Publications

Found 7 results
Author Title Type [ Year(Desc)]
Filters: Author is Noah Zaitlen  [Clear All Filters]
2005
Zaitlen, N., Kang H. Min, Feolo M. L., Sherry S. T., Halperin E., & Eskin E. (2005).  Inference and Analysis of Haplotypes from Combined Genotyping Studies Deposited in dbSNP. Genome Research. 15(11), 1594-1600.
2007
Zaitlen, N., Kang H. Min, Eskin E., & Halperin E. (2007).  Leveraging the HapMap Correlation Structure in Association Studies. American Journal of Human Genetics. 80, 683-691.
2010
Pasaniuc, B., Zaitlen N., & Halperin E. (2010).  Accurate Estimation of Expression Levels of Homologous Genes in RNA-Seq Experiments. 397-409.
Zaitlen, N., Pasaniuc B., Gur T., Ziv E., & Halperin E. (2010).  Leveraging Genetic Variability Across Populations for the Identification of Causal Variants. The American Journal of Human Genetics. 86(1), 23-33.
2011
Pasaniuc, B., Zaitlen N., & Halperin E. (2011).  Accurate Estimation of Expression Levels of Homologous Genes in RNA-Seq Experiments. 18(3), 459-468.
He, D., Zaitlen N., Pasaniuc B., Eskin E., & Halperin E. (2011).  Genotyping Common and Rare Variation Using Overlapping Pool Sequencing. BMC Informatics. 12,
He, D., Zaitlen N., Pasaniuc B., Eskin E., & Halperin E. (2011).  Genotyping Common and Rare Variation Using Overlapping Pool Sequencing. Proceedings of the First Annual RECOMB Satellite Workshop on Massively Parallel Sequencing (RECOMB-seq). 26-27.