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Journal Abstract Search
305 related items for PubMed ID: 17608949
1. Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation. Macconaill LE, Aldred MA, Lu X, Laframboise T. BMC Genomics; 2007 Jul 03; 8():211. PubMed ID: 17608949 [Abstract] [Full Text] [Related]
9. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, Hangaishi A, Kurokawa M, Chiba S, Bailey DK, Kennedy GC, Ogawa S. Cancer Res; 2005 Jul 15; 65(14):6071-9. PubMed ID: 16024607 [Abstract] [Full Text] [Related]
11. Computational identification of candidate loci for recessively inherited mutation using high-throughput SNP arrays. Laakso M, Tuupanen S, Karhu A, Lehtonen R, Aaltonen LA, Hautaniemi S. Bioinformatics; 2007 Aug 01; 23(15):1952-61. PubMed ID: 17510170 [Abstract] [Full Text] [Related]
12. SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery. Bell PA, Chaturvedi S, Gelfand CA, Huang CY, Kochersperger M, Kopla R, Modica F, Pohl M, Varde S, Zhao R, Zhao X, Boyce-Jacino MT, Yassen A. Biotechniques; 2002 Jun 01; Suppl():70-2, 74, 76-7. PubMed ID: 12083401 [Abstract] [Full Text] [Related]
19. Triallelic single nucleotide polymorphisms and genotyping error in genetic epidemiology studies: MDR1 (ABCB1) G2677/T/A as an example. Hüebner C, Petermann I, Browning BL, Shelling AN, Ferguson LR. Cancer Epidemiol Biomarkers Prev; 2007 Jun 21; 16(6):1185-92. PubMed ID: 17548683 [Abstract] [Full Text] [Related]
20. Detection of copy number variation using SNP genotyping. Cooper GM, Mefford HC. Methods Mol Biol; 2011 Jun 21; 767():243-52. PubMed ID: 21822880 [Abstract] [Full Text] [Related] Page: [Next] [New Search]