Whole-genome insight

See more in your DNA.

A comprehensive genome scan designed to look beyond the obvious — examining your DNA across all chromosomes and organizing relevant findings into a clear, human-readable report.

Explore DNA scans ↘ View sample report
Whole-genome analysis Known + research-stage findings Sample identity cross-checks
Genome signal / live view
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About us

Built to look deeper.

Chromosight is a young, ambitious genomics startup built around a simple idea: standard answers are not always enough. Our team brings together scientific curiosity, technology and laboratory biomedicine expertise to investigate genomic data with a broader perspective.

01 / OUR APPROACH

Question assumptions. Follow the data.

We combine established genomic knowledge with research-stage signals, aiming to surface information that narrower tests may not examine.

Comprehensive Designed around whole-genome data rather than a limited panel.
Curious We look beyond standard checklists and investigate context.
Scientific Evidence is separated by maturity, relevance and interpretation.
Human Results are structured to be clear enough to discuss and verify.
Laboratory biomedicine expertise

Our team includes people with a background connected to university-level laboratory biomedicine, bringing scientific discipline into the product.

Product

One scan. A much wider view.

Chromosight analyzes whole-genome data from chromosome to chromosome, screening observed variants against established pathology knowledge and research-stage evidence. The result is organized into a report designed for informed review — not a black box.

01

Whole-genome coverage

The analysis is designed around genome-wide data rather than a small set of predefined genes, providing a broader foundation for variant review.

02

Variant screening

Findings can be compared with curated knowledge on established pathogenic variants and relevant research-stage observations.

03

Identity cross-check

Selected genetically influenced traits can be included as an additional sample-consistency check, helping flag an accidental sample mix-up.

04

Telomere context

Where available, telomere-length information can be presented as a rough biomarker associated with cellular aging. It should not be interpreted as a standalone measure of biological age or overall health.

Genome-wide by design.

Across autosomes and sex chromosomes, subject to sample and sequencing quality.

23 chromosome pairs
DNA report sample

Complex data, made reviewable.

The report is designed to separate different kinds of findings clearly: established clinical relevance, research-stage signals, selected traits and quality/identity checks.

What the report can include

A structured overview helps you understand what was found, how strong the underlying evidence is, and which results may need professional clinical interpretation.

✓Genome-wide variant findings
✓Evidence and significance categories
✓Selected visual / biological traits for sample cross-checking
✓Telomere-length context where available
See sample report ↗
CHROMOSIGHT / DNA REPORT Sample

Genome overview

Illustrative report layout — not real patient data.
FindingCategoryEvidence
Example genomic variantReviewEstablished
Example research signalResearchEmerging
Example carrier findingCarrierEstablished

Sample consistency

Sex chromosome patternExample: XX
Hair pigmentationExample: dark
Telomere contextExample range
Prices

Choose your level of analysis.

Two clear options for customers who want a broad genomic overview or a more extensive premium analysis. Final scope, turnaround time and included report elements can be specified before launch.

Regular DNA analysis
990EUR

A comprehensive entry point for whole-genome analysis and structured reporting.

  • Whole-genome data analysis
  • Screening of relevant genomic variants
  • Structured digital DNA report
  • Selected sample-consistency traits
Ask about Regular
Premium Scan DNA analysis
2,490EUR

A deeper premium review for customers who want the broadest level of genomic investigation.

  • Everything in Regular analysis
  • Expanded review and interpretation workflow
  • Research-stage findings section
  • Extended report context
Ask about Premium
Contact

Ready to see your genome differently?

Talk to us about availability, sample collection, report scope and which analysis is the right fit for you.

Email Chromosight ↗ Compare scans
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Phone Phone to be confirmed