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Closing gaps in the human genome using sequencing by synthesis

Overview of attention for article published in Genome Biology, June 2009
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Citations

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102 Mendeley
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10 CiteULike
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Title
Closing gaps in the human genome using sequencing by synthesis
Published in
Genome Biology, June 2009
DOI 10.1186/gb-2009-10-6-r60
Pubmed ID
Authors

Manuel Garber, Michael C Zody, Harindra M Arachchi, Aaron Berlin, Sante Gnerre, Lisa M Green, Niall Lennon, Chad Nusbaum

Abstract

The most recent release of the finished human genome contains 260 euchromatic gaps (excluding chromosome Y). Recent work has helped explain a large number of these unresolved regions as 'structural' in nature. Another class of gaps is likely to be refractory to clone-based approaches, and cannot be approached in ways previously described. We present an approach for closing these gaps using 454 sequencing. As a proof of principle, we closed all three remaining non-structural gaps in chromosome 15.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 102 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Germany 4 4%
United States 3 3%
Italy 1 <1%
South Africa 1 <1%
China 1 <1%
United Kingdom 1 <1%
Russia 1 <1%
Philippines 1 <1%
Unknown 89 87%

Demographic breakdown

Readers by professional status Count As %
Researcher 33 32%
Student > Ph. D. Student 23 23%
Professor 9 9%
Professor > Associate Professor 8 8%
Student > Bachelor 6 6%
Other 14 14%
Unknown 9 9%
Readers by discipline Count As %
Agricultural and Biological Sciences 64 63%
Biochemistry, Genetics and Molecular Biology 14 14%
Computer Science 3 3%
Medicine and Dentistry 3 3%
Immunology and Microbiology 2 2%
Other 4 4%
Unknown 12 12%