The genetic contributions to disease have seen significant advancements due to recent breakthroughs in high-throughput genotyping and next-generation DNA sequencing technologies. These innovations have generated extensive datasets for genome-wide association studies and whole genome/exome sequencing studies..
salle de conférences de la Faculté des Sciences de la Nature et de la Vie
Université Constantine 1 Frères Mentouri.
26. 06. 2024
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PAVAL Lab Director ; Université Grenoble Alpes Saint Martin d'Hères, Gières, France
CRAPast, CNRST, ESSAIA
Neurology, Constantine University Hospital, Constantine, Algeria
