Abstract 2848: Severus: A tool for detecting and characterizing complex structural variants in cancer using long-read sequencing
Ayse Keskus(National Cancer Institute), Mikhail Kolmogorov(National Institutes of Health), Yuelin Liu(National Cancer Institute), Brandy McNulty(University of California, Santa Cruz), Isabel Rodriguez(National Institutes of Health), Irina Pushel(Children's Mercy Hospital), Xiwen Cui(National Cancer Institute), Anton Goretsky(National Cancer Institute), Nicolas Robine(New York Genome Center), Tomi Pastinen(Children's Mercy Hospital), Adrienne Helland(New York Genome Center), Daniel E. Cook(Google (United States)), Yongmei Zhao(Leidos (United States)), Erin K. Molloy(University of Maryland, College Park), Salem Malikić(Simon Fraser University), Jimin Park(University of California, Santa Cruz), Chi-Ping Day(National Cancer Institute), Pi-Chuan Chang(Google (United States)), Midhat S. Farooqi(Children's Mercy Hospital), Michael Dean(National Cancer Institute), Byunggil Yoo(Children's Mercy Hospital), Erin Guest(Children's Mercy Hospital), Benedict Paten(University of California, Santa Cruz), Karen H. Miga(University of California, Santa Cruz), Alexey Kolesnikov(Google (United States)), Andrew Carroll(Western NSW Local Health District), Sergey Aganezov(Oxford Nanopore Technologies (United Kingdom)), Joshua Gardner(University of California, Santa Cruz), Samuel Sacco(University of California, Santa Cruz), Kishwar Shafin(Google (United States)), Giuseppe Narzisi(Cold Spring Harbor Laboratory), Lisa A. Lansdon(Mercy Research), Jyoti Shetty(Leidos (United States)), S. Cenk Şahinalp(National Institutes of Health), Margaret Gibson(Children's Mercy Hospital), Tanveer Ahmad(National Cancer Institute), Asher Bryant(National Cancer Institute), Adam Walter(Children's Mercy Hospital), Ataberk Donmez(National Cancer Institute), Chengpeng Bi(Children's Mercy Hospital), Bao Tran(Leidos (United States))
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