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Postdoctoral Fellow for ongoing research in the area of cancer risk. Specifically, the study focuses on the identification of single nucleotide and structural polymorphisms associated with increased risk of developing the disease and on the association between germline variants and somatic aberrations. Genome-wide data are being generated using latest technology on a large collection of individuals within an international collaboration.
Requirements The candidate should have strong interest in genetics, biology, and quantitative data analysis. A candidate should be enthusiastic, accurate, flexible and able to work in team setting. Expertise in programming, statistical analysis, and computational genetics/genomics is required. Experience of work with large data sets, and familiarity with Linux environment is recommended. Candidates must have a Ph.D. in human genetics, natural sciences, mathematics, physics, bioinformatics or related fields.
Contact Information
Interested candidates should send a curriculum vitae and brief summary of research experience to:
Francesca Demichelis, Ph.D.
Department of Pathology and Laboratory Medicine
Institute for Computational Biomedicine
Weill Cornell Medical Center
1305 York Avenue, Room Y-1307, Box 140
New York, NY 10065
frd2004@med.cornell.edu |