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公开(公告)号:US20210047682A1
公开(公告)日:2021-02-18
申请号:US16591232
申请日:2019-10-02
Applicant: Seagate Technology LLC
Inventor: Gemma MENDONSA , Riyan A. MENDONSA , Krishnan SUBRAMANIAN
IPC: C12Q1/6869 , G01N33/487 , G01N27/72
Abstract: Method of utilizing a nanochannel in combination with at least one magnetic sensor for detecting (e.g., identifying) molecules, cells, and other analytes. Particularly, the method includes bringing molecules, labeled with magnetic nanoparticles (MNPs), in close proximity to the magnetic sensor to identify the molecules via an output signal from the magnetic sensor. The method is particularly suited for identifying nucleotides of DNA and RNA strands.
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公开(公告)号:US20210349054A1
公开(公告)日:2021-11-11
申请号:US16870580
申请日:2020-05-08
Applicant: Seagate Technology LLC
Inventor: Gemma MENDONSA , Tim RAUSCH , Riyan Alex MENDONSA
IPC: G01N27/447 , C12N15/10
Abstract: Systems and methods for identifying DNA strand size and purifying the DNA based on strand size using electrophoresis. The methods include moving, via voltage, a plurality of DNA strands through a separation gel from an inlet of a capillary or passage to either a first outlet or a second outlet dependent on the DNA strand length. In some implementations, the system is a capillary electrophoresis system. In other implementations, the system is a microfluidic lab-on-a-chip.
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公开(公告)号:US20220090157A1
公开(公告)日:2022-03-24
申请号:US17031664
申请日:2020-09-24
Applicant: Seagate Technology LLC
Inventor: Gemma MENDONSA , Riyan Alex MENDONSA , Tim RAUSCH
IPC: C12P19/34
Abstract: Methods of writing data to a DNA strand by inserting data-encoding oligos or symbols into a DNA backbone. One particular method of synthesizing a DNA strand encoding data includes cleaving a DNA backbone into multiple segments, and pasting a plurality of data-encoding oligo symbols between the multiple segments, with the terminal ends of the segments joining homologous terminal ends of the symbols, resulting in the DNA strand encoding data comprising alternating segments and symbols.
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公开(公告)号:US20210309991A1
公开(公告)日:2021-10-07
申请号:US17348642
申请日:2021-06-15
Applicant: Seagate Technology LLC
Inventor: Tim RAUSCH , Walter R EPPLER , Gemma MENDONSA
Abstract: A system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The symbol library has a number of DNA symbols each having a first overhanging end and a second overhanging end different than and non-complimentary to the first end, the first and second ends being the same nucleotides for each DNA symbol. The linker library has pairs of DNA linkers, a first linker of a pair having a first end and a second end and a second linker of the pair having a first end and a second end, the first end of the first linker being the same nucleotides for each first linker and the second end of the second linker being the same nucleotides for each second linker, wherein the second end of the first linker and the first end of the second linker have complementary nucleotides. The first linker joins to the first end of a DNA symbol and the second linker joins to the second end of another DNA symbol.
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公开(公告)号:US20210054364A1
公开(公告)日:2021-02-25
申请号:US16857006
申请日:2020-04-23
Applicant: Seagate Technology LLC
Inventor: Tim RAUSCH , Walter R EPPLER , Gemma MENDONSA
Abstract: A microfluidic lab-on-a-chip system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The lab-on-a-chip has a fluidic platform with a plurality of arrays operably connected to a voltage source and a controller for the voltage source, a set of first inlets operably connected to the fluidic platform, each first inlet for one DNA symbol from a DNA symbol library, a set of second inlets operably connected to the fluidic platform, each second inlet for one DNA linker from a DNA linker library, and a mixing area operably connected to the fluidic platform and to the plurality of first inlets and the plurality of second inlets.
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公开(公告)号:US20240282374A1
公开(公告)日:2024-08-22
申请号:US18638432
申请日:2024-04-17
Applicant: Seagate Technology LLC
Inventor: Gemma MENDONSA , Riyan Alex MENDONSA , Tim RAUSCH
Abstract: Methods of writing data to a DNA strand by inserting data-encoding oligos or symbols into a DNA backbone. One particular method of synthesizing a DNA strand encoding data includes cleaving a DNA backbone into multiple segments, and pasting a plurality of data-encoding oligo symbols between the multiple segments, with the terminal ends of the segments joining homologous terminal ends of the symbols, resulting in the DNA strand encoding data comprising alternating segments and symbols.
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公开(公告)号:US20210054368A1
公开(公告)日:2021-02-25
申请号:US16856947
申请日:2020-04-23
Applicant: Seagate Technology LLC
Inventor: Tim RAUSCH , Walter R EPPLER , Gemma MENDONSA
Abstract: A system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The symbol library has a number of DNA symbols each having a first overhanging end and a second overhanging end different than and non-complimentary to the first end, the first and second ends being the same nucleotides for each DNA symbol. The linker library has pairs of DNA linkers, a first linker of a pair having a first overhanging end and a second overhanging end and a second linker of the pair having a first overhanging end and a second overhanging end, the first end of the first linker being the same nucleotides for each first linker and the second end of the second linker being the same nucleotides for each second linker, wherein the second end of the first linker and the first end of the second linker have complementary nucleotides. The first linker joins to the first end of a DNA symbol and the second linker joins to the second end of another DNA symbol.
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公开(公告)号:US20210047681A1
公开(公告)日:2021-02-18
申请号:US16591162
申请日:2019-10-02
Applicant: Seagate Technology LLC
Inventor: Gemma MENDONSA , Riyan A. MENDONSA , Krishnan SUBRAMANIAN
IPC: C12Q1/6869 , C12Q1/6876
Abstract: Methods of DNA sequencing from a template strand via DNA polymerase immobilized on a magnetic sensor. The methods include forming a complementary strand by the DNA polymerase from individual magnetic nanoparticle (MNP)-labeled nucleotides, and obtaining a signal from the magnetic sensor to identify the MNP and thus the nucleotide. The process can be repeated until the entire complementary strand is formed and identified.
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