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™.
