JP2018514234A5 - - Google Patents
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- JP2018514234A5 JP2018514234A5 JP2018509952A JP2018509952A JP2018514234A5 JP 2018514234 A5 JP2018514234 A5 JP 2018514234A5 JP 2018509952 A JP2018509952 A JP 2018509952A JP 2018509952 A JP2018509952 A JP 2018509952A JP 2018514234 A5 JP2018514234 A5 JP 2018514234A5
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- 210000000349 chromosome Anatomy 0.000 claims description 434
- 239000012634 fragment Substances 0.000 claims description 244
- 238000004364 calculation method Methods 0.000 claims description 146
- 230000002159 abnormal effect Effects 0.000 claims description 141
- 238000012937 correction Methods 0.000 claims description 107
- 238000001514 detection method Methods 0.000 claims description 76
- 208000036878 aneuploidy Diseases 0.000 claims description 74
- 231100001075 aneuploidy Toxicity 0.000 claims description 73
- 230000002759 chromosomal effect Effects 0.000 claims description 61
- 238000000034 method Methods 0.000 claims description 42
- 230000001605 fetal effect Effects 0.000 claims description 40
- 230000005856 abnormality Effects 0.000 claims description 35
- 210000003754 fetus Anatomy 0.000 claims description 23
- 210000005259 peripheral blood Anatomy 0.000 claims description 23
- 239000011886 peripheral blood Substances 0.000 claims description 23
- 238000013507 mapping Methods 0.000 claims description 15
- 230000000694 effects Effects 0.000 claims description 13
- 238000012165 high-throughput sequencing Methods 0.000 claims description 11
- 238000004422 calculation algorithm Methods 0.000 claims description 10
- 238000012360 testing method Methods 0.000 claims description 9
- 238000001801 Z-test Methods 0.000 claims description 5
- 239000003153 chemical reaction reagent Substances 0.000 claims description 5
- 238000010606 normalization Methods 0.000 claims description 4
- 230000008774 maternal effect Effects 0.000 description 40
- 238000005259 measurement Methods 0.000 description 8
- 238000010586 diagram Methods 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 6
- 238000012545 processing Methods 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 4
- 230000035935 pregnancy Effects 0.000 description 4
- 230000011987 methylation Effects 0.000 description 3
- 238000007069 methylation reaction Methods 0.000 description 3
- 210000002826 placenta Anatomy 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 206010000234 Abortion spontaneous Diseases 0.000 description 2
- 210000001766 X chromosome Anatomy 0.000 description 2
- 238000003491 array Methods 0.000 description 2
- 238000002405 diagnostic procedure Methods 0.000 description 2
- 208000015994 miscarriage Diseases 0.000 description 2
- 238000012163 sequencing technique Methods 0.000 description 2
- 238000004088 simulation Methods 0.000 description 2
- 208000000995 spontaneous abortion Diseases 0.000 description 2
- 201000010374 Down Syndrome Diseases 0.000 description 1
- 201000006360 Edwards syndrome Diseases 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 208000024556 Mendelian disease Diseases 0.000 description 1
- 238000001190 Q-PCR Methods 0.000 description 1
- 208000037280 Trisomy Diseases 0.000 description 1
- 208000007159 Trisomy 18 Syndrome Diseases 0.000 description 1
- 206010044688 Trisomy 21 Diseases 0.000 description 1
- 206010000210 abortion Diseases 0.000 description 1
- 231100000176 abortion Toxicity 0.000 description 1
- 210000004381 amniotic fluid Anatomy 0.000 description 1
- 230000003322 aneuploid effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229960000074 biopharmaceutical Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 230000001416 effect on chromosomes Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 201000003738 orofaciodigital syndrome VIII Diseases 0.000 description 1
- 230000003169 placental effect Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 206010053884 trisomy 18 Diseases 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2015/078422 WO2016176847A1 (zh) | 2015-05-06 | 2015-05-06 | 检测染色体非整倍性的试剂盒、装置和方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018514234A JP2018514234A (ja) | 2018-06-07 |
| JP2018514234A5 true JP2018514234A5 (enExample) | 2019-10-17 |
| JP6623400B2 JP6623400B2 (ja) | 2019-12-25 |
Family
ID=57217322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018509952A Active JP6623400B2 (ja) | 2015-05-06 | 2015-05-06 | 染色体異数性を測定するためのキット、装置及び方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20180201990A1 (enExample) |
| EP (1) | EP3293270B1 (enExample) |
| JP (1) | JP6623400B2 (enExample) |
| SG (1) | SG11201709141YA (enExample) |
| WO (1) | WO2016176847A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20180190384A1 (en) * | 2017-01-05 | 2018-07-05 | Clear Genetics, Inc. | Automated genetic test counseling |
| CN112397148B (zh) * | 2019-08-23 | 2023-10-03 | 武汉希望组生物科技有限公司 | 序列比对方法、序列校正方法及其装置 |
| CN114585749B (zh) * | 2019-10-16 | 2024-09-03 | 斯蒂拉科技公司 | 核酸序列浓度的确定 |
| CN110993024B (zh) * | 2019-12-20 | 2023-08-22 | 北京科迅生物技术有限公司 | 建立胎儿浓度校正模型的方法及装置与胎儿浓度定量的方法及装置 |
| CN112037846A (zh) * | 2020-07-14 | 2020-12-04 | 广州市达瑞生物技术股份有限公司 | 一种cffDNA非整倍体检测方法、系统、储存介质以及检测设备 |
| CN114171118B (zh) * | 2021-11-15 | 2024-09-27 | 成都凡迪医疗器械有限公司 | 用于无创基因检测的数据处理方法和装置 |
| CN114792548B (zh) * | 2022-06-14 | 2022-09-09 | 北京贝瑞和康生物技术有限公司 | 校正测序数据、检测拷贝数变异的方法、设备和介质 |
| CN115132271B (zh) * | 2022-09-01 | 2023-07-04 | 北京中仪康卫医疗器械有限公司 | 一种基于批次内校正的cnv检测方法 |
| CN117095747B (zh) * | 2023-08-29 | 2024-04-30 | 广东省农业科学院水稻研究所 | 一种基于线性泛基因组和人工智能模型检测群体倒位或转座子端点基因型的方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2011365507A1 (en) * | 2011-04-14 | 2013-05-02 | Verinata Health, Inc. | Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies |
| CN104603284B (zh) * | 2012-09-12 | 2016-08-24 | 深圳华大基因研究院 | 利用基因组测序片段检测拷贝数变异的方法 |
| US10482994B2 (en) * | 2012-10-04 | 2019-11-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10319463B2 (en) * | 2015-01-23 | 2019-06-11 | The Chinese University Of Hong Kong | Combined size- and count-based analysis of maternal plasma for detection of fetal subchromosomal aberrations |
| CN104789686B (zh) * | 2015-05-06 | 2018-09-07 | 浙江安诺优达生物科技有限公司 | 检测染色体非整倍性的试剂盒和装置 |
| CN104789466B (zh) * | 2015-05-06 | 2018-03-13 | 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和装置 |
-
2015
- 2015-05-06 EP EP15891099.2A patent/EP3293270B1/en active Active
- 2015-05-06 WO PCT/CN2015/078422 patent/WO2016176847A1/zh not_active Ceased
- 2015-05-06 SG SG11201709141YA patent/SG11201709141YA/en unknown
- 2015-05-06 JP JP2018509952A patent/JP6623400B2/ja active Active
- 2015-05-06 US US15/571,859 patent/US20180201990A1/en not_active Abandoned
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