GenoSeq runs reproducible alignment, assembly, and variant-calling pipelines on managed cloud infrastructure — so your lab can go from FASTQ to insight without babysitting a cluster.
A complete toolkit for genomics workflows, from raw basecalling to annotated variant reports — all versioned, all reproducible.
Compose BWA, minimap2, GATK, and DeepVariant steps into shareable, parameterized workflows with one click.
Elastic GPU and CPU pools spin up per run. Pay only for the wall-clock minutes your samples actually use.
MultiQC-style dashboards, coverage plots, and VCF summaries generated automatically for every completed run.
HIPAA- and GDPR-aligned controls, encryption at rest, and full audit logs across every dataset and job.
Every analysis is pinned to exact tool versions and reference genomes. Rerun any job and get byte-identical output.
Share projects with collaborators, set fine-grained permissions, and publish results to your lab group in one click.
From upload to annotated report, GenoSeq handles orchestration so you can focus on the biology.
Upload FASTQ/BAM or pull directly from your sequencer or SRA.
Short- and long-read alignment against GRCh38 or custom references.
Germline and somatic variant calling with ensemble consensus.
ClinVar, gnomAD, and VEP annotation with filterable reports.
Free tier includes 50 GB of processing and 100 GB of storage. No credit card to start.
Create a free account