High-throughput polymorphism screening and genotyping with high-density oligonucleotide arrays

Ronald J. Sapolsky , Linda Hsie , Anthony Berno , Ghassan Ghandour , Michael Mittmann , Jian-Bing Fan
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引用次数: 91

Abstract

A highly reliable and efficient technology has been developed for high-throughput DNA polymorphism screening and large-scale genotyping. Photolithographic synthesis has been used to generate miniaturized, high-density oligonucleotide arrays. Dedicated instrumentation and software have been developed for array hybridization, fluorescent detection, and data acquisition and analysis. Specific oligonucleotide probe arrays have been designed to rapidly screen human STSs, known genes and full-length cDNAs. This has led to the identification of several thousand biallelic single-nucleotide polymorphisms (SNPs). Meanwhile, a rapid and robust method has been developed for genotyping these SNPs using oligonucleotide arrays. Each allele of an SNP marker is represented on the array by a set of perfect match and mismatch probes. Prototype genotyping chips have been produced to detect 400, 600 and 3000 of these SNPs. Based on the preliminary results, using oligonucleotide arrays to genotype several thousand polymorphic loci simultaneously appears feasible.

高密度寡核苷酸阵列的高通量多态性筛选和基因分型
为高通量DNA多态性筛选和大规模基因分型提供了一种可靠、高效的技术。光刻合成已被用于生成小型化、高密度的寡核苷酸阵列。专用仪器和软件已经开发用于阵列杂交,荧光检测,数据采集和分析。特定的寡核苷酸探针阵列已被设计用于快速筛选人类STSs,已知基因和全长cdna。这导致了数千个双等位基因单核苷酸多态性(SNPs)的鉴定。同时,利用寡核苷酸阵列对这些snp进行快速、可靠的基因分型。SNP标记的每个等位基因在阵列上由一组完全匹配和不匹配探针表示。基因分型芯片的原型已经生产出来,可以检测其中的400,600和3000个snp。基于初步结果,利用寡核苷酸阵列同时对数千个多态性位点进行基因分型似乎是可行的。
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