Result for 035B90727C3C28203A359169237FB1782D1C2B7A

Query result

Key Value
FileName./usr/lib64/R/library/qtl/R/qtl.rdx
FileSize5237
MD5C14FCA1459B365791D273C429D46D6A7
SHA-1035B90727C3C28203A359169237FB1782D1C2B7A
SHA-256A9F7ACEB6D8111085356A8874F2BB58C6151E57E6DDE6F71495866FBABA7D006
SSDEEP96:0kxhWkjtO8CMRAYgWmxbGeZQ86bcbrIlvaqhYAER1/2AbkZHlrQXLCNUlROeYtFn:Dfjt3zDybGrdbcbMlCqhYAERF/YlrQGR
TLSHT15AB1ADB76149B113B920874BF42FD86DE422E421BD2B48B05789712D1E397829CAD8A0
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
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