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公开(公告)号:US20130210182A1
公开(公告)日:2013-08-15
申请号:US13797871
申请日:2013-03-12
Applicant: Life Technologies Corporation
Inventor: Jonathan ROTHBERG , Wolfgang Hinz , John Davidson , Antoine van Oijen , John Leamon , Martin Huber
IPC: H01L21/82
CPC classification number: G01N27/4145 , C12Q1/6869 , C12Q1/6874 , G01N27/4148 , H01L21/82 , C12Q2565/607
Abstract: Methods and apparatus relating to FET arrays for monitoring chemical and/or biological reactions such as nucleic acid sequencing-by-synthesis reactions. Some methods provided herein relate to improving signal (and also signal to noise ratio) from released hydrogen ions during nucleic acid sequencing reactions.
Abstract translation: 与用于监测化学和/或生物反应的FET阵列相关的方法和装置,例如核酸序列合成反应。 本文提供的一些方法涉及在核酸测序反应期间从释放的氢离子改进信号(以及信噪比)。
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公开(公告)号:US20240085368A1
公开(公告)日:2024-03-14
申请号:US18324346
申请日:2023-05-26
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Mark MILGREW , Jonathan ROTHBERG , James BUSTILLO
IPC: G01N27/414 , C12Q1/6869 , C12Q1/6874 , G01N27/27
CPC classification number: G01N27/4145 , C12Q1/6869 , C12Q1/6874 , G01N27/27 , G01N27/414 , Y10T29/49002
Abstract: Methods and apparatus relating to FET arrays for monitoring chemical and/or biological reactions such as nucleic acid sequencing-by-synthesis reactions. Some methods provided herein relate to improving signal (and also signal to noise ratio) from released hydrogen ions during nucleic acid sequencing reactions.
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公开(公告)号:US20230058778A1
公开(公告)日:2023-02-23
申请号:US17820202
申请日:2022-08-16
Applicant: Life Technologies Corporation
Inventor: Jonathan ROTHBERG , Wolfgang HINZ , Kim JOHNSON , James BUSTILLO
IPC: G01N27/414 , C12Q1/6874 , H01L29/78 , H01L27/088 , C12Q1/6818 , G01N33/543
Abstract: Methods and apparatus relating to very large scale FET arrays for analyte measurements. ChemFET (e.g., ISFET) arrays may be fabricated using conventional CMOS processing techniques based on improved FET pixel and array designs that increase measurement sensitivity and accuracy, and at the same time facilitate significantly small pixel sizes and dense arrays. Improved array control techniques provide for rapid data acquisition from large and dense arrays. Such arrays may be employed to detect a presence and/or concentration changes of various analyte types in a wide variety of chemical and/or biological processes. In one example, chemFET arrays facilitate DNA sequencing techniques based on monitoring changes in hydrogen ion concentration (pH), changes in other analyte concentration, and/or binding events associated with chemical processes relating to DNA synthesis.
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公开(公告)号:US20210261929A1
公开(公告)日:2021-08-26
申请号:US17302192
申请日:2021-04-27
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chieh-Yuan LI , David RUFF , Shiaw-Min CHEN , Jennifer O'NEIL , Rachel KASINSKAS , Jonathan ROTHBERG , Bin LI , Kai Qin LAO
IPC: C12N9/12 , C12Q1/6853 , C12Q1/6844 , C12Q1/6855 , C12Q1/686
Abstract: The present disclosure provides methods, compositions, kits and systems for nucleic acid amplification. In some embodiments, nucleic acid amplification methods include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, nucleic acid amplification methods include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the nucleic acid amplification method employs an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel and/or in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer which can include a sieving agent and/or a diffusion-reducing agent.
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公开(公告)号:US20160272954A1
公开(公告)日:2016-09-22
申请号:US15091717
申请日:2016-04-06
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chieh-Yuan LI , David RUFF , Shiaw-Min CHEN , Jennifer O'NEIL , Rachel KASINSKAS , Jonathan ROTHBERG , Bin LI , Kai Qin LAO , Wolfgang HINZ
CPC classification number: C12N9/1252 , C12Q1/6846 , C12Q1/6853 , C12Q1/6855 , C12Q1/686 , C12Q1/6874 , C12Y207/07007 , C12Q2531/119 , C12Q2565/537
Abstract: In some embodiments, the present teachings provide methods for nucleic acid amplification, comprising forming a reaction mixture, and subjecting the reaction mixture to conditions suitable for nucleic acid amplification. In some embodiments, methods for nucleic acid amplification include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, methods for nucleic acid amplification include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the methods for nucleic acid amplification employ an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel. In some embodiments, methods for nucleic acid amplification can be conducted in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise a amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer. The polymer can include a sieving agent and/or a diffusion-reducing agent.
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公开(公告)号:US20160032375A1
公开(公告)日:2016-02-04
申请号:US14789922
申请日:2015-07-01
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chieh-Yuan LI , David RUFF , Jennifer O'NEIL , Rachel KASINSKAS , Shiaw-Min CHEN , Jonathan ROTHBERG
IPC: C12Q1/68
CPC classification number: C12Q1/6846 , C12Q1/6844 , C12Q1/6874 , C12Q2563/159 , C12Q2565/513 , C12Q2565/519 , C12Q2565/607
Abstract: In some embodiments, the present teachings provide methods for nucleic acid amplification, comprising forming a reaction mixture, and subjecting the reaction mixture to conditions suitable for nucleic acid amplification. In some embodiments, methods for nucleic acid amplification include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, methods for nucleic acid amplification include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the methods for nucleic acid amplification employ an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel. In some embodiments, methods for nucleic acid amplification can be conducted in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise a amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer. The polymer can include a sieving agent and/or a diffusion-reducing agent.
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公开(公告)号:US20130281307A1
公开(公告)日:2013-10-24
申请号:US13923232
申请日:2013-06-20
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chieh-Yuan LI , David RUFF , Jennifer O'NEIL , Rachel KASINSKAS , Shiaw-Min CHEN , Jonathan ROTHBERG
IPC: C12Q1/68
CPC classification number: C12Q1/6806 , C12Q1/6846 , C12Q1/6853 , C12Q1/686 , C12Q1/6874 , C12Q2531/119 , C12Q2565/537
Abstract: In some embodiments, the present teachings provide methods for nucleic acid amplification, comprising forming a reaction mixture, and subjecting the reaction mixture to conditions suitable for nucleic acid amplification. In some embodiments, methods for nucleic acid amplification include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, methods for nucleic acid amplification include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the methods for nucleic acid amplification employ an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel. In some embodiments, methods for nucleic acid amplification can be conducted in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise a amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer. The polymer can include a sieving agent and/or a diffusion-reducing agent.
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公开(公告)号:US20240426775A1
公开(公告)日:2024-12-26
申请号:US18732345
申请日:2024-06-03
Applicant: Life Technologies Corporation
Inventor: James BUSTILLO , Wolfgang HINZ , Kim JOHNSON , Jonathan ROTHBERG
IPC: G01N27/414 , C12Q1/6818 , C12Q1/6874 , G01N33/543 , H01L27/088 , H01L29/423 , H01L29/78
Abstract: Methods and apparatus relating to very large scale FET arrays for analyte measurements. ChemFET (e.g., ISFET) arrays may be fabricated using conventional CMOS processing techniques based on improved FET pixel and array designs that increase measurement sensitivity and accuracy, and at the same time facilitate significantly small pixel sizes and dense arrays. Improved array control techniques provide for rapid data acquisition from large and dense arrays. Such arrays may be employed to detect a presence and/or concentration changes of various analyte types in a wide variety of chemical and/or biological processes. In one example, chemFET arrays facilitate DNA sequencing techniques based on monitoring changes in hydrogen ion concentration (pH), changes in other analyte concentration, and/or binding events associated with chemical processes relating to DNA synthesis.
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公开(公告)号:US20240201126A1
公开(公告)日:2024-06-20
申请号:US18536131
申请日:2023-12-11
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: James BUSTILLO , Mark J. MILGREW , Wolfgang HINZ , John LEAMON , John DAVIDSON , Martin HUBER , Antoine M. VAN OIJEN , Jonathan ROTHBERG
IPC: G01N27/414 , C12Q1/6869 , C12Q1/6874 , H01L21/82
CPC classification number: G01N27/4145 , C12Q1/6869 , C12Q1/6874 , G01N27/4148 , H01L21/82
Abstract: Methods and apparatus relating to FET arrays for monitoring chemical and/or biological reactions such as nucleic acid sequencing-by-synthesis reactions. Some methods provided herein relate to improving signal (and also signal to noise ratio) from released hydrogen ions during nucleic acid sequencing reactions.
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公开(公告)号:US20240067939A1
公开(公告)日:2024-02-29
申请号:US18221099
申请日:2023-07-12
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chieh-Yuan LI , David RUFF , Shiaw-Min CHEN , Jennifer O'NEIL , Rachel KASINSKAS , Jonathan ROTHBERG , Bin LI , Kai Qin LAO
IPC: C12N9/12 , C12Q1/6844 , C12Q1/6853 , C12Q1/6855 , C12Q1/686
CPC classification number: C12N9/1252 , C12Q1/6846 , C12Q1/6853 , C12Q1/6855 , C12Q1/686 , C12Q1/6874
Abstract: The present disclosure provides methods, compositions, kits and systems for nucleic acid amplification. In some embodiments, nucleic acid amplification methods include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, nucleic acid amplification methods include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the nucleic acid amplification method employs an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel and/or in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer which can include a sieving agent and/or a diffusion-reducing agent.
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