In cancer genome sequencing, reference gaps and germline variants obscure detection of small and large somatic variants and methylation …
Justin Wagner,
Ayse G. Keskus,
Keisuke K. Oshima,
T. Rhyker Ranallo-Benavidez,
Jennifer McDaniel,
Mile Sikic,
Dehui Lin,
Luis F. Paulin,
Adam C. English,
Fritz J. Sedlazeck,
Elizabeth M. Munding,
J. Zachary Sanborn,
Andrew Carroll,
Pi-Chuan Chang,
Daniel E. Cook,
Kishwar Shafin,
Joep de Ligt,
Rayan Hassaine,
Daniel Cameron,
Severine Catreux,
Yeonghun Lee,
Lisa Murray,
Sean Truong,
Christian Brueffer,
Aleksey V. Zimin,
Erin Cross,
Matthew McGowan,
Michael Vernich,
Andrew S. Liss,
Jean-Pierre Kocher,
Zachary Stephens,
Tanveer Ahmad,
Asher Bryant,
Nathan Dwarshuis,
Hua-Jun He,
Zhiyong He,
Nathan D. Olson,
Francoise Thibaud-Nissen,
Dmitry Antipov,
Sergey Koren,
Adam Phillippy,
Rajeeva Lochan Musunuri,
Giuseppe Narzisi,
Miten Jain,
Aaron M. Wenger,
Stephen Eacker,
Sayed Mohammad Ebrahim Sahraeian,
Paul C. Boutros,
Yash Patel,
Takafumi N. Yamaguchi,
Joseph McConnell,
Matthew Borchers,
Jennifer L. Gerton,
Paxton Kostos,
Andrea Guarracino,
Maryam Jehangir,
Hila Benjamin,
Mohammed Faizal Eeman Mootor,
Yuan Xu,
Mobin Asri,
Karen H. Miga,
Jimin Park,
Benedict Paten,
Ruibang Luo,
Zhenxian Zheng,
Jae Young Choi,
Linh Nguyen,
Dan R. Robinson,
Josh N. Vo,
Shenghan Gao,
Ghulam Murtaza,
Christopher E. Mason,
Haoyu Cheng,
Floris P. Barthel,
Chunlin Xiao,
Glennis A. Logsdon,
Mikhail Kolmogorov,
Justin M. Zook