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1.发明申请Methods and kits for selectively amplifying, detecting or quantifying target DNA with specific end sequences 有权用于选择性扩增，检测或定量具有特定末端序列的靶DNA的方法和试剂盒公开(公告)号：US20090061425A1
公开(公告)日：2009-03-05
申请号：US11897654
申请日：2007-08-30
CPC分类号： C12Q1/686 , C12Q2525/301 , C12Q2521/331
摘要： Disclosed herein are methods and kits for selectively amplifying, detecting or quantifying a DNA fragment with a specific end sequence, especially generated following restriction enzyme digestion. This method can be used, for example, to detect a hypomethylated DNA fragment. This methods and kits are especially useful in detecting or quantifying a hypomethylated fetal DNA fragment in a maternal plasma sample containing a corresponding hypermethylated maternal DNA fragment.
摘要翻译： 本文公开了用于选择性扩增，检测或定量具有特异末端序列的DNA片段的方法和试剂盒，特别是在限制酶消化后产生。 该方法可用于例如检测低甲基化DNA片段。 该方法和试剂盒特别可用于检测或定量含有相应的高甲基化母体DNA片段的母体血浆样品中的低甲基化胎儿DNA片段。
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2.发明授权Methods and kits for selectively amplifying, detecting or quantifying target DNA with specific end sequences 有权用于选择性扩增，检测或定量具有特定末端序列的靶DNA的方法和试剂盒公开(公告)号：US08748100B2
公开(公告)日：2014-06-10
申请号：US11897654
申请日：2007-08-30
CPC分类号： C12Q1/686 , C12Q2525/301 , C12Q2521/331
摘要： Disclosed herein are methods and kits for selectively amplifying, detecting or quantifying a DNA fragment with a specific end sequence, especially generated following restriction enzyme digestion. This method can be used, for example, to detect a hypomethylated DNA fragment. This methods and kits are especially useful in detecting or quantifying a hypomethylated fetal DNA fragment in a maternal plasma sample containing a corresponding hypermethylated maternal DNA fragment.
摘要翻译： 本文公开了用于选择性扩增，检测或定量具有特异末端序列的DNA片段的方法和试剂盒，特别是在限制酶消化后产生。 该方法可用于例如检测低甲基化DNA片段。 该方法和试剂盒特别可用于检测或定量含有相应的高甲基化母体DNA片段的母体血浆样品中的低甲基化胎儿DNA片段。
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公开(公告)号：US08563242B2
公开(公告)日：2013-10-22
申请号：US12833460
申请日：2010-07-09
申请人： Yuk Ming Dennis Lo , Rossa Wai Kwun Chiu , Yu Kwan Tong , Shengnan Jin , Siu Chung Stephen Chim , Wai Yi Tsui
发明人： Yuk Ming Dennis Lo , Rossa Wai Kwun Chiu , Yu Kwan Tong , Shengnan Jin , Siu Chung Stephen Chim , Wai Yi Tsui
CPC分类号： C12Q1/6827 , C12Q2523/125
摘要： The present invention relates to a new, non-invasive method for detecting chromosomal aneuploidy by analyzing a sample from a pregnant woman. The detection is based on the ratio between the amount of a fetal methylation marker located on a chromosome relevant to the aneuploidy and the amount of a fetal genetic marker located on a reference chromosome, offering improved accuracy.
摘要翻译： 本发明涉及通过分析来自孕妇的样品来检测染色体非整倍体的新的非侵入性方法。 检测是基于位于与非整倍性相关的染色体上的胎儿甲基化标记的量与位于参考染色体上的胎儿遗传标记的量之间的比例，提供更高的准确度。
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公开(公告)号：US20110039724A1
公开(公告)日：2011-02-17
申请号：US12833460
申请日：2010-07-09
申请人： Yuk Ming Dennis Lo , Rossa Wai Kwun Chiu , Yu Kwan Tong , Shengnan Jin , Siu Chung Stephen Chim , Wai Yi Tsui
发明人： Yuk Ming Dennis Lo , Rossa Wai Kwun Chiu , Yu Kwan Tong , Shengnan Jin , Siu Chung Stephen Chim , Wai Yi Tsui
CPC分类号： C12Q1/6827 , C12Q2523/125
摘要： The present invention relates to a new, non-invasive method for detecting chromosomal aneuploidy by analyzing a sample from a pregnant woman. The detection is based on the ratio between the amount of a fetal methylation marker located on a chromosome relevant to the aneuploidy and the amount of a fetal genetic marker located on a reference chromosome, offering improved accuracy.
摘要翻译： 本发明涉及通过分析来自孕妇的样品来检测染色体非整倍体的新的非侵入性方法。 检测是基于位于与非整倍性相关的染色体上的胎儿甲基化标记的量与位于参考染色体上的胎儿遗传标记的量之间的比例，提供更高的准确性。
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