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Breakthrough Genomics

Irvine, United States (US) · Health and Medical

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Data quality

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#ai

#deep machine learning

#precision medicine

#improved diagnostic yields

#rare disease diagnosis

#whole genome

#early cancer detection

#cancer screening

#colon cancer

#pancreatic cancer

Breakthrough Genomics is a Health and Medical company based in Irvine, United States (US), founded in 2017, with 10-20 employees. Breakthrough Genomics's profile is verified on Enterprise League.

Overview

Breakthrough Genomics is an Irvine, California-based AI-powered clinical interpretation company specializing in genomic data analysis and rare disease diagnostics.

We serve healthcare providers, genetic counselors, and researchers seeking to accelerate and improve the accuracy of genetic testing. Our mission is to transform rare disease diagnostics and expand access to precision medicine through innovative technology.

Virtual Geneticist®, our proprietary AI platform, streamlines genomic data interpretation, prioritizing potential disease-causing variants with ACMG classifications and literature associations. We’ve been recognized for our innovation, including winning the 2024 Innovation Award for AI-Driven Rare Disease Diagnosis and Early Cancer Detection.

Breakthrough Genomics is dedicated to advancing the field of genomics and improving patient outcomes through cutting-edge technology and collaborative partnerships.
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Contact Details

+1949-229-0094
info@btgenomics.com

Irvine, United States (US), 2 Hughes

Founded

2017

Company Type

Private Limited Company

Employees

10-20

Categories

Biopharma
Life Science
Biotechnology

Keywords

#ai

#deep machine learning

#precision medicine

#improved diagnostic yields

#rare disease diagnosis

#whole genome

#early cancer detection

#cancer screening

#colon cancer

#pancreatic cancer

Awards

• 2026 OpenSee all

Services

Default Product Image
Virtual Geneticist™ VG Plus
Biotechnology

Virtual Geneticist™ VG Plus builds upon VG, offering enhanced features and expanded capabilities for complex genetic cases. It provides a more in-depth analysis and supports a wider range of sequencing technologies.

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