Juraj Gazdarica

发表

Adaptable Model Parameters in Non-Invasive Prenatal Testing Lead to More Stable Predictions

T. Szemeš, F. Duris, J. Turňa, 2019, International journal of molecular sciences.

Innovative method for reducing uninformative calls in non-invasive prenatal testing

Frantisek Duris, Marcel Kucharík, Lucia Strieskova, 2018, bioRxiv.

Repression of a large number of genes requires interplay between homologous recombination and HIRA

Z. Benko, T. Szemeš, L. Cipak, 2021, Nucleic acids research.

Telomere Length Changes in Cancer: Insights on Carcinogenesis and Potential for Non-Invasive Diagnostic Strategies

O. Pös, T. Szemeš, R. Saade, 2023, Genes.

Mean and variance of ratios of proportions from categories of a multinomial distribution

T. Szemeš, F. Duris, J. Turňa, 2018 .

SnakeLines: integrated set of computational pipelines for sequencing reads pdf

Frantisek Duris, Jaroslav Budis, Jan Radvanszky, 2021, J. Integr. Bioinform..

Evaluation and limitations of different approaches among COVID-19 fatal cases using whole-exome sequencing data

P. Babál, T. Szemeš, R. Hekel, 2023, BMC Genomics.

Seasonal changes of circulating 25-hydroxyvitamin D correlate with the lower gut microbiome composition in inflammatory bowel disease patients

T. Szemeš, J. Turňa, K. Šoltys, 2020, Scientific Reports.

On the critical evaluation and confirmation of germline sequence variants identified using massively parallel sequencing.

Frantisek Duris, Ludevit Kadasi, Jan Radvanszky, 2019, Journal of biotechnology.

Non-invasive prenatal testing as a valuable source of population specific allelic frequencies

T. Szemeš, B. Nagy, G. Minárik, 2018, bioRxiv.

Understanding genetic variability: exploring large-scale copy number variants through non-invasive prenatal testing in European populations

T. Szemeš, M. Kucharík, J. Budiš, 2024, BMC genomics.