Findingdiagnoses.cures.
Comprehensive Genetic Testing + Consultation
The only provider in the world to combine Long/Short Read Whole Genome Sequencing with Bionano Optical Genome Mapping and Transcriptome Sequencing.
NewsDr. Peter Nagy gives talk on Accelerating Prenatal Diagnostics!
Despite costly and extensive testing, nearly 50% of patients with an underlying genetic disease never receive a molecular diagnosis.
Even with breakthroughs that tailor each patient's treatment to their cancer's unique genetic profile, fewer than 10% of cancer patients undergo such testing.
We created Praxis Genomics to overcome these fundamental limitations in genetic diagnostics.
Our Unique Approach
As the only provider combining these three technologies, we investigate the genome at sequence, structure, and function levels simultaneously.
Optical Genome Mapping
Bionano Technology
Reveals structural variants and complex genomic rearrangements invisible to other methods.
Whole Genome Sequencing
Complete DNA Analysis
Comprehensive sequencing of all genetic material for maximum diagnostic sensitivity.
Whole Transcriptome Sequencing
RNA Expression Analysis
Captures gene expression and functional insights beyond DNA sequence alone.
Trusted Results. Proven Impact.
This unique approach provides unprecedented depth in cancer profiling and achieves an unsurpassed diagnosis rate for otherwise unsolved genetic disorders.
Our Services
Clinical Genetic Consulting
Expert guidance for complex genetic cases
Our board-certified geneticists and pathologists will review clinical history, help select the appropriate diagnostic tests, and explain the results in detail.
Clinical Genetic Testing
Unparalleled diagnostic accuracy
Our unique approach of combining Optical Genome Mapping, Whole Genome, and Whole Transcriptome Sequencing provides exceptional diagnostic sensitivity and accuracy.
Research Services
Advanced genomics for discovery
Our Optical Genome Mapping, Whole Genome and Transcriptome Sequencing platforms are available for custom basic science research applications.
Clinical Genetic Consulting
Expert guidance for complex genetic cases
Our board-certified geneticists and pathologists will review clinical history, help select the appropriate diagnostic tests, and explain the results in detail.
Clinical Genetic Consulting
Expert guidance for complex genetic cases
Our board-certified geneticists and pathologists will review clinical history, help select the appropriate diagnostic tests, and explain the results in detail.
Clinical Genetic Testing
Unparalleled diagnostic accuracy
Our unique approach of combining Optical Genome Mapping, Whole Genome, and Whole Transcriptome Sequencing provides exceptional diagnostic sensitivity and accuracy.
Research Services
Advanced genomics for discovery
Our Optical Genome Mapping, Whole Genome and Transcriptome Sequencing platforms are available for custom basic science research applications.
Download Our Brochures
Get detailed information about our genetic testing services
Leadership
Peter Lajos Nagy, MD, PhD
Chief Medical Officer
Paul Smith, MB (ASCP)CM
Director of Laboratory Operations
Nicholas Rouse, MS
Director of Bioinformatics
Michael F. Nagy, BA
Director of IT
Carl Woodham, PhD
Director of Business Development
Scientific Advisory Board
Ben Tycko, MD, PhD
Peter Underhill, PhD
Val Sheffield, MD, PhD
Howard J. Worman, MD
Michael L. Shelanski, MD, PhD
Uta Francke, MD
Mark Aurel Nagy, MD, PhD
For decades, our founders have been pioneers in the development of modern genome analysis techniques and informatics tools for clinical applications. They have been among the first in the country to introduce clinical microarray testing, to offer combined clinical DNA and RNA analysis for patients with pediatric malignancies and have been first in the world to introduce clinical grade whole-exome-based carrier testing.
Praxis Genomics LLC now builds on these accomplishments and pushes the boundaries of Molecular Medicine further to provide a genetic diagnosis for an ever-increasing percentage of patients.
Publications
News
Technology
Saphyr Whole Genome Optical Mapping Instrument
The Saphyr® Whole Genome Optical Mapping Instrument from Bionano Genomics provides a high level assessment of breaks, rearrangements and repeat expansions in the DNA that cannot be seen using sequencing
Learn About Saphyr
DNBSEQ-T7
DNBSEQ-T7 can generate 1-7Tb of high-quality data per day for a wide range of applications, including whole genome, deep exome, epigenome, transcriptome, and targeted panel sequencing projects.
Learn About DNBSEQ-T7NovaSeq 6000 System
The NovaSeq 6000 Sequencing System allows diagnosis of DNA mutations at the level of its building blocks
Learn About NovaSeq 6000
Oxford Nanopore Technologies PromethION
The PromethION sequencer allows diagnosis of DNA mutations that scale between the building block resolution and the high level assessment.
Learn About PromethIONOxford Nanopore Technologies minION
The minION combines long read sequencing technology with rapid data availability for fast variant confirmation.
Learn About minION
Illumina DRAGEN Bio-IT Platform
The Dragen analysis pipeline allows high sensitivity detection of mutations and instability in difficult to analyze repetitive regions
Learn About DRAGENContact
6115 Peachtree Dunwoody Road, Suite 220
Atlanta, GA
30328
(678) 837-4022
Monday - Friday
8AM - 6PM
CAP #: 8743866
CLIA ID #: 11D2178215
