Overview
Avanti is a cutting-edge, plug-and-play platform designed specifically to streamline and enhance the analysis and reporting processes for Next-Generation Sequencing (NGS) data. With the capacity to handle diverse data types from leading sequencing platforms such as Oxford Nanopore Technologies (ONT), Pacific Biosciences (PacBio), and Illumina, Avanti offers a versatile solution to the genomics community. This platform is engineered to accommodate the vast and varying data output by these technologies, providing comprehensive support for both long-read and short-read sequencing methods.
Key features of Avanti include its user-friendly interface, which allows researchers and clinicians alike to easily navigate through complex genomic data. It integrates advanced bioinformatics tools and algorithms, enabling the accurate identification, analysis, and reporting of genetic variations.
Highlights
- Quickly perform NGS secondary analyses from many popular sequencing platforms.
- Generate and download white-labelled PDF reports for 100+ hereditary predispositions and conditions
Details
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Features and programs
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Pricing
Dimension | Description | Cost/unit |
---|---|---|
Reports | A report is a genomic analysis | $0.001 |
Genomic Analysis | A genomic analysis produces an output file(s) | $0.001 |
Report Tokens | Each report is worth a certain amount of tokens | $0.10 |
Workflow Tokens | Each workflow is worth a certain amount of tokens | $0.10 |
Vendor refund policy
Refunds can be provided according to terms laid out in the terms and conditions of the product: https://shop.dantegenomics.com/pages/terms-and-conditions . Please contact contact@dantelabs.com for more information
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Support
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Support is available within the application and through our customer support team, which can be accessed at contact@dantelabs.comÂ
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