Enables analysis of over 200 genetic markers using a single, streamlined workflow.

Eliminate the need for multiple STR kits

• Interrogate up to 230 STR and SNP markers (plus Amelogenin), with 200 amplicons between 63 – 180 bp

Superior analysis of challenging samples

• Obtain discriminating profiles from low-level and/or degraded DNA

Turn cold cases into hot leads

• Generate phenotypic and ancestry estimations for investigative leads

Increased resolution for mixture samples

• Detect minor contributors at ~1% of major

STR data is compatible with current database formats

• Provides seamless link between CE-based and MPS data

Enables analysis of over 200 genetic markers using a single, streamlined workflow.

• Eliminate the need for multiple STR kits
• Superior analysis of challenging samples
• Turn cold cases into hot leads
• Increased resolution for mixture samples
• STR data is compatible with current database formats

The most complete, integrated workflow currently available, with the lowest base-by-base price.

The highest quality data on the market

• Produces the highest yield of error-free reads with the best performance in repetitive regions

Semi-automated and simple

• Intuitive touch screen and plug-and-play reagents make run set up a snap

All-in-one sequencing

• Automated on-board cluster generation and sequencing eliminates unnecessary down time

Flexible sequencing workflows

• Choose from pre-installed Forensic or Research workflows to accommodate your needs

The most widely adopted sequencing chemistry in the industry

• Highest quality MPS data on the market, lowest base-by-base price
• Most complete, integrated workflow; simple and easy to use
• Automated on-board cluster generation and sequencing
• Flexibility to choose from Forensic or Research workflows

Specifically designed to make forensic genomics data review easy and efficient.

See exactly what’s in your sample at every locus, at every base.

• Intuitive visualization of STR and SNP data at both sample and locus levels

Ensure the data is the highest quality for reliable results.

• Sample controls and Quality indicators simplify data analysis

Additional reporting for deeper insight

• Statistical estimates of ancestry, phenotype and profile frequencies can provide leads, even on cold cases

Because better data needs smarter software.

• See exactly what’s in your samples with intuitive visualization of STR and SNP data
• Simplify analysis with quality indicators and sample controls
• Increase resolution with tools for intra-STR and flanking region variant detection
• Gain deeper insights with statistical estimates of ancestry, phenotype and profile frequencies