Skip to main content

Bioinformatics Pipeline for Accurate Quantification of Fetal DNA Fraction in Maternal Plasma

  • Protocol
  • First Online:
Cell-free DNA as Diagnostic Markers

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1909))

Abstract

The discovery of circulating cell-free fetal DNA has profoundly transformed the landscape of noninvasive prenatal testing (NIPT) and rapidly found its way into global clinical applications. The fractional concentration of cell-free fetal DNA in plasma DNA of a pregnant woman is an important parameter for understanding and interpreting analytical results of NIPT. Thus, the accurate quantification of fetal DNA fraction is indispensable when NIPT is involved. In this protocol, we describe the bioinformatics workflow to calculate fetal DNA fraction using two programs developed by our group, which provide accurate estimation.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 139.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 179.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Lo YMD, Corbetta N, Chamberlain PF et al (1997) Presence of fetal DNA in maternal plasma and serum. Lancet 350:485–487

    Article  CAS  Google Scholar 

  2. Lo YMD, Hjelm NM, Fidler C et al (1998) Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N Engl J Med 339:1734–1738

    Article  CAS  Google Scholar 

  3. Chiu RWK, Chan KCA, Gao Y et al (2008) Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma. Proc Natl Acad Sci U S A 105:20458–20463

    Article  CAS  Google Scholar 

  4. Chen EZ, Chiu RWK, Sun H et al (2011) Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing. PLoS One 6:1–7

    Google Scholar 

  5. Costa J-M, Benachi A, Gautier E (2002) New strategy for prenatal diagnosis of X-linked disorders. N Engl J Med 346:1502–1502

    Article  Google Scholar 

  6. Hudecova I, Jiang P, Davies J, Lo YMD, Kadir RA, Chiu RWK (2017) Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers. Blood 130:340–347

    Article  CAS  Google Scholar 

  7. Hui WWI, Jiang P, Tong YK et al (2017) Universal haplotype-based noninvasive prenatal testing for single gene diseases. Clin Chem 63:513–524

    Article  CAS  Google Scholar 

  8. New MI, Tong YK, Yuen T et al (2014) Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma. J Clin Endocrinol Metab 99:E1022–E1030

    Article  CAS  Google Scholar 

  9. Lam KW, Jiang P, Liao GJ et al (2012) Noninvasive prenatal diagnosis of monogenic diseases by targeted massively parallel sequencing of maternal plasma: application to β-thalassemia. Clin Chem 58:1467–1475

    Article  CAS  Google Scholar 

  10. Allyse M, Minear MA, Berson E et al (2015) Non-invasive prenatal testing: a review of international implementation and challenges. Int J Womens Health 7:113–126

    Article  CAS  Google Scholar 

  11. Chandrasekharan S, Minear MA, Hung A, Allyse M (2014) Noninvasive prenatal testing goes global. Sci Transl Med 6:231fs15

    Article  Google Scholar 

  12. Palomaki GE, Deciu C, Kloza EM et al (2012) DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study. Genet Med 14:296–305

    Article  CAS  Google Scholar 

  13. Chiu RWKK, Akolekar R, Zheng YWLL et al (2011) Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study. BMJ 342:217

    Article  Google Scholar 

  14. Jiang P, Chan KCA, Liao GJW et al (2012) FetalQuant: deducing fractional fetal DNA concentration from massively parallel sequencing of DNA in maternal plasma. Bioinformatics 28:2883–2890

    Article  CAS  Google Scholar 

  15. Jiang P, Peng X, Su X et al (2016) FetalQuantSD: accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA. NPJ Genom Med 1:16013

    Article  Google Scholar 

Download references

Acknowledgments

P.J. is currently funded by the Innovation and Technology Fund (ITS/401/17), Hong Kong.

Conflict of Interest

P.J. is a consultant to GRAIL. P.J. has filed patents/patent applications regarding cell-free DNA molecules. The remaining authors declare no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Peiyong Jiang .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Science+Business Media, LLC, part of Springer Nature

About this protocol

Check for updates. Verify currency and authenticity via CrossMark

Cite this protocol

Ni, M., Peng, X.L., Jiang, P. (2019). Bioinformatics Pipeline for Accurate Quantification of Fetal DNA Fraction in Maternal Plasma. In: Casadio, V., Salvi, S. (eds) Cell-free DNA as Diagnostic Markers. Methods in Molecular Biology, vol 1909. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-8973-7_13

Download citation

  • DOI: https://doi.org/10.1007/978-1-4939-8973-7_13

  • Published:

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-8972-0

  • Online ISBN: 978-1-4939-8973-7

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics