RU2019138698A - Способы и композиции для днк-профилирования - Google Patents
Способы и композиции для днк-профилирования Download PDFInfo
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- RU2019138698A RU2019138698A RU2019138698A RU2019138698A RU2019138698A RU 2019138698 A RU2019138698 A RU 2019138698A RU 2019138698 A RU2019138698 A RU 2019138698A RU 2019138698 A RU2019138698 A RU 2019138698A RU 2019138698 A RU2019138698 A RU 2019138698A
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Claims (23)
1. Способ получения ДНК–профиля, включающий
обеспечение образца нуклеиновой кислоты,
амплификацию образца нуклеиновой кислоты с множеством праймеров, которые специфически гибридизуются по меньшей мере с одной последовательностью-мишенью, содержащей однонуклеотидный полиморфизм (SNP), и по меньшей мере с одной последовательностью-мишенью, содержащей тандемный повтор, в мультиплексной реакции с получением продуктов амплификации, где по меньшей мере один из множества праймеров имеет низкую температуру плавления, имеет длину по меньшей мере 24 нуклеотида или содержит гомополимерную нуклеотидную последовательность, или их комбинацию, и
определение в продуктах амплификации генотипов по меньшей мере одного SNP и по меньшей мере одного тандемного повтора, таким образом, получая ДНК-профиль образца нуклеиновой кислоты.
2. Способ по п.1, в котором образец нуклеиновой кислоты получают у человека.
3. Способ по п.1, в котором по меньшей мере один SNP включает SNP, который, как известно, указывает на родственную или фенотипическую характеристику источника образца нуклеиновой кислоты.
4. Способ по п. 1, в котором по меньшей мере один из множества праймеров содержит по меньшей мере 24 нуклеотида.
5. Способ по п.4, в котором по меньшей мере один из множества праймеров имеет температуру плавления менее 60°С.
6. Способ по п.1, в котором амплификация образца нуклеиновой кислоты включает проведение полимеразной цепной реакции (ПЦР) на образце нуклеиновой кислоты.
7. Способ по п.1, в котором множество праймеров специфически гибридизуются по меньшей мере с 30 SNP.
8. Способ по п.1, в котором множество праймеров специфически гибридизуются по меньшей мере с 24 последовательностями тандемных повторов.
9. Способ по п.1, в котором образец нуклеиновой кислоты содержит геномную ДНК.
10. Способ по п.9, в котором обеспечение образца нуклеиновой кислоты включает обеспечение криминалистического образца, содержащего нуклеиновую кислоту.
11. Способ по п.1, в котором определение генотипов включает определение по меньшей мере 90% генотипов по меньшей мере одного SNP и по меньшей мере одного тандемного повтора.
12. Способ по п.1, в котором, по меньшей мере, один из множества праймеров содержит одну или несколько последовательностей–меток, содержащих метку уникального молекулярного идентификатора.
13. Способ построения библиотеки нуклеиновых кислот, включающий: предоставление образца нуклеиновой кислоты и амплификацию образца нуклеиновой кислоты со множеством праймеров, которые специфически гибридизуются с по меньшей мере одним однонуклеотидным полиморфизмом (SNP) и по меньшей мере с одной последовательностью-мишенью, содержащей последовательность тандемного повтора в мультиплексной реакции для получения продуктов амплификации, где по меньшей мере один из множества праймеров имеет низкую температуру плавления, имеет длину по меньшей мере 24 нуклеотида или содержит гомополимерную нуклеотидную последовательность, или их комбинацию.
14. Способ по п.13, в котором по меньшей мере один SNP указывает на родственную или фенотипическую характеристику источника образца нуклеиновой кислоты.
15. Способ по п.13, в котором по меньшей мере один из множества праймеров содержит одну или несколько последовательностей-меток.
16. Способ по п.15, в котором одна или несколько последовательностей-меток содержат метку-праймер, метку для захвата, метку для секвенирования или метку уникального молекулярного идентификатора или их сочетание.
17. Способ по п.16, дополнительно включающий амплификацию продуктов амплификации со вторым множеством праймеров.
18. Способ по п.17, в котором по меньшей мере один из второго множества праймеров содержит часть, соответствующую метке-праймеру из множества праймеров и одной или нескольким последовательностям-меткам.
19. Способ по п.17, включающий добавление связывающего одноцепочечные ДНК белка (SSB) к продуктам амплификации.
20. Способ по п.13, в котором амплификация образца нуклеиновой кислоты включает амплификацию посредством полимеразной цепной реакции (ПЦР).
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461940942P | 2014-02-18 | 2014-02-18 | |
| US61/940,942 | 2014-02-18 | ||
| US201462043060P | 2014-08-28 | 2014-08-28 | |
| US62/043,060 | 2014-08-28 | ||
| US201562103524P | 2015-01-14 | 2015-01-14 | |
| US62/103,524 | 2015-01-14 |
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| Application Number | Title | Priority Date | Filing Date |
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| RU2016133987A Division RU2708337C2 (ru) | 2014-02-18 | 2015-02-13 | Способы и композиции для днк-профилирования |
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| Publication Number | Publication Date |
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| RU2019138698A true RU2019138698A (ru) | 2020-01-27 |
| RU2019138698A3 RU2019138698A3 (ru) | 2020-06-19 |
| RU2752700C2 RU2752700C2 (ru) | 2021-07-30 |
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| RU2016133987A RU2708337C2 (ru) | 2014-02-18 | 2015-02-13 | Способы и композиции для днк-профилирования |
| RU2019138698A RU2752700C2 (ru) | 2014-02-18 | 2015-02-13 | Способы и композиции для днк-профилирования |
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| Country | Link |
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| US (2) | US10422002B2 (ru) |
| EP (2) | EP3108009B1 (ru) |
| JP (3) | JP7011392B2 (ru) |
| CN (1) | CN106164298B (ru) |
| AU (2) | AU2015219289B2 (ru) |
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| MY (2) | MY200537A (ru) |
| NZ (1) | NZ723399A (ru) |
| PL (1) | PL3108009T3 (ru) |
| PT (1) | PT3108009T (ru) |
| RS (1) | RS61976B1 (ru) |
| RU (2) | RU2708337C2 (ru) |
| SA (1) | SA516371691B1 (ru) |
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| WO (1) | WO2015126766A1 (ru) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| RU2015144287A (ru) * | 2013-03-15 | 2017-04-24 | Эббви Дойчланд Гмбх Унд Ко. Кг | Составы конъюгата антитело против egfr-лекарственное средство |
| MY200537A (en) * | 2014-02-18 | 2024-01-02 | Illumina Inc | Methods and compositions for dna profiling |
| US10020300B2 (en) | 2014-12-18 | 2018-07-10 | Agilome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
| US9859394B2 (en) | 2014-12-18 | 2018-01-02 | Agilome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
| US10006910B2 (en) | 2014-12-18 | 2018-06-26 | Agilome, Inc. | Chemically-sensitive field effect transistors, systems, and methods for manufacturing and using the same |
| EP3235010A4 (en) | 2014-12-18 | 2018-08-29 | Agilome, Inc. | Chemically-sensitive field effect transistor |
| US9618474B2 (en) | 2014-12-18 | 2017-04-11 | Edico Genome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
| US9857328B2 (en) | 2014-12-18 | 2018-01-02 | Agilome, Inc. | Chemically-sensitive field effect transistors, systems and methods for manufacturing and using the same |
| EP3286338B1 (en) * | 2015-04-24 | 2023-11-01 | Atila Biosystems Incorporated | Amplification with primers of limited nucleotide composition |
| CN105755129B (zh) * | 2016-03-21 | 2020-03-31 | 北京市理化分析测试中心 | 基于新一代测序的基因座d8s1179的str分型方法 |
| WO2017196720A1 (en) * | 2016-05-13 | 2017-11-16 | Colorado State University Research Foundation | High throughput method to genotype plants |
| US10811539B2 (en) | 2016-05-16 | 2020-10-20 | Nanomedical Diagnostics, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
| US10822647B2 (en) * | 2016-07-12 | 2020-11-03 | Biodynamics S.R.L. | Methods for using long ssDNA polynucleotides as primers (superprimers) in PCR assays |
| IL266197B2 (en) * | 2016-10-24 | 2024-03-01 | Geneinfosec Inc | Hiding information contained within nucleic acids |
| WO2018175997A1 (en) * | 2017-03-23 | 2018-09-27 | University Of Washington | Methods for targeted nucleic acid sequence enrichment with applications to error corrected nucleic acid sequencing |
| CN106835292B (zh) * | 2017-04-05 | 2019-04-09 | 北京泛生子基因科技有限公司 | 一步法快速构建扩增子文库的方法 |
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