JP2020517304A5 - - Google Patents

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JP2020517304A5
JP2020517304A5 JP2020507747A JP2020507747A JP2020517304A5 JP 2020517304 A5 JP2020517304 A5 JP 2020517304A5 JP 2020507747 A JP2020507747 A JP 2020507747A JP 2020507747 A JP2020507747 A JP 2020507747A JP 2020517304 A5 JP2020517304 A5 JP 2020517304A5
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JP
Japan
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target
dna
fetal
read
probe
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JP2020507747A
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English (en)
Japanese (ja)
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JP7170711B2 (ja
JP2020517304A (ja
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Priority claimed from PCT/EP2018/059889 external-priority patent/WO2018192967A1/en
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Publication of JP2020517304A5 publication Critical patent/JP2020517304A5/ja
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JP2020507747A 2017-04-18 2018-04-18 Dna分析のためのオフターゲット配列の使用 Active JP7170711B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP17166836 2017-04-18
EP17166836.1 2017-04-18
PCT/EP2018/059889 WO2018192967A1 (en) 2017-04-18 2018-04-18 Use of off-target sequences for dna analysis

Publications (3)

Publication Number Publication Date
JP2020517304A JP2020517304A (ja) 2020-06-18
JP2020517304A5 true JP2020517304A5 (enExample) 2021-05-27
JP7170711B2 JP7170711B2 (ja) 2022-11-14

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JP2020507747A Active JP7170711B2 (ja) 2017-04-18 2018-04-18 Dna分析のためのオフターゲット配列の使用

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US (1) US20200048715A1 (enExample)
EP (2) EP3988672B1 (enExample)
JP (1) JP7170711B2 (enExample)
CN (1) CN110475874A (enExample)
CA (1) CA3058845A1 (enExample)
WO (1) WO2018192967A1 (enExample)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4305200A1 (en) * 2021-03-09 2024-01-17 Guardant Health, Inc. Detecting the presence of a tumor based on off-target polynucleotide sequencing data
CN114334007B (zh) * 2022-01-20 2024-10-18 腾讯科技(深圳)有限公司 基因脱靶预测模型训练方法、预测方法、装置及电子设备
CN119207553B (zh) * 2024-10-08 2025-10-10 上海唯可生物科技有限公司 一种基于靶向富集测序评估基因编辑脱靶风险的方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4074838A1 (en) * 2010-01-19 2022-10-19 Verinata Health, Inc. Novel protocol for preparing sequencing libraries
US11322224B2 (en) * 2010-05-18 2022-05-03 Natera, Inc. Methods for non-invasive prenatal ploidy calling
ES2651612T3 (es) * 2011-10-18 2018-01-29 Multiplicom Nv Diagnóstico de aneuploidía cromosómica fetal
AU2013245272B2 (en) * 2012-04-06 2018-04-05 The Chinese University Of Hong Kong Noninvasive prenatal diagnosis of fetal trisomy by allelic ratio analysis using targeted massively parallel sequencing
EP3409791B1 (en) * 2013-03-15 2021-06-30 Verinata Health, Inc. Generating cell-free dna libraries directly from blood
EP4567682A3 (en) 2013-08-30 2025-09-03 Personalis, Inc. Methods for genomic analysis
KR101721480B1 (ko) * 2016-06-02 2017-03-30 주식회사 랩 지노믹스 염색체 이상 검사 방법 및 시스템

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