Uncover hidden genomic variations.
Trait discovery can feel slow or complex. Our platform is designed to streamline the process and accelerate your breakthroughs. Unlock new genetic insights with greater speed and confidence, even when working with highly complex data.
Why Choose Pantograph?
Pantograph empowers you to:
Does scattered data hinder your progress?
Many organizations are dealing with genomics data scattered across different platforms, formats, and references creating obstacles for comprehensive analysis. Additionally, existing tools often lack intuitive workflows for building and exploring pangenomes, making trait discovery a lengthy and resource-intensive process.
Pantograph delivers a clear, comprehensive view of pangenomic data, including variation, gene annotations, and phenotypic traits as well as other omics data. Upload custom variation, annotation, and phenotype data to tailor Pantograph to your specific research needs. With unlimited user access, collaboration is effortless across teams.
Pantograph broadens your insights with multi-crop support for broader research applications across multiple species. Save valuable time and effort with advanced bioinformatics pipelines. Generate additional pangenomes and unlock the full genetic diversity using automated variant calling and genotyping.
Customer Quotes
“Pantograph helped us gain a much deeper understanding of our material's genomics.”
“Allows different expert profiles within the organization to access all genomic and omics data.”
Our interactive pangenome browser Pantograph offers a comprehensive trait and genomics knowledge base and can incorporate all your omics and phenotypic data to inspect, analyze and correlate in one place and with common and intuitive browser functionalities.
