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Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
BMC Medical Genomics volume 12, Article number: 65 (2019)
- The original article was published in BMC Medical Genomics 2019 12:59
Miller et al. BMC Medical Genomics (2019) 12:59.
https://doi.org/10.1186/s12920-019-0504-9
Following publication of the original article [1], the authors reported that Fig. 1 was not correctly processed during the production process. The correct Fig. 1 is given below.
The publishers apologise for the inconvenience caused. The original article [1] has been corrected.
Waterfall plot of all genes with pathogenic variants. Waterfall plot of all EMCA samples that contained rare variants that passed the filter from Additional file 1: Figure S1. The main heatmap contains columns which represent an individual participant (N = 86), and rows that represent genes, while the color that fills in the cell represents the type of variant present for a specific participant in a specific gene. The heatmap below illustrates that histology, cancer stage and patient survival status, each column represents a different participant. “Undiff” refers to undifferentiated histology. The graph to the left shows the percentage of participants who have a rare variant in a gene, relative to all participants with variants, while the bar plot above the main graph represents the variant burden for each participant
Reference
- 1.
Miller, et al. Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population. BMC Med Genet. 2019;12:59. https://doi.org/10.1186/s12920-019-0504-9.
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Miller, J.E., Metpally, R.P., Person, T.N. et al. Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population. BMC Med Genomics 12, 65 (2019). https://doi.org/10.1186/s12920-019-0523-6
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