JP2013517789A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013517789A5 JP2013517789A5 JP2012550529A JP2012550529A JP2013517789A5 JP 2013517789 A5 JP2013517789 A5 JP 2013517789A5 JP 2012550529 A JP2012550529 A JP 2012550529A JP 2012550529 A JP2012550529 A JP 2012550529A JP 2013517789 A5 JP2013517789 A5 JP 2013517789A5
- Authority
- JP
- Japan
- Prior art keywords
- seq
- base pair
- dna
- sample
- chromosome
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 claims description 56
- 210000000349 chromosome Anatomy 0.000 claims description 44
- 230000008774 maternal effect Effects 0.000 claims description 23
- 230000006607 hypermethylation Effects 0.000 claims description 20
- 210000004369 blood Anatomy 0.000 claims description 19
- 239000008280 blood Substances 0.000 claims description 19
- 230000011987 methylation Effects 0.000 claims description 12
- 238000007069 methylation reaction Methods 0.000 claims description 12
- 201000010374 Down Syndrome Diseases 0.000 claims description 11
- 206010044688 Trisomy 21 Diseases 0.000 claims description 11
- 208000036878 aneuploidy Diseases 0.000 claims description 10
- 231100001075 aneuploidy Toxicity 0.000 claims description 10
- 230000001605 fetal effect Effects 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 108020004707 nucleic acids Proteins 0.000 claims description 8
- 150000007523 nucleic acids Chemical class 0.000 claims description 8
- 102000039446 nucleic acids Human genes 0.000 claims description 8
- 210000005259 peripheral blood Anatomy 0.000 claims description 8
- 239000011886 peripheral blood Substances 0.000 claims description 8
- 239000002773 nucleotide Substances 0.000 claims description 6
- 125000003729 nucleotide group Chemical group 0.000 claims description 6
- 239000003155 DNA primer Substances 0.000 claims description 5
- 238000003745 diagnosis Methods 0.000 claims description 5
- 230000001404 mediated effect Effects 0.000 claims description 5
- 238000003752 polymerase chain reaction Methods 0.000 claims description 5
- 108091034117 Oligonucleotide Proteins 0.000 claims description 4
- 210000001766 X chromosome Anatomy 0.000 claims description 4
- 210000002593 Y chromosome Anatomy 0.000 claims description 4
- 238000003793 prenatal diagnosis Methods 0.000 claims description 4
- 238000003753 real-time PCR Methods 0.000 claims description 4
- 208000037280 Trisomy Diseases 0.000 claims description 3
- 239000012133 immunoprecipitate Substances 0.000 claims description 3
- 238000001114 immunoprecipitation Methods 0.000 claims description 3
- 238000009007 Diagnostic Kit Methods 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 208000030454 monosomy Diseases 0.000 claims description 2
- 230000003169 placental effect Effects 0.000 claims description 2
- 239000013615 primer Substances 0.000 claims description 2
- 238000001514 detection method Methods 0.000 claims 5
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 230000029087 digestion Effects 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29833910P | 2010-01-26 | 2010-01-26 | |
| US61/298,339 | 2010-01-26 | ||
| US40542110P | 2010-10-21 | 2010-10-21 | |
| US61/405,421 | 2010-10-21 | ||
| PCT/IB2011/000217 WO2011092592A2 (en) | 2010-01-26 | 2011-01-26 | Methods and compositions for noninvasive prenatal diagnosis of fetal aneuploidies |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013517789A JP2013517789A (ja) | 2013-05-20 |
| JP2013517789A5 true JP2013517789A5 (enExample) | 2014-03-13 |
Family
ID=44278821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012550529A Pending JP2013517789A (ja) | 2010-01-26 | 2011-01-26 | 胎児異数性の非侵襲性出生前診断の方法および組成物 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US9249462B2 (enExample) |
| EP (1) | EP2529032B1 (enExample) |
| JP (1) | JP2013517789A (enExample) |
| KR (1) | KR20120107512A (enExample) |
| CN (1) | CN102892899A (enExample) |
| AU (1) | AU2011210255B2 (enExample) |
| BR (1) | BR112012018458A2 (enExample) |
| CA (1) | CA2786174A1 (enExample) |
| CY (1) | CY1118864T1 (enExample) |
| DK (1) | DK2529032T3 (enExample) |
| EA (1) | EA023565B1 (enExample) |
| ES (1) | ES2623156T3 (enExample) |
| NZ (1) | NZ601079A (enExample) |
| PL (1) | PL2529032T3 (enExample) |
| PT (1) | PT2529032T (enExample) |
| SG (1) | SG182322A1 (enExample) |
| WO (1) | WO2011092592A2 (enExample) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101153336B (zh) | 2006-09-27 | 2011-09-07 | 香港中文大学 | 检测dna甲基化程度的方法和试剂盒 |
| US8476013B2 (en) | 2008-09-16 | 2013-07-02 | Sequenom, Inc. | Processes and compositions for methylation-based acid enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses |
| US8962247B2 (en) | 2008-09-16 | 2015-02-24 | Sequenom, Inc. | Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non invasive prenatal diagnoses |
| EP2516680B1 (en) | 2009-12-22 | 2016-04-06 | Sequenom, Inc. | Processes and kits for identifying aneuploidy |
| US9605313B2 (en) | 2012-03-02 | 2017-03-28 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US9920361B2 (en) | 2012-05-21 | 2018-03-20 | Sequenom, Inc. | Methods and compositions for analyzing nucleic acid |
| US10504613B2 (en) | 2012-12-20 | 2019-12-10 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP2872648B1 (en) | 2012-07-13 | 2019-09-04 | Sequenom, Inc. | Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses |
| US9732390B2 (en) | 2012-09-20 | 2017-08-15 | The Chinese University Of Hong Kong | Non-invasive determination of methylome of fetus or tumor from plasma |
| US10706957B2 (en) | 2012-09-20 | 2020-07-07 | The Chinese University Of Hong Kong | Non-invasive determination of methylome of tumor from plasma |
| FI4056712T3 (fi) * | 2012-09-20 | 2024-08-29 | Univ Hong Kong Chinese | Kasvaimen metyloomin nonivasiivinen määrittäminen plasmasta |
| CN104838013A (zh) * | 2012-09-26 | 2015-08-12 | 新加坡科技研究局 | 用于唐氏综合症产前诊断的生物标志物 |
| EP3597774A1 (en) | 2013-03-13 | 2020-01-22 | Sequenom, Inc. | Primers for dna methylation analysis |
| KR20140118682A (ko) | 2013-03-29 | 2014-10-08 | (주)셀트리온 | 2 이상의 인플루엔자 a 바이러스 중화 결합 분자를 포함하는 조성물 |
| EP3117011B1 (en) | 2014-03-13 | 2020-05-06 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| RU2583830C2 (ru) * | 2014-04-21 | 2016-05-10 | Закрытое акционерное общество "Геноаналитика" | Способ неинвазивной пренатальной диагностики анеуплоидий плода |
| EP2942401A1 (en) | 2014-05-09 | 2015-11-11 | Lifecodexx AG | Detection of DNA that originates from a specific cell-type |
| EP2942400A1 (en) | 2014-05-09 | 2015-11-11 | Lifecodexx AG | Multiplex detection of DNA that originates from a specific cell-type |
| EP3521454A1 (en) | 2014-05-09 | 2019-08-07 | LifeCodexx AG | Detection of dna that originates from a specific cell-type and related methods |
| US20180187267A1 (en) * | 2017-01-05 | 2018-07-05 | Michael J. Powell | Method for conducting early detection of colon cancer and/or of colon cancer precursor cells and for monitoring colon cancer recurrence |
| US10174383B2 (en) * | 2014-08-13 | 2019-01-08 | Vanadis Diagnostics | Method of estimating the amount of a methylated locus in a sample |
| WO2016176846A1 (zh) * | 2015-05-06 | 2016-11-10 | 安诺优达基因科技(北京)有限公司 | 检测染色体非整倍性的试剂盒、装置和方法 |
| WO2016189388A1 (en) | 2015-05-22 | 2016-12-01 | Nipd Genetics Ltd | Multiplexed parallel analysis of targeted genomic regions for non-invasive prenatal testing |
| DK3168309T3 (da) | 2015-11-10 | 2020-06-22 | Eurofins Lifecodexx Gmbh | Detektion af føtale kromosomale aneuploidier under anvendelse af dna-regioner med forskellig metylering mellem fosteret og det gravide hunkøn |
| SG11201804651XA (en) * | 2015-12-04 | 2018-07-30 | Green Cross Genome Corp | Method for determining copy-number variation in sample comprising mixture of nucleic acids |
| KR101817180B1 (ko) * | 2016-01-20 | 2018-01-10 | 이원다이애그노믹스(주) | 염색체 이상 판단 방법 |
| US10781490B2 (en) | 2016-05-30 | 2020-09-22 | The Chinese University Of Hong Kong | Detecting hematological disorders using cell-free DNA in blood |
| CN109112209B (zh) * | 2017-06-25 | 2022-06-24 | 国家卫生计生委科学技术研究所 | 用于无创产前检测胎儿非整倍体染色体的参考品 |
| US12027237B2 (en) | 2018-03-13 | 2024-07-02 | Grail, Llc | Anomalous fragment detection and classification |
| KR20200060969A (ko) | 2018-11-23 | 2020-06-02 | (주)셀트리온 | 인플루엔자 바이러스 질환을 치료하기 위한 투여 요법 |
| US12234514B2 (en) | 2018-12-21 | 2025-02-25 | Grail, Inc. | Source of origin deconvolution based on methylation fragments in cell-free DNA samples |
| US20230151409A1 (en) * | 2020-03-30 | 2023-05-18 | Vilnius University | Methods and compositions for noninvasive prenatal diagnosis through targeted covalent labeling of genomic sites |
| KR102332540B1 (ko) * | 2020-07-02 | 2021-11-29 | 의료법인 성광의료재단 | 다운증후군 특이적인 후성학적 마커를 이용한 다운증후군 진단 방법 |
| US20250079015A1 (en) * | 2022-01-10 | 2025-03-06 | Washington State University | Dna methylation biomarkers for preterm birth |
| WO2024216205A1 (en) * | 2023-04-14 | 2024-10-17 | Adela, Inc. | Methods and systems for cell-free nucleic acid processing |
| WO2025179073A1 (en) * | 2024-02-21 | 2025-08-28 | Adela, Inc. | Methods and systems for tissue informed differentially methylated region analysis |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6582908B2 (en) * | 1990-12-06 | 2003-06-24 | Affymetrix, Inc. | Oligonucleotides |
| JP5013869B2 (ja) * | 2003-09-22 | 2012-08-29 | トリソゲン バイオテクノロジー リミテッド パートナーシップ | 遺伝子座コピー数の変化を検出するのに有用な方法およびキット |
| US20050282213A1 (en) | 2003-09-22 | 2005-12-22 | Trisogen Biotechnology Limited Partnership | Methods and kits useful for detecting an alteration in a locus copy number |
| GB0413688D0 (en) | 2004-06-18 | 2004-07-21 | Novartis Forschungsstiftung | Analysis of methylated nucleic acid |
| AU2005308918B2 (en) | 2004-11-29 | 2012-09-27 | Sequenom, Inc. | Means and methods for detecting methylated DNA |
| WO2007044780A2 (en) | 2005-10-07 | 2007-04-19 | Emory University | Methods and systems for screening for and diagnosing dna methylation associated abnormalities and sex chromosome aneuploidies |
| US7901884B2 (en) * | 2006-05-03 | 2011-03-08 | The Chinese University Of Hong Kong | Markers for prenatal diagnosis and monitoring |
| EP3892736A1 (en) | 2007-07-23 | 2021-10-13 | The Chinese University of Hong Kong | Determining a nucleic acid sequence imbalance |
| JP5322471B2 (ja) | 2008-03-27 | 2013-10-23 | シスメックス株式会社 | メチル化dnaの解析方法及びプライマーセット |
| US8476013B2 (en) * | 2008-09-16 | 2013-07-02 | Sequenom, Inc. | Processes and compositions for methylation-based acid enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses |
-
2011
- 2011-01-26 NZ NZ601079A patent/NZ601079A/en unknown
- 2011-01-26 AU AU2011210255A patent/AU2011210255B2/en active Active
- 2011-01-26 EP EP11709465.6A patent/EP2529032B1/en active Active
- 2011-01-26 CN CN2011800097571A patent/CN102892899A/zh active Pending
- 2011-01-26 PT PT117094656T patent/PT2529032T/pt unknown
- 2011-01-26 ES ES11709465.6T patent/ES2623156T3/es active Active
- 2011-01-26 KR KR1020127020832A patent/KR20120107512A/ko not_active Withdrawn
- 2011-01-26 EA EA201290716A patent/EA023565B1/ru not_active IP Right Cessation
- 2011-01-26 DK DK11709465.6T patent/DK2529032T3/en active
- 2011-01-26 PL PL11709465T patent/PL2529032T3/pl unknown
- 2011-01-26 CA CA2786174A patent/CA2786174A1/en not_active Abandoned
- 2011-01-26 JP JP2012550529A patent/JP2013517789A/ja active Pending
- 2011-01-26 SG SG2012049003A patent/SG182322A1/en unknown
- 2011-01-26 BR BR112012018458A patent/BR112012018458A2/pt not_active IP Right Cessation
- 2011-01-26 US US13/520,708 patent/US9249462B2/en active Active
- 2011-01-26 WO PCT/IB2011/000217 patent/WO2011092592A2/en not_active Ceased
-
2017
- 2017-04-21 CY CY20171100452T patent/CY1118864T1/el unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013517789A5 (enExample) | ||
| AU2022202491B2 (en) | Probe set for analyzing a DNA sample and method for using the same | |
| US10711269B2 (en) | Method for making an asymmetrically-tagged sequencing library | |
| JP2019162102A (ja) | 末梢血中で、がんによって変化したrnaを検出するシステムおよび方法 | |
| US10876169B2 (en) | Method and kit for estimating the amount of a methylated locus in a sample | |
| JP2017506908A (ja) | 対象シークエンスを有する核酸の量の減少または増加の検出方法 | |
| JP2021511075A (ja) | 癌におけるマイクロサテライト不安定性を検出するためのバイオマーカーパネル及び方法 | |
| US20220364173A1 (en) | Methods and systems for detection of nucleic acid modifications | |
| EP3565906B1 (en) | Quantifying dna sequences | |
| WO2020159608A1 (en) | Cost-effective detection of low frequency genetic variation | |
| US20250154187A1 (en) | Compositions and methods related to modification and detection of pseudouridine and 5-hydroxymethylcytosine | |
| JP6468555B2 (ja) | 検出キット,及び検出方法 | |
| Cawthon | A novel PCR method directly quantifies sequence features that block primer extension | |
| EP3696279A1 (en) | Methods for noninvasive prenatal testing of fetal abnormalities | |
| HK1230651B (zh) | 分析dna样品的探针集合和使用所述探针集合的方法 | |
| WO2012072813A1 (en) | Genotyping application |