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    • 5. 发明授权
    • Combined CGH and allele specific hybridisation method
    • 组合CGH和等位基因特异性杂交方法
    • US09587278B2
    • 2017-03-07
    • US13520935
    • 2011-01-07
    • Douglas HurdEdwin Southern
    • Douglas HurdEdwin Southern
    • C12Q1/68
    • G06F19/20C12Q1/6837C12Q1/6883C12Q1/6886C12Q2600/156C12Q2600/172C12Q2525/151C12Q2535/131C12Q2537/16C12Q2539/115C12Q2565/513
    • The invention combines the fields of comparative genomic hybridization (CGH) analysis and SNP array analysis. It relates to methods for detecting and mapping genetic abnormalities associated with various diseases. In particular the invention provides a method for simultaneously performing array CGH and SNP array analysis on a genomic DNA sample comprising contacting a nucleic acid array which comprises a first probe set and a second probe set with a genomic DNA sample, comprising a test and reference sample, under hybridization conditions, comparing the amount of test sample and reference sample hybridized to the hybridization probes of the first probe set, comparing the amount of test sample and reference sample hybridized to the hybridization probes of the second probe set; and using the data obtained to determine the copy number of at least one locus; and at least one SNP in the genomic DNA sample.
    • 本发明结合了比较基因组杂交(CGH)分析和SNP阵列分析的领域。 它涉及检测和绘制与各种疾病相关的遗传异常的方法。 特别地,本发明提供了一种用于在基因组DNA样品上同时进行阵列CGH和SNP阵列分析的方法,包括使包含第一探针组和第二探针组的核酸阵列与基因组DNA样品接触,所述核酸阵列包含测试和参考样品 在杂交条件下,比较与第一探针组的杂交探针杂交的测试样品和参考样品的量,比较与第二探针组的杂交探针杂交的测试样品和参考样品的量; 并使用获得的数据来确定至少一个轨迹的拷贝数; 和基因组DNA样品中的至少一个SNP。