biostudies-literatureKolarikova KMinisterstvo Zdravotnictví Ceské RepublikyMinisterstvo Vnitra České RepublikyEuropean Regional Development Fund817713https://www.ebi.ac.uk/biostudies/studies/S-EPMC8968137biostudies-literatureUnknown16Parkinsonism belongs to the most common neurodegenerative disease. Genetic predisposition could be one of the significant risk factor for disease development. It has been described higher prevalence of parkinsonism in large pedigree from southeastern Moravia region. The study aims were to select accessible subfamily trios from the pedigree suitable for segregation genetic analyses to perform whole exome sequencing (WES) in trio individuals and further to evaluate genetic variants in the each trio. We used IonTorrent platform for WES for five subfamily trios (1-5). Each trio included two affected and one healthy person (as control). Found variants were filtered with respect to MAF < 1% (minor allele frequency), variants effect (based on prediction tools) and disease filter (Parkinsonism resFrontiers in neuroscienceWhole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development.PMC8968137CZ.02.1.01/0.0/0.0/16_019/0000868FNOL,00098892VI2017202010215-32715AVrtel RKolarikova KKanovsky PStellmachova JProchazka MMensikova KVodicka RfalseWhole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development.Parkinsonism belongs to the most common neurodegenerative disease. Genetic predisposition could be one of the significant risk factor for disease development. It has been described higher prevalence of parkinsonism in large pedigree from southeastern Moravia region. The study aims were to select accessible subfamily trios from the pedigree suitable for segregation genetic analyses to perform whole exome sequencing (WES) in trio individuals and further to evaluate genetic variants in the each trio. We used IonTorrent platform for WES for five subfamily trios (1-5). Each trio included two affected and one healthy person (as control). Found variants were filtered with respect to MAF < 1% (minor allele frequency), variants effect (based on prediction tools) and disease filter (Parkinsonism res2022-01-01T00:00:00Z20222025-04-05T11:03:18.28Z2025-04-05T11:03:18.28ZS-EPMC89681373536828810.3389/fnins.2022.817713