JP2018196379A5 - - Google Patents
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- JP2018196379A5 JP2018196379A5 JP2018121829A JP2018121829A JP2018196379A5 JP 2018196379 A5 JP2018196379 A5 JP 2018196379A5 JP 2018121829 A JP2018121829 A JP 2018121829A JP 2018121829 A JP2018121829 A JP 2018121829A JP 2018196379 A5 JP2018196379 A5 JP 2018196379A5
- Authority
- JP
- Japan
- Prior art keywords
- mutation
- primer
- amplification
- amplification reaction
- nucleic acid
- 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
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261652827P | 2012-05-29 | 2012-05-29 | |
| US61/652,827 | 2012-05-29 | ||
| US13/840,142 | 2013-03-15 | ||
| US13/840,142 US10077474B2 (en) | 2012-05-29 | 2013-03-15 | Method of designing primers, method of detecting single nucleotide polymorphisms (SNPs), method of distinguishing SNPs, and related primers, detectable oligonucleotides, and kits |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015515106A Division JP6448534B2 (ja) | 2012-05-29 | 2013-05-28 | ヒトｂｒａｆのコドン６００における一塩基多型（ｓｎｐ）を検出する方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2018196379A JP2018196379A (ja) | 2018-12-13 |
| JP2018196379A5 true JP2018196379A5 (enExample) | 2019-02-14 |
Family
ID=49670689
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015515106A Expired - Fee Related JP6448534B2 (ja) | 2012-05-29 | 2013-05-28 | ヒトｂｒａｆのコドン６００における一塩基多型（ｓｎｐ）を検出する方法 |
| JP2018121829A Pending JP2018196379A (ja) | 2012-05-29 | 2018-06-27 | ヒトｂｒａｆのコドン６００における一塩基多型（ｓｎｐ）を検出する方法 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015515106A Expired - Fee Related JP6448534B2 (ja) | 2012-05-29 | 2013-05-28 | ヒトｂｒａｆのコドン６００における一塩基多型（ｓｎｐ）を検出する方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US10077474B2 (enExample) |
| EP (2) | EP2855708B1 (enExample) |
| JP (2) | JP6448534B2 (enExample) |
| AU (2) | AU2013267660B2 (enExample) |
| CA (1) | CA2875281A1 (enExample) |
| ES (1) | ES2751371T3 (enExample) |
| WO (1) | WO2013181125A2 (enExample) |
Families Citing this family (35)
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| US11939634B2 (en) | 2010-05-18 | 2024-03-26 | Natera, Inc. | Methods for simultaneous amplification of target loci |
| US12221653B2 (en) | 2010-05-18 | 2025-02-11 | Natera, Inc. | Methods for simultaneous amplification of target loci |
| US12152275B2 (en) | 2010-05-18 | 2024-11-26 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| US20190010543A1 (en) | 2010-05-18 | 2019-01-10 | Natera, Inc. | Methods for simultaneous amplification of target loci |
| US9677118B2 (en) | 2014-04-21 | 2017-06-13 | Natera, Inc. | Methods for simultaneous amplification of target loci |
| US11322224B2 (en) | 2010-05-18 | 2022-05-03 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| US10316362B2 (en) | 2010-05-18 | 2019-06-11 | Natera, Inc. | Methods for simultaneous amplification of target loci |
| JP6153874B2 (ja) | 2011-02-09 | 2017-06-28 | ナテラ， インコーポレイテッド | 非侵襲的出生前倍数性呼び出しのための方法 |
| AU2013249012B2 (en) | 2012-04-19 | 2019-03-28 | The Medical College Of Wisconsin, Inc. | Highly sensitive surveillance using detection of cell free DNA |
| US20140100126A1 (en) | 2012-08-17 | 2014-04-10 | Natera, Inc. | Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data |
| CN104928355A (zh) * | 2014-03-19 | 2015-09-23 | 李跃 | 检测braf基因突变的方法及其试剂盒 |
| US12492429B2 (en) | 2014-04-21 | 2025-12-09 | Natera, Inc. | Detecting mutations and ploidy in chromosomal segments |
| CN113774132A (zh) | 2014-04-21 | 2021-12-10 | 纳特拉公司 | 检测染色体片段中的突变和倍性 |
| US20180173846A1 (en) | 2014-06-05 | 2018-06-21 | Natera, Inc. | Systems and Methods for Detection of Aneuploidy |
| DK3294906T3 (en) | 2015-05-11 | 2024-08-05 | Natera Inc | Methods for determining ploidy |
| EP3307911B1 (en) * | 2015-06-11 | 2020-12-09 | Bio-Rad Laboratories, Inc. | Amplification assay with a probe competitor |
| US11053542B2 (en) | 2015-12-31 | 2021-07-06 | Quest Diagnostics Investments Llc | Compositions and methods for screening mutations in thyroid cancer |
| DK3443119T3 (da) | 2016-04-15 | 2022-05-23 | Natera Inc | Fremgangsmåde til bestemmelse af lunge cancer |
| EA201892491A1 (ru) * | 2016-04-29 | 2019-06-28 | Дзе Медикал Колледж Оф Висконсин, Инк. | Пцр в реальном времени с мультиплексной оптимизированной амплификацией неправильно спаренных оснований (moma) для анализа злокачественных новообразований |
| CN105861689A (zh) * | 2016-05-06 | 2016-08-17 | 北京晋祺生物科技有限公司 | 一种cyp3a5*3的检测引物组合物、试剂盒及方法 |
| GB201618485D0 (en) | 2016-11-02 | 2016-12-14 | Ucl Business Plc | Method of detecting tumour recurrence |
| EP3642354B1 (en) | 2017-06-20 | 2022-08-03 | Bio-Rad Laboratories, Inc. | Digital amplification assays for genetic instability |
| JP2020524519A (ja) | 2017-06-20 | 2020-08-20 | ザ メディカル カレッジ オブ ウィスコンシン，インコーポレイテッドＴｈｅ Ｍｅｄｉｃａｌ Ｃｏｌｌｅｇｅ ｏｆ Ｗｉｓｃｏｎｓｉｎ， Ｉｎｃ． | 全セルフリーｄｎａによる移植合併症リスクの評価 |
| WO2019099420A1 (en) * | 2017-11-15 | 2019-05-23 | Yan Wang | A method for detecting multiple dna mutations and copy number variations |
| WO2019118926A1 (en) | 2017-12-14 | 2019-06-20 | Tai Diagnostics, Inc. | Assessing graft suitability for transplantation |
| DK3781714T3 (da) | 2018-04-14 | 2026-03-30 | Natera Inc | Fremgangsmåder til cancerpåvisning og -overvågning ved personlig påvisning af cirkulerende tumor-dna |
| US12234509B2 (en) | 2018-07-03 | 2025-02-25 | Natera, Inc. | Methods for detection of donor-derived cell-free DNA |
| CA3125435A1 (en) * | 2018-12-31 | 2020-07-09 | Abbott Molecular Inc. | Improved amplification of nucleic acids |
| WO2020145734A1 (ko) * | 2019-01-11 | 2020-07-16 | 주식회사 진캐스트 | Braf 돌연변이 검출을 위한 dna 중합효소 및 이를 포함하는 키트 |
| US11931674B2 (en) | 2019-04-04 | 2024-03-19 | Natera, Inc. | Materials and methods for processing blood samples |
| US20220333183A1 (en) * | 2019-10-02 | 2022-10-20 | Rutgers, The State University Of New Jersey | Assay methods and kits for detecting rare sequence variants |
| AU2021264510A1 (en) * | 2020-04-28 | 2022-12-01 | Cepheid | Pseudo-complementary bases in genotyping and nucleic acid sequencing |
| WO2023013421A1 (ja) * | 2021-08-03 | 2023-02-09 | 国立大学法人群馬大学 | 腫瘍マーカーｃａ１９－９によるがん診断の精度向上を目的とする血液型関連糖鎖遺伝子の迅速スクリーニングのための新規手法 |
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-
2013
- 2013-03-15 US US13/840,142 patent/US10077474B2/en not_active Expired - Fee Related
- 2013-05-28 JP JP2015515106A patent/JP6448534B2/ja not_active Expired - Fee Related
- 2013-05-28 EP EP13798093.4A patent/EP2855708B1/en active Active
- 2013-05-28 AU AU2013267660A patent/AU2013267660B2/en not_active Ceased
- 2013-05-28 CA CA2875281A patent/CA2875281A1/en not_active Abandoned
- 2013-05-28 ES ES13798093T patent/ES2751371T3/es active Active
- 2013-05-28 EP EP19187147.4A patent/EP3604552A1/en not_active Withdrawn
- 2013-05-28 WO PCT/US2013/042817 patent/WO2013181125A2/en not_active Ceased
-
2018
- 2018-06-27 JP JP2018121829A patent/JP2018196379A/ja active Pending
- 2018-08-20 US US16/105,057 patent/US20190032133A1/en not_active Abandoned
- 2018-10-19 AU AU2018250508A patent/AU2018250508A1/en not_active Abandoned
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