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BFAST: An Alignment Tool for Large Scale Genome Resequencing

Overview of attention for article published in PLOS ONE, November 2009
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Title
BFAST: An Alignment Tool for Large Scale Genome Resequencing
Published in
PLOS ONE, November 2009
DOI 10.1371/journal.pone.0007767
Pubmed ID
Authors

Nils Homer, Barry Merriman, Stanley F. Nelson

Abstract

The new generation of massively parallel DNA sequencers, combined with the challenge of whole human genome resequencing, result in the need for rapid and accurate alignment of billions of short DNA sequence reads to a large reference genome. Speed is obviously of great importance, but equally important is maintaining alignment accuracy of short reads, in the 25-100 base range, in the presence of errors and true biological variation.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 596 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 17 3%
Brazil 9 2%
United Kingdom 8 1%
Netherlands 7 1%
France 7 1%
Spain 7 1%
Italy 5 <1%
Norway 4 <1%
Belgium 4 <1%
Other 20 3%
Unknown 508 85%

Demographic breakdown

Readers by professional status Count As %
Researcher 186 31%
Student > Ph. D. Student 136 23%
Student > Master 67 11%
Other 33 6%
Professor > Associate Professor 28 5%
Other 107 18%
Unknown 39 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 333 56%
Computer Science 70 12%
Biochemistry, Genetics and Molecular Biology 64 11%
Medicine and Dentistry 28 5%
Engineering 11 2%
Other 41 7%
Unknown 49 8%