Nature Communications (Apr 2019)

Multi-platform discovery of haplotype-resolved structural variation in human genomes

  • Mark J. P. Chaisson,
  • Ashley D. Sanders,
  • Xuefang Zhao,
  • Ankit Malhotra,
  • David Porubsky,
  • Tobias Rausch,
  • Eugene J. Gardner,
  • Oscar L. Rodriguez,
  • Li Guo,
  • Ryan L. Collins,
  • Xian Fan,
  • Jia Wen,
  • Robert E. Handsaker,
  • Susan Fairley,
  • Zev N. Kronenberg,
  • Xiangmeng Kong,
  • Fereydoun Hormozdiari,
  • Dillon Lee,
  • Aaron M. Wenger,
  • Alex R. Hastie,
  • Danny Antaki,
  • Thomas Anantharaman,
  • Peter A. Audano,
  • Harrison Brand,
  • Stuart Cantsilieris,
  • Han Cao,
  • Eliza Cerveira,
  • Chong Chen,
  • Xintong Chen,
  • Chen-Shan Chin,
  • Zechen Chong,
  • Nelson T. Chuang,
  • Christine C. Lambert,
  • Deanna M. Church,
  • Laura Clarke,
  • Andrew Farrell,
  • Joey Flores,
  • Timur Galeev,
  • David U. Gorkin,
  • Madhusudan Gujral,
  • Victor Guryev,
  • William Haynes Heaton,
  • Jonas Korlach,
  • Sushant Kumar,
  • Jee Young Kwon,
  • Ernest T. Lam,
  • Jong Eun Lee,
  • Joyce Lee,
  • Wan-Ping Lee,
  • Sau Peng Lee,
  • Shantao Li,
  • Patrick Marks,
  • Karine Viaud-Martinez,
  • Sascha Meiers,
  • Katherine M. Munson,
  • Fabio C. P. Navarro,
  • Bradley J. Nelson,
  • Conor Nodzak,
  • Amina Noor,
  • Sofia Kyriazopoulou-Panagiotopoulou,
  • Andy W. C. Pang,
  • Yunjiang Qiu,
  • Gabriel Rosanio,
  • Mallory Ryan,
  • Adrian Stütz,
  • Diana C. J. Spierings,
  • Alistair Ward,
  • AnneMarie E. Welch,
  • Ming Xiao,
  • Wei Xu,
  • Chengsheng Zhang,
  • Qihui Zhu,
  • Xiangqun Zheng-Bradley,
  • Ernesto Lowy,
  • Sergei Yakneen,
  • Steven McCarroll,
  • Goo Jun,
  • Li Ding,
  • Chong Lek Koh,
  • Bing Ren,
  • Paul Flicek,
  • Ken Chen,
  • Mark B. Gerstein,
  • Pui-Yan Kwok,
  • Peter M. Lansdorp,
  • Gabor T. Marth,
  • Jonathan Sebat,
  • Xinghua Shi,
  • Ali Bashir,
  • Kai Ye,
  • Scott E. Devine,
  • Michael E. Talkowski,
  • Ryan E. Mills,
  • Tobias Marschall,
  • Jan O. Korbel,
  • Evan E. Eichler,
  • Charles Lee

DOI
https://doi.org/10.1038/s41467-018-08148-z
Journal volume & issue
Vol. 10, no. 1
pp. 1 – 16

Abstract

Read online

Structural variants (SVs) in human genomes contribute diversity and diseases. Here, the authors use a multi-platform strategy to generate haplotype-resolved SVs for three human parent–child trios.