Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail Kolmogorov(National Institutes of Health), Benedict Paten(University of California, Santa Cruz), Sairam Behera(Baylor College of Medicine), Jeshuwin Prabakaran(National Institutes of Health), Melissa Meredith(University of California, Santa Cruz), Miten Jain(Northeastern University), Mark Chaisson(University of Southern California), Pilar Álvarez Jerez(National Institute on Aging), Bryan J. Traynor(National Institutes of Health), Fritz J. Sedlazeck(Baylor College of Medicine), Ramita Dewan(National Institutes of Health), Ryan Lorig-Roach(Broad Institute), Karen H. Miga(University of California, Santa Cruz), Sonja W. Scholz(Johns Hopkins University), Jean Monlong(Inserm), Laksh Malik(National Institutes of Health), Xylena Reed(National Institutes of Health), Trevor Pesout(University of California, Santa Cruz), Kensuke Daida(National Institutes of Health), Mira Mastoras(University of California, Santa Cruz), P. Carnevali(Chan Zuckerberg Initiative (United States)), Cornelis Blauwendraat(National Institute of Neurological Disorders and Stroke), Arang Rhie(National Human Genome Research Institute), Kishwar Shafin(Google (United States)), Winston Timp(Johns Hopkins University), Adam M. Phillippy(National Human Genome Research Institute), Mobin Asri(University of California, Santa Cruz), Kimberley J. Billingsley(National Institutes of Health), Jianzhi Yang(University of Southern California), Rylee M. Genner(National Institutes of Health)
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