Correction: Digital PCR provides sensitive and absolute calibration for high throughput sequencing
- Equal contributors
Department of Bioengineering at Stanford University and Howard Hughes Medical Institute, Stanford, California 94305, USA
BMC Genomics 2009, 10:541 doi:10.1186/1471-2164-10-541Published: 19 November 2009
First paragraph (this article has no abstract)
After this article  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.