Structural variation and its potential impact on genome instability: Novel discoveries in the EGFR landscape by long-read sequencing.

Structural variation (SV) is typically defined as variation within the human genome that exceeds 50 base pairs (bp). SV may be copy number neutral or it may involve duplications, deletions, and complex rearrangements. Recent studies have shown SV to be associated with many human diseases. However, s...

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Bibliographic Details
Main Authors: George W Cook, Michael G Benton, Wallace Akerley, George F Mayhew, Cynthia Moehlenkamp, Denise Raterman, Daniel L Burgess, William J Rowell, Christine Lambert, Kevin Eng, Jenny Gu, Primo Baybayan, John T Fussell, Heath D Herbold, John M O'Shea, Thomas K Varghese, Lyska L Emerson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0226340