Other bioinformatics analysis
Our experts work directly on your Sanger, Roche or Illumina raw data: their experience ensures quality and help for results interpretation.
- Genomic capture : individual et comparative analysis of captured regions
- Mutations detection: genes, amplicons and post-exome analysis: assembly and mapping, listing and study of the mutations, position of the mutations according to the nomenclature, transcription in amino-acids
- ChipSeq: reference database creation, mapping, genes identification, comparison of the samples regulated by the same transcription factor
- Statistic analysis of Roche Diagnostics® genotyping results
- Analysis of BeadExpress®, Illumina® genotyping results, as well as other methods (imbalance linkage maps, haplotype…)
- Design of specific or multiplex primers
- MLST or MIRU-VNTR typing data analysis with data management
If you need any other analysis, please do not hesitate to contact us to discuss it.