The Future of Genomic Diagnostics

Advancing Precision Medicine
with Accessible NGS Solutions

The Foresee Genomics Advantage

Integrated Solution

Integrated Solution

Innovative molecular kit with cutting edge software for seamless operation

Precision Sequencing

Precision Sequencing

Highly accurate sequencing using Nanopore technology, ensuring reliable results

Proven Technology

Proven Technology

Validated technology, ensuring trust and reliability

Rapid Scalability

Rapid Scalability

Flexible solutions tailored to small and medium-sized labs

Professional Standards

Professional Standards

Tailored for CLIA/ISO15189 certified labs, an ideal choice for Laboratory Developed Tests (LDT)

User-Centric Design

User-Centric Design

Designed for customer ease and usability

Fast, Affordable and High-Precision NGS Solutions

Foresee Genomics is transforming genomic testing with our innovative Next Generation Sequencing (NGS) solutions. By combining proprietary molecular biology and bioinformatics software with fourth generation Nanopore sequencing technology, we empower small and medium labs to deliver fast, affordable and highly accurate diagnostics.

Re-envisioning NGS for Small-Medium Labs

Foresee Genomics simplifies and accelerates the NGS workflow to provide small- and medium-sized labs with access to life-changing information to drive precision medicine forward.  We provide NGS in a manner that is more affordable, with faster results, and the ability to run at lower volumes, making it ideal for clinical diagnostics in a small or medium lab setting.

Integrated
Molecular Kits

Streamlined sample preparation with user-friendly protocols

Sequencing
Technology

Real-time, high-accuracy sequencing adaptable for various diagnostic needs

Proprietary
Analysis Software

Automated data interpretation for actionable clinical insights

VALIDATED TECHNOLOGY

Foresee Genomics’ technology platform, SeqF, has been validated in numerous independent runs and
samples to deliver high-precision, accurate and reproducible results.

Comparisons with expected allele frequencies in synthetic and spiked samples, together with observed
allele frequencies from independent sequencing platforms (MiSeq and MGI) indicate the high accuracy and sensitivity of SeqF deployed with the MinION platform.

The figure presents an example of SeqF’s performance showcasing the identification of the IDH2 R172K mutation in the HD829 standard across three sequencing platforms, compared with the expected allele frequency.
SeqF consistently aligns with expected VAF, indicating its
capability in detecting low-frequency mutations in cancer genomics and precision medicine.

Foresee Genomics Provides Highly Accurate and Consistent Mutation Detection
Comparing Mutation Detection Across Sequencing Platforms

Graph