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公开(公告)号:US11713235B2
公开(公告)日:2023-08-01
申请号:US17559440
申请日:2021-12-22
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Todd Roswech , Jonathan Schultz , Chun Heen Ho
CPC classification number: B67D7/0266 , B01L3/502 , B01L3/523 , B67D7/0288 , B67D7/76 , B01L3/563 , B01L2200/026 , B01L2200/0684 , B01L2200/0689 , B01L2300/043 , B01L2400/0487 , B67D2210/0001 , G01N35/1002
Abstract: A fluidic interconnect includes a first interface including a liquid port, a gas port, and a cradle; a second interface including a liquid port, a gas port, and a swing bar to engage the cradle, a weight of a container attached to one of the first or second interfaces to drive the liquid port of the first interface into connection with the liquid port of the second interface and the gas port of the first interface into connection with the gas port of the second interface.
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公开(公告)号:US11386978B2
公开(公告)日:2022-07-12
申请号:US16195068
申请日:2018-11-19
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Todd Rearick , Jonathan Schultz
IPC: G16B40/10 , G16B40/00 , C12Q1/6869
Abstract: Mathematical models for the analysis of signal data generated by sequencing of a polynucleotide strand using a pH-based method of detecting nucleotide incorporation(s). In an embodiment, the measured output signal from the reaction confinement region of a reactor array is mathematically modeled. The output signal may be modeled as a linear combination of one or more signal components, including a background signal component. This model is solved to determine the nucleotide incorporation signal. In another embodiment, the incorporation signal from the reaction confinement region of a reactor array is mathematically modeled.
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公开(公告)号:US20210047686A1
公开(公告)日:2021-02-18
申请号:US16882414
申请日:2020-05-22
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Jonathan M. Rothberg , Wolfgang Hinz , Kim L. Johnson , James Bustillo , John Leamon , Jonathan Schultz
IPC: C12Q1/6874 , G01N27/414 , B01L3/00 , C12Q1/6869
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 the concentration of inorganic pyrophosphate (PPi), hydrogen ions, and nucleotide triphosphates.
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公开(公告)号:US10894982B2
公开(公告)日:2021-01-19
申请号:US16289508
申请日:2019-02-28
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Jonathan Schultz , Todd Roswech , Jon A. Hoshizaki , Albert L. Carrillo , James A. Ball
IPC: C12Q1/6869 , C12Q1/6806 , B01L3/00 , G01N27/414 , G01N35/10 , B01F5/06 , B01F11/00 , B01F1/00
Abstract: A method of preparing reagents includes inserting a cartridge into an instrument. The cartridge includes a plurality of reagent enclosures disposed in a cavity of the cartridge and exposing a port to an exterior of the cartridge. Each reagent enclosure includes a reagent container including a reagent and an internal cavity defining a compressible volume, an opening defined through the reagent container to the internal cavity. The method further includes connecting a plurality of fluid ports to the openings of the plurality of reagent enclosures; applying a solution through the fluid ports to at least partially fill the plurality of reagent enclosures; and cycling a pressure of the cavity, whereby for each of the reagent enclosures, during increasing pressure, the solution enters the internal cavity of the reagent container, combines with the reagent, and compresses the compressible volume, and during decreasing pressure, the compressible volume decreases and the reagent is ejected through the opening.
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公开(公告)号:US10781474B2
公开(公告)日:2020-09-22
申请号:US15133428
申请日:2016-04-20
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Kristopher Barbee , Ryan Jones , Sean McCusker , Maximilian Carpino , John Leamon , Jonathan Schultz
IPC: B04B5/04 , C12Q1/6806 , G01N35/00 , G01N35/10 , C12Q1/6869 , B04B13/00
Abstract: A sample preparation apparatus includes a robotic system providing movement in three orthogonal directions to an arm operable to receive a pipette tip and to facilitate movement of fluid into and out of the pipette tip. Optionally, the robot can include a gripper arm in addition to the pipette receiving arm. In addition, the sample preparation apparatus can include a tray for receiving pipette tips, receptacles for receiving tubes, an apparatus for forming an emulsion, a device for forming particles that include copies of the polynucleotide, a device for enriching the particles, as well as a centrifuge for loading such particles onto a sensor array. The sample preparation apparatus can further include receptacles for holding containers of reagent solutions.
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公开(公告)号:US10597711B2
公开(公告)日:2020-03-24
申请号:US13859360
申请日:2013-04-09
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Earl Hubbell , Jonathan Schultz
IPC: C12Q1/68 , C12Q1/6869 , C12Q1/6874
Abstract: A method for nucleic acid sequencing includes: disposing a plurality of template polynucleotide strands, sequencing primers, and polymerases in a plurality of defined spaces of a sensor array; exposing template polynucleotide strands to a series of flows of nucleotide species, the series comprising a sequence of random flows; and obtaining, for each of the series of flows of nucleotide species, a signal indicative of how many nucleotide incorporations occurred for that particular flow to determine a predicted sequence of nucleotides corresponding to the template polynucleotide strands.
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公开(公告)号:US10478816B2
公开(公告)日:2019-11-19
申请号:US15348907
申请日:2016-11-10
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Jonathan Schultz , David Marran
IPC: C12M1/00 , C12M3/00 , C12M1/34 , B01L3/00 , C12Q1/6869 , G01N27/447 , G01N35/10
Abstract: The invention provides a passive fluidics circuit for directing different fluids to a common volume, such as a reaction chamber or flow cell, without intermixing or cross contamination. The direction and rate of flow through junctions, nodes and passages of the fluidics circuit are controlled by the states of upstream valves (e.g. opened or closed), differential fluid pressures at circuit inlets or upstream reservoirs, flow path resistances, and the like. Free diffusion or leakage of fluids from unselected inlets into the common outlet or other inlets at junctions or nodes is prevented by the flow of the selected inlet fluid, a portion of which sweeps by the inlets of unselected fluids and exits the fluidics circuit by waste ports, thereby creating a barrier against undesired intermixing with the outlet flow through leakage or diffusion. The invention is particularly advantageous in apparatus for performing sensitive multistep reactions, such as pH-based DNA sequencing reactions.
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公开(公告)号:US09937494B2
公开(公告)日:2018-04-10
申请号:US14739974
申请日:2015-06-15
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Jonathan Schultz , Todd Roswech
CPC classification number: B01L3/502 , B01F11/0008 , B01F11/0065 , B01F15/0238 , B01F15/028 , B01L3/505 , B01L3/527 , B01L2200/04 , B01L2200/16 , B01L2300/022 , B01L2300/0681 , B01L2300/0861 , B01L2300/123 , B01L2400/0481 , B01L2400/0487 , B65D81/3272 , G01N35/1002 , Y10T436/2575
Abstract: An apparatus for preparing a reagent solution includes an enclosure and a container disposed within the enclosure. The container defines an internal cavity having a compressible volume and defines a passage providing fluidic communication between the internal cavity and the exterior of the container. Optionally, a compressible member is disposed within the internal cavity. A reagent is disposed within the internal cavity.
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公开(公告)号:US09901887B2
公开(公告)日:2018-02-27
申请号:US15282283
申请日:2016-09-30
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Jonathan Schultz , John Nobile , Brian Reed , Prasanna Thwar , Todd Roswech , John Andrew Sheridan
IPC: C12M1/00 , C12M3/00 , C12M1/34 , B01F3/08 , C12P19/34 , C12M1/26 , B01F15/00 , B04B11/02 , B01F5/04 , B01F13/00 , B01L3/00 , B01L7/00 , B04B5/04 , B04B7/02 , C12Q1/68
CPC classification number: B01F3/0807 , B01F5/0485 , B01F13/0059 , B01F15/00 , B01F2215/0037 , B01L3/5021 , B01L3/502784 , B01L7/52 , B01L2200/026 , B01L2300/046 , B01L2300/06 , B01L2300/18 , B01L2300/1822 , B01L2300/1827 , B01L2300/1838 , B01L2400/0409 , B04B5/0414 , B04B7/02 , B04B11/02 , B04B2007/025 , C12M33/10 , C12P19/34 , C12Q1/686 , C12Q2523/32 , C12Q2563/159 , C12Q2565/629
Abstract: An automated template bead preparation system is provided and includes a membrane-based emulsion generation subsystems, a thermal plate and subsystem, and a continuous centrifugation emulsion breaking and templated bead collection subsystem. The emulsion generation subsystem provides uniformity in the preparation of an inverse emulsion and may be used to create large or small volume inverse emulsions rapidly and reproducibly. An emulsion-generating device is provided that can supply a continuous stream of an inverse emulsion to a thermal subsystem, in automated fashion. The thermal subsystem can treat an inverse emulsion passed therethrough. The continuous centrifugation subsystem can continuously break a thermally cycled inverse emulsion and collect template beads formed in the aqueous microreactor droplets of the inverse emulsion.
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公开(公告)号:US09776146B2
公开(公告)日:2017-10-03
申请号:US14696642
申请日:2015-04-27
Applicant: LIFE TECHNOLOGIES CORPORATION
Inventor: Jonathan Schultz , John Nobile , Brian Reed , Prasanna Krishnan Thwar , Todd Roswech
IPC: B01F5/06 , C12M1/34 , C12M3/00 , B01F3/08 , B01F5/04 , B01F13/00 , B04B5/04 , B04B7/02 , B01L3/00
CPC classification number: B01F5/0602 , B01F3/0807 , B01F5/0485 , B01F13/0059 , B01F2215/0037 , B01L3/502784 , B04B5/0414 , B04B7/02
Abstract: An automated on-touch template bead preparation system is provided and includes a membrane-based emulsion generation subsystems, an emulsion PCR (ePCR) thermocycling plate and subsystem, and a continuous centrifugation emulsion breaking and templated bead collection subsystem. The emulsion generation subsystem provides uniformity in the preparation of an inverse emulsion and may be used to create large or small volume inverse emulsions rapidly and reproducibly. An emulsion-generating device is provided that can supply a continuous stream of an inverse emulsion to a thermocycling subsystem, in automated fashion. The ePCR subsystem can continuously thermocycle an inverse emulsion passed therethrough and includes static temperature zones and a consumable thermocycling plate. The continuous centrifugation subsystem can continuously break a thermally cycled inverse emulsion and collect template beads formed in the aqueous microreactor droplets of the inverse emulsion.
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