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Accessing genetic information with high-density DNA arrays.
Chee M, Yang R, Hubbell E, Berno A, Huang XC, Stern D, Winkler J, Lockhart DJ, Morris MS, Fodor SP. Chee M, et al. Science. 1996 Oct 25;274(5287):610-4. doi: 10.1126/science.274.5287.610. Science. 1996. PMID: 8849452
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.
Wang DG, Fan JB, Siao CJ, Berno A, Young P, Sapolsky R, Ghandour G, Perkins N, Winchester E, Spencer J, Kruglyak L, Stein L, Hsie L, Topaloglou T, Hubbell E, Robinson E, Mittmann M, Morris MS, Shen N, Kilburn D, Rioux J, Nusbaum C, Rozen S, Hudson TJ, Lipshutz R, Chee M, Lander ES. Wang DG, et al. Among authors: chee m. Science. 1998 May 15;280(5366):1077-82. doi: 10.1126/science.280.5366.1077. Science. 1998. PMID: 9582121
Mutation detection by ligation to complete n-mer DNA arrays.
Gunderson KL, Huang XC, Morris MS, Lipshutz RJ, Lockhart DJ, Chee MS. Gunderson KL, et al. Among authors: chee ms. Genome Res. 1998 Nov;8(11):1142-53. doi: 10.1101/gr.8.11.1142. Genome Res. 1998. PMID: 9847078 Free article.
A highly informative SNP linkage panel for human genetic studies.
Murray SS, Oliphant A, Shen R, McBride C, Steeke RJ, Shannon SG, Rubano T, Kermani BG, Fan JB, Chee MS, Hansen MS. Murray SS, et al. Nat Methods. 2004 Nov;1(2):113-7. doi: 10.1038/nmeth712. Epub 2004 Oct 21. Nat Methods. 2004. PMID: 15782173
498 results