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. 2018 Feb 23;9:794. doi: 10.1038/s41467-017-02621-x

Table 2.

Multivariate linear models explaining the evolutionary distance between samples

Predictor of evolutionary distance Estimate SE t-Value p
a) Single-crypt study (8 patients)
(Intercept) 14.06 12.27 1.15 0.5691
Progressor status (yes) 18.91 5.49 3.44 0.0017
Time point (second) 6.46 6.123 1.06 0.0537
Maximum distance from GEJ (cm) −1.48 0.52 −2.84 0.0088
Distance between biopsies (cm) −1.03 0.93 −1.11 0.2545
b) Large cohort (197 patients)
(Intercept) 4.54 1.50 3.03 0.0025
Progressor (yes) 12.75 0.78 16.30 <2e −16
Time point (second) −0.25 0.77 −0.33 0.7430
Maximum distance from GEJ (cm) −0.50 0.15 −3.21 0.0014
Distance between biopsies (cm) 0.57 0.20 2.81 0.0051

a) For the eight patients in our study, genetic distances between crypts are based on phylogenetic estimates of the number of genetic events that separate the samples. b) For the larger cohort of Barrett’s patients, the genetic distance between biopsies was calculated based on divergent copy number calls across 1 Mb windows as described in11. Values highlighted in bold pass the 0.05 threshold for statistical significance.