BCH 606 Advances in genomics and bioinformatics

Human molecular genetics, whole genome alignment, next generation sequencing data, comparative genomics, phylogenetic, biological database, system biology, simple Mendelian diseases, complex diseases, functional genomics, population genetics, epigenetics, SNPs, copy number and structural variations, personal and clinical genomics, cancer genomics. Metagenomics and metatranscriptomics.