Open Access

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

  • Richard A WhiteIII1,
  • Paul C Blainey1,
  • H Christina Fan1 and
  • Stephen R Quake1Email author
Contributed equally
BMC Genomics200910:541

DOI: 10.1186/1471-2164-10-541

Received: 11 August 2009

Accepted: 19 November 2009

Published: 19 November 2009

The Methodology article to this article has been published in BMC Genomics 2009 10:116

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.

Notes

Authors’ Affiliations

(1)
Department of Bioengineering at Stanford University and Howard Hughes Medical Institute

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: 116-10.1186/1471-2164-10-116.PubMed CentralView ArticlePubMed

Copyright

© White et al; licensee BioMed Central Ltd. 2009

This article is published under license to 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.

Advertisement