State-of-the-art genomic sequencing and analysis technologies powering precision diagnostics
Utilising a comprehensive suite of advanced platforms to deliver precise and reliable genetic diagnostics
High-throughput sequencing for comprehensive genetic diagnostics and research applications using GenoLabM and GeneStudio S5 Prime platforms.
Genome-wide analysis to detect copy number variations (CNVs) linked to genetic syndromes with 100-200kb resolution.
Gold-standard method for orthogonal confirmation of variants and familial mutation testing with >99.9% accuracy.
Sensitive absolute quantification and detection of rare variants and copy-number changes with high precision.
High-throughput mass-spectrometry genotyping of SNPs and mutations for pharmacogenomics and population studies.
Constitutional cytogenetic analysis for detecting aneuploidies and chromosomal rearrangements.
Advanced instruments ensuring precise and reliable results
High-throughput sequencing platform for large-scale genomic studies
Medium-throughput sequencing for targeted panels and confirmatory testing
Precision robotic system for high-throughput sample processing
MALDI-TOF mass spectrometry for high-throughput genotyping
High-resolution scanning for chromosomal microarray analysis
Quantitative PCR for gene expression and variant detection
All our platforms undergo rigorous validation and are maintained according to ISO 15189 standards. We participate in external quality assessment programs including CAP and GenQA to ensure the highest quality of results.
Contact our scientific team for detailed information about our platforms and validation data
Contact Our Team