Your genome already has a reference but you want to go further in it analysis by identifying small events (identification of SNPs, small insertions or deletions) or structural events (translocations, duplications, insertions or deletions) ?

According to your specific issues, our team will advise you on the most appropriate strategy considering your genome size and complexity.

Thus, the combination
of different existing libraries (Shotgun, Paired-End and Mate-Paired) and lengths of reads fromHiSeq2500 or GsFLX sequencerswill permit to offer you the methodology that best meets your needs and will provide quality results.

Our team of bioinformaticians can help you in analyzing your data. Find our solutions in bioinformatics

Do not hesitate to contact us for an appropriate training. Find our training solutions


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