Sequencing

NGS analysis software

for research and clinical applications

 accurate DNA variant analysis

NGS data interpretation

variant annotation and genetic variant management

high-throughput NGS sequencing system

large-scale genomic analysis

benchtop NGS sequencing platform

versatile medium-throughput

rapid and flexible genomic analysis

compact NGS sequencing platform

rapid targeted sequencing

flexible capacity

Fast and simple fragmentation

Fragment size easily controlled by incubation time

Ideal for NGS library preparation

Fast and simple fragmentation

Fragment size easily controlled by incubation time

Ideal for NGS library preparation

Fast and simple fragmentation

Fragment size easily controlled by incubation time

Ideal for NGS library preparation

High efficiency

Low GC bias

Input DNA: 500 pg to 1 µg

Fast and easy ligation

High efficiency

Optimized formulation

Fast and simple to use
Minimal DNA loss
Direct use of the product

Cost savings
Easy integration
High performance

Cost savings
Easy integration
High performance

Cost savings
Easy integration
High performance

Cost savings
Easy integration
High performance

Cost savings
Easy integration
High performance

Cost savings
Easy integration
High performance

Cost savings
Easy integration
High performance

DNA size > 10 kb

Magnetic bead technology

Long-read sequencing

DNA size > 5 kb

Magnetic bead technology (SPRI)

Long-read sequencing

DNA size 1-5 kb

Magnetic bead technology (SPRI)

Single or double-sided selection

DNA size 1-3 kb

Magnetic bead technology (SPRI)

Single or double-sided selection

DNA size 500-1000 bp

Magnetic bead technology (SPRI)

Single or double-sided selection

DNA size: 450-750 bp

Magnetic bead technology (SPRI)

DNA library PE300