Ch. 1: Introduction -- Ch. 2: Concepts of genetic epidemiology -- Ch. 3: Integration of linkage analysis and next-generation sequencing data -- Ch. 4: From family study to population study: a history of genetic mapping for nasopharyngeal carcinoma (NPC) -- Ch. 5: QTL mapping of molecular traits for studies of human complex diseases -- Ch. 6: Renewed interest in haplotype: from genetic marker to gene prediction -- Ch. 7: Analytical approaches for exome sequence data -- Ch. 8: Rare variants analysis in unrelated individuals -- Ch. 9: Gene duplication and functional consequences -- Ch. 10: From GWAS to next-generation sequencing on human complex diseases: the implications for translational medicine and therapeutics.
Electronic reproduction. Perth, W.A. Available via World Wide Web.