Methods of identifying markers of graft rejection

The present invention relates to polynucleotide probes, each comprising two strands that are perfectly complementary. In some embodiments, each of the strands comprises, in the 5'to 3 'direction, a) a first target hybridization sequence, b) a first digital tag sequence, c) a first Halo bar...

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Bibliographic Details
Main Authors KRISHNA KUMAR SURESH, LEE MEELAN, PALSGAARD PETER, MINDRINOS MARK N
Format Patent
LanguageChinese
English
Published 25.07.2023
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Summary:The present invention relates to polynucleotide probes, each comprising two strands that are perfectly complementary. In some embodiments, each of the strands comprises, in the 5'to 3 'direction, a) a first target hybridization sequence, b) a first digital tag sequence, c) a first Halo barcode sequence, d) a first Halo amplification primer sequence, e) a reverse second Halo amplification primer sequence, f) a reverse second Halo barcode sequence, g) a reverse second digital tag sequence, and h) a reverse second target hybridization sequence. The invention also relates to methods of using these novel probes to determine the level of a minor population of DNA in a mixture of DNA from two different sources. 本发明涉及多核苷酸探针,每个多核苷酸探针包含两条完美互补的链。在一些实施方案中,该链中的每一个以5'至3'方向包含,a)第一靶杂交序列,b)第一数字标签序列,c)第一Halo条形码序列,d)第一Halo扩增引物序列,e)反向第二Halo扩增引物序列,f)反向第二Halo条形码序列,g)反向第二数字标签序列,和h)反向第二靶杂交序列。本发明还涉及使用这些新的探针来确定来自两个不同来源的DNA的混合物中DNA次要群体的水平的方法。
Bibliography:Application Number: CN202180058047