Table 2.
Biopsy | Cell counts | All overlapping genes | COSMIC genes p < 0.05 and K* > 1 | ||||
---|---|---|---|---|---|---|---|
PIDa | Histology | RNA | DNA | No. any p and K* | No. p < 0.05 and K* > 1 | No. | Max K* (gene) |
20 | CARDb | 249 | 342 | 6671 | 98 | 7 | 1.12 (MUC1)c |
20 | ESOd | 181 | 339 | 7581 | 2 | 0 | — |
9 | NDBEe | 160 | 362 | 3783 | 35 | 4 | 1.01 (ERBB2) |
14 | NDBE | 259 | 200 | 9213 | 8 | 0 | — |
16 | NDBE | 237 | 227 | 7217 | 0 | 0 | — |
6 | LGDf | 221 | 353 | 7818 | 58 | 0 | — |
19 | LGD | 354 | 317 | 8566 | 5 | 0 | — |
6 | HGDg | 189 | 312 | 8308 | 485 | 35 | 1.54 (ERBB2) |
14 | HGD | 172 | 117 | 7282 | 2612 | 119 | 1.27 (CXCR4) |
20 | HGDh | 233 | 339 | 7148 | 416 | 39 | 1.33 (PTPRC) |
16 | EACi | 187 | 274 | 7713 | 244 | 20 | 1.46 (GNAS) |
We measured the contribution of genomic mutations to transcriptomic changes by K* index of phylogenetic signal49. For each gene, the p-value was estimated by a one-sided random permutation test with 999 repetitions to test K* index against the null hypothesis of the gene expression values being randomly distributed in the phylogeny (n = number of DNA cells per biopsy).
aPatient identification number from the original study.
bHealthy gastric cardia.
cThe gene names are italicized according to the organism-specific formatting guidelines for humans.
dHealthy esophagus.
eNon-dysplastic Barrett’s esophagus.
fLow-grade dysplastic Barrett’s esophagus.
gHigh-grade dysplastic Barrett’s esophagus.
hThe first of two HGD biopsies from this patient separated by at least 5 cm.
iEsophageal adenocarcinoma.