Session Abstract – PMWC 2026 Silicon Valley
The PMWC 2026 Genomic Profiling Showcase will provide a 15-30 min speaking opportunity for selected companies working with the latest technologies in nucleic acid sequencing such as NGS, providing instrumentation for genomic sequencing, and offering direct to consumer services. These companies will share their innovative products and services to an audience of leading investors, potential clients and partners. The Genomic Profiling Showcase will exhibit the latest innovations in methods and instruments used for DNA/ RNA sequencing to ascertain the genomic and transcriptional profile of a person in order to understand why some people get certain diseases while others do not, or why people react in different ways to the same drug. This information is also being used to develop new ways to diagnose, treat, and prevent diseases, such as cancer.
Confirmed Presenting Companies:
Speaker Profile
Biography
Dr. Anmol S. Kapoor is a cardiologist, entrepreneur, and founder of Bio Aro, a next-generation precision health company integrating genomics, multi-omics, and advanced AI to transform clinical care. Under his leadership, Bio Aro has built a global ecosystem spanning whole-genome and cancer sequencing, pharmacogenomics, microbiome testing, telomere biology, and longevity sciences. Driven to bridge the gaps of traditional medicine, Dr. Kapoor is advancing a prediction-, prevention-, and personalization-focused model that empowers clinicians across cardiology, oncology, dermatology, gastroenterology, gynecology, and longevity medicine. He also founded Pan OmiQ, an AI-powered therapy-selection and multi-omics platform, and pioneered BioEMRBioELR, next-generation electronic record systems integrating AI into everyday practice. Through Kapoor Wealth Partners, he supports breakthrough ventures in medtech, biotech, digital health, and longevity. Internationally recognized in digital health and multi-omics innovation, Dr. Kapoor is shaping the global adoption of data-driven, patient-centered healthcare.
Talk
MultiOmics and AI: Pioneering the future of Longevity
MultiOmics and AI are redefining longevity science by uncovering hidden drivers of aging and enabling ultra-personalized prevention. This talk explores how integrated genomics, proteomics, microbiome insights, and AI-driven prediction models are transforming early detection, therapeutic targeting, and real-time health optimization shaping a new era of precision, preventive, and proactive longevity medicine.
Genomic Profiling Showcase:
BioAro Inc.
BioAro advances longevity through AI, LLM-powered BioIntelligence, and Axion hardware, integrating genomics, multi-omics lab testing, and real-time analysis. Its PanOmiQ platform unifies DNA, microbiome, and metabolic insights to deliver predictive, personalized, and proactive precision health.
Speaker Profile
Biography
Dr. Smith obtained her PhD at Harvard University, and trained further at Insitut Pasteur, Paris and University of California, San Diego. Dr. Smith focuses on the development of disruptive technologies at the intersection of genomics, immunology, and virology. The primary goal of all of her work is to overcome prior technical limitations with innovative approaches that provideunparalleled resolution of the human immune system, enabling the development of effective and efficient precision therapeutic approaches.
Talk
Decoding immune diversity to deliver precision therapeutics
The Clairity platform delivers comprehensive personalized immune profiling enabling AIML-based modeling for targeted drug design, therapeutic response prediction, and autoimmunity risk assessment. We'll showcase key competitive differentiators, highlight multiple proven successes across diverse applications, and present our detailed roadmap toward companion diagnostics development, bridging immune diversity insights with precision medicine.
Genomic Profiling Showcase:
Clareo Biosciences, Inc.
Clareo Biosciences delivers the world's first comprehensive immune receptor profiling through the Clairty platform. Our complete immunogenomic intelligence enables companion diagnostics, predictive biomarkers, and precision drug design—accelerating therapeutic development, improving patient outcomes, and reducing adverse events across immunotherapy, vaccines, and autoimmunity.
Speaker Profile
Biography
Tarun leads the development of A IVA, a GenAI-powered agentic platform for genomic variant analysis and rare disease diagnosis. His research focuses on leveraging AI and machine learning to improve molecular diagnosis success rates for rare disease patients. His work has been cited over 300 times and he has presented at major conferences including the Indo US Bridging RARE Summit. He is passionate about making genomic diagnostics faster, more accurate, and affordable for diagnostic labs worldwide.
Talk
When an AI Clinical Analyst Joins the Genomics Team
What If Genomes Could Answer Back, Clinically? With AIVA, you could simply ask questions about patient's symptoms and get instant, source-verified answers. AIVA transforms genomic interpretation through conversational AI, enabling diagnostic labs to analyze variants in minutes instead of hours or weeks, with ACMG-compliant classifications and zero data retention.
Genomic Profiling Showcase:
Mamidi Health
Mamidi Health develops AIVA, an AI-powered platform that transforms genomic variant analysis for diagnostic labs. AIVA reduces diagnosis time from weeks to hours while delivering accurate ACMG-compliant classifications, making rare disease diagnosis faster, cheaper, and more accessible.
Speaker Profile
Biography
Dr. Karen E. Malone brings a strong combination of translational medicine and biomarker expertise, grounded in a clear commercial perspective, to drive science-based business programs. With over 15 years of industry experience across both CRO and pharmaceutical environments, she has progressed into senior, strategy-focused roles with increasing responsibility. Her work centers on new product planning and corporate strategy, with a particular emphasis on the rapidly evolving, high-technology field of rare disease therapeutics and diagnostics.
Talk
Diagnostic Integrity for Medically Actionable Inherited Diseases
GeneScape is developing the most advanced genetic diagnostic algorithms for inherited rare diseases to facilitate therapeutic development and bring potentially life changing therapies to the patients. Based on large-scale, diverse genomic datasets and proprietary expertly-curated patient databases, coupled with important strategic partnerships, GeneScape is poised to bring state-of-the-art, disease-specific diagnostic algorithms to global labs.
Genomic Profiling Showcase:
GeneScape
GeneScape currently offers services for precision medicine epidemiology focusing on genetically defined diseases. We have compiled a suite of unique data resources, including proprietary data, that we are now leveraging to develop specialized algorithms for genetic diagnosis in rare diseases to improve accuracy.
Speaker Profile
Biography
Dr. Tsimberidou is a Tenured Professor of Medical Oncology at MD Anderson. She has designed highly innovative clinical trials that have changed the standard of oncology practice. She pioneered the personalized medicine program for cancer that improved patient care and established a model for clinical trials at other institutions, nationally and internationally. She led multiple clinical trials and has published over 370 articles. She has been invited to present her work as a keynote speaker at national and international conferences. She has received many awards, including an ASCO Career Development Award. She chaired ASCO's Clinical Research Committee (2016-2017) and was appointed as a member of other committees. Because of her accomplishments in personalized medicine, she was elected a Fellow of the American Association for the Advancement of Science (FAAAS) and for her contributions to ASCO, she received the designation of Fellow of ASCO (FASCO). She is a Katherine Russell Dixie Distinguished Endowed Professor.
Talk
Concordance Analysis of DNA and RNA Profiling
In an analysis of genomic and transcriptomic alterations (tumor analysis, Tempus AI) of 253 patients with cancer treated in the IMPACT2 study, significant concordance was noted in the AR, AKT2, CDK4, CDKN2A, CDKN2B, ESR1, KRAS, and TP53 genes; and between TP53 alterations and VEGFA overexpression. High tumor transcriptional burden was associated with shorter overall survival.
Genomic Profiling Showcase:
MD Anderson Cancer Center
The mission of the University of Texas MD Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through education for undergraduate/graduate students, trainees, professionals, employees and the public.
Speaker Profile
Biography
Dr. Clark is the CEO and founder of Pavi Health, Inc, a precision medicine company focused on targeting treatment for patients with severe infections and sepsis. Dr. Clark previously co-founded and served as the Director for the Austere environments Consortium for Enhanced Sepsis Outcomes (A CESO), where she built an international consortium focused on developing tools and strategies for improving survival for patients with severe infections. She has spearheaded development of host-based diagnostic and prognostic assays using a multi-omic systems biology approach.
Talk
Reimagining Precision Medicine for Severe Infections
This talk will introduce the Pavi Health companion diagnostics platform, which utilizes the patients response to an infection to guide treatment selection. By incorporating information on the patients immune endotype and the therapeutic mechanism of action, the Pavi Health platform accurately predicts response to treatment to better inform care decisions.
Genomic Profiling Showcase:
Pavi Health, Inc.
Pavi Health is reimagining precision medicine for severe infections and sepsis, providing critical information to improve clinical outcomes and reduce costs.
Speaker Profile
Biography
Genomic Profiling Showcase:
EpiMethyl Analytics




