J. Hynšt

发表

Bioinformatic strategies for the analysis of genomic aberrations detected by targeted NGS panels with clinical application

Karol Pal, Jakub Hynst, Veronika Navrkalova, 2021, PeerJ.

Distinct p53 phosphorylation patterns in chronic lymphocytic leukemia patients are reflected in the activation of circumjacent pathways upon DNA damage

Š. Pospíšilová, S. Pavlova, V. Mancikova, 2022, Molecular oncology.

Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model

M. Brázdil, Š. Pospíšilová, P. Bencúrová, 2021, Scientific Reports.

Low-burden TP53 mutations in CLL: clinical impact and clonal evolution within the context of different treatment options

Š. Pospíšilová, S. Pavlova, L. Radová, 2021, Blood.

Nextflow in Bioinformatics: Executors Performance Comparison Using Genomics Data

L. Hejtmánek, J. Hynšt, Viktória Spišaková, 2023, Future Gener. Comput. Syst..

LYmphoid NeXt-Generation Sequencing (LYNX) Panel

Š. Pospíšilová, S. Pavlova, K. Plevova, 2021, The Journal of Molecular Diagnostics.

Hierarchical distribution of somatic variants in newly diagnosed chronic myeloid leukaemia at diagnosis and early follow‐up

J. Mayer, Z. Ráčil, Dagmar Smitalova, 2021, British journal of haematology.

Bioinformatic pipelines for whole transcriptome sequencing data exploitation in leukemia patients with complex structural variants

Š. Pospíšilová, L. Radová, V. Bystrý, 2019, PeerJ.

LYNX (LYmphoid NeXt-generation sequencing) panel: a comprehensive capture-based sequencing tool for the analysis of prognostic and predictive markers in lymphoid malignancies.

Š. Pospíšilová, S. Pavlova, K. Pal, 2021, The Journal of molecular diagnostics : JMD.