Result for 07788CE352FEE1497ABCDB362C12F59CC576EF0D

Query result

Key Value
FileName./usr/lib/R/library/qtl/libs/qtl.so
FileSize355896
MD56E0CAE1E5A3D494FF0FC2F6B065E6466
SHA-107788CE352FEE1497ABCDB362C12F59CC576EF0D
SHA-2562C44F0D7EF45AA98C0A7C8D5DC0DA25FB2E37F466CF2EE0EED45457F82EA902F
SSDEEP6144:lKcnj1kdqC22WOfZTs8oIGDeB2Ab4zUVM4XIgP4XPGOkATaB+eV7U:kcj1kc2WqxjGU2AJvIgAXuOcB+X
TLSHT13D74398B6D39CB63CDAA55361A3E4F9B776C6162143B0E5F4F0991F7088FA90B207E11
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
MD5836D1AF0BEF1C97B58A2BA5DFB707F39
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.fc22
PackageVersion1.36.6
SHA-13D48627A31F41CFE34E79A75D112353D19EEA6E8
SHA-25644E717E2D55EA8B122C1F3D9741E5D4601D38E8BEA7C4FC563CBEE143E2CD88A