INSC

mutation — cross-omics
Cross-omicsMUTATION → DRUGCell-linePairwise association · TCGA cohorts

Across TCGA cell cohorts, INSC mutation is significantly associated with the drug of many other genes, with 23 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible INSC-associated genes across cancer lineages are PD0325901, Trametinib, and GSK2801. Each is linked with INSC in more than 1 cancer types. Because this analysis shows association rather than direction, both INSC-to-partner and partner-to-INSC results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (INSC→partner) and Y-score (partner→INSC) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
LARGE_INTESTINEPD0325901 →-0.574-2.745.022.04731
LARGE_INTESTINETrametinib →-0.669-2.745.033.04731
LARGE_INTESTINEGSK2801 →+0.338+2.871.024.02131
LARGE_INTESTINEOxaliplatin →+0.538+2.871.032.02121
LARGE_INTESTINE729189 →+0.320+2.871.007.02121
LARGE_INTESTINECCT007093 →+0.402+2.649.006.04611
Each partner links to its Q-omics profile. Showing the 6 strongest of 23 associations by consensus.

Exploration