Single molecule sequencing of free DNA from maternal plasma for noninvasive trisomy 21 detection

Jessica M.E. Van Den Oever, Sahila Balkassmi, E. Joanne Verweij, Maarten Van Iterson, Phebe N.Adama Van Scheltema, Dick Oepkes, Jan M.M. Van Lith, Mariëtte J.V. Hoffer, Johan T. Den Dunnen, Egbert Bakker, Elles M.J. Boon*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


BACKGROUND: Noninvasive fetal aneuploidy detection by use of free DNA from maternal plasma has recently been shown to be achievable by whole genome shotgun sequencing. The high-throughput next-generation sequencing platforms previously tested use a PCR step during sample preparation, which results in amplification bias in GC-rich areas of the human genome. To eliminate this bias, and thereby experimental noise, we have used single molecule sequencing as an alternative method. METHODS: For noninvasive trisomy 21 detection, we performed single molecule sequencing on the Helicos platform using free DNA isolated from maternal plasma from 9 weeks of gestation onwards. Relative sequence tag density ratios were calculated and results were directly compared to the previously described Illumina GAII platform. RESULTS: Sequence data generated without an amplification step show no GC bias. Therefore, with the use of single molecule sequencing all trisomy 21 fetuses could be distinguished more clearly from euploid fetuses. CONCLUSIONS: This study shows for the first time that single molecule sequencing is an attractive and easy to use alternative for reliable noninvasive fetal aneuploidy detection in diagnostics. With this approach, previously described experimental noise associated with PCR amplification, such as GC bias, can be overcome.

Original languageEnglish
Pages (from-to)699-706
Number of pages8
JournalClinical Chemistry
Issue number4
Publication statusPublished - Apr 2012

Cite this