Powering Genomic Medicine

The best way to use DNA for preventive care

What We Do

HEALTHCARE NEEDS A GENOMIC MEDICINE PLATFORM

Genomics are healthcare’s most valuable asset for improving care and reducing costs. While sequencing costs have fallen dramatically, the cost and complexity associated with storing and analyzing the data have only increased. We need a platform for collaboration, data and process sharing, and machine learning to make precision medicine a part of everyday medical care.

PRACTICE SCIENTIFIC MEDICINE

Add value across the care continuum

PREVENTIVE CARE

Incorporate disease risks into care plans and promote personalized healthy behavior changes. Make your relationship with patients more consultative.

DIAGNOSIS AND TREATMENT

Rare diseases may not actually be rare. There may be as many as 7,000 rare diseases and the number of Americans living with a rare disease is estimated at between 25 and 30 million. 80% of rare diseases are genetic in origin. A patient’s DNA, RNA, proteins, and other molecular signals can improve early diagnoses and targeted treatments while reducing costs and clinician burden.

PATIENT SAFETY AND EXPERIENCE

The overall incidence of SADRs in hospitalized patients in the United States has been estimated at 6.2–6.7% and the incidence of fatal ADRs is estimated to be 0.15–0.3%. If these estimates are correct, then there are more than 2 million serious ADRs in hospitalized patients, causing over 100,000 deaths annually. This would make ADRs the 4th leading cause of death—ahead of pulmonary disease, diabetes, accidents, and automobile deaths. Of 27 drugs that are frequently cited in ADR studies, 59% are metabolized by at least one enzyme with a variant allele known to be associated with decreased drug metabolism.

Platform

THE OMIC PLATFORM

Genomic Medicine Engine

SECURELY STORE MULTI-OMIC DATA

Omic compresses raw genetic data 10X better than the leading standard.

BUILD, VALIDATE, AND SHARE PIPELINES

We are building the largest interconnected research network in the world to power complex analyses that can be configured in under a minute with mouse clicks – no coding required. These analyses run 30X faster than traditional methods and include actionability metrics.

INTEGRATE SEAMLESSLY INTO YOUR PROCESSES

We also have user-driven reporting and API-based integration, so the insights can be delivered flexibly to care teams and patients. These elements are what’s needed to make genomics cost-effective, trusted by medical staff, and actionable.

Platform
"Pediatric treatments improve through whole genome sequencing"
Children’s Mercy Hospital, Kansas City,
Our Work

SELECT ALLIANCES

Our Work
About Us

OUR STORY

We are a team of scientists, engineers, architects, and big data experts who have lost family members or been directly impacted by the lack of genomic medicine in healthcare today. Our mission is to improve healthcare and save lives through omics.

About Us
Join Our Team

Our Leadership

Our leadership team brings over 50 years of combined experience in genomics,
healthcare, and SaaS platforms to the table.

Hubs

Gabriel Richman

Founder & CEO

Gabe has a background in genetic research and experience as an engineer at Affymetrix, a genetic equipment and test manufacturing company. He has held leadership positions in SaaS companies and most recently led a team of software architects and digital strategy consultants at MuleSoft, the market-leading enterprise integration software company.

Steve

Steve Muller

VP Engineering

Steve has more than 15 years of experience in genomic data warehousing, analysis, architecture, and development operations. He most recently led data operations for Affymetrix manufacturing.

Join Our Team

LET'S COLLABORATE

Contact us for a free genomic opportunity analysis or to schedule a demo.