SG10202108175RA - Single cell whole genome libraries for methylation sequencing - Google Patents

Single cell whole genome libraries for methylation sequencing

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Publication number
SG10202108175RA
SG10202108175RA SG10202108175RA SG10202108175RA SG10202108175RA SG 10202108175R A SG10202108175R A SG 10202108175RA SG 10202108175R A SG10202108175R A SG 10202108175RA SG 10202108175R A SG10202108175R A SG 10202108175RA SG 10202108175R A SG10202108175R A SG 10202108175RA
Authority
SG
Singapore
Prior art keywords
single cell
whole genome
methylation sequencing
cell whole
genome libraries
Prior art date
Application number
SG10202108175RA
Inventor
Andrew C Adey
Ryan Mulqueen
Frank J Steemers
Dmitry K Pokholok
Steven Norberg
Original Assignee
Univ Oregon Health & Science
Illumina Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Univ Oregon Health & Science, Illumina Inc filed Critical Univ Oregon Health & Science
Publication of SG10202108175RA publication Critical patent/SG10202108175RA/en

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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/10Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/1034Isolating an individual clone by screening libraries
    • C12N15/1065Preparation or screening of tagged libraries, e.g. tagged microorganisms by STM-mutagenesis, tagged polynucleotides, gene tags
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/10Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/1034Isolating an individual clone by screening libraries
    • C12N15/1093General methods of preparing gene libraries, not provided for in other subgroups
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    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6806Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay
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    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6869Methods for sequencing
    • C12Q1/6874Methods for sequencing involving nucleic acid arrays, e.g. sequencing by hybridisation
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    • C12Q2523/00Reactions characterised by treatment of reaction samples
    • C12Q2523/10Characterised by chemical treatment
    • C12Q2523/101Crosslinking agents, e.g. psoralen
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12Q2523/00Reactions characterised by treatment of reaction samples
    • C12Q2523/10Characterised by chemical treatment
    • C12Q2523/125Bisulfite(s)
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/191Modifications characterised by incorporating an adaptor
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    • C12Q2535/00Reactions characterised by the assay type for determining the identity of a nucleotide base or a sequence of oligonucleotides
    • C12Q2535/122Massive parallel sequencing
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    • C12Q2537/00Reactions characterised by the reaction format or use of a specific feature
    • C12Q2537/10Reactions characterised by the reaction format or use of a specific feature the purpose or use of
    • C12Q2537/143Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
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    • C12Q2537/00Reactions characterised by the reaction format or use of a specific feature
    • C12Q2537/10Reactions characterised by the reaction format or use of a specific feature the purpose or use of
    • C12Q2537/159Reduction of complexity, e.g. amplification of subsets, removing duplicated genomic regions
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    • C12Q2563/00Nucleic acid detection characterized by the use of physical, structural and functional properties
    • C12Q2563/159Microreactors, e.g. emulsion PCR or sequencing, droplet PCR, microcapsules, i.e. non-liquid containers with a range of different permeability's for different reaction components
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    • C12Q2563/00Nucleic acid detection characterized by the use of physical, structural and functional properties
    • C12Q2563/179Nucleic acid detection characterized by the use of physical, structural and functional properties the label being a nucleic acid
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B50/00Methods of creating libraries, e.g. combinatorial synthesis
    • C40B50/14Solid phase synthesis, i.e. wherein one or more library building blocks are bound to a solid support during library creation; Particular methods of cleavage from the solid support
    • C40B50/18Solid phase synthesis, i.e. wherein one or more library building blocks are bound to a solid support during library creation; Particular methods of cleavage from the solid support using a particular method of attachment to the solid support
SG10202108175RA 2017-06-07 2018-06-05 Single cell whole genome libraries for methylation sequencing SG10202108175RA (en)

Applications Claiming Priority (1)

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US201762516324P 2017-06-07 2017-06-07

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US (1) US20180355348A1 (en)
EP (3) EP3981884B1 (en)
JP (2) JP7407597B2 (en)
KR (2) KR20240013852A (en)
CN (1) CN110997932A (en)
AU (1) AU2018280131A1 (en)
CA (1) CA3066424A1 (en)
DK (2) DK3981884T3 (en)
ES (2) ES2898250T3 (en)
FI (1) FI3981884T3 (en)
IL (2) IL271215A (en)
NZ (1) NZ759895A (en)
RU (1) RU2770879C2 (en)
SG (2) SG11201911730XA (en)
WO (1) WO2018226708A1 (en)

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EP4293122A3 (en) 2024-01-24
JP7407597B2 (en) 2024-01-04
EP3981884B1 (en) 2023-08-09
IL271241A (en) 2020-01-30
JP2023085466A (en) 2023-06-20
NZ759895A (en) 2023-05-26
EP3635136B1 (en) 2021-10-20
AU2018280131A1 (en) 2020-01-02
JP2020523011A (en) 2020-08-06
RU2019144026A3 (en) 2021-10-07
CN110997932A (en) 2020-04-10
DK3981884T3 (en) 2023-09-04
ES2959047T3 (en) 2024-02-19
EP3981884A1 (en) 2022-04-13
US20180355348A1 (en) 2018-12-13
FI3981884T3 (en) 2023-09-21
RU2770879C2 (en) 2022-04-22
EP4293122A2 (en) 2023-12-20
EP3635136A1 (en) 2020-04-15
KR20240013852A (en) 2024-01-30
ES2898250T3 (en) 2022-03-04
IL271215A (en) 2020-01-30
DK3635136T3 (en) 2022-01-10
CA3066424A1 (en) 2018-12-13
SG11201911730XA (en) 2020-01-30
KR20200016287A (en) 2020-02-14
KR102628035B1 (en) 2024-01-22
RU2019144026A (en) 2021-07-09
WO2018226708A1 (en) 2018-12-13

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