Result for 04A30BA7522E533E452EEAB7ABBE3B6533D1222F

Query result

Key Value
FileName./usr/lib64/R/library/qtl/html/convert.scanone.html
FileSize1783
MD5BED18EC49C7404639085EBB5269B51A4
SHA-104A30BA7522E533E452EEAB7ABBE3B6533D1222F
SHA-256E4E7CCD4A2E88E4BC96C0882507BAFC6D9A66FA23EEA6680229AFF8E3BAB249A
SSDEEP48:KpbseCQY+eCXFGHVGNxocQ0DNMUhJVCH97zxR2S2Ez87m:He7pAHVGHooMUHVCH97zn4E4C
TLSHT1BD31629495C3069B4123B36CAE2536DC7BCEC7A42EA409C06C5F9A0DC7D012E5329B8B
hashlookup:parent-total4
hashlookup:trust70

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Parents (Total: 4)

The searched file hash is included in 4 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
MD57E11E63E211156249326E0E8EC466F4D
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.fc20
PackageVersion1.28.19
SHA-10EC3C659ABDD78EFEF862C7193B80B5D080DF978
SHA-256255BE44F551362192BE44CDB096023CF7B2098E57104F23A5660848A5F6C619A
Key Value
MD5DA51743DD1D33DAA2749F42B82EC793E
PackageArchppc
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.fc20
PackageVersion1.28.19
SHA-1673CDFC0660BC20C3479DE9B42A79F881FE738F3
SHA-256A1B32275539008744E7123FA7C0C3DEFE6DE86C7B47530EA872B71A6BB7BE23C
Key Value
MD5A92612FBDFEBE3E5E3F43A0F93982C2E
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.fc20
PackageVersion1.28.19
SHA-1F5DC36798FBF4B7BCCFF0C0A91F84D0C0918900A
SHA-256391BB0821FE5DF69679E826DF746A4D52852554B3692C229E35BC7B9FDDF66CD
Key Value
MD5695643DDC2534B9AE4C89CBFD97972A2
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.fc20
PackageVersion1.28.19
SHA-12C74DCF84B133BA001F040C752C0FB327C41EEAA
SHA-256ACF372F6672E8E1B9EF6C0D2915A9197303D3C1808B0A8A935A65E248BE32C63