BR112018009105A8 - método para detectar anomalia cromossómica em embrião usando cultura de blastocisto - Google Patents
método para detectar anomalia cromossómica em embrião usando cultura de blastocistoInfo
- Publication number
- BR112018009105A8 BR112018009105A8 BR112018009105A BR112018009105A BR112018009105A8 BR 112018009105 A8 BR112018009105 A8 BR 112018009105A8 BR 112018009105 A BR112018009105 A BR 112018009105A BR 112018009105 A BR112018009105 A BR 112018009105A BR 112018009105 A8 BR112018009105 A8 BR 112018009105A8
- Authority
- BR
- Brazil
- Prior art keywords
- embryo
- blastocyst culture
- chromosomal abnormality
- culture
- blastocyst
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 210000002459 blastocyst Anatomy 0.000 title abstract 3
- 210000001161 mammalian embryo Anatomy 0.000 title abstract 3
- 208000031404 Chromosome Aberrations Diseases 0.000 title abstract 2
- 208000036878 aneuploidy Diseases 0.000 abstract 2
- 231100001075 aneuploidy Toxicity 0.000 abstract 2
- 230000003321 amplification Effects 0.000 abstract 1
- 230000002759 chromosomal effect Effects 0.000 abstract 1
- 210000002308 embryonic cell Anatomy 0.000 abstract 1
- 238000000338 in vitro Methods 0.000 abstract 1
- 238000007481 next generation sequencing Methods 0.000 abstract 1
- 238000003199 nucleic acid amplification method Methods 0.000 abstract 1
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Abstract
um método fornecido é para detectar uma anormalia cromossômica em um embrião usando cultura de blastocisto. o método compreende: detectar dna livre de células embrionárias circulantes em cultura in vitro embrionária inicial, isto é, cultura de blastocisto, realizando amplificação uniforme completa do genoma em dna traço, e então usando um método, como sequenciamento de próxima geração, para realizar análises no produto de dna amplificado, de modo a determinar uma condição cromossômica de um embrião, ou seja, se ocorre aneuploidia ou aneuploidia parcial de cormossomas.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510746098.XA CN105368936B (zh) | 2015-11-05 | 2015-11-05 | 一种利用囊胚培养液检测胚胎染色体异常的方法 |
PCT/CN2016/104753 WO2017076359A1 (zh) | 2015-11-05 | 2016-11-04 | 一种利用囊胚培养液检测胚胎染色体异常的方法 |
Publications (2)
Publication Number | Publication Date |
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BR112018009105A2 BR112018009105A2 (pt) | 2018-11-06 |
BR112018009105A8 true BR112018009105A8 (pt) | 2019-02-26 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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BR112018009105A BR112018009105A8 (pt) | 2015-11-05 | 2016-11-04 | método para detectar anomalia cromossómica em embrião usando cultura de blastocisto |
Country Status (9)
Country | Link |
---|---|
US (1) | US20180327821A1 (pt) |
EP (1) | EP3372690A4 (pt) |
JP (2) | JP2019506873A (pt) |
KR (2) | KR20200118221A (pt) |
CN (2) | CN105368936B (pt) |
AU (2) | AU2016351034B2 (pt) |
BR (1) | BR112018009105A8 (pt) |
TW (1) | TWI622651B (pt) |
WO (1) | WO2017076359A1 (pt) |
Families Citing this family (25)
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CN111621548A (zh) * | 2016-04-26 | 2020-09-04 | 序康医疗科技(苏州)有限公司 | 扩增dna的方法 |
CN106086199A (zh) * | 2016-07-05 | 2016-11-09 | 上海序康医疗科技有限公司 | 一种利用不含透明带的囊胚培养液检测胚胎染色体异常的方法 |
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WO2020061637A1 (en) * | 2018-09-27 | 2020-04-02 | Monash Ivf Group Limited | Dna from cell-free medium |
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CN111172259A (zh) * | 2020-03-09 | 2020-05-19 | 云南省第一人民医院 | 一种胚胎培养液的卵裂球期的胚胎染色体检测方法 |
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KR102310223B1 (ko) * | 2021-07-21 | 2021-10-08 | 주식회사 에이아이더뉴트리진 | 랩온페이퍼칩을 포함하는 구조물에 적용하기 위한 세포용해용 조성물 |
CN113957131B (zh) * | 2021-10-17 | 2024-03-19 | 合肥金域医学检验实验室有限公司 | 一种废旧芯片重新处理再利用的方法 |
CN116103280B (zh) * | 2022-12-28 | 2024-03-15 | 上海亿康医学检验所有限公司 | 样本保存液及其在染色体非整倍体筛查和/或转录组检测中的应用 |
CN117721222B (zh) * | 2024-02-07 | 2024-05-10 | 北京大学第三医院(北京大学第三临床医学院) | 一种单细胞转录组预测胚胎着床的方法及应用 |
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US20010044937A1 (en) * | 1999-12-17 | 2001-11-22 | Gerald Schatten | Methods for producing transgenic animals |
JP2006087394A (ja) * | 2004-09-27 | 2006-04-06 | Wako Pure Chem Ind Ltd | 核酸抽出方法および核酸抽出キット |
JP2008017851A (ja) * | 2007-09-10 | 2008-01-31 | Toyobo Co Ltd | Dna合成反応を促進する添加剤 |
WO2012166425A2 (en) * | 2011-05-27 | 2012-12-06 | President And Fellows Of Harvard College | Methods of amplifying whole genome of a single cell |
AT512417A1 (de) * | 2012-02-10 | 2013-08-15 | Ivf Zentren Prof Zech Bregenz Gmbh | Verfahren zur analyse fetaler nukleinsäuren |
EP4036250A1 (en) * | 2013-06-18 | 2022-08-03 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods for determining the quality of an embryo |
GB201319779D0 (en) * | 2013-11-08 | 2013-12-25 | Cartagenia N V | Genetic analysis method |
ES2796224T3 (es) * | 2014-01-30 | 2020-11-26 | Pecsi Tudomanyegyetem | Evaluación de embriones previa a la implantación a través de la detección de ADN embrionario libre |
CN105368936B (zh) * | 2015-11-05 | 2021-07-30 | 序康医疗科技(苏州)有限公司 | 一种利用囊胚培养液检测胚胎染色体异常的方法 |
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KR20180088830A (ko) | 2018-08-07 |
CN113684250B (zh) | 2024-08-20 |
AU2016351034B2 (en) | 2020-12-24 |
CN113684250A (zh) | 2021-11-23 |
WO2017076359A1 (zh) | 2017-05-11 |
KR20200118221A (ko) | 2020-10-14 |
BR112018009105A2 (pt) | 2018-11-06 |
JP2019506873A (ja) | 2019-03-14 |
CN105368936B (zh) | 2021-07-30 |
TW201716584A (zh) | 2017-05-16 |
JP2021007403A (ja) | 2021-01-28 |
EP3372690A1 (en) | 2018-09-12 |
CN105368936A (zh) | 2016-03-02 |
AU2016351034A1 (en) | 2018-06-28 |
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