Variant Analysis and Qualification, Simplified. For organizations that are conducting NGS based research or running clinical NGS tests, GenomePilot™ enables labs to automate the process of identifying reportable variants with an integrated, scalable and compliant data analysis platform.
For the staff that is working with NGS data but does not possess a bioinformatics skillset, GenomePilot™ bridges the gap between bioinformatics and the NGS lab making it much simpler to identify reportable variants from NGS datasets. With a focus on making the analysis of NGS data more approachable and accessible, GenomePilot integrates analytics, compliance and infrastructure into a single solution enabling labs to improve productivity and reduce costs associated with NGS based testing.
Enable all lab personnel to run NGS analyses without complicated scripting.
Execute quality, repeatable analyses on DNA-seq and RNA-seq data.
Scale and automate workflows for variant analysis, qualification and prioritization.
Track all activity and access full audit logs to meet compliance requirements.
GenomePilot can automate analyses and standardize day-to-day tasks resulting in a substantial productivity gain for the bioinformatician and NGS labs they support. Bioinformaticians can get back to novel discovery work while meeting the needs of the NGS lab.
Choose from industry-standard tools you trust to build best-practice analyses.
Streamline your processes for data refinement and validation.
Adjust parameters and choose tools specific to analysis needs.
Create version controlled pipelines for repeatable execution.
The analytics component of GenomePilot simplifies and automates how an organization works with NGS data, making the informatics and datasets more approachable and accessible.
For organizations who are processing clinical data, GenomePilot simplifies data management, workflows, and audit trailing to help labs achieve and maintain regulatory compliance such as CLIA. Through the easy-to-use interface, users can access full audit logs on all runs, data used, and output files, along with controlling user management to keep data, processes, and results secure.
Computation, processing, and storage capabilities are delivered in a single solution to simplify and increase productivity in analyzing NGS datasets. GenomePilot requires no specialized networking or complex IT expertise and can be set-up and generating results in less than a day.
REST based APIs connect with internal systems such as your sequencer, LIMS, or EMR to automate processes and streamline data analysis.
GenomePilot sits on top of a high-performance computing engine to enable robust and scalable execution of NGS datasets.
Easily integrate with a variety of standard storage solutions.
Easily grow the system as laboratory volumes change without reengineernig processes.
Labs can choose from flexible deployment and licensing options that can be tailored to meet the needs of your organization.
Tell us how many samples you plan to process and scale as your lab volume grows.
Customers can select from monthly or annual subscriptions to predict and control costs.
GenomePilot can be easily deployed as software only, an integrated hardware solution or in the cloud with no complex integration or set-up.
Dell has partnered with Appistry to deliver a turnkey solution integrating GenomePilot on robust Dell hardware. Available in two configurations, tower or rack, to assist small start-up labs and larger facilities that require higher processing capacity and throughput.
GenomePilot is designed to leverage the flexibility, cost-efficiency, and security of the Microsoft Azure Cloud. The pay-as-you go subscription model enables users to only pay for compute and storage resources when consumed.