Result for 047F7031FA03DA3E07F740E164904CF7BABB3559

Query result

Key Value
FileName./usr/lib/R/library/qtl/R/qtl.rdx
FileSize5153
MD55E4B2C4A79FA71FD7A2881581DEE8789
SHA-1047F7031FA03DA3E07F740E164904CF7BABB3559
SHA-2561763DFFEC7A56A7EFCE5453F080C9312AE1D8346E208A2AE0F1BCFD5331CB8C8
SSDEEP96:HNmPPx0TM/Xs6jDyxU68F9R53t3fDbFmGq0O2ueDfx+77U8+GkyjL0:tmRxXs6jOxj8F9rh991D8UXraL0
TLSHT1C0B16D66146D186D817B0352991F1A998EA2D77CE0BDC0C6932ADDC421C5A14F45BBD4
hashlookup:parent-total1
hashlookup:trust55

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Parents (Total: 1)

The searched file hash is included in 1 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
MD5C1731B51EB29EC42BF71387271CDA8A5
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.fc18
PackageVersion1.25.15
SHA-1D26199F3C04AD9833852309DF85A7CEEF6C73EFE
SHA-256F827652F344A2C4B306AC8E2D140D85479816D67B963D56BFFD4D01532A0C598