Ontology highlight
ABSTRACT:
SUBMITTER: Alpert T
PROVIDER: S-EPMC7885932 | biostudies-literature | 2021 Mar
REPOSITORIES: biostudies-literature
Alpert Tara T Brito Anderson F AF Lasek-Nesselquist Erica E Rothman Jessica J Valesano Andrew L AL MacKay Matthew J MJ Petrone Mary E ME Breban Mallery I MI Watkins Anne E AE Vogels Chantal B F CBF Kalinich Chaney C CC Dellicour Simon S Russell Alexis A Kelly John P JP Shudt Matthew M Plitnick Jonathan J Schneider Erasmus E Fitzsimmons William J WJ Khullar Gaurav G Metti Jessica J Dudley Joel T JT Nash Megan M Beaubier Nike N Wang Jianhui J Liu Chen C Hui Pei P Muyombwe Anthony A Downing Randy R Razeq Jafar J Bart Stephen M SM Grills Ardath A Morrison Stephanie M SM Murphy Steven S Neal Caleb C Laszlo Eva E Rennert Hanna H Cushing Melissa M Westblade Lars L Velu Priya P Craney Arryn A Fauntleroy Kathy A KA Peaper David R DR Landry Marie L ML Cook Peter W PW Fauver Joseph R JR Mason Christopher E CE Lauring Adam S AS George Kirsten St KS MacCannell Duncan R DR Grubaugh Nathan D ND
medRxiv : the preprint server for health sciences 20210311
The emergence and spread of SARS-CoV-2 lineage B.1.1.7, first detected in the United Kingdom, has become a global public health concern because of its increased transmissibility. Over 2500 COVID-19 cases associated with this variant have been detected in the US since December 2020, but the extent of establishment is relatively unknown. Using travel, genomic, and diagnostic data, we highlight the primary ports of entry for B.1.1.7 in the US and locations of possible underreporting of B.1.1.7 case ...[more]