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. 2021 May 6;23(7):1378. doi: 10.1038/s41436-021-01190-1

Correction to: Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy number variants

Erica Soster 1,, Theresa Boomer 1, Susan Hicks 1, Samantha Caldwell 1, Brittany Dyr 1, Jason Chibuk 1, Eyad Almasri 1
PMCID: PMC8257495  PMID: 33958750

Correction to: Genetics in Medicine 2021; 10.1038/s41436-021-01135-8; published online 17 March 2021

Unfortunately, an error occured in Fig. 2. The corrected Fig. 2 is given below.

Fig. 2. Graphic depicting the distribution of positives by year.

Fig. 2

Rare autosomal trisomies (RAT) also include two cases that were monosomies of autosomes. Microdeletions refer to the select list of microdeletions <7 Mb as described in “Materials and Methods”. Common/Genome refers to cases positive for a common trisomy and a genome-wide event, while Common/SCA refers to cases positive for a common trisomy and a sex chromosome aneuploidy. Categories with an asterisk (*) show a significant trend, although given the small sample size of the Common/Genome category, significance should be interpreted with caution. Corresponding Z-scores can be found in Table S3. CNV copy-number variant.

The original article has been corrected.


Articles from Genetics in Medicine are provided here courtesy of Nature Publishing Group

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