Clinical-Grade Whole Genome Sequencing and Interpration now at $400. 

PacBio Whole Genome Sequencing (WGS)



Whole Genome Sequencing Test

Whole Genome Sequencing is the analysis of the entire genome, including intronic and exonic regions of DNA. The data provided thanks to this method are useful tools to investigate inherited disorders and rare diseases, to develop targeted therapies and drugs, to study tumors and fight their progression. The WGS application can be extended to non-human genomes, for example for agricultural or bacteria segments, in fact it was widely used during the Covid-19 pandemic.

The analysis is powered by Next Generation Sequencing (NGS) technology, a powerful tool for research and clinics that can reduce costs in terms of money and time, and that can drive to terabytes of output.

The Extensa software, CE-IVD and ISO13485 certified, is the Dante Labs property system that intervenes in the bioinformatic process. The result is a comprehensive overview of the whole genome, with the highest level of accuracy and precision and, for human genomes, with the latest reference of comparison.


Sequel II


The Sequel IIE system, based on Single Molecule, Real-Time (SMRT®), provides highly accurate long reads,PacBio® HiFi reads, with uniform coverage and epigenetic characterization.

These end-to-end solutions ensure superior data quality with reduced cost and time.

The sharpness of HiFi readings, in fact, allows in a short time to receive in-depth results, with a high degree of accuracy of biological insights and a significantly reduced volume of data to be processed. Thanks to this technology, even the compute infrastructure and cloud-based platform also have a minor impact on the cost structure.

A variety of applications can be tailored to the Sequel IIE system to achieve a reliable, cost-effective, and high-throughput sequencing process.


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