Result for 0007FBA6FC2D35480018B536977958E3D35C34A9

Query result

Key Value
FileName./usr/lib64/R/library/qtl/html/badorder.html
FileSize1897
MD5074A0FFD097F1BC7EA488BA8C31818D0
SHA-10007FBA6FC2D35480018B536977958E3D35C34A9
SHA-256272EA4984A9CA083D10FD4777291D7C964DC01633B4D07102776EE07BB1A2F02
SSDEEP48:lmIbYJpmpeeUnY6FYNANsX45z7zxR2cbWhBOiEzhf3d36z3K:1bpeeUnJCNosX45z7zn6EBdh
TLSHT1D6416445F4C606868296F3BDA4526F283F5ED362E74C04C03C56912DC882669E22DB4F
hashlookup:parent-total5
hashlookup:trust75

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Parents (Total: 5)

The searched file hash is included in 5 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
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
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