The Center for Public Health Genomics is focused on the application of NextGen sequencing (NGS) on issues of public health importance. In particular, its aims are to develop methods to:
- Enhance the detection, diagnosis and tracking of bacterial, viral and fungal disease outbreaks.
- Improve the detection of drug-resistant variants and identification of new agents of disease.
- Enable the characterization and differentiation of organisms at a level not possible with existing technologies.
- Develop screening and confirmatory tests for genetic disorders of newborns that would not be possible with established methods.
- Provide the rapid monitoring and response to public health emergencies that only an on-site, dedicated facility can provide.
- Provide essential expertise for validation of consumer point-of-service genetic testing, proficiency testing and regulation of NGS laboratory testing.
Associated Researchers
Michele Caggana, Sc.D., FACMG
Deputy Director, Division of Genetics
Alexander T. Ciota, Ph.D.
Director, Arbovirus Laboratory
We study arbovirus adaptation and vector-virus interactions, focusing on West Nile virus and Culex mosquitoes. Areas of interest include mutant swarm dynamics, mechanisms of adaptation, microbial interactions and vectorial capacity.
Christina Egan, Ph.D.
Chief, Biodefense and Mycology Laboratories
We focus on the development and validation of assays to detect pathogens and toxins associated with bioterrorism or food-borne disease. We utilize methods such as real-time PCR, whole genome sequencing, and mass spectrometry for rapid detection of agents.
Vincent Escuyer, Ph.D.
Director, Mycobacteriology Laboratory
Todd Gray, Ph.D.
Molecular Genetics of Mycobacteria
We use innovative molecular genomic approaches to address fundamental questions of mycobacterial biology. Our findings shed new light on the evolution and function of mycobacterial genomes, accelerating tuberculosis research.
Bruce J. Herron, Ph.D.
Mammalian Genomics
We utilize an array of mammalian genomic tools to discover genetic modifiers that influence multifactorial diseases. These susceptibility loci are targets for diagnosis and treatment of similar disorders in humans.
Denise M. Kay, Ph.D.
Newborn Screening Program
We use targeted and genome-wide approaches to identify and characterize mutations/genes involved in diseases affecting children, including conditions screened by the NYS newborn screening program and birth defects.
Pascal Lapierre, Ph.D.
Bioinformatics and Statistics Core
Kimberlee A. Musser, Ph.D.
Clinical Director, Wadsworth Center David Axelrod Institute
We develop molecular diagnostic assays and reference testing for the detection and characterization of pathogenic bacteria and mycobacteria and to predict antibiotic resistance using real-time PCR and whole genome sequencing.
Kirsten St. George, Ph.D.
Chief, Laboratory of Viral Diseases
We develop viral detection and characterization assays and investigate new molecular chemistries and platforms. Research includes rhinovirus infection in transplant recipients, drug-resistant influenza and adenovirus evolution.
Joseph T. Wade, Ph.D.
Microbial Gene Expression
We study gene regulation in bacteria, with a focus on genome-scale approaches. We are interested in regulation of transcription, the function of non-coding RNAs, and leaderless translation initiation.
Keith M. Derbyshire, Ph.D.
Associate Director for Research and Technology
We study mycobacteria and use molecular genetic approaches to investigate: global gene expression, at both transcriptional and translational levels; the mechanism of distributive conjugal transfer; and synthetic genetic interactions.