GeneMind delivers a comprehensive range of NGS sequencers— from low to ultra-high throughput — with data outputs ranging from 2 Gb to 14 Tb per run to empower laboratories of every size.

Widely used across basic research, clinical diagnostics, public health, agriculture, and biotechnology, supports applications such as

• Whole genome sequencing (WGS),
• Whole exome sequencing (WES),
• Cancer panels,
• Single-cell & spatial transcriptomics sequencing,
• Epigenomics and metagenomics,
• Environmental DNA (eDNA)

In clinical and translational medicine, NGS plays a critical role in:

• Oncology, rare disease diagnosis,
• Hereditary disorder screening, gene panels, tumor profiling,
• Reproductive health: Non-invasive prenatal testing (NIPT) and PGT-A,
• Pharmacogenomics.

Explore advantages of GeneMind NGS Sequencing Platforms:

• Cost-effective solutions for diverse applications,
• High sequencing accuracy and data quality (Q30 > 95% and Q40 > 90%),
• Compatibility with mainstream NGS libraries (P5/P7 adapters),
• Flexible throughput across models,
• End-to-end workflows without third-party dependencies,
• Comprehensive life-long after sales service,
• Support with local Technical Service & Experienced Application Specialist.

LEARN MORE: ANALIS.COM/NGS

Come discuss your project with our experts at Laborama.

ANALIS - Namur 081 25 50 50 - Gent 09 243 77 10 - mail@analis.be