Result for 039046B2D8AF2F4C097AE06B87D8BBAD06978A54

Query result

Key Value
FileName./usr/lib/R/library/qtl/DESCRIPTION
FileSize716
MD555B6A1158D8BBD822BDF334CABB85979
SHA-1039046B2D8AF2F4C097AE06B87D8BBAD06978A54
SHA-256D18328F1D9625532CEEC87FB44019AAFB38B8F8DC308B34D9163C687B763FC20
SSDEEP12:06+BQxGXv2KW0ZeYXaMeP6O+G/b43bR/GA4EAamYpVkzctRqvTGrVb6sKoNyd+LO:QBQsXePSeEeiO7/sLRuA4pOkKqvyrF6h
TLSHT18D0165886A81515578C6495166F90BF9C380C38AF39880E891B88F269E01B06B27F2F9
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
MD57CCC28A36E0BF8D88BB4DD3259D37EB2
PackageArcharmv7hl
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-1B5B1CB57ED65E958EE0F8E27D88F1B5660B38F1B
SHA-2568767B1A10245F369AE193A55E1A652762BA1C59FAEB3940F992EEEF788F6E68F