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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


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2164/10/541


Received:11 August 2009
Accepted:19 November 2009
Published:19 November 2009

© 2009 White et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Correction

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.

References

  1. White RA, Blainey PC, Fan HC, Quake SR: Digital PCR provides sensitive and absolute calibration for high throughput sequencing.

    BMC Genomics 2009, 10:116. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL