Atlas targeted genomic newborn screening platform
Integrated DNA extraction, capture based library preparation and bioinformatics for newborn screening laboratories.
Your Laboratory needs?
The right platform for the right need
First tier targeted genomics to expand my program
Modular genomic newborn screening for sustainable program expansion.
Second tier confirmatory genetic testing for multi-ethnic populations
Comprehensive gene sequencing for cystic fibrosis, severe combined immunodeficiency, metabolic conditions, IEMs, lysosomal disorders.
The ATLAS platform includes
High sensitivity DNA Binding Probes
Comprehensive gene sequencing to identify exonic and non-coding variants in multi ethnic populations.
Validated analytical sensitivity greater than whole genome sequencing.
Scalable automation
Streamlined laboratory workflow from DNA extraction to report generation.
Low volume and high volume platforms.
World first software
Includes sample management, QC, bioinformatics and reporting.
Integrated primary, secondary and tertiary analysis of SNVs, in/dels, and CNVs including those in genes with high homology e.g. SMN1.
The Atlas Platform
With Atlas, we’re enabling high-throughput targeted gene sequencing from a heel prick dried blood spot sample that can be incorporated into newborn screening programs. The Atlas platform delivers a unique combination of simple setup processes, automation and user friendly software to simplify testing.