FamLBL 1.0 – Detecting Rare Haplotype Disease Association Based on Common SNPs Using Case-Parent Triads

FamLBL 1.0

:: DESCRIPTION

famLBL (family-triad-based logistic Bayesian Lasso) is an R package for estimating effects of haplotypes on complex diseases using SNP data.

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::DEVELOPER

Statistical Genetics and Bioinformatics Group

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

 FamLBL

:: MORE INFORMATION

Citation

Bioinformatics. 2014 May 21. pii: btu347. [Epub ahead of print]
FamLBL: Detecting Rare Haplotype Disease Association Based on Common SNPs Using Case-Parent Triads.
Wang M1, Lin S2.