CN108138226B - 单核苷酸多态性和插入缺失的多等位基因基因分型 - Google Patents

单核苷酸多态性和插入缺失的多等位基因基因分型 Download PDF

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CN108138226B
CN108138226B CN201680060855.0A CN201680060855A CN108138226B CN 108138226 B CN108138226 B CN 108138226B CN 201680060855 A CN201680060855 A CN 201680060855A CN 108138226 B CN108138226 B CN 108138226B
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allele
sample
signal
alleles
cluster
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CN108138226A (zh
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J·N·戈卢布
M·H·夏皮罗
D·奥利弗
D·布莱克
F·西迪基
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Affymetrix Inc
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CN201680060855.0A 2015-10-18 2016-10-18 单核苷酸多态性和插入缺失的多等位基因基因分型 Active CN108138226B (zh)

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US201562243078P 2015-10-18 2015-10-18
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PCT/US2016/057496 WO2017070096A1 (en) 2015-10-18 2016-10-18 Multiallelic genotyping of single nucleotide polymorphisms and indels

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CN110706746B (zh) * 2019-11-27 2021-09-17 北京博安智联科技有限公司 一种dna混合分型数据库比对算法
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
WO2024047168A1 (en) * 2022-08-31 2024-03-07 Saga Diagnostics Ab Multi-vector detection of variant sequences
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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