NGS Analysis, Simplified.

Automate your next-generation sequencing (NGS) workflows from sequencer to report with accessible, scalable and compliant genomics solutions for your lab.

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Process creation

Automate NGS Workflows From Reads to Reports.

Appistry helps clinical labs establish and expand their NGS based testing capabilities with solutions that automate variant identification, prioritization and interpretation to reduce turnaround and improve the profitability of NGS based testing.

Automate Variant Analysis

GenomePilotâ„¢ enables labs to automate the process of identifying reportable variants with an integrated, scalable and compliant data analysis platform.

Scale Clinical Reporting

GenomeNavigatorâ„¢ delivers an easy-to-use, interactive solution for molecular pathologists and clinical genomicists to interpret and report clinically relevant variants.

Expand NGS Capabilities

Appistry's Managed Workflow Services help your lab reduce the resources, cost and time required to launch or expand your NGS based testing capabilities.

Your Support and Innovation Partner.

With roots in high-performance computing, big data and health sciences Appistry brings a unique level of expertise to helping our customers establish and expand their genomics testing capabilities. We focus on partnering with our customers to build innovative solutions that enable more staff to work with genomics datasets, resulting in a faster path to clinical effectiveness and delivering answers to patients.

Learn How We Might Work Together.

We welcome the opportunity to talk and learn how we might work together. Please complete the below form and an Appistry representative will be in touch.

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