Publications

Found 17 results
Author Title Type [ Year(Desc)]
Filters: Author is Eleazar Eskin  [Clear All Filters]
2002
Eskin, E., Halperin E., & Karp R. M. (2002).  Large-Scale Reconstruction of Haplotype Structure via Perfect Phylogeny.
Halperin, E., & Eskin E. (2002).  Large-Scale Recovery of Haplotypes from Genotype Data Using Imperfect Phylogeny.
2003
Eskin, E., Halperin E., & Karp R. M. (2003).  Efficient Reconstruction of Haplotype Structure Via Perfect Phylogeny. Journal of Bioinformatics and Computational Biology. 1(1), 1-20.
Eskin, E., Halperin E., & Karp R. M. (2003).  Large Scale Reconstruction of Haplotypes from Genotype Data. Proceedings of the Seventh Conference on Research in Computational Biology (RECOMB).
2004
Halperin, E., & Eskin E. (2004).  Haplotype Reconstruction from Genotype Data Using Imperfect Phylogeny. Bioinformatics.
Eskin, E., Halperin E., & Sharan R. (2004).  Optimally Phasing Long Genomic Regions using Local Haplotype Predictions. Proceedings of the Second RECOMB Satellite Workshop on Computational Methods for SNPs and Haplotypes. 13-16.
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.
Hinds, D.. A., Stuve L.. L., Nilsen G.. B., Halperin E., Eskin E., Ballinger D.. G., et al. (2005).  Whole-Genome Patterns of Common DNA Variation in Three Human Populations. Science. 307(5712), 1072-1079.
2006
Marchini, J., Cutler D., Patterson N., Stephens M., Eskin E., Halperin E., et al. (2006).  A Comparison of Phasing Algorithms for Trios and Unrelated Individuals. American Journal of Human Genetics. 78(3), 437-450.
Eskin, E., Halperin E., & Sharan R. (2006).  A Note on Optimally Phasing Long Genomic Regions Using Local Haplotype Predictions. Journal of Bioinformatics and Computational Biology. 4(3), 639-647.
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.
2011
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.
He, D., Zaitlen N., Pasaniuc B., Eskin E., & Halperin E. (2011).  Genotyping Common and Rare Variation Using Overlapping Pool Sequencing. BMC Informatics. 12,
2012
Wang, Z., Hormozdiari F., Yang W-Y., Halperin E., & Eskin E. (2012).  CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping. 326-340.
Yang, W-Y., Novembre J., Eskin E., & Halperin E. (2012).  A Model-Based Approach for Analysis of Spatial Structure in Genetic Data.
Yang, W-Y., Novembre J., Eskin E., & Halperin E. (2012).  A Model-Based Approach for Analysis of Spatial Structure in Genetic Data. Nature Genetics. 44, 725-731.
Yang, W-Y., Novembre J., Eskin E., & Halperin E. (2012).  A Model-Based Approach for Analysis of Spatial Structure in Genetic Data. Nature Genetics. 44, 725-731.