GEL ELECTROPHORESIS FOR DNA PURIFICATION

    公开(公告)号:US20210349054A1

    公开(公告)日:2021-11-11

    申请号:US16870580

    申请日:2020-05-08

    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.

    DNA BACKBONE EDITING FOR DNA DATA STORAGE

    公开(公告)号:US20220090157A1

    公开(公告)日:2022-03-24

    申请号:US17031664

    申请日:2020-09-24

    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.

    METHODS OF GENE ASSEMBLY AND THEIR USE IN DNA DATA STORAGE

    公开(公告)号:US20210309991A1

    公开(公告)日:2021-10-07

    申请号:US17348642

    申请日:2021-06-15

    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.

    MICROFLUIDIC LAB-ON-A-CHIP FOR GENE SYNTHESIS

    公开(公告)号:US20210054364A1

    公开(公告)日:2021-02-25

    申请号:US16857006

    申请日:2020-04-23

    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.

    DNA BACKBONE EDITING FOR DNA DATA STORAGE
    6.
    发明公开

    公开(公告)号:US20240282374A1

    公开(公告)日:2024-08-22

    申请号:US18638432

    申请日:2024-04-17

    CPC classification number: G11C13/02 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.

    METHODS OF GENE ASSEMBLY AND THEIR USE IN DNA DATA STORAGE

    公开(公告)号:US20210054368A1

    公开(公告)日:2021-02-25

    申请号:US16856947

    申请日:2020-04-23

    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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