
Abstract
In this talk, we discuss some of the advantages of modern sequencing technologies including standard short-read and long-read sequencing technologies with applications to genome re-sequencing and variation discovery. We discuss the ability of these technologies in calling variants including structural variants in repeat regions of the genome. We also discuss potentials of short-read and long-read technologies in applications such as metagenomics and quantifying cancer evolution.
About the presenter
Iman Hajirasouliha
Associate Professor of Computational GenomicsWeill Cornell Medicine
