Eskin E - Search Results

1

A machine learning algorithm to increase COVID-19 inpatient diagnostic capacity.

Goodman-Meza D, Rudas A, Chiang JN, Adamson PC, Ebinger J, Sun N, Botting P, Fulcher JA, Saab FG, Brook R, Eskin E, An U, Kordi M, Jew B, Balliu B, Chen Z, Hill BL, Rahmani E, Halperin E, Manuel V. Goodman-Meza D, et al. Among authors: eskin e. PLoS One. 2020 Sep 22;15(9):e0239474. doi: 10.1371/journal.pone.0239474. eCollection 2020. PLoS One. 2020. PMID: 32960917 Free PMC article.

2

Haplotype reconstruction from genotype data using Imperfect Phylogeny.

Halperin E, Eskin E. Halperin E, et al. Among authors: eskin e. Bioinformatics. 2004 Aug 12;20(12):1842-9. doi: 10.1093/bioinformatics/bth149. Epub 2004 Feb 26. Bioinformatics. 2004. PMID: 14988101

3

Efficient reconstruction of haplotype structure via perfect phylogeny.

Eskin E, Halperin E, Karp RM. Eskin E, et al. J Bioinform Comput Biol. 2003 Apr;1(1):1-20. doi: 10.1142/s0219720003000174. J Bioinform Comput Biol. 2003. PMID: 15290779

4

A note on phasing long genomic regions using local haplotype predictions.

Eskin E, Sharan R, Halperin E. Eskin E, et al. J Bioinform Comput Biol. 2006 Jun;4(3):639-47. doi: 10.1142/s0219720006002272. J Bioinform Comput Biol. 2006. PMID: 16960967 Free article.

5

Leveraging the HapMap correlation structure in association studies.

Zaitlen N, Kang HM, Eskin E, Halperin E. Zaitlen N, et al. Among authors: eskin e. Am J Hum Genet. 2007 Apr;80(4):683-91. doi: 10.1086/513109. Epub 2007 Mar 2. Am J Hum Genet. 2007. PMID: 17357074 Free PMC article.

6

Genotyping common and rare variation using overlapping pool sequencing.

He D, Zaitlen N, Pasaniuc B, Eskin E, Halperin E. He D, et al. Among authors: eskin e. BMC Bioinformatics. 2011;12 Suppl 6(Suppl 6):S2. doi: 10.1186/1471-2105-12-S6-S2. Epub 2011 Jul 28. BMC Bioinformatics. 2011. PMID: 21989232 Free PMC article.

7

A model-based approach for analysis of spatial structure in genetic data.

Yang WY, Novembre J, Eskin E, Halperin E. Yang WY, et al. Among authors: eskin e. Nat Genet. 2012 May 20;44(6):725-31. doi: 10.1038/ng.2285. Nat Genet. 2012. PMID: 22610118 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

Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies.

Rahmani E, Zaitlen N, Baran Y, Eng C, Hu D, Galanter J, Oh S, Burchard EG, Eskin E, Zou J, Halperin E. Rahmani E, et al. Among authors: eskin e. Nat Methods. 2016 May;13(5):443-5. doi: 10.1038/nmeth.3809. Epub 2016 Mar 28. Nat Methods. 2016. PMID: 27018579 Free PMC article.

10

Correcting for cell-type heterogeneity in DNA methylation: a comprehensive evaluation.

Rahmani E, Zaitlen N, Baran Y, Eng C, Hu D, Galanter J, Oh S, Burchard EG, Eskin E, Zou J, Halperin E. Rahmani E, et al. Among authors: eskin e. Nat Methods. 2017 Feb 28;14(3):218-219. doi: 10.1038/nmeth.4190. Nat Methods. 2017. PMID: 28245214 Free PMC article. No abstract available.

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