SG11201811735WA - Method for producing dna library and method for analyzing genomic dna using the dna library - Google Patents

Method for producing dna library and method for analyzing genomic dna using the dna library

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Publication number
SG11201811735WA
SG11201811735WA SG11201811735WA SG11201811735WA SG11201811735WA SG 11201811735W A SG11201811735W A SG 11201811735WA SG 11201811735W A SG11201811735W A SG 11201811735WA SG 11201811735W A SG11201811735W A SG 11201811735WA SG 11201811735W A SG11201811735W A SG 11201811735WA
Authority
SG
Singapore
Prior art keywords
dna
dna library
library
producing
genomic dna
Prior art date
Application number
SG11201811735WA
Other languages
English (en)
Inventor
Hiroyuki Enoki
Yoshie Takeuchi
Original Assignee
Toyota Motor Co Ltd
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 Toyota Motor Co Ltd filed Critical Toyota Motor Co Ltd
Priority claimed from PCT/JP2017/013965 external-priority patent/WO2018003220A1/ja
Publication of SG11201811735WA publication Critical patent/SG11201811735WA/en

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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • 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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    • 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
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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
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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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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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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
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B40/00Libraries per se, e.g. arrays, mixtures
    • C40B40/04Libraries containing only organic compounds
    • C40B40/06Libraries containing nucleotides or polynucleotides, or derivatives thereof
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    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B50/00Methods of creating libraries, e.g. combinatorial synthesis
    • C40B50/06Biochemical methods, e.g. using enzymes or whole viable microorganisms
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    • C12Q2521/00Reaction characterised by the enzymatic activity
    • C12Q2521/10Nucleotidyl transfering
    • C12Q2521/101DNA polymerase
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/179Modifications characterised by incorporating arbitrary or random nucleotide sequences
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    • C12Q2525/00Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
    • C12Q2525/10Modifications characterised by
    • C12Q2525/204Modifications characterised by specific length of the oligonucleotides
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    • C12Q2527/00Reactions demanding special reaction conditions
    • C12Q2527/143Concentration of primer or probe
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    • C12Q2531/00Reactions of nucleic acids characterised by
    • C12Q2531/10Reactions of nucleic acids characterised by the purpose being amplify/increase the copy number of target nucleic acid
    • C12Q2531/113PCR
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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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    • C12Q2563/00Nucleic acid detection characterized by the use of physical, structural and functional properties
    • C12Q2563/107Nucleic acid detection characterized by the use of physical, structural and functional properties fluorescence
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    • C12Q2565/00Nucleic acid analysis characterised by mode or means of detection
    • C12Q2565/10Detection mode being characterised by the assay principle
    • C12Q2565/125Electrophoretic separation
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    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/16Primer sets for multiplex assays

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Microbiology (AREA)
  • Biomedical Technology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • General Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Analytical Chemistry (AREA)
  • Plant Pathology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Immunology (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
SG11201811735WA 2016-06-29 2017-04-03 Method for producing dna library and method for analyzing genomic dna using the dna library SG11201811735WA (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2016129048 2016-06-29
JP2016178528 2016-09-13
JP2017071020A JP7343264B2 (ja) 2016-06-29 2017-03-31 Dnaライブラリーの作製方法及びdnaライブラリーを用いたゲノムdna解析方法
PCT/JP2017/013965 WO2018003220A1 (ja) 2016-06-29 2017-04-03 Dnaライブラリーの作製方法及びdnaライブラリーを用いたゲノムdna解析方法

Publications (1)

Publication Number Publication Date
SG11201811735WA true SG11201811735WA (en) 2019-01-30

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Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201811735WA SG11201811735WA (en) 2016-06-29 2017-04-03 Method for producing dna library and method for analyzing genomic dna using the dna library

Country Status (11)

Country Link
US (1) US20190233889A1 (es)
EP (1) EP3480319A1 (es)
JP (1) JP7343264B2 (es)
KR (1) KR102298586B1 (es)
CN (1) CN109715798B (es)
AU (1) AU2017287059B2 (es)
CA (1) CA3029167C (es)
IL (1) IL263960A (es)
MX (1) MX2018015860A (es)
PH (1) PH12018502739A1 (es)
SG (1) SG11201811735WA (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106676099B (zh) * 2016-12-21 2019-07-02 中国水稻研究所 构建简化基因组文库的方法及试剂盒
JP7056012B2 (ja) * 2017-05-19 2022-04-19 トヨタ自動車株式会社 ランダムプライマーセット、及びこれを用いたdnaライブラリーの作製方法
JP7047373B2 (ja) 2017-12-25 2022-04-05 トヨタ自動車株式会社 次世代シーケンサー用プライマー並びにその製造方法、次世代シーケンサー用プライマーを用いたdnaライブラリー並びにその製造方法、及びdnaライブラリーを用いたゲノムdna解析方法
CN110256566A (zh) * 2019-05-10 2019-09-20 江苏苏博生物医学科技南京有限公司 Taq DNA聚合酶单链免疫球蛋白IgG抗体、制备方法及其在基因分型检测中的应用

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4255630B2 (ja) 2001-09-10 2009-04-15 独立行政法人農業・食品産業技術総合研究機構 米のdna食味判定技術及び籾/玄米半粒による良食味米選抜方法
DE03808546T1 (de) * 2002-12-23 2006-01-26 Agilent Technologies, Inc., Palo Alto Vergleichende genomischehybridisierungstests unter verwendung von merkmalen immobilisierteroligonukleotide sowie zusammensetzungen zur durchführung davon
EP1604040B1 (en) * 2003-03-07 2010-10-13 Rubicon Genomics, Inc. Amplification and analysis of whole genome and whole transcriptome libraries generated by a dna polymerization process
US8206913B1 (en) * 2003-03-07 2012-06-26 Rubicon Genomics, Inc. Amplification and analysis of whole genome and whole transcriptome libraries generated by a DNA polymerization process
WO2005003304A2 (en) * 2003-06-20 2005-01-13 Illumina, Inc. Methods and compositions for whole genome amplification and genotyping
US20040259100A1 (en) * 2003-06-20 2004-12-23 Illumina, Inc. Methods and compositions for whole genome amplification and genotyping
JP3972106B2 (ja) * 2004-03-03 2007-09-05 大学共同利用機関法人情報・システム研究機構 ゲノムライブラリー作製方法、および同方法により作製されたゲノムライブラリー
PT2963127T (pt) * 2006-04-04 2017-10-06 Keygene Nv Detecção de alto rendimento de marcadores moleculares com base em fragmentos de restrição

Also Published As

Publication number Publication date
BR112018077489A2 (pt) 2019-09-03
EP3480319A4 (en) 2019-05-08
US20190233889A1 (en) 2019-08-01
KR102298586B1 (ko) 2021-09-07
JP7343264B2 (ja) 2023-09-12
CN109715798B (zh) 2023-04-28
PH12018502739A1 (en) 2019-09-30
EP3480319A1 (en) 2019-05-08
KR20190020338A (ko) 2019-02-28
NZ749198A (en) 2021-01-29
AU2017287059B2 (en) 2021-06-10
MX2018015860A (es) 2019-03-28
JP2018042548A (ja) 2018-03-22
CA3029167C (en) 2022-06-21
CA3029167A1 (en) 2018-01-04
CN109715798A (zh) 2019-05-03
IL263960A (en) 2019-01-31

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