A Streamlined Method for Detecting Structural Variants in Cancer Genomes by Short Read Paired-End Sequencing

• Martina Mijušković,

  Affiliation Department of Pathology and Laboratory Medicine and Abramson Family Cancer Research Institute, Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America

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• Stuart M. Brown,

  Affiliation Center for Health Informatics and Bioinformatics, New York University Langone Medical Center, New York, New York, United States of America

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• Zuojian Tang,

  Affiliation Center for Health Informatics and Bioinformatics, New York University Langone Medical Center, New York, New York, United States of America

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• Cory R. Lindsay,

  Affiliation Department of Pathology and Laboratory Medicine and Abramson Family Cancer Research Institute, Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America

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• Efstratios Efstathiadis,

  Affiliation Center for Health Informatics and Bioinformatics, New York University Langone Medical Center, New York, New York, United States of America

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• Ludovic Deriano,

  Affiliations Department of Immunology, Institut Pasteur, Paris, France, Centre National de la Recherche Scientifique URA1961, Paris, France

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• David B. Roth

  * E-mail: David.Roth2@uphs.upenn.edu

  Affiliation Department of Pathology and Laboratory Medicine and Abramson Family Cancer Research Institute, Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America

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