Research Area

Agriculture & Evolutionary Biology

From a wild genome no one has assembled to a breeding program spanning thousands of individuals—non-model biology brings its own hard problems. We bring the computational depth to match: genome assembly, population genomics, phylogenomics, selection scans, and genomic selection, for research.

Any organism · non-model WGS · RAD-seq / GBS Assembly · popgen · breeding Research predictions · no guarantees
Sample genome synteny dot-plot An illustrative synteny dot-plot comparing two genomes: collinear syntenic blocks along the diagonal, an inverted block, and translocated blocks off the diagonal, coloured by rearrangement type. synteny · genome A × B · PRJ-2026-0417 genome A →genome B →
Illustrative sample output collinear inverted translocated
Overview

Genomics for the whole tree of life, not just the model organisms

Most genomics tooling assumes a polished reference genome and a human-shaped problem. Agriculture and evolutionary biology rarely offer either. Genomes are often large, repetitive, and polyploid; references may not exist; sampling spans hundreds of individuals across populations and environments; and the questions—diversity, adaptation, ancestry, breeding value—need population-scale and comparative methods rather than single-sample pipelines.

We work across that whole space. From de novo assembly and annotation of non-model genomes to population genomics, phylogenomics, selection scans, genomic selection, and conservation genetics, we apply established, peer-reviewed methods at population scale—and return results documented for reproducibility. Where we estimate breeding values or selection signals, we are clear that these are research predictions: they need validation, and field performance also depends on environment and management.

Applications

What we analyse in agriculture & evolution

The computational analyses that span assembly to breeding—from non-model genomes and population structure to selection and comparative genomics.

Genome assembly & annotation

De novo assembly of non-model genomes to chromosome scale, with completeness assessment and gene and repeat annotation.

hifiasm · BUSCO · BRAKER

Population genomics & diversity

Diversity and differentiation statistics, population structure, admixture, and effective-population-size estimation.

ANGSD · PLINK · ADMIXTURE

Phylogenomics & comparative

Orthology inference, gene and species trees, and comparative genomics across many taxa, including synteny.

OrthoFinder · IQ-TREE · ASTRAL

Selection & adaptation

Genome scans for selection, environmental-association analysis, and molecular-evolution tests of adaptation.

SweeD · BayPass · PAML

Genomic selection & breeding

GWAS and genomic-selection models to estimate breeding values (GEBVs)—research predictions, not guaranteed outcomes.

rrBLUP · GAPIT · BGLR

Conservation genomics

Runs of homozygosity, inbreeding, and effective-population-size estimation to inform conservation research.

ROH · GONE · inbreeding

Pangenomics

Graph pangenome construction and structural-variation analysis to capture diversity a single reference misses.

PGGB · minigraph-cactus · vg

Biodiversity & metabarcoding

eDNA and metabarcoding analysis for species identification and biodiversity assessment from environmental samples.

DADA2 · OBITools · BOLD

The Pipeline

A representative agri-genomics workflow

A transparent, organism-agnostic sequence from raw data to interpreted biology—each step suited to your species and question and documented for reproducibility.

Adapted to your study: reference vs. de novo, WGS vs. RAD/GBS, single population vs. many taxa, diversity vs. breeding. We confirm the plan with you before any compute begins.

Intake & QC

Raw reads are quality-checked—quality, adapters, contamination, and ploidy and genome-size estimation.

Tools: fastp · GenomeScope · MultiQC

Assembly / alignment & annotation

A genome is assembled and annotated, or reads aligned to a reference, with completeness assessed by BUSCO.

Tools: hifiasm · BWA-MEM2 · BRAKER

Variant calling & genotyping

Variants are called across individuals—including RAD-seq/GBS genotyping—then filtered for quality and missingness.

Tools: GATK · Stacks · bcftools

Population structure & diversity

Diversity, differentiation, structure, and admixture are estimated across populations and samples.

Tools: ANGSD · ADMIXTURE · PCA

Selection, phylogeny & breeding

Depending on the goal: selection scans, phylogenomic trees, or genomic-selection breeding-value models.

Tools: SweeD · IQ-TREE · rrBLUP

Comparative & functional context

Signals are placed in comparative and functional context—orthology, synteny, gene families, and enrichment.

Tools: OrthoFinder · CAFE · synteny

Integration & reporting

Results become structure plots, trees, synteny and selection figures, tables, and reproducible methods with every tool version.

Tools: ggplot2 · R · versioned manifest

Tools & Technologies

Established, peer-reviewed tools—matched to your data

We select from the field's standard toolkit rather than forcing every dataset through one pipeline. A representative set of what we work with:

Assembly & annotation

hifiasm Flye purge_dups BUSCO BRAKER

Variant & genotyping

GATK Stacks bcftools VCFtools

Population genomics

ANGSD PLINK ADMIXTURE PopLDdecay GONE

Phylogenomics

OrthoFinder IQ-TREE ASTRAL MAFFT

Selection & evolution

SweeD BayPass PAML CAFE

Genomic selection & breeding

rrBLUP BGLR GAPIT TASSEL

Pangenomics & SVs

PGGB minigraph-cactus vg MUMmer

Visualization & databases

ggplot2 Ensembl Plants Phytozome OrthoDB
Key Databases

The genomics resources we draw on

Cross-species analysis is powered by reference genomes, ortholog sets, and biodiversity databases. We build on the community's authoritative, versioned resources.

Ensembl Plants
Reference plant genomes, gene models, and comparative data.
Ensembl Metazoa
Reference genomes and annotation across animal taxa.
NCBI / GenBank
The primary archive of sequences and assemblies.
Phytozome
Plant genomes with gene families and comparative tools.
Gramene
Comparative plant genomics for crops and models.
OrthoDB
Hierarchical catalog of orthologs across the tree of life.
BUSCO lineages
Near-universal single-copy orthologs for completeness.
GBIF
Global biodiversity occurrence records for context.
BOLD
Barcode of Life reference library for species ID.
Choosing an Approach

RAD-seq/GBS vs. WGS resequencing vs. de novo

Different strategies trade cost against completeness. A quick orientation; we will help you match it to your study.

General comparison of sequencing strategies for non-model genomics. The right choice depends on budget, sample number, and question.
Dimension RAD-seq / GBS WGS resequencing De novo assembly
Genome coverage Reduced-representation Whole genome, needs reference Builds the reference
Cost / sample Lowest—many samples Moderate Highest, per genome
Reference needed Optional Yes No
Resolves SVs No Partially Yes
Best suited to Large population & breeding panels Diversity & selection scans New species & pangenomes
What You Receive

A complete, documented deliverable

Not just a VCF dropped in a folder—a coherent picture of your organisms and populations, documented so it reproduces.

  • Assembled, annotated genome with BUSCO completeness, where applicable
  • Filtered variant set & genotype matrix across individuals
  • Diversity, differentiation & population-structure results
  • Selection-scan or phylogenomic results, per your question
  • Estimated breeding values (GEBVs) with accuracy, where applicable
  • Structure, tree, synteny & scan figures (publication-quality)
  • Reproducible methods with every tool & reference version

Built for reproducibility, not just a result

Population-scale analysis follows documented best practices—ploidy and genome-size checks, careful variant filtering and relatedness control, assembly completeness assessed by BUSCO, and reference and database versions pinned—so a selection signal or a structure result is real signal, not a filtering artifact or reference bias. Where we estimate breeding values or predictive models, we are explicit that these are research predictions with a stated accuracy: they need independent validation, and real-world field or population outcomes also depend on environment, management, and factors outside the genome, so we make no guarantees.

The practical payoff: your methods section writes itself, a reviewer can re-run the analysis, and a result from today can be reproduced a year from now. We will also tell you honestly when a design or sample size won't support the conclusion you're after.

FAQ

Agriculture & evolutionary biology questions

What plant, animal, and evolutionary-biology teams most often ask before starting.

Any organism, model or non-model — plants, animals, crops, livestock, wild species. We handle whole-genome sequencing (short- and long-read), reduced-representation data (RAD-seq/GBS), resequencing panels, and RNA-seq, from raw reads or assemblies from your core or public repositories.
Yes. De novo assembly of non-model genomes is core to this work — we assemble from long or hybrid reads, scaffold to chromosome level, assess completeness with BUSCO, and annotate genes and repeats.
Yes. We compute diversity and differentiation statistics, infer population structure and admixture, estimate effective population size and inbreeding, and run selection and environmental-association scans.
Yes. We run GWAS and build genomic-selection models to estimate breeding values (GEBVs) for research and breeding programs. These are statistical predictions that need validation; real-world performance also depends on environment and management, so we make no guarantees of field outcomes.
Yes. We infer orthology, build gene and species trees (including coalescent methods), and run comparative and molecular-evolution analyses such as gene-family expansion and dN/dS.
Agriculture and evolutionary biology is a research area we support through our core services — chiefly Genomics & Variant Analysis, Biostatistics & Visualization, and Custom Pipelines & Software — applied to your organisms. This page shows how they come together.

Have genomes or populations to analyse?

Tell us your organism, data type, and question—we'll scope it honestly, including if a different design would serve you better.