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Nature Communications|September 6, 2022
Genomic surveillance of SARS-CoV-2 Omicron variants on a university campusAna A Weil, Kyle G Luiten, Amanda M Casto, et al.Medrxiv : the Preprint Server for Health Sciences|February 16, 2022
Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance dataRoy Burstein, Benjamin M Althouse, Amanda Adler, et al.Plos One|August 14, 2014
Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthmaCatarina D Campbell, Kiana Mohajeri, Maika Malig, et al.Nature Communications|April 28, 2026
Technical and biological sources of noise confound multiplexed enhancer AAV screeningAvery C Hunker, John K Mich, Naz Taskin, et al.The New England Journal of Medicine|August 21, 2014
Somatic mutations in cerebral cortical malformationsSaumya S Jamuar, Anh-Thu N Lam, Martin Kircher, et al.Cell|October 6, 2018
Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population HistorySiyang Liu, Shujia Huang, Fang Chen, et al.Cell|July 8, 2014
Disruptive CHD8 mutations define a subtype of autism early in developmentRaphael Bernier, Christelle Golzio, Bo Xiong, et al.Biorxiv : the Preprint Server for Biology|June 9, 2020
SwabExpress: An end-to-end protocol for extraction-free COVID-19 testingSanjay Srivatsan, Sarah Heidl, Brian Pfau, et al.Nature Genetics|May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.Genome Biology|September 16, 2011
Mutation discovery in mice by whole exome sequencingHeather Fairfield, Griffith J Gilbert, Mary Barter, et al.Pageof 47