KMD LABPUBLIC RESEARCH TOOL

Switchgrass RNA-seq Browser

Cold-acclimation expression, differential expression, and haplotype bias in one gene-centered view

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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 featureSourceReadiness
Gene and annotation searchv5.1↔haplotype mapping plus UniProt/GO fieldsReady
Five-timepoint expressionAP13 HAP1 v6.1 featureCounts, 30 samplesReady for exploratory CPM profiles
Differential expression343,326 significant gene-comparison rowsReady
Haplotype bias486,310 gene-context-time rowsReady
Transcript-level expressionNo transcript abundance matrix in the current browser inputsFuture extension