After publication of this Method , 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).
Garber M, Zody MC, Arachchi HM, Berlin A, Gnerre S, Green LM, Lennon N, Nusbaum C: Closing gaps in the human genome using sequencing by synthesis. Genome Biology. 2009, 10: R60-10.1186/gb-2009-10-6-r60.PubMedPubMed CentralView ArticleGoogle Scholar