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Scott Ferguson on Muck Rack

Scott Ferguson

  • Custom and Marketing Content Director, ALM Media
New Jersey
As seen in: ALM Media, Nature, CTV News, InformationWeek, Light Reading, The Indianapolis Star, BNN Bloomberg, CP24, MyCentralJersey, Dice Insights, BankInfoSecurity and
Director of Custom & Marketing Content @ALMMedia. Former editor with @ISMGCorp, @InformationWeek, @eWEEKNews and others.
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Articles

Un vol WestJet pour une destination canadienne interrompu en raison d’un «incident»

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By Melissa Gilligan Verified, Scott Ferguson
| Noovo Info Verified
Un vol de la compagnie WestJet qui devait décoller jeudi de Denver, dans le Colorado, à destination de Calgary n’a finalement jamais quitté la piste. Le transporteur aérien que le vol WS1571 a interrompu son décollage à la suite d’un «incident» survenu à l’aéroport international de Denver. «L’équipage a réagi rapidement, conformément aux procédures établies, et a déclaré l’état d’urgence; les équipes d’intervention sont immédiatement intervenues», a déclaré la compagnie aérienne.
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WestJet flight bound for Calgary aborted after ‘incident’ on Denver runway

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By Melissa Gilligan Verified, Scott Ferguson
| CP24 Verified
A WestJet flight scheduled to fly from Denver, Colo., to Calgary on Thursday never ended up leaving the runway. WestJet confirms flight WS1571 aborted takeoff after an “incident” at Denver International Airport. “The crew responded promptly in accordance with established procedures and declared an emergency, with response teams attending immediately,” the airline said.
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Recurrent structural variation and recent turnover at the 17q21.31 locus in humans and great apes

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By Samvardhini Sridharan, Runyang Nicolas Lou, Scott Ferguson, Joana Rocha, Rishi De-Kayne, Matthew Mitchell, Brenna M. Henn, Peter H. Sudmant, Alison N. Killilia
| Nature Verified
Abstract The 17q21.31 locus in humans harbors several complex structural haplotypes including a ~ 970 kb inversion. Different inversion haplotypes have been associated with susceptibility to microdeletions causing Koolen-de Vries syndrome and variation in fecundity and recombination rates. Here, using 210 haplotype-resolved human genome assemblies and pangenome graph-based approaches we characterize 11 distinct structural haplotypes, several of which have not been previously described.
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