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Open Access Correction

Correction: Digital PCR provides sensitive and absolute calibration for high throughput sequencing

Richard A White, Paul C Blainey, H Christina Fan and Stephen R Quake*

Author Affiliations

Department of Bioengineering at Stanford University and Howard Hughes Medical Institute, Stanford, California 94305, USA

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BMC Genomics 2009, 10:541  doi:10.1186/1471-2164-10-541

Published: 19 November 2009

First paragraph (this article has no abstract)

After this article [1] appeared online, an error was called to our attention. The "universal probe" sequence UPL #149 in Table 6 appears with the 5' and 3' ends reversed. The correct sequence of this locked nucleic acid (LNA) probe is 5'-TCGCCGCC-3'. This typographical error does not affect any of the conclusions drawn in the article.