scholarly journals Whole Genome Sequencing for Surveillance of Diphtheria in Low Incidence Settings

2019 ◽  
Vol 7 ◽  
Author(s):  
Helena M. B. Seth-Smith ◽  
Adrian Egli
Keyword(s):  
Whole Genome Sequencing ◽  
Genome Sequencing ◽  
Whole Genome ◽  
Low Incidence

scholarly journals Countrywide implementation of whole genome sequencing: an opportunity to improve tuberculosis management, surveillance and contact tracing in low incidence countries

2018 ◽  
Vol 51 (6) ◽  
pp. 1800387 ◽  
Author(s):  
Andrea Maurizio Cabibbe ◽  
Alberto Trovato ◽  
Maria Rosaria De Filippo ◽  
Arash Ghodousi ◽  
Laura Rindi ◽  
...  
Keyword(s):  
Whole Genome Sequencing ◽  
Genome Sequencing ◽  
Contact Tracing ◽  
Whole Genome ◽  
Low Incidence

scholarly journals Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing

2014 ◽  
Vol 15 (2) ◽  
pp. 254 ◽  
Author(s):  
Adrian Veres ◽  
Bridget S. Gosis ◽  
Qiurong Ding ◽  
Ryan Collins ◽  
Ashok Ragavendran ◽  
...  
Keyword(s):  
Stem Cell ◽  
Whole Genome Sequencing ◽  
Genome Sequencing ◽  
Whole Genome ◽  
Human Stem Cell ◽  
Cell Clones ◽  
Low Incidence

scholarly journals Whole-Genome Sequencing of Emerging Invasive Neisseria meningitidis Serogroup W in Sweden

2018 ◽  
Vol 56 (4) ◽  
Author(s):  
Lorraine Eriksson ◽  
Sara Thulin Hedberg ◽  
Susanne Jacobsson ◽  
Hans Fredlund ◽  
Paula Mölling ◽  
...  
Keyword(s):  
Neisseria Meningitidis ◽  
Whole Genome Sequencing ◽  
Genome Sequencing ◽  
Clonal Complex ◽  
Invasive Disease ◽  
South American ◽  
Whole Genome ◽  
The Novel ◽  
Content Type ◽  
Low Incidence

ABSTRACT Invasive disease caused by Neisseria meningitidis serogroup W (MenW) has historically had a low incidence in Sweden, with an average incidence of 0.03 case/100,000 population from 1995 to 2014. In recent years, a significant increase in the incidence of MenW has been noted in Sweden, to an average incidence of 0.15 case/100,000 population in 2015 to 2016. In 2017 (1 January to 30 June), 33% of invasive meningococcal disease cases (7/21 cases) were caused by MenW. In the present study, all invasive MenW isolates from Sweden collected in 1995 to June 2017 ( n = 86) were subjected to whole-genome sequencing to determine the population structure and to compare isolates from Sweden with historical and international cases. The increase of MenW in Sweden was determined to be due to isolates belonging to the South American sublineage of MenW clonal complex 11, namely, the novel U.K. 2013 lineage. This lineage was introduced in Sweden in 2013 and has since been the dominant lineage of MenW.

scholarly journals Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing

2014 ◽  
Vol 15 (1) ◽  
pp. 27-30 ◽  
Author(s):  
Adrian Veres ◽  
Bridget S. Gosis ◽  
Qiurong Ding ◽  
Ryan Collins ◽  
Ashok Ragavendran ◽  
...  
Keyword(s):  
Stem Cell ◽  
Whole Genome Sequencing ◽  
Genome Sequencing ◽  
Whole Genome ◽  
Human Stem Cell ◽  
Cell Clones ◽  
Low Incidence

Utility of Whole Genome Sequencing in diagnosing complex disorders: lesson from renal tubular disorders

2018 ◽  
Author(s):  
Mark Stevenson ◽  
Alistair T Pagnamenta ◽  
Heather G Mack ◽  
Judith A Savige ◽  
Kate E Lines ◽  
...  
Keyword(s):  
Whole Genome Sequencing ◽  
Genome Sequencing ◽  
Whole Genome ◽  
Complex Disorders ◽  
Tubular Disorders ◽  
Renal Tubular Disorders ◽  
Renal Tubular

0306 Exploring the feasibility of using copy number variants as genetic markers through large-scale whole genome sequencing experiments

2016 ◽  
Vol 94 (suppl_5) ◽  
pp. 146-146
Author(s):  
D. M. Bickhart ◽  
L. Xu ◽  
J. L. Hutchison ◽  
J. B. Cole ◽  
D. J. Null ◽  
...  
Keyword(s):  
Whole Genome Sequencing ◽  
Genetic Markers ◽  
Genome Sequencing ◽  
Copy Number ◽  
Large Scale ◽  
Copy Number Variants ◽  
Whole Genome
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