eDNA & metabarcoding
Detect which taxa are present from environmental DNA—ASV inference, taxonomic assignment, and diversity, with primer and reference caveats stated.
The ocean is mostly unsequenced, and its organisms rarely have a tidy reference. We bring the computational depth to match: environmental DNA and metabarcoding for biodiversity, marine metagenomics, population genomics, and aquaculture genomic selection—for research, with the limits stated as plainly as the results.
A single litre of seawater carries DNA from hundreds of species; a marine genome is often large, repetitive, and unreferenced; and the questions—what lives here, how populations connect, how a stock adapts—are ecological and population-scale rather than single-sample. Marine data also brings its own gaps: reference databases are patchier for marine taxa, and eDNA signals are shaped by primers, shedding, and currents.
We work across that space: environmental DNA and metabarcoding for biodiversity, marine metagenomics for microbial communities, population genomics for connectivity and adaptation, and aquaculture genomics for breeding. The work runs through our core metagenomics, genomics, and pipeline services. Where we estimate breeding values or read eDNA, we are clear these are research findings and predictions: eDNA is a detection signal, not a census, and breeding values need validation in your population.
The computational analyses that span a drop of seawater to a farmed genome—from biodiversity and community ecology to population connectivity and aquaculture breeding.
Detect which taxa are present from environmental DNA—ASV inference, taxonomic assignment, and diversity, with primer and reference caveats stated.
Alpha- and beta-diversity, rarefaction, and community comparison across sites, depths, and seasons.
Connectivity, structure, and adaptation across populations—robust even at the low coverage marine studies often have.
Genomic selection and breeding-value estimation for farmed species—framed as research predictions needing validation.
Host-symbiont (e.g. Symbiodiniaceae) analysis, disentangling holobiont partners in reef systems.
Community composition and function of marine microbiomes from metagenomic and amplicon data.
eDNA-based screening for target, invasive, or indicator species over space and time—research, not certified testing.
Mining marine metagenomes for novel enzymes, biosynthetic gene clusters, and functions of interest.
A transparent sequence from raw marine reads to an interpreted, reproducible result—methods and references chosen for the marker, organism, and question.
Steps adapt to your project: eDNA metabarcoding vs. metagenomics vs. population genomics vs. aquaculture selection. We agree the plan—and the caveats—with you first.
We agree the question and marker, and select reference databases—flagging where marine coverage is thin.
Inputs: reads · markers · plan
Reads are quality-checked, trimmed, and denoised; primers removed for metabarcoding.
Tools: fastp · cutadapt · DADA2
ASVs are assigned against SILVA/PR2/BOLD, or reads mapped and assembled for genomic work.
Tools: DADA2 · SILVA · BWA
Diversity and community structure, or population genomics—structure, connectivity, selection.
Tools: phyloseq · ANGSD · vegan
Aquaculture selection, coral holobiont, or bioprospecting analyses as the project requires.
Tools: rrBLUP · antiSMASH
Results are interpreted with limits stated—eDNA detection vs. abundance, reference gaps, prediction uncertainty.
Focus: honest interpretation
Figures, tables, and a written summary, with version-locked code and databases so it reproduces exactly.
Tools: Quarto · renv · conda
We select from the field's standard toolkit rather than forcing every dataset through one pipeline. A representative set of what we work with:
Cross-species analysis is powered by reference genomes, ortholog sets, and biodiversity databases. We build on the community's authoritative, versioned resources.
Three marine approaches answer different questions. A quick orientation; we will help you match it to your study.
| Dimension | eDNA / metabarcoding | Metagenomics | Population genomics |
|---|---|---|---|
| Answers | Which taxa are present? | What can the community do? | How do populations differ? |
| Input | Marker amplicons | Shotgun reads | WGS or RAD-seq of individuals |
| Key limit | Reference gaps; not a census | Assembly & depth | Sample number & coverage |
| Best for | Biodiversity & monitoring | Function & novel genes | Connectivity, adaptation, breeding |
Not just a taxa table dropped in a folder—a coherent picture of your samples, communities, or populations, documented so it reproduces.
Marine work carries two honest caveats we state up front. First, eDNA and metabarcoding measure detectability, not abundance or certainty of absence—results are shaped by primers, reference completeness, and how DNA disperses in water, so we report them as a biodiversity signal, not a headcount. Second, where we estimate aquaculture breeding values, these are statistical predictions with a stated accuracy that need validation in your population; field and production outcomes depend on environment and management, so we make no guarantees. We also flag where marine reference gaps limit what any method can resolve.
The practical payoff: you get results you can defend, with every tool and reference-database version recorded so the analysis reproduces exactly. And we will tell you plainly when sampling depth or reference coverage won't support the conclusion you're after.
What marine, ecology, and aquaculture teams most often ask before starting.
Send us your eDNA reads, metagenomes, or marine genotypes—we'll scope the analysis and tell you honestly what it can and can't show.