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

Whole Genome Sequencing Test for Researchers

SKU:
ILLUWGSB2B-90GB6WGDNOYOUR
Sale
$600.00
$400.00

Description

Short-reads Whole Genome Sequencing Test and Interpretation

  • Short-reads Whole Genome Sequencing.
  • Leverage the Dante experience with tens of thousands of whole genomes sequenced.
  • End-to-end solution, including data delivery via cloud, logistics, customer support

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.

The Turnaround Time starts from when your sample is received at the lab. Our labs process samples from Monday to Friday. 

Fully customizable

Dante Genomics solutions are fully customizable in all the features, you can choose: the sequencing platform, the turnaround time and the coverage. 

End-to-end solution

You will receive an End-to-end solution, including data delivery via cloud, logistics, and customer support.

Accessible Data
Download your data when you want, where you want, and get actionable insights for today and the future.

NovaSeq6000 Platform

 

The NovaSeq 6000 System provides throughput, speed, and flexibility to meet any studio needs. This technology supports multiple types of flow cells, two library load workflows, and various combinations of read lengths to enable the power of next generation sequencing (NGS) processes.

 

The flexibility released allows scaling up or down to complete several levels of complexity for application as whole genome sequencing (WGS), whole exome sequencing (WES), whole transcriptome sequencing, or even less data intensive methods that require easy operation and integration with data storage and analysis tools.

 

An output up to 6 Tb and 20B reads in < 2 days enable powerful, high-throughput genomics solutions that empower users to achieve their company or research objectives.

 

The NovaSeq 6000 System is even fully compatible with LIMS system, as BaseSpace™ Clarity

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