AI Tools in
Precision Medicine
Join us for an engaging session on AI-driven innovation, expert talks, and insightful discussions in precision medicine.
Co-organized with Bay Bifx!
Explore how automation and AI strengthen bioinformatics workflows for scaled clinical genomics, with sessions on AI in digital pathology and its use in the analysis of medically relevant genes that remain difficult to interpret, as well as an exciting, expert-led panel discussion. Co hosted by Myriad Genetics and Strand Life Sciences, this event brings together shared expertise in genomics, bioinformatics, and clinical diagnostics.
AI Tools in Precision Medicine
08th
April 2026
Venue
Myriad Genetics' SSF facility
Grand Nexus Building, 233 E Grand Ave., South San Francisco, CA
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Talk Details
Talk Details
Moderators
Jaya Singh
Associate Vice President, Strand Life Sciences
Radhakrishna (RK) Bettadapura
VP, Research Informatics
Connecting Metadata, Analytics, and AI to Accelerate Target and Drug Discovery
Shrutee Jakhanwal
Associate Director - Product
Management, Strand Life Sciences
Metadata harmonization, analysis pipelines, and AI foundational models together form the backbone of modern target discovery. By standardizing heterogeneous omics datasets, harmonized metadata enables meaningful cross-study comparisons and deeper biological context. Robust analysis pipelines ensure consistent, reproducible insights at scale, reducing time spent on data preprocessing. Building on this foundation, AI models can uncover hidden patterns, prioritize targets, and generate novel hypotheses. Collectively, these capabilities accelerate the transition from raw data to actionable insights, enabling more confident and efficient identification and validation of therapeutic targets in complex disease landscapes. This talk highlights our ongoing efforts to integrate these capabilities to accelerate target discovery.
AI-Native Operating System for Drug Development
Twesh Malkhani
Cheiron
This talk introduces Cheiron’s AI-native operating system for drug development, designed to unify scientific, clinical, regulatory, and competitive workflows. Powered by a Lifesciences Knowledge Graph, it connects diverse data sources and enables workflow-native AI agents, accelerating decision-making and streamlining biopharma processes from insight generation to execution.
Bioinformatics Workflows for Scaled Clinical Genomics
Sam Pearlman
Myriad Genetics
Sajja Vinay Kumar
Strand Life Sciences
Scaling clinical genomics requires workflows that ensure traceability, reproducibility, and regulatory alignment amid growing data complexity and diverse analytical platforms. In this talk, Strand will first present a framework that separates pipelines into independent repositories, and standardizes pipeline configuration, versioning, and release management across workflows, while centralizing configuration in ConfigDB, a database-backed service. Following this, we will hear perspectives from the Myriad Genetics team on the data complexity issue. We will look into how analysis is not limited to a single platform, while significant parts of those pipelines are functionally identical. This section of the talk will cover strategies to address some of the major challenges associated with complex bioinformatics pipelines and analyses, and support both Production and Research workflows.
DeepCAH: Deep Learning in Variant Calling for Difficult Genes
Jing Liu
Myriad Genetics
The genetic complexity of congenital adrenal hyperplasia (CAH) makes it difficult to call variants of the disease. We will explore how machine learning was utilized to make this process easier and to narrow down on diagnoses.
An expert-led Panel on AI Tools to Advance Precision Medicine
TO BE DECIDED
TBD
An expert panel discussion on the challenges in validation, integration and scalability of AI models will follow the above talks. This interactive session will unpack some of the key bottlenecks in deploying AI models for data curation, integrating scalable AI workflows and how GPT-based chatbots are influencing this dynamic space.
Resources
Resources
Single Cell Data Harmonization
Pharma and Biomarker Discovery Applications
07
Methylomics
Our