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公开(公告)号:US12234512B2
公开(公告)日:2025-02-25
申请号:US18164439
申请日:2023-02-03
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Shengrong Lin , Zhaohui Sun , Grace Qizhi Zhao , Paul Ling-Fung Tang
IPC: C12Q1/6874 , C12Q1/6827 , C12Q1/6869
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants in a nucleic acid sample. In some embodiments, a method comprises identifying sequence differences between sequencing reads and a reference sequence, and calling a sequence difference that occurs in at least two different circular polynucleotides, such as two circular polynucleotides having different junctions, as the sequence variant. In some aspects, the present disclosure provides compositions and systems useful in the described methods.
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公开(公告)号:US11427866B2
公开(公告)日:2022-08-30
申请号:US16301707
申请日:2017-05-16
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Malek Faham , Shengrong Lin , Ling Fung Tang , Yontao Lu , Zhaohui Sun , Yingyu Wang , Li Weng
IPC: C12Q1/6869 , C12Q1/6827 , C12Q1/6858 , C40B50/06
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants, as well as methods of determining copy number of a genetic locus in a sample. Systems and kits for performing methods of the disclosure, as well as compositions produced by or useful in methods of the disclosure are also provided. In some embodiments, methods comprise extending 3′ ends of polynucleotides by adding one or more pre-determined nucleotides. In some embodiments, methods comprise use of a strand-tagging sequence.
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公开(公告)号:US20190119743A1
公开(公告)日:2019-04-25
申请号:US16172310
申请日:2018-10-26
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Li Weng , Zhaohui Sun , Shengrong Lin
IPC: C12Q1/6869 , C12Q1/6806 , C12P19/34
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants in a nucleic acid sample. In some embodiments, a method comprises identifying sequence differences between sequencing reads and a reference sequence, and calling a sequence difference that occurs in at least two different circular polynucleotides, such as two circular polynucleotides having different junctions, or two different sheared polynucleotides as the sequence variant. In some aspects, the present disclosure provides compositions and systems useful in the described method.
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公开(公告)号:US10724088B2
公开(公告)日:2020-07-28
申请号:US16172310
申请日:2018-10-26
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Li Weng , Zhaohui Sun , Shengrong Lin
IPC: C12Q1/6869 , C12Q1/6806 , C12P19/34 , C12Q1/6816 , C12Q1/6827 , C12Q1/6858
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants in a nucleic acid sample. In some embodiments, a method comprises identifying sequence differences between sequencing reads and a reference sequence, and calling a sequence difference that occurs in at least two different circular polynucleotides, such as two circular polynucleotides having different junctions, or two different sheared polynucleotides as the sequence variant. In some aspects, the present disclosure provides compositions and systems useful in the described method.
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公开(公告)号:US10155980B2
公开(公告)日:2018-12-18
申请号:US15800558
申请日:2017-11-01
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Li Weng , Zhaohui Sun , Shengrong Lin
IPC: C12P19/34 , C12Q1/6806 , C12Q1/6869 , C12Q1/6816 , C12Q1/6827 , C12Q1/6858
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants in a nucleic acid sample. In some embodiments, a method comprises identifying sequence differences between sequencing reads and a reference sequence, and calling a sequence difference that occurs in at least two different circular polynucleotides, such as two circular polynucleotides having different junctions, or two different sheared polynucleotides as the sequence variant. In some aspects, the present disclosure provides compositions and systems useful in the described methods.
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公开(公告)号:US10767222B2
公开(公告)日:2020-09-08
申请号:US15102241
申请日:2014-12-11
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Shengrong Lin , Zhaohui Sun , Grace Qizhi Zhao , Paul Ling-Fung Tang
IPC: C12Q1/6874 , C12Q1/6827 , C12Q1/6869
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants in a nucleic acid sample. In some embodiments, a method comprises identifying sequence differences between sequencing reads and a reference sequence, and calling a sequence difference that occurs in at least two different circular polynucleotides, such as two circular polynucleotides having different junctions, as the sequence variant. In some aspects, the present disclosure provides compositions and systems useful in the described methods.
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公开(公告)号:US20180057871A1
公开(公告)日:2018-03-01
申请号:US15800558
申请日:2017-11-01
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Li Weng , Zhaohui Sun , Shengrong Lin
CPC classification number: C12Q1/6869 , C12P19/34 , C12Q1/6806 , C12Q1/6816 , C12Q1/6827 , C12Q1/6858 , C12Q2521/501 , C12Q2531/125 , C12Q2535/122
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants in a nucleic acid sample. In some embodiments, a method comprises identifying sequence differences between sequencing reads and a reference sequence, and calling a sequence difference that occurs in at least two different circular polynucleotides, such as two circular polynucleotides having different junctions, or two different sheared polynucleotides as the sequence variant. In some aspects, the present disclosure provides compositions and systems useful in the described methods.
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公开(公告)号:US11643683B2
公开(公告)日:2023-05-09
申请号:US16896073
申请日:2020-06-08
Applicant: ACCURAGEN HOLDINGS LIMITED
Inventor: Li Weng , Zhaohui Sun , Shengrong Lin
IPC: C12Q1/6806 , C12P19/34 , C12Q1/6816 , C12Q1/6827 , C12Q1/6869 , C12Q1/6858
CPC classification number: C12Q1/6869 , C12P19/34 , C12Q1/6806 , C12Q1/6816 , C12Q1/6827 , C12Q1/6858 , C12Q1/6806 , C12Q2521/501 , C12Q2531/125 , C12Q2535/122
Abstract: In some aspects, the present disclosure provides methods for identifying sequence variants in a nucleic acid sample. In some embodiments, a method comprises identifying sequence differences between sequencing reads and a reference sequence, and calling a sequence difference that occurs in at least two different circular polynucleotides, such as two circular polynucleotides having different junctions, or two different sheared polynucleotides as the sequence variant. In some aspects, the present disclosure provides compositions and systems useful in the described method.
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