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公开(公告)号:US12050196B2
公开(公告)日:2024-07-30
申请号:US17499676
申请日:2021-10-12
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chiu Tai Andrew Wong , Todd Rearick , John Donohue
IPC: G01N27/414 , G16B30/00
CPC classification number: G01N27/4145 , G16B30/00
Abstract: A method for correcting nucleotide incorporation signals for fluid potential effects or disturbances arising in nucleic acid sequencing-by-synthesis includes: disposing a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, the template polynucleotide strands having a sequencing primer and a polymerase bound therewith; exposing the template polynucleotide strands to a series of flows of nucleotide species flowed through a fluid manifold, the fluid manifold comprising passages for flowing nucleotide species and a branch passage for flowing a solution, the branch passage comprising a reference electrode and a sensing electrode; obtaining a plurality of nucleotide incorporation signals corresponding to the plurality of defined spaces, the nucleotide incorporation signals having a signal intensity related to a number of nucleotide incorporations; and correcting at least some of the plurality of nucleotide incorporation signals for fluid potential effects or disturbances.
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公开(公告)号:US11169111B2
公开(公告)日:2021-11-09
申请号:US16362367
申请日:2019-03-22
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chiu Tai Andrew Wong , Todd Rearick , John Donohue
IPC: G01N27/414 , G16B30/00
Abstract: A method for correcting nucleotide incorporation signals for fluid potential effects or disturbances arising in nucleic acid sequencing-by-synthesis includes: disposing a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, the template polynucleotide strands having a sequencing primer and a polymerase bound therewith; exposing the template polynucleotide strands to a series of flows of nucleotide species flowed through a fluid manifold, the fluid manifold comprising passages for flowing nucleotide species and a branch passage for flowing a solution, the branch passage comprising a reference electrode and a sensing electrode; obtaining a plurality of nucleotide incorporation signals corresponding to the plurality of defined spaces, the nucleotide incorporation signals having a signal intensity related to a number of nucleotide incorporations; and correcting at least some of the plurality of nucleotide incorporation signals for fluid potential effects or disturbances.
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公开(公告)号:US10416112B2
公开(公告)日:2019-09-17
申请号:US14853026
申请日:2015-09-14
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chiu Tai Andrew Wong , Todd Rearick , John Donohue
IPC: C12Q1/68 , G06F19/22 , G01N27/414
Abstract: A method for correcting nucleotide incorporation signals for fluid potential effects or disturbances arising in nucleic acid sequencing-by-synthesis includes: disposing a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, the template polynucleotide strands having a sequencing primer and a polymerase bound therewith; exposing the template polynucleotide strands to a series of flows of nucleotide species flowed through a fluid manifold, the fluid manifold comprising passages for flowing nucleotide species and a branch passage for flowing a solution, the branch passage comprising a reference electrode and a sensing electrode; obtaining a plurality of nucleotide incorporation signals corresponding to the plurality of defined spaces, the nucleotide incorporation signals having a signal intensity related to a number of nucleotide incorporations; and correcting at least some of the plurality of nucleotide incorporation signals for fluid potential effects or disturbances.
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公开(公告)号:US20240263168A1
公开(公告)日:2024-08-08
申请号:US18636580
申请日:2024-04-16
Applicant: Life Technologies Corporation
Inventor: Chiu Tai Andrew Wong , Mark Beauchemin , Shanti Shankar , Kylan Szeto
IPC: C12N15/10 , C12Q1/6825 , C12Q1/6874 , G01N35/10
CPC classification number: C12N15/1065 , C12Q1/6825 , C12Q1/6874 , G01N35/1081
Abstract: A method for sequencing a target polynucleotide includes detecting a first series of nucleotide incorporations complementary to at least a portion of the target polynucleotide. The first series of nucleotide incorporations forms a first complementary polynucleotide. The target nucleotide is secured to a substrate disposed in a sequencing zone of an assembly. The method further includes moving the substrate to which the target nucleotide is secured to a templating zone of the assembly; removing the first complementary polynucleotide when the substrate is disposed at the templating zone of the assembly, the target polynucleotide remaining secured to the substrate; following the removing, moving the substrate to which the target polynucleotide is secured to the sequencing zone; and detecting a second series of nucleotide incorporations complementary to at least a portion of the target polynucleotide, the second series of nucleotide incorporations forming a second complementary polynucleotide.
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公开(公告)号:US11959074B2
公开(公告)日:2024-04-16
申请号:US17525737
申请日:2021-11-12
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Chiu Tai Andrew Wong , Kylan Szeto , Shanti Shankar , Mark Beauchemin
IPC: C12N15/10 , C12Q1/6825 , C12Q1/6874 , G01N35/10
CPC classification number: C12N15/1065 , C12Q1/6825 , C12Q1/6874 , G01N35/1081
Abstract: A method for sequencing a target polynucleotide includes detecting a first series of nucleotide incorporations complementary to at least a portion of the target polynucleotide. The first series of nucleotide incorporations forms a first complementary polynucleotide. The target nucleotide is secured to a substrate disposed in a sequencing zone of an assembly. The method further includes moving the substrate to which the target nucleotide is secured to a templating zone of the assembly; removing the first complementary polynucleotide when the substrate is disposed at the templating zone of the assembly, the target polynucleotide remaining secured to the substrate; following the removing, moving the substrate to which the target polynucleotide is secured to the sequencing zone; and detecting a second series of nucleotide incorporations complementary to at least a portion of the target polynucleotide, the second series of nucleotide incorporations forming a second complementary polynucleotide.
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公开(公告)号:US20240182965A1
公开(公告)日:2024-06-06
申请号:US18437474
申请日:2024-02-09
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Mark Reed , Chiu Tai Andrew Wong , David Marran
IPC: C12Q1/6874
CPC classification number: C12Q1/6874
Abstract: A sequencing system includes an automated sequencing instrument adapted to determine variant calls for one or more extracted polynucleotide samples with a performance of at least 98.5% raw read accuracy and a run time in a range of 5 hours to 14 hours to determine variant calls for 4 extracted polynucleotide samples using a targeted assay with one DNA pool per sample and an average amplicon size in a range of 100 to 120 bases.
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公开(公告)号:US11905558B2
公开(公告)日:2024-02-20
申请号:US16994318
申请日:2020-08-14
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Mark Reed , Chiu Tai Andrew Wong , David Marran
IPC: C12Q1/6874
CPC classification number: C12Q1/6874
Abstract: A sequencing system includes an automated sequencing instrument adapted to determine variant calls for one or more extracted polynucleotide samples with a performance of at least 98.5% raw read accuracy and a run time in a range of 5 hours to 14 hours to determine variant calls for 4 extracted polynucleotide samples using a targeted assay with one DNA pool per sample and an average amplicon size in a range of 100 to 120 bases.
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