DeepNGS automates the workflow of gene analyses and can assist in diagnostic procedures.

In Next Generation Sequencing, the analysis of genomics data requires a standardised pipeline that will help clinicians and researchers obtain explicit and comprehensive information.

What is
What is

Achieve a higher level of accuracy by incorporating all the patient's genetic data in a secure, agile and easy-to-use platform. Capable of digesting information to ensure the accuracy of the final diagnosis and the adequacy of treatment recommendations.

Main Features

Optimized NGS pipeline

Processing multiple data sources and formats

Whole Genome & Exome/Targeted Sequencing files
Whole Genome & Exome/Targeted Sequencing files

Raw sequencing data (FASTQ)
Genetic variant files (VCF)
Sequence alignment maps (SAM, BAM)
Annotated files (VEP)

Medical records
Medical records

Genetic databases
Patient histories
Phenotypic data

Different sequence sources
Different sequence sources

Formalin-Fixed Paraffin-Embedded (FFPE) samples
Liquid biopsies/cfDNA (circulating free DNA)
Germline/hereditary diseases
Somatic abnormalities (tumor sequencing)

Detection of different variant types and mutations

  • Single Nucleotide Variants and INDELs (small insertions and deletions)
  • Large Structural Variants
  • Copy Number Variants
  • Genomic Fusions and Rearrangements

Automatic Analysis

Secondary and tertiary analysis of sequencing samples without having to manually modify the parameters

Automatic Analysis
Automatic Analysis

Intuitive design & Interactive graphics

  • Advanced visualization techniques
  • Fully optimized and adapted to the needs of genetic data
  • Simple and intuitive display of useful information
  • Comfortable & user-friendly interface