Breakthrough Genomics

We are Breakthrough Genomics, the pioneers in Clinical Exome and Whole Genome tests.

Why should you test with us?

- High diagnostic yield of 50-60% due to our advanced clinical - interpretation software
- Fast turnaround time of 7-10 working days
- Comprehensive detection of SNPs, Indel, CNVs, and Trinucleotide repeats
- Free genetic consultations

Choose us today for Rapid Whole Exome and Genome Testing!

Learn more: https://drive.google.com/file/d/1IxiszAnjX0p1kdQF1Apbj4neajnknC0T/view?usp=sharing

We also offer Genetic Panel Testing

Click below to see our catalog: https://drive.google.com/file/d/1hgNIoyaDtlIkxlSGV55rkojtVLNyeP2J/view?usp=sharing

Catalog of BTG Genetic Panel Testing 2022.pdf

We are so excited to share that Futurology.Life named Breakthrough Genomics as one of the Most Innovative Irvine Based Machine Learning Companies! Thank you Futurology.Life for recognizing us - it is such an honor!

25 Most Innovative Irvine Based Machine Learning Companies This article showcases our top picks for the best Irvine based Machine Learning companies. These startups and companies are taking a variety of approaches to innovating the Machine Learning industry, but are all exceptional companies well worth a follow. We tried to pick companies across the size

"Since the start of the pandemic, it has been our to provide accurate results in the shortest amount of time. Whether you're getting a -19 or genetic test, we strive to get you the answers you need in order to take the next steps for your health.
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Breakthrough Genomics is committed to supporting you in your goal to reintroduce in-person summer camp and school programs this year!

Why you should choose Breakthrough Genomics for your COVID-19 testing services:
(1) We have rich testing at all ages in the area (from elementary schools to high schools and ). We have tested Alhambra, Fullerton, and Coachella Valley school districts during the , allowing students to go back to school safely
(2) We offer kid-friendly, non-invasive saliva testing
(3) Our prices are competitive to the point where testing is FREE for and
(4) Our gold-standard PCR –19 testing results are delivered by email within 24 hours
(5) All information submitted for COVID-19 testing is kept strictly confidential

Contact us today [[email protected]] for more information!

We are so proud to work together with our partner EIS Consulting as the preferred testing provider at Willows Community School. Our priority is to help and return to the as safely as possible! Looking forward to a happy and healthy future!

Excited to be the first clinical lab in Southern California designated by the Yale School of Public Health to provide SalivaDirect - the very same test used to test NBA basketball teams across the country!

Why choose SalivaDirect with Breakthrough Genomics?
Results You Can Trust - High sensitivity and specificity.
Quickest and easiest sample collection - avoids unpleasant oral and nasopharyngeal swabbing.
FDA Emergency Use Authorized
Test results are typically available within 1 business day or less
User friendly portal provides secured results at your fingertips

Spots are filling up fast! Click the banner below to register for Wednesday's webinar co-hosted by Novogene Life Sciences, presented by our Founder and CEO Dr. Laura Li, PhD, FACMGG. We hope to see you there!

Welcome! You are invited to join a webinar: Diagnose Rare Diseases in Minutes - Clinical Whole Exome Sequencing and the AI/ML-powered ENLITER™ System. After registering, you will receive a confirmation email about joining the webinar. There are 30 million people within the US who carry rare diseases, and often the average time to receive an accurate diagnosis is 4.8 years. With the sequencing cost dropping rapidly, more and more people are doing whole exome sequencing testing for rare disease diagnosis. Whole exome sequencing is....

Want to learn how to efficiently diagnose genetic diseases? Join us on June 17th for an exclusive webinar co-hosted by Novogene Life Sciences and Breakthrough Genomics. The live webinar will be presented by our Founder and CEO, Dr. Laura Li, PhD, FACMGG. Register today by clicking the banner below!

Welcome! You are invited to join a webinar: Diagnose Rare Diseases in Minutes - Clinical Whole Exome Sequencing and the AI/ML-powered ENLITER™ System. After registering, you will receive a confirmation email about joining the webinar. There are 30 million people within the US who carry rare diseases, and often the average time to receive an accurate diagnosis is 4.8 years. With the sequencing cost dropping rapidly, more and more people are doing whole exome sequencing testing for rare disease diagnosis. Whole exome sequencing is....

Great to see Breakthrough Genomics' article on
GenomeWeb! In it, our Founder and CEO, Dr. Laura Li, discusses the development and implementation of a Susceptibility Assessment. We invite you to take a look:

Informatics Startup Breakthorugh Genomics Developing Coronavirus Susceptibility Assessment | Breakthrough Genomics Informatics Startup Breakthorugh Genomics Developing Coronavirus Susceptibility Assessment May 07, 2020 | Neil Versel | GenomeWeb CHICAGO – In responding to the COVID-19 pandemic, genomic interpretation software developer Breakthrough Genomics last month added a research-use-only coronavirus susce...

Great to see Breakthrough Genomics' article on
GenomeWeb! In it, our Founder and CEO, Dr. Laura Li, discusses the development and implementation of a Susceptibility Assessment. We invite you to take a look:

https://btgenomics.com/2020/05/informatics-startup-breakthorugh-genomics-developing-coronavirus-susceptibility-assessment/

Informatics Startup Breakthorugh Genomics Developing Coronavirus Susceptibility Assessment | Breakthrough Genomics Informatics Startup Breakthorugh Genomics Developing Coronavirus Susceptibility Assessment May 07, 2020 | Neil Versel | GenomeWeb CHICAGO – In responding to the COVID-19 pandemic, genomic interpretation software developer Breakthrough Genomics last month added a research-use-only coronavirus susce...

April 25th is National DNA Day celebrating the completion of the
Human Genome Project at National Human Genome Research Institute and the discovery of the double helix. The team at Breakthrough Genomics loves as we are using and MachineLearning to transform the way that genomic data is interpreted to enable faster and better diagnoses, treatment decisions, and earlier disease intervention. And yes we’ve identified some key that may influence how you respond to -19. Happy National DNA Day!

Women.in.science Bioinformatics

The Breakthrough Genomics team would like to share with you a message from our Chief Operating Officer, Maribeth Raines, PhD.:

"This is , a special time where we recognize our medical laboratory professionals for all of their hard work and commitment to patient care and excellence in laboratory testing. I am proud to have led many of you over the years and thank you for your extraordinary efforts during these most challenging and pressing times of . It is important to me that your efforts are recognized alongside all the other fighting the pandemic. Your efforts are much appreciated."

Lab Week 2020: Thank You, Medical Laboratory Team! This Lab Week might look different than past celebrations, but the message is still the same: without the lab, patients wouldn’t get the care they need. You ...

The Breakthrough Genomics team hopes this message finds you healthy and energized /engaged at home and supporting your great ecosystem and the community! These are truly uncharted times and we're all learning as we navigate together.

In response to the growing crisis, we want to share the attached press release on our launching of a Genetic Susceptibility Assessment as part of our Services. We invite you to take a few moments to read about Breakthrough Genomics' newest launch.

Best Regards & stay safe!
-BTG Team

Breakthrough Genomics Press Release BREAKTHROUGHGENOMICSPress ReleaseFor Immediate Release: April 2, 2020Breakthrough Genomics Launches a Coronavirus Genetic Susceptibility

Genomic analysis is key to diagnosing rare diseases and we at Breakthrough Genomics are enlightening the genome with our Enliter™ software and enabling labs throughout the world to diagnose rare diseases faster and more accurately than ever before. Our mission is to make whole genome analysis and rare disease testing affordable and accessible to everyone.

Please join us in participating in by wearing your stripes on February 29th.

Breakthrough Genomics updated their business hours.