Correction to: Genetics in Medicine 2019; https://doi.org/10.1038/s41436-019-0636-5; Article published online 30 August 2019.
After further review of the manuscript, the author decided to withdraw the NIH grant acknowledgment as the manuscript was not directly related to the specific aims of the grant. The PDF and HTML versions of the Article have now been modified accordingly.
Author information
Authors and Affiliations
Corresponding authors
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
About this article
Cite this article
Dang, M., Xu, H., Zhang, J. et al. Correction: Inferring fetal fractions from read heterozygosity empowers the noninvasive prenatal screening. Genet Med 22, 450 (2020). https://doi.org/10.1038/s41436-019-0728-2
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41436-019-0728-2
