Improving the calling of non-invasive prenatal testing on 13-/18-/21-trisomy by support vector machine discrimination
Abstract
With the advance of next-generation sequencing technologies, non-invasive prenatal testing (NIPT) has been developed and employed in fetal aneuploidy screening on 13-/18-/21-trisomies through detecting cell-free fetal DNA (cffDNA) in maternal blood. Although Z test is widely used in NIPT nowadays, there is still necessity to improve its accuracy for removing a) false negatives and false positives, and b) the ratio of unclassified data, so as to reduce the potential harm to patients caused by these inaccuracies as well as the induced cost of retests.\n\nEmploying multiple Z tests with machine-learning algorithm could provide a better prediction on NIPT data. Combining the multiple Z values with indexes of clinical signs and quality control, features were collected from the known samples and scaled for model training in support vector machine (SVM) discrimination. The trained model was applied to predict the unknown samples, which showed significant improvement. In 4752 qualified NIPT data, our method reached 100% accuracies on all three chromosomes, including 151 data that were grouped as unclassified by one-Z-value based method. Moreover, four false positives and four false negatives were corrected by using this machine-learning model.\n\nTo our knowledge, this is the first study to employ support vector machine in NIPT data analysis. It is expected to replace the current one-Z-value based NIPT analysis in clinical use.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 24
- FWCI
- 1.93
- Field percentile
- top 14%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- An Efficient Computational Method to Create Positive NIPT Samples with Autosomal Trisomy
Tinh H. Nguyen, Huynh V. Nguyen, … Vinh Sy Le·International Conference on Bioinformatics and Computational Biology (ICBCB)Peer-reviewed·Mar 18, 2024
- Computational framework for targeted high-coverage sequencing based NIPT
Hindrek Teder, Priit Paluoja, … Priit Palta·PLoS ONEPeer-reviewed·Jul 8, 2019
- Innovative method for reducing uninformative calls in non-invasive prenatal testing
Jaroslav Budiš, Juraj Gazdarica, … Tomáš Szemes·bioRxiv·Jun 22, 2018
- Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples
Priit Paluoja, Hindrek Teder, … Priit Palta·PLoS Computational BiologyPeer-reviewed·Dec 20, 2021
- Clinical Validation of a Non-Invasive Prenatal Test for Genome-Wide Detection of Fetal Copy Number Variants
Roy B Lefkowitz, John A Tynan, … Mathias Ehrich·bioRxiv·Dec 4, 2015
- Noninvasive Prenatal Screening at Low Fetal Fraction: Comparing Whole- Genome Sequencing and Single-Nucleotide Polymorphism Methods
Carlo G. Artieri, Carrie E. Haverty, … Dale Muzzey·Prenatal DiagnosisPeer-reviewed·Mar 20, 2017