SG10202104266VA - Methods of sequencing data read realignment - Google Patents

Methods of sequencing data read realignment

Info

Publication number
SG10202104266VA
SG10202104266VA SG10202104266VA SG10202104266VA SG10202104266VA SG 10202104266V A SG10202104266V A SG 10202104266VA SG 10202104266V A SG10202104266V A SG 10202104266VA SG 10202104266V A SG10202104266V A SG 10202104266VA SG 10202104266V A SG10202104266V A SG 10202104266VA
Authority
SG
Singapore
Prior art keywords
methods
data read
sequencing data
realignment
read realignment
Prior art date
Application number
SG10202104266VA
Inventor
Gwenn Berry
Han-Yu Chuang
Jessica Gordon
Xiao Chen
Stephen Tanner
Original Assignee
Illumina Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Illumina Inc filed Critical Illumina Inc
Publication of SG10202104266VA publication Critical patent/SG10202104266VA/en

Links

Classifications

    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B30/00ICT specially adapted for sequence analysis involving nucleotides or amino acids
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B30/00ICT specially adapted for sequence analysis involving nucleotides or amino acids
    • G16B30/10Sequence alignment; Homology search

Landscapes

  • Physics & Mathematics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biophysics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Biotechnology (AREA)
  • Evolutionary Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medical Informatics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Theoretical Computer Science (AREA)
  • Management, Administration, Business Operations System, And Electronic Commerce (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Magnetic Resonance Imaging Apparatus (AREA)
  • Eye Examination Apparatus (AREA)
  • Information Retrieval, Db Structures And Fs Structures Therefor (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
SG10202104266VA 2016-11-16 2017-11-15 Methods of sequencing data read realignment SG10202104266VA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662422841P 2016-11-16 2016-11-16
US201762447103P 2017-01-17 2017-01-17
US201762480330P 2017-03-31 2017-03-31

Publications (1)

Publication Number Publication Date
SG10202104266VA true SG10202104266VA (en) 2021-05-28

Family

ID=60543712

Family Applications (1)

Application Number Title Priority Date Filing Date
SG10202104266VA SG10202104266VA (en) 2016-11-16 2017-11-15 Methods of sequencing data read realignment

Country Status (10)

Country Link
US (1) US20190287647A1 (en)
EP (2) EP4300501A3 (en)
JP (1) JP7052955B2 (en)
KR (1) KR102425673B1 (en)
CN (2) CN110168647B (en)
AU (2) AU2017361069B2 (en)
BR (1) BR112019009830A2 (en)
CA (1) CA3043875A1 (en)
SG (1) SG10202104266VA (en)
WO (1) WO2018093804A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109754845B (en) * 2018-12-29 2020-02-28 浙江安诺优达生物科技有限公司 Method for simulating target disease simulation sequencing library and application thereof
CN109935275B (en) * 2018-12-29 2021-09-07 北京安诺优达医学检验实验室有限公司 Sequence variation verification method and device, method and device for producing variation sequence and electronic equipment
CN112825267B (en) * 2019-11-21 2024-05-14 深圳华大基因科技服务有限公司 Method for determining a collection of small nucleic acid sequences and use thereof
CN113574603A (en) * 2019-12-05 2021-10-29 因美纳有限公司 Rapid detection of gene fusion
CN112530522B (en) * 2020-12-15 2022-10-28 中国科学院深圳先进技术研究院 Sequence error correction method, device, equipment and storage medium

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011139797A2 (en) * 2010-04-27 2011-11-10 Spiral Genetics Inc. Method and system for analysis and error correction of biological sequences and inference of relationship for multiple samples
KR20140024270A (en) * 2010-12-30 2014-02-28 파운데이션 메디신 인코포레이티드 Optimization of multigene analysis of tumor samples
US20120203792A1 (en) * 2011-02-01 2012-08-09 Life Technologies Corporation Systems and methods for mapping sequence reads
JP2012235723A (en) * 2011-05-11 2012-12-06 National Cancer Center Large-scale base sequence analysis method, program, and apparatus
WO2014041380A1 (en) * 2012-09-11 2014-03-20 Kps Zrt. Method and computer program product for detecting mutation in a nucleotide sequence
US9916416B2 (en) * 2012-10-18 2018-03-13 Virginia Tech Intellectual Properties, Inc. System and method for genotyping using informed error profiles
KR101480897B1 (en) * 2012-10-29 2015-01-12 삼성에스디에스 주식회사 System and method for aligning genome sequence
WO2014099979A2 (en) * 2012-12-17 2014-06-26 Virginia Tech Intellectual Properties, Inc. Methods and compositions for identifying global microsatellite instability and for characterizing informative microsatellite loci
KR101482010B1 (en) * 2013-01-23 2015-01-14 숭실대학교산학협력단 Ultrafast general searching device and method for whole genome sequencing
CN103146823A (en) * 2013-02-27 2013-06-12 西北农林科技大学 Method for designing SNP (single-nucleotide polymorphism) molecular marker with base substitution or insertion deletion
US10191929B2 (en) * 2013-05-29 2019-01-29 Noblis, Inc. Systems and methods for SNP analysis and genome sequencing
US9898575B2 (en) * 2013-08-21 2018-02-20 Seven Bridges Genomics Inc. Methods and systems for aligning sequences
CN104834833B (en) * 2014-02-12 2017-12-05 深圳华大基因科技有限公司 The detection method and device of SNP
US10216895B2 (en) * 2014-05-12 2019-02-26 Roche Molecular Systems, Inc. Rare variant calls in ultra-deep sequencing
CN105989246B (en) * 2015-01-28 2018-10-26 深圳华大智造科技有限公司 A kind of mutation detection method and device based on genome assembling
CN104794371B (en) * 2015-04-29 2018-02-09 深圳华大生命科学研究院 The method and apparatus for detecting retrotransponsons insertion polymorphism
CN105631242B (en) * 2015-12-25 2018-09-11 中国农业大学 A method of identifying transgenic event using sequencing data of whole genome

Also Published As

Publication number Publication date
KR102425673B1 (en) 2022-07-26
AU2023266266A1 (en) 2023-12-07
EP4300501A3 (en) 2024-03-27
CA3043875A1 (en) 2018-05-24
JP7052955B2 (en) 2022-04-12
EP3542293B1 (en) 2023-12-27
EP3542293A1 (en) 2019-09-25
US20190287647A1 (en) 2019-09-19
JP2020506447A (en) 2020-02-27
KR20190082854A (en) 2019-07-10
EP4300501A2 (en) 2024-01-03
AU2017361069B2 (en) 2023-09-21
CN110168647B (en) 2023-10-31
CN110168647A (en) 2019-08-23
CN117457074A (en) 2024-01-26
BR112019009830A2 (en) 2019-08-13
WO2018093804A1 (en) 2018-05-24
AU2017361069A1 (en) 2019-06-06

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