DominantMapper: Rule-based analysis of SNP data for rapid mapping of dominant diseases in related nuclear families
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference12 articles.
1. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees;Abecasis;Nat Genet,2002
2. Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families;Carr;Hum Mutat,2006
3. Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps;Evans;Am J Hum Genet,2004
4. Application of genome-wide single nucleotide polymorphism typing: simple association and beyond;Gibbs;PLOS Genet,2006
5. Allegro, a new computer program for multipoint linkage analysis;Gudbjartsson;Nat Genet,2000
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