Nanopore Sequencing of 1000 Genomes Project Samples to Build a Comprehensive Catalog of Human Genetic Variation
Jonas A Gustafson,Sophia B Gibson,Nikhita Damaraju,Miranda Pg Zalusky,Kendra Hoekzema,David Twesigomwe,Lei Yang,Anthony A Snead, Phillip A Richmond,Wouter De Coster,Nathan D Olson,Andrea Guarracino, Qiuhui Li,Angela L Miller,Joy Goffena, Zachery Anderson, Sophie Hr Storz, Sydney A Ward, Maisha Sinha,Claudia Gonzaga-Jauregui,Wayne E Clarke,Anna O Basile,André Corvelo,Catherine Reeves,Adrienne Helland,Rajeeva Lochan Musunuri, Mahler Revsine,Karynne E Patterson,Cate R Paschal, Christina Zakarian,Sara Goodwin,Tanner D Jensen, Esther Robb, Genomes ONT Sequencing Consortium, University of Washington Center for Rare Disease Research (UW-CRDR), Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium,W Richard McCombie,Fritz J Sedlazeck,Justin M Zook,Stephen B Montgomery,Erik Garrison,Mikhail Kolmogorov,Michael C Schatz,Richard N McLaughlin,Harriet Dashnow,Michael C Zody,Matt Loose,Miten Jain,Evan E Eichler,Danny E Miller medRxiv the preprint server for health sciences（2024）
Key words
Exome Sequencing
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