SNPduo

SNPduo Publications

Reference:

Roberson EDO and Pevsner J. Visualization of Shared Genomic Regions and Meiotic Recombination in High-Density SNP Data Plos One, 2009 Aug 21;4:8. PMID: 19696932


Publications Citing SNPduo:

Ting JC, Roberson ED, Currier DG, Pevsner J. Locations and patterns of meiotic recombination in two-generation pedigrees. BMC Med Genet. 2009 Sep 17;10:93. PMID: 19761602

Goh L, Chen GB, Cutcutache I, Low B, Teh BT, Rozen S, Tan P. Assessing matched normal and tumor pairs in next-generation sequencing studies. PLoS One. 2011 Mar 18;6(3):e17810. PMID: 21445261

Lee YS, Chao A, Chen CH, Chou T, Wang SY, Wang TH. Analysis of human meiotic recombination events with a parent-sibling tracing approach. BMC Genomics. 2011 Aug 26;12:434. PMID: 21867557

Stevens EL, Heckenberg G, Roberson ED, Baugher JD, Downey TJ, Pevsner J. Inference of relationships in population data using identity-by-descent and identity-by-state. PLoS Genet. 2011 Sep;7(9):e1002287. PMID: 21966277

Stevens EL, Heckenberg G, Baugher JD, Roberson ED, Downey TJ, Pevsner J. Consanguinity in Centre d'Étude du Polymorphisme Humain (CEPH) pedigrees.Eur J Hum Genet. 2012 Jun;20(6):657-67. Epub 2012 Jan 25. PMID: 22274586

Calvo SE, Compton AG, Hershman SG, Lim SC, Lieber DS, Tucker EJ, Laskowski A, Garone C, Liu S, Jaffe DB, Christodoulou J, Fletcher JM, Bruno DL, Goldblatt J, Dimauro S, Thorburn DR, Mootha VK. Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. Sci Transl Med. 2012 Jan 25;4(118):118ra10. PMID: 22277967

Shirley MD, Baugher JD, Stevens EL, Tang Z, Gerry N, Beiswanger CM, Berlin DS, Pevsner J. Chromosomal variation in lymphoblastoid cell lines. Hum Mutat. 2012 Jul;33(7):1075-86. PMID: 22374857

Srebniak MI, Boter M, Oudesluijs GO, Cohen-Overbeek T, Govaerts LC, Diderich KE, Oegema R, Knapen MF, van de Laar IM, Joosten M, Van Opstal D, Galjaard RJ. Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities. Mol Cytogenet. 2012 Mar 13;5(1):14. PMID: 22413963

Harteveld CL, Refaldi C, Giambona A, Ruivenkamp CA, Hoffer MJ, Pijpe J, De Knijff P, Borgna-Pignatti C, Maggio A, Cappellini MD, Giordano PC. Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major. Haematologica. 2013 May;98(5):691-5. Epub 2012 Sep 14. PMID: 22983591

Stevens EL, Baugher JD, Shirley MD, Frelin LP, Pevsner J. Unexpected relationships and inbreeding in HapMap phase III populations. PLoS One. 2012;7(11):e49575. PMID: 23185369