PRICE LIST

We always strive to offer attractive prices with the highest analysis quality. Below you will find an excerpt from our portfolio. The complete current price list is available for download.

OUR CURRENT PRICE LIST

Should the desired analysis not be listed here, or if you have questions about our prices, please do not hesitate to contact us.

SINGLE GENE ANALYSES

Analysis of a predefined disease-relevant gene
€ 895 excl. VAT
  • Sequencing of all coding regions of the genome (exons) including flanking regions
  • Evaluation of a gene according to requirements
  • Detection of single nucleotide variants (SNVs), smaller insertions/deletions (Indels), and copy number variations (CNVs)
  • Medical-genetic specialist
    report
TO THE SERVICE CATALOG
for detailed information
NGS

PANEL ANALYSES

Analysis of predefined disease-relevant genes
€ 995 excl. VAT
  • Sequencing of all coding regions of the genome (exons) including flanking regions
  • Selection of genes to be evaluated (panels) based on suspected diagnosis using PanelApp UK
  • Detection of single nucleotide variants (SNVs), smaller insertions/deletions (Indels), and copy number variations (CNVs)
  • Medical-genetic specialist
    report
TO THE SERVICE CATALOG
for detailed information
NGS

EXOME ANALYSIS

Analysis of all phenotypically relevant genes
€ 1095 excl. VAT
  • Sequencing of all coding regions of the genome (exons) including flanking regions
  • Selection of genes to be evaluated based on clinical characteristics (phenotype) using HPO Terms
  • Detection of single nucleotide variants (SNVs), smaller insertions/deletions (Indels), and copy number variations (CNVs)
  • Medical-genetic specialist
    report
TO THE SERVICE CATALOG
for detailed information
NGS

TRIO EXOME ANALYSIS

Exome sequencing of a child and both parents
€ 2750 excl. VAT
  • Sequencing of all coding regions of the genome (exons) including flanking regions
  • Selection of genes to be evaluated based on clinical characteristics (phenotype) using HPO Terms
  • Detection of single nucleotide variants (SNVs), smaller insertions/deletions (Indels), and copy number variations (CNVs)
  • Targeted search for de novo variants (new mutations) and compound heterozygosity
TO THE SERVICE CATALOG
for detailed information
NGS

NGS Express Processing

If you require your patient’s NGS test results even faster (within approximately 10 working days), we offer the option of express processing

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