Mirxes provides high-quality, cost-efficient human whole genome sequencing (hWGS) to meet your research needs while driving down your sequencing costs.

Our DNBSEQ™ DNA nanoball sequencing technology, coupled with PCR-free library preparation, enables Mirxes to deliver highly accurate results with low sequencing artifacts—quickly and cost-effectively. Complementary variant calling based on best practices is included.

High-quality Data

Guaranteed Q30 score >80% for PE150 and PE100

Highly Scalable Capacity

Up to 640 genomes in a single run.

Reliable Service, Fast Turnaround

Optimized workflows ensure efficient sequencing and quick result delivery.

Strong Bioinformatics Support

Expert experimental planning and customized data analysis.
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