Analysis and Identification of Mutations in Affected or Carriers of Hereditary Pathology, Study and Determination of Mutations from Acquired Genetics (Tumors, Leukemia), Individual DNA Genotyping Molecular Tests; Microarrays: Principles, Applications and Analysis; DNA Sequencing: from the Classical Method to NGS Techniques, and Analysis of NGS Data and Their Problems, Diagnosis, Monitoring, Severity and Individual Variability by Molecular Deficiency; DNA Mitochondrial; Analysis and Interpretation of Results Identifying Healthy Carriers (Families, and Population Screening), Preclinical and / or Presintomatic Tests, Genetic Polymorphisms Associated with drugs Metabolism.
