Take reads to annotated variants
Upload FASTQ. Stop at BAM, VCF or annotated VCF.
Genomics & Life Sciences
From sequencing reads to reviewed results.
Five AI modules on one data layer, for people, horses and camels.
Start here
What do you want to do?
Interpret a VCF you already have
Get a reviewable report, every finding with its sources.
See the horse and camel tests
Whole genome, parentage, hereditary panels, markers.
Runs online today: the Human WGS pipeline.
Stop at any stage and download what it produced.
- 01
FASTQ
Your raw reads, R1 and R2.
- 02
BAM
Reads aligned to the reference.
- 03
VCF
Variants called.
- 04
Annotated VCF
Variants annotated.
- 05
Interpretation
Findings with evidence, for clinical review. Not a diagnosis.
Needs a connected Flopexa pipeline service. Without one, the page previews the flow and uploads nothing.
AI modules
Five AI modules. One data layer.
Each reads the same data at a different level, from raw reads to the patient.
For research labs
Research AI
Integrates sequencing and multi-omics data and proposes testable hypotheses, each with its sources.
Explore Research AIFor drug-discovery teams
Therapeutics AI
Ranks targets and biomarkers from genomic and pathway evidence, and models how candidates behave.
Explore Therapeutics AIFor regenerative-medicine labs
Stem Cell AI
Annotates every cell in a single-cell run, reconstructs lineages and compares runs.
Explore Stem Cell AIFor vets and breeders
Veterinary AI
Whole-genome tests for horses and camels, mapped to each species’ own genome.
Explore Veterinary AIFor clinical genetics teams
Clinical AI
Turns an annotated VCF into a reviewable variant report with sources. It informs the team’s judgement; it does not replace it.
Explore Clinical AIGenomic tests
Tests, by species.
Human · WGS runs online today. The other tests are arranged with our team.
Species
Whole-genome sequencing
Every base, coding and non-coding, in one pass.
Whole-exome sequencing
The protein-coding regions, at high depth.
Non-invasive prenatal testing
Fetal DNA read from a maternal blood sample.
Preimplantation testing for aneuploidy
Chromosome counts screened before transfer.
Whole-genome sequencing
Mapped to the horse reference genome, not a human one.
Parentage verification
Sire and dam confirmed from one sample.
Hereditary disease panel
Known variants of consequence for the breed.
Performance markers
Trait-associated variants, with their evidence.
Whole-genome sequencing
Mapped to the camel reference genome.
Parentage verification
Lineage confirmed from one sample.
Hereditary disease panel
Inherited risk screened from one sample.
Racing markers
Trait-associated variants, with their evidence.
Ready to run your first sample?
Start from FASTQ, or interpret a VCF you already have.