A complete reference genome improves analysis of human genetic variation
Sergey Aganezov(Oxford Nanopore Technologies (United Kingdom)), Michael C. Schatz(Johns Hopkins University), Melissa Meredith(University of California, Santa Cruz), Stephanie M. Yan(Johns Hopkins University), Melanie Kirsche(Johns Hopkins University), Jeffrey Rosenfeld(Zucker Hillside Hospital), Michael E.G. Sauria(Johns Hopkins University), Pavel Avdeyev(George Washington University), Fritz J. Sedlazeck(Baylor College of Medicine), Sergey Koren(National Human Genome Research Institute), Jennifer McDaniel(Material Measurement Laboratory), Karen H. Miga(University of California, Santa Cruz), Dylan J. Taylor(Johns Hopkins University), Nancy F. Hansen(National Institutes of Health), Justin M. Zook(National Cancer Institute), Benedict Paten(University of California, Santa Cruz), Danny E. Miller(Seattle Children's Hospital), Alaina Shumate(Dana-Farber Cancer Institute), Nathan D. Olson(Material Measurement Laboratory), Samantha Zarate(Johns Hopkins University), Daniela C. Soto(University of California, Davis), Megan Y. Dennis(University of California System), Chunlin Xiao, Ryan M. Layer(University of Colorado Boulder), Rajiv C. McCoy(Johns Hopkins University), Arang Rhie(National Human Genome Research Institute), Kishwar Shafin(Google (United States)), Skylar Martin(University of Colorado Boulder), Justin Wagner(National Institute of Standards and Technology), Adam M. Phillippy(National Human Genome Research Institute), Chen-Shan Chin(Program for Appropriate Technology in Health), Joyce Lee(BioNano Genomics (United States)), Mitchell R. Vollger(University of Utah)
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