AltaGene aims to facilitate the implementation of high-throughput sequencing (NGS) and bioinformatics methods in the medical sector across the regions of the Maghreb and North Africa. Our company provides you with a team of specialized experts in genomics and bioinformatics, boasting more than fourteen years of experience. We work together with you to propel the advancement of precision medicine for the betterment of your patients. As the exclusive representative of the company 3Billion. AltaGene offers high-throughput sequencing services, including:
•    Easy sample collection using DBS cards.
•    Genome sequencing reaching a minimum depth of coverage of 30X. Sequencing comes with a full report on SNVs, INDELs and structural variants such as CNVs.
•    Exome sequencing reaching a minimum depth of coverage of 100X. Sequencing comes with a full report on SNVs, INDELs and structural variants such as CNVs. 
•    Mitochondrial genome sequencing is provided free of charge with genome and exome sequencing reching a minimum depth of coverage of 1000X.
•    Bioinformatics analysis for prioritizing and classifying variants based on well maintaining and highly curated in house databases and using cutting edge AI algorithms of phenotype detection. All sequenced samples are regularly re-analyzed.