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Our Platform

Transforming healthcare with AI

We have developed novel technology that generates, collects, structures, and analyzes vast amounts of data and merged with the power of AI, we can advance precision medicine today, and in parallel, facilitate discovery, development, and delivery of optimal therapeutics for tomorrow.


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Our Solutions

GENOMIC PROFILING

Our genomic tests analyze somatic and germline information across DNA, RNA, and proteomic data to help identify treatment options tailored for the individual.
 

CLINICAL TRIAL MATCHING

Our proprietary trial matching software utilizes NGS as well as EHR integrations to identify patients that match to the right trial at the right time.

COMPANION DIAGNOSTICS

We integrate CDx claims into STAR Health Network assays which offer a validated and established sequencing platform to pursue companion diagnostic biomarkers

This is data-driven precision medicine.

This is the future of healthcare.

Our Platform

High throughput solutions provide comprehensive datasets for consumer, academic, and research needs.

 

We offer a broad range of technologies to support your high throughput needs, from genotyping to methylation to NGS.

 

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Our Solutions

Genotyping

We have a wide portfolio of genotyping solutions to fit the needs of small and high volume data projects.

Methylation

We have robust methylation solutions with an optimized workflow for high quality data.

NGS

Our lab has Illumina’s MiSeqs, NextSeqs and NovaSeqs to support all your sequencing needs.

Genotyping

Our wide portfolio of genotyping solutions fit the needs of small and high volume data projects:

 

Illumina
Medium to high throughput volumes

Multiple arrays for GWAS sample analysis

Arrays and boosters for a wide variety of testing such as PGx

Thermofisher
Medium to high throughput volumes

Enables GWAS, PGx and Gene Expression analysis

24, 96 sample formats

Methylation

We have robust methylation solutions with an optimized workflow for high quality data.

Extensive experience running Illumina Infinium EPIC 850k chips at high throughput

Capability to run customized methylation arrays to provide a range of medium to large data sets

Assay can provide data for research applications such as methylation profiling and biological age calculations

Supports data generation for EWAS analysis

NGS

Our lab has Illumina’s MiSeqs, NextSeqs and NovaSeqs to support all your sequencing needs.

 

Low Pass Whole Genome Sequencing

Cost effective to obtain large quantities of data

Combined with imputation across the whole genome

Low coverage combined with the NovaSeq enables very high throughput

Metagenomics
Supports microbiome analysis through shotgun metagenomics or 16s analysis.

16S rRNA sequencing analyzes the prokaryotic 16S ribosomal RNA gene (1500 bp), which contains 9 variable regions (species-specific)

Enables interrogation and monitoring aspects of variable regions on the bacteria.

Excellent resource for gut microbiome monitoring or ongoing research
 

Our Differentiators

Strong partnership

and collaboration to find tailored solutions for successful outcomes

High quality data

across multi-omic platforms

Fast turnaround time

on average 10 days from batch creation

Wide range of technology

from genotyping and sequencing to metagenomics and methylation

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