Result for 01C686B538DAB1447EE47DF4899D3DF1E83FAE16

Query result

Key Value
FileName./usr/lib64/R/library/qtl/Meta/package.rds
FileSize1131
MD561A35B028A7CFA9FCF0E3ACEE371F349
SHA-101C686B538DAB1447EE47DF4899D3DF1E83FAE16
SHA-256727C5118BDAD47B980F9DC98E8C9A08AAC74894ACFE40F89FF338FBBBA30F60A
SSDEEP24:XvFJKpXLW4XOAOfyig3d3RVdyVlpkxmTJg1QuTKUlcb4rPmn8OsQRfWhXPa1:Xix2AOfyJN3Rry7FNg2eKUlcB80RuhXM
TLSHT1A021F6B32E8C10179B2A13A22AFB421BA0CB89B756D3680C4DC812C085621A5A4DCA35
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
MD5B639DFFE61E1BA6AA9050B098A25F638
PackageArchx86_64
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.el8
PackageVersion1.46.2
SHA-10328667C94A7E2301C3B51FE383929AAA7246045
SHA-2561BB737356F4E368E1A83ACBDA7A76A47119BB47F30210903C2F44537DB537D02