Service
AVANTI Software Platform
Turn raw sequencing data into clinical-grade reports with zero setup and full scalability
Key advantages
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Free FASTQ to VCF conversion from any sequencer
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No installation required: works on any browser, instantly
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Pay-per-use model with no upfront costs or subscriptions
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Generate 180+ report types in parallel across unlimited samples
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Compatible with any data type: single gene to whole genome
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Fast turnaround: reports in minutes, not hours
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White-label option to customize reports with your branding
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Designed for labs, clinics, and research teams seeking fast, automated workflows
Technical specifications
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Input formats supported: FASTQ, VCF from any sequencing platform
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Output: Clinical-grade reports, VCF files, variant annotations
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Analysis pipeline: FASTQ-to-VCF conversion, variant annotation, report generation
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Report catalog: 180+ customizable reports (clinical, carrier screening, oncology, etc.)
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Interface: Web-based, compatible with all major browsers
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Scalability: Parallel analysis of multiple samples
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Security & privacy: GDPR-compliant infrastructure with secure cloud storage
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Branding: Customizable templates for clinics, labs, and institutions
