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

Timing

• 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

Support

• 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™.