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公开(公告)号:US20130338008A1
公开(公告)日:2013-12-19
申请号:US13905003
申请日:2013-05-29
Applicant: ILLUMINA, INC.
Inventor: Mostafa Ronaghi , Helmy A. Eltoukhy
IPC: C12Q1/68
CPC classification number: C12Q1/6874 , C12Q1/6837 , C12Q1/6869 , C12Q2535/122 , C12Q2565/543
Abstract: A method of making an array of nucleic acid colonies, including the steps of (a) providing a substrate having a patterned surface of features, wherein the features are spatially organized in a repeating pattern on the surface of the substrate; (b) contacting the substrate with a solution of different target nucleic acids to seed no more than a subset of the features that contact the solution; (c) amplifying the nucleic acids on the subset of features; and (d) repeating steps (b) and (c) to increase the number of features that are seeded with a nucleic acid, thereby making an array of nucleic acid colonies.
Abstract translation: 一种制备核酸集落阵列的方法,包括以下步骤:(a)提供具有图案化特征表面的基底,其中所述特征在空间上以基底表面上的重复图案组织; (b)使底物与不同靶核酸的溶液接触不超过接触溶液的特征的一部分; (c)扩增特征子集上的核酸; 和(d)重复步骤(b)和(c)以增加用核酸接种的特征的数量,由此形成核酸集落阵列。
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22.
公开(公告)号:US20230220462A1
公开(公告)日:2023-07-13
申请号:US18180622
申请日:2023-03-08
Applicant: ILLUMINA, INC.
Inventor: Tarun Kumar Khurana , Yir-Shyuan Wu , Xi-Jun Chen , Filiz Gorpe-Yasar , Yan-You Lin , Victoria Popic , Erich B. Jaeger , Mostafa Ronaghi
IPC: C12Q1/6874 , C12Q1/6813
CPC classification number: C12Q1/6874 , C12Q1/6813 , C12Q2600/156 , C12Q2565/514
Abstract: Implementations of a method for seeding sequence libraries on a surface of a sequencing flow cell that allow for spatial segregation of the libraries on the surface are provided. The spatial segregation can be used to index sequence reads from individual sequencing libraries to increase efficiency of subsequent data analysis. In some examples, hydrogel beads containing encapsulated sequencing libraries are captured on a sequencing flow cell and degraded in the presence of a liquid diffusion barrier to allow for the spatial segregation and seeding of the sequencing libraries on the surface of the flow cell. Additionally, examples of systems, methods and compositions are provided relating to flow cell devices configured for nucleic acid library preparation and single cell sequencing. Some examples include flow cell devices having a hydrogel with genetic material disposed therein, and which is retained within the hydrogel during nucleic acid processing.
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公开(公告)号:US11180752B2
公开(公告)日:2021-11-23
申请号:US16272870
申请日:2019-02-11
Applicant: Illumina, Inc.
Inventor: Yir-Shyuan Wu , Filiz Gorpe-Yasar , Tarun Kumar Khurana , Victoria Popic , Erich B. Jaeger , Mostafa Ronaghi
IPC: C12N15/10 , B01L3/00 , C12Q1/6834 , C12Q1/6806 , B01L7/00
Abstract: Systems, methods, and compositions provided herein relate to preparation of beads encapsulating long DNA fragments for high-throughput spatial indexing. Some embodiments include preparation of nucleic acid libraries within the bead, wherein the bead includes pores that allow diffusion of reagents while retaining genetic material.
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公开(公告)号:US10570447B2
公开(公告)日:2020-02-25
申请号:US15312851
申请日:2015-05-14
Applicant: Illumina, Inc.
Inventor: Mostafa Ronaghi , Molly He , Cheng-yao Chen , Michael Previte , M. Shane Bowen
IPC: C12Q1/6874 , B01J19/00
Abstract: A method for synthesizing a nucleic acid includes synthesizing one or more nucleic acid fragments on a substrate. The synthesized one or more nucleic acid fragments may be amplified on the substrate. The method also includes sequencing the synthesized or amplified one or more nucleic acid fragments on the substrate. The sequencing may provide feedback to designs of the one or more nucleic acid fragments. The method further includes harvesting the synthesized or amplified one or more nucleic acid fragments based on sequencing. The synthesized or amplified one or more nucleic acid fragments may be assembled to generate a target nucleic acid.
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公开(公告)号:US20200040386A1
公开(公告)日:2020-02-06
申请号:US16544670
申请日:2019-08-19
Applicant: Illumina, Inc.
Inventor: Min-Jui Richard Shen , Jonathan Mark Boutell , Kathryn M. Stephens , Mostafa Ronaghi , Kevin L. Gunderson , Bala Murali Venkatesan , M. Shane Bowen , Kandaswamy Vijayan
IPC: C12Q1/6848 , B01J19/00 , C12Q1/6844 , C12Q1/6874
Abstract: A method including (a) providing an amplification reagent including an array of sites, and a solution having different target nucleic acids; and (b) reacting the amplification reagent to produce amplification sites each having a clonal population of amplicons from a target nucleic acid from the solution. The reacting can include simultaneously transporting the nucleic acids to the sites at an average transport rate, and amplifying the nucleic acids that transport to the sites at an average amplification rate, wherein the average amplification rate exceeds the average transport rate. The reacting can include producing a first amplicon from a nucleic acid that transports to each of the sites, and producing subsequent amplicons from the nucleic acid or from the first amplicon, wherein the average rate at which the subsequent amplicons are generated exceeds the average rate at which the first amplicon is generated.
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公开(公告)号:US20190249171A1
公开(公告)日:2019-08-15
申请号:US16272870
申请日:2019-02-11
Applicant: Illumina, Inc.
Inventor: Yir-Shyuan Wu , Filiz Gorpe-Yasar , Tarun Kumar Khurana , Victoria Popic , Erich B. Jaeger , Mostafa Ronaghi
IPC: C12N15/10 , C12Q1/6806 , B01L3/00 , B01L7/00
CPC classification number: C12N15/1068 , B01L3/508 , B01L7/52 , B01L2200/141 , B01L2200/16 , B01L2300/123 , C12Q1/6806 , C12Q1/6834 , C12Q2523/101 , C12Q2527/156 , C12Q2531/119 , C12Q2535/122 , C12Q2563/149 , C12Q2563/159 , C12Q2565/629
Abstract: Systems, methods, and compositions provided herein relate to preparation of beads encapsulating long DNA fragments for high-throughput spatial indexing. Some embodiments include preparation of nucleic acid libraries within the bead, wherein the bead includes pores that allow diffusion of reagents while retaining genetic material.
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公开(公告)号:US09862998B2
公开(公告)日:2018-01-09
申请号:US15132662
申请日:2016-04-19
Applicant: Illumina, Inc.
Inventor: Molly He , Cheng-Yao Chen , Eric Kool , Mostafa Ronaghi , Michael Previte , Rigo Pantoja
CPC classification number: C12Q1/6874 , C12Q1/6806 , C12Q1/6818 , C12Q2565/133 , C12Q2563/125 , C12Q2525/101 , C12Q2565/1015
Abstract: This disclosure provides a method of determining a sequence of nucleotides for a nucleic acid template. The method can include the steps of contacting the nucleic acid template with a conformationally labeled polymerase and at least four different nucleotide species under conditions wherein the conformationally labeled polymerase catalyzes sequential addition of the nucleotide species to form a nucleic acid complement of the nucleic acid template, wherein the sequential addition of each different nucleotide species produces a conformational signal change from the conformationally labeled polymerase and wherein the rate or time duration for the conformational signal change is distinguishable for each different nucleotide species; detecting a series of changes in the signal from the conformationally labeled polymerase under the conditions; and determining the rates or time durations for the changes in the signal, thereby determining the sequence of nucleotides for the nucleic acid template.
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公开(公告)号:US09758816B2
公开(公告)日:2017-09-12
申请号:US14879932
申请日:2015-10-09
Applicant: Illumina, Inc.
Inventor: Min-Jui Richard Shen , Jonathan Mark Boutell , Kathryn M. Stephens , Mostafa Ronaghi , Kevin Gunderson , Bala Murali Venkatesan , M. Shane Bowen , Kandaswamy Vijayan
CPC classification number: C12Q1/6848 , B01J19/0046 , B01J2219/00585 , B01J2219/00587 , B01J2219/00608 , B01J2219/00621 , B01J2219/00637 , B01J2219/00653 , B01J2219/00675 , B01J2219/00722 , C12Q1/6844 , C12Q1/6874 , C12Q2521/507 , C12Q2527/101 , C12Q2527/113 , C12Q2535/122 , C12Q2565/513 , C12Q2565/537
Abstract: A method including (a) providing an amplification reagent including an array of sites, and a solution having different target nucleic acids; and (b) reacting the amplification reagent to produce amplification sites each having a clonal population of amplicons from a target nucleic acid from the solution. The reacting can include simultaneously transporting the nucleic acids to the sites at an average transport rate, and amplifying the nucleic acids that transport to the sites at an average amplification rate, wherein the average amplification rate exceeds the average transport rate. The reacting can include producing a first amplicon from a nucleic acid that transports to each of the sites, and producing subsequent amplicons from the nucleic acid or from the first amplicon, wherein the average rate at which the subsequent amplicons are generated exceeds the average rate at which the first amplicon is generated.
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公开(公告)号:US20160053310A1
公开(公告)日:2016-02-25
申请号:US14879932
申请日:2015-10-09
Applicant: ILLUMINA, INC.
Inventor: Min-Jui Richard Shen , Jonathan Mark Boutell , Kathryn M. Stephens , Mostafa Ronaghi , Kevin Gunderson , Bala Murali Venkatesan , M. Shane Bowen , Kandaswamy Vijayan
IPC: C12Q1/68
CPC classification number: C12Q1/6848 , B01J19/0046 , B01J2219/00585 , B01J2219/00587 , B01J2219/00608 , B01J2219/00621 , B01J2219/00637 , B01J2219/00653 , B01J2219/00675 , B01J2219/00722 , C12Q1/6844 , C12Q1/6874 , C12Q2521/507 , C12Q2527/101 , C12Q2527/113 , C12Q2535/122 , C12Q2565/513 , C12Q2565/537
Abstract: A method including (a) providing an amplification reagent including an array of sites, and a solution having different target nucleic acids; and (b) reacting the amplification reagent to produce amplification sites each having a clonal population of amplicons from a target nucleic acid from the solution. The reacting can include simultaneously transporting the nucleic acids to the sites at an average transport rate, and amplifying the nucleic acids that transport to the sites at an average amplification rate, wherein the average amplification rate exceeds the average transport rate. The reacting can include producing a first amplicon from a nucleic acid that transports to each of the sites, and producing subsequent amplicons from the nucleic acid or from the first amplicon, wherein the average rate at which the subsequent amplicons are generated exceeds the average rate at which the first amplicon is generated.
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30.
公开(公告)号:US09169513B2
公开(公告)日:2015-10-27
申请号:US14512693
申请日:2014-10-13
Applicant: ILLUMINA, INC.
Inventor: Min-Jui Richard Shen , Jonathan Mark Boutell , Kathryn M. Stephens , Mostafa Ronaghi , Kevin Gunderson , Bala Murali Venkatesan , M. Shane Bowen , Kandaswamy Vijayan
CPC classification number: C12Q1/6848 , B01J19/0046 , B01J2219/00585 , B01J2219/00587 , B01J2219/00608 , B01J2219/00621 , B01J2219/00637 , B01J2219/00653 , B01J2219/00675 , B01J2219/00722 , C12Q1/6844 , C12Q1/6874 , C12Q2521/507 , C12Q2527/101 , C12Q2527/113 , C12Q2535/122 , C12Q2565/513 , C12Q2565/537
Abstract: A method including (a) providing an amplification reagent including an array of sites, and a solution having different target nucleic acids; and (b) reacting the amplification reagent to produce amplification sites each having a clonal population of amplicons from a target nucleic acid from the solution. The reacting can include simultaneously transporting the nucleic acids to the sites at an average transport rate, and amplifying the nucleic acids that transport to the sites at an average amplification rate, wherein the average amplification rate exceeds the average transport rate. The reacting can include producing a first amplicon from a nucleic acid that transports to each of the sites, and producing subsequent amplicons from the nucleic acid or from the first amplicon, wherein the average rate at which the subsequent amplicons are generated exceeds the average rate at which the first amplicon is generated.
Abstract translation: 一种方法,包括(a)提供包含位点阵列的扩增试剂和具有不同靶核酸的溶液; 和(b)使扩增试剂反应以产生每个具有来自溶液的靶核酸的扩增子的克隆群的扩增位点。 反应可以包括以平均传输速率同时将核酸输送到位点,以及以平均扩增速率扩增转运到位点的核酸,其中平均扩增速率超过平均传输速率。 该反应可以包括从转运到每个位点的核酸产生第一扩增子,并产生来自核酸或第一扩增子的后续扩增子,其中后续扩增子产生的平均速率超过在 其中生成第一个扩增子。
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