Sequencing Technology Solutions

The gold-standard sequencing platform for fast, flexible analysis

Simple, fast, and flexible  benchtop sequencers for cancer, inherited disease, reproductive health, and microbial research

Flexible—combine Sanger sequencing and fragment analysis on the same plate

Easy to use—all-in-one cartridge takes setup from hours to minutes

Fast—runs in as little as 30 minutes

Connected—access your data anytime, anywhere*

*With internet connection and Thermo Fisher Cloud account

Accuracy—the ultimate sequencing verification tool

Speed and flexibility—run from 1 to 96 samples typically in <5 hours

Read length— highest read length capability, up to 1,000 bp

Flexibility—3 different instruments and 5 sequencing chips for flexible throughput and turnaround time

Simplicity— automated workflow solutions

Scalability— from 2M to 130M reads per run

Speed—DNA to data in as little as 24 hours with less than 45 min of hands-on time

Confirmation of NGS results

Plasmid sequencing

CRISPR-Cas9 genome editing analysis

Human cell line authentication

Applied Biosystems SNaPshot genotyping

Multiplex ligation–dependent analysis of human copy number variation

Confirmation of NGS results

Targeted amplicon resequencing

Bacterial, fungal, and viral identification

Fragment analysis

Microsatellite/STR analysis

Targeted RNA and DNA

Microbial

Transcriptome

Exome

RNA-seq