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Correction

Correction: Closing gaps in the human genome using sequencing by synthesis

Manuel Garber1, Michael C Zody12, Harindra C Arachchi1, Aaron Berlin1, Sante Gnerre1, Lisa M Green1, Niall Lennon1 and Chad Nusbaum1*

Author Affiliations

1 Genome Sequencing and Analysis Program, Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA

2 Department of Medical Biochemistry and Microbiology, Uppsala University, SE-751 24 Uppsala, Sweden

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Genome Biology 2011, 12:403  doi:10.1186/gb-2011-12-4-403

Published: 19 April 2011

First paragraph (this article has no abstract)

After publication of this Method [1], we noted errors to the legend of Figure 1. The labelling of the line representing the 454 reads and the line representing the small insert library reads was inverted (please see Figure 1 below, a corrected version of Figure 1).