Sold by: Innovare Genetics
Upload whole genomes, exomes or targeted gene panels (FASTQ, BAM or VCF) and get a review-ready analysis in one secure workspace: GPU-accelerated alignment and variant calling, ACMG/AMP classification with an auditable criteria ledger, integrated IGV, pharmacogenomics, HLA/KIR typing, repeat expansions, CNV/SV and ancestry-adjusted polygenic risk. Data hosted in the EU. For research use only.
Overview
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Real genome walkthrough (HG002), RUO
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From raw reads to interpreted variants
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Validated against ClinGen expert curation
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5.2 million variants to 97 for review
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Read-level review with embedded IGV
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36 virtual gene panels, ranked by score
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Pharmacogenomics with CPIC/DPWG/FDA actions
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Ancestry-adjusted polygenic risk scores
Innovare Genetics Portal turns raw sequencing data into a structured, review-ready genomic analysis. Research laboratories, hospital research groups, pharmaceutical teams and research centers upload whole-genome (WGS), whole-exome (WES) or targeted gene panel data as FASTQ, BAM or VCF, and the platform runs the complete analysis in the cloud: GPU-accelerated alignment and variant calling, annotation of millions of variants, and a prioritized shortlist for expert review. There is no bioinformatics infrastructure to install or maintain, and every organization works in its own isolated workspace.
Each analysis combines layers that are usually spread across several tools. A points-based ACMG/AMP classifier, calibrated to ClinGen recommendations, records every criterion it applies and every criterion it rejects, with the evidence and the reason, so each call can be audited. Variants are flagged when they fall in difficult regions (segmental duplications, low complexity), and reads can be reviewed in an embedded IGV viewer without downloading files. Depending on the assay, the portal also delivers 36 virtual gene panels ranked by a transparent score, pharmacogenomics for 23 genes with CPIC, DPWG and FDA recommendations per drug, HLA/KIR typing, repeat-expansion loci, pseudogene-aware analysis of genes such as SMN1/SMN2 and GBA, copy-number and structural variants with multi-caller consensus, carrier screening, quality and coverage metrics, and, for genome data, polygenic risk scores reported as ancestry-adjusted percentiles. Every module states what it covers and what it cannot exclude.
The classification engine has been benchmarked against the ClinGen Evidence Repository: on 1,232 expert-classified variants it reached 90.3% concordance with expert-panel classes, activated 100% of the expert criteria and produced no pathogenic-to-benign reversals. Data are processed and stored in the European Union (AWS Frankfurt). Plans are based on gigabytes of input data processed, with pay-as-you-go usage above the plan. Innovare Genetics Portal is for research use only. It is not intended for diagnostic use or for the diagnosis, treatment or prevention of disease, and its results are research estimates that require review by a qualified professional.
Highlights
- From raw reads to an interpreted result in one place: upload whole genomes, exomes or targeted gene panels (FASTQ, BAM or VCF) and get GPU-accelerated alignment and variant calling, annotation and a prioritized shortlist of variants for review, without managing any bioinformatics infrastructure.
- Auditable ACMG/AMP classification calibrated to ClinGen recommendations, benchmarked at 90.3% concordance with expert-panel classes on 1,232 ClinGen Evidence Repository variants, with an embedded IGV viewer for read-level review.
- Beyond SNVs and indels: pharmacogenomics (CPIC/DPWG/FDA), HLA/KIR typing, repeat expansions, pseudogene-aware genes, CNV/SV, carrier screening and ancestry-adjusted polygenic risk. EU data hosting. For research use only.
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Pricing
Pricing is based on the duration and terms of your contract with the vendor, and additional usage. You pay upfront or in installments according to your contract terms with the vendor. This entitles you to a specified quantity of use for the contract duration. Usage-based pricing is in effect for overages or additional usage not covered in the contract. These charges are applied on top of the contract price. If you choose not to renew or replace your contract before the contract end date, access to your entitlements will expire.
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Dimension | Description | Cost/month |
|---|---|---|
Starter 50 GB/month | 50 GB input/month (~1 WGS 30x). 20 GB minimum billed per sample. | $150.00 |
Lab 250 GB/month | 250 GB input/month (~5 WGS 30x). 20 GB minimum billed per sample. | $675.00 |
Pro 1,000 GB/month | 1,000 GB input/month (~20 WGS 30x). 20 GB minimum billed per sample. | $2,400.00 |
Dimension | Description | Cost/unit |
|---|---|---|
Additional GB processed | Per GB of input (FASTQ/BAM/VCF) above your plan. 20 GB minimum billed per sample. | $3.00 |
Dimensions summary
You buy a monthly plan based on how much sequencing input you process, measured in gigabytes of FASTQ, BAM, or VCF files. Three plans cover different volumes: Starter at 50 GB, Lab at 250 GB, and Pro at 1,000 GB per month. Each plan bills a 20 GB minimum per sample. When your input exceeds your plan's allowance, the Additional GB processed dimension charges per gigabyte above the included amount. You pick the plan matching your expected monthly volume, then pay the overage rate only if you go over.
Top-of-mind questions for buyers
Input GB measures the size of your uploaded sequencing files: FASTQ, BAM, or VCF. Each sample is billed at a minimum of 20 GB, even if the file is smaller. One whole-genome 30x run equals roughly 50 GB of input. Supported file types align with whole-exome, targeted panel, and microarray data.
When your input exceeds your plan allowance, the Additional GB processed dimension charges per gigabyte above the included amount. Only the overage is billed at the per-GB rate; your base plan fee stays the same. The 20 GB per-sample minimum still applies to each sample you submit.
Plans meter input measured in gigabytes of FASTQ, BAM, or VCF files. The marketplace dimensions bill by data volume, not by physical samples sent for sequencing. For cases starting from a saliva or blood sample where sequencing is not yet done, contact the vendor for scope and pricing.
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Vendor refund policy
Monthly plans can be cancelled at any time and are not renewed. 12-month plans can be refunded in full within 14 days of purchase if no data has been processed. GB already processed and pay-as-you-go usage are non-refundable. Plans can be upgraded at any time with prorated credit. To request a refund, email info@innovaregenetics.com with your AWS account ID and agreement ID; we reply within 2 business days.
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Delivery details
Software as a Service (SaaS)
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Support
Vendor support
Support is provided by email at info@innovaregenetics.com . We reply within 2 business days. Support covers account access and onboarding, use of the platform and its analysis modules, data upload, and reporting of technical issues.
AWS infrastructure support
AWS Support is a one-on-one, fast-response support channel that is staffed 24x7x365 with experienced and technical support engineers. The service helps customers of all sizes and technical abilities to successfully utilize the products and features provided by Amazon Web Services.
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