Presented by Dr. Lianrong Pu (Tel Aviv University) High-throughput sequencing techniques generate large volumes of DNA sequencing data at ultra-fast speed and extremely low cost. To handle the large datasets produced by these techniques, efficient data structures and algorithms are necessary and have been developed in recent decades. How to analyse these deep sequencing data by using graph algorithms and machine learning methods will be introduced. Specifically, a three-way classifier for metagenome assemblies will be the focus. Viruses and plasmids are part of microbial communities and play a major role in disease and in antibiotic resistance. In metagenome sequence assembly, identifying virus and plasmid contigs is a hard task, since they tend to form shorter contigs and are overwhelmed by a larger mass of bacterial contigs. 3CAC is a new classifier that builds on machine learning based classifiers and exploits the structure of assembly graph for the classification of contigs into bacterial, viral, plasmidic, and unknown contigs. In simulated and real metagenomes of short and long reads, 3CAC outperformed the state-of-the-art algorithms.