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Identifying structural variants using linked-read sequencing data

Bioinformatics

Nov 3, 2017

Rebecca ElyanowBenjamin J. Raphael

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Abstract

Structural variation, including large deletions, duplications, inversions, translocations, and other rearrangements, is common in human and cancer genomes. A number of methods have been developed to identify structural variants from Illumina short-read sequencing data. However, reliable...read more

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  • Identifying structural variants using linked-read sequencing data

    Bioinformatics

    Nov 3, 2017

    Rebecca ElyanowBenjamin J. Raphael

    PMID: 29112732

    DOI: 10.1093/bioinformatics/btx712

    Abstract

    Structural variation, including large deletions, duplications, inversions, translocations, and other rearrangements, is common in human and cancer genomes. A number of methods have been developed to identify structural variants from Illumina short-read sequencing data. However, reliable...read more

    9
    95
    Paper Details
    References
    • References33
    • Citations1
    • References33
    • Citations1
  • Get paper from

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