Open Access

Erratum to: Closing gaps in the human genome using sequencing by synthesis

  • Manuel Garber1,
  • Michael C Zody1, 2,
  • Harindra C Arachchi1,
  • Aaron Berlin1,
  • Sante Gnerre1,
  • Lisa M Green1,
  • Niall Lennon1 and
  • Chad Nusbaum1Email author
Genome Biology201112:403

DOI: 10.1186/gb-2011-12-4-403

Published: 19 April 2011

The original article was published in Genome Biology 2009 10:R60

Correction

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).
https://static-content.springer.com/image/art%3A10.1186%2Fgb-2011-12-4-403/MediaObjects/13059_2011_Article_2507_Fig1_HTML.jpg
Figure 1

Coverage of gap regions. Sequence coverage of the gap regions on human chromosome 15 is shown for gaps at (a) 24 Mb, (b) 25 Mb and (c) 96 Mb. The x-axis indicates base position in the local region containing each gap. The y-axis shows sequence coverage obtained in 454 reads (blue line) and small insert library reads (red line). Coverage was computed as the average in 10-base non-overlapping windows. Arrows indicate primers used to amplify the amplicons sequenced, color coded in pairs. Bars at top indicate bases present in the Celera (dark gray) and NCBI build 36 (light gray) assemblies.

Notes

Declarations

Authors’ Affiliations

(1)
Genome Sequencing and Analysis Program, Broad Institute of MIT and Harvard
(2)
Department of Medical Biochemistry and Microbiology, Uppsala University

References

  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

Copyright

© BioMed Central Ltd 2011

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