Memory-efficient RNA energy landscape exploration

por Mann, Martin, Kucharík, Marcel, Flamm, Christoph, Wolfinger, Michael T.
Publicado 2014

Pseudoknots in RNA folding landscapes

por Kucharík, Marcel, Hofacker, Ivo L., Stadler, Peter F., Qin, Jing
Publicado 2016

Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH

por Kucharík, Marcel, Budiš, Jaroslav, Hýblová, Michaela, Minárik, Gabriel, Szemes, Tomáš
Publicado 2021

Privacy-preserving storage of sequenced genomic data

por Hekel, Rastislav, Budis, Jaroslav, Kucharik, Marcel, Radvanszky, Jan, Pös, Zuzana, Szemes, Tomas
Publicado 2021

Maternal Copy Number Imbalances in Non-Invasive Prenatal Testing: Do They Matter?

por Hyblova, Michaela, Gnip, Andrej, Kucharik, Marcel, Budis, Jaroslav, Sekelska, Martina, Minarik, Gabriel
Publicado 2022

Identification of Structural Variation from NGS-Based Non-Invasive Prenatal Testing

por Pös, Ondrej, Budis, Jaroslav, Kubiritova, Zuzana, Kucharik, Marcel, Duris, Frantisek, Radvanszky, Jan, Szemes, Tomas
Publicado 2019

Validation of Copy Number Variants Detection from Pregnant Plasma Using Low-Pass Whole-Genome Sequencing in Noninvasive Prenatal Testing-Like Settings

por Hyblova, Michaela, Harsanyova, Maria, Nikulenkov-Grochova, Diana, Kadlecova, Jitka, Kucharik, Marcel, Budis, Jaroslav, Minarik, Gabriel
Publicado 2020

Combination of Fetal Fraction Estimators Based on Fragment Lengths and Fragment Counts in Non-Invasive Prenatal Testing

por Gazdarica, Juraj, Hekel, Rastislav, Budis, Jaroslav, Kucharik, Marcel, Duris, Frantisek, Radvanszky, Jan, Turna, Jan, Szemes, Tomas
Publicado 2019

Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions

por Kucharik, Marcel, Gnip, Andrej, Hyblova, Michaela, Budis, Jaroslav, Strieskova, Lucia, Harsanyova, Maria, Pös, Ondrej, Kubiritova, Zuzana, Radvanszky, Jan, Minarik, Gabriel, Szemes, Tomas
Publicado 2020

Result of Prospective Validation of the Trisomy Test(®) for the Detection of Chromosomal Trisomies

por Sekelska, Martina, Izsakova, Anita, Kubosova, Katarina, Tilandyova, Petra, Csekes, Erika, Kuchova, Zaneta, Hyblova, Michaela, Harsanyova, Maria, Kucharik, Marcel, Budis, Jaroslav, Szemes, Tomas, Minarik, Gabriel
Publicado 2019

Combination of expert guidelines-based and machine learning-based approaches leads to superior accuracy of automated prediction of clinical effect of copy number variations

por Sládeček, Tomáš, Gažiová, Michaela, Kucharík, Marcel, Zaťková, Andrea, Pös, Zuzana, Pös, Ondrej, Krampl, Werner, Tomková, Erika, Hýblová, Michaela, Minárik, Gabriel, Radvánszky, Ján, Budiš, Jaroslav, Szemes, Tomáš
Publicado 2023