JP2020515236A5 - - Google Patents

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JP2020515236A5
JP2020515236A5 JP2019537282A JP2019537282A JP2020515236A5 JP 2020515236 A5 JP2020515236 A5 JP 2020515236A5 JP 2019537282 A JP2019537282 A JP 2019537282A JP 2019537282 A JP2019537282 A JP 2019537282A JP 2020515236 A5 JP2020515236 A5 JP 2020515236A5
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Japan
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cell
composition
cells
epigenetic
genomic regions
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JP2019537282A
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JP2020515236A (ja
JP7429338B2 (ja
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Priority claimed from PCT/US2018/013227 external-priority patent/WO2018132518A1/en
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JP2019537282A 2017-01-10 2018-01-10 細胞療法および関連方法のエピジェネティック解析 Active JP7429338B2 (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US201762444802P 2017-01-10 2017-01-10
US62/444,802 2017-01-10
US201762551752P 2017-08-29 2017-08-29
US62/551,752 2017-08-29
US201762596662P 2017-12-08 2017-12-08
US62/596,662 2017-12-08
PCT/US2018/013227 WO2018132518A1 (en) 2017-01-10 2018-01-10 Epigenetic analysis of cell therapy and related methods

Publications (3)

Publication Number Publication Date
JP2020515236A JP2020515236A (ja) 2020-05-28
JP2020515236A5 true JP2020515236A5 (enExample) 2021-02-25
JP7429338B2 JP7429338B2 (ja) 2024-02-08

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JP2019537282A Active JP7429338B2 (ja) 2017-01-10 2018-01-10 細胞療法および関連方法のエピジェネティック解析

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US (2) US11821027B2 (enExample)
EP (1) EP3568414A1 (enExample)
JP (1) JP7429338B2 (enExample)
CN (1) CN110691792A (enExample)
AU (1) AU2018207305A1 (enExample)
CA (1) CA3049461A1 (enExample)
MA (1) MA47283A (enExample)
MX (1) MX2019008227A (enExample)
WO (1) WO2018132518A1 (enExample)

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WO2020198942A1 (zh) * 2019-03-29 2020-10-08 中国科学技术大学 基于峰聚类的单细胞染色质可及性测序数据分析方法和系统
EP4104177A1 (en) * 2020-02-13 2022-12-21 10X Genomics, Inc. Methods for characterizing cells using gene expression and chromatin accessibility
CN113436683B (zh) * 2020-03-23 2024-08-16 北京合生基因科技有限公司 筛选候选插入片段的方法和系统
WO2023069985A1 (en) * 2021-10-19 2023-04-27 Battelle Memorial Institute Technologies for genetic engineering detection
EP4659248A1 (en) * 2023-01-31 2025-12-10 Guardant Health, Inc. Non-invasive monitoring of genomic alterations induced by gene-editing therapies
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