Open AccesseP144: Long-read genome sequencing secondary processing pipelines provide variant call accuracy that exceeds current clinical standards for short-read genome sequencing
Author(s) -
James Holt,
Lori H. Handley,
James M.J. Lawlor,
Susan M. Hiatt,
Gregory M. Cooper,
Jane Grimwood,
Ghunwa Nakouzi
Publication year - 2022
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1016/j.gim.2022.01.180
Subject(s) - hybrid genome assembly , whole genome sequencing , genome , computational biology , exome sequencing , dna sequencing , deep sequencing , cancer genome sequencing , computer science , genetics , biology , gene , mutation
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom