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Genome Biology

, 12:403 | Cite as

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

  • Manuel Garber
  • Michael C Zody
  • Harindra C Arachchi
  • Aaron Berlin
  • Sante Gnerre
  • Lisa M Green
  • Niall Lennon
  • Chad Nusbaum
Erratum

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).
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.

Supplementary material

13059_2011_2507_MOESM1_ESM.pdf (261 kb)
Authors’ original file for figure 1

References

  1. 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.PubMedPubMedCentralCrossRefGoogle Scholar

Copyright information

© BioMed Central Ltd 2011

Authors and Affiliations

  • Manuel Garber
    • 1
  • Michael C Zody
    • 1
    • 2
  • Harindra C Arachchi
    • 1
  • Aaron Berlin
    • 1
  • Sante Gnerre
    • 1
  • Lisa M Green
    • 1
  • Niall Lennon
    • 1
  • Chad Nusbaum
    • 1
  1. 1.Genome Sequencing and Analysis ProgramBroad Institute of MIT and HarvardCambridgeUSA
  2. 2.Department of Medical Biochemistry and MicrobiologyUppsala UniversityUppsalaSweden

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