Discovering Novel Biofuels Using Machine Learning Software BioCompoundML
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2018 International Conference on Computing, Networking and Communications, ICNC 2018
In many organizations, intrusion detection and other related systems are tuned to generate security alerts, which are then manually inspected by cyber-security analysts. These analysts often devote a large portion of time to inspecting these alerts, most of which are innocuous. Thus, it would be greatly beneficial to reduce the number of innocuous alerts, allowing analysts to utilize their time and skills for other aspects of cyber defense. In this work, we devise several simple, fast, and easily understood models to cut back this manual inspection workload, while maintaining high true positive and true negative rates. We demonstrate their effectiveness on real data, and discuss their potential utility in application by others.
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Nucleic Acids Research
Virulence genes on mobile DNAs such as genomic islands (GIs) and plasmids promote bacterial pathogen emergence. Excision is an early step in GI mobilization, producing a circular GI and a deletion site in the chromosome; circular forms are also known for some bacterial insertion sequences (ISs). The recombinant sequence at the junctions of such circles and deletions can be detected sensitively in high-throughput sequencing data, using new computational methods that enable empirical discovery of mobile DNAs. For the rich mobilome of a hospital Klebsiella pneumoniae strain, circularization junctions (CJs) were detected for six GIs and seven IS types. Our methods revealed differential biology of multiple mobile DNAs, imprecision of integrases and transposases, and differential activity among identical IS copies for IS26, ISKpn18 and ISKpn21. Using the resistance of circular dsDNA molecules to exonuclease, internally calibrated with the native plasmids, showed that not all molecules bearing GI CJs were circular. Transpositions were also detected, revealing replicon preference (ISKpn18 prefers a conjugative IncA/C2 plasmid), local action (IS26), regional preferences, selection (against capsule synthesis) and IS polarity inversion. Efficient discovery and global characterization of numerous mobile elements per experiment improves accounting for the new gene combinations that arise in emerging pathogens.
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