4.7 Article

DNA methylation-based sex classifier to predict sex and identify sex chromosome aneuploidy

Journal

BMC GENOMICS
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12864-021-07675-2

Keywords

DNA methylation; Sex prediction; Aneuploidy

Funding

  1. Economic and Social Research Council [ES/M010236/1, ES/M008592/1]
  2. Medical Research Council [MR/R005176/1]
  3. Engineering and Physical Sciences Research Council [EP/V000462/1, EP/R02572X/1, EP/P017487/1]
  4. University of Essex
  5. EPSRC [EP/R02572X/1, EP/V000462/1, EP/P017487/1] Funding Source: UKRI
  6. ESRC [ES/M008592/1, ES/M010236/1] Funding Source: UKRI

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A novel method for predicting sex using DNA methylation beta values was presented, which can be applied to various formats of DNA methylation datasets. The sex classifier based on sex-associated CpG sites demonstrates good performance across different tissues and can be used to identify samples with sex chromosome aneuploidy.
Background: Sex is an important covariate of epigenome-wide association studies due to its strong influence on DNA methylation patterns across numerous genomic positions. Nevertheless, many samples on the Gene Expression Omnibus (GEO) frequently lack a sex annotation or are incorrectly labelled. Considering the influence that sex imposes on DNA methylation patterns, it is necessary to ensure that methods for filtering poor samples and checking of sex assignment are accurate and widely applicable. Results: Here we presented a novel method to predict sex using only DNA methylation beta values, which can be readily applied to almost all DNA methylation datasets of different formats (raw IDATs or text files with only signal intensities) uploaded to GEO. We identified 4345 significantly (p<0.01) sex-associated CpG sites present on both 450K and EPIC arrays, and constructed a sex classifier based on the two first principal components of the DNA methylation data of sex-associated probes mapped on sex chromosomes. The proposed method is constructed using whole blood samples and exhibits good performance across a wide range of tissues. We further demonstrated that our method can be used to identify samples with sex chromosome aneuploidy, this function is validated by five Turner syndrome cases and one Klinefelter syndrome case. Conclusions: This proposed sex classifier not only can be used for sex predictions but also applied to identify samples with sex chromosome aneuploidy, and it is freely and easily accessible by calling the 'estimateSex' function from the newest wateRmelon Bioconductor package (https://github.com/schalkwyk/wateRmelon).

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