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Indicative prices · VAT included

Transparency in pricing

All prices include sequencing, bioinformatic analysis and signed clinical report. Volume discounts and academic institution rates available.

For individuals

Clinical Exome

Diagnosis of genetic diseases

300
Medical prescription required
  • 20,000+ genes analyzed
  • ACMG variant classification
  • Complete clinical report
  • Genetic counseling
  • 4–6 week turnaround

Fertility Test

Carrier screening

200
Per person · Couple pack €350
  • 300+ recessive diseases
  • Couple analysis available
  • Integration with IVF clinics
  • Genetic counseling
  • 3–4 week turnaround

For researchers and centers

Whole Genome (WGS)

30x human · Extraction, library, DNBSEQ sequencing, FASTQ and optional bioinformatic analysis.

FROM 500 €
Volume discounts

Whole Exome (WES)

100x · Exonic capture, DNBSEQ sequencing, FASTQ and optional bioinformatic analysis.

FROM 300 €
Volume discounts

RNA-seq

mRNA / total RNA · Stranded library, PE150, 12 Gb/sample, optional differential expression analysis.

FROM 200 €
Per sample

Targeted panels

Custom or predesigned · Design, capture, deep sequencing (>500x), FASTQ and optional analysis.

FROM 200 €
Depending on panel and volume

Bioinformatics

Standalone analysis for existing NGS data. Alignment, variant calling, annotation, ACMG interpretation and report.

FROM 150 €
Per sample

Metagenomics

16S rRNA (V3–V4) or shotgun metagenomics. Taxonomic classification and functional analysis.

FROM 200 €
Per sample

Note — Prices are indicative and may vary depending on volume, project complexity and additional services. Discounts available for projects of more than 20 samples, academic institutions and long-term collaborations.

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OmicaLabs