6598081EE
Key Value
MD5B05FF82937A1D9B7D41B51303CADE312
PackageArchaarch64
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.fc23
PackageVersion1.37.11
SHA-13FC5A532DBAF3DC431E35BE2DD8B3D65452A40BA
SHA-2565E609328ADCF1FEE4C6514A769326FA290ED43E36AD5EB9DBA9F460C79A4B0E8
Key Value
MD575892274EE52833570F476D1B5535E12
PackageArchppc64
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.fc23
PackageVersion1.37.11
SHA-1573E6C75ECCE6411897E0630059F157428B966BF
SHA-256251F1859E29EF9FD073C3F70839B48137C01C087EDCA7411D4C2DF040B24E7B3