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Comparative genomic resequencing

机译:比较基因组重测序

摘要

The present invention is an improved method of resequencing DNA using microarrays to rapidly map and identify SNPs, deletions and amplification events present in the genome of an organism. The method is performed by hybridizing a reference and a test genome to two separate arrays with each array exhibiting a specific intensity pattern. The intensity differences between the reference and the test genome arrays are used to produce a mutation map. The mapped differences are resequenced on a set of resequencing arrays to identify specific genetic mutations.
机译:本发明是使用微阵列来快速定位和鉴定生物体基因组中存在的SNP,缺失和扩增事件的DNA重测序的改进方法。通过将参照物和测试基因组杂交到两个单独的阵列上来执行该方法,每个阵列均表现出特定的强度模式。参考和测试基因组阵列之间的强度差异用于产生突变图。在一组重测序阵列上对映射的差异进行重测序,以鉴定特定的基因突变。

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