JP2018500625A5 - - Google Patents

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JP2018500625A5
JP2018500625A5 JP2017518960A JP2017518960A JP2018500625A5 JP 2018500625 A5 JP2018500625 A5 JP 2018500625A5 JP 2017518960 A JP2017518960 A JP 2017518960A JP 2017518960 A JP2017518960 A JP 2017518960A JP 2018500625 A5 JP2018500625 A5 JP 2018500625A5
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JP
Japan
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lead
contigs
contig
nucleotides
generating
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JP2017518960A
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Japanese (ja)
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JP2018500625A (ja
JP6762932B2 (ja
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Priority claimed from PCT/IB2015/057716 external-priority patent/WO2016055971A2/en
Publication of JP2018500625A publication Critical patent/JP2018500625A/ja
Publication of JP2018500625A5 publication Critical patent/JP2018500625A5/ja
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JP2017518960A 2014-10-10 2015-10-09 シーケンシングリードのｄｅ ｎｏｖｏアセンブリーの方法、システム、およびプロセス Expired - Fee Related JP6762932B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462062636P 2014-10-10 2014-10-10
US62/062,636 2014-10-10
PCT/IB2015/057716 WO2016055971A2 (en) 2014-10-10 2015-10-09 Methods, systems and processes of de novo assembly of sequencing reads

Publications (3)

Publication Number Publication Date
JP2018500625A JP2018500625A (ja) 2018-01-11
JP2018500625A5 true JP2018500625A5 (https=) 2018-11-22
JP6762932B2 JP6762932B2 (ja) 2020-09-30

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JP2017518960A Expired - Fee Related JP6762932B2 (ja) 2014-10-10 2015-10-09 シーケンシングリードのｄｅ ｎｏｖｏアセンブリーの方法、システム、およびプロセス

Country Status (8)

Country Link
US (1) US20190244678A1 (https=)
EP (1) EP3204522A4 (https=)
JP (1) JP6762932B2 (https=)
CN (1) CN106795568A (https=)
BR (1) BR112017007282A2 (https=)
CA (1) CA2963868A1 (https=)
IL (1) IL251277B (https=)
WO (1) WO2016055971A2 (https=)

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Publication number Priority date Publication date Assignee Title
US10395759B2 (en) 2015-05-18 2019-08-27 Regeneron Pharmaceuticals, Inc. Methods and systems for copy number variant detection
US12071669B2 (en) 2016-02-12 2024-08-27 Regeneron Pharmaceuticals, Inc. Methods and systems for detection of abnormal karyotypes
WO2018057775A1 (en) * 2016-09-22 2018-03-29 Invitae Corporation Methods, systems and processes of identifying genetic variations
WO2019028189A2 (en) * 2017-08-01 2019-02-07 Human Longevity, Inc. DETERMINING THE STR LENGTH BY SHORT READ SEQUENCING
US11728007B2 (en) 2017-11-30 2023-08-15 Grail, Llc Methods and systems for analyzing nucleic acid sequences using mappability analysis and de novo sequence assembly
JP7361774B2 (ja) * 2018-07-27 2023-10-16 ミリアド・ウィメンズ・ヘルス・インコーポレーテッド シーケンスリードの独立したアラインメントおよびペアリングによって高度に相同なシーケンスにおける遺伝的変異を検出するための方法
EP3853763A1 (en) * 2018-09-20 2021-07-28 Aivf Ltd Image feature detection
BR112020026259A2 (pt) * 2018-11-01 2021-07-27 Illumina, Inc. métodos e composições para detecção de variante de linhagem germinativa
CN113557572B (zh) * 2019-01-25 2025-02-07 加利福尼亚太平洋生物科学股份有限公司 基于图的映射核酸片段的系统和方法
CN110060734B (zh) * 2019-03-29 2021-08-13 天津大学 一种高鲁棒性dna测序用条形码生成和读取方法
SG11202109079YA (en) * 2019-12-05 2021-09-29 Illumina Inc Rapid detection of gene fusions
US12093803B2 (en) * 2020-07-01 2024-09-17 International Business Machines Corporation Downsampling genomic sequence data
CA3184609A1 (en) * 2020-12-11 2022-06-16 Illumina Inc. Methods and systems for visualizing short reads in repetitive regions of the genome
US20240117445A1 (en) * 2021-03-16 2024-04-11 University Of North Texas Health Science Center At Fort Worth Macrohaplotypes for Forensic DNA Mixture Deconvolution
CN115938480B (zh) * 2021-09-23 2026-03-13 武汉华大基因技术服务有限公司 长读长测序对基因组组装结果纠错方法优化装置和系统
CN118380052B (zh) * 2024-06-24 2024-09-17 安诺优达基因科技(北京)有限公司 基因组结构预测的方法及电子装置

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8383345B2 (en) * 2008-09-12 2013-02-26 University Of Washington Sequence tag directed subassembly of short sequencing reads into long sequencing reads
EP2511843B1 (en) * 2009-04-29 2016-12-21 Complete Genomics, Inc. Method and system for calling variations in a sample polynucleotide sequence with respect to a reference polynucleotide sequence
US20110257889A1 (en) * 2010-02-24 2011-10-20 Pacific Biosciences Of California, Inc. Sequence assembly and consensus sequence determination
WO2012177774A2 (en) * 2011-06-21 2012-12-27 Life Technologies Corporation Systems and methods for hybrid assembly of nucleic acid sequences
WO2013103759A2 (en) * 2012-01-04 2013-07-11 Dow Agrosciences Llc Haplotype based pipeline for snp discovery and/or classification
US9916416B2 (en) * 2012-10-18 2018-03-13 Virginia Tech Intellectual Properties, Inc. System and method for genotyping using informed error profiles
CN103258145B (zh) * 2012-12-22 2016-06-29 中国科学院深圳先进技术研究院 一种基于De Bruijn图的并行基因拼接方法
CN103761453B (zh) * 2013-12-09 2017-10-27 天津工业大学 一种基于簇图结构的并行基因拼接方法

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