Erratum to: Closing gaps in the human genome using sequencing by synthesis
Published: 19 April 2011
The original article was published in Genome Biology 2009 10:R60
Correction
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.
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Authors’ Affiliations
References
- 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