One platform. From raw data to
biological understanding.

TraitSeq covers the entire analytical journey, from preprocessing, multi-method analysis, and AI-driven mechanistic interpretation, across all major omics types.

Transcriptomics Metabolomics Proteomics Phenomics Genomics

The full analytical landscape.

Every TraitSeq analysis applies the complete suite of methods to your data, across transcriptomics, metabolomics, and multi-omics, run in parallel, integrated across results, not siloed. The breadth is what makes the interpretation possible.

Understand what drives variation in your experiment.

Before any differential analysis, the platform maps your experiment’s global structure: which factors explain the most variance, whether samples cluster as expected, and where outliers sit. Data preprocessing, quality control, normalisation, and batch correction are all handled automatically.

Identify what changes between conditions.

Robust differential expression analysis with adaptive shrinkage for denoised effect sizes. Multi-factor designs, dose-response trends, interaction effects, and transcript-level isoform analysis, not just pairwise gene comparisons.

Map molecular changes to biological function.

Enrichment analysis with extensive biological annotation across transcription factors, hormone signalling, stress response pathways, protein domains, enzyme classes, and more. This breadth reveals biology insights that narrower analyses miss.

Find coordinated gene programmes and regulatory relationships.

Co-expression networks reveal groups of genes that respond together, often mapping to biological processes invisible in single-gene analysis. Regulatory network inference identifies which transcription factors are driving the response.

Deep characterisation reveals how genes connect into a mechanism.

Every significant gene is individually researched against the species knowledge graph to the same depth shown below. Select a gene to see how characterisation reveals its role, its relationship to other findings, and its contribution to answering the research question.

Showing 5 key genes of the thousands characterised in this analysis

01
Statistical result
02
Functional annotation
03
Cross-reference
04
Literature & validation
Detect
FLS2 Part of a 33-receptor expansion spanning both surface (PTI) and intracellular (ETI) immune detection systems. The plant is broadening its ability to perceive pathogen-associated signals.
Ethylene feeds back to upregulate more receptors
Relay
ACO1 → WRKY80 ACO1 produces ethylene, relaying the alarm through calcium waves and WRKY transcription factors. WRKY80 sustains the signal under both watering conditions at 24h, maintaining the primed state after the transient burst subsides.
Sustained WRKY80 activates defence genes and receptor production
Manufacture
BiP / GRP78 Part of a 13-gene ER secretory pipeline involved in folding, quality-checking, and deploying newly produced immune receptors, expanding the plant’s detection capacity.
Defence effectors manufactured and stockpiled
Arsenal
β-1,3-glucanase One of 28 defence effectors stockpiled by the plant. Pathway topology analysis shows the upstream MAPK cascade is activated but the downstream pathogen-response pathway is inhibited: armed, not firing.
Interpretation

A biological narrative answering your research question.

The mechanistic report synthesises findings from every analysis into an evidence-attributed narrative: executive summary, mechanistic model, biomarker panels, and actionable recommendations. Every claim links to the data that produced it. Publication-ready and designed to be handed directly to your board, regulatory team, or development programme.

Your R&D partner for omics interpretation.

Bring biological evidence to your decision making across the full development cycle: from early screening, through R&D, regulatory, product positioning, marketing, and customer use. Your product, your questions, your data, your insights.

Discuss your data →