Data scope
What this browser uses—and what each measurement means
This public browser is source-backed and reads a deployment copy of the analysis database. It does not alter the underlying analysis files.
Experimental design
Thirty biological samples cover five ordered conditions (NonA, 4h, 1d, 4d, 7d), two ecotypes (AP13 lowland and VS16 upland), and three biological replicates per ecotype-time group.
Total gene expression
The chart uses raw paired-end fragment counts from the AP13 HAP1 v6.1 featureCounts matrix. Each sample is divided by its assigned-fragment library size and multiplied by one million to produce CPM. This supports within-gene comparisons across samples and time.
CPM means counts per million assigned fragments. The default display applies log2(CPM + 1) so zero-expression observations can be shown and large expression ranges fit on one chart. These values are expression abundances, not fold changes.
Caution: AP13 HAP1 is a common reference for both ecotypes. Sequence divergence can create reference-alignment bias. Use the supplied differential-expression results for formal AP13-vs-VS16 inference and treat the CPM chart as an exploratory expression profile.
Differential expression
The browser imports the supplied rnaseq_all_comparisons_DE.csv. Every imported row has adjusted P ≤ 0.05; this is a significant-results table rather than a complete all-tested-gene table.
The readable comparison is shown as numerator vs denominator: positive DESeq2 log2FC means the numerator is higher, and negative means the denominator is higher. The original comparison code remains beneath the readable label for traceability. The supplied legacy codes for 4hvs1d and 4hvs4d use the opposite sign order from most within-ecotype codes, so the browser explicitly displays their verified biological direction.
Haplotype bias
The bias view uses strict one-to-one HAP1/HAP2 gene pairs across both AP13 and VS16 and all five time points. HAP1/HAP2 counts represent reads overlapping informative SNPs, not total transcript abundance. Low-total rows are shown explicitly so absence of evidence is not mistaken for balance.
Data readiness
| Website feature | Source | Readiness |
| Gene and annotation search | v5.1↔haplotype mapping plus UniProt/GO fields | Ready |
| Five-timepoint expression | AP13 HAP1 v6.1 featureCounts, 30 samples | Ready for exploratory CPM profiles |
| Differential expression | 343,326 significant gene-comparison rows | Ready |
| Haplotype bias | 486,310 gene-context-time rows | Ready |
| Transcript-level expression | No transcript abundance matrix in the current browser inputs | Future extension |