WO2010033578A3 - Noninvasive diagnosis of fetal aneuploidy by sequencing - Google Patents

Noninvasive diagnosis of fetal aneuploidy by sequencing Download PDF

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Publication number
WO2010033578A3
WO2010033578A3 PCT/US2009/057136 US2009057136W WO2010033578A3 WO 2010033578 A3 WO2010033578 A3 WO 2010033578A3 US 2009057136 W US2009057136 W US 2009057136W WO 2010033578 A3 WO2010033578 A3 WO 2010033578A3
Authority
WO
WIPO (PCT)
Prior art keywords
chromosome
sequence tags
dna
sequencing
counting
Prior art date
Application number
PCT/US2009/057136
Other languages
French (fr)
Other versions
WO2010033578A2 (en
Inventor
Hei-Mun Christina Fan
Stephen R. Quake
Original Assignee
The Board Of Trustees Of The Leland Stanford Junior University
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42040105&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2010033578(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to AU2009293354A priority Critical patent/AU2009293354B2/en
Priority to EP18156359.4A priority patent/EP3378951B1/en
Priority to LTEP09815105.3T priority patent/LT2334812T/en
Priority to EP20174078.4A priority patent/EP3751005A3/en
Priority to CA2737643A priority patent/CA2737643C/en
Priority to ES09815105.3T priority patent/ES2620012T3/en
Priority to SI200931631A priority patent/SI2334812T1/en
Priority to EP09815105.3A priority patent/EP2334812B1/en
Application filed by The Board Of Trustees Of The Leland Stanford Junior University filed Critical The Board Of Trustees Of The Leland Stanford Junior University
Priority to DK09815105.3T priority patent/DK2334812T3/en
Publication of WO2010033578A2 publication Critical patent/WO2010033578A2/en
Publication of WO2010033578A3 publication Critical patent/WO2010033578A3/en
Priority to IL211794A priority patent/IL211794A/en
Priority to AU2015202167A priority patent/AU2015202167B2/en
Priority to IL243655A priority patent/IL243655A/en
Priority to CY20171100339T priority patent/CY1118802T1/en
Priority to HRP20170435TT priority patent/HRP20170435T1/en
Priority to AU2018201920A priority patent/AU2018201920B2/en
Priority to AU2021200569A priority patent/AU2021200569B2/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING 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
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING 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
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6869—Methods for sequencing
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING 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
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/156—Polymorphic or mutational markers
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00—Detection or diagnosis of diseases
    • G01N2800/38—Pediatrics
    • G01N2800/385—Congenital anomalies
    • G01N2800/387—Down syndrome; Trisomy 18; Trisomy 13

Abstract

Disclosed is a method to achieve digital quantification of DNA (i.e., counting differences between identical sequences) using direct shotgun sequencing followed by mapping to the chromosome of origin and enumeration of fragments per chromosome. The preferred method uses massively parallel sequencing, which can produce tens of millions of short sequence tags in a single run and enabling a sampling that can be statistically evaluated. By counting the number of sequence tags mapped to a predefined window in each chromosome, the over- or under- representation of any chromosome in maternal plasma DNA contributed by an aneuploid fetus can be detected. This method does not require the differentiation of fetal versus maternal DNA. The median count of autosomal values is used as a normalization constant to account for differences in total number of sequence tags is used for comparison between samples and between chromosomes.
PCT/US2009/057136 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing WO2010033578A2 (en)

Priority Applications (16)

Application Number Priority Date Filing Date Title
DK09815105.3T DK2334812T3 (en) 2008-09-20 2009-09-16 Non-invasive diagnosis of fetal aneuploidy by sequencing
EP18156359.4A EP3378951B1 (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of aneuploidy by sequencing
LTEP09815105.3T LT2334812T (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing
EP20174078.4A EP3751005A3 (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing
CA2737643A CA2737643C (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing
AU2009293354A AU2009293354B2 (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing
ES09815105.3T ES2620012T3 (en) 2008-09-20 2009-09-16 Non-invasive diagnosis of fetal aneuploidy by sequencing
SI200931631A SI2334812T1 (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing
EP09815105.3A EP2334812B1 (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing
IL211794A IL211794A (en) 2008-09-20 2011-03-17 Noninvasive diagnosis of fetal aneuploidy by sequencing
AU2015202167A AU2015202167B2 (en) 2008-09-20 2015-04-28 Noninvasive diagnosis of fetal aneuploidy by sequencing
IL243655A IL243655A (en) 2008-09-20 2016-01-18 Noninvasive diagnosis of fetal aneuploidy by sequencing
CY20171100339T CY1118802T1 (en) 2008-09-20 2017-03-16 NON-INVESTIGATIVE DIAGNOSIS OF EMBRYOPATHIC DISEASE WITH CONTROL
HRP20170435TT HRP20170435T1 (en) 2008-09-20 2017-03-17 Noninvasive diagnosis of fetal aneuploidy by sequencing
AU2018201920A AU2018201920B2 (en) 2008-09-20 2018-03-16 Noninvasive diagnosis of fetal aneuploidy by sequencing
AU2021200569A AU2021200569B2 (en) 2008-09-20 2021-01-29 Noninvasive diagnosis of fetal aneuploidy by sequencing

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9875808P 2008-09-20 2008-09-20
US61/098,758 2008-09-20

Publications (2)

Publication Number Publication Date
WO2010033578A2 WO2010033578A2 (en) 2010-03-25
WO2010033578A3 true WO2010033578A3 (en) 2010-05-14

Family

ID=42040105

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2009/057136 WO2010033578A2 (en) 2008-09-20 2009-09-16 Noninvasive diagnosis of fetal aneuploidy by sequencing

Country Status (17)

Country Link
US (9) US20100112575A1 (en)
EP (5) EP3751005A3 (en)
AU (1) AU2009293354B2 (en)
CA (4) CA3069081C (en)
CY (2) CY1118802T1 (en)
DK (2) DK2334812T3 (en)
ES (2) ES2620294T3 (en)
HK (1) HK1217354A1 (en)
HR (2) HRP20170435T1 (en)
HU (2) HUE031848T2 (en)
IL (2) IL211794A (en)
LT (2) LT2334812T (en)
PL (2) PL2562268T3 (en)
PT (2) PT2562268T (en)
SG (1) SG10201500567VA (en)
SI (2) SI2334812T1 (en)
WO (1) WO2010033578A2 (en)

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CN111755068B (en) * 2020-06-19 2021-02-19 深圳吉因加医学检验实验室 Method and device for identifying tumor purity and absolute copy number based on sequencing data

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