There are errors in Table S1 of the published paper. Please view the correct Table S1 here.
There is an error in the Results. The Results should state that twenty of the 44 participants with severe adverse events carried at least one of the candidate predictive markers.
Supporting Information
S1 Table. The genotypes at the loci DPYD and TYMP for 44 participants who had grade 3, 4 or 5 adverse events within 12 weeks of starting the chemotherapeutic protocol.
Treatment regimes; 1 = 5-FU as monotherapy; 2 = 5FU in combination chemotherapy; 3 = capecitabine as monotherapy; 4 = capecitabine in combination chemotherapy. For the genotype data; 0 = homozygous for the minor allele; 1 = heterozygous; 2 = homozygous for the major (wild type) allele. The genotypes 1236G>A and c1129-5923C>G are in linkage disequilibrium.
LFT; liver function tests.
https://doi.org/10.1371/journal.pone.0124893.s001
(XLS)
Reference
Citation: Jennings BA, Loke YK, Skinner J, Keane M, Chu GS, Turner R, et al. (2015) Correction: Evaluating Predictive Pharmacogenetic Signatures of Adverse Events in Colorectal Cancer Patients Treated with Fluoropyrimidines. PLoS ONE 10(4): e0124893. https://doi.org/10.1371/journal.pone.0124893
Published: April 13, 2015
Copyright: © 2015 Jennings et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited