Introduction Version

ID Cards

Short description
OmiX is a suite of tools to perform classic omics data analysis.
How that works?
The OmiX brick allows for a wide variety of bioinformatics analysis, including:

  • Sequence alignment against gene, protein and genome databases
  • Mapping of sequencing data against genomic and gene sequences
  • Gene expression assessment
  • Genome annotation
  • Sequence assembly
  • Variant detection

Applications and benefits

  • Genes alignement against open databases (uniprot, ensembl, NCBI...)
  • Analysing genes expression across samples
  • Genome annotation
  • Genes motifs discovery (enzymes assessment... )
  • Variant calling (SNP, InDels, Structural variations...)
  • ...

Input data

  • Sequences (genes, proteins, sequences, sequencing datasets (genomic, transcriptomique) required


  • Variable analysis time depending on the size of the data, the type of analysis and the specification of the machine used to analyse the data


  • Gencovery team support (assembly, clustering, analysis)
  • Gencovery ecosystem support (we make the connection with the right expert)

Intellectual property

  • You keep IP on your proprietary data, and any related models or insights generated in Constellab™.
  • You keep IP on your custom pipelines, know-how, and bricks created in Constellab™.