Skip to main content

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

The Original Article was published on 19 March 2009

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: 116-10.1186/1471-2164-10-116.

    PubMed Central  Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Stephen R Quake.

Additional information

The online version of the original article can be found at 10.1186/1471-2164-10-116

Richard A White III, Paul C Blainey contributed equally to this work.

Rights and permissions

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

Reprints and Permissions

About this article

Cite this article

White, R.A., Blainey, P.C., Fan, H.C. et al. Erratum to: Digital PCR provides sensitive and absolute calibration for high throughput sequencing. BMC Genomics 10, 541 (2009). https://doi.org/10.1186/1471-2164-10-541

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1471-2164-10-541