Genomics Services
Decoding genomes. End-to-end genome analysis from raw reads to annotated assemblies and actionable variant interpretation.
What We Offer
Comprehensive Genomics Analysis
From assembly to annotation, variant calling to population analysis.
Genome Assembly
De novo and reference-guided assembly from short and long-read sequencing data.
Variant Calling
Detect SNPs, indels, and small variants with high sensitivity and specificity.
Structural Variants
Identify large deletions, insertions, inversions, and translocations.
Copy Number Analysis
Detect copy number variations and aneuploidies across the genome.
Comparative Genomics
Compare genomes across species or strains to identify evolutionary changes.
Population Genetics
Analyse genetic variation within and between populations.
Applications
Diverse Sequencing Applications
Whether you are sequencing a new genome for the first time or looking for disease-causing variants, we have the expertise to help.
Whole Genome Sequencing
Complete genome analysis
Exome Sequencing
Coding region focus
Targeted Panels
Gene panel analysis
Metagenomics
Community genomics
Resequencing
Variant discovery
De Novo Assembly
Novel genome assembly
Ready to Decode Your Genome?
From raw FASTQ files to publication-ready results, we handle the entire genomics analysis workflow.