JP2019500706A5 - - Google Patents

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JP2019500706A5
JP2019500706A5 JP2018539252A JP2018539252A JP2019500706A5 JP 2019500706 A5 JP2019500706 A5 JP 2019500706A5 JP 2018539252 A JP2018539252 A JP 2018539252A JP 2018539252 A JP2018539252 A JP 2018539252A JP 2019500706 A5 JP2019500706 A5 JP 2019500706A5
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allele
sample
signal
background
call
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JP2018539252A
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JP2019500706A (ja
JP6858783B2 (ja
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Priority claimed from PCT/US2016/057496 external-priority patent/WO2017070096A1/en
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JP2018539252A 2015-10-18 2016-10-18 一塩基多型及びインデルの複対立遺伝子遺伝子型決定 Active JP6858783B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562243078P 2015-10-18 2015-10-18
US62/243,078 2015-10-18
PCT/US2016/057496 WO2017070096A1 (en) 2015-10-18 2016-10-18 Multiallelic genotyping of single nucleotide polymorphisms and indels

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JP2019500706A JP2019500706A (ja) 2019-01-10
JP2019500706A5 true JP2019500706A5 (enExample) 2019-06-13
JP6858783B2 JP6858783B2 (ja) 2021-04-14

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JP2018539252A Active JP6858783B2 (ja) 2015-10-18 2016-10-18 一塩基多型及びインデルの複対立遺伝子遺伝子型決定

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US (1) US20180305748A1 (enExample)
EP (2) EP3901279B1 (enExample)
JP (1) JP6858783B2 (enExample)
KR (1) KR20180071299A (enExample)
CN (1) CN108138226B (enExample)
AU (2) AU2016341845B2 (enExample)
IL (2) IL296418A (enExample)
RU (1) RU2706203C1 (enExample)
WO (1) WO2017070096A1 (enExample)

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US20210285042A1 (en) * 2020-02-28 2021-09-16 Grail, Inc. Systems and methods for calling variants using methylation sequencing data
CN114645080A (zh) * 2020-12-21 2022-06-21 高嵩 一种利用多态性位点和靶位点测序检测胎儿遗传变异的方法
CN114300045B (zh) * 2022-01-04 2025-03-07 杭州博日科技股份有限公司 基于对照组的半监督snp分型方法、装置和电子设备
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CN119673273A (zh) * 2024-11-29 2025-03-21 中国科学院北京基因组研究所(国家生物信息中心) 一种应用于二代测序数据的str分型方法

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