Bioinformatics Services
HPC-backed bioinformatics — assembly, variant calling, RNA-Seq, metagenomics and pharmacogenomics — delivering publication-ready, fully interpreted results.
Turn your sequencing data into insight
Send us your data or study design and our bioinformatics team will scope the right analysis pipeline.
Explore Bioinformatics Services
Analysis pipelines for genomes, transcriptomes and clinical data.
Whole Genome Assembly
De novo and reference-guided assembly of sequencing reads into complete, contiguous genomes.
Transcriptome Analysis (RNA-Seq)
Differential expression, transcript quantification and functional annotation from RNA-Seq data.
Metagenomics Analysis
Taxonomic and functional profiling of microbial communities from shotgun or amplicon sequencing.
Whole Exome Analysis
Variant calling, annotation and filtering across protein-coding regions to identify disease-relevant mutations.
Pharmacogenomics Analysis
Analysis of genetic variants influencing drug response to support personalised treatment decisions.
Human Whole Genome Analysis
Comprehensive interpretation of human whole-genome data, from SNVs and indels to structural variants.