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

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. 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.

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Correspondence to Stephen R Quake.

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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.

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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

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