Result for 029572A6AF77E7C3A2D32FB8B53C493E0E2F3817

Query result

Key Value
FileName./usr/lib/R/library/qtl/DESCRIPTION
FileSize710
MD538C20B2C321C741CB327646DFF19AEC8
SHA-1029572A6AF77E7C3A2D32FB8B53C493E0E2F3817
SHA-256C71200A2CF05AA47C990C1EC869F4CDB9C9D34C8897AB7004EDA2D4CE31DDCF1
SSDEEP12:06+BQxGXv2KW0ZeYXaMeP6O+G/b43bR/GA4EAamYpVkzctRqvTGrVb6sKormIFO:QBQsXePSeEeiO7/sLRuA4pOkKqvyrF6T
TLSHT1C50165485A85519468C6485216B90BFDC384C396F39884E891A88B364E41F0AB26B2F9
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