Eskin E - Search Results

1

Privacy preserving protocol for detecting genetic relatives using rare variants.

Hormozdiari F, Joo JW, Wadia A, Guan F, Ostrosky R, Sahai A, Eskin E. Hormozdiari F, et al. Among authors: eskin e. Bioinformatics. 2014 Jun 15;30(12):i204-11. doi: 10.1093/bioinformatics/btu294. Bioinformatics. 2014. PMID: 24931985 Free PMC article.

2

Optimal algorithms for haplotype assembly from whole-genome sequence data.

He D, Choi A, Pipatsrisawat K, Darwiche A, Eskin E. He D, et al. Among authors: eskin e. Bioinformatics. 2010 Jun 15;26(12):i183-90. doi: 10.1093/bioinformatics/btq215. Bioinformatics. 2010. PMID: 20529904 Free PMC article.

3

An optimal weighted aggregated association test for identification of rare variants involved in common diseases.

Sul JH, Han B, He D, Eskin E. Sul JH, et al. Among authors: eskin e. Genetics. 2011 May;188(1):181-8. doi: 10.1534/genetics.110.125070. Epub 2011 Mar 2. Genetics. 2011. PMID: 21368279 Free PMC article.

4

Efficient algorithms for tandem copy number variation reconstruction in repeat-rich regions.

He D, Hormozdiari F, Furlotte N, Eskin E. He D, et al. Among authors: eskin e. Bioinformatics. 2011 Jun 1;27(11):1513-20. doi: 10.1093/bioinformatics/btr169. Epub 2011 Apr 19. Bioinformatics. 2011. PMID: 21505028 Free PMC article.

5

Assembly of non-unique insertion content using next-generation sequencing.

Parrish N, Hormozdiari F, Eskin E. Parrish N, et al. Among authors: eskin e. BMC Bioinformatics. 2011;12 Suppl 6(Suppl 6):S3. doi: 10.1186/1471-2105-12-S6-S3. Epub 2011 Jul 28. BMC Bioinformatics. 2011. PMID: 21989261 Free PMC article.

6

Incorporating prior information into association studies.

Darnell G, Duong D, Han B, Eskin E. Darnell G, et al. Among authors: eskin e. Bioinformatics. 2012 Jun 15;28(12):i147-53. doi: 10.1093/bioinformatics/bts235. Bioinformatics. 2012. PMID: 22689754 Free PMC article.

7

Limited RNA editing in exons of mouse liver and adipose.

Lagarrigue S, Hormozdiari F, Martin LJ, Lecerf F, Hasin Y, Rau C, Hagopian R, Xiao Y, Yan J, Drake TA, Ghazalpour A, Eskin E, Lusis AJ. Lagarrigue S, et al. Among authors: eskin e. Genetics. 2013 Apr;193(4):1107-15. doi: 10.1534/genetics.112.149054. Epub 2013 Feb 14. Genetics. 2013. PMID: 23410828 Free PMC article.

8

CNVeM: copy number variation detection using uncertainty of read mapping.

Wang Z, Hormozdiari F, Yang WY, Halperin E, Eskin E. Wang Z, et al. Among authors: eskin e. J Comput Biol. 2013 Mar;20(3):224-36. doi: 10.1089/cmb.2012.0258. Epub 2013 Feb 19. J Comput Biol. 2013. PMID: 23421794 Free PMC article.

9

Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data.

Yang WY, Hormozdiari F, Wang Z, He D, Pasaniuc B, Eskin E. Yang WY, et al. Among authors: eskin e. Bioinformatics. 2013 Sep 15;29(18):2245-52. doi: 10.1093/bioinformatics/btt386. Epub 2013 Jul 3. Bioinformatics. 2013. PMID: 23825370 Free PMC article.

10

eALPS: estimating abundance levels in pooled sequencing using available genotyping data.

Eskin I, Hormozdiari F, Conde L, Riby J, Skibola CF, Eskin E, Halperin E. Eskin I, et al. Among authors: eskin e. J Comput Biol. 2013 Nov;20(11):861-77. doi: 10.1089/cmb.2013.0105. Epub 2013 Oct 21. J Comput Biol. 2013. PMID: 24144111 Free PMC article.

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