Correction
Correction: Closing gaps in the human genome using sequencing by synthesis
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
Genome Biology 2011, 12:403 doi:10.1186/gb-2011-12-4-403
Published: 19 April 2011First 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).
