01 Whole genome sequencing
02 Whole exome sequencing
03 Targeted sequencing
04 Sanger sequencing
05 Transcriptomics
06 Metagenomics
07 Proteomics
08 Metabolomics
09 Oligo synthesis
10 AI research project support
11 Sample to results, end to end
DNA 01 / 11
Whole genome sequencing
Read the full genome, coding and non-coding, to see every kind of variation in one experiment.
What it finds
Single-nucleotide variants and indels Structural variants and copy-number changes Repeat expansions and non-coding variants Ancestry and population structure
What you receive
Raw reads and alignments Annotated variant calls (VCF) Quality-control summary Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input High-quality genomic DNA from blood, tissue, cells or saliva.
Best for Rare-disease and cohort studies, population genetics, and new or improved reference genomes.
DNA 02 / 11
Whole exome sequencing
Sequence the protein-coding exons, where most known disease-causing variants sit, at a fraction of the cost of a full genome.
What it finds
Single-nucleotide variants and indels in coding regions Known and novel pathogenic variants Copy-number changes across exons Variants filtered by gene, inheritance and population frequency
What you receive
Raw reads and alignments Annotated, filtered variant calls (VCF) Coverage and quality-control summary Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Genomic DNA from blood, tissue, cells or saliva.
Best for Rare and inherited disease, family (trio) studies, and cost-effective cohort screening.
DNA 03 / 11
Targeted sequencing
Sequence only the genes or regions you choose, at very high depth, to catch low-frequency variants.
What it finds
Variants in a defined gene panel or amplicon set Low-frequency and somatic variants Marker genes for species and strain identification Confirmation of variants found by other methods
What you receive
Raw reads and alignments Variant calls or amplicon tables Per-target coverage report Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input DNA from tissue, blood, cultures or environmental samples. Low input amounts are often fine.
Best for Gene panels, validation studies, pathogen and strain typing, and large sample numbers on a budget.
DNA 04 / 11
Sanger sequencing
Standard and MID Sanger sequencing for accurate reads of PCR products and plasmids, ideal for confirming a sequence or checking a few samples.
What it finds
Confirmation of variants found by NGS Plasmid, clone and insert verification Species and strain identification from marker genes Mutations in a single gene or amplicon
What you receive
Raw trace files (.ab1) Base-called sequences (FASTA) Alignment to your reference sequence Read quality summary In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Purified PCR products or plasmid DNA, with sequencing primers.
Best for Validating NGS results, checking clones and constructs, and small numbers of samples.
RNA 05 / 11
Transcriptomics
Measure which genes are switched on, by how much, and how that changes between conditions.
What it finds
Differentially expressed genes Alternative splicing and isoforms Pathway and gene-set enrichment Cell types and states, with single-cell RNA-seq
What you receive
Raw reads and count matrices Differential expression tables PCA, heatmap and volcano plots Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Total RNA, or tissue and cells stored in an RNA-stabilising reagent.
Best for Treatment-response studies, disease versus healthy comparisons, and biomarker discovery.
DNA 06 / 11
Metagenomics
Identify and quantify the microbes in a sample, from gut and soil to water and air.
What it finds
Which bacteria, fungi and other microbes are present Relative abundance and diversity Functional genes and pathways Antimicrobial-resistance genes
What you receive
Raw reads Taxonomic and functional profiles Diversity and comparison plots Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Stool, soil, water, swabs, air filters or extracted DNA.
Best for Microbiome studies, environmental and eDNA monitoring, and food or agricultural samples.
Protein 07 / 11
Proteomics
Identify and quantify the proteins cells actually make, using mass spectrometry.
What it finds
Protein identities across the sample Changes in protein abundance between groups Post-translational modifications Candidate protein biomarkers
What you receive
Raw mass-spectrometry files Protein identification and quantification tables Pathway and enrichment analysis Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Cells, tissue, plasma, serum or purified protein.
Best for Mechanism studies, biomarker discovery, and checking whether gene-level changes reach the protein.
Metabolites 08 / 11
Metabolomics
Identify and measure the small molecules in a sample, from sugars and lipids to drug metabolites, using LC-MS and GC-MS.
What it finds
Metabolites present in the sample Changes in metabolite levels between groups Affected metabolic pathways Candidate metabolic biomarkers
What you receive
Raw mass-spectrometry files Metabolite identification and quantification tables Pathway and statistical analysis Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Plasma, serum, urine, tissue, cells, plant material or culture media.
Best for Disease and treatment studies, nutrition and plant research, and biomarker discovery.
DNA 09 / 11
Oligo synthesis
Custom DNA oligonucleotides for PCR, sequencing and probes, with desalt or HPLC purification.
What we make
PCR and qPCR primers Sequencing primers Probes and adapters Desalted or HPLC-purified oligos, to match your application
What you receive
Oligos with the purification you chose Quality-control data Sequence and yield information for each oligo
Typical input Your oligo sequences, the scale you need and the purification (desalt or HPLC).
Best for PCR and qPCR assays, sequencing, cloning and probe-based experiments.
AI 10 / 11
AI research project support
Hands-on machine-learning support for your own data, from study design to models you can defend.
What we cover
Study design and feature selection Predictive models and biomarker panels Integration of multi-omics data Validation, benchmarking and interpretation
What you receive
Cleaned, documented datasets Trained models and code Performance and validation report Methods text for your paper In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Data you already have: sequencing, expression, clinical or other tabular data.
Best for Labs with data but no in-house ML team, thesis and grant projects, and multi-omics studies.
End to end 11 / 11
Sample to results, end to end
Hand us your samples and your question. We run every step and deliver the answer.
What we cover
Choosing the right assay and depth Extraction, quality control and library preparation Sequencing or mass spectrometry Analysis and interpretation, with AI where it helps
What you receive
One project plan and point of contact All raw and processed data Figures ready for papers and reports Written findings report In alignment with the stated project objectives, comprehensive bioinformatics deliverables will be generated and provided.
Typical input Your samples, a sample sheet and a short description of your question.
Best for Teams without a core facility, first omics projects, and studies that combine several assays.
