Dr. Fann, Cathy S.-J.
Research Fellow
- 02-27899144 (Lab) (Room No: 100)
- 02-27823047 (Fax)
-
Specialty:
- Genetic Statistics
- Genetic Epidemiology
Education and Positions:
Division of Biostatistics, Department of Preventive Medicine and Environmental Health,
Ph.D. University of Iowa, Iowa City, Iowa, US
Highlight Detail
Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
Dr. Fann, Cathy S.-J.
Hum Mutat., May 09, 2008Copy number variation (CNV) has become an important genomic structure element in the human population, and some CNVs are related to specific traits and diseases. Moreover, analysis of human genomes has been potentiated by the use of high-resolution microarrays that assess single nucleotide polymorphisms (SNPs).