| 活動說明 |
In the post-genome era, a wealth of information is now available concerning variations in the human genome, including single nucleotide polymorphisms, rare variants, copy number variations, and gene expressions. In this talk, I will introduce how this information is useful for characterizing the genome itself as well as for applying to medical genomics and population genomics. I will illustrate several practical applications, including genome-wide association study, chromosomal aberration detection, gene-gene interaction analysis, expression quantitative trait locus mapping, characterization of homozygosity disequilibrium, identification of ancestry information marker, and integrative genomic analysis. In addition, statistical methods and user-friendly analysis software developed by us will also be introduced. |
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