GenomePilot™ enables any researcher to define and execute complex NGS analysis processes using an intuitive, browser-based interface.

Point and click to select which best-practice processes to run on your datasets—no scripting required. GenomePilot will enable your team to turn raw sequencing data into relevant variants and help your lab

Reduce implementation and overhead
Streamline the entire analysis process
Maximize use of sequencing instrumentation
Deliver high quality, more accurate results

Key Features

Diversified analysis toolset containing industry standard tools in ready-to-use, pre-validated processes.
Ready-to-use analyses include processes for alignment, quality control, single sample, tumor normal, and tumor-unmatched normal.
Easy-to-use interface allows users to quickly create, change parameters, and execute a process through guided prompts without scripting or command lines.
End-to-end analysis enables users to get data off the sequencer and determine causal variants without having to monitor your analysis at every step.
Multi-job processing maximizes performance and speeds analysis.
Real time monitoring and controls with built in tracking and auditing of all runs and data used, which is critical for CLIA certification.

GenomePilot - NGS Analysis SimplifiedAppistry

GenomePilot - NGS Analysis Simplified

Appistry

GenomePilot - NGS Analysis Simplified

Appistry

GenomePilot - NGS Analysis Simplified
Appistry