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METHODS OF ASSESSING EPIGENETIC REGULATION OF GENOME FUNCTION VIA DNA METHYLATION STATUS AND SYSTEMS AND KITS THEREFOR

机译:通过DNA甲基化状态,系统及其套件评估基因组功能的抗原调控的方法。

摘要

Systems, kits and methods are disclosed for assessing epigenetic regulation of genome function via deoxyribonucleic acid (DNA) methylation status. The systems, kits and methods rely on a covert then capture concept in which unmethylated cytosine residues in a nucleic acid sequence are first converted to uracil residues and then captured for subsequent analysis. The systems, kits and method use a solution-phase capture probe pool having a mixture of at least three (3) types of capture probes. One type is “wobble” probes, in which some cytosine residues in a nucleic acid sequence are randomly assumed to be unmethylated and thus converted to uracil residues, while other cytosine residues are assumed to be methylated and thus conserved as cytosine residues. Moreover, each type of probe can include a mixture of probes that bind/hybridize to one or the other strand of a nucleic acid sequence of interest, thereby improving sequencing depth and reliability.
机译:公开了用于通过脱氧核糖核酸(DNA)甲基化状态评估基因组功能的表观遗传调控的系统,试剂盒和方法。该系统,试剂盒和方法依赖于隐蔽然后捕获的概念,其中核酸序列中未甲基化的胞嘧啶残基首先被转化为尿嘧啶残基,然后被捕获用于后续分析。该系统,试剂盒和方法使用具有至少三(3)种类型的捕获探针的混合物的溶液相捕获探针池。一种类型是“摆动”探针,其中核酸序列中的一些胞嘧啶残基被随机假定为未甲基化并因此转化为尿嘧啶残基,而其他胞嘧啶残基被假定为甲基化并因此保守为胞嘧啶残基。此外,每种类型的探针可包括与目标核酸序列的一条或另一条链结合/杂交的探针混合物,从而改善测序深度和可靠性。

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