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公开(公告)号:US20130296173A1
公开(公告)日:2013-11-07
申请号:US13868000
申请日:2013-04-22
Applicant: Complete Genomics, Inc.
Inventor: Matthew Callow , Linsu Chen , Dennis Ballinger
IPC: C12Q1/68
CPC classification number: C12Q1/6874 , C12Q2527/125
Abstract: The present invention is directed to compositions and methods for improving the discordance rate and mapping yield in nucleic acid sequencing reactions.
Abstract translation: 本发明涉及用于提高核酸测序反应中不一致率和测绘产率的组合物和方法。
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公开(公告)号:US11835437B2
公开(公告)日:2023-12-05
申请号:US17094523
申请日:2020-11-10
Applicant: Complete Genomics, Inc.
Inventor: Norman Lee Burns , Jay Willis Shafto
IPC: C12Q1/68 , G01N1/30 , B01J19/00 , C12Q1/6837
CPC classification number: G01N1/30 , B01J19/0046 , B01J2219/00529 , B01J2219/00608 , B01J2219/00637 , B01J2219/00659 , B01J2219/00722 , C12Q1/6837
Abstract: The present invention is directed to treatment of nucleic acid molecules that are attached or associated with solid supports for biochemical analysis, including nucleic acid sequencing. After loading on the solid support, the nucleic acid molecules are treated with a composition comprising a condensing agent, a volume excluding agent, or both, then treated with a composition comprising a protein.
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公开(公告)号:US20230323445A1
公开(公告)日:2023-10-12
申请号:US18144124
申请日:2023-05-05
Applicant: MGI TECH CO., LTD. , COMPLETE GENOMICS, INC.
Inventor: Jin YANG , Xun XU , Hui WANG , Bin XIE , Zhuokun LI , Shengming ZHAO , Ao CHEN , Chongjun XU , Wenwei ZHANG , Ming NI
IPC: C12Q1/6869 , C12Q1/6876 , G01N21/64
CPC classification number: C12Q1/6869 , C12Q1/6876 , G01N21/6486 , B01L2200/10
Abstract: The present invention provides a method for sequencing a nucleic acid using an immersion reaction protocol. The immersion reaction protocol comprises sequentially immersing a solid support having nucleic acid molecules immobilized thereon in different reaction containers to realize nucleic acid sequencing.
FIG. 1 is published together with the abstract-
44.
公开(公告)号:US20220362735A1
公开(公告)日:2022-11-17
申请号:US17840843
申请日:2022-06-15
Applicant: Complete Genomics, Inc.
Inventor: Radoje Drmanac , Brock A. Peters , Andrei Alexeev , Peter Hong
IPC: B01J19/00 , C12P19/34 , C12Q1/6869 , C12N15/10 , C12Q1/6874
Abstract: This disclosure provides methods and compositions for long fragment read sequencing. Technology is described for preparing long fragments of genomic DNA, for processing genomic DNA for long fragment read sequencing methods, as well as software and algorithms for processing and analyzing sequence data. Combinatorial oligonucleotide bar codes are used to label fragments from nearby portions of the genome, which facilitate computational assembly of sequence reads to obtain the genome sequence. This improves efficiency and accuracy of sequencing, whereby an entire sequence can be obtained from fragments that constitute a lower coverage amount of the genome.
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公开(公告)号:US11485966B2
公开(公告)日:2022-11-01
申请号:US16754713
申请日:2017-10-11
Applicant: MGI TECH CO., LTD. , COMPLETE GENOMICS, INC.
Inventor: Hui Wang , Xun Xu , Jin Yang , Ao Chen , Chongjun Xu , Wenwei Zhang
Abstract: The present invention provides a method for improving the loading of nucleic acid on a solid support by contacting the solid support with a poloxamer-containing reagent. The present invention also provides a method for improving the stability of a nucleic acid on a solid support, comprising contacting a nucleic acid molecule with a partially double-strand oligonucleotide before or after loading the nucleic acid molecule on a solid support, so as to cause the nucleic acid molecule to hybridize with the oligonucleotide. The present invention also provides a combined use of the two methods.
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公开(公告)号:US11414702B2
公开(公告)日:2022-08-16
申请号:US16730829
申请日:2019-12-30
Applicant: Complete Genomics, Inc.
Inventor: Radoje Drmanac
IPC: C12Q1/6869 , C12Q1/6806 , C12Q1/6874 , C12Q1/682 , C12Q1/6837 , C07H21/04 , C07K1/04 , G01N15/14
Abstract: The invention provides methods and kits for ordering sequence information derived from one or more target polynucleotides. In one aspect, one or more tiers or levels of fragmentation and aliquoting are generated, after which sequence information is obtained from fragments in a final level or tier. Each fragment in such final tier is from a particular aliquot, which, in turn, is from a particular aliquot of a prior tier, and so on. For every fragment of an aliquot in the final tier, the aliquots from which it was derived at every prior tier is known, or can be discerned. Thus, identical sequences from overlapping fragments from different aliquots can be distinguished and grouped as being derived from the same or different fragments from prior tiers. When the fragments in the final tier are sequenced, overlapping sequence regions of fragments in different aliquots are used to register the fragments so that non-overlapping regions are ordered. In one aspect, this process is carried out in a hierarchical fashion until the one or more target polynucleotides are characterized, e.g. by their nucleic acid sequences, or by an ordering of sequence segments, or by an ordering of single nucleotide polymorphisms (SNPs), or the like.
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公开(公告)号:US20220186309A1
公开(公告)日:2022-06-16
申请号:US17407935
申请日:2021-08-20
Applicant: Complete Genomics, Inc.
Inventor: Radoje Drmanac
IPC: C12Q1/6874 , C12Q1/6876 , C12Q1/6869 , C12Q1/686
Abstract: The present invention is directed to methods and compositions for acquiring nucleotide sequence information of target sequences. In particular, the present invention provides methods and compositions for improving the efficiency of sequencing reactions by using fewer labels to distinguish between nucleotides and by detecting nucleotides at multiple detection positions in a target sequence.
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公开(公告)号:US20210131924A1
公开(公告)日:2021-05-06
申请号:US17094523
申请日:2020-11-10
Applicant: Complete Genomics, Inc.
Inventor: Norman Lee Burns , Jay Willis Shafto
Abstract: The present invention is directed to treatment of nucleic acid molecules that are attached or associated with solid supports for biochemical analysis, including nucleic acid sequencing. After loading on the solid support, the nucleic acid molecules are treated with a composition comprising a condensing agent, a volume excluding agent, or both, then treated with a composition comprising a protein.
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公开(公告)号:US20200318177A1
公开(公告)日:2020-10-08
申请号:US16635131
申请日:2017-08-01
Applicant: MGI TECH CO., LTD. , COMPLETE GENOMICS, INC.
Inventor: Jin YANG , Xun XU , Hui WANG , Bin XIE , Zhuokun LI , Shengming ZHAO , Ao CHEN , Chongjun XU , Wenwei ZHANG , Ming NI
IPC: C12Q1/6869 , C12Q1/6876 , G01N21/64
Abstract: The present invention provides a method for sequencing a nucleic acid using an immersion reaction protocol. The immersion reaction protocol comprises sequentially immersing a solid support having nucleic acid molecules immobilized thereon in different reaction containers to realize nucleic acid sequencing.
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公开(公告)号:US10784103B2
公开(公告)日:2020-09-22
申请号:US16128120
申请日:2018-09-11
Applicant: Complete Genomics, Inc.
Inventor: Shifeng Li , Jian Gong , Yan-You Lin , Cheng Frank Zhong
Abstract: A method for forming sequencing flow cells can include providing a semiconductor wafer covered with a dielectric layer, and forming a patterned layer on the dielectric layer. The patterned layer has a differential surface that includes alternating first surface regions and second surface regions. The method can also include attaching a cover wafer to the semiconductor wafer to form a composite wafer structure including a plurality of flow cells. The composite wafer structure can then be singulated to form a plurality of dies. Each die forms a sequencing flow cell. The sequencing flow cell can include a flow channel between a portion of the patterned layer and a portion of the cover wafer, an inlet, and an outlet. Further, the method can include functionalizing the sequencing flow cell to create differential surfaces.
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