Highly-accurate long-read sequencing improves variant detection and assembly of a human genome
Aaron M. Wenger(Stanford University), Michael W. Hunkapiller, William J. Rowell(Pacific Biosciences (United States)), Fritz J. Sedlazeck(Baylor College of Medicine), Medhat Mahmoud(Baylor College of Medicine), Sergey Koren(National Human Genome Research Institute), Gregory T. Concepcion(Pacific Biosciences (United States)), Arkarachai Fungtammasan(DNAnexus (United States)), Mark A. DePristo(Google (United States)), Pi-Chuan Chang(Google (United States)), Michael C. Schatz(Johns Hopkins University), Justin M. Zook(National Cancer Institute), David R. Rank(Pacific Biosciences (United States)), Armin Töpfer(Pacific Biosciences (United States)), Alexey Kolesnikov(Google (United States)), Nathan D. Olson(Material Measurement Laboratory), Tobias Marschall(Heinrich Heine University Düsseldorf), Andrew Carroll(Western NSW Local Health District), Michael Alonge(Johns Hopkins University), Jana Ebler(Research Institute of Molecular Pathology), Y. Qian(Pacific Biosciences (United States)), Adam M. Phillippy(National Human Genome Research Institute), Jue Ruan(Agricultural Genomics Institute at Shenzhen), Heng Li(Air Force Medical University), Richard Hall(Pacific Biosciences (United States)), Chen-Shan Chin(Program for Appropriate Technology in Health), Gene Myers(Max Planck Institute of Molecular Cell Biology and Genetics), Paul Peluso(Pacific Biosciences (United States))
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