Skip to main content
BMC Medical Genomics logoLink to BMC Medical Genomics
. 2019 May 22;12:65. doi: 10.1186/s12920-019-0523-6

Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population

Jason E Miller 1, Raghu P Metpally 2, Thomas N Person 2, Sarathbabu Krishnamurthy 3, Venkata Ramesh Dasari 3, Manu Shivakumar 2, Daniel R Lavage 2, Adam M Cook 3, David J Carey 3, Marylyn D Ritchie 1, Dokyoon Kim 2,4,5,6, Radhika Gogoi 3,; on behalf of the DiscovEHR collaboration
PMCID: PMC6530188  PMID: 31118041

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.

Fig. 1.

Fig. 1

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. doi: 10.1186/s12920-019-0504-9. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from BMC Medical Genomics are provided here courtesy of BMC

RESOURCES