• Human genetic diagnostic services

    Gene panels, targeted sequencing, WES, WGS

Identify the cause of genetic diseases!

omics2view.consulting GbR and our partners have long-standing experience in NGS diagnostics. We recommend whole-genome or whole-exome sequencing to investigate a broad spectrum of genes for possible causes of diverse genetic diseases. Alternatively, the following gene panels are available for specific entities:

  • Comprehensive Tumor Panel (636 genes)*
  • Hereditary Cancer Panel (f 74 genes, m 79 genes)
  • Hereditary Breast and Ovarian Cancer (26 genes)
  • BRCA1 & BCRA2 (2 genes)
  • Gastric Cancer (14 genes)
  • Renal Carcinoma (11 genes)
  • Prostate Cancer (13 genes)
  • Melanoma (2 genes)
  • Multiple Endocrine Neoplasia (3 genes)
  • Thyroid Cancer (2 genes)

Material: Saliva, blood, DNA
*Material: Tissue, Liquid biopsy sample (whole blood)

  • Parathyroid Carcinoma (2 genes)
  • Familial Paraganglioma (5 genes)
  • Retinoblastoma (1 gene)
  • Chondrosarcoma (2 genes)
  • Colorectal Cancer (23 genes)
  • Pancreatic Cancer (12 genes)
  • Endometrial Cancer (11 genes)
  • Gastrointestinal Stromal Tumor (7 genes)
  • Neurofibromatosis (2 genes)
  • Pheochromocytoma (9 genes)

Consulting

Aspects of subsequent bioinformatic and statistical data analysis must be taken into account as early as the project planning stage. Get profound assistance to lead your project to success.