Enrichment of the fetal fraction in non-invasive prenatal screening reduces maternal background interference
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-35738-0.pdf
Reference27 articles.
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2. Yin, A. H. et al. Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA. Proceedings of the National Academy of Sciences of the United States of America 112, 14670–14675, https://doi.org/10.1073/pnas.1518151112 (2015).
3. Li, R. et al. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies. Ultrasound in obstetrics & gynecology: the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 47, 53–57, https://doi.org/10.1002/uog.14911 (2016).
4. Peters, D. et al. Noninvasive prenatal diagnosis of a fetal microdeletion syndrome. The New England journal of medicine 365, 1847–1848, https://doi.org/10.1056/NEJMc1106975 (2011).
5. Rampasek, L., Arbabi, A. & Brudno, M. Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencing. Bioinformatics 30, i212–218, https://doi.org/10.1093/bioinformatics/btu292 (2014).
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