Author

Martina Sekelská

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:DNA methylation· 1 Organism:human· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Bálint NagyiD· 2 shared František ĎurišiD· 2 shared Gabriel MinárikiD· 2 shared Iveta Gazdaricova· 2 shared Ján RadvánszkyiD· 2 shared Jaroslav BudišiD· 2 shared Juraj GazdaricaiD· 2 shared Lucia Striešková· 2 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Bálint NagyORCID

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2 papers

Recent·Most cited

GenomicsJournal of BiotechnologyPeer-reviewedMay 1, 2019

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

Jaroslav Budiš, Juraj Gazdarica, Ján Radvánszky…·Tomáš Szemes

This study uses NIPT data to determine population-specific allelic frequencies of small DNA variants at low cost, showing high reliability through in silico and wet lab validation.

28 citations

humanwhole-genome sequencing

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BioinformaticsbioRxivPreprintJun 22, 2018

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

Jaroslav Budiš, Juraj Gazdarica, Ján Radvánszky…·Tomáš Szemes

The paper introduces a method to reduce uninformative calls in NIPT by analyzing the length profile of circulating cell-free DNA, improving resolution of ambiguous results when combined with z-scores.

1 citation

DNA methylationstatistical model

𝕏 PostBluesky