SRR

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

Across TCGA patient cohorts, SRR mutation is significantly associated with the RNA expression of many other genes, with 2,520 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SRR-associated genes across cancer lineages are SNORD116-10, RN7SL685P, and RNU6ATAC29P. Each is linked with SRR in more than 1 cancer types. Because this analysis shows association rather than direction, both SRR-to-partner and partner-to-SRR results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNORD116-10 grouped by SRR-low versus SRR-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SRR→partner) and Y-score (partner→SRR) 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
BLCASNORD116-10 →+0.343+4.289<.001.00732
BLCARN7SL685P →+0.223+4.850<.001<.00132
UCECRNU6ATAC29P →+0.261+2.163.007.00532
HNSCKRTAP22-2 →+0.279+7.954<.001.00831
BLCAOR13J1 →+0.176+3.773<.001.00631
BLCAINSL5 →+0.146+3.725.001.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,520 associations by consensus.

SNORD116-10 by SRR expression — BLCA

Box plot of SNORD116-10 in SRR-low vs SRR-high samples in BLCA.

Explore this box plot interactively →

Exploration