Simple. Intelligent. Connected.

One Solution that Simplifies the Process of Translating Complex Genomic Data into Actionable Intelligence


WHAT WE DO

One Solution, One Space for Enabling Precision Medicine

PierianDx solves the problem of translating complex genomic data into actionable clinical insight to advance precision medicine. We do this through a cloud-based clinical genomics software platform that simplifies the process of taking DNA sequencing data though analysis, interpretation and final report. This is made possible through Actionable Intelligence derived from our comprehensive knowledgebase supplemented by human clinical expertise.

Request Demo

WHAT WE DO

SIMPLE


SIMPLE

We make it easier to access vast amounts of genomic data and translate that data into actionable insight.

Learn More

  • Streamline the entire clinical lab end-to-end workflow, from initial DNA sample to final clinical report

  • Includes an intuitive interface and easy-to-understand clinical reports

  • Supported by a range of services to help you ramp up your in-house genomic testing

  • Assay agnostic to make it easier to incorporate a range of somatic and constitutional testing

INTELLIGENT


INTELLIGENT

We use automated Actionable Intelligence through our knowledgebase to produce patient-specific reports and data visualization.

Learn More

  • PierianDx’s Clinical Genomics KnowledgeSpace translates millions of complex biomedical findings from public sources, highly curated sources, shared interpretations and more into simplified reports that can be shared with patients.

  • Our KnowledgeSpace is enhanced with human expertise – a team of variant scientists and medical directors who contribute to these shared interpretations and support our customers with validation and interpretation services.

CONNECTED


CONNECTED

PierianDx’s solution allows you to connect to an entire technology and collaboration ecosystem to advance your precision medicine program.

Learn More

  • Provides HL-7 integration and connects with all major Electronic Health Record systems, Lab Information Systems (LIS), and Lab Management Systems (LMS)

  • Our Partner Sharing Network facilitates shared clinical interpretations and precision medicine best practices

  • Our secure, HIPAA-compliant, web-based service offers secure access from anywhere with an internet connection

WHAT DRIVES US

We are driven by a quest to make it simpler for our customers to save more lives with precision medicine. United by this mission, PierianDx’s team of dedicated medical professionals, scientists, genomics experts and developers help our customers advance precision medicine by simplifying the process of turning DNA into actionable clinical insight.

HISTORY

A Legacy of Innovation

Through the completion of the Human Genome project to 2011, our founder Rakesh Nagarajan led a multi-disciplinary team of scientists, bioinformaticians, engineers, and biostatisticians at Washington University in St. Louis to solve a problem – handling and integrating the vast amounts of clinical and translational research data and turning it into actionable insights. This data included medical records, clinical trials, patient registries, biospecimen repositories, and genomics data generated from Next Generation Sequencing (NGS). In 2011, Rakesh and his team set their sights on solving this problem clinically and invented one of the first clinical bioinformatics platforms in the industry capable of enabling labs to perform NGS testing. Since spinning out of Washington University in 2014, PierianDx has extended the capability of its knowledgebase and clinical workflow, building one of the most comprehensive clinical genomics platforms in the industry. Today, health systems, academic medical centers, cancer centers and children’s hospitals worldwide are using PierianDx’s Clinical Genomics KnowledgeSpace™ and WorkSpace™ to advance precision medicine.

Timeline

CUSTOMERS

JOIN OUR GROWING PARTNER NETWORK

By becoming a PierianDx customer you join an expanding list of precision medicine leaders who contribute to one of the most extensive knowledgebases in the industry. By sharing medical interpretations, variant classifications, and aggregated variant and clinical data, each customer added to the PierianDx community expands the intelligence of the PierianDx Clinical Genomics KnowledgeSpace™. PierianDx’s knowledgebase is comprehensive database containing millions of biomedical findings that are constantly updated. Join the growing team of health systems, academic medical centers, cancer centers, children’s hospitals and commercial labs who have turned to PierianDx for a complete solution to their NGS testing needs.

Cleveland Clinic
Cleveland, OH

Aventus Biolabs
Winter Springs, FL

Dartmouth-Hitchcock
Bedford, NH

Human Longevity Inc.
Los Angeles, CA

UAB Lab
Birmingham

Cedars-Sinai Medical Center
Los Angeles, CA

Next Molecular
Chester, VA

University of Arkansas
Fayetteville, AR

ARUP Laboratories
Salt Lake City, UT

Wake Forest Baptist Health
Winston-Salem, NC

Florida Hospital
Orlando, FL

Siteman Cancer Center
St. Louis, MO

St.Luke’s Hospital
Chesterfield, MO

Q² Solutions
Durham, NC

Alpha Genomix Laboratory
Lawrenceville, GA

CHEO/NSO
Ontario, CA

GenLives
Montevideo, Uruguay

PrimBio
Exton, PA

BYU
Provo, UT

PacGenomics
Agoura Hills, CA

TriCore Reference Laboratories
Albuquerque, New Mexico

Partners

Archer
Boulder, CO

ARUP Laboratories
Salt Lake City, UT

Syapse
Palo Alto, CA

REAN Cloud
Herndon, Virginia

AWS

Search Job Listings

CAREERS

GOT WHAT IT TAKES?

Join PierianDx and help us simplify genomic insights in order to make precision medicine possible.

PierianDx is a fast-paced rapidly growing healthcare technology company with an expert team of professionals with deep experience in genomics, healthcare technology and clinical lab management. Our team is on the forefront of clinically Actionable Intelligence (AI), the leading technology that enables precision medicine and more patient-specific treatments and diagnoses.

If you’d like to join our team, we’d like to hear from you.

MEET THE TEAM

PierianDx is a dedicated team of medical professionals, scientists, genomics experts and developers who are driven by one goal – to advance precision medicine by simplifying the process of turning DNA into meaningful clinical insight.

Leadership Team

Rakesh Nagarajan, MD, PhD
Rakesh Nagarajan, MD, PhD
Founder and Executive Chairman
Michael L. Sanderson
Michael L. Sanderson
Chief Executive Officer
Chris Callahan, MBA
Chris Callahan, MBA
Chief Commercial Officer
Shalini Verma, MD, FCAP
Shalini Verma, MD, FCAP
Laboratory and Medical Director
Bryce Daines, PhD
Bryce Daines, PhD
VP Product Development
Andy Bredemeyer, PhD
Andy Bredemeyer, PhD
Vice President, Product
Mukesh Sharma, PhD
Mukesh Sharma, PhD
Vice President, Product
Josh Forsythe
Josh Forsythe
Vice President, Marketing
Aditya Phatak
Aditya Phatak
Director and Centre Head
Sumit Deshmukh
Sumit Deshmukh
Head of Delivery
Lisa Weingartner, MBA
Lisa Weingartner, MBA
Regional VP - NGS Solutions

Clinical Genomics Directors

Our Clinical Genomics Directors guide our customers through the process of accelerating their precision medicine programs. They assist during the planning, implementation and utilization stages, leveraging PierianDx solutions to achieve customer goals.

Will Moller, MS
Will Moller, MS
Director, Customer Success
Tyler Marquart, PhD
Tyler Marquart, PhD
Clinical Genomics Director

Advisors

John D. Pfeifer M.D., Ph.D.

View Bio

Karl V. Voelkerding M.D., FCAP

View Bio

Kai Wang, PhD

View Bio

Jonathan Heusel M.D., Ph.D.

View Bio

Allie Grossmann M.D., Ph.D.

View Bio

Board Members

Charles Boorady

View Bio

Bryan Carey

View Bio

Rakesh Nagarajan M.D., Ph.D.

View Bio

Frederick A. Hessler

View Bio

Pete Jobse

View Bio

Reid Robison, MD, MBA

View Bio

Michael L. Sanderson

View Bio