When Jeremy Luban first looked over the genetic sequence of the Omicron variant on his phone one day last November, it was five o’clock in the morning. But even at that hour, the University of Massachusetts virus expert knew right away Omicron was a problem. First, there was the sheer number of new mutations—by some counts, as many as 50, with 30 of them in the critical places that vaccines and drug treatments target.

Topics:  massachusetts    ldquo;it’s   achilles&rsquo   covid-19&rsquo   covid-19&mdash   you should not try   february   the covid-19   let&rsquo   viruses   textbooks   dwayne   senior&mdash   bloomberg/getty imagesa   cape flats development association cafda    egoli   cape town   nov   south african   california los   angeles   actually worries u.s doctors about   u.k     ldquo;all   start thinking differently about breakthrough infections    ldquo;one   nadia roan   gladstone institutes   california   san   francisco    ldquo;this   jeremy farrar   trust   we learned about genetic sequencing during covid-19 could revolutionize public health   angola   kevin   frayer&mdash   getty imagessecurity   january   beijing    ldquo;there   broad institute   harvard   mit ldquo;that’s   let s not be fatalistic about   know how   fight it   u.s   centers   disease   control&rsquo   strain surveillance   experts     ldquo;the   dr warner green   virology   immunology   ho ldquo;what   jeremy   luban   omicron   university   sars-cov-2   covid-19   read   scenario   the   south africa   delta   yang   california    u.s     in   that&rsquo   gladstone institute   china    ldquo;the   sabeti    how   beginning   pandemic   people   infected   variant   cases   vaccinated   variants   endemic   immune   population   host   previous   immunity   cells   common   causing   version   hosts   transmissible   good   point   transmissibility   doesn’t   suggests   live   cell   mild   human   virus’s   symptoms   world   year   mutating   including   explain   evidence   vaccines   weakened   unpredictable   severe   dangerous   viral   years   identify   scientists   sick   sequence   system   cold   immunized   respiratory   positive   protection   perfect   helped   efficiently   eventually   replicate   week   reason   part   turn   high   build   led   global   hurrah   tract   inflammation   community   vaccination   testing   major   models   unvaccinated   recovered   glimmer   hope   globe   villains   hit   problem   herd   outbreaks   mutation   shift   versions   isn’t   path   time   effects   magical   vulnerable   deal   virulent   protected   replicating   goal   can’t   efficient   mutations   lines   opportunities   information   kill   virus-making   infects   possibility   efforts   wouldn’t   immunocompromised   investigator   systems   developing   continue   odds   result   professor   months   potentially   highly   reported   speed   early   small   lineage   quickly   fusion   possibly   mutate   world’s   vaccine   balance   history   changing   copies   genomic   
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