Platform

A complete genomics toolkit.

Industry-standard tools, wrapped in a managed, reproducible runtime. Pick a workflow, point it at your data, and let GenoSeq handle orchestration, scaling, and reporting.

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Alignment

BWA-MEM2 and minimap2 for short and long reads, with automatic duplicate marking and sorting.

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Variant calling

GATK HaplotypeCaller, DeepVariant, and Strelka2 with ensemble consensus for germline and somatic calls.

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De novo assembly

SPAdes, Flye, and hifiasm assemblies with HiC scaffolding and BUSCO quality assessment.

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Quality control

FastQC, MultiQC, and custom coverage/Q-metrics rolled into a single interactive report.

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Annotation

VEP- and ANNOVAR-based annotation against ClinVar, gnomAD, dbSNP, and custom panels.

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Workflow engine

WDL and Nextflow-compatible runtime with retry, caching, and scatter-gather out of the box.

Pricing that scales with your lab

Start free. Upgrade when your sample volume grows.

Free

$0

50 GB processing / month · 100 GB storage · Community support.

Team

$290 / mo

2 TB processing · 1 TB storage · Priority queues · Shared projects.

Enterprise

Custom

Dedicated compute · SSO & audit logs · On-prem option · 24/7 support.

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