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Correction: Whole-exome sequencing of BRCA-negative breast cancer patients and case–control analyses identify variants associated with breast cancer susceptibility
Human Genomics volume 16, Article number: 68 (2022)
The Original Article was published on 23 November 2022
Correction: Human Genomics (2022) 16:61 https://doi.org/10.1186/s40246-022-00435-7
Following publication of the original article [1], the authors reported Fig. 1 is not the updated version. The correct Fig. 1 has been provided in this Correction.
Study design for the selection of variants and genes. aList of known or candidate cancer genes in the Network of Cancer Genes [9]. bThe Cancer Gene Census list of the Catalogue of Somatic Mutations in Cancer (COSMIC) [10]. cList of cancer driver genes from Bailey et al. [38]. dList of cancer driver genes inferred with nucleotide context from Dietlein et al. [11]
The original article [1] has been corrected.
Reference
Lee NY, Hum M, Amali AA, et al. Whole-exome sequencing of BRCA-negative breast cancer patients and case–control analyses identify variants associated with breast cancer susceptibility. Hum Genomics. 2022;16:61. https://doi.org/10.1186/s40246-022-00435-7.
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Lee, N.Y., Hum, M., Amali, A.A. et al. Correction: Whole-exome sequencing of BRCA-negative breast cancer patients and case–control analyses identify variants associated with breast cancer susceptibility. Hum Genomics 16, 68 (2022). https://doi.org/10.1186/s40246-022-00443-7
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DOI: https://doi.org/10.1186/s40246-022-00443-7