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Realising the potential of genomic newborn screening
 
 
 
 

Atlas software integrates the entire inherited disease testing workflow

Uniting DNA extraction, capture based library preparation and bioinformatics for high throughput testing.

 
 
 
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How does it work?

Intuitive software to reduce hands on time and automate testing

 
 

Faster, easier library prep with fewer errors

Eliminating spreadsheets, improving traceability, automating calculations

Integrated genomic data analysis and reporting

Drag and drop FASTQs into integrated highthrough-put secondary, tertiary and Quaternary Analysisᵀᴹ

 
 
 

CLINICALLY VALIDATED

 
 

SUITABLE FOR ALL LIBRARY PREPARATION KITS

  • Autoassigns molecular barcodes

  • Integrates QC metrics

  • Reduces repetitive work

 
 

automation agnostic

  • Compatible with all liquid handling instruments

  • Autocalculates pipetting volumes

 
 

World first software

  • Drag and drop analysis

  • No command line needed

  • Validated data analysis and reporting

 
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Atlas powering genomic newborn screening

With Atlas, we’re enabling integrated genomic newborn screening from a heel prick dried blood spot sample, delivering a unique combination of simple setup processes, automation and user friendly software to simplify testing.

TECHNICALLY validated

High throughput

Cost effective